Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 80157 |
| ensemblid | ENSG00000109182.12 |
| hgncid | 26133 |
| symbol | CWH43 |
| name | cell wall biogenesis 43 C-terminal homolog |
| refseq_nuc | NM_025087.3 |
| refseq_prot | NP_079363.2 |
| ensembl_nuc | ENST00000226432.9 |
| ensembl_prot | ENSP00000226432.4 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 48986275 |
| end | 49062079 |
| strand | + |
| ver | v1.2 |
| region | chr4:48986275-49062079 |
| region5000 | chr4:48981275-49067079 |
| regionname0 | CWH43_chr4_48986275_49062079 |
| regionname5000 | CWH43_chr4_48981275_49067079 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 699 | 126 | 48 | 6 | 55 | 1 | 14 | 43 | CWH43_chr4_48981275_49067079 | CWH43 | MPSLW others(694): Show |
chr4 | 48981275 | 49067079 |
| a0002 | 0/0 | 699 | 85 | 10 | 26 | 33 | 7 | 9 | 25 | CWH43_chr4_48981275_49067079 | CWH43 | MTSLW others(694): Show |
chr4 | 48981275 | 49067079 |
| a0003 | 0/0 | 699 | 67 | 7 | 18 | 29 | 6 | 7 | 20 | CWH43_chr4_48981275_49067079 | CWH43 | MPSLW others(694): Show |
chr4 | 48981275 | 49067079 |
| a0004 | 0/0 | 532 | 9 | 0 | 5 | 1 | 2 | 1 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | MPSLW others(527): Show |
chr4 | 48981275 | 49067079 |
| a0005 | 0/0 | 699 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | MPSLW others(694): Show |
chr4 | 48981275 | 49067079 |
| a0006 | 0/0 | 699 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | MTSLW others(694): Show |
chr4 | 48981275 | 49067079 |
| a0007 | 0/0 | 699 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | MPSLW others(694): Show |
chr4 | 48981275 | 49067079 |
| a0008 | 0/0 | 699 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | MPSLW others(694): Show |
chr4 | 48981275 | 49067079 |
| a0009 | 0/0 | 699 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | MPSLW others(694): Show |
chr4 | 48981275 | 49067079 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2097 | 124 | 48 | 6 | 55 | 1 | 12 | CWH43_chr4_48981275_49067079 | CWH43 | ATGCC others(2092): Show |
chr4 | 48981275 | 49067079 | ||
| a0001c0007 | 0/0 | 2097 | 2 | 0 | 0 | 0 | 0 | 2 | CWH43_chr4_48981275_49067079 | CWH43 | ATGCC others(2092): Show |
chr4 | 48981275 | 49067079 | ||
| a0002c0002 | 0/0 | 2097 | 85 | 10 | 26 | 33 | 7 | 9 | CWH43_chr4_48981275_49067079 | CWH43 | ATGAC others(2092): Show |
chr4 | 48981275 | 49067079 | ||
| a0003c0003 | 0/0 | 2097 | 67 | 7 | 18 | 29 | 6 | 7 | CWH43_chr4_48981275_49067079 | CWH43 | ATGCC others(2092): Show |
chr4 | 48981275 | 49067079 | ||
| a0004c0004 | 0/0 | 2096 | 9 | 0 | 5 | 1 | 2 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | ATGCC others(2091): Show |
chr4 | 48981275 | 49067079 | ||
| a0005c0005 | 0/0 | 2097 | 3 | 0 | 3 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | ATGCC others(2092): Show |
chr4 | 48981275 | 49067079 | ||
| a0006c0006 | 0/0 | 2097 | 2 | 0 | 2 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | ATGAC others(2092): Show |
chr4 | 48981275 | 49067079 | ||
| a0007c0008 | 0/0 | 2097 | 2 | 2 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | ATGCC others(2092): Show |
chr4 | 48981275 | 49067079 | ||
| a0008c0009 | 0/0 | 2097 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | ATGCC others(2092): Show |
chr4 | 48981275 | 49067079 | ||
| a0009c0010 | 0/0 | 2097 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | ATGCC others(2092): Show |
chr4 | 48981275 | 49067079 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2444 | 122 | 46 | 6 | 55 | 1 | 12 | CWH43_chr4_48981275_49067079 | CWH43 | AGTTG others(2439): Show |
chr4 | 48981275 | 49067079 |
| a0001c0001t0003 | 0/0 | 2444 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | AGTTG others(2439): Show |
chr4 | 48981275 | 49067079 |
| a0001c0001t0004 | 0/0 | 2444 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | AGTTG others(2439): Show |
chr4 | 48981275 | 49067079 |
| a0001c0007t0001 | 0/0 | 2444 | 2 | 0 | 0 | 0 | 0 | 2 | CWH43_chr4_48981275_49067079 | CWH43 | AGTTG others(2439): Show |
chr4 | 48981275 | 49067079 |
| a0002c0002t0001 | 0/0 | 2444 | 85 | 10 | 26 | 33 | 7 | 9 | CWH43_chr4_48981275_49067079 | CWH43 | AGTTG others(2439): Show |
chr4 | 48981275 | 49067079 |
| a0003c0003t0001 | 0/0 | 2444 | 64 | 7 | 18 | 27 | 6 | 6 | CWH43_chr4_48981275_49067079 | CWH43 | AGTTG others(2439): Show |
chr4 | 48981275 | 49067079 |
| a0003c0003t0002 | 0/0 | 2444 | 3 | 0 | 0 | 2 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | AGTTG others(2439): Show |
chr4 | 48981275 | 49067079 |
| a0004c0004t0001 | 0/0 | 2443 | 9 | 0 | 5 | 1 | 2 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | AGTTG others(2438): Show |
chr4 | 48981275 | 49067079 |
| a0005c0005t0001 | 0/0 | 2444 | 3 | 0 | 3 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | AGTTG others(2439): Show |
chr4 | 48981275 | 49067079 |
| a0006c0006t0001 | 0/0 | 2444 | 2 | 0 | 2 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | AGTTG others(2439): Show |
chr4 | 48981275 | 49067079 |
| a0007c0008t0001 | 0/0 | 2444 | 2 | 2 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | AGTTG others(2439): Show |
chr4 | 48981275 | 49067079 |
| a0008c0009t0001 | 0/0 | 2444 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | AGTTG others(2439): Show |
chr4 | 48981275 | 49067079 |
| a0009c0010t0001 | 0/0 | 2444 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | AGTTG others(2439): Show |
chr4 | 48981275 | 49067079 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0240 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0001t0004g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0001c0007t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0002c0002t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0003c0003t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0004c0004t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0004c0004t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0004c0004t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0004c0004t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0004c0004t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0004c0004t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0004c0004t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0005c0005t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0005c0005t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0006c0006t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0006c0006t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0007c0008t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0007c0008t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0008c0009t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| a0009c0010t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0003 | c0003 | t0001 | g0189 | EUR | GBR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG00099 | hp2 | a0002 | c0002 | t0001 | g0102 | EUR | GBR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0264 | EUR | GBR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0086 | EUR | GBR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0112 | EUR | FIN | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG00280 | hp2 | a0003 | c0003 | t0001 | g0035 | EUR | FIN | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0106 | EUR | FIN | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG00323 | hp2 | a0003 | c0003 | t0001 | g0031 | EUR | FIN | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG00408 | hp1 | a0002 | c0002 | t0001 | g0076 | EAS | CHS | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0064 | EAS | CHS | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0066 | EAS | CHS | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG00438 | hp1 | a0002 | c0002 | t0001 | g0063 | EAS | CHS | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | CHS | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | CHS | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG00558 | hp2 | a0003 | c0003 | t0001 | g0133 | EAS | CHS | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0075 | EAS | CHS | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | CHS | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG00639 | hp1 | a0003 | c0003 | t0001 | g0116 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0074 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG00735 | hp1 | a0003 | c0003 | t0001 | g0044 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG00735 | hp2 | a0006 | c0006 | t0001 | g0144 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0093 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG00738 | hp2 | a0004 | c0004 | t0001 | g0154 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG00741 | hp1 | a0003 | c0003 | t0001 | g0127 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG00741 | hp2 | a0003 | c0003 | t0001 | g0188 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0067 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01069 | hp2 | a0004 | c0004 | t0001 | g0011 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01070 | hp1 | a0003 | c0003 | t0001 | g0001 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0090 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01071 | hp1 | a0003 | c0003 | t0001 | g0001 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0062 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01074 | hp1 | a0003 | c0003 | t0001 | g0121 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01074 | hp2 | a0006 | c0006 | t0001 | g0134 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0103 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01109 | hp1 | a0004 | c0004 | t0001 | g0011 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0111 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01167 | hp2 | a0003 | c0003 | t0001 | g0043 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01175 | hp2 | a0002 | c0002 | t0001 | g0142 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01192 | hp1 | a0003 | c0003 | t0001 | g0024 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0105 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0109 | AMR | PUR | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01255 | hp2 | a0002 | c0002 | t0001 | g0143 | AMR | CLM | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01257 | hp1 | a0004 | c0004 | t0001 | g0012 | AMR | CLM | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0104 | AMR | CLM | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0101 | AMR | CLM | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01258 | hp2 | a0004 | c0004 | t0001 | g0012 | AMR | CLM | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0009 | AMR | CLM | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01346 | hp2 | a0003 | c0003 | t0001 | g0141 | AMR | CLM | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0087 | AMR | CLM | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01358 | hp2 | a0003 | c0003 | t0001 | g0005 | AMR | CLM | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01361 | hp1 | a0003 | c0003 | t0001 | g0005 | AMR | CLM | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0009 | AMR | CLM | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0088 | AMR | CLM | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01433 | hp2 | a0003 | c0003 | t0001 | g0029 | AMR | CLM | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0092 | AMR | CLM | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01496 | hp2 | a0003 | c0003 | t0001 | g0140 | AMR | CLM | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0113 | EUR | IBS | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01515 | hp2 | a0003 | c0003 | t0001 | g0003 | EUR | IBS | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01517 | hp1 | a0003 | c0003 | t0001 | g0003 | EUR | IBS | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01517 | hp2 | a0002 | c0002 | t0001 | g0073 | EUR | IBS | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01884 | hp1 | a0007 | c0008 | t0001 | g0146 | AFR | ACB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | ACB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01891 | hp2 | a0003 | c0003 | t0001 | g0058 | AFR | ACB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01928 | hp1 | a0005 | c0005 | t0001 | g0244 | AMR | PEL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0007 | AMR | PEL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01952 | hp1 | a0002 | c0002 | t0001 | g0095 | AMR | PEL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01952 | hp2 | a0003 | c0003 | t0001 | g0001 | AMR | PEL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01975 | hp1 | a0005 | c0005 | t0001 | g0020 | AMR | PEL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01975 | hp2 | a0002 | c0002 | t0001 | g0089 | AMR | PEL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01978 | hp1 | a0003 | c0003 | t0001 | g0030 | AMR | PEL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01978 | hp2 | a0002 | c0002 | t0001 | g0007 | AMR | PEL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01981 | hp1 | a0005 | c0005 | t0001 | g0020 | AMR | PEL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01981 | hp2 | a0002 | c0002 | t0001 | g0096 | AMR | PEL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01993 | hp1 | a0003 | c0003 | t0001 | g0045 | AMR | PEL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0094 | AMR | PEL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02004 | hp1 | a0003 | c0003 | t0001 | g0128 | AMR | PEL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0078 | AMR | PEL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0080 | EAS | KHV | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02027 | hp2 | a0004 | c0004 | t0001 | g0150 | EAS | KHV | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02055 | hp1 | a0002 | c0002 | t0001 | g0110 | AFR | ACB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | ACB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02056 | hp1 | a0003 | c0003 | t0001 | g0038 | EAS | KHV | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02056 | hp2 | a0003 | c0003 | t0001 | g0185 | EAS | KHV | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02071 | hp1 | a0002 | c0002 | t0001 | g0025 | EAS | KHV | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | KHV | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02129 | hp1 | a0003 | c0003 | t0001 | g0132 | EAS | KHV | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02129 | hp2 | a0003 | c0003 | t0001 | g0046 | EAS | KHV | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | KHV | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02132 | hp2 | a0003 | c0003 | t0002 | g0153 | EAS | KHV | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02145 | hp1 | a0002 | c0002 | t0001 | g0138 | AFR | ACB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02155 | hp1 | a0003 | c0003 | t0001 | g0184 | EAS | CDX | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02155 | hp2 | a0003 | c0003 | t0001 | g0026 | EAS | CDX | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0270 | AFR | ACB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0097 | AFR | ACB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02300 | hp1 | a0002 | c0002 | t0001 | g0070 | AMR | PEL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02523 | hp1 | a0003 | c0003 | t0001 | g0123 | EAS | KHV | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02572 | hp2 | a0003 | c0003 | t0001 | g0118 | AFR | GWD | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02630 | hp2 | a0003 | c0003 | t0001 | g0119 | AFR | GWD | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | PJL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02698 | hp2 | a0008 | c0009 | t0001 | g0033 | SAS | PJL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02735 | hp1 | a0003 | c0003 | t0001 | g0120 | SAS | PJL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02735 | hp2 | a0003 | c0003 | t0001 | g0028 | SAS | PJL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0049 | SAS | PJL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0114 | AFR | GWD | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ESN | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | ESN | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02965 | hp1 | a0002 | c0002 | t0001 | g0115 | AFR | ESN | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | ESN | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG03017 | hp2 | a0002 | c0002 | t0001 | g0052 | SAS | PJL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | GWD | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | MSL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG03130 | hp1 | a0007 | c0008 | t0001 | g0147 | AFR | ESN | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ESN | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0108 | AFR | ESN | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ESN | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | ESN | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0100 | AFR | ESN | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG03209 | hp1 | a0002 | c0002 | t0001 | g0099 | AFR | MSL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | MSL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | MSL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | MSL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | MSL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0139 | AFR | MSL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0010 | SAS | PJL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG03490 | hp2 | a0004 | c0004 | t0001 | g0155 | SAS | PJL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0010 | SAS | PJL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | ESN | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0048 | SAS | PJL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG03654 | hp2 | a0003 | c0003 | t0001 | g0039 | SAS | PJL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG03710 | hp1 | a0003 | c0003 | t0001 | g0034 | SAS | PJL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0055 | SAS | BEB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG03831 | hp2 | a0001 | c0007 | t0001 | g0015 | SAS | BEB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | BEB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG03834 | hp2 | a0003 | c0003 | t0001 | g0124 | SAS | BEB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | BEB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG03927 | hp2 | a0003 | c0003 | t0002 | g0157 | SAS | BEB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | BEB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG03942 | hp2 | a0003 | c0003 | t0001 | g0027 | SAS | BEB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | STU | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG04115 | hp2 | a0002 | c0002 | t0001 | g0117 | SAS | STU | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG04184 | hp1 | a0002 | c0002 | t0001 | g0071 | SAS | BEB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | BEB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG04204 | hp1 | a0002 | c0002 | t0001 | g0084 | SAS | STU | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG04204 | hp2 | a0001 | c0007 | t0001 | g0015 | SAS | STU | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18522 | hp1 | a0003 | c0003 | t0001 | g0158 | AFR | YRI | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | YRI | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CHB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0081 | EAS | CHB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | CHB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | YRI | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | YRI | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18940 | hp1 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18943 | hp1 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18946 | hp2 | a0003 | c0003 | t0001 | g0014 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18951 | hp1 | a0003 | c0003 | t0001 | g0032 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18954 | hp1 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18956 | hp1 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0051 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18959 | hp1 | a0003 | c0003 | t0001 | g0211 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18960 | hp2 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18964 | hp1 | a0002 | c0002 | t0001 | g0077 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0069 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18968 | hp1 | a0003 | c0003 | t0001 | g0190 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18969 | hp2 | a0003 | c0003 | t0001 | g0126 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18971 | hp1 | a0003 | c0003 | t0001 | g0037 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18971 | hp2 | a0003 | c0003 | t0001 | g0191 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18980 | hp2 | a0003 | c0003 | t0001 | g0187 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0083 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0068 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18983 | hp2 | a0003 | c0003 | t0001 | g0210 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18986 | hp2 | a0003 | c0003 | t0001 | g0042 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18990 | hp2 | a0003 | c0003 | t0001 | g0014 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18997 | hp2 | a0002 | c0002 | t0001 | g0137 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18999 | hp1 | a0002 | c0002 | t0001 | g0054 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18999 | hp2 | a0003 | c0003 | t0001 | g0186 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA19000 | hp1 | a0003 | c0003 | t0002 | g0156 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA19001 | hp1 | a0002 | c0002 | t0001 | g0079 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0059 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA19006 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA19011 | hp2 | a0003 | c0003 | t0001 | g0183 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | LWK | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA19030 | hp2 | a0003 | c0003 | t0001 | g0085 | AFR | LWK | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | LWK | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA19043 | hp2 | a0009 | c0010 | t0001 | g0145 | AFR | LWK | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA19056 | hp2 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0047 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA19070 | hp1 | a0003 | c0003 | t0001 | g0036 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA19075 | hp2 | a0002 | c0002 | t0001 | g0056 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA19076 | hp1 | a0002 | c0002 | t0001 | g0072 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA19079 | hp1 | a0002 | c0002 | t0001 | g0061 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA19082 | hp2 | a0003 | c0003 | t0001 | g0122 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA19083 | hp1 | a0002 | c0002 | t0001 | g0135 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA19091 | hp1 | a0003 | c0003 | t0001 | g0041 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ASW | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0107 | AFR | ASW | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA20752 | hp1 | a0004 | c0004 | t0001 | g0151 | EUR | TSI | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0091 | EUR | TSI | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA20805 | hp1 | a0003 | c0003 | t0001 | g0131 | EUR | TSI | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA20805 | hp2 | a0004 | c0004 | t0001 | g0152 | EUR | TSI | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0220 | AFR | ACB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | USA | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| HG06807 | hp2 | a0003 | c0003 | t0001 | g0159 | AFR | USA | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18955 | hp1 | a0003 | c0003 | t0001 | g0125 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA20300 | hp1 | a0003 | c0003 | t0001 | g0023 | AFR | USA | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | USA | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0240 | REF | REF | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0002 | REF | REF | CWH43_chr4_48981275_49067079 | CWH43 | chr4 | 48981275 | 49067079 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:48986433 | C | A | 2 | a0002 a0006 |
