Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 3426 |
| ensemblid | ENSG00000205403.15 |
| hgncid | 5394 |
| symbol | CFI |
| name | complement factor I |
| refseq_nuc | NM_000204.5 |
| refseq_prot | NP_000195.3 |
| ensembl_nuc | ENST00000394634.7 |
| ensembl_prot | ENSP00000378130.2 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 109740695 |
| end | 109801999 |
| strand | - |
| ver | v1.2 |
| region | chr4:109740695-109801999 |
| region5000 | chr4:109735695-109806999 |
| regionname0 | CFI_chr4_109740695_109801999 |
| regionname5000 | CFI_chr4_109735695_109806999 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 583 | 310 | 77 | 63 | 134 | 14 | 21 | 108 | CFI_chr4_109735695_109806999 | CFI | MKLLH others(578): Show |
chr4 | 109735695 | 109806999 |
| a0002 | 0/0 | 583 | 17 | 0 | 0 | 15 | 0 | 2 | 9 | CFI_chr4_109735695_109806999 | CFI | MKLLH others(578): Show |
chr4 | 109735695 | 109806999 |
| a0003 | 1/0 | 583 | 15 | 13 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | MKLLH others(578): Show |
chr4 | 109735695 | 109806999 |
| a0004 | 0/0 | 583 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | CFI_chr4_109735695_109806999 | CFI | MKLLH others(578): Show |
chr4 | 109735695 | 109806999 |
| a0005 | 0/0 | 583 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | MKLLH others(578): Show |
chr4 | 109735695 | 109806999 |
| a0006 | 0/0 | 583 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | MKLLH others(578): Show |
chr4 | 109735695 | 109806999 |
| a0007 | 0/0 | 583 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | MKLLH others(578): Show |
chr4 | 109735695 | 109806999 |
| a0008 | 0/0 | 583 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | MKLLH others(578): Show |
chr4 | 109735695 | 109806999 |
| a0009 | 0/0 | 583 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CFI_chr4_109735695_109806999 | CFI | MKLLH others(578): Show |
chr4 | 109735695 | 109806999 |
| a0010 | 0/0 | 583 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | MKLLH others(578): Show |
chr4 | 109735695 | 109806999 |
| a0011 | 0/0 | 583 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | MKLLH others(578): Show |
chr4 | 109735695 | 109806999 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1749 | 182 | 48 | 32 | 72 | 12 | 17 | CFI_chr4_109735695_109806999 | CFI | ATGAA others(1744): Show |
chr4 | 109735695 | 109806999 | ||
| a0001c0002 | 0/0 | 1749 | 124 | 25 | 31 | 62 | 2 | 4 | CFI_chr4_109735695_109806999 | CFI | ATGAA others(1744): Show |
chr4 | 109735695 | 109806999 | ||
| a0001c0006 | 0/0 | 1749 | 2 | 2 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | ATGAA others(1744): Show |
chr4 | 109735695 | 109806999 | ||
| a0001c0008 | 0/0 | 1749 | 2 | 2 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | ATGAA others(1744): Show |
chr4 | 109735695 | 109806999 | ||
| a0002c0003 | 0/0 | 1749 | 17 | 0 | 0 | 15 | 0 | 2 | CFI_chr4_109735695_109806999 | CFI | ATGAA others(1744): Show |
chr4 | 109735695 | 109806999 | ||
| a0003c0004 | 1/0 | 1749 | 15 | 13 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | ATGAA others(1744): Show |
chr4 | 109735695 | 109806999 | ||
| a0004c0005 | 0/0 | 1749 | 4 | 0 | 0 | 4 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | ATGAA others(1744): Show |
chr4 | 109735695 | 109806999 | ||
| a0005c0007 | 0/0 | 1749 | 2 | 0 | 2 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | ATGAA others(1744): Show |
chr4 | 109735695 | 109806999 | ||
| a0006c0014 | 0/0 | 1749 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | ATGAA others(1744): Show |
chr4 | 109735695 | 109806999 | ||
| a0007c0013 | 0/0 | 1749 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | ATGAA others(1744): Show |
chr4 | 109735695 | 109806999 | ||
| a0008c0011 | 0/0 | 1749 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | ATGAA others(1744): Show |
chr4 | 109735695 | 109806999 | ||
| a0009c0010 | 0/0 | 1749 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | ATGAA others(1744): Show |
chr4 | 109735695 | 109806999 | ||
| a0010c0012 | 0/0 | 1749 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | ATGAA others(1744): Show |
chr4 | 109735695 | 109806999 | ||
| a0011c0009 | 0/0 | 1749 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | ATGAA others(1744): Show |
chr4 | 109735695 | 109806999 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1978 | 174 | 40 | 32 | 72 | 12 | 17 | CFI_chr4_109735695_109806999 | CFI | AGAGA others(1973): Show |
chr4 | 109735695 | 109806999 |
| a0001c0001t0002 | 0/0 | 1978 | 3 | 3 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | AGAGA others(1973): Show |
chr4 | 109735695 | 109806999 |
| a0001c0001t0003 | 0/0 | 1978 | 5 | 5 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | AGAGA others(1973): Show |
chr4 | 109735695 | 109806999 |
| a0001c0002t0001 | 0/0 | 1978 | 114 | 19 | 27 | 62 | 2 | 4 | CFI_chr4_109735695_109806999 | CFI | AGAGA others(1973): Show |
chr4 | 109735695 | 109806999 |
| a0001c0002t0002 | 0/0 | 1978 | 6 | 5 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | AGAGA others(1973): Show |
chr4 | 109735695 | 109806999 |
| a0001c0002t0003 | 0/0 | 1978 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | AGAGA others(1973): Show |
chr4 | 109735695 | 109806999 |
| a0001c0002t0004 | 0/0 | 1978 | 3 | 0 | 3 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | AGAGA others(1973): Show |
chr4 | 109735695 | 109806999 |
| a0001c0006t0005 | 0/0 | 1978 | 2 | 2 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | AGAGA others(1973): Show |
chr4 | 109735695 | 109806999 |
| a0001c0008t0001 | 0/0 | 1978 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | AGAGA others(1973): Show |
chr4 | 109735695 | 109806999 |
| a0001c0008t0002 | 0/0 | 1978 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | AGAGA others(1973): Show |
chr4 | 109735695 | 109806999 |
| a0002c0003t0001 | 0/0 | 1978 | 17 | 0 | 0 | 15 | 0 | 2 | CFI_chr4_109735695_109806999 | CFI | AGAGA others(1973): Show |
chr4 | 109735695 | 109806999 |
| a0003c0004t0001 | 0/0 | 1978 | 12 | 11 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | AGAGA others(1973): Show |
chr4 | 109735695 | 109806999 |
| a0003c0004t0002 | 1/0 | 1978 | 3 | 2 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | AGAGA others(1973): Show |
chr4 | 109735695 | 109806999 |
| a0004c0005t0001 | 0/0 | 1978 | 4 | 0 | 0 | 4 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | AGAGA others(1973): Show |
chr4 | 109735695 | 109806999 |
| a0005c0007t0001 | 0/0 | 1978 | 2 | 0 | 2 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | AGAGA others(1973): Show |
chr4 | 109735695 | 109806999 |
| a0006c0014t0001 | 0/0 | 1978 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | AGAGA others(1973): Show |
chr4 | 109735695 | 109806999 |
| a0007c0013t0001 | 0/0 | 1978 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | AGAGA others(1973): Show |
chr4 | 109735695 | 109806999 |
| a0008c0011t0001 | 0/0 | 1978 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | AGAGA others(1973): Show |
chr4 | 109735695 | 109806999 |
| a0009c0010t0001 | 0/0 | 1978 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | AGAGA others(1973): Show |
chr4 | 109735695 | 109806999 |
| a0010c0012t0001 | 0/0 | 1978 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | AGAGA others(1973): Show |
chr4 | 109735695 | 109806999 |
| a0011c0009t0001 | 0/0 | 1978 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | AGAGA others(1973): Show |
chr4 | 109735695 | 109806999 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0298 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0002g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0003g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0003g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0001t0003g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0004g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0004g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0002t0004g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0006t0005g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0006t0005g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0008t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0001c0008t0002g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0002c0003t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0002c0003t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0002c0003t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0002c0003t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0002c0003t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0002c0003t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0002c0003t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0002c0003t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0002c0003t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0002c0003t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0002c0003t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0002c0003t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0002c0003t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0002c0003t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0002c0003t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0002c0003t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0002c0003t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0003c0004t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0003c0004t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0003c0004t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0003c0004t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0003c0004t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0003c0004t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0003c0004t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0003c0004t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0003c0004t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0003c0004t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0003c0004t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0003c0004t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0003c0004t0002g0026 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0003c0004t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0004c0005t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0004c0005t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0004c0005t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0004c0005t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0005c0007t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0005c0007t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0006c0014t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0007c0013t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0008c0011t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0009c0010t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0010c0012t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| a0011c0009t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0267 | EUR | GBR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0261 | EUR | GBR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0170 | EUR | FIN | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0203 | EUR | FIN | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0035 | EUR | FIN | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0202 | EUR | FIN | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | CHS | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | CHS | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0052 | EAS | CHS | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0125 | EAS | CHS | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0113 | EAS | CHS | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG00609 | hp2 | a0001 | c0002 | t0001 | g0137 | EAS | CHS | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG00673 | hp1 | a0002 | c0003 | t0001 | g0300 | EAS | CHS | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0116 | EAS | CHS | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0043 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0291 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG00738 | hp1 | a0003 | c0004 | t0001 | g0155 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0075 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0040 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01070 | hp1 | a0001 | c0002 | t0004 | g0018 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0127 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01071 | hp1 | a0001 | c0002 | t0004 | g0017 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0079 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01074 | hp1 | a0005 | c0007 | t0001 | g0047 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01074 | hp2 | a0001 | c0002 | t0001 | g0196 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01081 | hp1 | a0005 | c0007 | t0001 | g0046 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0076 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0045 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01106 | hp2 | a0006 | c0014 | t0001 | g0038 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0321 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0072 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0094 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0119 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01243 | hp2 | a0001 | c0002 | t0001 | g0134 | AMR | PUR | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | CLM | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01255 | hp2 | a0001 | c0002 | t0002 | g0107 | AMR | CLM | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | CLM | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0048 | AMR | CLM | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01257 | hp2 | a0001 | c0002 | t0004 | g0016 | AMR | CLM | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0049 | AMR | CLM | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | CLM | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0077 | AMR | CLM | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | CLM | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | CLM | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0084 | EUR | IBS | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0215 | EUR | IBS | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | IBS | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0198 | EUR | IBS | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0085 | EUR | IBS | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | IBS | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01891 | hp2 | a0003 | c0004 | t0002 | g0024 | AFR | ACB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0078 | AMR | PEL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01975 | hp1 | a0007 | c0013 | t0001 | g0290 | AMR | PEL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0059 | AMR | PEL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01978 | hp1 | a0001 | c0002 | t0001 | g0044 | AMR | PEL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0141 | AMR | PEL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0050 | AMR | PEL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0037 | AMR | PEL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0089 | AMR | PEL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PEL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0069 | EAS | KHV | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0022 | EAS | KHV | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0138 | EAS | KHV | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02027 | hp2 | a0002 | c0003 | t0001 | g0307 | EAS | KHV | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0288 | AFR | ACB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02055 | hp2 | a0003 | c0004 | t0001 | g0031 | AFR | ACB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0143 | EAS | KHV | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0130 | EAS | KHV | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0122 | EAS | KHV | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0053 | EAS | KHV | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02080 | hp2 | a0002 | c0003 | t0001 | g0312 | EAS | KHV | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0105 | AFR | ACB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02148 | hp1 | a0001 | c0002 | t0001 | g0093 | AMR | PEL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | PEL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02155 | hp1 | a0002 | c0003 | t0001 | g0299 | EAS | CDX | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | CDX | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0083 | EAS | CDX | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | CDX | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02257 | hp1 | a0003 | c0004 | t0001 | g0030 | AFR | ACB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02257 | hp2 | a0001 | c0002 | t0002 | g0023 | AFR | ACB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0090 | AFR | ACB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02258 | hp2 | a0001 | c0001 | t0003 | g0013 | AFR | ACB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0289 | AFR | ACB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02280 | hp2 | a0001 | c0002 | t0001 | g0140 | AFR | ACB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | PEL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0074 | AMR | PEL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02451 | hp2 | a0001 | c0002 | t0001 | g0106 | AFR | ACB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02523 | hp1 | a0002 | c0003 | t0001 | g0314 | EAS | KHV | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | KHV | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02615 | hp1 | a0008 | c0011 | t0001 | g0108 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0332 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0323 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02622 | hp2 | a0003 | c0004 | t0001 | g0003 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02630 | hp1 | a0003 | c0004 | t0001 | g0032 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02647 | hp1 | a0001 | c0006 | t0005 | g0098 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02647 | hp2 | a0003 | c0004 | t0001 | g0025 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0080 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0316 | SAS | PJL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02738 | hp2 | a0009 | c0010 | t0001 | g0036 | SAS | PJL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02809 | hp1 | a0001 | c0002 | t0003 | g0280 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0320 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0041 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02886 | hp2 | a0003 | c0004 | t0001 | g0154 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0337 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02896 | hp2 | a0003 | c0004 | t0001 | g0027 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02897 | hp1 | a0003 | c0004 | t0001 | g0028 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0158 | AFR | ESN | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0324 | AFR | ESN | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02970 | hp1 | a0003 | c0004 | t0001 | g0157 | AFR | ESN | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0326 | AFR | ESN | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0287 | AFR | ESN | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ESN | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03041 | hp1 | a0001 | c0006 | t0005 | g0099 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0112 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0327 | AFR | MSL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0334 | AFR | ESN | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03130 | hp2 | a0003 | c0004 | t0002 | g0029 | AFR | ESN | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0286 | AFR | ESN | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0322 | AFR | ESN | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0153 | AFR | ESN | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | ESN | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0329 | AFR | MSL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03209 | hp2 | a0001 | c0002 | t0002 | g0100 | AFR | MSL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | MSL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0281 | AFR | MSL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0128 | SAS | PJL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03239 | hp2 | a0002 | c0003 | t0001 | g0315 | SAS | PJL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03453 | hp1 | a0001 | c0002 | t0002 | g0126 | AFR | MSL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0330 | AFR | MSL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0292 | AFR | MSL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | MSL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0042 | AFR | ESN | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03516 | hp2 | a0001 | c0008 | t0002 | g0271 | AFR | ESN | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0139 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03540 | hp2 | a0003 | c0004 | t0001 | g0003 | AFR | GWD | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03579 | hp1 | a0001 | c0008 | t0001 | g0272 | AFR | MSL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03579 | hp2 | a0003 | c0004 | t0001 | g0297 | AFR | MSL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0039 | SAS | PJL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03831 | hp1 | a0002 | c0003 | t0001 | g0317 | SAS | BEB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0274 | SAS | BEB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0152 | SAS | BEB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | BEB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0270 | SAS | STU | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | STU | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | BEB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG04184 | hp2 | a0001 | c0002 | t0001 | g0102 | SAS | BEB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0264 | SAS | STU | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0197 | SAS | STU | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0266 | SAS | STU | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | STU | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | YRI | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0133 | AFR | YRI | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0135 | EAS | CHB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | CHB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0054 | EAS | CHB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18747 | hp2 | a0002 | c0003 | t0001 | g0305 | EAS | CHB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | YRI | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0285 | AFR | YRI | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18939 | hp2 | a0001 | c0002 | t0001 | g0103 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18941 | hp2 | a0004 | c0005 | t0001 | g0086 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18946 | hp2 | a0001 | c0002 | t0001 | g0057 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18950 | hp2 | a0002 | c0003 | t0001 | g0248 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18952 | hp1 | a0002 | c0003 | t0001 | g0308 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18952 | hp2 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18954 | hp1 | a0002 | c0003 | t0001 | g0306 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18954 | hp2 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18956 | hp2 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18959 | hp1 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0277 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18960 | hp2 | a0001 | c0002 | t0001 | g0276 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0124 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18968 | hp1 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18970 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18972 | hp1 | a0001 | c0002 | t0001 | g0051 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18972 | hp2 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18978 | hp1 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18978 | hp2 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18979 | hp2 | a0002 | c0003 | t0001 | g0310 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0104 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18980 | hp2 | a0001 | c0002 | t0001 | g0279 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18982 | hp2 | a0002 | c0003 | t0001 | g0313 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18985 | hp1 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18989 | hp2 | a0010 | c0012 | t0001 | g0166 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18991 | hp2 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18994 | hp1 | a0002 | c0003 | t0001 | g0301 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0142 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA18999 | hp2 | a0004 | c0005 | t0001 | g0088 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19000 | hp1 | a0004 | c0005 | t0001 | g0095 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19002 | hp1 | a0001 | c0002 | t0001 | g0278 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19002 | hp2 | a0002 | c0003 | t0001 | g0302 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19003 | hp1 | a0001 | c0002 | t0001 | g0275 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0333 | AFR | LWK | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | LWK | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0121 | AFR | LWK | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0331 | AFR | LWK | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19063 | hp2 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19064 | hp2 | a0002 | c0003 | t0001 | g0309 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0144 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0136 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19070 | hp2 | a0004 | c0005 | t0001 | g0087 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19072 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19077 | hp1 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19078 | hp2 | a0001 | c0002 | t0001 | g0111 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19080 | hp2 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19081 | hp2 | a0002 | c0003 | t0001 | g0318 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19082 | hp1 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19085 | hp2 | a0001 | c0002 | t0001 | g0071 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19087 | hp1 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | YRI | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | YRI | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0060 | AFR | ASW | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ASW | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0234 | EUR | TSI | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA20752 | hp2 | a0001 | c0002 | t0001 | g0034 | EUR | TSI | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | ACB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0336 | AFR | ACB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0335 | AFR | ACB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0325 | AFR | ACB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02559 | hp1 | a0001 | c0002 | t0002 | g0109 | AFR | ACB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | ACB | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0328 | AFR | MSL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG03471 | hp2 | a0001 | c0002 | t0002 | g0101 | AFR | MSL | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | USA | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | USA | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | USA | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| NA20300 | hp2 | a0011 | c0009 | t0001 | g0092 | AFR | USA | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0298 | REF | REF | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| homoSapiens | grch38p0 | a0003 | c0004 | t0002 | g0026 | REF | REF | CFI_chr4_109735695_109806999 | CFI | chr4 | 109735695 | 109806999 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:109740897 | A | G | 1 | a0010 | 1 | NA18989.hp2 | missense_variant | MODERATE | c.1748T>C | p.Val583Ala | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 13/13 | 1776/1978 | 1748/1752 | 583/583 | chr4 | 109740897 | |||
| chr4:109740964 | T | C | 1 | a0009 | 1 | HG02738.hp2 | missense_variant | MODERATE | c.1681A>G | p.Lys561Glu | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 13/13 | 1709/1978 | 1681/1752 | 561/583 | chr4 | 109740964 | |||
| chr4:109746405 | T | G | 1 | a0008 | 1 | HG02615.hp1 | missense_variant | MODERATE | c.1246A>C | p.Ile416Leu | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/13 | 1274/1978 | 1246/1752 | 416/583 | chr4 | 109746405 | |||
| chr4:109746434 | C | T | 1 | a0002 | 17 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(14): Show |
missense_variant | MODERATE | c.1217G>A | p.Arg406His | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/13 | 1245/1978 | 1217/1752 | 406/583 | chr4 | 109746434 | |||
| chr4:109752492 | T | C | 1 | a0007 | 1 | HG01975.hp1 | missense_variant | MODERATE | c.916A>G | p.Ile306Val | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/13 | 944/1978 | 916/1752 | 306/583 | chr4 | 109752492 | |||
| chr4:109757769 | T | C | 10 | a0001 a0002 a0004 others(7): Show |
338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): Show |
missense_variant | MODERATE | c.898A>G | p.Thr300Ala | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/13 | 926/1978 | 898/1752 | 300/583 | chr4 | 109757769 | |||
| chr4:109760294 | C | T | 1 | a0011 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.859G>A | p.Gly287Arg | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/13 | 887/1978 | 859/1752 | 287/583 | chr4 | 109760294 | |||
| chr4:109761572 | T | G | 1 | a0004 | 4 | NA18941.hp2 NA18999.hp2 NA19000.hp1 others(1): Show |
missense_variant | MODERATE | c.603A>C | p.Arg201Ser | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 4/13 | 631/1978 | 603/1752 | 201/583 | chr4 | 109761572 | |||
| chr4:109761605 | C | A | 1 | a0006 | 1 | HG01106.hp2 | missense_variant | MODERATE | c.570G>T | p.Glu190Asp | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 4/13 | 598/1978 | 570/1752 | 190/583 | chr4 | 109761605 | |||
| chr4:109761673 | T | C | 1 | a0005 | 2 | HG01074.hp1 HG01081.hp1 |
missense_variant | MODERATE | c.502A>G | p.Arg168Gly | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 4/13 | 530/1978 | 502/1752 | 168/583 | chr4 | 109761673 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:109746445 | G | A | 1 | a0001c0006 | 2 | HG02647.hp1 HG03041.hp1 |
synonymous_variant | LOW | c.1206C>T | p.Pro402Pro | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/13 | 1234/1978 | 1206/1752 | 402/583 | chr4 | 109746445 | |||
| chr4:109760349 | C | T | 9 | a0001c0002 a0001c0006 a0001c0008 others(6): Show |
138 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(135): Show |
synonymous_variant | LOW | c.804G>A | p.Ser268Ser | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/13 | 832/1978 | 804/1752 | 268/583 | chr4 | 109760349 | |||
| chr4:109766567 | T | A | 1 | a0001c0008 | 2 | HG03516.hp2 HG03579.hp1 |
synonymous_variant | LOW | c.315A>T | p.Thr105Thr | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 2/13 | 343/1978 | 315/1752 | 105/583 | chr4 | 109766567 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:109740749 | A | G | 1 | a0001c0006t0005 | 2 | HG02647.hp1 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*144T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 13/13 | 144 | chr4 | 109740749 | ||||||
| chr4:109740781 | G | A | 17 | a0001c0001t0001 a0001c0001t0003 a0001c0002t0001 others(14): Show |
340 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(337): Show |
3_prime_UTR_variant | MODIFIER | c.*112C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 13/13 | 112 | chr4 | 109740781 | ||||||
| chr4:109740886 | C | A | 2 | a0001c0001t0003 a0001c0002t0003 |
6 | HG02258.hp2 HG02486.hp1 HG02809.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*7G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 13/13 | 7 | chr4 | 109740886 | ||||||
| chr4:109801984 | C | T | 1 | a0001c0002t0004 | 3 | HG01070.hp1 HG01071.hp1 HG01257.hp2 |
5_prime_UTR_variant | MODIFIER | c.-13G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/13 | 13 | chr4 | 109801984 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:109741297 | C | T | 2 | a0001c0001t0001g0233 a0001c0001t0001g0237 |
2 | HG02572.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1535-187G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 12/12 | chr4 | 109741297 | |||||||
| chr4:109741593 | A | G | 9 | a0001c0001t0001g0320 a0001c0001t0001g0323 a0001c0001t0001g0325 others(6): Show |
9 | HG01975.hp1 HG02486.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1535-483T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 12/12 | chr4 | 109741593 | |||||||
| chr4:109741777 | T | C | 3 | a0003c0004t0001g0154 a0003c0004t0001g0155 a0003c0004t0001g0297 |
3 | HG00738.hp1 HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1535-667A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 12/12 | chr4 | 109741777 | |||||||
| chr4:109741982 | A | G | 2 | a0001c0001t0001g0224 a0001c0001t0001g0239 |
2 | HG00741.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.1534+509T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 12/12 | chr4 | 109741982 | |||||||
| chr4:109741993 | A | AATTTACT others(37): Show |
1 | a0001c0001t0001g0283 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1534+454_1534+497d others(46): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 12/12 | chr4 | 109741993 | |||||||
| chr4:109742038 | A | T | 1 | a0001c0001t0001g0148 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1534+453T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 12/12 | chr4 | 109742038 | |||||||
| chr4:109742250 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1534+241C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 12/12 | chr4 | 109742250 | |||||||
| chr4:109742285 | C | T | 3 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 |
3 | HG02559.hp2 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1534+206G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 12/12 | chr4 | 109742285 | |||||||
| chr4:109742313 | T | A | 1 | a0001c0002t0001g0081 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1534+178A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 12/12 | chr4 | 109742313 | |||||||
| chr4:109742354 | G | A | 1 | a0001c0002t0001g0134 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1534+137C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 12/12 | chr4 | 109742354 | |||||||
| chr4:109742708 | A | G | 5 | a0001c0001t0001g0164 a0001c0001t0001g0169 a0001c0001t0001g0219 others(2): Show |
5 | HG01123.hp1 HG01168.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.1430-113T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109742708 | |||||||
| chr4:109742735 | G | A | 1 | a0001c0002t0003g0280 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1430-140C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109742735 | |||||||
| chr4:109742841 | T | C | 333 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(330): Show |
350 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(347): Show |
intron_variant | MODIFIER | c.1430-246A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109742841 | |||||||
| chr4:109742901 | A | G | 3 | a0001c0001t0001g0205 a0001c0001t0001g0208 a0001c0001t0001g0210 |
3 | HG02155.hp2 NA19080.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.1430-306T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109742901 | |||||||
| chr4:109743047 | G | T | 5 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0003c0004t0001g0154 others(2): Show |
5 | HG00738.hp1 HG02886.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1430-452C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109743047 | |||||||
| chr4:109743474 | T | C | 251 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(248): Show |
265 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.1430-879A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109743474 | |||||||
| chr4:109743480 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1430-885C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109743480 | |||||||
| chr4:109743561 | T | C | 8 | a0001c0001t0001g0145 a0001c0001t0001g0173 a0001c0001t0001g0225 others(5): Show |
8 | HG02572.hp1 HG02630.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1430-966A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109743561 | |||||||
| chr4:109743641 | C | A | 28 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0145 others(25): Show |
30 | HG00099.hp1 HG00438.hp1 HG00639.hp1 others(27): Show |
intron_variant | MODIFIER | c.1430-1046G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109743641 | |||||||
| chr4:109743727 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1430-1132G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109743727 | |||||||
| chr4:109743859 | A | G | 6 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(3): Show |
6 | HG02723.hp2 HG02897.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1430-1264T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109743859 | |||||||
| chr4:109743903 | T | G | 1 | a0001c0001t0001g0218 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1430-1308A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109743903 | |||||||
| chr4:109744056 | CCATTCTC others(21): Show |
C | 1 | a0001c0002t0001g0019 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1430-1489_1430-146 others(32): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109744056 | |||||||
| chr4:109744073 | T | C | 3 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0002t0001g0133 |
3 | HG02723.hp2 HG03486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1430-1478A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109744073 | |||||||
| chr4:109744085 | A | G | 1 | a0001c0001t0001g0226 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1430-1490T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109744085 | |||||||
| chr4:109744091 | A | C | 19 | a0001c0001t0001g0172 a0001c0001t0001g0304 a0002c0003t0001g0248 others(16): Show |
19 | HG00544.hp2 HG00673.hp1 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.1430-1496T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109744091 | |||||||
| chr4:109744254 | G | A | 1 | a0001c0002t0001g0196 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1430-1659C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109744254 | |||||||
| chr4:109744325 | T | C | 101 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0176 others(98): Show |
103 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(100): Show |
intron_variant | MODIFIER | c.1430-1730A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109744325 | |||||||
| chr4:109744393 | C | G | 2 | a0001c0001t0001g0171 a0001c0001t0001g0187 |
2 | NA19068.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1430-1798G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109744393 | |||||||
| chr4:109744486 | A | G | 2 | a0001c0001t0001g0010 a0001c0001t0001g0263 |
3 | HG00438.hp1 NA18945.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.1429+1736T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109744486 | |||||||
| chr4:109744622 | C | T | 1 | a0001c0001t0001g0009 | 2 | HG00438.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.1429+1600G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109744622 | |||||||
| chr4:109745015 | T | A | 200 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(197): Show |
214 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(211): Show |
intron_variant | MODIFIER | c.1429+1207A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109745015 | |||||||
| chr4:109745115 | C | T | 1 | a0001c0002t0001g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1429+1107G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109745115 | |||||||
| chr4:109745136 | G | A | 128 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(125): Show |
139 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.1429+1086C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109745136 | |||||||
| chr4:109745152 | A | G | 3 | a0001c0002t0001g0289 a0001c0002t0001g0291 a0001c0002t0001g0292 |
3 | HG00735.hp2 HG02280.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1429+1070T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109745152 | |||||||
| chr4:109745171 | C | T | 306 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(303): Show |
323 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.1429+1051G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109745171 | |||||||
| chr4:109745275 | C | T | 311 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(308): Show |
328 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.1429+947G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109745275 | |||||||
| chr4:109745326 | G | C | 1 | a0001c0001t0003g0013 | 2 | HG02258.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1429+896C>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109745326 | |||||||
| chr4:109745392 | T | A | 1 | a0008c0011t0001g0108 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1429+830A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109745392 | |||||||
| chr4:109745687 | G | A | 2 | a0001c0008t0001g0272 a0001c0008t0002g0271 |
2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1429+535C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109745687 | |||||||
| chr4:109745723 | C | T | 4 | a0001c0002t0001g0112 a0001c0002t0001g0121 a0003c0004t0001g0027 others(1): Show |
4 | HG02896.hp2 HG02897.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1429+499G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109745723 | |||||||
| chr4:109746144 | G | A | 1 | a0001c0002t0001g0062 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1429+78C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109746144 | |||||||
| chr4:109746189 | T | C | 43 | a0001c0001t0001g0082 a0001c0001t0001g0145 a0001c0001t0001g0146 others(40): Show |
