Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 90288 |
| ensemblid | ENSG00000172771.13 |
| hgncid | 28061 |
| symbol | EFCAB12 |
| name | EF-hand calcium binding domain 12 |
| refseq_nuc | NM_207307.3 |
| refseq_prot | NP_997190.1 |
| ensembl_nuc | ENST00000505956.6 |
| ensembl_prot | ENSP00000420854.1 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 129401321 |
| end | 129428636 |
| strand | - |
| ver | v1.2 |
| region | chr3:129401321-129428636 |
| region5000 | chr3:129396321-129433636 |
| regionname0 | EFCAB12_chr3_129401321_129428636 |
| regionname5000 | EFCAB12_chr3_129396321_129433636 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 572 | 177 | 31 | 44 | 62 | 13 | 26 | 48 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | MDDDY others(567): Show |
chr3 | 129396321 | 129433636 |
| a0002 | 0/0 | 572 | 91 | 12 | 13 | 61 | 0 | 5 | 43 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | MDDDY others(567): Show |
chr3 | 129396321 | 129433636 |
| a0003 | 0/0 | 572 | 32 | 2 | 2 | 27 | 0 | 1 | 19 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | MDDDY others(567): Show |
chr3 | 129396321 | 129433636 |
| a0004 | 0/1 | 572 | 23 | 7 | 6 | 3 | 2 | 4 | 1 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | MDDDY others(567): Show |
chr3 | 129396321 | 129433636 |
| a0005 | 0/0 | 572 | 16 | 7 | 1 | 3 | 0 | 5 | 1 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | MDDDY others(567): Show |
chr3 | 129396321 | 129433636 |
| a0006 | 0/0 | 572 | 15 | 11 | 4 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | MDDDY others(567): Show |
chr3 | 129396321 | 129433636 |
| a0007 | 0/0 | 572 | 6 | 0 | 4 | 0 | 1 | 1 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | MDDDY others(567): Show |
chr3 | 129396321 | 129433636 |
| a0008 | 0/0 | 572 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | MDDDY others(567): Show |
chr3 | 129396321 | 129433636 |
| a0009 | 0/0 | 572 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | MDDDY others(567): Show |
chr3 | 129396321 | 129433636 |
| a0010 | 0/0 | 572 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | MDDDY others(567): Show |
chr3 | 129396321 | 129433636 |
| a0011 | 0/0 | 572 | 3 | 2 | 0 | 1 | 0 | 0 | 1 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | MDDDY others(567): Show |
chr3 | 129396321 | 129433636 |
| a0012 | 0/0 | 572 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | MDDDY others(567): Show |
chr3 | 129396321 | 129433636 |
| a0013 | 0/0 | 572 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | MDDDY others(567): Show |
chr3 | 129396321 | 129433636 |
| a0014 | 0/0 | 572 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | MDDDY others(567): Show |
chr3 | 129396321 | 129433636 |
| a0015 | 0/0 | 572 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | MDDDY others(567): Show |
chr3 | 129396321 | 129433636 |
| a0016 | 0/0 | 572 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | MDDDY others(567): Show |
chr3 | 129396321 | 129433636 |
| a0017 | 0/0 | 572 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | MDDDY others(567): Show |
chr3 | 129396321 | 129433636 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1716 | 165 | 25 | 40 | 61 | 12 | 26 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | ATGGA others(1711): Show |
chr3 | 129396321 | 129433636 | ||
| a0001c0007 | 0/0 | 1716 | 10 | 5 | 4 | 0 | 1 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | ATGGA others(1711): Show |
chr3 | 129396321 | 129433636 | ||
| a0001c0018 | 0/0 | 1716 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | ATGGA others(1711): Show |
chr3 | 129396321 | 129433636 | ||
| a0001c0020 | 0/0 | 1716 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | ATGGA others(1711): Show |
chr3 | 129396321 | 129433636 | ||
| a0002c0002 | 0/0 | 1716 | 90 | 12 | 12 | 61 | 0 | 5 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | ATGGA others(1711): Show |
chr3 | 129396321 | 129433636 | ||
| a0002c0016 | 0/0 | 1716 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | ATGGA others(1711): Show |
chr3 | 129396321 | 129433636 | ||
| a0003c0003 | 0/0 | 1716 | 32 | 2 | 2 | 27 | 0 | 1 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | ATGGA others(1711): Show |
chr3 | 129396321 | 129433636 | ||
| a0004c0004 | 0/1 | 1716 | 23 | 7 | 6 | 3 | 2 | 4 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | ATGGA others(1711): Show |
chr3 | 129396321 | 129433636 | ||
| a0005c0006 | 0/0 | 1716 | 14 | 7 | 1 | 2 | 0 | 4 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | ATGGA others(1711): Show |
chr3 | 129396321 | 129433636 | ||
| a0005c0015 | 0/0 | 1716 | 2 | 0 | 0 | 1 | 0 | 1 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | ATGGA others(1711): Show |
chr3 | 129396321 | 129433636 | ||
| a0006c0005 | 0/0 | 1716 | 15 | 11 | 4 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | ATGGA others(1711): Show |
chr3 | 129396321 | 129433636 | ||
| a0007c0008 | 0/0 | 1716 | 6 | 0 | 4 | 0 | 1 | 1 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | ATGGA others(1711): Show |
chr3 | 129396321 | 129433636 | ||
| a0008c0009 | 0/0 | 1716 | 6 | 6 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | ATGGA others(1711): Show |
chr3 | 129396321 | 129433636 | ||
| a0009c0010 | 0/0 | 1716 | 5 | 4 | 1 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | ATGGA others(1711): Show |
chr3 | 129396321 | 129433636 | ||
| a0010c0011 | 0/0 | 1716 | 4 | 4 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | ATGGA others(1711): Show |
chr3 | 129396321 | 129433636 | ||
| a0011c0014 | 0/0 | 1716 | 2 | 2 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | ATGGA others(1711): Show |
chr3 | 129396321 | 129433636 | ||
| a0011c0021 | 0/0 | 1716 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | ATGGA others(1711): Show |
chr3 | 129396321 | 129433636 | ||
| a0012c0012 | 0/0 | 1716 | 2 | 2 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | ATGGA others(1711): Show |
chr3 | 129396321 | 129433636 | ||
| a0013c0013 | 0/0 | 1716 | 2 | 2 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | ATGGA others(1711): Show |
chr3 | 129396321 | 129433636 | ||
| a0014c0023 | 0/0 | 1716 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | ATGGA others(1711): Show |
chr3 | 129396321 | 129433636 | ||
| a0015c0022 | 0/0 | 1716 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | ATGGA others(1711): Show |