87 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(84): Show |
missense_variant | MODERATE | c.4C>A | p.Pro2Thr | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 1/16 | 159/2444 | 4/2100 | 2/699 | chr4 | 48986433 | |||
| chr4:48988665 | A | G | 2 | a0007 a0009 |
3 | HG01884.hp1 HG03130.hp1 NA19043.hp2 |
missense_variant | MODERATE | c.232A>G | p.Ile78Val | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 2/16 | 387/2444 | 232/2100 | 78/699 | chr4 | 48988665 | |||
| chr4:48992079 | G | A | 1 | a0008 | 1 | HG02698.hp2 | missense_variant | MODERATE | c.500G>A | p.Arg167His | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 4/16 | 655/2444 | 500/2100 | 167/699 | chr4 | 48992079 | |||
| chr4:49032652 | CA | C | 1 | a0004 | 9 | HG00738.hp2 HG01069.hp2 HG01109.hp1 others(6): Show |
frameshift_variant | HIGH | c.1596delA | p.Leu533fs | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/16 | 1751/2444 | 1596/2100 | 532/699 | chr4 | 49032652 | |||
| chr4:49050705 | C | T | 1 | a0005 | 3 | HG01928.hp1 HG01975.hp1 HG01981.hp1 |
missense_variant | MODERATE | c.1877C>T | p.Ala626Val | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/16 | 2032/2444 | 1877/2100 | 626/699 | chr4 | 49050705 | |||
| chr4:49061855 | C | A | 4 | a0002 a0003 a0008 others(1): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
missense_variant | MODERATE | c.2065C>A | p.His689Asn | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 16/16 | 2220/2444 | 2065/2100 | 689/699 | chr4 | 49061855 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:48986462 | G | A | 1 | a0001c0007 | 2 | HG03831.hp2 HG04204.hp2 |
synonymous_variant | LOW | c.33G>A | p.Glu11Glu | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 1/16 | 188/2444 | 33/2100 | 11/699 | chr4 | 48986462 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:49061941 | T | C | 1 | a0001c0001t0003 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*51T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 16/16 | 51 | chr4 | 49061941 | ||||||
| chr4:49062016 | T | A | 1 | a0003c0003t0002 | 3 | HG02132.hp2 HG03927.hp2 NA19000.hp1 |
3_prime_UTR_variant | MODIFIER | c.*126T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 16/16 | 126 | chr4 | 49062016 | ||||||
| chr4:49062018 | T | C | 1 | a0001c0001t0004 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*128T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 16/16 | 128 | chr4 | 49062018 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:48986554 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.43+82G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 1/15 | chr4 | 48986554 | |||||||
| chr4:48986556 | T | G | 1 | a0001c0001t0001g0022 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.43+84T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 1/15 | chr4 | 48986556 | |||||||
| chr4:48986588 | G | T | 1 | a0001c0001t0001g0274 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.43+116G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 1/15 | chr4 | 48986588 | |||||||
| chr4:48986657 | G | A | 1 | a0003c0003t0001g0023 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.43+185G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 1/15 | chr4 | 48986657 | |||||||
| chr4:48986688 | G | A | 131 | a0001c0001t0001g0040 a0001c0001t0001g0129 a0001c0001t0001g0130 others(128): Show |
141 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.43+216G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 1/15 | chr4 | 48986688 | |||||||
| chr4:48986876 | C | T | 1 | a0006c0006t0001g0144 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.43+404C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 1/15 | chr4 | 48986876 | |||||||
| chr4:48987244 | C | T | 131 | a0001c0001t0001g0040 a0001c0001t0001g0129 a0001c0001t0001g0130 others(128): Show |
141 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.43+772C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 1/15 | chr4 | 48987244 | |||||||
| chr4:48987341 | A | G | 131 | a0001c0001t0001g0040 a0001c0001t0001g0129 a0001c0001t0001g0130 others(128): Show |
141 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.43+869A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 1/15 | chr4 | 48987341 | |||||||
| chr4:48987591 | C | T | 1 | a0002c0002t0001g0143 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.44-886C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 1/15 | chr4 | 48987591 | |||||||
| chr4:48987707 | A | G | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.44-770A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 1/15 | chr4 | 48987707 | |||||||
| chr4:48987837 | C | T | 4 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 others(1): Show |
4 | HG02258.hp2 HG03540.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.44-640C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 1/15 | chr4 | 48987837 | |||||||
| chr4:48988084 | C | CA | 3 | a0007c0008t0001g0146 a0007c0008t0001g0147 a0009c0010t0001g0145 |
3 | HG01884.hp1 HG03130.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.44-392dupA | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 48988084 | ||||||
| chr4:48988222 | G | A | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG01099.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.44-255G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 1/15 | chr4 | 48988222 | |||||||
| chr4:48988291 | C | T | 1 | a0002c0002t0001g0142 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.44-186C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 1/15 | chr4 | 48988291 | |||||||
| chr4:48988459 | CT | C | 132 | a0001c0001t0001g0021 a0001c0001t0001g0040 a0001c0001t0001g0129 others(129): Show |
142 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(139): Show |
splice_region_variant&intron_variant | LOW | c.44-5delT | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr4 | 48988459 | ||||||
| chr4:48988868 | T | G | 165 | a0001c0001t0001g0021 a0001c0001t0001g0040 a0001c0001t0001g0129 others(162): Show |
177 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(174): Show |
intron_variant | MODIFIER | c.235+200T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 2/15 | chr4 | 48988868 | |||||||
| chr4:48988994 | A | G | 133 | a0001c0001t0001g0040 a0001c0001t0001g0129 a0001c0001t0001g0130 others(130): Show |
143 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.235+326A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 2/15 | chr4 | 48988994 | |||||||
| chr4:48989140 | A | G | 2 | a0003c0003t0001g0140 a0003c0003t0001g0141 |
2 | HG01346.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.235+472A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 2/15 | chr4 | 48989140 | |||||||
| chr4:48989165 | A | C | 134 | a0001c0001t0001g0021 a0001c0001t0001g0040 a0001c0001t0001g0129 others(131): Show |
144 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.235+497A>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 2/15 | chr4 | 48989165 | |||||||
| chr4:48989474 | A | G | 2 | a0007c0008t0001g0146 a0007c0008t0001g0147 |
2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.235+806A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 2/15 | chr4 | 48989474 | |||||||
| chr4:48989494 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.235+826G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 2/15 | chr4 | 48989494 | |||||||
| chr4:48989523 | G | A | 131 | a0001c0001t0001g0040 a0001c0001t0001g0129 a0001c0001t0001g0130 others(128): Show |
141 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.235+855G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 2/15 | chr4 | 48989523 | |||||||
| chr4:48989535 | C | T | 1 | a0002c0002t0001g0139 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.235+867C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 2/15 | chr4 | 48989535 | |||||||
| chr4:48989556 | T | C | 9 | a0001c0001t0001g0013 a0001c0001t0001g0174 a0001c0001t0001g0175 others(6): Show |
10 | NA18968.hp2 NA18980.hp1 NA18982.hp2 others(7): Show |
intron_variant | MODIFIER | c.235+888T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 2/15 | chr4 | 48989556 | |||||||
| chr4:48989582 | A | G | 1 | a0001c0001t0001g0173 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.235+914A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 2/15 | chr4 | 48989582 | |||||||
| chr4:48989809 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.235+1141C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 2/15 | chr4 | 48989809 | |||||||
| chr4:48989820 | G | C | 131 | a0001c0001t0001g0040 a0001c0001t0001g0129 a0001c0001t0001g0130 others(128): Show |
141 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.235+1152G>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 2/15 | chr4 | 48989820 | |||||||
| chr4:48989872 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.235+1204A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 2/15 | chr4 | 48989872 | |||||||
| chr4:48989876 | T | G | 2 | a0003c0003t0001g0001 a0003c0003t0001g0024 |
4 | HG01070.hp1 HG01071.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.235+1208T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 2/15 | chr4 | 48989876 | |||||||
| chr4:48989881 | C | A | 1 | a0002c0002t0001g0025 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.235+1213C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 2/15 | chr4 | 48989881 | |||||||
| chr4:48989910 | C | T | 1 | a0001c0001t0001g0269 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.235+1242C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 2/15 | chr4 | 48989910 | |||||||
| chr4:48989992 | G | A | 2 | a0007c0008t0001g0146 a0007c0008t0001g0147 |
2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.235+1324G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 2/15 | chr4 | 48989992 | |||||||
| chr4:48990175 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.236-1279G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 2/15 | chr4 | 48990175 | |||||||
| chr4:48990239 | A | C | 132 | a0001c0001t0001g0021 a0001c0001t0001g0040 a0001c0001t0001g0129 others(129): Show |
142 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.236-1215A>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 2/15 | chr4 | 48990239 | |||||||
| chr4:48990331 | C | T | 1 | a0002c0002t0001g0138 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.236-1123C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 2/15 | chr4 | 48990331 | |||||||
| chr4:48990401 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.236-1053C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 2/15 | chr4 | 48990401 | |||||||
| chr4:48990731 | G | A | 131 | a0001c0001t0001g0040 a0001c0001t0001g0129 a0001c0001t0001g0130 others(128): Show |
141 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.236-723G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 2/15 | chr4 | 48990731 | |||||||
| chr4:48990744 | T | A | 132 | a0001c0001t0001g0021 a0001c0001t0001g0040 a0001c0001t0001g0129 others(129): Show |
142 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.236-710T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 2/15 | chr4 | 48990744 | |||||||
| chr4:48990756 | A | T | 1 | a0001c0001t0001g0169 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.236-698A>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 2/15 | chr4 | 48990756 | |||||||
| chr4:48991001 | G | T | 2 | a0007c0008t0001g0146 a0007c0008t0001g0147 |
2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.236-453G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 2/15 | chr4 | 48991001 | |||||||
| chr4:48991593 | G | A | 9 | a0003c0003t0002g0153 a0003c0003t0002g0156 a0004c0004t0001g0011 others(6): Show |
11 | HG00738.hp2 HG01069.hp2 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.356+19G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 3/15 | chr4 | 48991593 | |||||||
| chr4:48991600 | T | C | 1 | a0003c0003t0001g0026 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.356+26T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 3/15 | chr4 | 48991600 | |||||||
| chr4:48991724 | A | T | 1 | a0003c0003t0002g0156 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.356+150A>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 3/15 | chr4 | 48991724 | |||||||
| chr4:48991790 | T | C | 1 | a0003c0003t0001g0027 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.357-146T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 3/15 | chr4 | 48991790 | |||||||
| chr4:48991879 | G | T | 1 | a0001c0001t0001g0168 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.357-57G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 3/15 | chr4 | 48991879 | |||||||
| chr4:48991893 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.357-43G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 3/15 | chr4 | 48991893 | |||||||
| chr4:48992121 | G | T | 131 | a0001c0001t0001g0040 a0001c0001t0001g0129 a0001c0001t0001g0130 others(128): Show |
141 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.511+31G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 4/15 | chr4 | 48992121 | |||||||
| chr4:48992147 | G | A | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.511+57G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 4/15 | chr4 | 48992147 | |||||||
| chr4:48992376 | A | G | 1 | a0002c0002t0001g0137 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.511+286A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 4/15 | chr4 | 48992376 | |||||||
| chr4:48992450 | C | A | 1 | a0004c0004t0001g0150 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.511+360C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 4/15 | chr4 | 48992450 | |||||||
| chr4:48992470 | TAAC | T | 3 | a0007c0008t0001g0146 a0007c0008t0001g0147 a0009c0010t0001g0145 |
3 | HG01884.hp1 HG03130.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.511+382_511+384del others(3): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr4 | 48992470 | ||||||
| chr4:48992729 | G | T | 12 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(9): Show |
12 | HG02145.hp2 HG02258.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.511+639G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 4/15 | chr4 | 48992729 | |||||||
| chr4:48992857 | G | A | 3 | a0007c0008t0001g0146 a0007c0008t0001g0147 a0009c0010t0001g0145 |
3 | HG01884.hp1 HG03130.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.511+767G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 4/15 | chr4 | 48992857 | |||||||
| chr4:48993026 | A | G | 1 | a0001c0001t0001g0267 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.511+936A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 4/15 | chr4 | 48993026 | |||||||
| chr4:48993269 | T | G | 27 | a0001c0001t0001g0040 a0003c0003t0001g0001 a0003c0003t0001g0003 others(24): Show |
32 | HG00280.hp2 HG00323.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.511+1179T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 4/15 | chr4 | 48993269 | |||||||
| chr4:48993366 | C | T | 1 | a0001c0001t0001g0266 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.512-1253C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 4/15 | chr4 | 48993366 | |||||||
| chr4:48993482 | T | C | 160 | a0001c0001t0001g0021 a0001c0001t0001g0040 a0001c0001t0001g0129 others(157): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.512-1137T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 4/15 | chr4 | 48993482 | |||||||
| chr4:48993599 | G | A | 141 | a0001c0001t0001g0040 a0001c0001t0001g0129 a0001c0001t0001g0130 others(138): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(149): Show |
intron_variant | MODIFIER | c.512-1020G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 4/15 | chr4 | 48993599 | |||||||
| chr4:48993683 | G | A | 140 | a0001c0001t0001g0040 a0001c0001t0001g0129 a0001c0001t0001g0130 others(137): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.512-936G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 4/15 | chr4 | 48993683 | |||||||
| chr4:48993707 | A | G | 1 | a0002c0002t0001g0135 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.512-912A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 4/15 | chr4 | 48993707 | |||||||
| chr4:48993784 | C | T | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.512-835C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 4/15 | chr4 | 48993784 | |||||||
| chr4:48993795 | C | G | 2 | a0001c0001t0001g0166 a0001c0001t0001g0167 |
2 | HG02258.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.512-824C>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 4/15 | chr4 | 48993795 | |||||||
| chr4:48994099 | C | A | 140 | a0001c0001t0001g0040 a0001c0001t0001g0129 a0001c0001t0001g0130 others(137): Show |
151 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(148): Show |
intron_variant | MODIFIER | c.512-520C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 4/15 | chr4 | 48994099 | |||||||
| chr4:48994159 | G | A | 3 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 |
3 | HG01255.hp1 HG02897.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.512-460G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 4/15 | chr4 | 48994159 | |||||||
| chr4:48994349 | C | A | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.512-270C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 4/15 | chr4 | 48994349 | |||||||
| chr4:48994390 | C | G | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.512-229C>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 4/15 | chr4 | 48994390 | |||||||
| chr4:48994604 | A | G | 1 | a0001c0001t0001g0265 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.512-15A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 4/15 | chr4 | 48994604 | |||||||
| chr4:48994882 | C | T | 1 | a0001c0001t0001g0264 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.713+62C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | chr4 | 48994882 | |||||||
| chr4:48995103 | A | T | 1 | a0003c0003t0001g0046 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.713+283A>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | chr4 | 48995103 | |||||||
| chr4:48995195 | T | G | 3 | a0001c0001t0001g0160 a0001c0001t0001g0166 a0001c0001t0001g0167 |
3 | HG02258.hp1 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.713+375T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | chr4 | 48995195 | |||||||
| chr4:48995333 | T | A | 147 | a0001c0001t0001g0021 a0001c0001t0001g0040 a0001c0001t0001g0129 others(144): Show |
158 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.713+513T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | chr4 | 48995333 | |||||||
| chr4:48995613 | C | T | 4 | a0003c0003t0001g0005 a0003c0003t0001g0043 a0003c0003t0001g0044 others(1): Show |
5 | HG00735.hp1 HG01167.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.713+793C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | chr4 | 48995613 | |||||||
| chr4:48996241 | T | A | 1 | a0001c0001t0001g0196 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.713+1421T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | chr4 | 48996241 | |||||||
| chr4:48996298 | T | TAC | 13 | a0001c0001t0001g0021 a0001c0001t0001g0148 a0001c0001t0001g0149 others(10): Show |
13 | HG00609.hp2 HG01099.hp1 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.713+1510_713+1511d others(4): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr4 | 48996298 | ||||||
| chr4:48996298 | TAC | T | 15 | a0001c0001t0001g0168 a0001c0001t0001g0171 a0001c0001t0001g0260 others(12): Show |
15 | HG01884.hp1 HG02258.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.713+1510_713+1511d others(4): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr4 | 48996298 | ||||||
| chr4:48996298 | TACAC | T | 2 | a0002c0002t0001g0047 a0004c0004t0001g0012 |
3 | HG01257.hp1 HG01258.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.713+1508_713+1511d others(6): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr4 | 48996298 | ||||||