44 | HG00558.hp2 HG00609.hp2 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.1429+33A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 11/12 | chr4 | 109746189 | |||||||
| chr4:109746530 | A | G | 2 | a0001c0002t0001g0139 a0001c0002t0001g0140 |
2 | HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1149-28T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109746530 | |||||||
| chr4:109746663 | G | C | 2 | a0001c0001t0001g0217 a0001c0001t0001g0230 |
2 | NA18979.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.1149-161C>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109746663 | |||||||
| chr4:109746710 | G | A | 3 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 |
3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1149-208C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109746710 | |||||||
| chr4:109746806 | G | C | 1 | a0001c0002t0001g0122 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1149-304C>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109746806 | |||||||
| chr4:109746972 | T | C | 3 | a0003c0004t0001g0154 a0003c0004t0001g0155 a0003c0004t0001g0297 |
3 | HG00738.hp1 HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1149-470A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109746972 | |||||||
| chr4:109746998 | C | A | 1 | a0001c0001t0001g0186 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1149-496G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109746998 | |||||||
| chr4:109747150 | C | T | 3 | a0001c0002t0004g0016 a0001c0002t0004g0017 a0001c0002t0004g0018 |
3 | HG01070.hp1 HG01071.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.1149-648G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109747150 | |||||||
| chr4:109747158 | C | T | 1 | a0003c0004t0001g0297 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1149-656G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109747158 | |||||||
| chr4:109747172 | G | A | 240 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(237): Show |
255 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.1149-670C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109747172 | |||||||
| chr4:109747354 | T | TA | 6 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(3): Show |
6 | HG02723.hp2 HG02897.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1149-853dupT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109747354 | |||||||
| chr4:109747361 | A | AT | 322 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(319): Show |
339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.1149-860dupA | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109747361 | |||||||
| chr4:109747373 | A | G | 3 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 |
3 | HG02559.hp2 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1149-871T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109747373 | |||||||
| chr4:109747495 | G | A | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(123): Show |
136 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1149-993C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109747495 | |||||||
| chr4:109747531 | T | A | 1 | a0001c0002t0001g0289 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1149-1029A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109747531 | |||||||
| chr4:109747564 | T | G | 1 | a0001c0002t0001g0019 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1149-1062A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109747564 | |||||||
| chr4:109747566 | G | T | 1 | a0001c0002t0001g0019 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1149-1064C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109747566 | |||||||
| chr4:109747744 | G | A | 3 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 |
3 | HG02559.hp2 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1149-1242C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109747744 | |||||||
| chr4:109747801 | G | A | 1 | a0001c0002t0001g0131 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1149-1299C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109747801 | |||||||
| chr4:109747824 | C | G | 328 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(325): Show |
345 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.1149-1322G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109747824 | |||||||
| chr4:109747992 | G | C | 1 | a0002c0003t0001g0305 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1148+1226C>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109747992 | |||||||
| chr4:109748045 | C | A | 1 | a0001c0001t0002g0158 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1148+1173G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109748045 | |||||||
| chr4:109748105 | A | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(123): Show |
136 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.1148+1113T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109748105 | |||||||
| chr4:109748199 | G | A | 1 | a0001c0001t0001g0232 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1148+1019C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109748199 | |||||||
| chr4:109748264 | T | C | 85 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0019 others(82): Show |
87 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.1148+954A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109748264 | |||||||
| chr4:109748457 | C | A | 1 | a0001c0002t0001g0051 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1148+761G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109748457 | |||||||
| chr4:109748639 | G | A | 1 | a0001c0002t0001g0141 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1148+579C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109748639 | |||||||
| chr4:109748644 | A | G | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(234): Show |
252 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.1148+574T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109748644 | |||||||
| chr4:109748692 | G | A | 1 | a0002c0003t0001g0317 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1148+526C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109748692 | |||||||
| chr4:109748696 | C | T | 237 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(234): Show |
252 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(249): Show |
intron_variant | MODIFIER | c.1148+522G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109748696 | |||||||
| chr4:109748769 | G | A | 2 | a0003c0004t0001g0154 a0003c0004t0001g0155 |
2 | HG00738.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1148+449C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109748769 | |||||||
| chr4:109748818 | T | C | 2 | a0003c0004t0001g0154 a0003c0004t0001g0155 |
2 | HG00738.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1148+400A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109748818 | |||||||
| chr4:109748876 | C | T | 4 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0197 others(1): Show |
4 | HG01256.hp1 HG03491.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.1148+342G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109748876 | |||||||
| chr4:109749183 | C | T | 3 | a0001c0001t0003g0334 a0001c0001t0003g0335 a0007c0013t0001g0290 |
3 | HG01975.hp1 HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1148+35G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 10/12 | chr4 | 109749183 | |||||||
| chr4:109749651 | G | C | 325 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(322): Show |
342 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(339): Show |
intron_variant | MODIFIER | c.941-49C>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109749651 | |||||||
| chr4:109749747 | C | T | 19 | a0001c0001t0001g0303 a0001c0001t0001g0311 a0002c0003t0001g0248 others(16): Show |
19 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.941-145G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109749747 | |||||||
| chr4:109749873 | C | T | 4 | a0001c0002t0001g0288 a0001c0002t0001g0289 a0001c0002t0001g0291 others(1): Show |
4 | HG00735.hp2 HG02055.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.941-271G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109749873 | |||||||
| chr4:109750003 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.941-401A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109750003 | |||||||
| chr4:109750027 | C | T | 1 | a0001c0001t0003g0334 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.941-425G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109750027 | |||||||
| chr4:109750082 | C | T | 85 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0019 others(82): Show |
87 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.941-480G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109750082 | |||||||
| chr4:109750154 | G | A | 3 | a0001c0002t0001g0075 a0001c0002t0001g0076 a0001c0002t0001g0079 |
3 | HG01069.hp1 HG01071.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.941-552C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109750154 | |||||||
| chr4:109750280 | A | G | 325 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(322): Show |
341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.941-678T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109750280 | |||||||
| chr4:109750384 | A | G | 4 | a0001c0002t0001g0288 a0001c0002t0001g0289 a0001c0002t0001g0291 others(1): Show |
4 | HG00735.hp2 HG02055.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.941-782T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109750384 | |||||||
| chr4:109750385 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.941-783A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109750385 | |||||||
| chr4:109750545 | C | T | 85 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0019 others(82): Show |
87 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.941-943G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109750545 | |||||||
| chr4:109750567 | C | G | 2 | a0005c0007t0001g0046 a0005c0007t0001g0047 |
2 | HG01074.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.941-965G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109750567 | |||||||
| chr4:109750577 | A | T | 1 | a0001c0001t0001g0216 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.941-975T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109750577 | |||||||
| chr4:109750709 | C | T | 3 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 |
3 | HG02559.hp2 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.941-1107G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109750709 | |||||||
| chr4:109750722 | G | T | 3 | a0001c0002t0001g0119 a0001c0002t0001g0128 a0001c0002t0001g0196 |
3 | HG01074.hp2 HG01243.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.941-1120C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109750722 | |||||||
| chr4:109750770 | A | T | 14 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0156 others(11): Show |
16 | HG00099.hp1 HG00438.hp1 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.941-1168T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109750770 | |||||||
| chr4:109751039 | A | T | 1 | a0001c0001t0001g0242 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.940+1429T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109751039 | |||||||
| chr4:109751070 | CACAGACC others(27): Show |
C | 4 | a0001c0002t0001g0288 a0001c0002t0001g0289 a0001c0002t0001g0291 others(1): Show |
4 | HG00735.hp2 HG02055.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.940+1364_940+1397d others(36): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109751070 | |||||||
| chr4:109751128 | C | T | 322 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(319): Show |
338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.940+1340G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109751128 | |||||||
| chr4:109751129 | A | G | 85 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0019 others(82): Show |
87 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.940+1339T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109751129 | |||||||
| chr4:109751384 | G | A | 1 | a0001c0001t0001g0009 | 2 | HG00438.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.940+1084C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109751384 | |||||||
| chr4:109751413 | A | C | 1 | a0007c0013t0001g0290 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.940+1055T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109751413 | |||||||
| chr4:109751426 | C | T | 2 | a0001c0001t0001g0304 a0010c0012t0001g0166 |
2 | NA18989.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.940+1042G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109751426 | |||||||
| chr4:109751438 | C | CT | 139 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(136): Show |
152 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.940+1029dupA | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109751438 | |||||||
| chr4:109751438 | C | CTT | 38 | a0001c0001t0001g0161 a0001c0001t0001g0165 a0001c0001t0001g0167 others(35): Show |
38 | HG00544.hp1 HG00673.hp1 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.940+1028_940+1029d others(4): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109751438 | |||||||
| chr4:109751438 | CT | C | 79 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0033 others(76): Show |
81 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(78): Show |
intron_variant | MODIFIER | c.940+1029delA | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109751438 | |||||||
| chr4:109751614 | A | G | 126 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(123): Show |
136 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.940+854T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109751614 | |||||||
| chr4:109751629 | T | A | 85 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0019 others(82): Show |
87 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.940+839A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109751629 | |||||||
| chr4:109751646 | G | GGCCAGGC others(10): Show |
1 | a0002c0003t0001g0307 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.940+805_940+821dup others(17): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109751646 | |||||||
| chr4:109752041 | C | A | 57 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(54): Show |
58 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.940+427G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109752041 | |||||||
| chr4:109752158 | C | T | 19 | a0001c0001t0001g0303 a0001c0001t0001g0311 a0002c0003t0001g0248 others(16): Show |
19 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.940+310G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 8/12 | chr4 | 109752158 | |||||||
| chr4:109752647 | G | C | 4 | a0001c0002t0001g0288 a0001c0002t0001g0289 a0001c0002t0001g0291 others(1): Show |
4 | HG00735.hp2 HG02055.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.905-144C>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752647 | |||||||
| chr4:109752729 | CTA | C | 3 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 |
3 | HG02559.hp2 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.905-228_905-227del others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752729 | |||||||
| chr4:109752797 | C | G | 321 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(318): Show |
337 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.905-294G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752797 | |||||||
| chr4:109752864 | A | G | 8 | a0001c0001t0001g0082 a0001c0001t0001g0273 a0001c0001t0001g0321 others(5): Show |
9 | HG01109.hp2 HG02258.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.905-361T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752864 | |||||||
| chr4:109752882 | A | ATATAATA others(25): Show |
4 | a0001c0001t0001g0330 a0001c0001t0003g0153 a0001c0002t0001g0112 others(1): Show |
4 | HG03041.hp2 HG03195.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.905-411_905-380dup others(32): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752882 | |||||||
| chr4:109752890 | T | TATATTTA others(25): Show |
1 | a0007c0013t0001g0290 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.905-388_905-387ins others(32): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752890 | |||||||
| chr4:109752927 | T | C | 19 | a0001c0001t0001g0303 a0001c0001t0001g0311 a0002c0003t0001g0248 others(16): Show |
19 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.905-424A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752927 | |||||||
| chr4:109752935 | TA | T | 5 | a0001c0002t0001g0005 a0001c0002t0001g0041 a0001c0002t0001g0052 others(2): Show |
6 | HG00558.hp1 HG01167.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.905-433delT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752935 | |||||||
| chr4:109752936 | A | ATTTATTA others(4): Show |
83 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(80): Show |
84 | HG00323.hp1 HG00733.hp1 HG00735.hp2 others(81): Show |
intron_variant | MODIFIER | c.905-434_905-433ins others(11): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752936 | |||||||
| chr4:109752936 | A | G | 20 | a0001c0001t0001g0185 a0001c0001t0001g0303 a0001c0001t0001g0311 others(17): Show |
20 | HG00673.hp1 HG02027.hp2 HG02056.hp2 others(17): Show |
intron_variant | MODIFIER | c.905-433T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752936 | |||||||
| chr4:109752938 | A | T | 5 | a0001c0002t0001g0005 a0001c0002t0001g0041 a0001c0002t0001g0052 others(2): Show |
6 | HG00558.hp1 HG01167.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.905-435T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752938 | |||||||
| chr4:109752940 | A | T | 5 | a0001c0002t0001g0005 a0001c0002t0001g0041 a0001c0002t0001g0052 others(2): Show |
6 | HG00558.hp1 HG01167.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.905-437T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752940 | |||||||
| chr4:109752942 | A | T | 5 | a0001c0002t0001g0005 a0001c0002t0001g0041 a0001c0002t0001g0052 others(2): Show |
6 | HG00558.hp1 HG01167.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.905-439T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752942 | |||||||
| chr4:109752946 | T | A | 5 | a0001c0002t0001g0005 a0001c0002t0001g0041 a0001c0002t0001g0052 others(2): Show |
6 | HG00558.hp1 HG01167.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.905-443A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752946 | |||||||
| chr4:109752947 | TA | T | 5 | a0001c0002t0001g0005 a0001c0002t0001g0041 a0001c0002t0001g0052 others(2): Show |
6 | HG00558.hp1 HG01167.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.905-445delT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752947 | |||||||
| chr4:109752949 | T | G | 5 | a0001c0002t0001g0005 a0001c0002t0001g0041 a0001c0002t0001g0052 others(2): Show |
6 | HG00558.hp1 HG01167.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.905-446A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752949 | |||||||
| chr4:109752951 | ATACATAT others(4): Show |
A | 34 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0063 others(31): Show |
36 | HG00438.hp2 HG00544.hp1 HG01123.hp2 others(33): Show |
intron_variant | MODIFIER | c.905-459_905-449del others(11): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752951 | |||||||
| chr4:109752953 | A | C | 1 | a0007c0013t0001g0290 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.905-450T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752953 | |||||||
| chr4:109752954 | C | A | 5 | a0001c0002t0001g0005 a0001c0002t0001g0041 a0001c0002t0001g0052 others(2): Show |
6 | HG00558.hp1 HG01167.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.905-451G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752954 | |||||||
| chr4:109752954 | C | G | 1 | a0001c0002t0001g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.905-451G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752954 | |||||||
| chr4:109752954 | C | T | 283 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(280): Show |
296 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.905-451G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752954 | |||||||
| chr4:109752962 | T | TAA | 5 | a0001c0002t0001g0005 a0001c0002t0001g0041 a0001c0002t0001g0052 others(2): Show |
6 | HG00558.hp1 HG01167.hp2 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.905-460_905-459ins others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752962 | |||||||
| chr4:109752962 | T | TTATATAA others(14): Show |
79 | a0001c0001t0001g0020 a0001c0001t0001g0194 a0001c0002t0001g0004 others(76): Show |
80 | HG00323.hp1 HG00733.hp1 HG00735.hp2 others(77): Show |
intron_variant | MODIFIER | c.905-460_905-459ins others(21): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752962 | |||||||
| chr4:109752962 | T | TTATATAA others(46): Show |
3 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 |
3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-460_905-459ins others(53): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752962 | |||||||
| chr4:109752962 | T | TTATATGA others(57): Show |
1 | a0001c0001t0001g0168 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.905-460_905-459ins others(64): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752962 | |||||||
| chr4:109752965 | T | TATGAATA others(1): Show |
17 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0167 others(14): Show |
17 | HG00639.hp2 HG01256.hp1 HG03017.hp2 others(14): Show |
intron_variant | MODIFIER | c.905-463_905-462ins others(8): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752965 | |||||||
| chr4:109752974 | T | A | 18 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0167 others(15): Show |
18 | HG00639.hp2 HG01256.hp1 HG03017.hp2 others(15): Show |
intron_variant | MODIFIER | c.905-471A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752974 | |||||||
| chr4:109752977 | A | ATATAT | 18 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0167 others(15): Show |
18 | HG00639.hp2 HG01256.hp1 HG03017.hp2 others(15): Show |
intron_variant | MODIFIER | c.905-475_905-474ins others(5): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752977 | |||||||
| chr4:109752979 | G | A | 89 | a0001c0001t0001g0225 a0001c0001t0001g0282 a0001c0001t0001g0283 others(86): Show |
91 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(88): Show |
intron_variant | MODIFIER | c.905-476C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752979 | |||||||
| chr4:109752979 | G | T | 18 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0167 others(15): Show |
18 | HG00639.hp2 HG01256.hp1 HG03017.hp2 others(15): Show |
intron_variant | MODIFIER | c.905-476C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752979 | |||||||
| chr4:109752981 | A | T | 18 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0167 others(15): Show |
18 | HG00639.hp2 HG01256.hp1 HG03017.hp2 others(15): Show |
intron_variant | MODIFIER | c.905-478T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752981 | |||||||
| chr4:109752984 | A | T | 18 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0167 others(15): Show |
18 | HG00639.hp2 HG01256.hp1 HG03017.hp2 others(15): Show |
intron_variant | MODIFIER | c.905-481T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752984 | |||||||
| chr4:109752992 | T | TTATATA | 18 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0167 others(15): Show |
18 | HG00639.hp2 HG01256.hp1 HG03017.hp2 others(15): Show |
intron_variant | MODIFIER | c.905-490_905-489ins others(6): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752992 | |||||||
| chr4:109752994 | ATATATAT others(4): Show |
A | 1 | a0001c0002t0001g0041 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.905-502_905-492del others(11): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752994 | |||||||
| chr4:109752997 | T | A | 18 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0167 others(15): Show |
18 | HG00639.hp2 HG01256.hp1 HG03017.hp2 others(15): Show |
intron_variant | MODIFIER | c.905-494A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109752997 | |||||||
| chr4:109753005 | T | TAA | 18 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0167 others(15): Show |
18 | HG00639.hp2 HG01256.hp1 HG03017.hp2 others(15): Show |
intron_variant | MODIFIER | c.905-503_905-502ins others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753005 | |||||||
| chr4:109753005 | T | TTATATAA others(14): Show |
6 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(3): Show |
6 | HG00558.hp1 HG02559.hp2 NA18906.hp1 others(3): Show |
intron_variant | MODIFIER | c.905-503_905-502ins others(21): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753005 | |||||||
| chr4:109753005 | T | TTATATAT others(25): Show |
51 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(48): Show |
55 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.905-534_905-503dup others(32): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753005 | |||||||
| chr4:109753014 | TA | T | 3 | a0001c0002t0001g0033 a0001c0002t0001g0037 a0001c0002t0001g0055 |
3 | HG01993.hp2 NA18945.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.905-512delT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753014 | |||||||
| chr4:109753015 | AT | A | 74 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0019 others(71): Show |
76 | HG00323.hp1 HG00733.hp1 HG00735.hp2 others(73): Show |
intron_variant | MODIFIER | c.905-513delA | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753015 | |||||||
| chr4:109753022 | A | G | 58 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(55): Show |
59 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.905-519T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753022 | |||||||
| chr4:109753025 | T | C | 4 | a0001c0002t0001g0288 a0001c0002t0001g0289 a0001c0002t0001g0291 others(1): Show |
4 | HG00735.hp2 HG02055.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.905-522A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753025 | |||||||
| chr4:109753048 | T | TTATATAA others(14): Show |
11 | a0001c0002t0001g0035 a0001c0002t0001g0039 a0001c0002t0001g0040 others(8): Show |
11 | HG00323.hp1 HG01069.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.905-546_905-545ins others(21): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753048 | |||||||
| chr4:109753048 | T | TTATATAA others(110): Show |
1 | a0001c0008t0001g0272 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.905-546_905-545ins others(117): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753048 | |||||||
| chr4:109753048 | T | TTATATAA others(142): Show |
1 | a0001c0008t0002g0271 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.905-546_905-545ins others(149): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753048 | |||||||
| chr4:109753048 | T | TTATATAA others(46): Show |
5 | a0001c0002t0001g0065 a0001c0002t0001g0288 a0001c0002t0001g0289 others(2): Show |
5 | HG00735.hp2 HG02055.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.905-546_905-545ins others(53): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753048 | |||||||
| chr4:109753048 | T | TTATATAA others(14): Show |
3 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 |
3 | HG02559.hp2 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.905-546_905-545ins others(21): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753048 | |||||||
| chr4:109753048 | T | TTATATAA others(78): Show |
2 | a0001c0006t0005g0098 a0001c0006t0005g0099 |
2 | HG02647.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.905-546_905-545ins others(85): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753048 | |||||||
| chr4:109753048 | T | TTATATAA others(120): Show |
8 | a0002c0003t0001g0300 a0002c0003t0001g0301 a0002c0003t0001g0302 others(5): Show |
8 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.905-546_905-545ins others(127): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753048 | |||||||
| chr4:109753048 | T | TTATATAA others(87): Show |
2 | a0001c0001t0001g0171 a0001c0001t0001g0187 |
2 | NA19068.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.905-546_905-545ins others(94): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753048 | |||||||
| chr4:109753048 | T | TTATATAA others(55): Show |
77 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(74): Show |
83 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(80): Show |
intron_variant | MODIFIER | c.905-546_905-545ins others(62): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753048 | |||||||
| chr4:109753048 | T | TTATATAA others(87): Show |
9 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0200 others(6): Show |
11 | HG00741.hp2 HG02145.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.905-546_905-545ins others(94): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753048 | |||||||
| chr4:109753048 | T | TTATATAA others(119): Show |
1 | a0001c0001t0001g0273 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.905-546_905-545ins others(126): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753048 | |||||||
| chr4:109753048 | T | TTATATAA others(87): Show |
1 | a0001c0001t0001g0321 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.905-546_905-545ins others(94): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753048 | |||||||
| chr4:109753048 | TTATATAT others(3): Show |
T | 66 | a0001c0001t0001g0320 a0001c0001t0001g0323 a0001c0001t0001g0324 others(63): Show |
68 | HG00733.hp1 HG01069.hp1 HG01070.hp1 others(65): Show |
intron_variant | MODIFIER | c.905-555_905-546del others(10): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753048 | |||||||
| chr4:109753049 | T | A | 4 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 others(1): Show |
4 | HG02257.hp2 HG02976.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.905-546A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753049 | |||||||
| chr4:109753058 | A | AT | 133 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(130): Show |
141 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.905-556dupA | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753058 | |||||||
| chr4:109753058 | A | ATTATAAA others(195): Show |
1 | a0001c0002t0001g0113 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.905-556_905-555ins others(202): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753058 | |||||||
| chr4:109753058 | A | ATTATATA others(163): Show |
8 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(5): Show |
8 | HG02723.hp2 HG02897.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.905-556_905-555ins others(170): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753058 | |||||||
| chr4:109753058 | A | ATTATATA others(195): Show |
38 | a0001c0002t0001g0006 a0001c0002t0001g0021 a0001c0002t0001g0022 others(35): Show |
39 | HG00558.hp2 HG00609.hp2 HG00673.hp2 others(36): Show |
intron_variant | MODIFIER | c.905-556_905-555ins others(202): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753058 | |||||||
| chr4:109753058 | A | ATTATATA others(227): Show |
1 | a0001c0002t0001g0134 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.905-556_905-555ins others(234): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753058 | |||||||
| chr4:109753058 | A | ATTATATA others(132): Show |
1 | a0002c0003t0001g0309 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.905-556_905-555ins others(139): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753058 | |||||||
| chr4:109753058 | A | ATTATGTA others(99): Show |
1 | a0001c0001t0003g0153 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.905-556_905-555ins others(106): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753058 | |||||||
| chr4:109753063 | TA | T | 62 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(59): Show |
67 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.905-561delT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753063 | |||||||
| chr4:109753067 | T | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(132): Show |
143 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.905-564A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753067 | |||||||
| chr4:109753095 | TA | T | 4 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 others(1): Show |
4 | HG02257.hp2 HG02976.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.905-593delT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753095 | |||||||
| chr4:109753099 | C | CAAATATT others(25): Show |
5 | a0003c0004t0001g0027 a0003c0004t0001g0028 a0003c0004t0001g0030 others(2): Show |
5 | HG02257.hp1 HG02630.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.905-628_905-597dup others(32): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753099 | |||||||
| chr4:109753099 | C | CAAATATT others(24): Show |
1 | a0003c0004t0001g0031 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.905-597_905-596ins others(31): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753099 | |||||||
| chr4:109753099 | C | T | 247 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(244): Show |
258 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(255): Show |
intron_variant | MODIFIER | c.905-596G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753099 | |||||||
| chr4:109753125 | TATAA | T | 4 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 others(1): Show |
4 | HG02257.hp2 HG02976.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.905-626_905-623del others(4): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753125 | |||||||
| chr4:109753128 | A | ATTTATAT others(2): Show |
8 | a0001c0001t0001g0148 a0001c0002t0001g0119 a0001c0002t0001g0121 others(5): Show |
8 | HG01074.hp2 HG01243.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.905-626_905-625ins others(9): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753128 | |||||||
| chr4:109753131 | T | C | 10 | a0001c0001t0001g0303 a0001c0001t0001g0311 a0002c0003t0001g0248 others(7): Show |
10 | HG02155.hp1 HG02523.hp1 HG03831.hp1 others(7): Show |
intron_variant | MODIFIER | c.905-628A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753131 | |||||||
| chr4:109753134 | ATATTTAT others(10): Show |
A | 9 | a0001c0001t0001g0320 a0001c0001t0001g0323 a0001c0001t0001g0324 others(6): Show |
9 | HG02486.hp2 HG02622.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.905-648_905-632del others(17): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753134 | |||||||
| chr4:109753150 | TTTA | T | 4 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 others(1): Show |
4 | HG02257.hp2 HG02976.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.905-650_905-648del others(3): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753150 | |||||||
| chr4:109753151 | T | G | 1 | a0003c0004t0001g0297 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.905-648A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753151 | |||||||
| chr4:109753159 | TA | T | 4 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 others(1): Show |
4 | HG02257.hp2 HG02976.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.905-657delT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753159 | |||||||
| chr4:109753160 | A | G | 1 | a0007c0013t0001g0290 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.905-657T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753160 | |||||||
| chr4:109753163 | T | C | 9 | a0001c0001t0001g0148 a0001c0002t0001g0119 a0001c0002t0001g0121 others(6): Show |
9 | HG01074.hp2 HG01243.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.905-660A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753163 | |||||||
| chr4:109753174 | A | AAC | 9 | a0001c0001t0001g0320 a0001c0001t0001g0323 a0001c0001t0001g0324 others(6): Show |
9 | HG02486.hp2 HG02622.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.905-672_905-671ins others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753174 | |||||||
| chr4:109753174 | A | AAT | 295 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(292): Show |
309 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.905-673_905-672dup others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753174 | |||||||
| chr4:109753174 | A | AATATATA others(42): Show |
1 | a0001c0001t0001g0147 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.905-672_905-671ins others(49): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753174 | |||||||
| chr4:109753174 | A | AATATATA others(106): Show |
1 | a0001c0008t0001g0272 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.905-672_905-671ins others(113): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753174 | |||||||
| chr4:109753174 | A | AATATATA others(74): Show |
2 | a0001c0001t0001g0265 a0001c0001t0001g0270 |
2 | HG03927.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.905-672_905-671ins others(81): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753174 | |||||||
| chr4:109753174 | A | AATATATA others(138): Show |
4 | a0001c0001t0001g0002 a0001c0001t0001g0294 a0001c0001t0001g0295 others(1): Show |
6 | HG01261.hp1 HG01433.hp1 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.905-672_905-671ins others(145): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753174 | |||||||
| chr4:109753174 | A | AATATATA others(170): Show |
1 | a0002c0003t0001g0314 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.905-672_905-671ins others(177): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753174 | |||||||
| chr4:109753174 | A | AATATATA others(106): Show |
5 | a0001c0001t0001g0199 a0001c0001t0001g0201 a0001c0001t0001g0212 others(2): Show |
5 | HG00735.hp1 HG00738.hp2 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.905-672_905-671ins others(113): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753174 | |||||||
| chr4:109753174 | A | AATATATA others(112): Show |
1 | a0007c0013t0001g0290 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.905-672_905-671ins others(119): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753174 | |||||||
| chr4:109753181 | T | G | 1 | a0003c0004t0001g0297 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.905-678A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753181 | |||||||
| chr4:109753183 | A | C | 5 | a0001c0001t0001g0171 a0001c0001t0001g0187 a0001c0001t0001g0189 others(2): Show |
5 | HG01175.hp1 HG01256.hp1 NA18994.hp2 others(2): Show |
intron_variant | MODIFIER | c.905-680T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753183 | |||||||
| chr4:109753189 | TA | T | 4 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 others(1): Show |
4 | HG02257.hp2 HG02976.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.905-687delT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753189 | |||||||
| chr4:109753193 | T | C | 8 | a0001c0001t0001g0148 a0001c0002t0001g0119 a0001c0002t0001g0121 others(5): Show |
8 | HG01074.hp2 HG01243.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.905-690A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753193 | |||||||
| chr4:109753195 | AATATTTA others(6): Show |
A | 1 | a0003c0004t0001g0154 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.905-705_905-693del others(13): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753195 | |||||||
| chr4:109753200 | T | TA | 60 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0145 others(57): Show |
63 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.905-698_905-697ins others(1): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753200 | |||||||
| chr4:109753203 | T | TA | 60 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0145 others(57): Show |
63 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.905-701dupT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753203 | |||||||
| chr4:109753204 | AAT | A | 3 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 |
3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-703_905-702del others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753204 | |||||||
| chr4:109753206 | TATATATT others(4): Show |
T | 3 | a0001c0002t0001g0139 a0001c0002t0001g0140 a0003c0004t0001g0155 |
3 | HG00738.hp1 HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.905-714_905-704del others(11): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753206 | |||||||
| chr4:109753208 | T | A | 60 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0145 others(57): Show |
63 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.905-705A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753208 | |||||||
| chr4:109753213 | T | G | 1 | a0003c0004t0001g0297 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.905-710A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753213 | |||||||
| chr4:109753215 | A | C | 79 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(76): Show |
85 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.905-712T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753215 | |||||||
| chr4:109753216 | T | TTATATAA others(14): Show |
5 | a0001c0002t0001g0119 a0001c0002t0001g0121 a0001c0002t0001g0128 others(2): Show |
5 | HG01074.hp2 HG01243.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.905-714_905-713ins others(21): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753216 | |||||||
| chr4:109753216 | T | TTATATAA others(14): Show |
15 | a0001c0001t0001g0082 a0001c0001t0001g0148 a0001c0001t0001g0303 others(12): Show |
16 | HG02109.hp2 HG02155.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.905-714_905-713ins others(21): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753216 | |||||||
| chr4:109753216 | T | TTATATAA others(46): Show |
1 | a0001c0001t0003g0334 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.905-714_905-713ins others(53): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753216 | |||||||
| chr4:109753216 | T | TTATATAA others(93): Show |
2 | a0002c0003t0001g0308 a0002c0003t0001g0310 |
2 | NA18952.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.905-714_905-713ins others(100): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753216 | |||||||
| chr4:109753216 | T | TTATATAA others(61): Show |
18 | a0001c0001t0001g0020 a0001c0001t0001g0160 a0001c0001t0001g0162 others(15): Show |
18 | HG00280.hp2 HG00639.hp2 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.905-714_905-713ins others(68): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753216 | |||||||
| chr4:109753217 | A | AAC | 60 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0145 others(57): Show |
63 | HG00323.hp1 HG00558.hp2 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.905-715_905-714ins others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753217 | |||||||
| chr4:109753217 | A | C | 20 | a0001c0001t0001g0020 a0001c0001t0001g0160 a0001c0001t0001g0162 others(17): Show |
20 | HG00280.hp2 HG00639.hp2 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.905-714T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753217 | |||||||
| chr4:109753217 | A | T | 240 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(237): Show |