chr3 | 129396321 | 129433636 | ||
| a0016c0019 | 0/0 | 1716 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | ATGGA others(1711): Show |
chr3 | 129396321 | 129433636 | ||
| a0017c0017 | 0/0 | 1716 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | ATGGA others(1711): Show |
chr3 | 129396321 | 129433636 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2139 | 119 | 18 | 21 | 55 | 10 | 14 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | AACAG others(2134): Show |
chr3 | 129396321 | 129433636 |
| a0001c0001t0002 | 0/0 | 2139 | 6 | 6 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | AACAG others(2134): Show |
chr3 | 129396321 | 129433636 |
| a0001c0001t0003 | 0/0 | 2139 | 39 | 1 | 19 | 6 | 2 | 11 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | AACAG others(2134): Show |
chr3 | 129396321 | 129433636 |
| a0001c0001t0005 | 0/0 | 2139 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | AACAG others(2134): Show |
chr3 | 129396321 | 129433636 |
| a0001c0007t0001 | 0/0 | 2139 | 10 | 5 | 4 | 0 | 1 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | AACAG others(2134): Show |
chr3 | 129396321 | 129433636 |
| a0001c0018t0001 | 0/0 | 2139 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | AACAG others(2134): Show |
chr3 | 129396321 | 129433636 |
| a0001c0020t0001 | 0/0 | 2139 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | AACAG others(2134): Show |
chr3 | 129396321 | 129433636 |
| a0002c0002t0001 | 0/0 | 2139 | 88 | 11 | 12 | 61 | 0 | 4 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | AACAG others(2134): Show |
chr3 | 129396321 | 129433636 |
| a0002c0002t0002 | 0/0 | 2139 | 2 | 1 | 0 | 0 | 0 | 1 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | AACAG others(2134): Show |
chr3 | 129396321 | 129433636 |
| a0002c0016t0001 | 0/0 | 2139 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | AACAG others(2134): Show |
chr3 | 129396321 | 129433636 |
| a0003c0003t0002 | 0/0 | 2139 | 32 | 2 | 2 | 27 | 0 | 1 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | AACAG others(2134): Show |
chr3 | 129396321 | 129433636 |
| a0004c0004t0001 | 0/1 | 2139 | 23 | 7 | 6 | 3 | 2 | 4 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | AACAG others(2134): Show |
chr3 | 129396321 | 129433636 |
| a0005c0006t0001 | 0/0 | 2139 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | AACAG others(2134): Show |
chr3 | 129396321 | 129433636 |
| a0005c0006t0002 | 0/0 | 2139 | 13 | 7 | 1 | 1 | 0 | 4 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | AACAG others(2134): Show |
chr3 | 129396321 | 129433636 |
| a0005c0015t0001 | 0/0 | 2139 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | AACAG others(2134): Show |
chr3 | 129396321 | 129433636 |
| a0005c0015t0002 | 0/0 | 2139 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | AACAG others(2134): Show |
chr3 | 129396321 | 129433636 |
| a0006c0005t0001 | 0/0 | 2139 | 15 | 11 | 4 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | AACAG others(2134): Show |
chr3 | 129396321 | 129433636 |
| a0007c0008t0001 | 0/0 | 2139 | 6 | 0 | 4 | 0 | 1 | 1 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | AACAG others(2134): Show |
chr3 | 129396321 | 129433636 |
| a0008c0009t0001 | 0/0 | 2139 | 6 | 6 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | AACAG others(2134): Show |
chr3 | 129396321 | 129433636 |
| a0009c0010t0001 | 0/0 | 2139 | 5 | 4 | 1 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | AACAG others(2134): Show |
chr3 | 129396321 | 129433636 |
| a0010c0011t0001 | 0/0 | 2139 | 4 | 4 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | AACAG others(2134): Show |
chr3 | 129396321 | 129433636 |
| a0011c0014t0001 | 0/0 | 2139 | 2 | 2 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | AACAG others(2134): Show |
chr3 | 129396321 | 129433636 |
| a0011c0021t0001 | 0/0 | 2139 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | AACAG others(2134): Show |
chr3 | 129396321 | 129433636 |
| a0012c0012t0001 | 0/0 | 2139 | 2 | 2 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | AACAG others(2134): Show |
chr3 | 129396321 | 129433636 |
| a0013c0013t0001 | 0/0 | 2139 | 2 | 2 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | AACAG others(2134): Show |
chr3 | 129396321 | 129433636 |
| a0014c0023t0004 | 0/0 | 2139 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | AACAG others(2134): Show |
chr3 | 129396321 | 129433636 |
| a0015c0022t0002 | 0/0 | 2139 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | AACAG others(2134): Show |
chr3 | 129396321 | 129433636 |
| a0016c0019t0001 | 0/0 | 2139 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | AACAG others(2134): Show |
chr3 | 129396321 | 129433636 |
| a0017c0017t0001 | 0/0 | 2139 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | AACAG others(2134): Show |
chr3 | 129396321 | 129433636 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/0 | 38 | 1 | 13 | 16 | 3 | 4 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0002g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0003g0004 | 0/0 | 14 | 0 | 3 | 3 | 2 | 6 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0003g0013 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0003g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0003g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0003g0044 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0001t0005g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0007t0001g0041 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0007t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0007t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0007t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0007t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0007t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0007t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0007t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0007t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0018t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0001c0020t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0001g0002 | 0/0 | 18 | 0 | 6 | 11 | 0 | 1 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0001g0006 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0002t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0002c0016t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0003c0003t0002g0003 | 0/0 | 15 | 1 | 2 | 11 | 0 | 1 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0003c0003t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0003c0003t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0003c0003t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0003c0003t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0003c0003t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0003c0003t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0003c0003t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0003c0003t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0003c0003t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0003c0003t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0003c0003t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0003c0003t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0003c0003t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0003c0003t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0003c0003t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0003c0003t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0004c0004t0001g0007 | 0/0 | 7 | 0 | 4 | 0 | 2 | 1 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0004c0004t0001g0022 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0004c0004t0001g0039 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0004c0004t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0004c0004t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0004c0004t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0004c0004t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0004c0004t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0004c0004t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0004c0004t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0004c0004t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0004c0004t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0004c0004t0001g0197 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0004c0004t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0005c0006t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0005c0006t0002g0021 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0005c0006t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0005c0006t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0005c0006t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0005c0006t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0005c0006t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0005c0006t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0005c0006t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0005c0006t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0005c0006t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0005c0006t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0005c0015t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0005c0015t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0006c0005t0001g0005 | 0/0 | 9 | 5 | 4 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0006c0005t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0006c0005t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0006c0005t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0006c0005t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0006c0005t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0006c0005t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0007c0008t0001g0008 | 0/0 | 6 | 0 | 4 | 0 | 1 | 1 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0008c0009t0001g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0008c0009t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0008c0009t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0009c0010t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0009c0010t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0009c0010t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0009c0010t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0010c0011t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0010c0011t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0010c0011t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0011c0014t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0011c0014t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0011c0021t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0012c0012t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0012c0012t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0013c0013t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0014c0023t0004g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0015c0022t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0016c0019t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| a0017c0017t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0007 | t0001 | g0041 | EUR | GBR | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0074 | EUR | GBR | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG00280 | hp1 | a0007 | c0008 | t0001 | g0008 | EUR | FIN | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0004 | EUR | FIN | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | FIN | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0004 | EUR | FIN | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG00408 | hp1 | a0004 | c0004 | t0001 | g0039 | EAS | CHS | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG00423 | hp1 | a0003 | c0003 | t0002 | g0003 | EAS | CHS | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG00544 | hp1 | a0002 | c0002 | t0001 | g0032 | EAS | CHS | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0195 | EAS | CHS | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0110 | EAS | CHS | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG00597 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | CHS | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | CHS | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG00621 | hp1 | a0003 | c0003 | t0002 | g0003 | EAS | CHS | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG00621 | hp2 | a0004 | c0004 | t0001 | g0185 | EAS | CHS | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0044 | AMR | PUR | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG00639 | hp2 | a0003 | c0003 | t0002 | g0003 | AMR | PUR | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG00642 | hp1 | a0004 | c0004 | t0001 | g0007 | AMR | PUR | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG00642 | hp2 | a0007 | c0008 | t0001 | g0008 | AMR | PUR | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG00673 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CHS | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG00735 | hp1 | a0001 | c0007 | t0001 | g0205 | AMR | PUR | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG00738 | hp1 | a0001 | c0007 | t0001 | g0200 | AMR | PUR | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG00738 | hp2 | a0006 | c0005 | t0001 | g0005 | AMR | PUR | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG00741 | hp2 | a0007 | c0008 | t0001 | g0008 | AMR | PUR | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01070 | hp1 | a0004 | c0004 | t0001 | g0007 | AMR | PUR | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0095 | AMR | PUR | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01071 | hp1 | a0004 | c0004 | t0001 | g0007 | AMR | PUR | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0094 | AMR | PUR | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0212 | AMR | PUR | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01099 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01099 | hp2 | a0007 | c0008 | t0001 | g0008 | AMR | PUR | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01109 | hp2 | a0009 | c0010 | t0001 | g0131 | AMR | PUR | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01167 | hp2 | a0006 | c0005 | t0001 | g0005 | AMR | PUR | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01168 | hp1 | a0004 | c0004 | t0001 | g0022 | AMR | PUR | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0042 | AMR | PUR | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0042 | AMR | PUR | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01169 | hp2 | a0006 | c0005 | t0001 | g0005 | AMR | PUR | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01175 | hp1 | a0001 | c0007 | t0001 | g0184 | AMR | PUR | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0220 | AMR | PUR | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01192 | hp1 | a0004 | c0004 | t0001 | g0007 | AMR | PUR | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01255 | hp1 | a0002 | c0016 | t0001 | g0098 | AMR | CLM | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01255 | hp2 | a0005 | c0006 | t0002 | g0021 | AMR | CLM | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01256 | hp2 | a0001 | c0001 | t0003 | g0213 | AMR | CLM | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0118 | AMR | CLM | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01346 | hp1 | a0006 | c0005 | t0001 | g0005 | AMR | CLM | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01358 | hp2 | a0001 | c0001 | t0003 | g0221 | AMR | CLM | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0122 | AMR | CLM | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01361 | hp2 | a0001 | c0007 | t0001 | g0201 | AMR | CLM | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01433 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01433 | hp2 | a0004 | c0004 | t0001 | g0022 | AMR | CLM | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01496 | hp1 | a0014 | c0023 | t0004 | g0209 | AMR | CLM | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0138 | EUR | IBS | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | IBS | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01516 | hp2 | a0004 | c0004 | t0001 | g0007 | EUR | IBS | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0029 | EUR | IBS | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01517 | hp2 | a0004 | c0004 | t0001 | g0007 | EUR | IBS | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01884 | hp1 | a0001 | c0007 | t0001 | g0199 | AFR | ACB | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0126 | AFR | ACB | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01891 | hp1 | a0010 | c0011 | t0001 | g0038 | AFR | ACB | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01891 | hp2 | a0004 | c0004 | t0001 | g0047 | AFR | ACB | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01928 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01934 | hp1 | a0001 | c0001 | t0003 | g0013 | AMR | PEL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0223 | AMR | PEL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0214 | AMR | PEL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0117 | AMR | PEL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0013 | AMR | PEL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0043 | AMR | PEL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01981 | hp1 | a0003 | c0003 | t0002 | g0003 | AMR | PEL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0224 | AMR | PEL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0013 | AMR | PEL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0040 | EAS | KHV | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02015 | hp2 | a0002 | c0002 | t0001 | g0096 | EAS | KHV | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | KHV | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02055 | hp2 | a0005 | c0006 | t0002 | g0178 | AFR | ACB | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0192 | EAS | KHV | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02071 | hp1 | a0003 | c0003 | t0002 | g0145 | EAS | KHV | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02071 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0210 | EAS | KHV | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0222 | EAS | KHV | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02083 | hp2 | a0005 | c0015 | t0001 | g0171 | EAS | KHV | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | KHV | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02129 | hp2 | a0003 | c0003 | t0002 | g0003 | EAS | KHV | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02132 | hp1 | a0003 | c0003 | t0002 | g0003 | EAS | KHV | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | KHV | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02135 | hp1 | a0003 | c0003 | t0002 | g0148 | EAS | KHV | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02135 | hp2 | a0005 | c0006 | t0002 | g0173 | EAS | KHV | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02145 | hp2 | a0001 | c0007 | t0001 | g0041 | AFR | ACB | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CDX | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0102 | EAS | CDX | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02257 | hp1 | a0012 | c0012 | t0001 | g0156 | AFR | ACB | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02257 | hp2 | a0001 | c0007 | t0001 | g0203 | AFR | ACB | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02258 | hp2 | a0001 | c0007 | t0001 | g0202 | AFR | ACB | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0013 | AMR | PEL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02280 | hp1 | a0008 | c0009 | t0001 | g0049 | AFR | ACB | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02280 | hp2 | a0011 | c0014 | t0001 | g0100 | AFR | ACB | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02300 | hp1 | a0007 | c0008 | t0001 | g0008 | AMR | PEL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02451 | hp1 | a0010 | c0011 | t0001 | g0038 | AFR | ACB | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02451 | hp2 | a0013 | c0013 | t0001 | g0033 | AFR | ACB | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02523 | hp1 | a0002 | c0002 | t0001 | g0104 | EAS | KHV | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02523 | hp2 | a0003 | c0003 | t0002 | g0078 | EAS | KHV | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02572 | hp2 | a0008 | c0009 | t0001 | g0009 | AFR | GWD | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0217 | SAS | PJL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02615 | hp1 | a0008 | c0009 | t0001 | g0009 | AFR | GWD | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02615 | hp2 | a0005 | c0006 | t0002 | g0021 | AFR | GWD | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02622 | hp1 | a0002 | c0002 | t0002 | g0046 | AFR | GWD | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02630 | hp1 | a0003 | c0003 | t0002 | g0153 | AFR | GWD | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02630 | hp2 | a0006 | c0005 | t0001 | g0127 | AFR | GWD | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | GWD | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02698 | hp2 | a0007 | c0008 | t0001 | g0008 | SAS | PJL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02717 | hp1 | a0006 | c0005 | t0001 | g0005 | AFR | GWD | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | GWD | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0154 | AFR | GWD | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0211 | SAS | PJL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02809 | hp1 | a0010 | c0011 | t0001 | g0181 | AFR | GWD | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0124 | AFR | GWD | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02818 | hp1 | a0006 | c0005 | t0001 | g0135 | AFR | GWD | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02818 | hp2 | a0008 | c0009 | t0001 | g0009 | AFR | GWD | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | GWD | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02886 | hp2 | a0004 | c0004 | t0001 | g0022 | AFR | GWD | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02895 | hp1 | a0001 | c0007 | t0001 | g0091 | AFR | GWD | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02895 | hp2 | a0006 | c0005 | t0001 | g0005 | AFR | GWD | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02896 | hp1 | a0006 | c0005 | t0001 | g0167 | AFR | GWD | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0024 | AFR | GWD | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0023 | AFR | ESN | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02922 | hp2 | a0012 | c0012 | t0001 | g0155 | AFR | ESN | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02965 | hp1 | a0002 | c0002 | t0001 | g0023 | AFR | ESN | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02965 | hp2 | a0004 | c0004 | t0001 | g0187 | AFR | ESN | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0161 | AFR | ESN | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02970 | hp2 | a0004 | c0004 | t0001 | g0039 | AFR | ESN | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02976 | hp1 | a0016 | c0019 | t0001 | g0129 | AFR | ESN | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0160 | AFR | ESN | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG03041 | hp2 | a0010 | c0011 | t0001 | g0182 | AFR | GWD | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG03098 | hp1 | a0013 | c0013 | t0001 | g0033 | AFR | MSL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | MSL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG03139 | hp2 | a0003 | c0003 | t0002 | g0003 | AFR | ESN | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG03195 | hp1 | a0006 | c0005 | t0001 | g0005 | AFR | ESN | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | ESN | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG03209 | hp1 | a0009 | c0010 | t0001 | g0034 | AFR | MSL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG03209 | hp2 | a0008 | c0009 | t0001 | g0050 | AFR | MSL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG03225 | hp1 | a0009 | c0010 | t0001 | g0132 | AFR | MSL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG03225 | hp2 | a0004 | c0004 | t0001 | g0186 | AFR | MSL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG03239 | hp1 | a0004 | c0004 | t0001 | g0007 | SAS | PJL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG03453 | hp1 | a0005 | c0006 | t0002 | g0168 | AFR | MSL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG03453 | hp2 | a0006 | c0005 | t0001 | g0005 | AFR | MSL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | MSL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0024 | AFR | MSL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG03490 | hp1 | a0002 | c0002 | t0001 | g0031 | SAS | PJL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG03491 | hp1 | a0005 | c0006 | t0002 | g0174 | SAS | PJL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG03491 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG03492 | hp1 | a0002 | c0002 | t0001 | g0031 | SAS | PJL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG03516 | hp1 | a0002 | c0002 | t0001 | g0048 | AFR | ESN | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0159 | AFR | ESN | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | MSL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | MSL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG03654 | hp1 | a0002 | c0002 | t0001 | g0006 | SAS | PJL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0044 | SAS | PJL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG03669 | hp1 | a0003 | c0003 | t0002 | g0003 | SAS | PJL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | STU | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG03688 | hp2 | a0004 | c0004 | t0001 | g0189 | SAS | STU | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG03710 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | BEB | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG03831 | hp2 | a0001 | c0001 | t0005 | g0225 | SAS | BEB | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG03834 | hp1 | a0005 | c0015 | t0002 | g0170 | SAS | BEB | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0219 | SAS | BEB | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG03927 | hp2 | a0004 | c0004 | t0001 | g0183 | SAS | BEB | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG03942 | hp1 | a0005 | c0006 | t0002 | g0177 | SAS | BEB | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | BEB | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | STU | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG04115 | hp2 | a0005 | c0006 | t0002 | g0166 | SAS | STU | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG04204 | hp1 | a0004 | c0004 | t0001 | g0190 | SAS | STU | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | STU | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG04228 | hp1 | a0002 | c0002 | t0002 | g0193 | SAS | STU | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | STU | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18522 | hp1 | a0005 | c0006 | t0002 | g0021 | AFR | YRI | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | YRI | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18612 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CHB | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18612 | hp2 | a0003 | c0003 | t0002 | g0003 | EAS | CHB | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | CHB | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0032 | EAS | CHB | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18906 | hp1 | a0006 | c0005 | t0001 | g0085 | AFR | YRI | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18906 | hp2 | a0004 | c0004 | t0001 | g0188 | AFR | YRI | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0120 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18944 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18947 | hp2 | a0011 | c0021 | t0001 | g0111 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0040 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0101 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18952 | hp2 | a0005 | c0006 | t0001 | g0179 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18957 | hp1 | a0003 | c0003 | t0002 | g0079 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18959 | hp1 | a0017 | c0017 | t0001 | g0099 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18962 | hp2 | a0003 | c0003 | t0002 | g0163 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0113 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18966 | hp2 | a0003 | c0003 | t0002 | g0146 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18968 | hp1 | a0002 | c0002 | t0001 | g0109 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18968 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18971 | hp2 | a0003 | c0003 | t0002 | g0003 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18973 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18975 | hp1 | a0003 | c0003 | t0002 | g0037 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0108 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18978 | hp2 | a0002 | c0002 | t0001 | g0114 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18979 | hp1 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0123 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18984 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18988 | hp2 | a0002 | c0002 | t0001 | g0121 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18989 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18989 | hp2 | a0003 | c0003 | t0002 | g0150 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18992 | hp2 | a0001 | c0018 | t0001 | g0137 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18993 | hp1 | a0002 | c0002 | t0001 | g0105 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18994 | hp1 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18997 | hp2 | a0003 | c0003 | t0002 | g0003 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18999 | hp1 | a0002 | c0002 | t0001 | g0196 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19000 | hp1 | a0003 | c0003 | t0002 | g0089 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19001 | hp1 | a0002 | c0002 | t0001 | g0128 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0116 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19005 | hp1 | a0003 | c0003 | t0002 | g0003 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19005 | hp2 | a0002 | c0002 | t0001 | g0097 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19007 | hp2 | a0003 | c0003 | t0002 | g0003 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19009 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19011 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19011 | hp2 | a0003 | c0003 | t0002 | g0164 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19030 | hp1 | a0009 | c0010 | t0001 | g0086 | AFR | LWK | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19030 | hp2 | a0011 | c0014 | t0001 | g0081 | AFR | LWK | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19043 | hp1 | a0005 | c0006 | t0002 | g0176 | AFR | LWK | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19043 | hp2 | a0004 | c0004 | t0001 | g0045 | AFR | LWK | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19054 | hp2 | a0002 | c0002 | t0001 | g0084 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19055 | hp1 | a0003 | c0003 | t0002 | g0144 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19056 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19056 | hp2 | a0003 | c0003 | t0002 | g0147 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19058 | hp1 | a0003 | c0003 | t0002 | g0130 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19058 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19060 | hp1 | a0004 | c0004 | t0001 | g0198 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19060 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19063 | hp2 | a0002 | c0002 | t0001 | g0107 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19065 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19066 | hp1 | a0002 | c0002 | t0001 | g0194 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19067 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0106 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19074 | hp2 | a0003 | c0003 | t0002 | g0003 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19077 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19079 | hp1 | a0003 | c0003 | t0002 | g0149 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19079 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19081 | hp1 | a0003 | c0003 | t0002 | g0162 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19081 | hp2 | a0002 | c0002 | t0001 | g0115 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19084 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19084 | hp2 | a0003 | c0003 | t0002 | g0003 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19089 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0119 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19091 | hp1 | a0003 | c0003 | t0002 | g0037 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19240 | hp1 | a0005 | c0006 | t0002 | g0172 | AFR | YRI | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0191 | AFR | YRI | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ASW | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA20129 | hp2 | a0006 | c0005 | t0001 | g0088 | AFR | ASW | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | TSI | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0142 | EUR | TSI | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA20905 | hp1 | a0005 | c0006 | t0002 | g0180 | SAS | GIH | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0218 | SAS | GIH | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0043 | AMR | CLM | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0204 | AMR | CLM | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02109 | hp1 | a0008 | c0009 | t0001 | g0009 | AFR | ACB | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02109 | hp2 | a0006 | c0005 | t0001 | g0005 | AFR | ACB | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0103 | AFR | ACB | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02486 | hp2 | a0006 | c0005 | t0001 | g0083 | AFR | ACB | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | ACB | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG02559 | hp2 | a0015 | c0022 | t0002 | g0169 | AFR | ACB | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG03471 | hp1 | a0001 | c0020 | t0001 | g0206 | AFR | MSL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| HG03471 | hp2 | a0009 | c0010 | t0001 | g0034 | AFR | MSL | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA20300 | hp1 | a0005 | c0006 | t0002 | g0175 | AFR | USA | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0216 | AFR | USA | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0125 | AFR | LWK | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | LWK | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| homoSapiens | chm13v2 | a0004 | c0004 | t0001 | g0197 | REF | REF | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | EFCAB12_chr3_129396321_129433636 | EFCAB12 | chr3 | 129396321 | 129433636 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:129401726 | A | G | 1 | a0012 | 2 | HG02257.hp1 HG02922.hp2 |
missense_variant | MODERATE | c.1586T>C | p.Leu529Pro | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 9/9 | 1734/2139 | 1586/1719 | 529/572 | chr3 | 129401726 | |||
| chr3:129401780 | A | G | 1 | a0016 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.1532T>C | p.Leu511Pro | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 9/9 | 1680/2139 | 1532/1719 | 511/572 | chr3 | 129401780 | |||
| chr3:129411175 | G | A | 3 | a0004 a0010 a0013 |
28 | HG00408.hp1 HG00621.hp2 HG00642.hp1 others(25): Show |
missense_variant | MODERATE | c.1018C>T | p.Arg340Trp | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 5/9 | 1166/2139 | 1018/1719 | 340/572 | chr3 | 129411175 | |||
| chr3:129411180 | C | T | 1 | a0011 | 2 | HG02280.hp2 NA19030.hp2 |
missense_variant | MODERATE | c.1013G>A | p.Arg338His | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 5/9 | 1161/2139 | 1013/1719 | 338/572 | chr3 | 129411180 | |||
| chr3:129411181 | G | A | 1 | a0011 | 1 | NA18947.hp2 | missense_variant | MODERATE | c.1012C>T | p.Arg338Cys | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 5/9 | 1160/2139 | 1012/1719 | 338/572 | chr3 | 129411181 | |||
| chr3:129411228 | G | A | 1 | a0009 | 5 | HG01109.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
missense_variant | MODERATE | c.965C>T | p.Thr322Met | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 5/9 | 1113/2139 | 965/1719 | 322/572 | chr3 | 129411228 | |||
| chr3:129411244 | C | T | 1 | a0003 | 32 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(29): Show |
missense_variant | MODERATE | c.949G>A | p.Asp317Asn | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 5/9 | 1097/2139 | 949/1719 | 317/572 | chr3 | 129411244 | |||
| chr3:129411354 | T | C | 3 | a0002 a0011 a0017 |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
missense_variant&splice_region_variant | MODERATE | c.839A>G | p.His280Arg | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 5/9 | 987/2139 | 839/1719 | 280/572 | chr3 | 129411354 | |||
| chr3:129418292 | T | C | 1 | a0008 | 6 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
missense_variant | MODERATE | c.643A>G | p.Arg215Gly | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/9 | 791/2139 | 643/1719 | 215/572 | chr3 | 129418292 | |||
| chr3:129418345 | C | T | 1 | a0007 | 6 | HG00280.hp1 HG00642.hp2 HG00741.hp2 others(3): Show |
missense_variant | MODERATE | c.590G>A | p.Arg197His | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/9 | 738/2139 | 590/1719 | 197/572 | chr3 | 129418345 | |||
| chr3:129418402 | T | G | 2 | a0006 a0013 |
17 | HG00738.hp2 HG01167.hp2 HG01169.hp2 others(14): Show |
missense_variant | MODERATE | c.533A>C | p.Gln178Pro | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/9 | 681/2139 | 533/1719 | 178/572 | chr3 | 129418402 | |||