| chr4:48996298 | TACACAC | T | 94 | a0002c0002t0001g0006 a0002c0002t0001g0007 a0002c0002t0001g0008 others(91): Show |
100 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.713+1506_713+1511d others(8): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr4 | 48996298 | ||||||
| chr4:48996298 | TACACACA others(1): Show |
T | 3 | a0002c0002t0001g0117 a0003c0003t0001g0116 a0009c0010t0001g0145 |
3 | HG00639.hp1 HG04115.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.713+1504_713+1511d others(10): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr4 | 48996298 | ||||||
| chr4:48996298 | TACACACA others(3): Show |
T | 42 | a0001c0001t0001g0040 a0001c0001t0001g0129 a0001c0001t0001g0130 others(39): Show |
47 | HG00280.hp2 HG00323.hp2 HG00558.hp2 others(44): Show |
intron_variant | MODIFIER | c.713+1502_713+1511d others(12): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr4 | 48996298 | ||||||
| chr4:48996328 | C | T | 3 | a0003c0003t0001g0026 a0003c0003t0001g0132 a0003c0003t0001g0133 |
3 | HG00558.hp2 HG02129.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.713+1508C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | chr4 | 48996328 | |||||||
| chr4:48996330 | C | T | 123 | a0001c0001t0001g0040 a0001c0001t0001g0129 a0001c0001t0001g0130 others(120): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.713+1510C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | chr4 | 48996330 | |||||||
| chr4:48996715 | T | C | 2 | a0003c0003t0001g0027 a0003c0003t0001g0028 |
2 | HG02735.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.714-1745T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | chr4 | 48996715 | |||||||
| chr4:48996757 | A | T | 139 | a0001c0001t0001g0040 a0001c0001t0001g0129 a0001c0001t0001g0130 others(136): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.714-1703A>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | chr4 | 48996757 | |||||||
| chr4:48996984 | G | C | 12 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(9): Show |
12 | HG02145.hp2 HG02258.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.714-1476G>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | chr4 | 48996984 | |||||||
| chr4:48997082 | A | G | 2 | a0002c0002t0001g0114 a0002c0002t0001g0115 |
2 | HG02886.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.714-1378A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | chr4 | 48997082 | |||||||
| chr4:48997225 | C | CT | 158 | a0001c0001t0001g0021 a0001c0001t0001g0040 a0001c0001t0001g0129 others(155): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.714-1221dupT | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr4 | 48997225 | ||||||
| chr4:48997319 | A | G | 12 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(9): Show |
12 | HG02145.hp2 HG02258.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.714-1141A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | chr4 | 48997319 | |||||||
| chr4:48997418 | C | G | 1 | a0001c0001t0001g0259 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.714-1042C>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | chr4 | 48997418 | |||||||
| chr4:48997669 | A | G | 1 | a0004c0004t0001g0155 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.714-791A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | chr4 | 48997669 | |||||||
| chr4:48997704 | T | C | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.714-756T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | chr4 | 48997704 | |||||||
| chr4:48997711 | C | T | 1 | a0001c0001t0001g0169 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.714-749C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | chr4 | 48997711 | |||||||
| chr4:48997825 | G | A | 159 | a0001c0001t0001g0021 a0001c0001t0001g0040 a0001c0001t0001g0129 others(156): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.714-635G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | chr4 | 48997825 | |||||||
| chr4:48997946 | C | T | 139 | a0001c0001t0001g0040 a0001c0001t0001g0129 a0001c0001t0001g0130 others(136): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.714-514C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | chr4 | 48997946 | |||||||
| chr4:48998235 | T | C | 4 | a0003c0003t0002g0153 a0003c0003t0002g0156 a0003c0003t0002g0157 others(1): Show |
4 | HG02027.hp2 HG02132.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.714-225T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 5/15 | chr4 | 48998235 | |||||||
| chr4:48998582 | T | A | 1 | a0003c0003t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.802+34T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 48998582 | |||||||
| chr4:48998623 | G | A | 12 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(9): Show |
12 | HG02145.hp2 HG02258.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.802+75G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 48998623 | |||||||
| chr4:48998635 | A | T | 2 | a0002c0002t0001g0112 a0002c0002t0001g0113 |
2 | HG00280.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.802+87A>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 48998635 | |||||||
| chr4:48998754 | C | T | 7 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 others(4): Show |
7 | HG01884.hp1 HG02258.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.802+206C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 48998754 | |||||||
| chr4:48998833 | A | G | 143 | a0001c0001t0001g0040 a0001c0001t0001g0129 a0001c0001t0001g0130 others(140): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.802+285A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 48998833 | |||||||
| chr4:48998935 | C | T | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.802+387C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 48998935 | |||||||
| chr4:48998974 | T | G | 2 | a0002c0002t0001g0056 a0002c0002t0001g0057 |
2 | NA19010.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.802+426T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 48998974 | |||||||
| chr4:48999046 | A | G | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.802+498A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 48999046 | |||||||
| chr4:48999327 | A | G | 1 | a0003c0003t0001g0131 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.802+779A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 48999327 | |||||||
| chr4:48999388 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.802+840C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 48999388 | |||||||
| chr4:48999610 | C | G | 8 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(5): Show |
8 | HG01255.hp1 HG01884.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.802+1062C>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 48999610 | |||||||
| chr4:48999761 | C | T | 1 | a0001c0001t0001g0254 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.802+1213C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 48999761 | |||||||
| chr4:48999790 | G | T | 157 | a0001c0001t0001g0040 a0001c0001t0001g0129 a0001c0001t0001g0130 others(154): Show |
168 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.802+1242G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 48999790 | |||||||
| chr4:48999917 | G | T | 1 | a0002c0002t0001g0113 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.802+1369G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 48999917 | |||||||
| chr4:48999962 | G | A | 2 | a0003c0003t0001g0188 a0003c0003t0001g0189 |
2 | HG00099.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.802+1414G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 48999962 | |||||||
| chr4:49000066 | A | C | 1 | a0003c0003t0001g0029 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.802+1518A>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 49000066 | |||||||
| chr4:49000067 | C | A | 1 | a0001c0001t0001g0271 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.802+1519C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 49000067 | |||||||
| chr4:49000204 | T | A | 139 | a0001c0001t0001g0040 a0001c0001t0001g0129 a0001c0001t0001g0130 others(136): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.802+1656T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 49000204 | |||||||
| chr4:49000241 | T | C | 1 | a0001c0001t0001g0197 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.802+1693T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 49000241 | |||||||
| chr4:49000337 | G | A | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.802+1789G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 49000337 | |||||||
| chr4:49000529 | T | C | 1 | a0001c0001t0001g0206 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.802+1981T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 49000529 | |||||||
| chr4:49000839 | ACT | A | 139 | a0001c0001t0001g0040 a0001c0001t0001g0129 a0001c0001t0001g0130 others(136): Show |
150 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(147): Show |
intron_variant | MODIFIER | c.802+2294_802+2295d others(4): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 49000839 | ||||||
| chr4:49001034 | C | CTG | 19 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 others(16): Show |
19 | HG01884.hp1 HG02145.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.802+2489_802+2490d others(4): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr4 | 49001034 | ||||||
| chr4:49001172 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.803-2563G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 49001172 | |||||||
| chr4:49001206 | A | T | 7 | a0001c0001t0001g0021 a0001c0001t0001g0250 a0001c0001t0001g0251 others(4): Show |
7 | HG01243.hp1 HG02615.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.803-2529A>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 49001206 | |||||||
| chr4:49001222 | T | C | 1 | a0002c0002t0001g0138 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.803-2513T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 49001222 | |||||||
| chr4:49001365 | T | C | 3 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0209 |
3 | HG02572.hp1 HG03130.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.803-2370T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 49001365 | |||||||
| chr4:49001520 | T | C | 2 | a0007c0008t0001g0146 a0007c0008t0001g0147 |
2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.803-2215T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 49001520 | |||||||
| chr4:49001871 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.803-1864G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 49001871 | |||||||
| chr4:49001972 | C | T | 3 | a0003c0003t0001g0004 a0003c0003t0001g0041 a0003c0003t0001g0042 |
4 | NA18954.hp1 NA18956.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.803-1763C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 49001972 | |||||||
| chr4:49002150 | T | A | 1 | a0003c0003t0001g0058 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.803-1585T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 49002150 | |||||||
| chr4:49002414 | A | G | 3 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 |
3 | HG03540.hp2 HG03669.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.803-1321A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 49002414 | |||||||
| chr4:49002642 | A | T | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.803-1093A>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 49002642 | |||||||
| chr4:49002817 | C | T | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.803-918C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 49002817 | |||||||
| chr4:49002831 | G | A | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.803-904G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 49002831 | |||||||
| chr4:49002846 | G | A | 16 | a0002c0002t0001g0006 a0002c0002t0001g0007 a0002c0002t0001g0059 others(13): Show |
18 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(15): Show |
intron_variant | MODIFIER | c.803-889G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 49002846 | |||||||
| chr4:49003224 | A | G | 3 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 |
3 | NA18986.hp1 NA19011.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.803-511A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 49003224 | |||||||
| chr4:49003281 | T | C | 6 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 others(3): Show |
6 | HG01884.hp1 HG03130.hp1 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.803-454T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 49003281 | |||||||
| chr4:49003505 | T | C | 1 | a0001c0001t0001g0168 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.803-230T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 49003505 | |||||||
| chr4:49003600 | G | C | 1 | a0003c0003t0001g0210 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.803-135G>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 6/15 | chr4 | 49003600 | |||||||
| chr4:49004168 | T | C | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1060+176T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 7/15 | chr4 | 49004168 | |||||||
| chr4:49004374 | T | A | 1 | a0001c0001t0001g0264 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1060+382T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 7/15 | chr4 | 49004374 | |||||||
| chr4:49004614 | T | G | 155 | a0001c0001t0001g0021 a0001c0001t0001g0040 a0001c0001t0001g0129 others(152): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(163): Show |
intron_variant | MODIFIER | c.1060+622T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 7/15 | chr4 | 49004614 | |||||||
| chr4:49004665 | C | G | 8 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(5): Show |
8 | HG01255.hp1 HG01884.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.1060+673C>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 7/15 | chr4 | 49004665 | |||||||
| chr4:49004739 | G | C | 1 | a0002c0002t0001g0070 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1060+747G>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 7/15 | chr4 | 49004739 | |||||||
| chr4:49004799 | A | T | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1060+807A>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 7/15 | chr4 | 49004799 | |||||||
| chr4:49004951 | T | C | 162 | a0001c0001t0001g0021 a0001c0001t0001g0040 a0001c0001t0001g0129 others(159): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.1060+959T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 7/15 | chr4 | 49004951 | |||||||
| chr4:49005100 | A | C | 1 | a0001c0001t0001g0249 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1060+1108A>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 7/15 | chr4 | 49005100 | |||||||
| chr4:49005391 | A | G | 2 | a0004c0004t0001g0151 a0004c0004t0001g0152 |
2 | NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1060+1399A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 7/15 | chr4 | 49005391 | |||||||
| chr4:49005433 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1060+1441C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 7/15 | chr4 | 49005433 | |||||||
| chr4:49005563 | CT | C | 6 | a0001c0001t0001g0161 a0001c0001t0001g0170 a0002c0002t0001g0056 others(3): Show |
6 | HG02145.hp2 HG03041.hp1 HG04184.hp1 others(3): Show |
intron_variant | MODIFIER | c.1060+1585delT | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr4 | 49005563 | ||||||
| chr4:49005757 | C | T | 1 | a0003c0003t0001g0058 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1061-1444C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 7/15 | chr4 | 49005757 | |||||||
| chr4:49005810 | G | C | 2 | a0001c0001t0001g0165 a0001c0001t0001g0170 |
2 | HG03041.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1061-1391G>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 7/15 | chr4 | 49005810 | |||||||
| chr4:49005958 | A | C | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1061-1243A>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 7/15 | chr4 | 49005958 | |||||||
| chr4:49005996 | T | C | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | NA18946.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.1061-1205T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 7/15 | chr4 | 49005996 | |||||||
| chr4:49006013 | C | G | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1061-1188C>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 7/15 | chr4 | 49006013 | |||||||
| chr4:49006412 | T | C | 2 | a0002c0002t0001g0073 a0002c0002t0001g0074 |
2 | HG00639.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1061-789T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 7/15 | chr4 | 49006412 | |||||||
| chr4:49006558 | T | C | 1 | a0001c0001t0001g0214 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1061-643T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 7/15 | chr4 | 49006558 | |||||||
| chr4:49006600 | T | G | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1061-601T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 7/15 | chr4 | 49006600 | |||||||
| chr4:49006639 | T | A | 2 | a0003c0003t0001g0118 a0003c0003t0001g0119 |
2 | HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1061-562T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 7/15 | chr4 | 49006639 | |||||||
| chr4:49006639 | T | G | 2 | a0001c0001t0001g0271 a0001c0001t0001g0272 |
2 | HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1061-562T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 7/15 | chr4 | 49006639 | |||||||
| chr4:49006749 | A | T | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1061-452A>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 7/15 | chr4 | 49006749 | |||||||
| chr4:49006892 | C | G | 1 | a0001c0001t0001g0130 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1061-309C>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 7/15 | chr4 | 49006892 | |||||||
| chr4:49006957 | A | G | 1 | a0003c0003t0001g0210 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1061-244A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 7/15 | chr4 | 49006957 | |||||||
| chr4:49007161 | G | C | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1061-40G>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 7/15 | chr4 | 49007161 | |||||||
| chr4:49007543 | G | A | 1 | a0002c0002t0001g0142 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1186+217G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49007543 | |||||||
| chr4:49007625 | C | T | 2 | a0001c0001t0001g0129 a0001c0001t0001g0181 |
2 | NA18612.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.1186+299C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49007625 | |||||||
| chr4:49007750 | T | G | 1 | a0001c0001t0001g0215 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1186+424T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49007750 | |||||||
| chr4:49007816 | G | T | 2 | a0001c0001t0001g0165 a0001c0001t0001g0170 |
2 | HG03041.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1186+490G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49007816 | |||||||
| chr4:49007832 | T | C | 1 | a0003c0003t0001g0058 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1186+506T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49007832 | |||||||
| chr4:49007871 | T | C | 1 | a0002c0002t0001g0049 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1186+545T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49007871 | |||||||
| chr4:49007933 | C | T | 3 | a0001c0001t0001g0160 a0001c0001t0001g0166 a0001c0001t0001g0167 |
3 | HG02258.hp1 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1186+607C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49007933 | |||||||
| chr4:49008094 | T | C | 56 | a0002c0002t0001g0008 a0002c0002t0001g0075 a0002c0002t0001g0076 others(53): Show |
62 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.1186+768T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49008094 | |||||||
| chr4:49008243 | T | A | 1 | a0001c0001t0001g0160 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1186+917T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49008243 | |||||||
| chr4:49008514 | G | A | 2 | a0003c0003t0001g0132 a0003c0003t0001g0133 |
2 | HG00558.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.1186+1188G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49008514 | |||||||
| chr4:49008521 | T | C | 3 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 |
3 | HG03540.hp2 HG03669.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1186+1195T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49008521 | |||||||
| chr4:49008598 | A | G | 4 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(1): Show |
4 | HG02145.hp2 HG02486.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1186+1272A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49008598 | |||||||
| chr4:49008734 | C | G | 1 | a0003c0003t0001g0039 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1186+1408C>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49008734 | |||||||
| chr4:49008907 | C | A | 1 | a0001c0001t0001g0265 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1186+1581C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49008907 | |||||||
| chr4:49008935 | C | T | 151 | a0001c0001t0001g0021 a0001c0001t0001g0271 a0001c0001t0001g0272 others(148): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.1186+1609C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49008935 | |||||||
| chr4:49008957 | G | T | 3 | a0003c0003t0001g0014 a0003c0003t0001g0186 a0003c0003t0001g0187 |
4 | NA18946.hp2 NA18980.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.1186+1631G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49008957 | |||||||
| chr4:49008991 | G | C | 1 | a0002c0002t0001g0070 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1186+1665G>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49008991 | |||||||
| chr4:49009103 | A | G | 1 | a0003c0003t0001g0038 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1186+1777A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49009103 | |||||||
| chr4:49009116 | A | G | 6 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 others(3): Show |
6 | HG01884.hp1 HG02258.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1186+1790A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49009116 | |||||||