253 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
intron_variant | MODIFIER | c.905-714T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753217 | |||||||
| chr4:109753219 | T | A | 1 | a0001c0002t0002g0023 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.905-716A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753219 | |||||||
| chr4:109753219 | T | TATAA | 181 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(178): Show |
191 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.905-717_905-716ins others(4): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753219 | |||||||
| chr4:109753223 | T | A | 193 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(190): Show |
203 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.905-720A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753223 | |||||||
| chr4:109753224 | T | A | 190 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(187): Show |
200 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.905-721A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753224 | |||||||
| chr4:109753225 | T | A | 3 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 |
3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-722A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753225 | |||||||
| chr4:109753226 | AT | A | 9 | a0001c0001t0001g0163 a0001c0001t0001g0170 a0001c0001t0001g0177 others(6): Show |
9 | HG00280.hp1 HG01081.hp2 HG03579.hp2 others(6): Show |
intron_variant | MODIFIER | c.905-724delA | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753226 | |||||||
| chr4:109753227 | T | A | 3 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 |
3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-724A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753227 | |||||||
| chr4:109753228 | A | AATATATA others(21): Show |
1 | a0001c0002t0001g0279 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.905-726_905-725ins others(28): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753228 | |||||||
| chr4:109753228 | A | AATATATA others(21): Show |
1 | a0001c0001t0001g0192 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.905-726_905-725ins others(28): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753228 | |||||||
| chr4:109753228 | A | T | 312 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(309): Show |
328 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(325): Show |
intron_variant | MODIFIER | c.905-725T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753228 | |||||||
| chr4:109753231 | A | T | 3 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 |
3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-728T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753231 | |||||||
| chr4:109753232 | T | TTTA | 9 | a0001c0001t0001g0163 a0001c0001t0001g0170 a0001c0001t0001g0177 others(6): Show |
9 | HG00280.hp1 HG01081.hp2 HG03579.hp2 others(6): Show |
intron_variant | MODIFIER | c.905-730_905-729ins others(3): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753232 | |||||||
| chr4:109753233 | A | AAATAAAT others(24): Show |
2 | a0003c0004t0001g0025 a0003c0004t0002g0024 |
2 | HG01891.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.905-761_905-731dup others(31): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753233 | |||||||
| chr4:109753233 | A | T | 9 | a0001c0001t0001g0163 a0001c0001t0001g0170 a0001c0001t0001g0177 others(6): Show |
9 | HG00280.hp1 HG01081.hp2 HG03579.hp2 others(6): Show |
intron_variant | MODIFIER | c.905-730T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753233 | |||||||
| chr4:109753234 | A | T | 3 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 |
3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-731T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753234 | |||||||
| chr4:109753235 | A | T | 1 | a0001c0002t0001g0128 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.905-732T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753235 | |||||||
| chr4:109753236 | T | C | 2 | a0001c0002t0001g0139 a0001c0002t0001g0140 |
2 | HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.905-733A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753236 | |||||||
| chr4:109753238 | A | T | 12 | a0001c0001t0001g0163 a0001c0001t0001g0170 a0001c0001t0001g0177 others(9): Show |
12 | HG00280.hp1 HG01081.hp2 HG02976.hp1 others(9): Show |
intron_variant | MODIFIER | c.905-735T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753238 | |||||||
| chr4:109753245 | A | C | 6 | a0001c0001t0001g0163 a0001c0001t0001g0170 a0001c0001t0001g0177 others(3): Show |
6 | HG00280.hp1 NA18983.hp1 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.905-742T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753245 | |||||||
| chr4:109753247 | A | T | 8 | a0001c0001t0001g0163 a0001c0001t0001g0170 a0001c0001t0001g0177 others(5): Show |
8 | HG00280.hp1 HG01081.hp2 NA18959.hp2 others(5): Show |
intron_variant | MODIFIER | c.905-744T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753247 | |||||||
| chr4:109753248 | A | T | 3 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 |
3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-745T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753248 | |||||||
| chr4:109753249 | T | C | 183 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(180): Show |
193 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.905-746A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753249 | |||||||
| chr4:109753249 | T | TATATATT others(4): Show |
1 | a0001c0008t0001g0272 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.905-747_905-746ins others(11): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753249 | |||||||
| chr4:109753250 | AT | A | 3 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 |
3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-748delA | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753250 | |||||||
| chr4:109753251 | T | TAA | 8 | a0001c0001t0001g0163 a0001c0001t0001g0170 a0001c0001t0001g0177 others(5): Show |
8 | HG00280.hp1 HG01081.hp2 NA18959.hp2 others(5): Show |
intron_variant | MODIFIER | c.905-749_905-748ins others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753251 | |||||||
| chr4:109753254 | A | T | 1 | a0003c0004t0001g0297 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.905-751T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753254 | |||||||
| chr4:109753255 | T | A | 11 | a0001c0001t0001g0163 a0001c0001t0001g0170 a0001c0001t0001g0177 others(8): Show |
11 | HG00280.hp1 HG01081.hp2 HG02976.hp1 others(8): Show |
intron_variant | MODIFIER | c.905-752A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753255 | |||||||
| chr4:109753256 | T | A | 12 | a0001c0001t0001g0163 a0001c0001t0001g0170 a0001c0001t0001g0177 others(9): Show |
12 | HG00280.hp1 HG01081.hp2 HG02976.hp1 others(9): Show |
intron_variant | MODIFIER | c.905-753A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753256 | |||||||
| chr4:109753259 | T | A | 1 | a0003c0004t0001g0297 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.905-756A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753259 | |||||||
| chr4:109753260 | T | A | 23 | a0001c0001t0001g0002 a0001c0001t0001g0147 a0001c0001t0001g0199 others(20): Show |
25 | HG00735.hp1 HG00738.hp2 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.905-757A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753260 | |||||||
| chr4:109753260 | TA | T | 3 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 |
3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-758delT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753260 | |||||||
| chr4:109753264 | T | TA | 233 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(230): Show |
244 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.905-762dupT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753264 | |||||||
| chr4:109753264 | T | TATTTATT others(5): Show |
64 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0020 others(61): Show |
67 | HG00280.hp2 HG00558.hp2 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.905-762_905-761ins others(12): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753264 | |||||||
| chr4:109753265 | A | ATTTATTA others(1): Show |
22 | a0001c0001t0001g0002 a0001c0001t0001g0147 a0001c0001t0001g0199 others(19): Show |
24 | HG00735.hp1 HG00738.hp2 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.905-763_905-762ins others(8): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753265 | |||||||
| chr4:109753267 | T | C | 1 | a0007c0013t0001g0290 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.905-764A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753267 | |||||||
| chr4:109753269 | A | T | 3 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 |
3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-766T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753269 | |||||||
| chr4:109753278 | AAT | A | 3 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 |
3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-777_905-776del others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753278 | |||||||
| chr4:109753279 | A | ATATATAT others(4): Show |
1 | a0001c0002t0001g0068 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.905-787_905-777dup others(11): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753279 | |||||||
| chr4:109753280 | T | C | 24 | a0001c0001t0001g0001 a0001c0001t0001g0163 a0001c0001t0001g0170 others(21): Show |
24 | HG00280.hp1 HG00544.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.905-777A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753280 | |||||||
| chr4:109753283 | ATATTTAT others(5): Show |
A | 1 | a0003c0004t0001g0154 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.905-792_905-781del others(12): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753283 | |||||||
| chr4:109753291 | T | A | 67 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0020 others(64): Show |
70 | HG00280.hp2 HG00558.hp2 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.905-788A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753291 | |||||||
| chr4:109753293 | TATA | T | 19 | a0001c0001t0001g0002 a0001c0001t0001g0212 a0001c0001t0001g0232 others(16): Show |
21 | HG01261.hp1 HG01433.hp1 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.905-793_905-791del others(3): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753293 | |||||||
| chr4:109753295 | T | TA | 102 | a0001c0001t0001g0148 a0001c0001t0001g0163 a0001c0001t0001g0170 others(99): Show |
104 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(101): Show |
intron_variant | MODIFIER | c.905-793dupT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753295 | |||||||
| chr4:109753295 | T | TAAATAAA others(9): Show |
2 | a0001c0001t0003g0153 a0002c0003t0001g0248 |
2 | HG03195.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.905-793_905-792ins others(16): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753295 | |||||||
| chr4:109753295 | T | TATTTATA others(5): Show |
1 | a0003c0004t0001g0155 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.905-793_905-792ins others(12): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753295 | |||||||
| chr4:109753295 | T | TATTTATT others(5): Show |
99 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(96): Show |
106 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.905-793_905-792ins others(12): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753295 | |||||||
| chr4:109753296 | A | AAATAAAT others(123): Show |
11 | a0001c0001t0001g0082 a0001c0001t0001g0303 a0001c0001t0001g0311 others(8): Show |
12 | HG02109.hp2 HG02258.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.905-794_905-793ins others(130): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753296 | |||||||
| chr4:109753296 | A | AAATATTT others(44): Show |
1 | a0001c0001t0001g0147 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.905-794_905-793ins others(51): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753296 | |||||||
| chr4:109753296 | A | ATTTATTA others(1): Show |
66 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0020 others(63): Show |
69 | HG00280.hp2 HG00558.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.905-794_905-793ins others(8): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753296 | |||||||
| chr4:109753296 | A | ATTTATTA others(44): Show |
20 | a0001c0001t0001g0011 a0001c0001t0001g0264 a0001c0001t0001g0266 others(17): Show |
21 | HG00099.hp1 HG00639.hp1 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.905-794_905-793ins others(51): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753296 | |||||||
| chr4:109753310 | A | AATAAATA others(93): Show |
1 | a0002c0003t0001g0299 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.905-808_905-807ins others(100): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753310 | |||||||
| chr4:109753310 | A | ACATATAT others(4): Show |
1 | a0001c0001t0001g0236 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.905-808_905-807ins others(11): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753310 | |||||||
| chr4:109753311 | T | A | 1 | a0001c0001t0001g0236 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.905-808A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753311 | |||||||
| chr4:109753311 | T | C | 4 | a0001c0001t0001g0257 a0001c0001t0001g0259 a0001c0001t0003g0153 others(1): Show |
4 | HG03195.hp1 NA18950.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.905-808A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753311 | |||||||
| chr4:109753311 | T | TATATATT others(4): Show |
98 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(95): Show |
105 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.905-809_905-808ins others(11): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753311 | |||||||
| chr4:109753311 | T | TATATATT others(126): Show |
1 | a0002c0003t0001g0317 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.905-809_905-808ins others(133): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753311 | |||||||
| chr4:109753322 | T | A | 1 | a0001c0002t0001g0068 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.905-819A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753322 | |||||||
| chr4:109753324 | T | TATA | 3 | a0003c0004t0001g0154 a0003c0004t0001g0155 a0003c0004t0001g0297 |
3 | HG00738.hp1 HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.905-824_905-822dup others(3): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753324 | |||||||
| chr4:109753324 | T | TATAA | 84 | a0001c0001t0003g0153 a0001c0002t0001g0004 a0001c0002t0001g0005 others(81): Show |
86 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(83): Show |
intron_variant | MODIFIER | c.905-825_905-822dup others(4): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753324 | |||||||
| chr4:109753324 | T | TATAAATA others(87): Show |
2 | a0001c0001t0001g0148 a0002c0003t0001g0305 |
2 | HG03486.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.905-822_905-821ins others(94): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753324 | |||||||
| chr4:109753324 | T | TATATTTA others(7): Show |
2 | a0001c0002t0001g0068 a0001c0002t0001g0144 |
2 | NA18978.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.905-822_905-821ins others(14): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753324 | |||||||
| chr4:109753324 | T | TATATTTA others(8): Show |
7 | a0001c0001t0001g0163 a0001c0001t0001g0170 a0001c0001t0001g0177 others(4): Show |
7 | HG00280.hp1 HG01081.hp2 NA18983.hp1 others(4): Show |
intron_variant | MODIFIER | c.905-822_905-821ins others(15): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753324 | |||||||
| chr4:109753324 | T | TATATTTA others(50): Show |
7 | a0001c0002t0001g0288 a0001c0002t0001g0289 a0001c0002t0001g0291 others(4): Show |
7 | HG00735.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.905-822_905-821ins others(57): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753324 | |||||||
| chr4:109753328 | A | T | 1 | a0001c0002t0001g0277 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.905-825T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753328 | |||||||
| chr4:109753329 | A | T | 1 | a0001c0002t0001g0277 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.905-826T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753329 | |||||||
| chr4:109753338 | A | ATATATAT others(4): Show |
68 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0019 others(65): Show |
70 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.905-846_905-836dup others(11): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753338 | |||||||
| chr4:109753339 | T | TATATATT others(4): Show |
1 | a0001c0002t0001g0144 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.905-837_905-836ins others(11): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753339 | |||||||
| chr4:109753341 | T | A | 1 | a0001c0002t0001g0277 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.905-838A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753341 | |||||||
| chr4:109753350 | T | A | 9 | a0001c0001t0001g0148 a0001c0001t0001g0163 a0001c0001t0001g0170 others(6): Show |
9 | HG00280.hp1 HG01081.hp2 HG03486.hp2 others(6): Show |
intron_variant | MODIFIER | c.905-847A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753350 | |||||||
| chr4:109753352 | TATA | T | 212 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(209): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.905-852_905-850del others(3): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753352 | |||||||
| chr4:109753354 | T | TA | 8 | a0001c0002t0001g0139 a0001c0002t0001g0140 a0001c0002t0001g0285 others(5): Show |
8 | HG01975.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.905-852dupT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753354 | |||||||
| chr4:109753354 | T | TAAATAAA others(9): Show |
1 | a0001c0002t0001g0121 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.905-852_905-851ins others(16): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753354 | |||||||
| chr4:109753354 | T | TATTTATT others(5): Show |
3 | a0001c0001t0003g0153 a0001c0002t0001g0041 a0001c0002t0001g0042 |
3 | HG02886.hp1 HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.905-852_905-851ins others(12): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753354 | |||||||
| chr4:109753355 | A | AAATAAAT others(123): Show |
3 | a0001c0002t0001g0119 a0001c0002t0001g0128 a0001c0002t0001g0196 |
3 | HG01074.hp2 HG01243.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.905-853_905-852ins others(130): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753355 | |||||||
| chr4:109753355 | A | AAATATTT others(16): Show |
1 | a0002c0003t0001g0314 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.905-853_905-852ins others(23): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753355 | |||||||
| chr4:109753355 | A | AAATATTT others(44): Show |
4 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0149 others(1): Show |
4 | HG02723.hp2 HG03098.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.905-853_905-852ins others(51): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753355 | |||||||
| chr4:109753355 | A | ATTTATTA others(1): Show |
9 | a0001c0001t0001g0148 a0001c0001t0001g0163 a0001c0001t0001g0170 others(6): Show |
9 | HG00280.hp1 HG01081.hp2 HG03486.hp2 others(6): Show |
intron_variant | MODIFIER | c.905-853_905-852ins others(8): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753355 | |||||||
| chr4:109753355 | A | ATTTATTA others(44): Show |
1 | a0002c0003t0001g0248 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.905-853_905-852ins others(51): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753355 | |||||||
| chr4:109753356 | A | T | 9 | a0001c0001t0001g0320 a0001c0001t0001g0323 a0001c0001t0001g0324 others(6): Show |
9 | HG02486.hp2 HG02622.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.905-853T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753356 | |||||||
| chr4:109753358 | A | T | 1 | a0001c0001t0001g0221 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.905-855T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753358 | |||||||
| chr4:109753359 | A | T | 1 | a0001c0002t0001g0277 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.905-856T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753359 | |||||||
| chr4:109753370 | T | C | 1 | a0001c0002t0001g0121 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.905-867A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753370 | |||||||
| chr4:109753370 | T | TATATATT others(4): Show |
1 | a0001c0001t0003g0153 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.905-868_905-867ins others(11): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753370 | |||||||
| chr4:109753381 | T | A | 68 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0019 others(65): Show |
70 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(67): Show |
intron_variant | MODIFIER | c.905-878A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753381 | |||||||
| chr4:109753383 | T | TATA | 5 | a0001c0001t0001g0212 a0001c0001t0001g0232 a0001c0001t0001g0240 others(2): Show |
5 | NA18959.hp2 NA18982.hp1 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.905-883_905-881dup others(3): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753383 | |||||||
| chr4:109753383 | T | TATAA | 8 | a0001c0002t0001g0121 a0001c0002t0001g0139 a0001c0002t0001g0140 others(5): Show |
8 | HG01975.hp1 HG02280.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.905-884_905-881dup others(4): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753383 | |||||||
| chr4:109753383 | T | TATATTTA others(7): Show |
70 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0019 others(67): Show |
72 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.905-881_905-880ins others(14): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753383 | |||||||
| chr4:109753387 | A | T | 1 | a0001c0002t0002g0023 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.905-884T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753387 | |||||||
| chr4:109753388 | A | T | 1 | a0001c0002t0002g0023 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.905-885T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753388 | |||||||
| chr4:109753397 | A | ATATATAT others(4): Show |
1 | a0001c0002t0001g0121 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.905-905_905-895dup others(11): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753397 | |||||||
| chr4:109753401 | A | G | 1 | a0001c0002t0002g0023 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.905-898T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753401 | |||||||
| chr4:109753404 | TTTA | T | 5 | a0001c0002t0001g0068 a0001c0006t0005g0098 a0001c0006t0005g0099 others(2): Show |
5 | HG02647.hp1 HG03041.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.905-904_905-902del others(3): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753404 | |||||||
| chr4:109753404 | TTTATTAT others(7): Show |
T | 1 | a0001c0002t0002g0023 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.905-915_905-902del others(14): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753404 | |||||||
| chr4:109753405 | T | TTATTATA others(8): Show |
2 | a0001c0002t0001g0139 a0001c0002t0001g0140 |
2 | HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.905-917_905-903dup others(15): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753405 | |||||||
| chr4:109753411 | TATAA | T | 115 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(112): Show |
122 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.905-912_905-909del others(4): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753411 | |||||||
| chr4:109753412 | A | G | 1 | a0001c0001t0001g0228 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.905-909T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753412 | |||||||
| chr4:109753413 | TA | T | 178 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0014 others(175): Show |
187 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.905-911delT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753413 | |||||||
| chr4:109753415 | A | T | 3 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 |
3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-912T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753415 | |||||||
| chr4:109753416 | A | T | 3 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 |
3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-913T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753416 | |||||||
| chr4:109753418 | A | ATTAT | 3 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 |
3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-916_905-915ins others(4): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753418 | |||||||
| chr4:109753418 | A | ATTTAT | 18 | a0001c0001t0001g0303 a0001c0001t0001g0311 a0002c0003t0001g0299 others(15): Show |
18 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.905-916_905-915ins others(5): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753418 | |||||||
| chr4:109753419 | A | T | 1 | a0001c0001t0003g0153 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.905-916T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753419 | |||||||
| chr4:109753424 | T | A | 18 | a0001c0001t0001g0303 a0001c0001t0001g0311 a0002c0003t0001g0299 others(15): Show |
18 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.905-921A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753424 | |||||||
| chr4:109753424 | T | G | 3 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 |
3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-921A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753424 | |||||||
| chr4:109753428 | A | AAT | 184 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(181): Show |
193 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.905-927_905-926dup others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753428 | |||||||
| chr4:109753428 | A | T | 1 | a0001c0001t0003g0153 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.905-925T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753428 | |||||||
| chr4:109753429 | A | ATTT | 3 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 |
3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-927_905-926ins others(3): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753429 | |||||||
| chr4:109753429 | A | T | 19 | a0001c0001t0001g0303 a0001c0001t0001g0311 a0001c0002t0002g0023 others(16): Show |
19 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.905-926T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753429 | |||||||
| chr4:109753433 | ATT | A | 7 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(4): Show |
7 | HG02257.hp2 HG02717.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.905-932_905-931del others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753433 | |||||||
| chr4:109753434 | T | A | 1 | a0001c0001t0003g0153 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.905-931A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753434 | |||||||
| chr4:109753435 | T | A | 20 | a0001c0001t0001g0303 a0001c0001t0001g0311 a0001c0001t0003g0153 others(17): Show |
20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.905-932A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753435 | |||||||
| chr4:109753435 | T | TATA | 3 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 |
3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-933_905-932ins others(3): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753435 | |||||||
| chr4:109753436 | T | A | 18 | a0001c0001t0001g0303 a0001c0001t0001g0311 a0002c0003t0001g0299 others(15): Show |
18 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.905-933A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753436 | |||||||
| chr4:109753438 | T | TA | 18 | a0001c0001t0001g0303 a0001c0001t0001g0311 a0002c0003t0001g0299 others(15): Show |
18 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.905-936_905-935ins others(1): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753438 | |||||||
| chr4:109753439 | T | A | 1 | a0001c0002t0001g0121 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.905-936A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753439 | |||||||
| chr4:109753440 | A | T | 18 | a0001c0001t0001g0303 a0001c0001t0001g0311 a0002c0003t0001g0299 others(15): Show |
18 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.905-937T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753440 | |||||||
| chr4:109753441 | TATA | T | 83 | a0001c0001t0001g0163 a0001c0001t0001g0170 a0001c0001t0001g0176 others(80): Show |
85 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.905-941_905-939del others(3): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753441 | |||||||
| chr4:109753443 | T | TA | 3 | a0001c0002t0001g0139 a0001c0002t0001g0140 a0007c0013t0001g0290 |
3 | HG01975.hp1 HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.905-941dupT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753443 | |||||||
| chr4:109753443 | T | TAAATAAA others(9): Show |
1 | a0001c0002t0003g0280 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.905-941_905-940ins others(16): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753443 | |||||||
| chr4:109753446 | T | G | 1 | a0001c0002t0001g0060 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.905-943A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753446 | |||||||
| chr4:109753447 | A | G | 4 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 others(1): Show |
4 | HG02257.hp2 HG02976.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.905-944T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753447 | |||||||
| chr4:109753448 | A | T | 26 | a0001c0001t0001g0148 a0001c0001t0001g0303 a0001c0001t0001g0311 others(23): Show |
26 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(23): Show |
intron_variant | MODIFIER | c.905-945T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753448 | |||||||
| chr4:109753449 | A | T | 1 | a0001c0002t0001g0068 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.905-946T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753449 | |||||||
| chr4:109753452 | T | A | 4 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 others(1): Show |
4 | HG02257.hp2 HG02976.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.905-949A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753452 | |||||||
| chr4:109753452 | T | TTTA | 19 | a0001c0001t0001g0303 a0001c0001t0001g0311 a0001c0001t0003g0153 others(16): Show |
19 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.905-952_905-950dup others(3): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753452 | |||||||
| chr4:109753453 | T | A | 1 | a0001c0002t0001g0068 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.905-950A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753453 | |||||||
| chr4:109753453 | T | TTA | 61 | a0001c0001t0001g0011 a0001c0001t0001g0264 a0001c0001t0001g0265 others(58): Show |
63 | HG00099.hp1 HG00558.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.905-952_905-951dup others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753453 | |||||||
| chr4:109753455 | A | T | 4 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 others(1): Show |
4 | HG02257.hp2 HG02976.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.905-952T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753455 | |||||||
| chr4:109753456 | T | TA | 86 | a0001c0001t0001g0163 a0001c0001t0001g0170 a0001c0001t0001g0176 others(83): Show |
88 | HG00280.hp1 HG00323.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.905-954dupT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753456 | |||||||
| chr4:109753457 | A | AATATATA others(5): Show |
2 | a0001c0002t0001g0139 a0001c0002t0001g0140 |
2 | HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.905-955_905-954ins others(12): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753457 | |||||||
| chr4:109753457 | AT | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
103 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.905-955delA | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753457 | |||||||
| chr4:109753459 | A | AT | 3 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 |
3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-957dupA | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753459 | |||||||
| chr4:109753460 | T | A | 20 | a0001c0001t0001g0303 a0001c0001t0001g0311 a0001c0001t0003g0153 others(17): Show |
20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.905-957A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753460 | |||||||
| chr4:109753462 | T | A | 1 | a0001c0001t0001g0148 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.905-959A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753462 | |||||||
| chr4:109753463 | A | T | 1 | a0001c0002t0003g0280 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.905-960T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753463 | |||||||
| chr4:109753464 | T | TA | 5 | a0001c0002t0001g0281 a0001c0002t0001g0285 a0001c0002t0001g0286 others(2): Show |
5 | HG02809.hp1 HG02976.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.905-962_905-961ins others(1): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753464 | |||||||
| chr4:109753464 | T | TTTATTAT others(114): Show |
1 | a0007c0013t0001g0290 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.905-962_905-961ins others(121): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753464 | |||||||
| chr4:109753465 | T | A | 3 | a0001c0001t0001g0148 a0001c0002t0002g0023 a0002c0003t0001g0248 |
3 | HG02257.hp2 HG03486.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.905-962A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753465 | |||||||
| chr4:109753467 | A | AT | 4 | a0001c0001t0001g0199 a0001c0002t0001g0119 a0001c0002t0001g0128 others(1): Show |
4 | HG00738.hp2 HG01074.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.905-965dupA | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753467 | |||||||
| chr4:109753467 | A | T | 1 | a0001c0001t0001g0148 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.905-964T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753467 | |||||||
| chr4:109753468 | TATTAATA others(4): Show |
T | 103 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(100): Show |
110 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.905-976_905-966del others(11): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753468 | |||||||
| chr4:109753469 | AT | A | 75 | a0001c0001t0001g0148 a0001c0002t0001g0004 a0001c0002t0001g0005 others(72): Show |
77 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(74): Show |
intron_variant | MODIFIER | c.905-967delA | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753469 | |||||||
| chr4:109753470 | T | A | 20 | a0001c0001t0001g0303 a0001c0001t0001g0311 a0001c0001t0003g0153 others(17): Show |
20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.905-967A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753470 | |||||||
| chr4:109753470 | T | TA | 4 | a0001c0001t0001g0199 a0001c0002t0001g0119 a0001c0002t0001g0128 others(1): Show |
4 | HG00738.hp2 HG01074.hp2 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.905-968_905-967ins others(1): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753470 | |||||||
| chr4:109753471 | T | A | 6 | a0001c0002t0001g0121 a0001c0002t0001g0139 a0001c0002t0001g0140 others(3): Show |
6 | HG01975.hp1 HG02280.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.905-968A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753471 | |||||||
| chr4:109753472 | A | AT | 20 | a0001c0001t0001g0303 a0001c0001t0001g0311 a0001c0001t0003g0153 others(17): Show |
20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.905-970_905-969ins others(1): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753472 | |||||||
| chr4:109753472 | A | T | 3 | a0001c0001t0001g0220 a0001c0002t0001g0121 a0001c0002t0001g0144 |
3 | HG01167.hp1 NA19043.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.905-969T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753472 | |||||||
| chr4:109753475 | A | G | 3 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 |
3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-972T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753475 | |||||||
| chr4:109753476 | A | T | 26 | a0001c0001t0001g0148 a0001c0001t0001g0303 a0001c0001t0001g0311 others(23): Show |
26 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(23): Show |
intron_variant | MODIFIER | c.905-973T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753476 | |||||||
| chr4:109753477 | A | T | 20 | a0001c0001t0001g0303 a0001c0001t0001g0311 a0001c0001t0003g0153 others(17): Show |
20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.905-974T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753477 | |||||||
| chr4:109753479 | A | AAT | 3 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 |
3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-977_905-976ins others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753479 | |||||||
| chr4:109753479 | A | T | 1 | a0001c0002t0001g0144 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.905-976T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753479 | |||||||
| chr4:109753481 | T | A | 104 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(101): Show |
111 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.905-978A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753481 | |||||||
| chr4:109753481 | T | G | 1 | a0001c0002t0002g0023 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.905-978A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753481 | |||||||
| chr4:109753481 | T | TA | 20 | a0001c0001t0001g0303 a0001c0001t0001g0311 a0001c0001t0003g0153 others(17): Show |
20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.905-979_905-978ins others(1): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753481 | |||||||
| chr4:109753481 | T | TTATAATA others(9): Show |
3 | a0001c0002t0001g0119 a0001c0002t0001g0128 a0001c0002t0001g0196 |
3 | HG01074.hp2 HG01243.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.905-979_905-978ins others(16): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753481 | |||||||
| chr4:109753485 | A | T | 5 | a0001c0001t0001g0148 a0001c0002t0001g0288 a0001c0002t0001g0289 others(2): Show |
5 | HG00735.hp2 HG02055.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.905-982T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753485 | |||||||
| chr4:109753486 | A | T | 3 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 |
3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-983T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753486 | |||||||
| chr4:109753489 | A | T | 191 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0014 others(188): Show |
200 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(197): Show |
intron_variant | MODIFIER | c.905-986T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753489 | |||||||
| chr4:109753490 | A | ATT | 72 | a0001c0001t0001g0199 a0001c0002t0001g0004 a0001c0002t0001g0005 others(69): Show |
74 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(71): Show |
intron_variant | MODIFIER | c.905-988_905-987ins others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753490 | |||||||
| chr4:109753493 | TTTATAAT others(7): Show |
T | 4 | a0001c0002t0001g0288 a0001c0002t0001g0289 a0001c0002t0001g0291 others(1): Show |
4 | HG00735.hp2 HG02055.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.905-1004_905-991de others(15): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753493 | |||||||
| chr4:109753494 | T | TA | 75 | a0001c0001t0001g0199 a0001c0002t0001g0004 a0001c0002t0001g0005 others(72): Show |
77 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(74): Show |
intron_variant | MODIFIER | c.905-992_905-991ins others(1): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753494 | |||||||
| chr4:109753496 | A | C | 3 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 |
3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-993T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753496 | |||||||
| chr4:109753497 | TA | T | 89 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(86): Show |
95 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.905-995delT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753497 | |||||||
| chr4:109753498 | A | AT | 11 | a0001c0001t0001g0010 a0001c0001t0001g0156 a0001c0001t0001g0262 others(8): Show |
12 | HG00438.hp1 HG01074.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.905-996_905-995ins others(1): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753498 | |||||||
| chr4:109753498 | A | T | 4 | a0001c0002t0001g0121 a0001c0002t0003g0280 a0002c0003t0001g0248 others(1): Show |
4 | HG01975.hp1 HG02809.hp1 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.905-995T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753498 | |||||||
| chr4:109753499 | A | G | 1 | a0001c0002t0001g0068 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.905-996T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753499 | |||||||
| chr4:109753499 | A | T | 1 | a0001c0002t0002g0023 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.905-996T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753499 | |||||||
| chr4:109753500 | T | TAA | 72 | a0001c0001t0001g0199 a0001c0002t0001g0004 a0001c0002t0001g0005 others(69): Show |
74 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(71): Show |
intron_variant | MODIFIER | c.905-998_905-997ins others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753500 | |||||||
| chr4:109753501 | A | G | 3 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 |
3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-998T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753501 | |||||||
| chr4:109753503 | A | G | 2 | a0001c0001t0001g0173 a0001c0001t0001g0236 |
2 | HG02818.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.905-1000T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753503 | |||||||
| chr4:109753503 | AT | A | 3 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 |
3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-1001delA | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753503 | |||||||
| chr4:109753504 | T | A | 1 | a0001c0002t0001g0121 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.905-1001A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753504 | |||||||
| chr4:109753505 | T | A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(97): Show |
107 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.905-1002A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753505 | |||||||
| chr4:109753506 | T | A | 3 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 |
3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-1003A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753506 | |||||||
| chr4:109753506 | TA | T | 99 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(96): Show |
106 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.905-1004delT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753506 | |||||||
| chr4:109753507 | A | ATATATAT | 67 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0019 others(64): Show |
69 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(66): Show |
intron_variant | MODIFIER | c.905-1005_905-1004i others(9): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753507 | |||||||
| chr4:109753507 | A | ATGTATAT | 4 | a0001c0002t0001g0058 a0001c0002t0001g0062 a0001c0002t0001g0066 others(1): Show |
4 | NA18956.hp2 NA18969.hp2 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.905-1005_905-1004i others(9): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753507 | |||||||
| chr4:109753509 | T | A | 1 | a0002c0003t0001g0248 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.905-1006A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753509 | |||||||
| chr4:109753510 | A | T | 3 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 |
3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-1007T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753510 | |||||||
| chr4:109753512 | A | C | 1 | a0001c0002t0002g0023 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.905-1009T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753512 | |||||||
| chr4:109753513 | TA | T | 13 | a0001c0001t0001g0148 a0001c0001t0001g0163 a0001c0001t0001g0170 others(10): Show |
13 | HG00280.hp1 HG01081.hp2 HG02976.hp1 others(10): Show |
intron_variant | MODIFIER | c.905-1011delT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753513 | |||||||
| chr4:109753514 | A | AAATAAAT others(184): Show |
1 | a0007c0013t0001g0290 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.905-1012_905-1011i others(193): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753514 | |||||||
| chr4:109753514 | A | AATAAATA others(18): Show |
1 | a0001c0002t0001g0144 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.905-1012_905-1011i others(27): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753514 | |||||||
| chr4:109753514 | A | T | 176 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(173): Show |
185 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.905-1011T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753514 | |||||||
| chr4:109753515 | A | AATATTTA others(73): Show |
2 | a0001c0002t0001g0139 a0001c0002t0001g0140 |
2 | HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.905-1013_905-1012i others(82): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753515 | |||||||
| chr4:109753515 | A | ATAAATAT others(19): Show |
18 | a0001c0001t0001g0303 a0001c0001t0001g0311 a0002c0003t0001g0299 others(15): Show |
18 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.905-1013_905-1012i others(28): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753515 | |||||||
| chr4:109753515 | A | T | 1 | a0002c0003t0001g0248 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.905-1012T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753515 | |||||||
| chr4:109753516 | A | G | 1 | a0001c0002t0002g0023 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.905-1013T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753516 | |||||||
| chr4:109753516 | A | T | 3 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 |
3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-1013T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753516 | |||||||
| chr4:109753518 | A | T | 1 | a0002c0003t0001g0248 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.905-1015T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753518 | |||||||
| chr4:109753519 | A | T | 6 | a0001c0002t0001g0121 a0001c0002t0001g0285 a0001c0002t0001g0286 others(3): Show |
6 | HG02257.hp2 HG02976.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.905-1016T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753519 | |||||||
| chr4:109753520 | A | T | 1 | a0001c0002t0001g0121 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.905-1017T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753520 | |||||||
| chr4:109753521 | T | A | 1 | a0001c0002t0002g0023 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.905-1018A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753521 | |||||||
| chr4:109753522 | A | T | 1 | a0001c0002t0002g0023 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.905-1019T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753522 | |||||||
| chr4:109753524 | T | A | 3 | a0001c0002t0001g0139 a0001c0002t0001g0140 a0002c0003t0001g0248 |
3 | HG02280.hp2 HG03540.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.905-1021A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753524 | |||||||
| chr4:109753524 | T | TA | 4 | a0001c0002t0001g0121 a0001c0002t0001g0285 a0001c0002t0001g0286 others(1): Show |
4 | HG02976.hp1 HG03139.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.905-1022_905-1021i others(3): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753524 | |||||||
| chr4:109753526 | A | C | 3 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 |
3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-1023T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753526 | |||||||
| chr4:109753527 | TA | T | 9 | a0001c0001t0001g0163 a0001c0001t0001g0170 a0001c0001t0001g0176 others(6): Show |
9 | HG00280.hp1 HG01081.hp2 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.905-1025delT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753527 | |||||||
| chr4:109753529 | A | T | 1 | a0001c0002t0002g0023 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.905-1026T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753529 | |||||||
| chr4:109753530 | TAAATATT others(4): Show |
T | 4 | a0001c0006t0005g0098 a0001c0006t0005g0099 a0001c0008t0001g0272 others(1): Show |
4 | HG02647.hp1 HG03041.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.905-1038_905-1028d others(13): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753530 | |||||||
| chr4:109753531 | A | G | 3 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 |
3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-1028T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753531 | |||||||
| chr4:109753532 | A | T | 314 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(311): Show |
330 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(327): Show |
intron_variant | MODIFIER | c.905-1029T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753532 | |||||||
| chr4:109753535 | A | AAT | 3 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 |
3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-1033_905-1032i others(4): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753535 | |||||||
| chr4:109753539 | A | C | 1 | a0001c0002t0002g0023 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.905-1036T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753539 | |||||||
| chr4:109753541 | A | AT | 3 | a0001c0002t0001g0121 a0001c0002t0001g0139 a0001c0002t0001g0140 |
3 | HG02280.hp2 HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.905-1039_905-1038i others(3): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753541 | |||||||
| chr4:109753541 | A | T | 103 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0014 others(100): Show |
110 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.905-1038T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753541 | |||||||
| chr4:109753542 | A | T | 12 | a0001c0001t0001g0163 a0001c0001t0001g0170 a0001c0001t0001g0176 others(9): Show |
12 | HG00280.hp1 HG01081.hp2 HG02976.hp1 others(9): Show |
intron_variant | MODIFIER | c.905-1039T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753542 | |||||||
| chr4:109753543 | T | TA | 9 | a0001c0001t0001g0163 a0001c0001t0001g0170 a0001c0001t0001g0176 others(6): Show |
9 | HG00280.hp1 HG01081.hp2 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.905-1041dupT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753543 | |||||||
| chr4:109753544 | A | G | 1 | a0001c0002t0002g0023 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.905-1041T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753544 | |||||||
| chr4:109753546 | ATT | A | 3 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 |
3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-1045_905-1044d others(4): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753546 | |||||||
| chr4:109753547 | T | A | 9 | a0001c0001t0001g0163 a0001c0001t0001g0170 a0001c0001t0001g0176 others(6): Show |
9 | HG00280.hp1 HG01081.hp2 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.905-1044A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753547 | |||||||
| chr4:109753548 | T | A | 12 | a0001c0001t0001g0163 a0001c0001t0001g0170 a0001c0001t0001g0176 others(9): Show |
12 | HG00280.hp1 HG01081.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.905-1045A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753548 | |||||||
| chr4:109753549 | T | A | 1 | a0001c0002t0002g0023 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.905-1046A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753549 | |||||||
| chr4:109753549 | TA | T | 3 | a0001c0002t0001g0121 a0001c0002t0001g0139 a0001c0002t0001g0140 |
3 | HG02280.hp2 HG03540.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.905-1047delT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753549 | |||||||
| chr4:109753552 | TA | T | 9 | a0001c0001t0001g0163 a0001c0001t0001g0170 a0001c0001t0001g0176 others(6): Show |
9 | HG00280.hp1 HG01081.hp2 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.905-1050delT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753552 | |||||||
| chr4:109753553 | A | T | 1 | a0001c0002t0002g0023 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.905-1050T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753553 | |||||||
| chr4:109753554 | T | TA | 21 | a0001c0001t0001g0145 a0001c0001t0001g0160 a0001c0001t0001g0233 others(18): Show |
22 | HG00639.hp2 HG01070.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.905-1052dupT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753554 | |||||||
| chr4:109753554 | TATAAATA | T | 81 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0014 others(78): Show |
87 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.905-1058_905-1052d others(9): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753554 | |||||||
| chr4:109753555 | A | C | 3 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 |
3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-1052T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753555 | |||||||
| chr4:109753556 | TA | T | 11 | a0001c0001t0001g0163 a0001c0001t0001g0170 a0001c0001t0001g0176 others(8): Show |
11 | HG00280.hp1 HG01081.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.905-1054delT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753556 | |||||||
| chr4:109753557 | A | AAATATTT others(163): Show |
1 | a0001c0002t0003g0280 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.905-1055_905-1054i others(172): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753557 | |||||||
| chr4:109753557 | A | T | 4 | a0001c0001t0001g0148 a0001c0002t0001g0121 a0001c0002t0001g0139 others(1): Show |
4 | HG02280.hp2 HG03486.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.905-1054T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753557 | |||||||
| chr4:109753558 | A | ATGT | 3 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 |
3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-1056_905-1055i others(5): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753558 | |||||||
| chr4:109753558 | A | T | 22 | a0001c0001t0001g0145 a0001c0001t0001g0160 a0001c0001t0001g0221 others(19): Show |
23 | HG00639.hp2 HG01070.hp2 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.905-1055T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753558 | |||||||
| chr4:109753559 | A | G | 22 | a0001c0001t0001g0145 a0001c0001t0001g0160 a0001c0001t0001g0221 others(19): Show |
23 | HG00639.hp2 HG01070.hp2 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.905-1056T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753559 | |||||||
| chr4:109753559 | A | T | 1 | a0001c0002t0002g0023 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.905-1056T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753559 | |||||||
| chr4:109753562 | A | T | 32 | a0001c0001t0001g0145 a0001c0001t0001g0160 a0001c0001t0001g0163 others(29): Show |
33 | HG00280.hp1 HG00639.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.905-1059T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753562 | |||||||
| chr4:109753563 | A | T | 3 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 |
3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-1060T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753563 | |||||||
| chr4:109753564 | T | A | 22 | a0001c0001t0001g0145 a0001c0001t0001g0160 a0001c0001t0001g0221 others(19): Show |
23 | HG00639.hp2 HG01070.hp2 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.905-1061A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753564 | |||||||
| chr4:109753565 | A | T | 25 | a0001c0001t0001g0145 a0001c0001t0001g0160 a0001c0001t0001g0221 others(22): Show |
26 | HG00639.hp2 HG01070.hp2 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.905-1062T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753565 | |||||||
| chr4:109753567 | T | A | 3 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 |
3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-1064A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753567 | |||||||
| chr4:109753567 | T | G | 81 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0014 others(78): Show |
87 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.905-1064A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753567 | |||||||
| chr4:109753569 | A | C | 1 | a0001c0002t0002g0023 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.905-1066T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753569 | |||||||
| chr4:109753571 | A | T | 3 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 |
3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-1068T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753571 | |||||||
| chr4:109753571 | AAT | A | 9 | a0001c0001t0001g0163 a0001c0001t0001g0170 a0001c0001t0001g0176 others(6): Show |
9 | HG00280.hp1 HG01081.hp2 HG03195.hp1 others(6): Show |
intron_variant | MODIFIER | c.905-1070_905-1069d others(4): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753571 | |||||||
| chr4:109753572 | A | T | 22 | a0001c0001t0001g0145 a0001c0001t0001g0160 a0001c0001t0001g0221 others(19): Show |
23 | HG00639.hp2 HG01070.hp2 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.905-1069T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753572 | |||||||
| chr4:109753573 | T | TATATATT others(4): Show |
5 | a0001c0001t0001g0148 a0001c0002t0001g0121 a0001c0002t0001g0139 others(2): Show |
5 | HG02280.hp2 HG02809.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.905-1071_905-1070i others(13): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753573 | |||||||
| chr4:109753573 | TATA | T | 81 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0014 others(78): Show |
87 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.905-1073_905-1071d others(5): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753573 | |||||||
| chr4:109753574 | A | G | 1 | a0001c0002t0002g0023 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.905-1071T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753574 | |||||||
| chr4:109753576 | A | AT | 3 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 |
3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-1074dupA | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753576 | |||||||
| chr4:109753576 | ATATTTAT others(40): Show |
A | 1 | a0001c0001t0001g0221 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.905-1120_905-1074d others(49): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753576 | |||||||
| chr4:109753578 | A | T | 81 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0014 others(78): Show |
87 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.905-1075T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753578 | |||||||
| chr4:109753579 | T | A | 1 | a0001c0002t0002g0023 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.905-1076A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753579 | |||||||
| chr4:109753580 | T | A | 81 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0014 others(78): Show |
87 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.905-1077A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753580 | |||||||
| chr4:109753580 | T | C | 3 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 |
3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.905-1077A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753580 | |||||||
| chr4:109753580 | T | TATA | 10 | a0001c0001t0001g0145 a0001c0001t0001g0160 a0001c0001t0001g0233 others(7): Show |
11 | HG00639.hp2 HG01070.hp2 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.905-1078_905-1077i others(5): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753580 | |||||||
| chr4:109753580 | T | TATATAAT others(18): Show |
10 | a0001c0001t0001g0273 a0001c0001t0001g0320 a0001c0001t0001g0323 others(7): Show |
10 | HG02615.hp2 HG02622.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.905-1078_905-1077i others(27): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753580 | |||||||
| chr4:109753580 | T | TATATAAT others(40): Show |
1 | a0001c0002t0001g0138 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.905-1078_905-1077i others(49): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753580 | |||||||
| chr4:109753583 | T | A | 13 | a0001c0001t0001g0145 a0001c0001t0001g0160 a0001c0001t0001g0233 others(10): Show |
14 | HG00639.hp2 HG01070.hp2 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.905-1080A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753583 | |||||||
| chr4:109753584 | T | A | 1 | a0002c0003t0001g0248 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.905-1081A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753584 | |||||||
| chr4:109753585 | A | G | 13 | a0001c0001t0001g0145 a0001c0001t0001g0160 a0001c0001t0001g0233 others(10): Show |
14 | HG00639.hp2 HG01070.hp2 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.905-1082T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753585 | |||||||
| chr4:109753585 | A | T | 1 | a0002c0003t0001g0248 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.905-1082T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753585 | |||||||
| chr4:109753589 | AAATAAAT | A | 81 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0014 others(78): Show |
87 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.905-1093_905-1087d others(9): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753589 | |||||||
| chr4:109753590 | A | AT | 10 | a0001c0001t0001g0273 a0001c0001t0001g0320 a0001c0001t0001g0323 others(7): Show |
10 | HG02615.hp2 HG02622.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.905-1088_905-1087i others(3): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753590 | |||||||
| chr4:109753590 | A | T | 97 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(94): Show |
104 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.905-1087T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753590 | |||||||
| chr4:109753591 | A | G | 10 | a0001c0001t0001g0273 a0001c0001t0001g0320 a0001c0001t0001g0323 others(7): Show |
10 | HG02615.hp2 HG02622.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.905-1088T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753591 | |||||||
| chr4:109753591 | A | T | 110 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(107): Show |
118 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.905-1088T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753591 | |||||||
| chr4:109753593 | A | G | 1 | a0001c0002t0001g0138 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.905-1090T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753593 | |||||||
| chr4:109753593 | A | T | 13 | a0001c0001t0001g0145 a0001c0001t0001g0160 a0001c0001t0001g0233 others(10): Show |
14 | HG00639.hp2 HG01070.hp2 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.905-1090T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753593 | |||||||
| chr4:109753593 | AAATAT | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
103 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.905-1095_905-1091d others(7): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753593 | |||||||
| chr4:109753594 | A | T | 26 | a0001c0001t0001g0145 a0001c0001t0001g0160 a0001c0001t0001g0233 others(23): Show |
27 | HG00639.hp2 HG01070.hp2 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.905-1091T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753594 | |||||||
| chr4:109753595 | A | G | 1 | a0003c0004t0001g0297 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.905-1092T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753595 | |||||||
| chr4:109753596 | T | A | 10 | a0001c0001t0001g0273 a0001c0001t0001g0320 a0001c0001t0001g0323 others(7): Show |
10 | HG02615.hp2 HG02622.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.905-1093A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753596 | |||||||
| chr4:109753597 | A | T | 91 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0014 others(88): Show |
97 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.905-1094T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753597 | |||||||
| chr4:109753599 | T | A | 81 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0014 others(78): Show |
87 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.905-1096A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753599 | |||||||
| chr4:109753599 | T | G | 1 | a0001c0001t0001g0179 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.905-1096A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753599 | |||||||
| chr4:109753599 | T | TA | 14 | a0001c0001t0001g0145 a0001c0001t0001g0160 a0001c0001t0001g0233 others(11): Show |
15 | HG00639.hp2 HG01070.hp2 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.905-1097_905-1096i others(3): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753599 | |||||||
| chr4:109753601 | A | C | 4 | a0001c0002t0001g0124 a0001c0002t0001g0134 a0001c0002t0002g0023 others(1): Show |
4 | HG01243.hp2 HG01255.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.905-1098T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753601 | |||||||
| chr4:109753604 | A | T | 25 | a0001c0001t0001g0145 a0001c0001t0001g0160 a0001c0001t0001g0233 others(22): Show |
26 | HG00639.hp2 HG01070.hp2 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.905-1101T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753604 | |||||||
| chr4:109753606 | A | G | 82 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0014 others(79): Show |
88 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.905-1103T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753606 | |||||||
| chr4:109753608 | A | C | 6 | a0001c0001t0001g0145 a0001c0002t0001g0127 a0001c0002t0001g0141 others(3): Show |
6 | HG01070.hp2 HG01978.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.905-1105T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753608 | |||||||
| chr4:109753608 | A | G | 96 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
103 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.905-1105T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753608 | |||||||
| chr4:109753610 | A | T | 1 | a0001c0001t0001g0179 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.905-1107T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753610 | |||||||
| chr4:109753611 | T | A | 95 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0014 others(92): Show |
102 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.905-1108A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753611 | |||||||
| chr4:109753611 | T | TA | 96 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
103 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.905-1109_905-1108i others(3): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753611 | |||||||
| chr4:109753612 | T | A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(94): Show |
104 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.905-1109A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753612 | |||||||
| chr4:109753612 | T | TATATAAT others(6): Show |
1 | a0003c0004t0001g0297 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.905-1110_905-1109i others(15): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753612 | |||||||
| chr4:109753612 | T | TATCTAAT others(6): Show |
11 | a0001c0001t0001g0273 a0001c0001t0001g0320 a0001c0001t0001g0323 others(8): Show |
11 | HG02027.hp1 HG02615.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.905-1110_905-1109i others(15): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753612 | |||||||
| chr4:109753612 | T | TGTATAA | 12 | a0001c0001t0001g0145 a0001c0001t0001g0160 a0001c0001t0001g0233 others(9): Show |
13 | HG00639.hp2 HG01070.hp2 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.905-1110_905-1109i others(8): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753612 | |||||||
| chr4:109753612 | T | TGTATAAT others(86): Show |
1 | a0001c0001t0001g0325 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.905-1110_905-1109i others(95): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753612 | |||||||
| chr4:109753613 | TA | T | 82 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0014 others(79): Show |
88 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(85): Show |
intron_variant | MODIFIER | c.905-1111delT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753613 | |||||||
| chr4:109753614 | A | T | 121 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(118): Show |
129 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(126): Show |
intron_variant | MODIFIER | c.905-1111T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753614 | |||||||
| chr4:109753616 | T | A | 1 | a0002c0003t0001g0248 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.905-1113A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753616 | |||||||
| chr4:109753619 | A | AT | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(200): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.905-1117dupA | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753619 | |||||||
| chr4:109753623 | T | A | 203 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(200): Show |
217 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.905-1120A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753623 | |||||||
| chr4:109753630 | A | C | 78 | a0001c0001t0001g0011 a0001c0001t0001g0145 a0001c0001t0001g0146 others(75): Show |
81 | HG00099.hp1 HG00558.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.905-1127T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753630 | |||||||
| chr4:109753631 | A | T | 204 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(201): Show |
218 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.905-1128T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753631 | |||||||
| chr4:109753632 | T | A | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(202): Show |
219 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(216): Show |
intron_variant | MODIFIER | c.905-1129A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753632 | |||||||
| chr4:109753632 | T | TATGTATA others(80): Show |
1 | a0007c0013t0001g0290 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.905-1130_905-1129i others(89): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753632 | |||||||
| chr4:109753635 | G | T | 1 | a0002c0003t0001g0248 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.905-1132C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753635 | |||||||
| chr4:109753643 | T | A | 1 | a0002c0003t0001g0248 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.905-1140A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753643 | |||||||
| chr4:109753645 | A | T | 1 | a0002c0003t0001g0248 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.905-1142T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753645 | |||||||
| chr4:109753655 | T | A | 1 | a0002c0003t0001g0248 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.905-1152A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753655 | |||||||
| chr4:109753657 | A | T | 1 | a0002c0003t0001g0248 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.905-1154T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753657 | |||||||
| chr4:109753659 | A | ATAATGTA others(51): Show |
1 | a0001c0001t0001g0148 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.905-1157_905-1156i others(60): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753659 | |||||||
| chr4:109753659 | A | ATAATGTA others(80): Show |
1 | a0001c0002t0003g0280 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.905-1157_905-1156i others(89): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753659 | |||||||
| chr4:109753659 | A | ATAATGTA others(109): Show |
1 | a0001c0002t0001g0140 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.905-1157_905-1156i others(118): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753659 | |||||||
| chr4:109753659 | A | ATAATGTA others(167): Show |
5 | a0001c0002t0001g0275 a0001c0002t0001g0276 a0001c0002t0001g0277 others(2): Show |
5 | NA18959.hp2 NA18960.hp2 NA18980.hp2 others(2): Show |
intron_variant | MODIFIER | c.905-1157_905-1156i others(176): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753659 | |||||||
| chr4:109753659 | A | ATAATGTA others(167): Show |
1 | a0001c0002t0001g0077 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.905-1157_905-1156i others(176): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753659 | |||||||
| chr4:109753659 | A | C | 128 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(125): Show |
136 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(133): Show |
intron_variant | MODIFIER | c.905-1156T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753659 | |||||||
| chr4:109753663 | T | C | 3 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 |
3 | HG02559.hp2 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.905-1160A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753663 | |||||||
| chr4:109753664 | G | A | 1 | a0002c0003t0001g0248 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.905-1161C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753664 | |||||||
| chr4:109753669 | A | T | 1 | a0002c0003t0001g0248 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.905-1166T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753669 | |||||||
| chr4:109753681 | A | T | 1 | a0002c0003t0001g0248 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.905-1178T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753681 | |||||||
| chr4:109753688 | A | ATAATGTA others(51): Show |
1 | a0001c0002t0001g0121 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.905-1186_905-1185i others(60): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753688 | |||||||
| chr4:109753688 | A | ATAATGTA others(196): Show |
4 | a0004c0005t0001g0086 a0004c0005t0001g0087 a0004c0005t0001g0088 others(1): Show |
4 | NA18941.hp2 NA18999.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.905-1186_905-1185i others(205): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753688 | |||||||
| chr4:109753688 | A | ATAATGTA others(225): Show |
2 | a0001c0002t0001g0041 a0001c0002t0001g0042 |
2 | HG02886.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.905-1186_905-1185i others(234): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753688 | |||||||
| chr4:109753688 | A | ATAATGTA others(167): Show |
7 | a0001c0002t0001g0005 a0001c0002t0001g0019 a0001c0002t0001g0051 others(4): Show |
8 | HG00558.hp1 HG01167.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.905-1186_905-1185i others(176): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753688 | |||||||
| chr4:109753688 | A | ATAATGTA others(196): Show |
1 | a0001c0002t0001g0043 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.905-1186_905-1185i others(205): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753688 | |||||||
| chr4:109753688 | A | C | 242 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(239): Show |
256 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.905-1185T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753688 | |||||||
| chr4:109753689 | T | A | 1 | a0002c0003t0001g0248 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.905-1186A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753689 | |||||||
| chr4:109753690 | A | T | 1 | a0002c0003t0001g0248 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.905-1187T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753690 | |||||||
| chr4:109753692 | T | C | 3 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 |
3 | HG02559.hp2 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.905-1189A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753692 | |||||||
| chr4:109753700 | T | C | 1 | a0003c0004t0001g0297 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.905-1197A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753700 | |||||||
| chr4:109753713 | T | TTATCTAA others(225): Show |
1 | a0001c0002t0001g0068 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.905-1211_905-1210i others(234): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753713 | |||||||
| chr4:109753717 | A | C | 301 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(298): Show |
316 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.905-1214T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753717 | |||||||
| chr4:109753717 | ATAATGTA others(22): Show |
A | 2 | a0003c0004t0001g0154 a0003c0004t0001g0155 |
2 | HG00738.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.905-1243_905-1215d others(31): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753717 | |||||||
| chr4:109753721 | T | C | 3 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 |
3 | HG02559.hp2 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.905-1218A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753721 | |||||||
| chr4:109753729 | T | C | 1 | a0003c0004t0001g0297 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.905-1226A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753729 | |||||||
| chr4:109753742 | T | A | 18 | a0001c0002t0001g0005 a0001c0002t0001g0019 a0001c0002t0001g0043 others(15): Show |
19 | HG00558.hp1 HG00733.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.905-1239A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753742 | |||||||
| chr4:109753746 | C | A | 2 | a0001c0002t0001g0061 a0003c0004t0001g0297 |
2 | HG03579.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.905-1243G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753746 | |||||||
| chr4:109753750 | T | C | 3 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 |
3 | HG02559.hp2 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.905-1247A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753750 | |||||||
| chr4:109753758 | T | C | 1 | a0003c0004t0001g0297 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.905-1255A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753758 | |||||||
| chr4:109753775 | C | A | 4 | a0001c0001t0001g0201 a0001c0001t0001g0226 a0001c0001t0001g0228 others(1): Show |
4 | HG00735.hp1 HG01123.hp1 HG03017.hp2 others(1): Show |
intron_variant | MODIFIER | c.905-1272G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753775 | |||||||
| chr4:109753787 | T | C | 1 | a0003c0004t0001g0297 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.905-1284A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753787 | |||||||
| chr4:109753804 | C | A | 114 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(111): Show |
124 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.905-1301G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753804 | |||||||
| chr4:109753816 | T | C | 3 | a0003c0004t0001g0154 a0003c0004t0001g0155 a0003c0004t0001g0297 |
3 | HG00738.hp1 HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.905-1313A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753816 | |||||||
| chr4:109753816 | TTTATATT others(22): Show |
T | 23 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(20): Show |
23 | HG00673.hp1 HG00735.hp2 HG02027.hp2 others(20): Show |
intron_variant | MODIFIER | c.905-1342_905-1314d others(31): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753816 | |||||||
| chr4:109753825 | T | C | 2 | a0001c0001t0003g0334 a0001c0001t0003g0335 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.905-1322A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753825 | |||||||
| chr4:109753833 | A | ATAATGTA others(195): Show |
1 | a0001c0002t0001g0067 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.905-1331_905-1330i others(204): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753833 | |||||||
| chr4:109753833 | A | ATAATGTA others(196): Show |
41 | a0001c0002t0001g0004 a0001c0002t0001g0033 a0001c0002t0001g0034 others(38): Show |
42 | HG01069.hp1 HG01070.hp1 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.905-1331_905-1330i others(205): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753833 | |||||||
| chr4:109753833 | A | ATAATGTA others(225): Show |
2 | a0001c0002t0001g0065 a0001c0002t0001g0081 |
2 | NA18966.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.905-1331_905-1330i others(234): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753833 | |||||||
| chr4:109753833 | A | ATAATGTA others(196): Show |
1 | a0001c0002t0001g0083 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.905-1331_905-1330i others(205): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753833 | |||||||
| chr4:109753833 | A | ATAATGTA others(22): Show |
1 | a0001c0001t0003g0013 | 2 | HG02258.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.905-1331_905-1330i others(31): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753833 | |||||||
| chr4:109753833 | A | ATAATGTA others(109): Show |
2 | a0001c0008t0001g0272 a0001c0008t0002g0271 |
2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.905-1331_905-1330i others(118): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753833 | |||||||
| chr4:109753833 | A | C | 76 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0156 others(73): Show |
79 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.905-1330T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753833 | |||||||
| chr4:109753845 | C | T | 299 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(296): Show |
315 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.905-1342G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753845 | |||||||
| chr4:109753857 | A | AATATCTA others(195): Show |
1 | a0001c0002t0001g0056 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.905-1355_905-1354i others(204): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753857 | |||||||
| chr4:109753858 | T | A | 1 | a0001c0002t0001g0056 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.905-1355A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753858 | |||||||
| chr4:109753862 | A | ATAATGTA others(225): Show |
3 | a0001c0002t0001g0039 a0001c0002t0001g0040 a0006c0014t0001g0038 |
3 | HG01069.hp2 HG01106.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.905-1360_905-1359i others(234): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753862 | |||||||
| chr4:109753862 | A | ATAATGTA others(225): Show |
1 | a0001c0002t0001g0035 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.905-1360_905-1359i others(234): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753862 | |||||||
| chr4:109753862 | A | ATAATGTA others(225): Show |
2 | a0001c0002t0001g0061 a0001c0002t0001g0073 |
2 | NA18950.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.905-1360_905-1359i others(234): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753862 | |||||||
| chr4:109753862 | A | C | 282 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(279): Show |
298 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(295): Show |
intron_variant | MODIFIER | c.905-1359T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753862 | |||||||
| chr4:109753874 | T | C | 2 | a0003c0004t0001g0154 a0003c0004t0001g0155 |
2 | HG00738.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.905-1371A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753874 | |||||||
| chr4:109753891 | A | C | 293 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(290): Show |
308 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(305): Show |
intron_variant | MODIFIER | c.905-1388T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753891 | |||||||
| chr4:109753895 | T | TGTATAAT others(51): Show |
1 | a0001c0002t0001g0139 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.905-1393_905-1392i others(60): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753895 | |||||||
| chr4:109753920 | C | A | 3 | a0002c0003t0001g0310 a0003c0004t0001g0154 a0003c0004t0001g0155 |
3 | HG00738.hp1 HG02886.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.905-1417G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753920 | |||||||
| chr4:109753935 | A | ATATTATA others(138): Show |
2 | a0001c0006t0005g0098 a0001c0006t0005g0099 |
2 | HG02647.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.905-1433_905-1432i others(147): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753935 | |||||||
| chr4:109753984 | T | A | 14 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0156 others(11): Show |
16 | HG00099.hp1 HG00438.hp1 HG00639.hp1 others(13): Show |
intron_variant | MODIFIER | c.905-1481A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109753984 | |||||||
| chr4:109754038 | C | T | 1 | a0001c0002t0001g0037 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.905-1535G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109754038 | |||||||
| chr4:109754069 | C | T | 1 | a0001c0002t0001g0139 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.905-1566G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109754069 | |||||||
| chr4:109754086 | C | T | 4 | a0001c0002t0001g0288 a0001c0002t0001g0289 a0001c0002t0001g0291 others(1): Show |
4 | HG00735.hp2 HG02055.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.905-1583G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109754086 | |||||||
| chr4:109754109 | G | C | 1 | a0007c0013t0001g0290 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.905-1606C>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109754109 | |||||||