| chr4:49009412 | C | T | 1 | a0002c0002t0001g0117 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1186+2086C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49009412 | |||||||
| chr4:49009564 | C | T | 3 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 |
3 | HG03540.hp2 HG03669.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1186+2238C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49009564 | |||||||
| chr4:49009645 | A | G | 152 | a0001c0001t0001g0021 a0001c0001t0001g0149 a0001c0001t0001g0271 others(149): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1186+2319A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49009645 | |||||||
| chr4:49009813 | C | T | 145 | a0001c0001t0001g0021 a0002c0002t0001g0006 a0002c0002t0001g0007 others(142): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.1186+2487C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49009813 | |||||||
| chr4:49010009 | T | G | 1 | a0003c0003t0001g0023 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1186+2683T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49010009 | |||||||
| chr4:49010115 | T | G | 145 | a0001c0001t0001g0149 a0002c0002t0001g0006 a0002c0002t0001g0007 others(142): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.1186+2789T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49010115 | |||||||
| chr4:49010229 | A | G | 1 | a0002c0002t0001g0069 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1186+2903A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49010229 | |||||||
| chr4:49010334 | T | C | 2 | a0007c0008t0001g0146 a0007c0008t0001g0147 |
2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1186+3008T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49010334 | |||||||
| chr4:49010776 | T | C | 1 | a0002c0002t0001g0084 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1186+3450T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49010776 | |||||||
| chr4:49010794 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1186+3468G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49010794 | |||||||
| chr4:49010823 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1186+3497G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49010823 | |||||||
| chr4:49010847 | G | T | 1 | a0001c0001t0001g0247 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1186+3521G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49010847 | |||||||
| chr4:49011153 | G | A | 1 | a0007c0008t0001g0146 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1186+3827G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49011153 | |||||||
| chr4:49011173 | A | G | 1 | a0002c0002t0001g0083 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1186+3847A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49011173 | |||||||
| chr4:49011841 | C | T | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1186+4515C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49011841 | |||||||
| chr4:49011922 | A | G | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1186+4596A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49011922 | |||||||
| chr4:49011959 | G | A | 1 | a0003c0003t0001g0085 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1186+4633G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49011959 | |||||||
| chr4:49012039 | G | C | 1 | a0002c0002t0001g0070 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1186+4713G>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49012039 | |||||||
| chr4:49012075 | C | T | 1 | a0003c0003t0001g0058 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1186+4749C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49012075 | |||||||
| chr4:49012370 | G | C | 3 | a0003c0003t0001g0116 a0003c0003t0001g0120 a0003c0003t0001g0131 |
3 | HG00639.hp1 HG02735.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1187-4879G>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49012370 | |||||||
| chr4:49012668 | C | T | 1 | a0002c0002t0001g0111 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1187-4581C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49012668 | |||||||
| chr4:49012674 | T | G | 1 | a0002c0002t0001g0111 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1187-4575T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49012674 | |||||||
| chr4:49012777 | G | A | 2 | a0002c0002t0001g0075 a0002c0002t0001g0076 |
2 | HG00408.hp1 HG00609.hp1 |
intron_variant | MODIFIER | c.1187-4472G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49012777 | |||||||
| chr4:49012786 | G | A | 3 | a0003c0003t0001g0116 a0003c0003t0001g0120 a0003c0003t0001g0131 |
3 | HG00639.hp1 HG02735.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1187-4463G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49012786 | |||||||
| chr4:49012921 | G | A | 2 | a0007c0008t0001g0146 a0007c0008t0001g0147 |
2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1187-4328G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49012921 | |||||||
| chr4:49012937 | A | G | 1 | a0002c0002t0001g0082 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1187-4312A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49012937 | |||||||
| chr4:49012997 | G | A | 1 | a0001c0001t0001g0254 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1187-4252G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49012997 | |||||||
| chr4:49013147 | C | T | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1187-4102C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49013147 | |||||||
| chr4:49013226 | C | T | 1 | a0003c0003t0001g0119 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1187-4023C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49013226 | |||||||
| chr4:49013227 | G | T | 2 | a0002c0002t0001g0112 a0002c0002t0001g0113 |
2 | HG00280.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.1187-4022G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49013227 | |||||||
| chr4:49013364 | C | T | 3 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 |
3 | HG03540.hp2 HG03669.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1187-3885C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49013364 | |||||||
| chr4:49013421 | G | A | 1 | a0002c0002t0001g0117 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1187-3828G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49013421 | |||||||
| chr4:49013467 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1187-3782C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49013467 | |||||||
| chr4:49013500 | C | T | 1 | a0001c0001t0001g0022 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1187-3749C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49013500 | |||||||
| chr4:49013595 | A | C | 3 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 |
3 | HG03540.hp2 HG03669.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1187-3654A>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49013595 | |||||||
| chr4:49013631 | CT | C | 152 | a0001c0001t0001g0021 a0001c0001t0001g0130 a0001c0001t0001g0271 others(149): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1187-3608delT | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 49013631 | ||||||
| chr4:49013654 | A | C | 1 | a0001c0001t0001g0246 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1187-3595A>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49013654 | |||||||
| chr4:49013802 | T | C | 1 | a0002c0002t0001g0086 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1187-3447T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49013802 | |||||||
| chr4:49013818 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1187-3431G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49013818 | |||||||
| chr4:49013896 | A | C | 6 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 others(3): Show |
6 | HG01243.hp1 HG02622.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1187-3353A>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49013896 | |||||||
| chr4:49014035 | A | G | 1 | a0001c0001t0001g0268 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1187-3214A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49014035 | |||||||
| chr4:49014139 | T | A | 2 | a0001c0001t0001g0203 a0001c0001t0001g0204 |
2 | NA19011.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.1187-3110T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49014139 | |||||||
| chr4:49014290 | A | C | 1 | a0001c0001t0001g0196 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1187-2959A>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49014290 | |||||||
| chr4:49014360 | C | A | 1 | a0001c0001t0001g0130 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1187-2889C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49014360 | |||||||
| chr4:49014439 | A | T | 1 | a0002c0002t0001g0055 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1187-2810A>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49014439 | |||||||
| chr4:49014443 | A | C | 1 | a0002c0002t0001g0055 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1187-2806A>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49014443 | |||||||
| chr4:49014458 | C | CA | 113 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0017 others(110): Show |
122 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.1187-2774dupA | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 49014458 | ||||||
| chr4:49014465 | A | G | 145 | a0001c0001t0001g0021 a0002c0002t0001g0006 a0002c0002t0001g0007 others(142): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.1187-2784A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49014465 | |||||||
| chr4:49014656 | C | A | 2 | a0001c0001t0001g0216 a0001c0001t0001g0217 |
2 | HG01891.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1187-2593C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49014656 | |||||||
| chr4:49014744 | A | G | 145 | a0001c0001t0001g0021 a0002c0002t0001g0006 a0002c0002t0001g0007 others(142): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.1187-2505A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49014744 | |||||||
| chr4:49014977 | T | A | 1 | a0001c0001t0001g0130 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1187-2272T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49014977 | |||||||
| chr4:49015055 | C | A | 9 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(6): Show |
9 | HG01255.hp1 HG01884.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1187-2194C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49015055 | |||||||
| chr4:49015071 | G | A | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1187-2178G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49015071 | |||||||
| chr4:49015202 | T | C | 1 | a0001c0001t0001g0172 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1187-2047T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49015202 | |||||||
| chr4:49015262 | GT | G | 7 | a0001c0001t0001g0013 a0001c0001t0001g0174 a0001c0001t0001g0175 others(4): Show |
8 | HG02258.hp2 NA18968.hp2 NA18980.hp1 others(5): Show |
intron_variant | MODIFIER | c.1187-1977delT | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr4 | 49015262 | ||||||
| chr4:49015441 | A | C | 3 | a0003c0003t0001g0014 a0003c0003t0001g0186 a0003c0003t0001g0187 |
4 | NA18946.hp2 NA18980.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.1187-1808A>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49015441 | |||||||
| chr4:49015714 | C | T | 3 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 |
3 | HG03540.hp2 HG03669.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1187-1535C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49015714 | |||||||
| chr4:49015824 | A | G | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1187-1425A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49015824 | |||||||
| chr4:49016289 | T | C | 146 | a0001c0001t0001g0021 a0001c0001t0001g0149 a0002c0002t0001g0006 others(143): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1187-960T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49016289 | |||||||
| chr4:49016317 | G | C | 146 | a0001c0001t0001g0021 a0001c0001t0001g0149 a0002c0002t0001g0006 others(143): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1187-932G>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49016317 | |||||||
| chr4:49016417 | G | A | 1 | a0001c0001t0001g0248 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1187-832G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49016417 | |||||||
| chr4:49016427 | C | T | 1 | a0001c0001t0001g0178 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1187-822C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49016427 | |||||||
| chr4:49016439 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1187-810G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49016439 | |||||||
| chr4:49016654 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1187-595G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49016654 | |||||||
| chr4:49016754 | C | G | 1 | a0001c0001t0001g0040 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1187-495C>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49016754 | |||||||
| chr4:49016764 | A | G | 1 | a0001c0001t0001g0178 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1187-485A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49016764 | |||||||
| chr4:49016790 | T | A | 1 | a0001c0001t0001g0161 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1187-459T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49016790 | |||||||
| chr4:49016869 | G | A | 3 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 |
3 | HG03540.hp2 HG03669.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1187-380G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49016869 | |||||||
| chr4:49016897 | T | C | 152 | a0001c0001t0001g0021 a0001c0001t0001g0149 a0001c0001t0001g0271 others(149): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1187-352T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49016897 | |||||||
| chr4:49016915 | C | T | 2 | a0007c0008t0001g0146 a0007c0008t0001g0147 |
2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1187-334C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49016915 | |||||||
| chr4:49016958 | G | A | 1 | a0002c0002t0001g0059 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1187-291G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49016958 | |||||||
| chr4:49017101 | T | A | 4 | a0004c0004t0001g0011 a0004c0004t0001g0012 a0004c0004t0001g0154 others(1): Show |
6 | HG00738.hp2 HG01069.hp2 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.1187-148T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49017101 | |||||||
| chr4:49017130 | A | G | 1 | a0003c0003t0001g0189 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1187-119A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49017130 | |||||||
| chr4:49017215 | T | A | 56 | a0002c0002t0001g0008 a0002c0002t0001g0075 a0002c0002t0001g0076 others(53): Show |
62 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.1187-34T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 8/15 | chr4 | 49017215 | |||||||
| chr4:49017588 | T | G | 1 | a0001c0001t0001g0040 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1266+260T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49017588 | |||||||
| chr4:49017682 | C | G | 145 | a0001c0001t0001g0149 a0002c0002t0001g0006 a0002c0002t0001g0007 others(142): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.1266+354C>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49017682 | |||||||
| chr4:49017685 | T | C | 152 | a0001c0001t0001g0021 a0001c0001t0001g0149 a0001c0001t0001g0271 others(149): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1266+357T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49017685 | |||||||
| chr4:49017875 | G | A | 1 | a0002c0002t0001g0087 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1266+547G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49017875 | |||||||
| chr4:49017897 | C | T | 3 | a0001c0001t0001g0263 a0005c0005t0001g0020 a0005c0005t0001g0244 |
4 | HG01928.hp1 HG01975.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.1266+569C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49017897 | |||||||
| chr4:49018031 | G | A | 4 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(1): Show |
4 | HG02145.hp2 HG02486.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1266+703G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49018031 | |||||||
| chr4:49018089 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1266+761C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49018089 | |||||||
| chr4:49018106 | A | G | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1266+778A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49018106 | |||||||
| chr4:49018154 | C | G | 146 | a0001c0001t0001g0021 a0001c0001t0001g0149 a0002c0002t0001g0006 others(143): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1266+826C>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49018154 | |||||||
| chr4:49018214 | C | CATTT | 2 | a0003c0003t0001g0003 a0003c0003t0001g0029 |
3 | HG01433.hp2 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1266+906_1266+909d others(6): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 49018214 | ||||||
| chr4:49018333 | T | C | 1 | a0003c0003t0001g0030 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1266+1005T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49018333 | |||||||
| chr4:49018649 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1266+1321C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49018649 | |||||||
| chr4:49018761 | C | T | 2 | a0007c0008t0001g0146 a0007c0008t0001g0147 |
2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1266+1433C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49018761 | |||||||
| chr4:49018762 | G | A | 1 | a0001c0001t0003g0220 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1266+1434G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49018762 | |||||||
| chr4:49018792 | A | T | 1 | a0001c0001t0001g0168 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1266+1464A>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49018792 | |||||||
| chr4:49019082 | A | G | 152 | a0001c0001t0001g0021 a0001c0001t0001g0149 a0001c0001t0001g0271 others(149): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1266+1754A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49019082 | |||||||
| chr4:49019094 | A | G | 1 | a0002c0002t0001g0137 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1266+1766A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49019094 | |||||||
| chr4:49019243 | G | A | 1 | a0003c0003t0001g0039 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1266+1915G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49019243 | |||||||
| chr4:49019243 | G | T | 1 | a0002c0002t0001g0054 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1266+1915G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49019243 | |||||||
| chr4:49019462 | T | C | 3 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 |
3 | HG03540.hp2 HG03669.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1266+2134T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49019462 | |||||||
| chr4:49019465 | C | T | 1 | a0001c0001t0001g0243 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1266+2137C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49019465 | |||||||
| chr4:49019511 | T | C | 1 | a0002c0002t0001g0077 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1266+2183T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49019511 | |||||||
| chr4:49019569 | A | G | 1 | a0002c0002t0001g0137 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1266+2241A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49019569 | |||||||
| chr4:49019724 | C | T | 3 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 |
3 | HG03540.hp2 HG03669.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1266+2396C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49019724 | |||||||
| chr4:49019741 | A | G | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1266+2413A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49019741 | |||||||
| chr4:49019890 | G | A | 4 | a0002c0002t0001g0088 a0002c0002t0001g0089 a0002c0002t0001g0090 others(1): Show |
4 | HG01070.hp2 HG01433.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.1266+2562G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49019890 | |||||||
| chr4:49020039 | A | G | 1 | a0001c0001t0001g0242 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1266+2711A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49020039 | |||||||
| chr4:49020289 | G | A | 7 | a0004c0004t0001g0011 a0004c0004t0001g0012 a0004c0004t0001g0150 others(4): Show |
9 | HG00738.hp2 HG01069.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1266+2961G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49020289 | |||||||
| chr4:49020306 | G | A | 145 | a0001c0001t0001g0021 a0002c0002t0001g0006 a0002c0002t0001g0007 others(142): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.1266+2978G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49020306 | |||||||
| chr4:49020326 | C | G | 1 | a0001c0001t0001g0182 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1266+2998C>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49020326 | |||||||
| chr4:49020384 | T | TAC | 5 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0221 others(2): Show |
5 | HG00558.hp1 HG02523.hp2 HG03942.hp1 others(2): Show |
intron_variant | MODIFIER | c.1266+3088_1266+308 others(6): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 49020384 | ||||||
| chr4:49020384 | T | TACAC | 6 | a0001c0001t0001g0148 a0001c0001t0001g0207 a0001c0001t0001g0208 others(3): Show |
6 | HG01891.hp1 HG02572.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1266+3086_1266+308 others(8): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 49020384 | ||||||
| chr4:49020384 | TAC | T | 8 | a0001c0001t0001g0040 a0001c0001t0001g0170 a0001c0001t0001g0202 others(5): Show |
8 | HG01074.hp2 HG02738.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.1266+3088_1266+308 others(6): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 49020384 | ||||||
| chr4:49020384 | TACAC | T | 5 | a0001c0001t0001g0195 a0001c0001t0001g0263 a0002c0002t0001g0081 others(2): Show |