| chr4:109754200 | T | C | 236 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(233): Show |
250 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.905-1697A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109754200 | |||||||
| chr4:109754209 | C | T | 19 | a0001c0001t0001g0303 a0001c0001t0001g0311 a0002c0003t0001g0248 others(16): Show |
19 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.905-1706G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109754209 | |||||||
| chr4:109754217 | C | T | 2 | a0001c0006t0005g0098 a0001c0006t0005g0099 |
2 | HG02647.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.905-1714G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109754217 | |||||||
| chr4:109754229 | G | A | 12 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 others(9): Show |
12 | HG00735.hp2 HG02055.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.905-1726C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109754229 | |||||||
| chr4:109754412 | T | TA | 104 | a0001c0001t0001g0178 a0001c0001t0001g0311 a0001c0001t0001g0321 others(101): Show |
106 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(103): Show |
intron_variant | MODIFIER | c.905-1910dupT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109754412 | |||||||
| chr4:109754412 | T | TAA | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(207): Show |
224 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.905-1911_905-1910d others(4): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109754412 | |||||||
| chr4:109754412 | T | TAAA | 6 | a0001c0001t0001g0251 a0001c0001t0001g0253 a0001c0001t0001g0263 others(3): Show |
6 | HG00438.hp1 HG02109.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.905-1912_905-1910d others(5): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109754412 | |||||||
| chr4:109754427 | G | A | 19 | a0001c0001t0001g0303 a0001c0001t0001g0311 a0002c0003t0001g0248 others(16): Show |
19 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.905-1924C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109754427 | |||||||
| chr4:109754429 | A | G | 6 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(3): Show |
6 | HG02572.hp1 HG02723.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.905-1926T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109754429 | |||||||
| chr4:109754434 | C | CT | 85 | a0001c0001t0001g0245 a0001c0001t0001g0282 a0001c0001t0001g0283 others(82): Show |
87 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.905-1932dupA | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109754434 | |||||||
| chr4:109754434 | CT | C | 6 | a0001c0001t0001g0162 a0001c0001t0001g0205 a0001c0001t0001g0208 others(3): Show |
6 | HG02109.hp2 HG02155.hp2 NA19043.hp2 others(3): Show |
intron_variant | MODIFIER | c.905-1932delA | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109754434 | |||||||
| chr4:109754583 | G | C | 1 | a0003c0004t0001g0297 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.905-2080C>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109754583 | |||||||
| chr4:109754621 | C | T | 1 | a0001c0001t0003g0153 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.905-2118G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109754621 | |||||||
| chr4:109754630 | G | GCAATCCT others(15): Show |
1 | a0001c0001t0001g0186 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.905-2149_905-2128d others(24): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109754630 | |||||||
| chr4:109754699 | C | T | 1 | a0001c0001t0001g0206 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.905-2196G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109754699 | |||||||
| chr4:109754762 | G | C | 322 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(319): Show |
338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.905-2259C>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109754762 | |||||||
| chr4:109754986 | C | A | 333 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(330): Show |
350 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(347): Show |
intron_variant | MODIFIER | c.905-2483G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109754986 | |||||||
| chr4:109755287 | A | G | 322 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(319): Show |
338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.904+2476T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109755287 | |||||||
| chr4:109755317 | G | A | 19 | a0001c0001t0001g0303 a0001c0001t0001g0311 a0002c0003t0001g0248 others(16): Show |
19 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.904+2446C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109755317 | |||||||
| chr4:109755502 | T | C | 19 | a0001c0001t0001g0303 a0001c0001t0001g0311 a0002c0003t0001g0248 others(16): Show |
19 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.904+2261A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109755502 | |||||||
| chr4:109755607 | G | C | 1 | a0001c0001t0003g0013 | 2 | HG02258.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.904+2156C>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109755607 | |||||||
| chr4:109755898 | A | G | 1 | a0007c0013t0001g0290 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.904+1865T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109755898 | |||||||
| chr4:109755965 | C | G | 1 | a0001c0002t0001g0287 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.904+1798G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109755965 | |||||||
| chr4:109756071 | A | G | 1 | a0003c0004t0001g0157 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.904+1692T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756071 | |||||||
| chr4:109756206 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.904+1557C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756206 | |||||||
| chr4:109756253 | G | A | 1 | a0007c0013t0001g0290 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.904+1510C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756253 | |||||||
| chr4:109756278 | C | A | 1 | a0002c0003t0001g0300 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.904+1485G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756278 | |||||||
| chr4:109756289 | G | A | 1 | a0002c0003t0001g0300 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.904+1474C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756289 | |||||||
| chr4:109756310 | A | C | 4 | a0001c0002t0001g0288 a0001c0002t0001g0289 a0001c0002t0001g0291 others(1): Show |
4 | HG00735.hp2 HG02055.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.904+1453T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756310 | |||||||
| chr4:109756374 | C | T | 19 | a0001c0001t0001g0303 a0001c0001t0001g0311 a0002c0003t0001g0248 others(16): Show |
19 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.904+1389G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756374 | |||||||
| chr4:109756387 | GGAA | G | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(153): Show |
169 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.904+1373_904+1375d others(5): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756387 | |||||||
| chr4:109756401 | A | T | 1 | a0001c0002t0001g0083 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.904+1362T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756401 | |||||||
| chr4:109756440 | AAGG | A | 75 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0019 others(72): Show |
77 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(74): Show |
intron_variant | MODIFIER | c.904+1320_904+1322d others(5): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756440 | |||||||
| chr4:109756573 | C | G | 85 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0019 others(82): Show |
87 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.904+1190G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756573 | |||||||
| chr4:109756752 | C | A | 6 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0269 others(3): Show |
6 | HG02165.hp2 HG02698.hp1 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.904+1011G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756752 | |||||||
| chr4:109756769 | G | T | 1 | a0001c0001t0001g0336 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.904+994C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756769 | |||||||
| chr4:109756837 | CTACAAGA others(5): Show |
C | 1 | a0001c0002t0001g0097 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.904+914_904+925del others(12): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756837 | |||||||
| chr4:109756875 | AGAAAGAA others(6): Show |
A | 1 | a0001c0001t0001g0208 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.904+875_904+887del others(13): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756875 | |||||||
| chr4:109756880 | GAAAGAAA others(7): Show |
G | 1 | a0001c0002t0001g0142 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.904+869_904+882del others(14): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756880 | |||||||
| chr4:109756885 | A | G | 19 | a0001c0001t0001g0303 a0001c0001t0001g0311 a0002c0003t0001g0248 others(16): Show |
19 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.904+878T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756885 | |||||||
| chr4:109756888 | G | A | 19 | a0001c0001t0001g0303 a0001c0001t0001g0311 a0002c0003t0001g0248 others(16): Show |
19 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.904+875C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756888 | |||||||
| chr4:109756888 | G | GGAAA | 18 | a0001c0001t0001g0014 a0001c0001t0001g0156 a0001c0001t0001g0179 others(15): Show |
18 | HG00323.hp2 HG00733.hp1 HG01109.hp2 others(15): Show |
intron_variant | MODIFIER | c.904+871_904+874dup others(4): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756888 | |||||||
| chr4:109756888 | G | GGAAAGAA | 3 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0003g0153 |
3 | HG02723.hp2 HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.904+868_904+874dup others(7): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756888 | |||||||
| chr4:109756888 | G | GGAAAGAA others(1): Show |
14 | a0001c0001t0001g0014 a0001c0001t0001g0201 a0001c0001t0001g0267 others(11): Show |
14 | HG00099.hp1 HG00735.hp1 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.904+867_904+874dup others(8): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756888 | |||||||
| chr4:109756888 | G | GGAAAGAA others(5): Show |
4 | a0001c0001t0001g0151 a0001c0001t0001g0245 a0001c0002t0001g0104 others(1): Show |
4 | HG01109.hp1 HG02622.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.904+863_904+874dup others(12): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756888 | |||||||
| chr4:109756888 | G | GGAAAGAA others(9): Show |
7 | a0001c0001t0001g0230 a0001c0002t0001g0041 a0001c0002t0001g0052 others(4): Show |
7 | HG00558.hp1 HG02055.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.904+859_904+874dup others(16): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756888 | |||||||
| chr4:109756888 | G | GGAAAGAA others(13): Show |
3 | a0001c0002t0001g0062 a0001c0002t0001g0093 a0004c0005t0001g0086 |
3 | HG02148.hp1 NA18941.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.904+855_904+874dup others(20): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756888 | |||||||
| chr4:109756888 | G | GGAAAGAA others(17): Show |
1 | a0004c0005t0001g0095 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.904+851_904+874dup others(24): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756888 | |||||||
| chr4:109756888 | G | GGAAAGAA others(4): Show |
1 | a0001c0001t0001g0145 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.904+874_904+875ins others(11): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756888 | |||||||
| chr4:109756888 | G | GGAAAGAA others(8): Show |
1 | a0001c0001t0001g0146 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.904+874_904+875ins others(15): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756888 | |||||||
| chr4:109756888 | G | GGAAAGAA others(12): Show |
1 | a0001c0001t0001g0147 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.904+874_904+875ins others(19): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756888 | |||||||
| chr4:109756888 | G | GGAAAGAA others(24): Show |
1 | a0001c0001t0001g0150 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.904+874_904+875ins others(31): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756888 | |||||||
| chr4:109756888 | GGAAA | G | 42 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0015 others(39): Show |
44 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.904+871_904+874del others(4): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756888 | |||||||
| chr4:109756888 | GGAAAGAA others(1): Show |
G | 39 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0015 others(36): Show |
40 | HG00280.hp2 HG00673.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.904+867_904+874del others(8): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756888 | |||||||
| chr4:109756888 | GGAAAGAA others(5): Show |
G | 42 | a0001c0001t0001g0008 a0001c0001t0001g0084 a0001c0001t0001g0085 others(39): Show |
42 | HG00544.hp1 HG00733.hp2 HG00741.hp1 others(39): Show |
intron_variant | MODIFIER | c.904+863_904+874del others(12): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756888 | |||||||
| chr4:109756888 | GGAAAGAA others(9): Show |
G | 31 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(28): Show |
33 | HG00099.hp2 HG01168.hp2 HG01257.hp1 others(30): Show |
intron_variant | MODIFIER | c.904+859_904+874del others(16): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756888 | |||||||
| chr4:109756888 | GGAAAGAA others(13): Show |
G | 35 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0197 others(32): Show |
35 | HG00438.hp2 HG00558.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.904+855_904+874del others(20): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756888 | |||||||
| chr4:109756888 | GGAAAGAA others(17): Show |
G | 22 | a0001c0001t0001g0161 a0001c0001t0001g0164 a0001c0001t0001g0169 others(19): Show |
22 | HG01070.hp2 HG01168.hp1 HG01169.hp2 others(19): Show |
intron_variant | MODIFIER | c.904+851_904+874del others(24): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756888 | |||||||
| chr4:109756888 | GGAAAGAA others(21): Show |
G | 3 | a0001c0001t0001g0195 a0001c0002t0001g0123 a0001c0002t0002g0126 |
3 | HG03453.hp1 HG03491.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.904+847_904+874del others(28): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756888 | |||||||
| chr4:109756888 | GGAAAGAA others(25): Show |
G | 6 | a0001c0001t0001g0193 a0001c0002t0001g0061 a0001c0002t0001g0073 others(3): Show |
6 | HG01255.hp2 HG01346.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.904+843_904+874del others(32): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756888 | |||||||
| chr4:109756888 | GGAAAGAA others(37): Show |
G | 1 | a0001c0002t0001g0006 | 2 | NA18970.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.904+831_904+874del others(44): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756888 | |||||||
| chr4:109756889 | GAAAGAAA others(7): Show |
G | 1 | a0001c0001t0001g0192 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.904+860_904+873del others(14): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756889 | |||||||
| chr4:109756889 | GAAAGAAA others(10): Show |
G | 1 | a0001c0001t0001g0246 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.904+857_904+873del others(17): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756889 | |||||||
| chr4:109756898 | A | G | 1 | a0003c0004t0001g0155 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.904+865T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756898 | |||||||
| chr4:109756906 | A | G | 1 | a0003c0004t0001g0154 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.904+857T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756906 | |||||||
| chr4:109756918 | A | AAAGAAAG others(87): Show |
1 | a0002c0003t0001g0299 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.904+844_904+845ins others(94): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756918 | |||||||
| chr4:109756918 | A | AAAGAAAG others(98): Show |
1 | a0002c0003t0001g0312 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.904+844_904+845ins others(105): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756918 | |||||||
| chr4:109756922 | A | AAAGAAAG others(100): Show |
1 | a0002c0003t0001g0302 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.904+840_904+841ins others(107): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756922 | |||||||
| chr4:109756922 | A | AAAGAAAG others(96): Show |
1 | a0002c0003t0001g0305 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.904+840_904+841ins others(103): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756922 | |||||||
| chr4:109756926 | A | AAAGAAAG others(90): Show |
1 | a0002c0003t0001g0301 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.904+836_904+837ins others(97): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756926 | |||||||
| chr4:109756930 | A | AAAGAAAG others(96): Show |
1 | a0001c0001t0001g0311 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.904+832_904+833ins others(103): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756930 | |||||||
| chr4:109756930 | A | AAAGAAAG others(100): Show |
1 | a0001c0001t0001g0303 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.904+832_904+833ins others(107): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756930 | |||||||
| chr4:109756934 | A | AAAGAAAG others(112): Show |
1 | a0002c0003t0001g0317 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.904+828_904+829ins others(119): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756934 | |||||||
| chr4:109756934 | A | AAAGAAAG others(107): Show |
1 | a0002c0003t0001g0307 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.904+828_904+829ins others(114): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756934 | |||||||
| chr4:109756934 | A | AAAGAAAG others(96): Show |
1 | a0002c0003t0001g0313 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.904+828_904+829ins others(103): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756934 | |||||||
| chr4:109756934 | A | AAAGAAAG others(88): Show |
1 | a0002c0003t0001g0306 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.904+828_904+829ins others(95): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756934 | |||||||
| chr4:109756934 | A | AAAGAAAG others(80): Show |
1 | a0002c0003t0001g0318 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.904+828_904+829ins others(87): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756934 | |||||||
| chr4:109756934 | A | AAAGAAAG others(84): Show |
1 | a0002c0003t0001g0248 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.904+828_904+829ins others(91): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756934 | |||||||
| chr4:109756934 | A | AAAGAAAG others(75): Show |
1 | a0002c0003t0001g0309 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.904+828_904+829ins others(82): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756934 | |||||||
| chr4:109756934 | A | AAAGAAAG others(76): Show |
1 | a0002c0003t0001g0308 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.904+828_904+829ins others(83): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756934 | |||||||
| chr4:109756934 | A | AAAGAAAG others(80): Show |
1 | a0002c0003t0001g0310 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.904+828_904+829ins others(87): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756934 | |||||||
| chr4:109756938 | A | AAAGAAAG others(72): Show |
1 | a0002c0003t0001g0314 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.904+824_904+825ins others(79): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756938 | |||||||
| chr4:109756942 | A | AAAGAAAG others(76): Show |
1 | a0002c0003t0001g0315 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.904+820_904+821ins others(83): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756942 | |||||||
| chr4:109756949 | G | GGAAGGAA others(91): Show |
1 | a0002c0003t0001g0300 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.904+813_904+814ins others(98): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756949 | |||||||
| chr4:109756955 | AAGAAAGA others(15): Show |
A | 1 | a0001c0001t0001g0172 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.904+786_904+807del others(22): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756955 | |||||||
| chr4:109756961 | G | T | 1 | a0001c0002t0002g0107 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.904+802C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756961 | |||||||
| chr4:109756965 | G | T | 1 | a0001c0002t0002g0107 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.904+798C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756965 | |||||||
| chr4:109756967 | AAGAAAGA others(3): Show |
A | 1 | a0001c0002t0001g0288 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.904+786_904+795del others(10): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756967 | |||||||
| chr4:109756969 | G | T | 3 | a0001c0002t0002g0101 a0001c0002t0002g0107 a0001c0002t0002g0126 |
3 | HG01255.hp2 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.904+794C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756969 | |||||||
| chr4:109756970 | A | G | 3 | a0001c0001t0001g0273 a0001c0001t0001g0316 a0001c0001t0002g0332 |
3 | HG02615.hp2 HG02738.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.904+793T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756970 | |||||||
| chr4:109756973 | G | T | 16 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0162 others(13): Show |
16 | HG01255.hp2 HG01515.hp1 HG01515.hp2 others(13): Show |
intron_variant | MODIFIER | c.904+790C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756973 | |||||||
| chr4:109756977 | G | T | 77 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0012 others(74): Show |
79 | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.904+786C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756977 | |||||||
| chr4:109756978 | A | T | 2 | a0001c0001t0001g0172 a0003c0004t0001g0154 |
2 | HG00544.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.904+785T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756978 | |||||||
| chr4:109756979 | A | AAGAAAGA others(19): Show |
1 | a0004c0005t0001g0088 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.904+783_904+784ins others(26): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109756979 | |||||||
| chr4:109757195 | AT | A | 6 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 others(3): Show |
6 | HG00738.hp1 HG02257.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.904+567delA | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109757195 | |||||||
| chr4:109757275 | C | T | 4 | a0001c0001t0001g0063 a0001c0001t0001g0084 a0001c0001t0001g0085 others(1): Show |
4 | HG01123.hp2 HG01515.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.904+488G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109757275 | |||||||
| chr4:109757276 | C | CA | 73 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0019 others(70): Show |
75 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(72): Show |
intron_variant | MODIFIER | c.904+486dupT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109757276 | |||||||
| chr4:109757420 | C | T | 1 | a0001c0002t0001g0121 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.904+343G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109757420 | |||||||
| chr4:109757663 | CA | C | 135 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(132): Show |
138 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.904+99delT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 7/12 | chr4 | 109757663 | |||||||
| chr4:109757790 | A | G | 10 | a0001c0002t0001g0005 a0001c0002t0001g0019 a0001c0002t0001g0043 others(7): Show |
11 | HG00558.hp1 HG00733.hp1 HG01167.hp2 others(8): Show |
splice_region_variant&intron_variant | LOW | c.884-7T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109757790 | |||||||
| chr4:109757801 | A | C | 1 | a0001c0001t0001g0146 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.884-18T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109757801 | |||||||
| chr4:109757823 | T | TTTTAA | 321 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(318): Show |
337 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.884-41_884-40insTT others(3): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109757823 | |||||||
| chr4:109757827 | G | T | 1 | a0001c0001t0001g0146 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.884-44C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109757827 | |||||||
| chr4:109757829 | A | G | 1 | a0001c0001t0001g0146 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.884-46T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109757829 | |||||||
| chr4:109757846 | G | T | 322 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(319): Show |
338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.884-63C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109757846 | |||||||
| chr4:109758043 | C | G | 3 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 |
3 | HG02559.hp2 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.884-260G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109758043 | |||||||
| chr4:109758060 | T | C | 1 | a0007c0013t0001g0290 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.884-277A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109758060 | |||||||
| chr4:109758113 | C | T | 1 | a0007c0013t0001g0290 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.884-330G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109758113 | |||||||
| chr4:109758222 | T | C | 322 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(319): Show |
338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.884-439A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109758222 | |||||||
| chr4:109758300 | C | T | 1 | a0001c0002t0001g0034 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.884-517G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109758300 | |||||||
| chr4:109758814 | C | T | 1 | a0001c0001t0001g0162 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.884-1031G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109758814 | |||||||
| chr4:109758836 | T | C | 21 | a0001c0001t0001g0163 a0001c0001t0001g0303 a0001c0001t0001g0304 others(18): Show |
21 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.884-1053A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109758836 | |||||||
| chr4:109758861 | G | T | 1 | a0001c0001t0001g0186 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.884-1078C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109758861 | |||||||
| chr4:109758891 | G | A | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(183): Show |
199 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.884-1108C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109758891 | |||||||
| chr4:109758968 | C | A | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.884-1185G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109758968 | |||||||
| chr4:109759222 | C | A | 322 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(319): Show |
338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.883+1048G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109759222 | |||||||
| chr4:109759253 | TA | T | 80 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0019 others(77): Show |
82 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.883+1016delT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109759253 | |||||||
| chr4:109759265 | A | AT | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(150): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.883+1004_883+1005i others(3): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109759265 | |||||||
| chr4:109759265 | A | T | 166 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(163): Show |
169 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(166): Show |
intron_variant | MODIFIER | c.883+1005T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109759265 | |||||||
| chr4:109759476 | A | G | 1 | a0001c0001t0001g0220 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.883+794T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109759476 | |||||||
| chr4:109759515 | A | G | 327 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(324): Show |
343 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(340): Show |
intron_variant | MODIFIER | c.883+755T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109759515 | |||||||
| chr4:109759515 | A | T | 2 | a0001c0006t0005g0098 a0001c0006t0005g0099 |
2 | HG02647.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.883+755T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109759515 | |||||||
| chr4:109759642 | C | T | 3 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 |
3 | HG02559.hp2 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.883+628G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109759642 | |||||||
| chr4:109759837 | T | C | 329 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(326): Show |
345 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.883+433A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109759837 | |||||||
| chr4:109759936 | T | TACAA | 322 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(319): Show |
338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.883+330_883+333dup others(4): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109759936 | |||||||
| chr4:109759965 | G | A | 322 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(319): Show |
338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.883+305C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109759965 | |||||||
| chr4:109759980 | T | G | 10 | a0001c0002t0001g0035 a0001c0002t0001g0039 a0001c0002t0001g0040 others(7): Show |
10 | HG00323.hp1 HG01069.hp2 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.883+290A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109759980 | |||||||
| chr4:109759984 | A | C | 3 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 |
3 | HG02559.hp2 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.883+286T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109759984 | |||||||
| chr4:109759992 | G | T | 1 | a0001c0001t0001g0148 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.883+278C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109759992 | |||||||
| chr4:109760101 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.883+169C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 6/12 | chr4 | 109760101 | |||||||
| chr4:109760462 | C | T | 322 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(319): Show |
338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.772+61G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 5/12 | chr4 | 109760462 | |||||||
| chr4:109760727 | A | C | 1 | a0001c0001t0001g0171 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.659-91T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 4/12 | chr4 | 109760727 | |||||||
| chr4:109760903 | C | T | 3 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0150 |
3 | HG02897.hp2 NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.659-267G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 4/12 | chr4 | 109760903 | |||||||
| chr4:109760984 | G | C | 1 | a0001c0001t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.659-348C>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 4/12 | chr4 | 109760984 | |||||||
| chr4:109761331 | T | C | 113 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(110): Show |
119 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.658+186A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 4/12 | chr4 | 109761331 | |||||||
| chr4:109761448 | T | A | 1 | a0007c0013t0001g0290 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.658+69A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 4/12 | chr4 | 109761448 | |||||||
| chr4:109761720 | G | A | 1 | a0007c0013t0001g0290 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.483-28C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109761720 | |||||||
| chr4:109761797 | A | G | 73 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0019 others(70): Show |
75 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(72): Show |
intron_variant | MODIFIER | c.483-105T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109761797 | |||||||
| chr4:109761927 | C | T | 2 | a0001c0002t0001g0115 a0001c0002t0001g0116 |
2 | HG00673.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.483-235G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109761927 | |||||||
| chr4:109761982 | G | C | 1 | a0001c0002t0001g0121 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.483-290C>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109761982 | |||||||
| chr4:109761982 | G | T | 322 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(319): Show |
338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.483-290C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109761982 | |||||||
| chr4:109762189 | T | TAAA | 11 | a0001c0001t0001g0171 a0001c0001t0001g0176 a0001c0001t0001g0205 others(8): Show |
11 | HG02004.hp1 HG02109.hp2 HG02155.hp1 others(8): Show |
intron_variant | MODIFIER | c.483-500_483-498dup others(3): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109762189 | |||||||
| chr4:109762189 | T | TAAAA | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(214): Show |
232 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.483-501_483-498dup others(4): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109762189 | |||||||
| chr4:109762189 | T | TAAAAA | 35 | a0001c0001t0001g0150 a0001c0001t0001g0159 a0001c0001t0001g0183 others(32): Show |
35 | HG00673.hp1 HG00735.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.483-502_483-498dup others(5): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109762189 | |||||||
| chr4:109762189 | T | TAAAAAA | 49 | a0001c0002t0001g0006 a0001c0002t0001g0021 a0001c0002t0001g0022 others(46): Show |
50 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.483-503_483-498dup others(6): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109762189 | |||||||
| chr4:109762189 | T | TAAAAAAA | 10 | a0001c0001t0001g0283 a0001c0001t0001g0284 a0001c0002t0001g0111 others(7): Show |
10 | HG01243.hp2 HG02027.hp1 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.483-504_483-498dup others(7): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109762189 | |||||||
| chr4:109762224 | T | C | 1 | a0001c0001t0003g0153 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.483-532A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109762224 | |||||||
| chr4:109762298 | G | A | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(176): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.483-606C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109762298 | |||||||
| chr4:109762323 | G | A | 2 | a0001c0006t0005g0098 a0001c0006t0005g0099 |
2 | HG02647.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.483-631C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109762323 | |||||||
| chr4:109762338 | A | C | 1 | a0003c0004t0001g0032 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.483-646T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109762338 | |||||||
| chr4:109762389 | G | A | 4 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 others(1): Show |
4 | HG02257.hp2 HG02976.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.483-697C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109762389 | |||||||
| chr4:109762390 | G | A | 1 | a0001c0001t0001g0311 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.483-698C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109762390 | |||||||
| chr4:109762394 | C | T | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(176): Show |
192 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.483-702G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109762394 | |||||||
| chr4:109762498 | T | G | 8 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(5): Show |
8 | HG02723.hp2 HG02897.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.483-806A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109762498 | |||||||
| chr4:109762517 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.483-825G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109762517 | |||||||
| chr4:109762591 | T | C | 20 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0311 others(17): Show |
20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.483-899A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109762591 | |||||||
| chr4:109762656 | T | C | 4 | a0003c0004t0001g0030 a0003c0004t0001g0031 a0003c0004t0001g0032 others(1): Show |
4 | HG02055.hp2 HG02257.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.483-964A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109762656 | |||||||
| chr4:109762656 | T | G | 325 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(322): Show |
341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.483-964A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109762656 | |||||||
| chr4:109763029 | T | C | 20 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0311 others(17): Show |
20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.483-1337A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109763029 | |||||||
| chr4:109763067 | G | T | 11 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0082 others(8): Show |
14 | HG02109.hp2 HG02145.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.483-1375C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109763067 | |||||||
| chr4:109763154 | T | C | 325 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(322): Show |
341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.482+1383A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109763154 | |||||||
| chr4:109763194 | C | G | 3 | a0002c0003t0001g0248 a0002c0003t0001g0306 a0002c0003t0001g0307 |
3 | HG02027.hp2 NA18950.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.482+1343G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109763194 | |||||||
| chr4:109763220 | G | T | 7 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(4): Show |
7 | HG02723.hp2 HG02897.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.482+1317C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109763220 | |||||||
| chr4:109763239 | T | C | 4 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(1): Show |
4 | HG02559.hp2 HG03579.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.482+1298A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109763239 | |||||||
| chr4:109763421 | A | G | 3 | a0001c0001t0001g0082 a0001c0001t0001g0273 a0001c0001t0002g0332 |
3 | HG02615.hp2 HG02818.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.482+1116T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109763421 | |||||||
| chr4:109763575 | G | A | 1 | a0001c0002t0002g0023 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.482+962C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109763575 | |||||||
| chr4:109763588 | T | C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(152): Show |
168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.482+949A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109763588 | |||||||
| chr4:109763631 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.482+906T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109763631 | |||||||
| chr4:109763714 | G | A | 1 | a0001c0002t0001g0060 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.482+823C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109763714 | |||||||
| chr4:109763892 | A | G | 1 | a0001c0002t0001g0119 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.482+645T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109763892 | |||||||
| chr4:109763940 | C | T | 323 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(320): Show |
339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.482+597G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109763940 | |||||||
| chr4:109763946 | C | T | 4 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(1): Show |
4 | HG02559.hp2 HG03579.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.482+591G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109763946 | |||||||
| chr4:109764190 | A | G | 2 | a0001c0001t0001g0190 a0001c0001t0001g0191 |
2 | NA18969.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.482+347T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109764190 | |||||||
| chr4:109764523 | A | T | 4 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 others(1): Show |
4 | HG02257.hp2 HG02976.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.482+14T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109764523 | |||||||
| chr4:109764531 | G | A | 14 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0082 others(11): Show |
17 | HG02109.hp2 HG02145.hp1 HG02258.hp2 others(14): Show |
splice_region_variant&intron_variant | LOW | c.482+6C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109764531 | |||||||
| chr4:109764531 | G | T | 3 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0150 |
3 | HG02897.hp2 NA19030.hp2 NA20129.hp2 |
splice_region_variant&intron_variant | LOW | c.482+6C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 3/12 | chr4 | 109764531 | |||||||
| chr4:109764806 | C | G | 20 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0311 others(17): Show |
20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.329-116G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 2/12 | chr4 | 109764806 | |||||||
| chr4:109764845 | A | G | 323 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(320): Show |
339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.329-155T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 2/12 | chr4 | 109764845 | |||||||
| chr4:109764898 | A | C | 323 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(320): Show |
339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.329-208T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 2/12 | chr4 | 109764898 | |||||||
| chr4:109764923 | A | G | 20 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0311 others(17): Show |
20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.329-233T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 2/12 | chr4 | 109764923 | |||||||
| chr4:109764928 | A | G | 323 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(320): Show |
339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.329-238T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 2/12 | chr4 | 109764928 | |||||||
| chr4:109764954 | C | G | 1 | a0001c0002t0002g0109 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.329-264G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 2/12 | chr4 | 109764954 | |||||||
| chr4:109765013 | A | T | 2 | a0001c0002t0002g0100 a0001c0002t0002g0101 |
2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.329-323T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 2/12 | chr4 | 109765013 | |||||||
| chr4:109765040 | C | T | 13 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0156 others(10): Show |
15 | HG00099.hp1 HG00438.hp1 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.329-350G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 2/12 | chr4 | 109765040 | |||||||
| chr4:109765151 | T | C | 4 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0209 others(1): Show |
4 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(1): Show |
intron_variant | MODIFIER | c.329-461A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 2/12 | chr4 | 109765151 | |||||||
| chr4:109765257 | T | A | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(152): Show |
168 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.329-567A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 2/12 | chr4 | 109765257 | |||||||
| chr4:109765620 | C | G | 135 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0006 others(132): Show |
138 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.329-930G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 2/12 | chr4 | 109765620 | |||||||
| chr4:109765703 | G | A | 1 | a0001c0002t0001g0057 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.328+851C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 2/12 | chr4 | 109765703 | |||||||
| chr4:109765776 | TG | T | 136 | a0001c0001t0003g0013 a0001c0002t0001g0004 a0001c0002t0001g0005 others(133): Show |
140 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(137): Show |
intron_variant | MODIFIER | c.328+777delC | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 2/12 | chr4 | 109765776 | |||||||
| chr4:109765803 | G | C | 155 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(152): Show |
167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.328+751C>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 2/12 | chr4 | 109765803 | |||||||
| chr4:109765839 | C | G | 20 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0311 others(17): Show |
20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.328+715G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 2/12 | chr4 | 109765839 | |||||||
| chr4:109765893 | C | T | 157 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(154): Show |
170 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.328+661G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 2/12 | chr4 | 109765893 | |||||||
| chr4:109766016 | G | T | 20 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0311 others(17): Show |
20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.328+538C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 2/12 | chr4 | 109766016 | |||||||
| chr4:109766113 | G | A | 4 | a0001c0002t0001g0288 a0001c0002t0001g0289 a0001c0002t0001g0291 others(1): Show |
4 | HG00735.hp2 HG02055.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.328+441C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 2/12 | chr4 | 109766113 | |||||||
| chr4:109766356 | C | T | 1 | a0001c0001t0001g0250 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.328+198G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 2/12 | chr4 | 109766356 | |||||||
| chr4:109766872 | C | T | 1 | a0001c0001t0001g0331 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.58-48G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109766872 | |||||||
| chr4:109766911 | G | T | 1 | a0001c0002t0001g0113 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.58-87C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109766911 | |||||||
| chr4:109766963 | C | G | 20 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0311 others(17): Show |
20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.58-139G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109766963 | |||||||
| chr4:109766976 | G | A | 1 | a0007c0013t0001g0290 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.58-152C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109766976 | |||||||
| chr4:109767005 | A | T | 1 | a0001c0001t0002g0158 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.58-181T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109767005 | |||||||
| chr4:109767169 | A | G | 6 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(3): Show |
6 | HG02723.hp2 HG02897.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.58-345T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109767169 | |||||||
| chr4:109767206 | A | T | 323 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(320): Show |
339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.58-382T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109767206 | |||||||
| chr4:109767270 | A | C | 10 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0001t0001g0323 others(7): Show |
10 | HG01109.hp2 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.58-446T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109767270 | |||||||
| chr4:109767334 | G | A | 1 | a0007c0013t0001g0290 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.58-510C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109767334 | |||||||
| chr4:109767348 | C | T | 323 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(320): Show |
339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.58-524G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109767348 | |||||||
| chr4:109767419 | T | A | 4 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(1): Show |
4 | HG02559.hp2 HG03579.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-595A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109767419 | |||||||
| chr4:109767463 | T | G | 2 | a0001c0002t0001g0133 a0001c0002t0001g0134 |
2 | HG01243.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.58-639A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109767463 | |||||||
| chr4:109767476 | T | C | 2 | a0001c0002t0001g0105 a0001c0002t0001g0106 |
2 | HG02145.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.58-652A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109767476 | |||||||
| chr4:109767480 | C | G | 1 | a0001c0001t0003g0153 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.58-656G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109767480 | |||||||
| chr4:109767486 | T | C | 1 | a0001c0001t0003g0153 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.58-662A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109767486 | |||||||
| chr4:109767556 | G | A | 13 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0156 others(10): Show |
15 | HG00099.hp1 HG00438.hp1 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.58-732C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109767556 | |||||||
| chr4:109767608 | C | T | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(175): Show |
191 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.58-784G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109767608 | |||||||
| chr4:109767609 | G | A | 1 | a0007c0013t0001g0290 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.58-785C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109767609 | |||||||
| chr4:109767611 | T | A | 2 | a0001c0001t0001g0151 a0001c0001t0003g0153 |
2 | HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.58-787A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109767611 | |||||||
| chr4:109767656 | C | A | 323 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(320): Show |
339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.58-832G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109767656 | |||||||
| chr4:109767659 | T | C | 323 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(320): Show |
339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.58-835A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109767659 | |||||||
| chr4:109767771 | C | T | 62 | a0001c0002t0001g0006 a0001c0002t0001g0021 a0001c0002t0001g0022 others(59): Show |
63 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.58-947G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109767771 | |||||||
| chr4:109767918 | G | A | 20 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0311 others(17): Show |
20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.58-1094C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109767918 | |||||||
| chr4:109767931 | A | C | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(151): Show |
167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.58-1107T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109767931 | |||||||
| chr4:109767967 | T | C | 323 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(320): Show |
339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.58-1143A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109767967 | |||||||
| chr4:109767988 | T | C | 322 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(319): Show |
338 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(335): Show |
intron_variant | MODIFIER | c.58-1164A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109767988 | |||||||
| chr4:109768100 | G | A | 1 | a0001c0001t0003g0335 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.58-1276C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768100 | |||||||
| chr4:109768188 | C | T | 2 | a0001c0001t0001g0273 a0001c0001t0002g0332 |
2 | HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.58-1364G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768188 | |||||||
| chr4:109768201 | G | A | 4 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(1): Show |
4 | HG02559.hp2 HG03579.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-1377C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768201 | |||||||
| chr4:109768278 | C | CA | 44 | a0001c0002t0001g0021 a0001c0002t0001g0022 a0001c0002t0001g0044 others(41): Show |
44 | HG00558.hp2 HG00609.hp2 HG00673.hp2 others(41): Show |
intron_variant | MODIFIER | c.58-1455dupT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768278 | |||||||
| chr4:109768278 | CA | C | 20 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(17): Show |
21 | HG00735.hp2 HG01081.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.58-1455delT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768278 | |||||||
| chr4:109768278 | CAA | C | 178 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(175): Show |
190 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.58-1456_58-1455del others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768278 | |||||||
| chr4:109768318 | G | C | 1 | a0001c0001t0001g0171 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.58-1494C>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768318 | |||||||
| chr4:109768334 | T | TA | 9 | a0001c0001t0001g0151 a0001c0001t0001g0186 a0001c0001t0001g0214 others(6): Show |
9 | HG00639.hp2 HG01891.hp1 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.58-1511dupT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768334 | |||||||
| chr4:109768334 | T | TAA | 15 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(12): Show |
15 | HG00323.hp1 HG01069.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.58-1512_58-1511dup others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768334 | |||||||
| chr4:109768334 | T | TAAA | 62 | a0001c0001t0001g0082 a0001c0002t0001g0004 a0001c0002t0001g0005 others(59): Show |
64 | HG00558.hp1 HG00733.hp1 HG01069.hp2 others(61): Show |
intron_variant | MODIFIER | c.58-1513_58-1511dup others(3): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768334 | |||||||
| chr4:109768334 | TA | T | 12 | a0001c0001t0001g0159 a0001c0001t0001g0163 a0001c0001t0001g0164 others(9): Show |
12 | HG00673.hp2 HG01168.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.58-1511delT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768334 | |||||||
| chr4:109768401 | T | G | 113 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(110): Show |
119 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(116): Show |
intron_variant | MODIFIER | c.58-1577A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768401 | |||||||
| chr4:109768440 | C | T | 1 | a0001c0002t0001g0139 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.58-1616G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768440 | |||||||
| chr4:109768455 | C | T | 2 | a0001c0008t0001g0272 a0001c0008t0002g0271 |
2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.58-1631G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768455 | |||||||
| chr4:109768478 | A | G | 1 | a0001c0002t0001g0045 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.58-1654T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768478 | |||||||
| chr4:109768583 | A | G | 2 | a0001c0001t0001g0151 a0001c0001t0003g0153 |
2 | HG03195.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.58-1759T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768583 | |||||||
| chr4:109768614 | C | T | 323 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(320): Show |
339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.58-1790G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768614 | |||||||
| chr4:109768633 | C | G | 1 | a0001c0001t0001g0266 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.58-1809G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768633 | |||||||
| chr4:109768645 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.58-1821G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768645 | |||||||
| chr4:109768718 | C | T | 1 | a0001c0002t0001g0277 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.58-1894G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768718 | |||||||
| chr4:109768739 | T | C | 323 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(320): Show |
339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.58-1915A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768739 | |||||||
| chr4:109768781 | T | C | 4 | a0001c0002t0001g0288 a0001c0002t0001g0289 a0001c0002t0001g0291 others(1): Show |
4 | HG00735.hp2 HG02055.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-1957A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768781 | |||||||
| chr4:109768845 | A | G | 1 | a0001c0001t0001g0316 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.58-2021T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768845 | |||||||
| chr4:109768893 | T | TAC | 220 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(217): Show |
234 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(231): Show |
intron_variant | MODIFIER | c.58-2071_58-2070dup others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768893 | |||||||
| chr4:109768972 | C | G | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(151): Show |
167 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(164): Show |
intron_variant | MODIFIER | c.58-2148G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768972 | |||||||
| chr4:109768978 | C | T | 2 | a0003c0004t0001g0154 a0003c0004t0001g0155 |
2 | HG00738.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.58-2154G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768978 | |||||||
| chr4:109768979 | G | A | 323 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(320): Show |
339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.58-2155C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109768979 | |||||||
| chr4:109769099 | T | G | 323 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(320): Show |
339 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.58-2275A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109769099 | |||||||
| chr4:109769181 | T | C | 1 | a0001c0001t0002g0158 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.58-2357A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109769181 | |||||||
| chr4:109769430 | C | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(146): Show |
160 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.58-2606G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109769430 | |||||||
| chr4:109769480 | T | A | 82 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(79): Show |
83 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.58-2656A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109769480 | |||||||
| chr4:109769503 | A | T | 81 | a0001c0001t0001g0082 a0001c0001t0001g0145 a0001c0001t0001g0146 others(78): Show |
83 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(80): Show |
intron_variant | MODIFIER | c.58-2679T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109769503 | |||||||
| chr4:109769529 | C | T | 1 | a0001c0001t0001g0294 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.58-2705G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109769529 | |||||||
| chr4:109769584 | G | T | 1 | a0001c0002t0001g0143 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.58-2760C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109769584 | |||||||
| chr4:109769778 | C | T | 1 | a0001c0002t0001g0122 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.58-2954G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109769778 | |||||||
| chr4:109769862 | A | G | 11 | a0001c0001t0001g0002 a0001c0001t0001g0293 a0001c0001t0001g0294 others(8): Show |
13 | HG01261.hp1 HG01433.hp1 HG01928.hp1 others(10): Show |
intron_variant | MODIFIER | c.58-3038T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109769862 | |||||||
| chr4:109769880 | C | T | 1 | a0007c0013t0001g0290 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.58-3056G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109769880 | |||||||
| chr4:109769960 | G | A | 1 | a0008c0011t0001g0108 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.58-3136C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109769960 | |||||||
| chr4:109770011 | C | A | 2 | a0001c0002t0001g0044 a0001c0002t0001g0050 |
2 | HG01978.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.58-3187G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109770011 | |||||||
| chr4:109770067 | C | T | 20 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0311 others(17): Show |
20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.58-3243G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109770067 | |||||||
| chr4:109770095 | C | T | 1 | a0001c0002t0001g0139 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.58-3271G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109770095 | |||||||
| chr4:109770349 | C | T | 13 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0156 others(10): Show |
15 | HG00099.hp1 HG00438.hp1 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.58-3525G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109770349 | |||||||
| chr4:109770502 | GC | G | 4 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 others(1): Show |
4 | HG02257.hp2 HG02976.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-3679delG | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109770502 | |||||||
| chr4:109770507 | G | A | 4 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 others(1): Show |
4 | HG02257.hp2 HG02976.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-3683C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109770507 | |||||||
| chr4:109770515 | C | G | 1 | a0001c0001t0001g0304 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.58-3691G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109770515 | |||||||
| chr4:109770556 | TA | T | 312 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(309): Show |
328 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.58-3733delT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109770556 | |||||||
| chr4:109770590 | T | C | 2 | a0001c0002t0001g0019 a0001c0002t0001g0059 |
2 | HG01975.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.58-3766A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109770590 | |||||||
| chr4:109770633 | G | GA | 48 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0014 others(45): Show |
53 | HG00099.hp1 HG00438.hp1 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.58-3810dupT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109770633 | |||||||
| chr4:109770633 | GA | G | 21 | a0001c0001t0001g0002 a0001c0001t0001g0084 a0001c0001t0001g0164 others(18): Show |
23 | HG00735.hp2 HG01081.hp1 HG01168.hp1 others(20): Show |
intron_variant | MODIFIER | c.58-3810delT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109770633 | |||||||
| chr4:109770827 | G | T | 5 | a0001c0002t0001g0288 a0001c0002t0001g0289 a0001c0002t0001g0291 others(2): Show |
5 | HG00735.hp2 HG01975.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.58-4003C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109770827 | |||||||
| chr4:109770860 | A | C | 1 | a0001c0001t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.58-4036T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109770860 | |||||||
| chr4:109770879 | C | T | 1 | a0001c0001t0001g0331 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.58-4055G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109770879 | |||||||
| chr4:109770902 | G | A | 1 | a0001c0002t0001g0041 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.58-4078C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109770902 | |||||||
| chr4:109771075 | G | A | 99 | a0001c0001t0001g0063 a0001c0001t0001g0082 a0001c0001t0001g0084 others(96): Show |
101 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(98): Show |
intron_variant | MODIFIER | c.58-4251C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109771075 | |||||||
| chr4:109771098 | G | A | 4 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0200 others(1): Show |
4 | HG00735.hp1 HG00738.hp2 HG00741.hp2 others(1): Show |
intron_variant | MODIFIER | c.58-4274C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109771098 | |||||||
| chr4:109771112 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.58-4288G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109771112 | |||||||
| chr4:109771284 | T | G | 2 | a0001c0008t0001g0272 a0001c0008t0002g0271 |
2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.58-4460A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109771284 | |||||||
| chr4:109771354 | C | T | 1 | a0001c0001t0001g0336 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.58-4530G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109771354 | |||||||
| chr4:109771400 | T | TA | 55 | a0001c0002t0001g0006 a0001c0002t0001g0021 a0001c0002t0001g0022 others(52): Show |
56 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.58-4577dupT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109771400 | |||||||
| chr4:109771522 | T | C | 1 | a0001c0001t0001g0189 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.58-4698A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109771522 | |||||||
| chr4:109771541 | C | T | 2 | a0003c0004t0001g0154 a0003c0004t0001g0155 |
2 | HG00738.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.58-4717G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109771541 | |||||||
| chr4:109771550 | C | CA | 29 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(26): Show |
29 | HG00544.hp2 HG00738.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.58-4727dupT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109771550 | |||||||
| chr4:109771550 | C | CAA | 36 | a0001c0002t0001g0006 a0001c0002t0001g0021 a0001c0002t0001g0022 others(33): Show |
37 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.58-4728_58-4727dup others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109771550 | |||||||
| chr4:109771596 | C | A | 55 | a0001c0002t0001g0006 a0001c0002t0001g0021 a0001c0002t0001g0022 others(52): Show |
56 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.58-4772G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109771596 | |||||||
| chr4:109771714 | C | CA | 40 | a0001c0001t0001g0015 a0001c0001t0001g0168 a0001c0001t0001g0169 others(37): Show |
41 | HG00438.hp1 HG00741.hp1 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.58-4891dupT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109771714 | |||||||
| chr4:109771714 | C | CAA | 88 | a0001c0001t0001g0063 a0001c0001t0001g0084 a0001c0001t0001g0085 others(85): Show |
91 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.58-4892_58-4891dup others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109771714 | |||||||
| chr4:109771714 | C | CAAA | 33 | a0001c0002t0001g0019 a0001c0002t0001g0034 a0001c0002t0001g0040 others(30): Show |
33 | HG01069.hp2 HG01081.hp1 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.58-4893_58-4891dup others(3): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109771714 | |||||||
| chr4:109771714 | C | CAAAA | 6 | a0001c0001t0001g0082 a0001c0002t0001g0043 a0001c0002t0001g0044 others(3): Show |
6 | HG00733.hp1 HG01978.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.58-4894_58-4891dup others(4): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109771714 | |||||||
| chr4:109771714 | CA | C | 14 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(11): Show |
14 | HG00323.hp2 HG00738.hp1 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.58-4891delT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109771714 | |||||||
| chr4:109771714 | CAAA | C | 9 | a0001c0001t0001g0002 a0001c0001t0001g0282 a0001c0001t0001g0283 others(6): Show |
11 | HG01433.hp1 HG01928.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.58-4893_58-4891del others(3): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109771714 | |||||||
| chr4:109771845 | A | G | 3 | a0001c0002t0001g0075 a0001c0002t0001g0076 a0001c0002t0001g0079 |
3 | HG01069.hp1 HG01071.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.58-5021T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109771845 | |||||||
| chr4:109771935 | T | A | 1 | a0001c0001t0001g0333 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.58-5111A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109771935 | |||||||
| chr4:109772279 | G | A | 1 | a0001c0001t0003g0153 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.58-5455C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109772279 | |||||||
| chr4:109772294 | T | C | 63 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(60): Show |
64 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.58-5470A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109772294 | |||||||
| chr4:109772379 | G | A | 54 | a0001c0002t0001g0006 a0001c0002t0001g0021 a0001c0002t0001g0022 others(51): Show |
55 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.58-5555C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109772379 | |||||||
| chr4:109772391 | C | T | 5 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(2): Show |
5 | HG02723.hp2 HG02897.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.58-5567G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109772391 | |||||||
| chr4:109772413 | G | A | 110 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(107): Show |
116 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.58-5589C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109772413 | |||||||
| chr4:109772580 | C | T | 1 | a0001c0001t0001g0296 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.58-5756G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109772580 | |||||||
| chr4:109772581 | G | GT | 136 | a0001c0001t0001g0063 a0001c0001t0001g0082 a0001c0001t0001g0084 others(133): Show |
139 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(136): Show |
intron_variant | MODIFIER | c.58-5758dupA | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109772581 | |||||||
| chr4:109772653 | A | C | 4 | a0001c0002t0001g0288 a0001c0002t0001g0289 a0001c0002t0001g0291 others(1): Show |
4 | HG00735.hp2 HG02055.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-5829T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109772653 | |||||||
| chr4:109772667 | C | A | 78 | a0001c0001t0001g0063 a0001c0001t0001g0082 a0001c0001t0001g0084 others(75): Show |
80 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.58-5843G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109772667 | |||||||
| chr4:109772784 | A | G | 78 | a0001c0001t0001g0063 a0001c0001t0001g0082 a0001c0001t0001g0084 others(75): Show |
80 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.58-5960T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109772784 | |||||||
| chr4:109772823 | A | G | 49 | a0001c0002t0001g0006 a0001c0002t0001g0021 a0001c0002t0001g0022 others(46): Show |
50 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.58-5999T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109772823 | |||||||
| chr4:109773213 | C | G | 8 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(5): Show |
8 | HG00738.hp1 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.58-6389G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109773213 | |||||||
| chr4:109773253 | C | T | 20 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0311 others(17): Show |
20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.58-6429G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109773253 | |||||||
| chr4:109773265 | C | T | 1 | a0001c0002t0001g0021 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.58-6441G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109773265 | |||||||
| chr4:109773300 | G | A | 1 | a0001c0002t0001g0091 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.58-6476C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109773300 | |||||||
| chr4:109773384 | C | T | 1 | a0001c0001t0001g0270 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.58-6560G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109773384 | |||||||
| chr4:109773385 | G | A | 1 | a0001c0002t0002g0023 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.58-6561C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109773385 | |||||||
| chr4:109773415 | C | A | 1 | a0001c0002t0001g0006 | 2 | NA18970.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.58-6591G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109773415 | |||||||
| chr4:109773465 | G | A | 63 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(60): Show |
64 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.58-6641C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109773465 | |||||||
| chr4:109773473 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.58-6649C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109773473 | |||||||
| chr4:109773493 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.58-6669G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109773493 | |||||||
| chr4:109773597 | T | C | 1 | a0001c0001t0001g0267 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.58-6773A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109773597 | |||||||
| chr4:109773608 | C | T | 6 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(3): Show |
6 | HG02723.hp2 HG02897.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.58-6784G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109773608 | |||||||
| chr4:109773638 | T | C | 1 | a0001c0002t0001g0094 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.58-6814A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109773638 | |||||||
| chr4:109773650 | T | C | 2 | a0001c0001t0001g0329 a0001c0001t0002g0322 |
2 | HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.58-6826A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109773650 | |||||||
| chr4:109773666 | T | C | 2 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
2 | NA18962.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.58-6842A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109773666 | |||||||
| chr4:109773811 | C | T | 162 | a0001c0001t0001g0063 a0001c0001t0001g0082 a0001c0001t0001g0084 others(159): Show |
165 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(162): Show |
intron_variant | MODIFIER | c.58-6987G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109773811 | |||||||
| chr4:109774100 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.58-7276A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109774100 | |||||||
| chr4:109774205 | T | C | 1 | a0001c0001t0001g0296 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.58-7381A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109774205 | |||||||
| chr4:109774404 | GAGCA | G | 55 | a0001c0002t0001g0006 a0001c0002t0001g0021 a0001c0002t0001g0022 others(52): Show |
56 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.58-7584_58-7581del others(4): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109774404 | |||||||
| chr4:109774434 | G | A | 98 | a0001c0001t0001g0063 a0001c0001t0001g0082 a0001c0001t0001g0084 others(95): Show |
100 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(97): Show |
intron_variant | MODIFIER | c.58-7610C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109774434 | |||||||
| chr4:109774558 | G | A | 2 | a0001c0001t0003g0334 a0001c0001t0003g0335 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.58-7734C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109774558 | |||||||
| chr4:109774595 | G | A | 3 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 |
3 | HG02559.hp2 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.58-7771C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109774595 | |||||||
| chr4:109774664 | C | A | 55 | a0001c0002t0001g0006 a0001c0002t0001g0021 a0001c0002t0001g0022 others(52): Show |
56 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.58-7840G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109774664 | |||||||
| chr4:109774783 | A | C | 2 | a0001c0001t0001g0176 a0001c0001t0001g0177 |
2 | NA18962.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.58-7959T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109774783 | |||||||
| chr4:109774913 | T | C | 2 | a0001c0006t0005g0098 a0001c0006t0005g0099 |
2 | HG02647.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.58-8089A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109774913 | |||||||
| chr4:109775016 | A | G | 1 | a0001c0002t0001g0043 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.58-8192T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109775016 | |||||||
| chr4:109775063 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.58-8239A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109775063 | |||||||
| chr4:109775069 | C | T | 3 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 |
3 | HG02559.hp2 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.58-8245G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109775069 | |||||||
| chr4:109775102 | G | A | 55 | a0001c0002t0001g0006 a0001c0002t0001g0021 a0001c0002t0001g0022 others(52): Show |
56 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.58-8278C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109775102 | |||||||
| chr4:109775110 | C | T | 1 | a0001c0001t0001g0213 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.58-8286G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109775110 | |||||||
| chr4:109775112 | G | A | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG02717.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.58-8288C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109775112 | |||||||
| chr4:109775183 | C | G | 49 | a0001c0002t0001g0006 a0001c0002t0001g0021 a0001c0002t0001g0022 others(46): Show |
50 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.58-8359G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109775183 | |||||||
| chr4:109775213 | G | A | 2 | a0001c0006t0005g0098 a0001c0006t0005g0099 |
2 | HG02647.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.58-8389C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109775213 | |||||||
| chr4:109775333 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.58-8509C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109775333 | |||||||
| chr4:109775394 | C | T | 1 | a0001c0002t0002g0023 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.58-8570G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109775394 | |||||||
| chr4:109775619 | A | G | 2 | a0001c0008t0001g0272 a0001c0008t0002g0271 |
2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.58-8795T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109775619 | |||||||
| chr4:109775755 | T | C | 154 | a0001c0001t0001g0063 a0001c0001t0001g0082 a0001c0001t0001g0084 others(151): Show |
157 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(154): Show |
intron_variant | MODIFIER | c.58-8931A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109775755 | |||||||
| chr4:109775776 | G | A | 1 | a0001c0002t0001g0056 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.58-8952C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109775776 | |||||||
| chr4:109775820 | T | A | 1 | a0001c0001t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.58-8996A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109775820 | |||||||
| chr4:109775860 | T | C | 1 | a0001c0001t0001g0268 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.58-9036A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109775860 | |||||||
| chr4:109775889 | C | G | 133 | a0001c0001t0001g0063 a0001c0001t0001g0082 a0001c0001t0001g0084 others(130): Show |
136 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(133): Show |
intron_variant | MODIFIER | c.58-9065G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109775889 | |||||||
| chr4:109775993 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.58-9169T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109775993 | |||||||
| chr4:109776071 | G | A | 49 | a0001c0002t0001g0006 a0001c0002t0001g0021 a0001c0002t0001g0022 others(46): Show |
50 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.58-9247C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109776071 | |||||||
| chr4:109776166 | A | G | 1 | a0001c0001t0001g0212 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.58-9342T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109776166 | |||||||
| chr4:109776288 | G | T | 1 | a0001c0001t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.58-9464C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109776288 | |||||||
| chr4:109776313 | T | C | 3 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 |
3 | HG02559.hp2 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.58-9489A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109776313 | |||||||
| chr4:109776316 | T | C | 1 | a0001c0002t0001g0040 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.58-9492A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109776316 | |||||||
| chr4:109776366 | G | C | 1 | a0001c0001t0003g0013 | 2 | HG02258.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.58-9542C>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109776366 | |||||||
| chr4:109776402 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.58-9578G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109776402 | |||||||
| chr4:109776413 | G | A | 1 | a0001c0002t0001g0067 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.58-9589C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109776413 | |||||||
| chr4:109776470 | T | C | 1 | a0007c0013t0001g0290 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.58-9646A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109776470 | |||||||
| chr4:109776499 | A | G | 175 | a0001c0001t0001g0002 a0001c0001t0001g0063 a0001c0001t0001g0082 others(172): Show |
180 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(177): Show |
intron_variant | MODIFIER | c.58-9675T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109776499 | |||||||
| chr4:109776631 | G | C | 1 | a0001c0001t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.58-9807C>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109776631 | |||||||
| chr4:109776767 | G | A | 22 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0311 others(19): Show |
22 | HG00673.hp1 HG00738.hp1 HG02027.hp2 others(19): Show |
intron_variant | MODIFIER | c.58-9943C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109776767 | |||||||
| chr4:109776801 | G | C | 1 | a0001c0001t0001g0187 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.58-9977C>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109776801 | |||||||
| chr4:109776853 | T | C | 20 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0311 others(17): Show |
20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.58-10029A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109776853 | |||||||
| chr4:109776972 | A | G | 175 | a0001c0001t0001g0002 a0001c0001t0001g0063 a0001c0001t0001g0082 others(172): Show |
180 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(177): Show |
intron_variant | MODIFIER | c.58-10148T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109776972 | |||||||
| chr4:109777068 | C | T | 4 | a0001c0002t0001g0288 a0001c0002t0001g0289 a0001c0002t0001g0291 others(1): Show |
4 | HG00735.hp2 HG02055.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-10244G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109777068 | |||||||
| chr4:109777130 | C | A | 1 | a0001c0001t0003g0153 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.58-10306G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109777130 | |||||||
| chr4:109777130 | C | T | 1 | a0001c0002t0001g0062 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.58-10306G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109777130 | |||||||
| chr4:109777185 | A | T | 1 | a0003c0004t0001g0031 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.58-10361T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109777185 | |||||||
| chr4:109777249 | C | T | 4 | a0001c0001t0001g0063 a0001c0001t0001g0084 a0001c0001t0001g0085 others(1): Show |
4 | HG01123.hp2 HG01515.hp1 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-10425G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109777249 | |||||||
| chr4:109777293 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.58-10469A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109777293 | |||||||
| chr4:109777336 | T | C | 1 | a0001c0001t0001g0331 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.58-10512A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109777336 | |||||||
| chr4:109777340 | G | A | 3 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 |
3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.58-10516C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109777340 | |||||||
| chr4:109777342 | A | G | 55 | a0001c0002t0001g0006 a0001c0002t0001g0021 a0001c0002t0001g0022 others(52): Show |