6 | HG01928.hp1 HG01975.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.1266+3086_1266+308 others(8): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 49020384 | ||||||
| chr4:49020384 | TACACACA others(3): Show |
T | 1 | a0001c0001t0001g0169 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1266+3080_1266+308 others(14): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 49020384 | ||||||
| chr4:49020414 | C | CATATAT | 3 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 |
3 | HG03540.hp2 HG03669.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1266+3087_1266+308 others(10): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 49020414 | ||||||
| chr4:49020414 | C | T | 1 | a0002c0002t0001g0081 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1266+3086C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49020414 | |||||||
| chr4:49020416 | C | CACACACA others(15): Show |
1 | a0002c0002t0001g0078 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1266+3089_1266+309 others(26): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 49020416 | ||||||
| chr4:49020416 | C | CACACACA others(17): Show |
2 | a0002c0002t0001g0006 a0002c0002t0001g0060 |
3 | NA18940.hp1 NA18994.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.1266+3089_1266+309 others(28): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 49020416 | ||||||
| chr4:49020416 | C | CACACACA others(13): Show |
1 | a0003c0003t0001g0183 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1266+3089_1266+309 others(24): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 49020416 | ||||||
| chr4:49020416 | C | CACACACA others(15): Show |
5 | a0002c0002t0001g0092 a0002c0002t0001g0093 a0002c0002t0001g0113 others(2): Show |
5 | HG00738.hp1 HG01496.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.1266+3089_1266+309 others(26): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 49020416 | ||||||
| chr4:49020416 | C | CACACACA others(11): Show |
1 | a0003c0003t0001g0121 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1266+3089_1266+309 others(22): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 49020416 | ||||||
| chr4:49020416 | C | CACACACA others(13): Show |
20 | a0002c0002t0001g0047 a0002c0002t0001g0048 a0002c0002t0001g0061 others(17): Show |
20 | HG00099.hp1 HG00280.hp1 HG00741.hp2 others(17): Show |
intron_variant | MODIFIER | c.1266+3089_1266+309 others(24): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 49020416 | ||||||
| chr4:49020416 | C | CACACACA others(9): Show |
1 | a0003c0003t0001g0123 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1266+3089_1266+309 others(20): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 49020416 | ||||||
| chr4:49020416 | C | CACACACA others(11): Show |
65 | a0001c0001t0001g0021 a0001c0001t0004g0270 a0002c0002t0001g0007 others(62): Show |
72 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.1266+3089_1266+309 others(22): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 49020416 | ||||||
| chr4:49020416 | C | CACACACA others(13): Show |
1 | a0003c0003t0001g0118 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1266+3089_1266+309 others(24): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 49020416 | ||||||
| chr4:49020416 | C | CACACACA others(7): Show |
2 | a0003c0003t0001g0085 a0003c0003t0001g0127 |
2 | HG00741.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1266+3089_1266+309 others(18): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 49020416 | ||||||
| chr4:49020416 | C | CACACACA others(9): Show |
28 | a0002c0002t0001g0010 a0002c0002t0001g0069 a0002c0002t0001g0070 others(25): Show |
30 | HG00323.hp1 HG01109.hp2 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.1266+3089_1266+309 others(20): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 49020416 | ||||||
| chr4:49020416 | C | CACACACA others(11): Show |
2 | a0002c0002t0001g0068 a0009c0010t0001g0145 |
2 | NA18982.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1266+3089_1266+309 others(22): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 49020416 | ||||||
| chr4:49020416 | C | CACACACA others(7): Show |
13 | a0002c0002t0001g0008 a0002c0002t0001g0055 a0002c0002t0001g0072 others(10): Show |
14 | HG00558.hp2 HG00735.hp2 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.1266+3089_1266+309 others(18): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 49020416 | ||||||
| chr4:49020416 | C | CACACACA others(9): Show |
2 | a0002c0002t0001g0090 a0002c0002t0001g0091 |
2 | HG01070.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1266+3089_1266+309 others(20): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 49020416 | ||||||
| chr4:49020416 | C | CACACACA others(3): Show |
1 | a0001c0001t0001g0163 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1266+3089_1266+309 others(14): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 49020416 | ||||||
| chr4:49020416 | C | CACACACA others(5): Show |
1 | a0002c0002t0001g0110 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1266+3089_1266+309 others(16): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 49020416 | ||||||
| chr4:49020416 | C | CACACACA others(3): Show |
2 | a0007c0008t0001g0146 a0007c0008t0001g0147 |
2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1266+3089_1266+309 others(14): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 49020416 | ||||||
| chr4:49020416 | C | CACAT | 8 | a0001c0001t0001g0130 a0001c0001t0001g0168 a0004c0004t0001g0011 others(5): Show |
10 | HG00738.hp2 HG01069.hp2 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1266+3089_1266+309 others(8): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 49020416 | ||||||
| chr4:49020416 | C | CAT | 4 | a0001c0001t0001g0160 a0001c0001t0001g0165 a0001c0001t0001g0166 others(1): Show |
4 | HG02258.hp1 HG02922.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1266+3100_1266+310 others(6): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr4 | 49020416 | ||||||
| chr4:49020416 | C | T | 8 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0169 others(5): Show |
8 | HG02145.hp2 HG03041.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.1266+3088C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49020416 | |||||||
| chr4:49020453 | G | T | 2 | a0007c0008t0001g0146 a0007c0008t0001g0147 |
2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1266+3125G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49020453 | |||||||
| chr4:49020638 | T | A | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1266+3310T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49020638 | |||||||
| chr4:49020742 | T | G | 4 | a0002c0002t0001g0070 a0002c0002t0001g0106 a0002c0002t0001g0111 others(1): Show |
4 | HG00323.hp1 HG01109.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.1266+3414T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49020742 | |||||||
| chr4:49021161 | G | A | 1 | a0001c0001t0001g0271 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1266+3833G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49021161 | |||||||
| chr4:49021189 | G | T | 1 | a0001c0001t0001g0243 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1266+3861G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49021189 | |||||||
| chr4:49021315 | T | C | 1 | a0001c0001t0001g0174 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1266+3987T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49021315 | |||||||
| chr4:49021407 | C | G | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1266+4079C>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49021407 | |||||||
| chr4:49021435 | T | A | 1 | a0003c0003t0001g0124 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1266+4107T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49021435 | |||||||
| chr4:49021999 | C | A | 4 | a0001c0001t0001g0130 a0001c0001t0001g0165 a0001c0001t0001g0169 others(1): Show |
4 | HG03041.hp1 HG03139.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1266+4671C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49021999 | |||||||
| chr4:49022002 | C | T | 1 | a0001c0001t0001g0209 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1266+4674C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49022002 | |||||||
| chr4:49022173 | T | C | 1 | a0001c0001t0001g0196 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1266+4845T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49022173 | |||||||
| chr4:49022340 | G | T | 1 | a0001c0001t0001g0241 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1266+5012G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49022340 | |||||||
| chr4:49022415 | G | A | 2 | a0002c0002t0001g0112 a0002c0002t0001g0113 |
2 | HG00280.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.1266+5087G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49022415 | |||||||
| chr4:49022438 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1266+5110G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49022438 | |||||||
| chr4:49022532 | A | G | 1 | a0001c0001t0001g0259 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1266+5204A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49022532 | |||||||
| chr4:49022836 | A | G | 5 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 others(2): Show |
5 | HG01884.hp1 HG03130.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.1266+5508A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49022836 | |||||||
| chr4:49022870 | A | G | 4 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(1): Show |
4 | HG02145.hp2 HG02486.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1266+5542A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49022870 | |||||||
| chr4:49023062 | C | A | 3 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 |
3 | HG03540.hp2 HG03669.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1267-5567C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49023062 | |||||||
| chr4:49023248 | T | A | 4 | a0002c0002t0001g0078 a0003c0003t0001g0121 a0003c0003t0001g0123 others(1): Show |
4 | HG00741.hp1 HG01074.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.1267-5381T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49023248 | |||||||
| chr4:49023258 | G | A | 2 | a0007c0008t0001g0146 a0007c0008t0001g0147 |
2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1267-5371G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49023258 | |||||||
| chr4:49023566 | G | A | 1 | a0002c0002t0001g0107 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1267-5063G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49023566 | |||||||
| chr4:49023704 | C | T | 9 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(6): Show |
9 | HG01255.hp1 HG01884.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1267-4925C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49023704 | |||||||
| chr4:49023951 | C | A | 8 | a0002c0002t0001g0087 a0002c0002t0001g0092 a0002c0002t0001g0094 others(5): Show |
8 | HG01358.hp1 HG01496.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.1267-4678C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49023951 | |||||||
| chr4:49024078 | C | T | 1 | a0002c0002t0001g0053 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1267-4551C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49024078 | |||||||
| chr4:49024087 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1267-4542G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49024087 | |||||||
| chr4:49024195 | A | T | 3 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 |
3 | HG03540.hp2 HG03669.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1267-4434A>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49024195 | |||||||
| chr4:49024270 | A | G | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1267-4359A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49024270 | |||||||
| chr4:49024359 | C | T | 1 | a0001c0001t0001g0224 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1267-4270C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49024359 | |||||||
| chr4:49024579 | T | A | 152 | a0001c0001t0001g0021 a0001c0001t0001g0149 a0001c0001t0001g0271 others(149): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1267-4050T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49024579 | |||||||
| chr4:49024582 | T | A | 152 | a0001c0001t0001g0021 a0001c0001t0001g0149 a0001c0001t0001g0271 others(149): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1267-4047T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49024582 | |||||||
| chr4:49024714 | T | A | 152 | a0001c0001t0001g0021 a0001c0001t0001g0149 a0001c0001t0001g0271 others(149): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1267-3915T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49024714 | |||||||
| chr4:49025060 | C | A | 1 | a0001c0001t0001g0168 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1267-3569C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49025060 | |||||||
| chr4:49025127 | T | C | 1 | a0001c0001t0001g0259 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1267-3502T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49025127 | |||||||
| chr4:49025159 | G | A | 2 | a0007c0008t0001g0146 a0007c0008t0001g0147 |
2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1267-3470G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49025159 | |||||||
| chr4:49025173 | T | C | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1267-3456T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49025173 | |||||||
| chr4:49025179 | C | T | 3 | a0002c0002t0001g0115 a0003c0003t0001g0034 a0003c0003t0001g0035 |
3 | HG00280.hp2 HG02965.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1267-3450C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49025179 | |||||||
| chr4:49025251 | A | G | 1 | a0001c0001t0001g0130 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1267-3378A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49025251 | |||||||
| chr4:49025384 | A | G | 1 | a0002c0002t0001g0056 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1267-3245A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49025384 | |||||||
| chr4:49025516 | G | A | 3 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 |
3 | HG03540.hp2 HG03669.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1267-3113G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49025516 | |||||||
| chr4:49025539 | T | C | 1 | a0003c0003t0001g0085 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1267-3090T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49025539 | |||||||
| chr4:49025621 | T | C | 152 | a0001c0001t0001g0021 a0001c0001t0001g0149 a0001c0001t0001g0271 others(149): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1267-3008T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49025621 | |||||||
| chr4:49025698 | G | A | 3 | a0001c0001t0004g0270 a0007c0008t0001g0146 a0007c0008t0001g0147 |
3 | HG01884.hp1 HG02258.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1267-2931G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49025698 | |||||||
| chr4:49025823 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1267-2806G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49025823 | |||||||
| chr4:49025936 | G | T | 1 | a0001c0001t0001g0269 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1267-2693G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49025936 | |||||||
| chr4:49025968 | T | C | 1 | a0003c0003t0001g0123 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1267-2661T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49025968 | |||||||
| chr4:49025989 | C | T | 144 | a0002c0002t0001g0006 a0002c0002t0001g0007 a0002c0002t0001g0008 others(141): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.1267-2640C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49025989 | |||||||
| chr4:49025999 | A | T | 1 | a0002c0002t0001g0109 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1267-2630A>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49025999 | |||||||
| chr4:49026053 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1267-2576C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49026053 | |||||||
| chr4:49026100 | T | C | 1 | a0001c0001t0001g0196 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1267-2529T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49026100 | |||||||
| chr4:49026120 | A | G | 152 | a0001c0001t0001g0021 a0001c0001t0001g0149 a0001c0001t0001g0271 others(149): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1267-2509A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49026120 | |||||||
| chr4:49026202 | C | T | 1 | a0001c0001t0001g0266 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1267-2427C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49026202 | |||||||
| chr4:49026632 | C | T | 7 | a0001c0001t0001g0261 a0001c0001t0001g0271 a0001c0001t0001g0272 others(4): Show |
7 | HG01884.hp1 HG02258.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1267-1997C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49026632 | |||||||
| chr4:49027121 | C | T | 4 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0254 others(1): Show |
4 | HG02622.hp2 HG03516.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1267-1508C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49027121 | |||||||
| chr4:49027328 | T | C | 1 | a0002c0002t0001g0070 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1267-1301T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49027328 | |||||||
| chr4:49027406 | G | A | 4 | a0003c0003t0001g0005 a0003c0003t0001g0043 a0003c0003t0001g0044 others(1): Show |
5 | HG00735.hp1 HG01167.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.1267-1223G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49027406 | |||||||
| chr4:49027474 | C | T | 2 | a0007c0008t0001g0146 a0007c0008t0001g0147 |
2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1267-1155C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49027474 | |||||||
| chr4:49027552 | A | T | 2 | a0001c0001t0001g0237 a0001c0001t0001g0242 |
2 | NA19002.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1267-1077A>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49027552 | |||||||
| chr4:49027683 | G | A | 1 | a0003c0003t0001g0184 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1267-946G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49027683 | |||||||
| chr4:49027690 | A | G | 3 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 |
3 | HG03540.hp2 HG03669.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1267-939A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49027690 | |||||||
| chr4:49027884 | C | T | 151 | a0001c0001t0001g0021 a0001c0001t0001g0271 a0001c0001t0001g0272 others(148): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.1267-745C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49027884 | |||||||
| chr4:49027957 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1267-672C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49027957 | |||||||
| chr4:49028213 | T | A | 1 | a0002c0002t0001g0114 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1267-416T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49028213 | |||||||
| chr4:49028222 | A | G | 2 | a0002c0002t0001g0112 a0002c0002t0001g0113 |
2 | HG00280.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.1267-407A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49028222 | |||||||
| chr4:49028446 | G | T | 3 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 |
3 | HG03540.hp2 HG03669.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1267-183G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49028446 | |||||||
| chr4:49028566 | G | A | 1 | a0003c0003t0001g0085 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1267-63G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 9/15 | chr4 | 49028566 | |||||||
| chr4:49028854 | G | A | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1372+120G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 10/15 | chr4 | 49028854 | |||||||
| chr4:49028985 | A | G | 1 | a0003c0003t0001g0190 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1372+251A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 10/15 | chr4 | 49028985 | |||||||
| chr4:49029409 | G | C | 3 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 |
3 | HG03540.hp2 HG03669.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1372+675G>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 10/15 | chr4 | 49029409 | |||||||
| chr4:49029690 | G | A | 1 | a0002c0002t0001g0111 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1372+956G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 10/15 | chr4 | 49029690 | |||||||
| chr4:49029838 | G | A | 143 | a0002c0002t0001g0006 a0002c0002t0001g0007 a0002c0002t0001g0008 others(140): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1373-987G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 10/15 | chr4 | 49029838 | |||||||
| chr4:49029849 | G | A | 1 | a0001c0001t0001g0175 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1373-976G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 10/15 | chr4 | 49029849 | |||||||
| chr4:49029910 | T | C | 1 | a0003c0003t0001g0041 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1373-915T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 10/15 | chr4 | 49029910 | |||||||
| chr4:49030055 | T | A | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1373-770T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 10/15 | chr4 | 49030055 | |||||||
| chr4:49030303 | G | C | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1373-522G>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 10/15 | chr4 | 49030303 | |||||||
| chr4:49030336 | T | G | 3 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 |
3 | HG03540.hp2 HG03669.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1373-489T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 10/15 | chr4 | 49030336 | |||||||
| chr4:49030378 | T | C | 1 | a0001c0001t0001g0221 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1373-447T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 10/15 | chr4 | 49030378 | |||||||
| chr4:49030465 | T | G | 2 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