56 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.58-10518T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109777342 | |||||||
| chr4:109777360 | C | T | 20 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0311 others(17): Show |
20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.58-10536G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109777360 | |||||||
| chr4:109777388 | T | C | 154 | a0001c0001t0001g0063 a0001c0001t0001g0082 a0001c0001t0001g0084 others(151): Show |
157 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(154): Show |
intron_variant | MODIFIER | c.58-10564A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109777388 | |||||||
| chr4:109777419 | C | T | 133 | a0001c0001t0001g0063 a0001c0001t0001g0082 a0001c0001t0001g0084 others(130): Show |
136 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(133): Show |
intron_variant | MODIFIER | c.58-10595G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109777419 | |||||||
| chr4:109777450 | T | C | 175 | a0001c0001t0001g0002 a0001c0001t0001g0063 a0001c0001t0001g0082 others(172): Show |
180 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(177): Show |
intron_variant | MODIFIER | c.58-10626A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109777450 | |||||||
| chr4:109777522 | C | CAATAATA others(2): Show |
10 | a0001c0001t0001g0002 a0001c0001t0001g0282 a0001c0001t0001g0283 others(7): Show |
12 | HG01261.hp1 HG01433.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.58-10699_58-10698i others(11): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109777522 | |||||||
| chr4:109777530 | A | T | 10 | a0001c0001t0001g0002 a0001c0001t0001g0282 a0001c0001t0001g0283 others(7): Show |
12 | HG01261.hp1 HG01433.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.58-10706T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109777530 | |||||||
| chr4:109777691 | A | G | 24 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0311 others(21): Show |
24 | HG00673.hp1 HG00735.hp2 HG02027.hp2 others(21): Show |
intron_variant | MODIFIER | c.58-10867T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109777691 | |||||||
| chr4:109777708 | C | T | 3 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 |
3 | HG02559.hp2 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.58-10884G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109777708 | |||||||
| chr4:109777853 | G | A | 5 | a0001c0002t0001g0288 a0001c0002t0001g0289 a0001c0002t0001g0291 others(2): Show |
5 | HG00735.hp2 HG01975.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.58-11029C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109777853 | |||||||
| chr4:109777873 | C | T | 175 | a0001c0001t0001g0002 a0001c0001t0001g0063 a0001c0001t0001g0082 others(172): Show |
180 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(177): Show |
intron_variant | MODIFIER | c.58-11049G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109777873 | |||||||
| chr4:109777874 | G | T | 1 | a0001c0001t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.58-11050C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109777874 | |||||||
| chr4:109777934 | T | C | 110 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(107): Show |
116 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.58-11110A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109777934 | |||||||
| chr4:109777942 | A | G | 1 | a0001c0001t0001g0255 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.58-11118T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109777942 | |||||||
| chr4:109778001 | A | G | 2 | a0001c0001t0001g0202 a0001c0001t0001g0203 |
2 | HG00280.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.58-11177T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109778001 | |||||||
| chr4:109778036 | A | T | 2 | a0001c0001t0001g0171 a0001c0001t0001g0187 |
2 | NA19068.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.58-11212T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109778036 | |||||||
| chr4:109778047 | A | T | 10 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0273 others(7): Show |
13 | HG02109.hp2 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.58-11223T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109778047 | |||||||
| chr4:109778081 | G | C | 1 | a0001c0002t0001g0061 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.58-11257C>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109778081 | |||||||
| chr4:109778103 | G | C | 1 | a0002c0003t0001g0315 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.58-11279C>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109778103 | |||||||
| chr4:109778195 | A | C | 20 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0311 others(17): Show |
20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.58-11371T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109778195 | |||||||
| chr4:109778274 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.58-11450A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109778274 | |||||||
| chr4:109778275 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.58-11451C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109778275 | |||||||
| chr4:109778332 | A | T | 4 | a0001c0002t0001g0105 a0001c0002t0001g0106 a0001c0002t0001g0133 others(1): Show |
4 | HG01243.hp2 HG02145.hp2 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.58-11508T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109778332 | |||||||
| chr4:109778683 | A | G | 163 | a0001c0001t0001g0063 a0001c0001t0001g0082 a0001c0001t0001g0084 others(160): Show |
166 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(163): Show |
intron_variant | MODIFIER | c.58-11859T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109778683 | |||||||
| chr4:109778784 | T | C | 329 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(326): Show |
345 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(342): Show |
intron_variant | MODIFIER | c.58-11960A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109778784 | |||||||
| chr4:109778816 | G | T | 2 | a0001c0001t0001g0329 a0001c0001t0002g0322 |
2 | HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.58-11992C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109778816 | |||||||
| chr4:109778977 | G | A | 78 | a0001c0001t0001g0063 a0001c0001t0001g0082 a0001c0001t0001g0084 others(75): Show |
80 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.58-12153C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109778977 | |||||||
| chr4:109779085 | C | T | 1 | a0001c0001t0001g0163 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.58-12261G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109779085 | |||||||
| chr4:109779129 | A | C | 163 | a0001c0001t0001g0063 a0001c0001t0001g0082 a0001c0001t0001g0084 others(160): Show |
166 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(163): Show |
intron_variant | MODIFIER | c.58-12305T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109779129 | |||||||
| chr4:109779151 | A | G | 6 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(3): Show |
6 | HG02723.hp2 HG02897.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.58-12327T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109779151 | |||||||
| chr4:109779169 | A | G | 110 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(107): Show |
116 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(113): Show |
intron_variant | MODIFIER | c.58-12345T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109779169 | |||||||
| chr4:109779182 | T | G | 163 | a0001c0001t0001g0063 a0001c0001t0001g0082 a0001c0001t0001g0084 others(160): Show |
166 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(163): Show |
intron_variant | MODIFIER | c.58-12358A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109779182 | |||||||
| chr4:109779218 | G | T | 1 | a0001c0001t0003g0013 | 2 | HG02258.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.58-12394C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109779218 | |||||||
| chr4:109779344 | C | T | 28 | a0001c0001t0001g0001 a0001c0001t0001g0172 a0001c0001t0001g0174 others(25): Show |
30 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.58-12520G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109779344 | |||||||
| chr4:109779371 | C | A | 13 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0156 others(10): Show |
15 | HG00099.hp1 HG00438.hp1 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.58-12547G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109779371 | |||||||
| chr4:109779693 | A | C | 1 | a0001c0001t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.58-12869T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109779693 | |||||||
| chr4:109779699 | A | G | 4 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 others(1): Show |
4 | HG02257.hp2 HG02976.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-12875T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109779699 | |||||||
| chr4:109779724 | C | T | 13 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0156 others(10): Show |
15 | HG00099.hp1 HG00438.hp1 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.58-12900G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109779724 | |||||||
| chr4:109779778 | A | G | 142 | a0001c0001t0001g0063 a0001c0001t0001g0082 a0001c0001t0001g0084 others(139): Show |
145 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(142): Show |
intron_variant | MODIFIER | c.58-12954T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109779778 | |||||||
| chr4:109779799 | C | T | 8 | a0001c0002t0001g0044 a0001c0002t0001g0045 a0001c0002t0001g0048 others(5): Show |
8 | HG01074.hp1 HG01081.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.58-12975G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109779799 | |||||||
| chr4:109779805 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.58-12981T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109779805 | |||||||
| chr4:109779828 | T | C | 163 | a0001c0001t0001g0063 a0001c0001t0001g0082 a0001c0001t0001g0084 others(160): Show |
166 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(163): Show |
intron_variant | MODIFIER | c.58-13004A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109779828 | |||||||
| chr4:109779911 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.58-13087C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109779911 | |||||||
| chr4:109779923 | G | A | 1 | a0001c0002t0001g0111 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.58-13099C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109779923 | |||||||
| chr4:109779924 | C | A | 3 | a0001c0002t0001g0093 a0001c0002t0001g0094 a0011c0009t0001g0092 |
3 | HG01175.hp2 HG02148.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.58-13100G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109779924 | |||||||
| chr4:109779954 | TCCTTATA others(15): Show |
T | 20 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0311 others(17): Show |
20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.58-13152_58-13131d others(24): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109779954 | |||||||
| chr4:109780022 | G | A | 1 | a0007c0013t0001g0290 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.58-13198C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109780022 | |||||||
| chr4:109780165 | G | C | 1 | a0001c0002t0001g0034 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.58-13341C>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109780165 | |||||||
| chr4:109780252 | C | T | 1 | a0003c0004t0001g0030 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.58-13428G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109780252 | |||||||
| chr4:109780331 | T | G | 184 | a0001c0001t0001g0002 a0001c0001t0001g0063 a0001c0001t0001g0082 others(181): Show |
189 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(186): Show |
intron_variant | MODIFIER | c.58-13507A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109780331 | |||||||
| chr4:109780333 | G | A | 4 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(1): Show |
4 | HG02559.hp2 HG03195.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-13509C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109780333 | |||||||
| chr4:109780500 | G | A | 1 | a0001c0001t0002g0158 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.58-13676C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109780500 | |||||||
| chr4:109780625 | G | C | 2 | a0001c0008t0001g0272 a0001c0008t0002g0271 |
2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.58-13801C>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109780625 | |||||||
| chr4:109780631 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.58-13807C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109780631 | |||||||
| chr4:109780824 | T | A | 325 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(322): Show |
341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.58-14000A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109780824 | |||||||
| chr4:109780969 | G | T | 20 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0311 others(17): Show |
20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.58-14145C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109780969 | |||||||
| chr4:109781049 | T | C | 78 | a0001c0001t0001g0063 a0001c0001t0001g0082 a0001c0001t0001g0084 others(75): Show |
80 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.58-14225A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109781049 | |||||||
| chr4:109781085 | A | G | 20 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0311 others(17): Show |
20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.58-14261T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109781085 | |||||||
| chr4:109781238 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.58-14414A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109781238 | |||||||
| chr4:109781354 | C | T | 2 | a0001c0001t0001g0273 a0001c0001t0002g0332 |
2 | HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.58-14530G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109781354 | |||||||
| chr4:109781369 | G | A | 78 | a0001c0001t0001g0063 a0001c0001t0001g0082 a0001c0001t0001g0084 others(75): Show |
80 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.58-14545C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109781369 | |||||||
| chr4:109781380 | A | G | 1 | a0001c0002t0001g0140 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.58-14556T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109781380 | |||||||
| chr4:109781500 | A | G | 4 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0200 others(1): Show |
4 | HG00735.hp1 HG00738.hp2 HG00741.hp2 others(1): Show |
intron_variant | MODIFIER | c.58-14676T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109781500 | |||||||
| chr4:109781795 | A | T | 4 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 others(1): Show |
4 | HG02257.hp2 HG02976.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-14971T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109781795 | |||||||
| chr4:109781819 | G | A | 55 | a0001c0002t0001g0006 a0001c0002t0001g0021 a0001c0002t0001g0022 others(52): Show |
56 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.58-14995C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109781819 | |||||||
| chr4:109781879 | CACA | C | 11 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0001c0001t0001g0192 others(8): Show |
11 | HG00639.hp2 HG01074.hp2 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.58-15058_58-15056d others(5): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109781879 | |||||||
| chr4:109781904 | A | G | 13 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0273 others(10): Show |
16 | HG02109.hp2 HG02145.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.58-15080T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109781904 | |||||||
| chr4:109781907 | G | A | 325 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(322): Show |
341 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.58-15083C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109781907 | |||||||
| chr4:109782092 | A | T | 55 | a0001c0002t0001g0006 a0001c0002t0001g0021 a0001c0002t0001g0022 others(52): Show |
56 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.58-15268T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109782092 | |||||||
| chr4:109782116 | C | T | 4 | a0001c0002t0001g0288 a0001c0002t0001g0289 a0001c0002t0001g0291 others(1): Show |
4 | HG00735.hp2 HG02055.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-15292G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109782116 | |||||||
| chr4:109782209 | C | G | 1 | a0001c0002t0001g0138 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.58-15385G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109782209 | |||||||
| chr4:109782406 | A | G | 1 | a0001c0001t0001g0331 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.58-15582T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109782406 | |||||||
| chr4:109782431 | C | CA | 67 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(64): Show |
68 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.58-15608dupT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109782431 | |||||||
| chr4:109782431 | C | CAA | 119 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(116): Show |
128 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.58-15609_58-15608d others(4): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109782431 | |||||||
| chr4:109782431 | C | CAAA | 13 | a0001c0001t0001g0082 a0001c0001t0001g0159 a0001c0001t0001g0160 others(10): Show |
13 | HG01175.hp1 HG01975.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.58-15610_58-15608d others(5): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109782431 | |||||||
| chr4:109782431 | C | CAAAA | 106 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(103): Show |
112 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.58-15611_58-15608d others(6): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109782431 | |||||||
| chr4:109782446 | T | A | 1 | a0001c0002t0001g0069 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.58-15622A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109782446 | |||||||
| chr4:109782597 | C | T | 2 | a0003c0004t0001g0154 a0003c0004t0001g0155 |
2 | HG00738.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.58-15773G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109782597 | |||||||
| chr4:109782741 | G | A | 5 | a0001c0002t0001g0288 a0001c0002t0001g0289 a0001c0002t0001g0291 others(2): Show |
5 | HG00735.hp2 HG01975.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.58-15917C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109782741 | |||||||
| chr4:109782936 | C | A | 2 | a0001c0001t0001g0171 a0001c0001t0001g0187 |
2 | NA19068.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.58-16112G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109782936 | |||||||
| chr4:109782976 | T | C | 78 | a0001c0001t0001g0063 a0001c0001t0001g0082 a0001c0001t0001g0084 others(75): Show |
80 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.58-16152A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109782976 | |||||||
| chr4:109783201 | C | A | 1 | a0006c0014t0001g0038 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.58-16377G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783201 | |||||||
| chr4:109783277 | C | T | 1 | a0001c0002t0001g0093 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.58-16453G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783277 | |||||||
| chr4:109783372 | T | C | 2 | a0001c0001t0001g0336 a0001c0001t0001g0337 |
2 | HG02109.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.58-16548A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783372 | |||||||
| chr4:109783411 | A | G | 20 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0311 others(17): Show |
20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.58-16587T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783411 | |||||||
| chr4:109783811 | T | TAATATAT others(3): Show |
18 | a0001c0002t0001g0006 a0001c0002t0001g0022 a0001c0002t0001g0121 others(15): Show |
19 | HG00558.hp2 HG01070.hp2 HG02015.hp2 others(16): Show |
intron_variant | MODIFIER | c.58-16988_58-16987i others(12): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783811 | |||||||
| chr4:109783811 | T | TAATATAT others(5): Show |
12 | a0001c0002t0001g0102 a0001c0002t0001g0103 a0001c0002t0001g0104 others(9): Show |
12 | HG00609.hp2 HG00673.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.58-16988_58-16987i others(14): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783811 | |||||||
| chr4:109783811 | T | TAATATAT others(7): Show |
4 | a0001c0002t0001g0112 a0001c0002t0001g0113 a0001c0002t0001g0114 others(1): Show |
4 | HG00609.hp1 HG01978.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.58-16988_58-16987i others(16): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783811 | |||||||
| chr4:109783811 | T | TAATATAT others(9): Show |
1 | a0001c0002t0001g0111 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.58-16988_58-16987i others(18): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783811 | |||||||
| chr4:109783811 | T | TAATATAT others(15): Show |
1 | a0001c0002t0001g0110 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.58-16988_58-16987i others(24): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783811 | |||||||
| chr4:109783811 | T | TAATATAT others(17): Show |
2 | a0001c0002t0002g0101 a0001c0002t0002g0109 |
2 | HG02559.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.58-16988_58-16987i others(26): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783811 | |||||||
| chr4:109783811 | T | TAATATAT others(19): Show |
1 | a0001c0002t0002g0100 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.58-16988_58-16987i others(28): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783811 | |||||||
| chr4:109783811 | T | TAATATAT others(23): Show |
2 | a0001c0002t0001g0140 a0008c0011t0001g0108 |
2 | HG02280.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.58-16988_58-16987i others(32): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783811 | |||||||
| chr4:109783811 | T | TAATATAT others(25): Show |
1 | a0001c0002t0003g0280 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.58-16988_58-16987i others(34): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783811 | |||||||
| chr4:109783811 | T | TAATATAT others(27): Show |
2 | a0001c0002t0001g0139 a0001c0002t0002g0107 |
2 | HG01255.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.58-16988_58-16987i others(36): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783811 | |||||||
| chr4:109783811 | T | TAATATAT others(33): Show |
2 | a0001c0002t0001g0133 a0001c0002t0001g0134 |
2 | HG01243.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.58-16988_58-16987i others(42): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783811 | |||||||
| chr4:109783811 | T | TAATATAT others(35): Show |
1 | a0001c0002t0002g0023 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.58-16988_58-16987i others(44): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783811 | |||||||
| chr4:109783811 | T | TAATATAT others(37): Show |
1 | a0001c0002t0001g0106 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.58-16988_58-16987i others(46): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783811 | |||||||
| chr4:109783811 | T | TAATATAT others(39): Show |
1 | a0001c0006t0005g0099 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.58-16988_58-16987i others(48): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783811 | |||||||
| chr4:109783811 | T | TAATATAT others(41): Show |
1 | a0001c0002t0001g0105 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.58-16988_58-16987i others(50): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783811 | |||||||
| chr4:109783812 | G | A | 1 | a0001c0002t0001g0287 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.58-16988C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783812 | |||||||
| chr4:109783812 | G | GAGATATT others(3): Show |
16 | a0001c0001t0001g0304 a0001c0001t0001g0311 a0002c0003t0001g0248 others(13): Show |
16 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(13): Show |
intron_variant | MODIFIER | c.58-16989_58-16988i others(12): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783812 | |||||||
| chr4:109783812 | G | GAGATATT others(5): Show |
2 | a0001c0001t0001g0303 a0002c0003t0001g0317 |
2 | HG03831.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.58-16989_58-16988i others(14): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783812 | |||||||
| chr4:109783812 | G | GAGATATT others(9): Show |
2 | a0002c0003t0001g0301 a0002c0003t0001g0302 |
2 | NA18994.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.58-16989_58-16988i others(18): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783812 | |||||||
| chr4:109783812 | G | GAT | 25 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(22): Show |
25 | HG00544.hp1 HG01109.hp2 HG02056.hp2 others(22): Show |
intron_variant | MODIFIER | c.58-16990_58-16989d others(4): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783812 | |||||||
| chr4:109783812 | G | GATATATA others(1): Show |
3 | a0001c0002t0001g0089 a0001c0002t0001g0090 a0001c0002t0001g0097 |
3 | HG02004.hp1 HG02258.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.58-16996_58-16989d others(10): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783812 | |||||||
| chr4:109783812 | G | GATATATA others(5): Show |
1 | a0001c0002t0001g0291 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.58-17000_58-16989d others(14): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783812 | |||||||
| chr4:109783812 | G | GATATATA others(7): Show |
4 | a0004c0005t0001g0086 a0004c0005t0001g0087 a0004c0005t0001g0088 others(1): Show |
4 | NA18941.hp2 NA18999.hp2 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.58-17002_58-16989d others(16): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783812 | |||||||
| chr4:109783812 | G | GATATATA others(9): Show |
2 | a0001c0002t0001g0050 a0007c0013t0001g0290 |
2 | HG01975.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.58-17004_58-16989d others(18): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783812 | |||||||
| chr4:109783812 | G | GATATATA others(15): Show |
2 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.58-17010_58-16989d others(24): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783812 | |||||||
| chr4:109783812 | G | GATATATA others(17): Show |
1 | a0001c0002t0001g0042 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.58-16989_58-16988i others(26): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783812 | |||||||
| chr4:109783812 | G | GATATATA others(19): Show |
1 | a0001c0002t0001g0083 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.58-16989_58-16988i others(28): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783812 | |||||||
| chr4:109783812 | G | GATATATA others(27): Show |
3 | a0001c0002t0001g0048 a0001c0002t0001g0049 a0001c0002t0004g0018 |
3 | HG01070.hp1 HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.58-16989_58-16988i others(36): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783812 | |||||||
| chr4:109783812 | G | GATATATA others(29): Show |
7 | a0001c0001t0001g0082 a0001c0002t0001g0019 a0001c0002t0001g0034 others(4): Show |
7 | HG01071.hp1 HG01071.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.58-16989_58-16988i others(38): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783812 | |||||||
| chr4:109783812 | G | GATATATA others(31): Show |
7 | a0001c0002t0001g0074 a0001c0002t0001g0075 a0001c0002t0001g0076 others(4): Show |
7 | HG01069.hp1 HG01074.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.58-16989_58-16988i others(40): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783812 | |||||||
| chr4:109783812 | G | GATATATA others(33): Show |
9 | a0001c0001t0001g0096 a0001c0002t0001g0037 a0001c0002t0001g0040 others(6): Show |
9 | HG01069.hp2 HG01081.hp1 HG01993.hp2 others(6): Show |
intron_variant | MODIFIER | c.58-16989_58-16988i others(42): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783812 | |||||||
| chr4:109783812 | G | GATATATA others(35): Show |
11 | a0001c0002t0001g0005 a0001c0002t0001g0033 a0001c0002t0001g0039 others(8): Show |
12 | HG00733.hp1 HG01167.hp2 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.58-16989_58-16988i others(44): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783812 | |||||||
| chr4:109783812 | G | GATATATA others(37): Show |
10 | a0001c0001t0001g0063 a0001c0002t0001g0064 a0001c0002t0001g0065 others(7): Show |
10 | HG01123.hp2 HG01257.hp2 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.58-16989_58-16988i others(46): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783812 | |||||||
| chr4:109783812 | G | GATATATA others(39): Show |
12 | a0001c0002t0001g0035 a0001c0002t0001g0045 a0001c0002t0001g0057 others(9): Show |
12 | HG00323.hp1 HG01106.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.58-16989_58-16988i others(48): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783812 | |||||||
| chr4:109783812 | G | GATATATA others(41): Show |
5 | a0001c0002t0001g0004 a0001c0002t0001g0054 a0001c0002t0001g0055 others(2): Show |
6 | NA18747.hp1 NA18984.hp2 NA19062.hp1 others(3): Show |
intron_variant | MODIFIER | c.58-16989_58-16988i others(50): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783812 | |||||||
| chr4:109783812 | G | GATATATA others(43): Show |
1 | a0001c0002t0001g0053 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.58-16989_58-16988i others(52): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783812 | |||||||
| chr4:109783812 | G | GATATATA others(49): Show |
2 | a0001c0002t0001g0051 a0001c0002t0001g0052 |
2 | HG00558.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.58-16989_58-16988i others(58): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783812 | |||||||
| chr4:109783812 | G | GATATATA others(51): Show |
1 | a0001c0002t0001g0044 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.58-16989_58-16988i others(60): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783812 | |||||||
| chr4:109783812 | G | T | 54 | a0001c0002t0001g0006 a0001c0002t0001g0021 a0001c0002t0001g0022 others(51): Show |
55 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.58-16988C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783812 | |||||||
| chr4:109783812 | GAT | G | 5 | a0001c0001t0001g0002 a0001c0001t0001g0293 a0001c0001t0001g0294 others(2): Show |
7 | HG01261.hp1 HG01433.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.58-16990_58-16989d others(4): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783812 | |||||||
| chr4:109783812 | GATAT | G | 5 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(2): Show |
5 | HG02559.hp2 HG03195.hp1 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.58-16992_58-16989d others(6): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783812 | |||||||
| chr4:109783975 | G | A | 78 | a0001c0001t0001g0063 a0001c0001t0001g0082 a0001c0001t0001g0084 others(75): Show |
80 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.58-17151C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109783975 | |||||||
| chr4:109784084 | G | A | 2 | a0001c0002t0001g0133 a0001c0002t0001g0134 |
2 | HG01243.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.58-17260C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109784084 | |||||||
| chr4:109784093 | T | G | 1 | a0001c0001t0003g0013 | 2 | HG02258.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.58-17269A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109784093 | |||||||
| chr4:109784095 | G | T | 1 | a0001c0001t0003g0013 | 2 | HG02258.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.58-17271C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109784095 | |||||||
| chr4:109784148 | T | A | 1 | a0003c0004t0001g0155 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.58-17324A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109784148 | |||||||
| chr4:109784472 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.57+17443T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109784472 | |||||||
| chr4:109784893 | GA | G | 185 | a0001c0001t0001g0002 a0001c0001t0001g0063 a0001c0001t0001g0082 others(182): Show |
190 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(187): Show |
intron_variant | MODIFIER | c.57+17021delT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109784893 | |||||||
| chr4:109784993 | G | C | 1 | a0001c0001t0001g0181 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.57+16922C>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109784993 | |||||||
| chr4:109785016 | C | A | 1 | a0002c0003t0001g0317 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.57+16899G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109785016 | |||||||
| chr4:109785021 | G | A | 7 | a0001c0001t0001g0151 a0001c0001t0001g0254 a0001c0001t0001g0255 others(4): Show |
7 | HG06807.hp1 NA18961.hp2 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.57+16894C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109785021 | |||||||
| chr4:109785052 | C | A | 77 | a0001c0001t0001g0063 a0001c0001t0001g0082 a0001c0001t0001g0084 others(74): Show |
79 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(76): Show |
intron_variant | MODIFIER | c.57+16863G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109785052 | |||||||
| chr4:109785091 | A | C | 163 | a0001c0001t0001g0063 a0001c0001t0001g0082 a0001c0001t0001g0084 others(160): Show |
166 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(163): Show |
intron_variant | MODIFIER | c.57+16824T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109785091 | |||||||
| chr4:109785108 | A | T | 20 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0311 others(17): Show |
20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.57+16807T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109785108 | |||||||
| chr4:109785183 | G | A | 77 | a0001c0001t0001g0063 a0001c0001t0001g0082 a0001c0001t0001g0084 others(74): Show |
79 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(76): Show |
intron_variant | MODIFIER | c.57+16732C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109785183 | |||||||
| chr4:109785296 | G | A | 77 | a0001c0001t0001g0063 a0001c0001t0001g0082 a0001c0001t0001g0084 others(74): Show |
79 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(76): Show |
intron_variant | MODIFIER | c.57+16619C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109785296 | |||||||
| chr4:109785328 | T | C | 2 | a0001c0006t0005g0098 a0001c0006t0005g0099 |
2 | HG02647.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.57+16587A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109785328 | |||||||
| chr4:109785375 | T | C | 66 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0001t0001g0323 others(63): Show |
67 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.57+16540A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109785375 | |||||||
| chr4:109785480 | T | C | 21 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 others(18): Show |
23 | HG00735.hp2 HG01261.hp1 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.57+16435A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109785480 | |||||||
| chr4:109786051 | A | C | 66 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0001t0001g0323 others(63): Show |
67 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.57+15864T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109786051 | |||||||
| chr4:109786077 | A | C | 1 | a0001c0001t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.57+15838T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109786077 | |||||||
| chr4:109786082 | G | A | 4 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 others(1): Show |
4 | HG02257.hp2 HG02976.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.57+15833C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109786082 | |||||||
| chr4:109786223 | G | A | 1 | a0001c0001t0001g0316 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.57+15692C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109786223 | |||||||
| chr4:109786225 | T | C | 21 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0311 others(18): Show |
21 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.57+15690A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109786225 | |||||||
| chr4:109786239 | C | T | 1 | a0001c0002t0001g0275 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.57+15676G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109786239 | |||||||
| chr4:109786277 | C | T | 2 | a0001c0001t0001g0162 a0001c0001t0001g0181 |
2 | NA18970.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.57+15638G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109786277 | |||||||
| chr4:109786385 | T | G | 7 | a0001c0001t0001g0002 a0001c0001t0001g0293 a0001c0001t0001g0294 others(4): Show |
9 | HG01261.hp1 HG01433.hp1 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.57+15530A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109786385 | |||||||
| chr4:109786390 | C | CT | 5 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(2): Show |
5 | HG02723.hp2 HG02897.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.57+15524dupA | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109786390 | |||||||
| chr4:109786413 | C | A | 9 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(6): Show |
9 | HG02559.hp2 HG02723.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.57+15502G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109786413 | |||||||
| chr4:109786518 | C | A | 2 | a0003c0004t0001g0154 a0003c0004t0001g0155 |
2 | HG00738.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.57+15397G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109786518 | |||||||
| chr4:109786583 | C | A | 99 | a0001c0001t0001g0063 a0001c0001t0001g0082 a0001c0001t0001g0084 others(96): Show |
101 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(98): Show |
intron_variant | MODIFIER | c.57+15332G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109786583 | |||||||
| chr4:109786610 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.57+15305C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109786610 | |||||||
| chr4:109786694 | G | A | 1 | a0001c0001t0001g0012 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.57+15221C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109786694 | |||||||
| chr4:109786727 | A | G | 5 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(2): Show |
5 | NA18956.hp1 NA18962.hp2 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.57+15188T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109786727 | |||||||
| chr4:109786823 | A | G | 21 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0311 others(18): Show |
21 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(18): Show |
intron_variant | MODIFIER | c.57+15092T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109786823 | |||||||
| chr4:109786869 | T | C | 78 | a0001c0001t0001g0063 a0001c0001t0001g0082 a0001c0001t0001g0084 others(75): Show |
80 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(77): Show |
intron_variant | MODIFIER | c.57+15046A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109786869 | |||||||
| chr4:109786977 | G | A | 9 | a0001c0001t0001g0320 a0001c0001t0001g0323 a0001c0001t0001g0324 others(6): Show |
9 | HG02486.hp2 HG02622.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.57+14938C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109786977 | |||||||
| chr4:109787127 | C | A | 1 | a0001c0002t0001g0135 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.57+14788G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109787127 | |||||||
| chr4:109787147 | T | G | 77 | a0001c0001t0001g0063 a0001c0001t0001g0082 a0001c0001t0001g0084 others(74): Show |
79 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(76): Show |
intron_variant | MODIFIER | c.57+14768A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109787147 | |||||||
| chr4:109787250 | T | C | 98 | a0001c0001t0001g0063 a0001c0001t0001g0082 a0001c0001t0001g0084 others(95): Show |
100 | HG00323.hp1 HG00558.hp1 HG00673.hp1 others(97): Show |
intron_variant | MODIFIER | c.57+14665A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109787250 | |||||||
| chr4:109787264 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.57+14651C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109787264 | |||||||
| chr4:109787304 | C | T | 1 | a0002c0003t0001g0300 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.57+14611G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109787304 | |||||||
| chr4:109787361 | A | C | 77 | a0001c0001t0001g0063 a0001c0001t0001g0082 a0001c0001t0001g0084 others(74): Show |
79 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(76): Show |
intron_variant | MODIFIER | c.57+14554T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109787361 | |||||||
| chr4:109787417 | G | A | 100 | a0001c0001t0001g0002 a0001c0001t0001g0063 a0001c0001t0001g0082 others(97): Show |
104 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(101): Show |
intron_variant | MODIFIER | c.57+14498C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109787417 | |||||||
| chr4:109787474 | C | T | 66 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0001t0001g0323 others(63): Show |
67 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.57+14441G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109787474 | |||||||
| chr4:109787480 | A | G | 109 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 others(106): Show |
112 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(109): Show |
intron_variant | MODIFIER | c.57+14435T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109787480 | |||||||
| chr4:109787514 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.57+14401T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109787514 | |||||||
| chr4:109787588 | G | A | 1 | a0001c0001t0001g0242 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.57+14327C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109787588 | |||||||
| chr4:109787595 | T | A | 3 | a0001c0002t0001g0093 a0001c0002t0001g0094 a0011c0009t0001g0092 |
3 | HG01175.hp2 HG02148.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.57+14320A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109787595 | |||||||
| chr4:109787720 | A | C | 1 | a0001c0001t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.57+14195T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109787720 | |||||||
| chr4:109787796 | A | T | 1 | a0001c0001t0003g0153 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.57+14119T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109787796 | |||||||