2 | HG01167.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1373-360T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 10/15 | chr4 | 49030465 | |||||||
| chr4:49030806 | CT | C | 4 | a0002c0002t0001g0062 a0002c0002t0001g0090 a0003c0003t0001g0001 others(1): Show |
6 | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.1373-9delT | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr4 | 49030806 | ||||||
| chr4:49031197 | C | A | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1508+237C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 11/15 | chr4 | 49031197 | |||||||
| chr4:49031348 | G | T | 1 | a0001c0001t0001g0243 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1508+388G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 11/15 | chr4 | 49031348 | |||||||
| chr4:49031378 | T | C | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1508+418T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 11/15 | chr4 | 49031378 | |||||||
| chr4:49031511 | TG | T | 146 | a0001c0001t0001g0021 a0001c0001t0001g0237 a0001c0001t0001g0242 others(143): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1508+557delG | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr4 | 49031511 | ||||||
| chr4:49031525 | G | A | 1 | a0003c0003t0001g0185 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1508+565G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 11/15 | chr4 | 49031525 | |||||||
| chr4:49031854 | C | T | 3 | a0002c0002t0001g0048 a0002c0002t0001g0052 a0002c0002t0001g0055 |
3 | HG03017.hp2 HG03654.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1509-712C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 11/15 | chr4 | 49031854 | |||||||
| chr4:49031915 | A | C | 1 | a0004c0004t0001g0154 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1509-651A>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 11/15 | chr4 | 49031915 | |||||||
| chr4:49032206 | G | A | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1509-360G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 11/15 | chr4 | 49032206 | |||||||
| chr4:49032279 | C | T | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1509-287C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 11/15 | chr4 | 49032279 | |||||||
| chr4:49032291 | G | T | 3 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 |
3 | HG03540.hp2 HG03669.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1509-275G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 11/15 | chr4 | 49032291 | |||||||
| chr4:49032538 | G | A | 3 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 |
3 | HG03540.hp2 HG03669.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1509-28G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 11/15 | chr4 | 49032538 | |||||||
| chr4:49032891 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1658+176G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49032891 | |||||||
| chr4:49032915 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1658+200C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49032915 | |||||||
| chr4:49032933 | C | T | 1 | a0003c0003t0001g0026 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1658+218C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49032933 | |||||||
| chr4:49033105 | T | C | 2 | a0001c0001t0001g0216 a0001c0001t0001g0217 |
2 | HG01891.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1658+390T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49033105 | |||||||
| chr4:49033204 | A | G | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1658+489A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49033204 | |||||||
| chr4:49033356 | T | A | 1 | a0001c0001t0001g0195 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1658+641T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49033356 | |||||||
| chr4:49033377 | A | G | 1 | a0003c0003t0001g0005 | 2 | HG01358.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1658+662A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49033377 | |||||||
| chr4:49033470 | C | T | 2 | a0007c0008t0001g0146 a0007c0008t0001g0147 |
2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1658+755C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49033470 | |||||||
| chr4:49033672 | C | A | 2 | a0007c0008t0001g0146 a0007c0008t0001g0147 |
2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1658+957C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49033672 | |||||||
| chr4:49033801 | A | G | 3 | a0001c0001t0001g0019 a0001c0001t0001g0249 a0001c0001t0001g0265 |
4 | HG02074.hp2 NA18956.hp2 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1658+1086A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49033801 | |||||||
| chr4:49033916 | A | G | 1 | a0002c0002t0001g0109 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1658+1201A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49033916 | |||||||
| chr4:49034035 | C | G | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1658+1320C>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49034035 | |||||||
| chr4:49034273 | T | C | 144 | a0001c0001t0001g0149 a0002c0002t0001g0006 a0002c0002t0001g0007 others(141): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.1658+1558T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49034273 | |||||||
| chr4:49034868 | A | T | 1 | a0001c0001t0001g0214 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1658+2153A>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49034868 | |||||||
| chr4:49034906 | G | T | 7 | a0004c0004t0001g0011 a0004c0004t0001g0012 a0004c0004t0001g0150 others(4): Show |
9 | HG00738.hp2 HG01069.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1658+2191G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49034906 | |||||||
| chr4:49035022 | A | G | 1 | a0001c0001t0001g0221 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1658+2307A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49035022 | |||||||
| chr4:49035078 | C | A | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1658+2363C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49035078 | |||||||
| chr4:49035094 | G | A | 8 | a0001c0001t0001g0219 a0001c0001t0001g0226 a0001c0001t0001g0227 others(5): Show |
9 | HG00140.hp1 HG01175.hp1 HG02300.hp2 others(6): Show |
intron_variant | MODIFIER | c.1658+2379G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49035094 | |||||||
| chr4:49035203 | C | T | 1 | a0006c0006t0001g0134 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1658+2488C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49035203 | |||||||
| chr4:49035571 | T | C | 151 | a0001c0001t0001g0021 a0001c0001t0001g0149 a0001c0001t0001g0271 others(148): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.1659-2465T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49035571 | |||||||
| chr4:49035634 | C | A | 1 | a0002c0002t0001g0050 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1659-2402C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49035634 | |||||||
| chr4:49035924 | T | C | 151 | a0001c0001t0001g0021 a0001c0001t0001g0149 a0001c0001t0001g0271 others(148): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.1659-2112T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49035924 | |||||||
| chr4:49036029 | G | A | 2 | a0002c0002t0001g0112 a0002c0002t0001g0113 |
2 | HG00280.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.1659-2007G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49036029 | |||||||
| chr4:49036039 | C | A | 1 | a0003c0003t0001g0116 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1659-1997C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49036039 | |||||||
| chr4:49036039 | C | T | 9 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(6): Show |
9 | HG01255.hp1 HG01884.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1659-1997C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49036039 | |||||||
| chr4:49036296 | A | C | 1 | a0001c0001t0001g0236 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1659-1740A>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49036296 | |||||||
| chr4:49036334 | A | G | 7 | a0001c0001t0001g0021 a0001c0001t0001g0271 a0001c0001t0001g0272 others(4): Show |
7 | HG01884.hp1 HG02258.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1659-1702A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49036334 | |||||||
| chr4:49036851 | G | T | 1 | a0001c0001t0001g0019 | 2 | NA18956.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.1659-1185G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49036851 | |||||||
| chr4:49037174 | G | C | 1 | a0001c0001t0001g0198 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1659-862G>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49037174 | |||||||
| chr4:49037185 | A | T | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1659-851A>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49037185 | |||||||
| chr4:49037233 | G | A | 2 | a0007c0008t0001g0146 a0007c0008t0001g0147 |
2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1659-803G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49037233 | |||||||
| chr4:49037424 | G | A | 1 | a0002c0002t0001g0087 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1659-612G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49037424 | |||||||
| chr4:49037569 | C | CA | 152 | a0001c0001t0001g0021 a0001c0001t0001g0149 a0001c0001t0001g0202 others(149): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1659-453dupA | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr4 | 49037569 | ||||||
| chr4:49037652 | T | A | 1 | a0001c0001t0001g0149 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1659-384T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49037652 | |||||||
| chr4:49037791 | T | C | 3 | a0002c0002t0001g0008 a0002c0002t0001g0077 a0002c0002t0001g0082 |
4 | NA18943.hp1 NA18964.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.1659-245T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49037791 | |||||||
| chr4:49037913 | C | T | 1 | a0007c0008t0001g0146 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1659-123C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49037913 | |||||||
| chr4:49037941 | C | G | 5 | a0003c0003t0001g0001 a0003c0003t0001g0024 a0003c0003t0001g0027 others(2): Show |
7 | HG01070.hp1 HG01071.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.1659-95C>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49037941 | |||||||
| chr4:49037942 | T | C | 4 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0001c0001t0001g0231 others(1): Show |
4 | HG02486.hp1 HG03486.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1659-94T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49037942 | |||||||
| chr4:49037958 | T | C | 1 | a0001c0001t0001g0232 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1659-78T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49037958 | |||||||
| chr4:49038008 | T | C | 2 | a0003c0003t0001g0014 a0003c0003t0001g0186 |
3 | NA18946.hp2 NA18990.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.1659-28T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 12/15 | chr4 | 49038008 | |||||||
| chr4:49038647 | T | G | 150 | a0001c0001t0001g0021 a0001c0001t0001g0271 a0001c0001t0001g0272 others(147): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.1803+467T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49038647 | |||||||
| chr4:49038914 | C | T | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1803+734C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49038914 | |||||||
| chr4:49038940 | C | A | 1 | a0001c0001t0001g0193 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1803+760C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49038940 | |||||||
| chr4:49039051 | C | G | 1 | a0001c0001t0001g0214 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.1803+871C>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49039051 | |||||||
| chr4:49039076 | A | T | 1 | a0002c0002t0001g0098 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1803+896A>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49039076 | |||||||
| chr4:49039077 | TTAAA | T | 143 | a0002c0002t0001g0006 a0002c0002t0001g0007 a0002c0002t0001g0008 others(140): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1803+917_1803+920d others(6): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039077 | ||||||
| chr4:49039082 | T | A | 1 | a0003c0003t0001g0085 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1803+902T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49039082 | |||||||
| chr4:49039083 | AAATAAAT others(8): Show |
A | 2 | a0001c0001t0001g0267 a0001c0007t0001g0015 |
3 | HG03831.hp2 HG04115.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1803+918_1803+932d others(17): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039083 | ||||||
| chr4:49039186 | C | A | 2 | a0002c0002t0001g0088 a0002c0002t0001g0089 |
2 | HG01433.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.1803+1006C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49039186 | |||||||
| chr4:49039306 | G | GAGATATA others(15): Show |
2 | a0007c0008t0001g0146 a0007c0008t0001g0147 |
2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1803+1127_1803+112 others(26): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039306 | ||||||
| chr4:49039306 | G | GATATATA others(1): Show |
3 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0229 |
3 | HG06807.hp1 NA18968.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.1803+1146_1803+115 others(12): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039306 | ||||||
| chr4:49039306 | G | GATATATA others(7): Show |
2 | a0001c0001t0001g0170 a0001c0001t0001g0225 |
2 | HG03041.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.1803+1140_1803+115 others(18): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039306 | ||||||
| chr4:49039306 | G | GATATATA others(9): Show |
1 | a0001c0001t0001g0197 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1803+1138_1803+115 others(20): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039306 | ||||||
| chr4:49039306 | G | GATATATA others(11): Show |
9 | a0001c0001t0001g0016 a0001c0001t0001g0219 a0001c0001t0001g0224 others(6): Show |
10 | HG00140.hp1 HG00438.hp2 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.1803+1136_1803+115 others(22): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039306 | ||||||
| chr4:49039306 | G | GATATATA others(13): Show |
9 | a0001c0001t0001g0017 a0001c0001t0001g0174 a0001c0001t0001g0192 others(6): Show |
10 | HG00639.hp1 HG01074.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.1803+1134_1803+115 others(24): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039306 | ||||||
| chr4:49039306 | G | GATATATA others(15): Show |
21 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0019 others(18): Show |
25 | HG01175.hp1 HG01975.hp1 HG01981.hp1 others(22): Show |
intron_variant | MODIFIER | c.1803+1132_1803+115 others(26): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039306 | ||||||
| chr4:49039306 | G | GATATATA others(17): Show |
20 | a0001c0001t0001g0162 a0001c0001t0001g0171 a0001c0001t0001g0173 others(17): Show |
20 | HG00423.hp1 HG01167.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.1803+1130_1803+115 others(28): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039306 | ||||||
| chr4:49039306 | G | GATATATA others(19): Show |
20 | a0001c0001t0001g0040 a0001c0001t0001g0136 a0001c0001t0001g0149 others(17): Show |
21 | HG00609.hp2 HG01099.hp1 HG02071.hp2 others(18): Show |
intron_variant | MODIFIER | c.1803+1128_1803+115 others(30): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039306 | ||||||
| chr4:49039306 | G | GATATATA others(21): Show |
10 | a0001c0001t0001g0022 a0001c0001t0001g0130 a0001c0001t0001g0160 others(7): Show |
10 | HG00558.hp1 HG02258.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1803+1153_1803+115 others(32): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039306 | ||||||
| chr4:49039306 | G | GATATATA others(23): Show |
3 | a0001c0001t0001g0235 a0001c0001t0001g0262 a0001c0001t0001g0266 |
3 | HG02132.hp1 HG02622.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1803+1153_1803+115 others(34): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039306 | ||||||
| chr4:49039306 | G | GATATATA others(25): Show |
2 | a0001c0001t0001g0193 a0001c0001t0001g0251 |
2 | HG01255.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1803+1153_1803+115 others(36): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039306 | ||||||
| chr4:49039306 | G | GATATATA others(27): Show |
2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | HG02615.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1803+1153_1803+115 others(38): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039306 | ||||||
| chr4:49039306 | G | GATATATA others(31): Show |
1 | a0001c0001t0001g0194 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1803+1153_1803+115 others(42): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039306 | ||||||
| chr4:49039306 | G | GATATATA others(35): Show |
1 | a0001c0001t0001g0177 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1803+1153_1803+115 others(46): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039306 | ||||||
| chr4:49039306 | GATATATA others(7): Show |
G | 1 | a0001c0001t0001g0215 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1803+1140_1803+115 others(18): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039306 | ||||||
| chr4:49039311 | A | ATATATAT others(29): Show |
1 | a0006c0006t0001g0144 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1803+1153_1803+115 others(40): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039311 | ||||||
| chr4:49039311 | A | ATATATAT others(21): Show |
1 | a0001c0001t0001g0269 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1803+1153_1803+115 others(32): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039311 | ||||||
| chr4:49039320 | T | G | 1 | a0003c0003t0001g0131 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1803+1140T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49039320 | |||||||
| chr4:49039320 | T | TATATATA others(7): Show |
1 | a0002c0002t0001g0052 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1803+1151_1803+115 others(18): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039320 | ||||||
| chr4:49039320 | T | TATATATA others(9): Show |
3 | a0002c0002t0001g0078 a0003c0003t0001g0118 a0003c0003t0001g0119 |
3 | HG02004.hp2 HG02572.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1803+1143_1803+115 others(20): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039320 | ||||||
| chr4:49039320 | T | TATATATA others(11): Show |
2 | a0002c0002t0001g0099 a0003c0003t0001g0190 |
2 | HG03209.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.1803+1153_1803+115 others(22): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039320 | ||||||
| chr4:49039320 | T | TATATATA others(13): Show |
1 | a0002c0002t0001g0117 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1803+1153_1803+115 others(24): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039320 | ||||||
| chr4:49039320 | T | TATATATA others(17): Show |
1 | a0003c0003t0001g0140 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1803+1153_1803+115 others(28): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039320 | ||||||
| chr4:49039320 | T | TATATATA others(25): Show |
11 | a0002c0002t0001g0094 a0003c0003t0001g0004 a0003c0003t0001g0027 others(8): Show |
12 | HG00735.hp1 HG01167.hp2 HG01993.hp2 others(9): Show |
intron_variant | MODIFIER | c.1803+1153_1803+115 others(36): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039320 | ||||||
| chr4:49039320 | T | TATATATA others(27): Show |
16 | a0002c0002t0001g0063 a0002c0002t0001g0064 a0002c0002t0001g0087 others(13): Show |
16 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(13): Show |
intron_variant | MODIFIER | c.1803+1153_1803+115 others(38): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039320 | ||||||
| chr4:49039320 | T | TATATATA others(33): Show |
1 | a0002c0002t0001g0049 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1803+1153_1803+115 others(44): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039320 | ||||||
| chr4:49039320 | T | TATATATA others(29): Show |
13 | a0002c0002t0001g0008 a0002c0002t0001g0075 a0002c0002t0001g0081 others(10): Show |
15 | HG00609.hp1 HG00741.hp2 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.1803+1153_1803+115 others(40): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039320 | ||||||
| chr4:49039320 | T | TATATATA others(31): Show |
20 | a0002c0002t0001g0070 a0002c0002t0001g0073 a0002c0002t0001g0074 others(17): Show |
20 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(17): Show |
intron_variant | MODIFIER | c.1803+1153_1803+115 others(42): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039320 | ||||||
| chr4:49039320 | T | TATATATA others(69): Show |
1 | a0003c0003t0001g0210 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1803+1153_1803+115 others(80): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039320 | ||||||
| chr4:49039320 | T | TATATATA others(33): Show |
26 | a0002c0002t0001g0050 a0002c0002t0001g0051 a0002c0002t0001g0053 others(23): Show |
27 | HG00099.hp2 HG00280.hp1 HG00423.hp2 others(24): Show |
intron_variant | MODIFIER | c.1803+1153_1803+115 others(44): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039320 | ||||||
| chr4:49039320 | T | TATATATA others(65): Show |
1 | a0003c0003t0001g0032 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1803+1153_1803+115 others(76): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039320 | ||||||
| chr4:49039320 | T | TATATATA others(35): Show |
29 | a0002c0002t0001g0006 a0002c0002t0001g0007 a0002c0002t0001g0009 others(26): Show |
33 | HG00140.hp2 HG00741.hp1 HG01099.hp2 others(30): Show |
intron_variant | MODIFIER | c.1803+1153_1803+115 others(46): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039320 | ||||||
| chr4:49039320 | T | TATATATA others(37): Show |
9 | a0002c0002t0001g0061 a0002c0002t0001g0062 a0002c0002t0001g0067 others(6): Show |
10 | HG01069.hp1 HG01071.hp2 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.1803+1153_1803+115 others(48): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039320 | ||||||
| chr4:49039320 | T | TATATATA others(39): Show |
2 | a0002c0002t0001g0060 a0002c0002t0001g0105 |
2 | HG01192.hp2 NA18940.hp1 |
intron_variant | MODIFIER | c.1803+1153_1803+115 others(50): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039320 | ||||||
| chr4:49039320 | T | TATATATA others(108): Show |
1 | a0001c0001t0001g0271 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1803+1153_1803+115 others(119): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039320 | ||||||
| chr4:49039320 | T | TATATATA others(158): Show |
1 | a0001c0001t0001g0273 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1803+1153_1803+115 others(169): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039320 | ||||||
| chr4:49039322 | T | A | 1 | a0001c0001t0001g0272 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1803+1142T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49039322 | |||||||
| chr4:49039322 | T | TATATATA others(21): Show |
1 | a0004c0004t0001g0155 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1803+1151_1803+115 others(32): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039322 | ||||||
| chr4:49039322 | T | TATATATA others(59): Show |
1 | a0003c0003t0001g0141 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1803+1153_1803+115 others(70): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039322 | ||||||
| chr4:49039322 | T | TATATATA others(43): Show |
1 | a0004c0004t0001g0150 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1803+1153_1803+115 others(54): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039322 | ||||||
| chr4:49039322 | T | TATATATA others(45): Show |
2 | a0001c0001t0001g0208 a0004c0004t0001g0151 |
2 | HG03195.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.1803+1153_1803+115 others(56): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039322 | ||||||
| chr4:49039322 | T | TATATATA others(47): Show |
1 | a0004c0004t0001g0152 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1803+1153_1803+115 others(58): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039322 | ||||||
| chr4:49039322 | T | TATATATA others(49): Show |
3 | a0004c0004t0001g0011 a0004c0004t0001g0012 a0004c0004t0001g0154 |
5 | HG00738.hp2 HG01069.hp2 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.1803+1153_1803+115 others(60): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039322 | ||||||
| chr4:49039322 | T | TATATATA others(41): Show |
1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1803+1153_1803+115 others(52): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039322 | ||||||
| chr4:49039332 | T | TATATATA others(17): Show |
1 | a0003c0003t0001g0001 | 3 | HG01070.hp1 HG01071.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.1803+1153_1803+115 others(28): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039332 | ||||||
| chr4:49039332 | T | TATATATA others(19): Show |
1 | a0003c0003t0001g0024 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1803+1153_1803+115 others(30): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039332 | ||||||
| chr4:49039332 | T | TATATATA others(19): Show |
1 | a0001c0001t0001g0252 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1803+1153_1803+115 others(30): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039332 | ||||||
| chr4:49039332 | T | TATATATA others(21): Show |
1 | a0001c0001t0001g0253 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1803+1153_1803+115 others(32): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039332 | ||||||
| chr4:49039332 | T | TATATATA others(23): Show |
1 | a0003c0003t0001g0058 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1803+1153_1803+115 others(34): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039332 | ||||||
| chr4:49039333 | A | ATATATAT others(16): Show |
1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1803+1153_1803+115 others(27): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49039333 | |||||||
| chr4:49039334 | C | A | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1803+1154C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49039334 | |||||||
| chr4:49039334 | C | T | 3 | a0003c0003t0001g0001 a0003c0003t0001g0024 a0003c0003t0001g0058 |
5 | HG01070.hp1 HG01071.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.1803+1154C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49039334 | |||||||
| chr4:49039337 | A | ATATATAT others(93): Show |
1 | a0001c0001t0001g0272 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1803+1158_1803+115 others(104): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039337 | ||||||
| chr4:49039339 | G | A | 2 | a0001c0001t0001g0272 a0003c0003t0001g0116 |
2 | HG00639.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1803+1159G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49039339 | |||||||
| chr4:49039352 | G | GAT | 8 | a0001c0001t0001g0021 a0001c0001t0001g0271 a0001c0001t0001g0272 others(5): Show |
8 | HG00639.hp1 HG01884.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1803+1182_1803+118 others(6): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039352 | ||||||
| chr4:49039369 | G | A | 1 | a0003c0003t0001g0141 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1803+1189G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49039369 | |||||||
| chr4:49039382 | G | GAT | 125 | a0001c0001t0001g0021 a0001c0001t0001g0271 a0001c0001t0001g0272 others(122): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.1803+1212_1803+121 others(6): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039382 | ||||||
| chr4:49039431 | T | TTA | 7 | a0001c0001t0001g0233 a0001c0001t0001g0246 a0001c0001t0001g0266 others(4): Show |
7 | HG02132.hp1 HG02258.hp2 HG03540.hp2 others(4): Show |
intron_variant | MODIFIER | c.1803+1268_1803+126 others(6): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039431 | ||||||
| chr4:49039431 | T | TTATA | 4 | a0001c0001t0001g0021 a0001c0001t0001g0168 a0007c0008t0001g0146 others(1): Show |
4 | HG01884.hp1 HG02615.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1803+1266_1803+126 others(8): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr4 | 49039431 | ||||||
| chr4:49039448 | T | C | 6 | a0002c0002t0001g0084 a0002c0002t0001g0088 a0002c0002t0001g0089 others(3): Show |
6 | HG01070.hp2 HG01433.hp1 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.1803+1268T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49039448 | |||||||
| chr4:49039735 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1803+1555G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49039735 | |||||||
| chr4:49039742 | T | A | 1 | a0003c0003t0001g0058 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1803+1562T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49039742 | |||||||
| chr4:49039743 | T | A | 143 | a0001c0001t0004g0270 a0002c0002t0001g0006 a0002c0002t0001g0007 others(140): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1803+1563T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49039743 | |||||||
| chr4:49039792 | T | C | 4 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(1): Show |
4 | HG02145.hp2 HG02486.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1803+1612T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49039792 | |||||||
| chr4:49040304 | T | C | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1803+2124T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49040304 | |||||||
| chr4:49040393 | C | T | 5 | a0002c0002t0001g0009 a0002c0002t0001g0086 a0002c0002t0001g0102 others(2): Show |
6 | HG00099.hp2 HG00140.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.1803+2213C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49040393 | |||||||
| chr4:49040913 | T | C | 1 | a0001c0001t0001g0272 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1803+2733T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49040913 | |||||||
| chr4:49040985 | A | C | 1 | a0001c0001t0001g0169 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1803+2805A>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49040985 | |||||||
| chr4:49041055 | A | G | 152 | a0001c0001t0001g0021 a0001c0001t0001g0040 a0001c0001t0001g0200 others(149): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1803+2875A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49041055 | |||||||
| chr4:49041088 | C | G | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1803+2908C>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49041088 | |||||||
| chr4:49041183 | T | G | 1 | a0002c0002t0001g0100 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1803+3003T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49041183 | |||||||
| chr4:49041317 | G | C | 3 | a0001c0001t0001g0160 a0001c0001t0001g0166 a0001c0001t0001g0167 |
3 | HG02258.hp1 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1803+3137G>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49041317 | |||||||
| chr4:49041330 | T | G | 1 | a0003c0003t0001g0001 | 3 | HG01070.hp1 HG01071.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.1803+3150T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49041330 | |||||||
| chr4:49041650 | T | C | 1 | a0002c0002t0001g0025 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1804-3136T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49041650 | |||||||
| chr4:49041729 | A | C | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1804-3057A>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49041729 | |||||||
| chr4:49041770 | T | C | 1 | a0002c0002t0001g0104 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1804-3016T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49041770 | |||||||
| chr4:49041823 | G | A | 1 | a0002c0002t0001g0051 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1804-2963G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49041823 | |||||||
| chr4:49041908 | T | C | 151 | a0001c0001t0001g0021 a0001c0001t0001g0224 a0001c0001t0001g0271 others(148): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.1804-2878T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49041908 | |||||||
| chr4:49042262 | C | T | 1 | a0003c0003t0001g0118 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1804-2524C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49042262 | |||||||
| chr4:49042306 | C | G | 1 | a0001c0001t0001g0149 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1804-2480C>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49042306 | |||||||
| chr4:49042311 | A | G | 144 | a0001c0001t0001g0040 a0002c0002t0001g0006 a0002c0002t0001g0007 others(141): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.1804-2475A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49042311 | |||||||
| chr4:49042335 | C | A | 1 | a0001c0001t0001g0171 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1804-2451C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49042335 | |||||||
| chr4:49042481 | T | C | 151 | a0001c0001t0001g0021 a0001c0001t0001g0040 a0001c0001t0001g0271 others(148): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.1804-2305T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49042481 | |||||||
| chr4:49042548 | T | C | 6 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0252 others(3): Show |
6 | HG01243.hp1 HG02622.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1804-2238T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49042548 | |||||||
| chr4:49042912 | T | C | 1 | a0002c0002t0001g0050 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1804-1874T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49042912 | |||||||
| chr4:49043007 | C | T | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1804-1779C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49043007 | |||||||
| chr4:49043151 | G | A | 143 | a0002c0002t0001g0006 a0002c0002t0001g0007 a0002c0002t0001g0008 others(140): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1804-1635G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49043151 | |||||||
| chr4:49043219 | C | A | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1804-1567C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49043219 | |||||||
| chr4:49043286 | G | A | 2 | a0002c0002t0001g0056 a0002c0002t0001g0057 |
2 | NA19010.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.1804-1500G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49043286 | |||||||
| chr4:49043356 | G | A | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1804-1430G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49043356 | |||||||
| chr4:49043585 | T | C | 1 | a0001c0001t0001g0268 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1804-1201T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49043585 | |||||||
| chr4:49043764 | C | A | 1 | a0001c0001t0001g0249 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1804-1022C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49043764 | |||||||
| chr4:49043879 | G | T | 1 | a0002c0002t0001g0049 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1804-907G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49043879 | |||||||
| chr4:49044089 | C | A | 1 | a0001c0001t0001g0171 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1804-697C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49044089 | |||||||
| chr4:49044135 | T | C | 1 | a0002c0002t0001g0106 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1804-651T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49044135 | |||||||
| chr4:49044542 | C | T | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1804-244C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49044542 | |||||||
| chr4:49044553 | C | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0200 a0001c0001t0001g0234 others(1): Show |
5 | NA18941.hp2 NA18957.hp1 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.1804-233C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49044553 | |||||||
| chr4:49044592 | G | T | 2 | a0007c0008t0001g0146 a0007c0008t0001g0147 |
2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1804-194G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49044592 | |||||||
| chr4:49044658 | T | C | 1 | a0002c0002t0001g0094 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1804-128T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49044658 | |||||||
| chr4:49044739 | G | A | 1 | a0001c0001t0001g0257 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1804-47G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 13/15 | chr4 | 49044739 | |||||||
| chr4:49044906 | G | C | 2 | a0003c0003t0001g0027 a0003c0003t0001g0028 |
2 | HG02735.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1865+59G>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49044906 | |||||||
| chr4:49044923 | A | G | 1 | a0002c0002t0001g0089 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1865+76A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49044923 | |||||||
| chr4:49045102 | G | A | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1865+255G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49045102 | |||||||
| chr4:49045354 | C | T | 150 | a0001c0001t0001g0021 a0001c0001t0001g0271 a0001c0001t0001g0272 others(147): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.1865+507C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49045354 | |||||||
| chr4:49045678 | A | C | 1 | a0003c0003t0001g0031 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1865+831A>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49045678 | |||||||
| chr4:49045990 | C | T | 3 | a0001c0001t0001g0160 a0001c0001t0001g0166 a0001c0001t0001g0167 |
3 | HG02258.hp1 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1865+1143C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49045990 | |||||||
| chr4:49046031 | T | C | 2 | a0007c0008t0001g0146 a0007c0008t0001g0147 |
2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1865+1184T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49046031 | |||||||
| chr4:49046033 | G | C | 1 | a0001c0001t0001g0168 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1865+1186G>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49046033 | |||||||
| chr4:49046129 | C | T | 3 | a0002c0002t0001g0078 a0003c0003t0001g0121 a0003c0003t0001g0127 |
3 | HG00741.hp1 HG01074.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.1865+1282C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49046129 | |||||||
| chr4:49046144 | A | T | 4 | a0001c0001t0001g0130 a0001c0001t0001g0165 a0001c0001t0001g0169 others(1): Show |
4 | HG03041.hp1 HG03139.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1865+1297A>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49046144 | |||||||
| chr4:49046308 | CCATT | C | 146 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 others(143): Show |
157 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.1865+1490_1865+149 others(8): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr4 | 49046308 | ||||||
| chr4:49046314 | A | G | 1 | a0001c0001t0001g0206 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1865+1467A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49046314 | |||||||
| chr4:49046510 | T | C | 1 | a0002c0002t0001g0139 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1865+1663T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49046510 | |||||||
| chr4:49046580 | T | C | 1 | a0001c0001t0001g0237 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1865+1733T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49046580 | |||||||
| chr4:49046688 | G | A | 6 | a0003c0003t0001g0014 a0003c0003t0001g0183 a0003c0003t0001g0184 others(3): Show |
7 | HG02056.hp2 HG02155.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.1865+1841G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49046688 | |||||||
| chr4:49046756 | A | G | 1 | a0001c0001t0001g0224 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1865+1909A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49046756 | |||||||
| chr4:49046993 | T | A | 170 | a0001c0001t0001g0021 a0001c0001t0001g0130 a0001c0001t0001g0160 others(167): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.1865+2146T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49046993 | |||||||
| chr4:49047005 | G | A | 1 | a0006c0006t0001g0134 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1865+2158G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49047005 | |||||||
| chr4:49047084 | G | A | 143 | a0002c0002t0001g0006 a0002c0002t0001g0007 a0002c0002t0001g0008 others(140): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1865+2237G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49047084 | |||||||
| chr4:49047152 | T | G | 1 | a0003c0003t0001g0028 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1865+2305T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49047152 | |||||||
| chr4:49047189 | C | T | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1865+2342C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49047189 | |||||||
| chr4:49047285 | A | G | 143 | a0002c0002t0001g0006 a0002c0002t0001g0007 a0002c0002t0001g0008 others(140): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1865+2438A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49047285 | |||||||
| chr4:49047481 | G | T | 3 | a0001c0001t0001g0165 a0001c0001t0001g0169 a0001c0001t0001g0170 |
3 | HG03041.hp1 HG03139.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1865+2634G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49047481 | |||||||
| chr4:49047507 | G | A | 1 | a0003c0003t0001g0188 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1865+2660G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49047507 | |||||||
| chr4:49047617 | C | T | 1 | a0002c0002t0001g0054 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1865+2770C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49047617 | |||||||
| chr4:49047793 | T | C | 1 | a0008c0009t0001g0033 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1866-2901T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49047793 | |||||||
| chr4:49048122 | A | G | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | NA19062.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1866-2572A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49048122 | |||||||
| chr4:49048143 | AG | A | 4 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 others(1): Show |
4 | HG02258.hp2 HG03540.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.1866-2549delG | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr4 | 49048143 | ||||||
| chr4:49048182 | G | A | 3 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 |
3 | HG03540.hp2 HG03669.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1866-2512G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49048182 | |||||||
| chr4:49048405 | T | C | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1866-2289T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49048405 | |||||||
| chr4:49048425 | ATATT | A | 7 | a0001c0001t0001g0021 a0001c0001t0001g0271 a0001c0001t0001g0272 others(4): Show |
7 | HG01884.hp1 HG02258.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1866-2261_1866-225 others(8): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr4 | 49048425 | ||||||
| chr4:49048665 | G | T | 5 | a0002c0002t0001g0087 a0002c0002t0001g0092 a0002c0002t0001g0094 others(2): Show |
5 | HG01358.hp1 HG01496.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.1866-2029G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49048665 | |||||||
| chr4:49048957 | A | G | 1 | a0001c0001t0001g0225 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1866-1737A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49048957 | |||||||
| chr4:49048988 | T | C | 1 | a0003c0003t0001g0190 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1866-1706T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49048988 | |||||||
| chr4:49049108 | G | T | 143 | a0002c0002t0001g0006 a0002c0002t0001g0007 a0002c0002t0001g0008 others(140): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.1866-1586G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49049108 | |||||||
| chr4:49049120 | C | G | 1 | a0003c0003t0001g0046 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1866-1574C>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49049120 | |||||||
| chr4:49049137 | C | A | 2 | a0001c0001t0001g0165 a0001c0001t0001g0170 |