| chr4:109787865 | T | A | 5 | a0001c0001t0001g0002 a0001c0001t0001g0293 a0001c0001t0001g0294 others(2): Show |
7 | HG01261.hp1 HG01433.hp1 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.57+14050A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109787865 | |||||||
| chr4:109787892 | G | T | 20 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0311 others(17): Show |
20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.57+14023C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109787892 | |||||||
| chr4:109788006 | A | G | 8 | a0001c0002t0001g0044 a0001c0002t0001g0045 a0001c0002t0001g0048 others(5): Show |
8 | HG01074.hp1 HG01081.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.57+13909T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109788006 | |||||||
| chr4:109788044 | T | C | 1 | a0001c0001t0001g0243 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.57+13871A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109788044 | |||||||
| chr4:109788137 | A | G | 188 | a0001c0001t0001g0002 a0001c0001t0001g0063 a0001c0001t0001g0082 others(185): Show |
193 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(190): Show |
intron_variant | MODIFIER | c.57+13778T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109788137 | |||||||
| chr4:109788376 | G | T | 1 | a0001c0001t0001g0175 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.57+13539C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109788376 | |||||||
| chr4:109788501 | C | T | 20 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0311 others(17): Show |
20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.57+13414G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109788501 | |||||||
| chr4:109788517 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.57+13398A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109788517 | |||||||
| chr4:109788718 | G | T | 1 | a0002c0003t0001g0299 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.57+13197C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109788718 | |||||||
| chr4:109788723 | G | A | 80 | a0001c0001t0001g0063 a0001c0001t0001g0082 a0001c0001t0001g0084 others(77): Show |
82 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.57+13192C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109788723 | |||||||
| chr4:109788861 | G | C | 1 | a0001c0001t0001g0316 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.57+13054C>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109788861 | |||||||
| chr4:109788878 | C | T | 79 | a0001c0001t0001g0063 a0001c0001t0001g0082 a0001c0001t0001g0084 others(76): Show |
81 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(78): Show |
intron_variant | MODIFIER | c.57+13037G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109788878 | |||||||
| chr4:109788890 | C | T | 1 | a0001c0002t0001g0043 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.57+13025G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109788890 | |||||||
| chr4:109788951 | A | G | 313 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(310): Show |
327 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(324): Show |
intron_variant | MODIFIER | c.57+12964T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109788951 | |||||||
| chr4:109789020 | G | T | 80 | a0001c0001t0001g0063 a0001c0001t0001g0082 a0001c0001t0001g0084 others(77): Show |
82 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(79): Show |
intron_variant | MODIFIER | c.57+12895C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109789020 | |||||||
| chr4:109789038 | C | A | 5 | a0001c0002t0001g0021 a0001c0002t0001g0022 a0001c0002t0001g0136 others(2): Show |
5 | HG00609.hp2 HG02015.hp2 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.57+12877G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109789038 | |||||||
| chr4:109789042 | T | C | 1 | a0001c0001t0001g0270 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.57+12873A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109789042 | |||||||
| chr4:109789134 | A | G | 1 | a0001c0001t0003g0153 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.57+12781T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109789134 | |||||||
| chr4:109789160 | A | G | 79 | a0001c0001t0001g0063 a0001c0001t0001g0082 a0001c0001t0001g0084 others(76): Show |
81 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(78): Show |
intron_variant | MODIFIER | c.57+12755T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109789160 | |||||||
| chr4:109789249 | A | C | 1 | a0001c0001t0001g0174 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.57+12666T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109789249 | |||||||
| chr4:109789386 | A | G | 1 | a0001c0001t0001g0173 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.57+12529T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109789386 | |||||||
| chr4:109789423 | A | G | 3 | a0001c0001t0001g0273 a0001c0008t0001g0272 a0001c0008t0002g0271 |
3 | HG03516.hp2 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.57+12492T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109789423 | |||||||
| chr4:109789441 | G | GAC | 108 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 others(105): Show |
111 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.57+12472_57+12473d others(4): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109789441 | |||||||
| chr4:109789461 | G | A | 20 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0311 others(17): Show |
20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.57+12454C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109789461 | |||||||
| chr4:109789552 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.57+12363T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109789552 | |||||||
| chr4:109789568 | T | C | 188 | a0001c0001t0001g0002 a0001c0001t0001g0063 a0001c0001t0001g0082 others(185): Show |
193 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(190): Show |
intron_variant | MODIFIER | c.57+12347A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109789568 | |||||||
| chr4:109789830 | G | A | 3 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 |
3 | HG02559.hp2 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.57+12085C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109789830 | |||||||
| chr4:109789925 | G | A | 107 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 others(104): Show |
110 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.57+11990C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109789925 | |||||||
| chr4:109789938 | G | A | 1 | a0001c0002t0001g0292 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.57+11977C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109789938 | |||||||
| chr4:109790007 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.57+11908A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109790007 | |||||||
| chr4:109790256 | G | A | 20 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0311 others(17): Show |
20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.57+11659C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109790256 | |||||||
| chr4:109790467 | T | C | 188 | a0001c0001t0001g0002 a0001c0001t0001g0063 a0001c0001t0001g0082 others(185): Show |
193 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(190): Show |
intron_variant | MODIFIER | c.57+11448A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109790467 | |||||||
| chr4:109790512 | G | C | 1 | a0001c0002t0001g0037 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.57+11403C>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109790512 | |||||||
| chr4:109790531 | C | G | 1 | a0001c0001t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.57+11384G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109790531 | |||||||
| chr4:109790741 | C | T | 2 | a0001c0002t0001g0041 a0001c0002t0001g0042 |
2 | HG02886.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.57+11174G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109790741 | |||||||
| chr4:109790791 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.57+11124C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109790791 | |||||||
| chr4:109790837 | C | G | 5 | a0001c0002t0001g0288 a0001c0002t0001g0289 a0001c0002t0001g0291 others(2): Show |
5 | HG00735.hp2 HG01975.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.57+11078G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109790837 | |||||||
| chr4:109790910 | T | C | 1 | a0001c0002t0001g0097 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.57+11005A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109790910 | |||||||
| chr4:109790952 | A | G | 2 | a0001c0001t0001g0249 a0002c0003t0001g0248 |
2 | NA18950.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.57+10963T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109790952 | |||||||
| chr4:109791166 | T | C | 2 | a0001c0001t0001g0336 a0001c0001t0001g0337 |
2 | HG02109.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.57+10749A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109791166 | |||||||
| chr4:109791203 | G | A | 9 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(6): Show |
9 | HG02559.hp2 HG02723.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.57+10712C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109791203 | |||||||
| chr4:109791432 | G | T | 1 | a0001c0001t0001g0171 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.57+10483C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109791432 | |||||||
| chr4:109791729 | T | G | 5 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0001g0148 others(2): Show |
5 | HG02723.hp2 HG02897.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.57+10186A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109791729 | |||||||
| chr4:109791738 | A | T | 2 | a0001c0001t0001g0336 a0001c0001t0001g0337 |
2 | HG02109.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.57+10177T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109791738 | |||||||
| chr4:109791927 | G | C | 1 | a0001c0001t0001g0244 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.57+9988C>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109791927 | |||||||
| chr4:109792069 | T | C | 2 | a0001c0001t0001g0245 a0001c0001t0001g0246 |
2 | HG01109.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.57+9846A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109792069 | |||||||
| chr4:109792091 | C | T | 79 | a0001c0001t0001g0063 a0001c0001t0001g0082 a0001c0001t0001g0084 others(76): Show |
81 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(78): Show |
intron_variant | MODIFIER | c.57+9824G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109792091 | |||||||
| chr4:109792119 | C | A | 3 | a0001c0002t0001g0285 a0001c0002t0001g0286 a0001c0002t0001g0287 |
3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.57+9796G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109792119 | |||||||
| chr4:109792327 | T | C | 187 | a0001c0001t0001g0002 a0001c0001t0001g0063 a0001c0001t0001g0082 others(184): Show |
192 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(189): Show |
intron_variant | MODIFIER | c.57+9588A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109792327 | |||||||
| chr4:109792376 | G | A | 107 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 others(104): Show |
110 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.57+9539C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109792376 | |||||||
| chr4:109792447 | A | C | 66 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0001t0001g0323 others(63): Show |
67 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.57+9468T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109792447 | |||||||
| chr4:109792523 | C | T | 79 | a0001c0001t0001g0063 a0001c0001t0001g0082 a0001c0001t0001g0084 others(76): Show |
81 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(78): Show |
intron_variant | MODIFIER | c.57+9392G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109792523 | |||||||
| chr4:109792545 | A | G | 2 | a0001c0002t0001g0105 a0001c0002t0001g0106 |
2 | HG02145.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.57+9370T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109792545 | |||||||
| chr4:109792592 | C | G | 2 | a0001c0001t0003g0334 a0001c0001t0003g0335 |
2 | HG02486.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.57+9323G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109792592 | |||||||
| chr4:109792697 | C | T | 9 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(6): Show |
9 | HG02559.hp2 HG02723.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.57+9218G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109792697 | |||||||
| chr4:109792728 | T | C | 2 | a0001c0002t0001g0139 a0001c0002t0001g0140 |
2 | HG02280.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.57+9187A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109792728 | |||||||
| chr4:109792747 | C | T | 2 | a0001c0002t0001g0103 a0001c0002t0001g0104 |
2 | NA18939.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.57+9168G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109792747 | |||||||
| chr4:109792748 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.57+9167C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109792748 | |||||||
| chr4:109792755 | G | C | 77 | a0001c0001t0001g0063 a0001c0001t0001g0082 a0001c0001t0001g0084 others(74): Show |
79 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(76): Show |
intron_variant | MODIFIER | c.57+9160C>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109792755 | |||||||
| chr4:109792782 | A | G | 1 | a0001c0001t0003g0153 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.57+9133T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109792782 | |||||||
| chr4:109792783 | G | A | 1 | a0001c0001t0001g0246 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.57+9132C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109792783 | |||||||
| chr4:109792789 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.57+9126G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109792789 | |||||||
| chr4:109792808 | A | G | 108 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 others(105): Show |
111 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.57+9107T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109792808 | |||||||
| chr4:109792865 | C | T | 9 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(6): Show |
9 | HG02559.hp2 HG02723.hp2 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.57+9050G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109792865 | |||||||
| chr4:109792907 | T | G | 108 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 others(105): Show |
111 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.57+9008A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109792907 | |||||||
| chr4:109792912 | C | A | 1 | a0003c0004t0001g0297 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.57+9003G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109792912 | |||||||
| chr4:109792941 | T | A | 3 | a0003c0004t0001g0030 a0003c0004t0001g0031 a0003c0004t0001g0032 |
3 | HG02055.hp2 HG02257.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.57+8974A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109792941 | |||||||
| chr4:109793147 | C | T | 5 | a0001c0001t0001g0170 a0001c0001t0001g0247 a0001c0001t0001g0273 others(2): Show |
5 | HG00280.hp1 HG01081.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.57+8768G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109793147 | |||||||
| chr4:109793203 | T | C | 1 | a0001c0001t0001g0247 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.57+8712A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109793203 | |||||||
| chr4:109793251 | C | T | 3 | a0001c0001t0001g0273 a0001c0008t0001g0272 a0001c0008t0002g0271 |
3 | HG03516.hp2 HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.57+8664G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109793251 | |||||||
| chr4:109793293 | T | C | 1 | a0001c0002t0001g0141 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.57+8622A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109793293 | |||||||
| chr4:109793370 | G | A | 1 | a0004c0005t0001g0095 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.57+8545C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109793370 | |||||||
| chr4:109793581 | G | A | 12 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0251 others(9): Show |
12 | HG02004.hp2 NA18942.hp2 NA18950.hp2 others(9): Show |
intron_variant | MODIFIER | c.57+8334C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109793581 | |||||||
| chr4:109793656 | T | C | 107 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 others(104): Show |
110 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.57+8259A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109793656 | |||||||
| chr4:109793748 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.57+8167G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109793748 | |||||||
| chr4:109793854 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.57+8061A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109793854 | |||||||
| chr4:109793994 | C | T | 4 | a0001c0002t0001g0035 a0001c0002t0001g0039 a0001c0002t0001g0040 others(1): Show |
4 | HG00323.hp1 HG01069.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.57+7921G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109793994 | |||||||
| chr4:109794033 | C | T | 1 | a0001c0001t0003g0153 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.57+7882G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109794033 | |||||||
| chr4:109794063 | C | T | 1 | a0001c0002t0001g0281 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.57+7852G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109794063 | |||||||
| chr4:109794129 | T | A | 20 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0311 others(17): Show |
20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.57+7786A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109794129 | |||||||
| chr4:109794237 | T | C | 1 | a0001c0001t0003g0153 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.57+7678A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109794237 | |||||||
| chr4:109794303 | G | T | 77 | a0001c0001t0001g0063 a0001c0001t0001g0082 a0001c0001t0001g0084 others(74): Show |
79 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(76): Show |
intron_variant | MODIFIER | c.57+7612C>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109794303 | |||||||
| chr4:109794317 | C | T | 108 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 others(105): Show |
111 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.57+7598G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109794317 | |||||||
| chr4:109794535 | T | C | 5 | a0001c0002t0001g0288 a0001c0002t0001g0289 a0001c0002t0001g0291 others(2): Show |
5 | HG00735.hp2 HG01975.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.57+7380A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109794535 | |||||||
| chr4:109794786 | C | G | 1 | a0001c0001t0001g0330 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.57+7129G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109794786 | |||||||
| chr4:109794889 | G | A | 23 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0156 others(20): Show |
25 | HG00099.hp1 HG00438.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.57+7026C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109794889 | |||||||
| chr4:109794892 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.57+7023A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109794892 | |||||||
| chr4:109794896 | A | C | 108 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 others(105): Show |
111 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.57+7019T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109794896 | |||||||
| chr4:109794914 | C | G | 1 | a0001c0002t0001g0037 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.57+7001G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109794914 | |||||||
| chr4:109795016 | C | T | 1 | a0009c0010t0001g0036 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.57+6899G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109795016 | |||||||
| chr4:109795135 | G | A | 1 | a0002c0003t0001g0317 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.57+6780C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109795135 | |||||||
| chr4:109795204 | A | T | 79 | a0001c0001t0001g0063 a0001c0001t0001g0082 a0001c0001t0001g0084 others(76): Show |
81 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(78): Show |
intron_variant | MODIFIER | c.57+6711T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109795204 | |||||||
| chr4:109795236 | C | A | 1 | a0001c0002t0001g0281 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.57+6679G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109795236 | |||||||
| chr4:109795251 | C | T | 66 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0001t0001g0323 others(63): Show |
67 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.57+6664G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109795251 | |||||||
| chr4:109795252 | G | A | 1 | a0001c0001t0001g0260 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.57+6663C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109795252 | |||||||
| chr4:109795311 | G | A | 107 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 others(104): Show |
110 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.57+6604C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109795311 | |||||||
| chr4:109795323 | C | G | 13 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0156 others(10): Show |
15 | HG00099.hp1 HG00438.hp1 HG00639.hp1 others(12): Show |
intron_variant | MODIFIER | c.57+6592G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109795323 | |||||||
| chr4:109795341 | C | T | 107 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 others(104): Show |
110 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.57+6574G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109795341 | |||||||
| chr4:109795362 | T | C | 1 | a0001c0001t0001g0273 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.57+6553A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109795362 | |||||||
| chr4:109795447 | T | C | 108 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 others(105): Show |
111 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.57+6468A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109795447 | |||||||
| chr4:109795488 | C | A | 107 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 others(104): Show |
110 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.57+6427G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109795488 | |||||||
| chr4:109795604 | C | T | 20 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0311 others(17): Show |
20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.57+6311G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109795604 | |||||||
| chr4:109795731 | T | C | 86 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0311 others(83): Show |
87 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.57+6184A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109795731 | |||||||
| chr4:109795742 | T | A | 108 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 others(105): Show |
111 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.57+6173A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109795742 | |||||||
| chr4:109795751 | C | T | 66 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0001t0001g0323 others(63): Show |
67 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.57+6164G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109795751 | |||||||
| chr4:109795862 | C | A | 108 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 others(105): Show |
111 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.57+6053G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109795862 | |||||||
| chr4:109796003 | C | T | 2 | a0003c0004t0001g0157 a0003c0004t0001g0297 |
2 | HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.57+5912G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109796003 | |||||||
| chr4:109796087 | G | A | 107 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 others(104): Show |
110 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.57+5828C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109796087 | |||||||
| chr4:109796216 | A | C | 2 | a0003c0004t0001g0154 a0003c0004t0001g0155 |
2 | HG00738.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.57+5699T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109796216 | |||||||
| chr4:109796222 | A | C | 1 | a0001c0001t0001g0161 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.57+5693T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109796222 | |||||||
| chr4:109796235 | G | A | 3 | a0001c0002t0001g0142 a0001c0002t0001g0143 a0002c0003t0001g0318 |
3 | HG02056.hp1 NA18998.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.57+5680C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109796235 | |||||||
| chr4:109796422 | C | T | 108 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 others(105): Show |
111 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(108): Show |
intron_variant | MODIFIER | c.57+5493G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109796422 | |||||||
| chr4:109796495 | G | A | 5 | a0001c0002t0001g0288 a0001c0002t0001g0289 a0001c0002t0001g0291 others(2): Show |
5 | HG00735.hp2 HG01975.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.57+5420C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109796495 | |||||||
| chr4:109796547 | T | A | 107 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 others(104): Show |
110 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.57+5368A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109796547 | |||||||
| chr4:109796551 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.57+5364G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109796551 | |||||||
| chr4:109796682 | T | C | 107 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 others(104): Show |
110 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.57+5233A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109796682 | |||||||
| chr4:109796749 | A | C | 1 | a0001c0002t0001g0102 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.57+5166T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109796749 | |||||||
| chr4:109796812 | A | G | 3 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 |
3 | HG02559.hp2 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.57+5103T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109796812 | |||||||
| chr4:109797088 | T | C | 66 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0001t0001g0323 others(63): Show |
67 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.57+4827A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109797088 | |||||||
| chr4:109797156 | C | A | 187 | a0001c0001t0001g0002 a0001c0001t0001g0063 a0001c0001t0001g0082 others(184): Show |
192 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(189): Show |
intron_variant | MODIFIER | c.57+4759G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109797156 | |||||||
| chr4:109797299 | C | T | 77 | a0001c0001t0001g0063 a0001c0001t0001g0082 a0001c0001t0001g0084 others(74): Show |
79 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(76): Show |
intron_variant | MODIFIER | c.57+4616G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109797299 | |||||||
| chr4:109797538 | A | G | 2 | a0003c0004t0001g0154 a0003c0004t0001g0155 |
2 | HG00738.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.57+4377T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109797538 | |||||||
| chr4:109797544 | G | A | 86 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0311 others(83): Show |
87 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.57+4371C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109797544 | |||||||
| chr4:109797561 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.57+4354T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109797561 | |||||||
| chr4:109797568 | GAC | G | 107 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 others(104): Show |
110 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.57+4345_57+4346del others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109797568 | |||||||
| chr4:109797574 | T | C | 187 | a0001c0001t0001g0002 a0001c0001t0001g0063 a0001c0001t0001g0082 others(184): Show |
192 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(189): Show |
intron_variant | MODIFIER | c.57+4341A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109797574 | |||||||
| chr4:109797708 | A | C | 107 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 others(104): Show |
110 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.57+4207T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109797708 | |||||||
| chr4:109797728 | T | C | 1 | a0001c0001t0003g0153 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.57+4187A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109797728 | |||||||
| chr4:109797765 | A | G | 107 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 others(104): Show |
110 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.57+4150T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109797765 | |||||||
| chr4:109797786 | G | A | 7 | a0001c0001t0001g0002 a0001c0001t0001g0293 a0001c0001t0001g0294 others(4): Show |
9 | HG01261.hp1 HG01433.hp1 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.57+4129C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109797786 | |||||||
| chr4:109797916 | A | C | 1 | a0001c0001t0001g0320 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.57+3999T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109797916 | |||||||
| chr4:109797930 | A | C | 1 | a0001c0002t0001g0035 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.57+3985T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109797930 | |||||||
| chr4:109798008 | A | G | 107 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 others(104): Show |
110 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.57+3907T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109798008 | |||||||
| chr4:109798198 | G | A | 1 | a0001c0002t0001g0144 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.57+3717C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109798198 | |||||||
| chr4:109798217 | A | G | 6 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(3): Show |
6 | HG02723.hp2 HG02897.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.57+3698T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109798217 | |||||||
| chr4:109798303 | C | T | 107 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 others(104): Show |
110 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.57+3612G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109798303 | |||||||
| chr4:109798378 | T | C | 107 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 others(104): Show |
110 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.57+3537A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109798378 | |||||||
| chr4:109798471 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.57+3444A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109798471 | |||||||
| chr4:109798508 | G | GT | 19 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0156 others(16): Show |
21 | HG00099.hp1 HG00438.hp1 HG00639.hp1 others(18): Show |
intron_variant | MODIFIER | c.57+3406dupA | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109798508 | |||||||
| chr4:109798508 | G | GTT | 10 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0264 others(7): Show |
13 | HG02109.hp2 HG02145.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.57+3405_57+3406dup others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109798508 | |||||||
| chr4:109798508 | GT | G | 107 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 others(104): Show |
110 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.57+3406delA | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109798508 | |||||||
| chr4:109798519 | T | A | 107 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 others(104): Show |
110 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.57+3396A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109798519 | |||||||
| chr4:109798520 | T | A | 108 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 others(105): Show |
111 | HG00099.hp2 HG00558.hp2 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.57+3395A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109798520 | |||||||
| chr4:109798520 | T | TA | 100 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(97): Show |
106 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.57+3394dupT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109798520 | |||||||
| chr4:109798520 | T | TTA | 85 | a0001c0001t0001g0063 a0001c0001t0001g0082 a0001c0001t0001g0084 others(82): Show |
87 | HG00323.hp1 HG00558.hp1 HG00733.hp1 others(84): Show |
intron_variant | MODIFIER | c.57+3394_57+3395ins others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109798520 | |||||||
| chr4:109798521 | A | T | 6 | a0001c0001t0001g0010 a0001c0001t0001g0156 a0001c0001t0001g0262 others(3): Show |
7 | HG00438.hp1 HG02109.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.57+3394T>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109798521 | |||||||
| chr4:109798789 | CA | C | 3 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 |
3 | HG02559.hp2 NA18906.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.57+3125delT | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109798789 | |||||||
| chr4:109798879 | A | G | 50 | a0001c0002t0001g0006 a0001c0002t0001g0021 a0001c0002t0001g0022 others(47): Show |
51 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.57+3036T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109798879 | |||||||
| chr4:109798881 | AGGAG | A | 107 | a0001c0001t0001g0002 a0001c0001t0001g0145 a0001c0001t0001g0146 others(104): Show |
110 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.57+3030_57+3033del others(4): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109798881 | |||||||
| chr4:109798916 | C | T | 2 | a0001c0002t0002g0100 a0001c0002t0002g0101 |
2 | HG03209.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.57+2999G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109798916 | |||||||
| chr4:109799137 | T | C | 1 | a0001c0001t0001g0329 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.57+2778A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109799137 | |||||||
| chr4:109799365 | A | G | 67 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0001t0001g0323 others(64): Show |
68 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.57+2550T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109799365 | |||||||
| chr4:109799432 | C | A | 204 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(201): Show |
211 | HG00099.hp1 HG00323.hp1 HG00438.hp1 others(208): Show |
intron_variant | MODIFIER | c.57+2483G>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109799432 | |||||||
| chr4:109799432 | C | T | 1 | a0001c0001t0001g0330 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.57+2483G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109799432 | |||||||
| chr4:109799824 | A | C | 2 | a0001c0006t0005g0098 a0001c0006t0005g0099 |
2 | HG02647.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.57+2091T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109799824 | |||||||
| chr4:109799830 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.57+2085A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109799830 | |||||||
| chr4:109799835 | T | A | 92 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(89): Show |
93 | HG00558.hp2 HG00609.hp1 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.57+2080A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109799835 | |||||||
| chr4:109799902 | G | A | 314 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(311): Show |
327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.57+2013C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109799902 | |||||||
| chr4:109799929 | T | G | 1 | a0001c0001t0001g0012 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.57+1986A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109799929 | |||||||
| chr4:109800048 | A | ATTTTTGG | 3 | a0001c0002t0002g0023 a0003c0004t0001g0154 a0003c0004t0001g0155 |
3 | HG00738.hp1 HG02257.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.57+1860_57+1866dup others(7): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109800048 | |||||||
| chr4:109800055 | G | GTT | 20 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0311 others(17): Show |
20 | HG00673.hp1 HG02027.hp2 HG02080.hp2 others(17): Show |
intron_variant | MODIFIER | c.57+1858_57+1859dup others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109800055 | |||||||
| chr4:109800056 | T | TTTTTGG | 27 | a0001c0001t0001g0002 a0001c0001t0001g0151 a0001c0001t0001g0293 others(24): Show |
29 | HG00735.hp2 HG01109.hp2 HG01261.hp1 others(26): Show |
intron_variant | MODIFIER | c.57+1853_57+1858dup others(6): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109800056 | |||||||
| chr4:109800094 | G | A | 2 | a0003c0004t0001g0157 a0003c0004t0001g0297 |
2 | HG02970.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.57+1821C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109800094 | |||||||
| chr4:109800293 | C | CATAATTA others(16): Show |
6 | a0001c0001t0001g0002 a0001c0001t0001g0294 a0001c0001t0001g0295 others(3): Show |
8 | HG01261.hp1 HG01433.hp1 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.57+1621_57+1622ins others(23): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109800293 | |||||||
| chr4:109800321 | G | GT | 9 | a0001c0001t0001g0333 a0001c0002t0001g0042 a0001c0002t0002g0100 others(6): Show |
9 | HG01255.hp2 HG02055.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.57+1593dupA | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109800321 | |||||||
| chr4:109800321 | G | GTT | 7 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(4): Show |
7 | HG02257.hp1 HG02630.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.57+1592_57+1593dup others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109800321 | |||||||
| chr4:109800321 | GT | G | 206 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(203): Show |
213 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.57+1593delA | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109800321 | |||||||
| chr4:109800321 | GTT | G | 40 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(37): Show |
44 | HG00099.hp1 HG00438.hp1 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.57+1592_57+1593del others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109800321 | |||||||
| chr4:109800321 | GTTT | G | 10 | a0001c0001t0001g0215 a0001c0001t0001g0320 a0001c0001t0001g0323 others(7): Show |
10 | HG01515.hp2 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.57+1591_57+1593del others(3): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109800321 | |||||||
| chr4:109800321 | GTTTTTTT others(8): Show |
G | 1 | a0001c0001t0001g0151 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.57+1579_57+1593del others(15): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109800321 | |||||||
| chr4:109800378 | C | G | 1 | a0003c0004t0001g0157 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.57+1537G>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109800378 | |||||||
| chr4:109800752 | T | C | 2 | a0001c0001t0001g0336 a0001c0001t0001g0337 |
2 | HG02109.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.57+1163A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109800752 | |||||||
| chr4:109800753 | T | A | 1 | a0001c0002t0001g0152 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.57+1162A>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109800753 | |||||||
| chr4:109800755 | A | G | 1 | a0001c0001t0003g0013 | 2 | HG02258.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.57+1160T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109800755 | |||||||
| chr4:109800756 | T | C | 1 | a0001c0001t0003g0153 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.57+1159A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109800756 | |||||||
| chr4:109800780 | CAT | C | 22 | a0001c0001t0001g0303 a0001c0001t0001g0304 a0001c0001t0001g0311 others(19): Show |
22 | HG00673.hp1 HG00738.hp1 HG02027.hp2 others(19): Show |
intron_variant | MODIFIER | c.57+1133_57+1134del others(2): Show |
CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109800780 | |||||||
| chr4:109800868 | T | G | 1 | a0001c0001t0001g0319 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.57+1047A>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109800868 | |||||||
| chr4:109800920 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.57+995G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109800920 | |||||||
| chr4:109801224 | A | C | 1 | a0001c0002t0002g0023 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.57+691T>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109801224 | |||||||
| chr4:109801349 | G | A | 10 | a0001c0001t0001g0320 a0001c0001t0001g0321 a0001c0001t0001g0323 others(7): Show |
10 | HG01109.hp2 HG02486.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.57+566C>T | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109801349 | |||||||
| chr4:109801590 | C | T | 13 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0330 others(10): Show |
16 | HG02015.hp2 HG02109.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.57+325G>A | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109801590 | |||||||
| chr4:109801730 | T | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(190): Show |
206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.57+185A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109801730 | |||||||
| chr4:109801755 | A | G | 1 | a0001c0001t0001g0020 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.57+160T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109801755 | |||||||
| chr4:109801861 | T | C | 11 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0330 others(8): Show |
14 | HG02109.hp2 HG02145.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.57+54A>G | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109801861 | |||||||
| chr4:109801906 | A | G | 1 | a0001c0002t0001g0019 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.57+9T>C | CFI | ENSG00000205403.15 | transcript | ENST00000394634.7 | protein_coding | 1/12 | chr4 | 109801906 |