2 | HG03041.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1866-1557C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49049137 | |||||||
| chr4:49049165 | C | T | 7 | a0001c0001t0001g0021 a0001c0001t0001g0271 a0001c0001t0001g0272 others(4): Show |
7 | HG01884.hp1 HG02258.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1866-1529C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49049165 | |||||||
| chr4:49049203 | T | C | 1 | a0002c0002t0001g0080 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1866-1491T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49049203 | |||||||
| chr4:49049413 | T | A | 1 | a0002c0002t0001g0052 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1866-1281T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49049413 | |||||||
| chr4:49049520 | T | A | 1 | a0001c0001t0001g0198 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1866-1174T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49049520 | |||||||
| chr4:49049531 | A | G | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1866-1163A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49049531 | |||||||
| chr4:49049534 | G | A | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1866-1160G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49049534 | |||||||
| chr4:49049748 | C | T | 144 | a0001c0001t0001g0272 a0002c0002t0001g0006 a0002c0002t0001g0007 others(141): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.1866-946C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49049748 | |||||||
| chr4:49049910 | T | C | 1 | a0001c0001t0001g0224 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1866-784T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49049910 | |||||||
| chr4:49049920 | T | A | 1 | a0001c0001t0001g0268 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1866-774T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49049920 | |||||||
| chr4:49049955 | A | T | 1 | a0002c0002t0001g0074 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1866-739A>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49049955 | |||||||
| chr4:49050147 | C | T | 2 | a0002c0002t0001g0143 a0003c0003t0001g0031 |
2 | HG00323.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.1866-547C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49050147 | |||||||
| chr4:49050523 | G | A | 1 | a0003c0003t0001g0085 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1866-171G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49050523 | |||||||
| chr4:49050523 | G | T | 1 | a0003c0003t0001g0035 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1866-171G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49050523 | |||||||
| chr4:49050637 | C | T | 2 | a0001c0001t0001g0267 a0001c0007t0001g0015 |
3 | HG03831.hp2 HG04115.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1866-57C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 14/15 | chr4 | 49050637 | |||||||
| chr4:49050947 | C | T | 4 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(1): Show |
4 | HG02145.hp2 HG02486.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2021+98C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49050947 | |||||||
| chr4:49051195 | C | G | 1 | a0002c0002t0001g0055 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2021+346C>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49051195 | |||||||
| chr4:49051370 | C | T | 2 | a0007c0008t0001g0146 a0007c0008t0001g0147 |
2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2021+521C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49051370 | |||||||
| chr4:49051505 | G | A | 143 | a0002c0002t0001g0006 a0002c0002t0001g0007 a0002c0002t0001g0008 others(140): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.2021+656G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49051505 | |||||||
| chr4:49051782 | G | A | 1 | a0004c0004t0001g0150 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2021+933G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49051782 | |||||||
| chr4:49051796 | C | T | 1 | a0003c0003t0001g0085 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2021+947C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49051796 | |||||||
| chr4:49051840 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2021+991G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49051840 | |||||||
| chr4:49052050 | A | G | 1 | a0001c0001t0001g0202 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2021+1201A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49052050 | |||||||
| chr4:49052069 | G | T | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2021+1220G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49052069 | |||||||
| chr4:49052535 | A | G | 3 | a0002c0002t0001g0064 a0002c0002t0001g0075 a0002c0002t0001g0079 |
3 | HG00408.hp2 HG00609.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.2021+1686A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49052535 | |||||||
| chr4:49052590 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2021+1741G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49052590 | |||||||
| chr4:49052663 | T | G | 88 | a0002c0002t0001g0006 a0002c0002t0001g0007 a0002c0002t0001g0009 others(85): Show |
93 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.2021+1814T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49052663 | |||||||
| chr4:49052747 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2021+1898C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49052747 | |||||||
| chr4:49053377 | A | C | 1 | a0001c0001t0001g0171 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2021+2528A>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49053377 | |||||||
| chr4:49053458 | G | A | 4 | a0002c0002t0001g0099 a0002c0002t0001g0100 a0002c0002t0001g0108 others(1): Show |
4 | HG03139.hp1 HG03195.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2021+2609G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49053458 | |||||||
| chr4:49054315 | G | C | 1 | a0001c0001t0001g0229 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2021+3466G>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49054315 | |||||||
| chr4:49054467 | T | C | 4 | a0002c0002t0001g0047 a0002c0002t0001g0050 a0002c0002t0001g0053 others(1): Show |
4 | NA18941.hp1 NA18999.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.2021+3618T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49054467 | |||||||
| chr4:49054709 | C | T | 1 | a0003c0003t0001g0119 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2021+3860C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49054709 | |||||||
| chr4:49054814 | C | T | 1 | a0003c0003t0001g0187 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2021+3965C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49054814 | |||||||
| chr4:49054864 | A | C | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2021+4015A>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49054864 | |||||||
| chr4:49054918 | G | GAT | 6 | a0001c0001t0001g0021 a0001c0001t0001g0161 a0001c0001t0001g0271 others(3): Show |
6 | HG02145.hp2 HG02615.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.2021+4085_2021+408 others(6): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr4 | 49054918 | ||||||
| chr4:49054994 | T | G | 1 | a0003c0003t0002g0156 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2021+4145T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49054994 | |||||||
| chr4:49055284 | C | G | 1 | a0001c0001t0001g0182 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2021+4435C>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49055284 | |||||||
| chr4:49055385 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2021+4536G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49055385 | |||||||
| chr4:49055407 | A | T | 151 | a0001c0001t0001g0021 a0001c0001t0001g0171 a0001c0001t0001g0271 others(148): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.2021+4558A>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49055407 | |||||||
| chr4:49055479 | T | A | 3 | a0001c0001t0001g0171 a0007c0008t0001g0146 a0007c0008t0001g0147 |
3 | HG01884.hp1 HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2021+4630T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49055479 | |||||||
| chr4:49055591 | AT | A | 145 | a0001c0001t0001g0021 a0001c0001t0001g0130 a0001c0001t0001g0171 others(142): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(153): Show |
intron_variant | MODIFIER | c.2021+4757delT | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr4 | 49055591 | ||||||
| chr4:49055725 | G | T | 1 | a0001c0001t0001g0225 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2021+4876G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49055725 | |||||||
| chr4:49055728 | T | A | 1 | a0001c0001t0001g0272 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2021+4879T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49055728 | |||||||
| chr4:49055876 | C | T | 3 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 |
3 | HG03540.hp2 HG03669.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2021+5027C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49055876 | |||||||
| chr4:49055882 | C | T | 2 | a0002c0002t0001g0062 a0002c0002t0001g0067 |
2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2021+5033C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49055882 | |||||||
| chr4:49055895 | T | C | 151 | a0001c0001t0001g0021 a0001c0001t0001g0171 a0001c0001t0001g0271 others(148): Show |
162 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.2021+5046T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49055895 | |||||||
| chr4:49055913 | CT | C | 129 | a0001c0001t0001g0165 a0001c0001t0001g0170 a0001c0001t0001g0206 others(126): Show |
137 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.2021+5078delT | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr4 | 49055913 | ||||||
| chr4:49055913 | CTT | C | 16 | a0002c0002t0001g0006 a0002c0002t0001g0007 a0002c0002t0001g0059 others(13): Show |
18 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(15): Show |
intron_variant | MODIFIER | c.2021+5077_2021+507 others(6): Show |
CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr4 | 49055913 | ||||||
| chr4:49055914 | T | C | 1 | a0003c0003t0001g0005 | 2 | HG01358.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.2021+5065T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49055914 | |||||||
| chr4:49055968 | G | C | 1 | a0003c0003t0001g0058 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2021+5119G>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49055968 | |||||||
| chr4:49056004 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2021+5155C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49056004 | |||||||
| chr4:49056018 | C | A | 270 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0017 others(267): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(287): Show |
intron_variant | MODIFIER | c.2021+5169C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49056018 | |||||||
| chr4:49056069 | C | T | 16 | a0002c0002t0001g0006 a0002c0002t0001g0007 a0002c0002t0001g0055 others(13): Show |
18 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(15): Show |
intron_variant | MODIFIER | c.2021+5220C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49056069 | |||||||
| chr4:49056177 | G | A | 2 | a0001c0001t0001g0161 a0001c0001t0001g0162 |
2 | HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.2021+5328G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49056177 | |||||||
| chr4:49056184 | C | T | 4 | a0001c0001t0001g0224 a0001c0001t0001g0271 a0001c0001t0001g0272 others(1): Show |
4 | HG00438.hp2 HG03540.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.2021+5335C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49056184 | |||||||
| chr4:49056230 | A | G | 1 | a0003c0003t0001g0005 | 2 | HG01358.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.2021+5381A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49056230 | |||||||
| chr4:49056278 | A | G | 143 | a0002c0002t0001g0006 a0002c0002t0001g0007 a0002c0002t0001g0008 others(140): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.2021+5429A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49056278 | |||||||
| chr4:49056331 | C | A | 2 | a0007c0008t0001g0146 a0007c0008t0001g0147 |
2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2022-5481C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49056331 | |||||||
| chr4:49056463 | G | T | 1 | a0001c0001t0003g0220 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2022-5349G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49056463 | |||||||
| chr4:49056467 | A | C | 2 | a0001c0001t0001g0269 a0006c0006t0001g0144 |
2 | HG00735.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2022-5345A>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49056467 | |||||||
| chr4:49056471 | T | C | 1 | a0003c0003t0001g0120 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2022-5341T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49056471 | |||||||
| chr4:49056535 | T | A | 1 | a0004c0004t0001g0011 | 2 | HG01069.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.2022-5277T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49056535 | |||||||
| chr4:49056682 | A | G | 144 | a0001c0001t0001g0021 a0002c0002t0001g0006 a0002c0002t0001g0007 others(141): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.2022-5130A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49056682 | |||||||
| chr4:49056877 | A | C | 1 | a0002c0002t0001g0142 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2022-4935A>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49056877 | |||||||
| chr4:49056879 | A | G | 1 | a0003c0003t0001g0038 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2022-4933A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49056879 | |||||||
| chr4:49056985 | T | C | 3 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 |
3 | HG03540.hp2 HG03669.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2022-4827T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49056985 | |||||||
| chr4:49056997 | G | T | 4 | a0002c0002t0001g0088 a0002c0002t0001g0089 a0002c0002t0001g0090 others(1): Show |
4 | HG01070.hp2 HG01433.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.2022-4815G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49056997 | |||||||
| chr4:49057069 | A | T | 1 | a0003c0003t0001g0039 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2022-4743A>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49057069 | |||||||
| chr4:49057298 | C | T | 5 | a0002c0002t0001g0087 a0002c0002t0001g0092 a0002c0002t0001g0094 others(2): Show |
5 | HG01358.hp1 HG01496.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.2022-4514C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49057298 | |||||||
| chr4:49057337 | C | T | 3 | a0002c0002t0001g0078 a0003c0003t0001g0121 a0003c0003t0001g0127 |
3 | HG00741.hp1 HG01074.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.2022-4475C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49057337 | |||||||
| chr4:49057367 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2022-4445G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49057367 | |||||||
| chr4:49057480 | C | G | 1 | a0001c0001t0001g0171 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2022-4332C>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49057480 | |||||||
| chr4:49057590 | C | T | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2022-4222C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49057590 | |||||||
| chr4:49057677 | T | G | 9 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 others(6): Show |
9 | HG02132.hp1 HG02523.hp2 NA18940.hp2 others(6): Show |
intron_variant | MODIFIER | c.2022-4135T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49057677 | |||||||
| chr4:49058027 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2022-3785C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49058027 | |||||||
| chr4:49058082 | A | G | 1 | a0002c0002t0001g0083 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2022-3730A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49058082 | |||||||
| chr4:49058136 | A | G | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2022-3676A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49058136 | |||||||
| chr4:49058259 | A | G | 3 | a0001c0001t0001g0171 a0007c0008t0001g0146 a0007c0008t0001g0147 |
3 | HG01884.hp1 HG02559.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2022-3553A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49058259 | |||||||
| chr4:49058298 | A | G | 1 | a0001c0001t0001g0206 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2022-3514A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49058298 | |||||||
| chr4:49058674 | T | G | 4 | a0001c0001t0001g0198 a0001c0001t0001g0200 a0001c0001t0001g0234 others(1): Show |
4 | HG00609.hp2 NA18941.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.2022-3138T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49058674 | |||||||
| chr4:49058679 | T | C | 1 | a0003c0003t0001g0124 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2022-3133T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49058679 | |||||||
| chr4:49058884 | T | C | 1 | a0003c0003t0001g0125 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2022-2928T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49058884 | |||||||
| chr4:49059041 | T | A | 1 | a0009c0010t0001g0145 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2022-2771T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49059041 | |||||||
| chr4:49059068 | T | C | 1 | a0003c0003t0001g0085 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2022-2744T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49059068 | |||||||
| chr4:49059124 | T | C | 100 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0017 others(97): Show |
107 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.2022-2688T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49059124 | |||||||
| chr4:49059587 | G | A | 120 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0017 others(117): Show |
129 | HG00140.hp1 HG00423.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.2022-2225G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49059587 | |||||||
| chr4:49059831 | C | T | 54 | a0002c0002t0001g0008 a0002c0002t0001g0064 a0002c0002t0001g0075 others(51): Show |
60 | HG00280.hp2 HG00323.hp2 HG00408.hp2 others(57): Show |
intron_variant | MODIFIER | c.2022-1981C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49059831 | |||||||
| chr4:49059855 | G | T | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2022-1957G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49059855 | |||||||
| chr4:49059870 | C | T | 2 | a0002c0002t0001g0093 a0002c0002t0001g0097 |
2 | HG00738.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.2022-1942C>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49059870 | |||||||
| chr4:49059889 | C | A | 3 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 |
3 | HG03540.hp2 HG03669.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2022-1923C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49059889 | |||||||
| chr4:49060134 | A | G | 1 | a0001c0001t0004g0270 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2022-1678A>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49060134 | |||||||
| chr4:49060135 | T | A | 1 | a0001c0001t0001g0021 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2022-1677T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49060135 | |||||||
| chr4:49060351 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2022-1461G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49060351 | |||||||
| chr4:49060359 | C | A | 1 | a0003c0003t0001g0183 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.2022-1453C>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49060359 | |||||||
| chr4:49060792 | A | C | 1 | a0001c0001t0001g0162 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2022-1020A>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49060792 | |||||||
| chr4:49060794 | T | G | 1 | a0001c0001t0001g0169 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2022-1018T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49060794 | |||||||
| chr4:49060875 | G | A | 2 | a0003c0003t0001g0188 a0003c0003t0001g0189 |
2 | HG00099.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.2022-937G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49060875 | |||||||
| chr4:49060878 | T | A | 2 | a0007c0008t0001g0146 a0007c0008t0001g0147 |
2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2022-934T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49060878 | |||||||
| chr4:49060911 | T | C | 1 | a0003c0003t0001g0124 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2022-901T>C | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49060911 | |||||||
| chr4:49061107 | G | A | 2 | a0007c0008t0001g0146 a0007c0008t0001g0147 |
2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2022-705G>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49061107 | |||||||
| chr4:49061143 | T | G | 1 | a0001c0001t0003g0220 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2022-669T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49061143 | |||||||
| chr4:49061462 | C | G | 82 | a0002c0002t0001g0006 a0002c0002t0001g0007 a0002c0002t0001g0009 others(79): Show |
87 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(84): Show |
intron_variant | MODIFIER | c.2022-350C>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49061462 | |||||||
| chr4:49061479 | T | A | 2 | a0007c0008t0001g0146 a0007c0008t0001g0147 |
2 | HG01884.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2022-333T>A | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49061479 | |||||||
| chr4:49061617 | G | T | 1 | a0001c0001t0001g0130 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2022-195G>T | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49061617 | |||||||
| chr4:49061721 | T | G | 2 | a0002c0002t0001g0098 a0003c0003t0001g0191 |
2 | NA18971.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.2022-91T>G | CWH43 | ENSG00000109182.12 | transcript | ENST00000226432.9 | protein_coding | 15/15 | chr4 | 49061721 |