| chr3:129418417 | C | T | 1 | a0010 | 4 | HG01891.hp1 HG02451.hp1 HG02809.hp1 others(1): Show |
missense_variant | MODERATE | c.518G>A | p.Arg173His | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/9 | 666/2139 | 518/1719 | 173/572 | chr3 | 129418417 | |||
| chr3:129421656 | T | C | 3 | a0002 a0011 a0017 |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
missense_variant | MODERATE | c.197A>G | p.Glu66Gly | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 2/9 | 345/2139 | 197/1719 | 66/572 | chr3 | 129421656 | |||
| chr3:129421662 | C | T | 1 | a0017 | 1 | NA18959.hp1 | missense_variant | MODERATE | c.191G>A | p.Arg64His | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 2/9 | 339/2139 | 191/1719 | 64/572 | chr3 | 129421662 | |||
| chr3:129421683 | C | T | 1 | a0015 | 1 | HG02559.hp2 | missense_variant | MODERATE | c.170G>A | p.Arg57Gln | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 2/9 | 318/2139 | 170/1719 | 57/572 | chr3 | 129421683 | |||
| chr3:129421746 | G | A | 2 | a0005 a0015 |
17 | HG01255.hp2 HG02055.hp2 HG02083.hp2 others(14): Show |
missense_variant | MODERATE | c.107C>T | p.Pro36Leu | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 2/9 | 255/2139 | 107/1719 | 36/572 | chr3 | 129421746 | |||
| chr3:129421791 | G | C | 1 | a0014 | 1 | HG01496.hp1 | missense_variant | MODERATE | c.62C>G | p.Ser21Cys | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 2/9 | 210/2139 | 62/1719 | 21/572 | chr3 | 129421791 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:129411227 | C | T | 1 | a0005c0015 | 2 | HG02083.hp2 HG03834.hp1 |
synonymous_variant | LOW | c.966G>A | p.Thr322Thr | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 5/9 | 1114/2139 | 966/1719 | 322/572 | chr3 | 129411227 | |||
| chr3:129411302 | C | T | 1 | a0001c0020 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.891G>A | p.Gln297Gln | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 5/9 | 1039/2139 | 891/1719 | 297/572 | chr3 | 129411302 | |||
| chr3:129415399 | G | A | 5 | a0002c0002 a0002c0016 a0011c0014 others(2): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
splice_region_variant&synonymous_variant | LOW | c.684C>T | p.Val228Val | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/9 | 832/2139 | 684/1719 | 228/572 | chr3 | 129415399 | |||
| chr3:129418284 | G | A | 5 | a0002c0002 a0002c0016 a0011c0014 others(2): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
synonymous_variant | LOW | c.651C>T | p.Thr217Thr | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/9 | 799/2139 | 651/1719 | 217/572 | chr3 | 129418284 | |||
| chr3:129421388 | C | T | 1 | a0001c0018 | 1 | NA18992.hp2 | synonymous_variant | LOW | c.465G>A | p.Gln155Gln | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 2/9 | 613/2139 | 465/1719 | 155/572 | chr3 | 129421388 | |||
| chr3:129421646 | T | C | 6 | a0001c0007 a0001c0020 a0004c0004 others(3): Show |
54 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(51): Show |
synonymous_variant | LOW | c.207A>G | p.Thr69Thr | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 2/9 | 355/2139 | 207/1719 | 69/572 | chr3 | 129421646 | |||
| chr3:129421793 | C | T | 1 | a0002c0016 | 1 | HG01255.hp1 | synonymous_variant | LOW | c.60G>A | p.Pro20Pro | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 2/9 | 208/2139 | 60/1719 | 20/572 | chr3 | 129421793 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:129401334 | A | G | 6 | a0001c0001t0002 a0002c0002t0002 a0003c0003t0002 others(3): Show |
55 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*259T>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 9/9 | 259 | chr3 | 129401334 | ||||||
| chr3:129428527 | G | A | 1 | a0001c0001t0005 | 1 | HG03831.hp2 | 5_prime_UTR_variant | MODIFIER | c.-39C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/9 | 39 | chr3 | 129428527 | ||||||
| chr3:129428554 | C | A | 1 | a0014c0023t0004 | 1 | HG01496.hp1 | 5_prime_UTR_variant | MODIFIER | c.-66G>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/9 | 66 | chr3 | 129428554 | ||||||
| chr3:129428575 | G | A | 2 | a0001c0001t0003 a0001c0001t0005 |
40 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(37): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-87C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/9 | chr3 | 129428575 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:129401900 | A | G | 140 | a0001c0001t0001g0019 a0001c0001t0001g0035 a0001c0001t0001g0036 others(137): Show |
218 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(215): Show |
intron_variant | MODIFIER | c.1461-49T>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 8/8 | chr3 | 129401900 | |||||||
| chr3:129401933 | G | A | 1 | a0005c0006t0002g0176 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1461-82C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 8/8 | chr3 | 129401933 | |||||||
| chr3:129401972 | C | T | 1 | a0002c0002t0001g0097 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1461-121G>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 8/8 | chr3 | 129401972 | |||||||
| chr3:129401974 | C | T | 1 | a0002c0002t0001g0097 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1461-123G>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 8/8 | chr3 | 129401974 | |||||||
| chr3:129402057 | C | T | 2 | a0001c0001t0001g0080 a0001c0001t0001g0087 |
2 | HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1461-206G>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 8/8 | chr3 | 129402057 | |||||||
| chr3:129402060 | C | T | 1 | a0001c0007t0001g0203 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1461-209G>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 8/8 | chr3 | 129402060 | |||||||
| chr3:129402081 | A | G | 2 | a0002c0002t0001g0108 a0002c0002t0001g0109 |
2 | NA18968.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.1461-230T>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 8/8 | chr3 | 129402081 | |||||||
| chr3:129402202 | G | T | 22 | a0001c0001t0001g0157 a0001c0001t0001g0165 a0001c0001t0001g0207 others(19): Show |
39 | HG00423.hp1 HG00597.hp1 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.1460+321C>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 8/8 | chr3 | 129402202 | |||||||
| chr3:129402238 | G | A | 4 | a0002c0002t0001g0023 a0002c0002t0001g0024 a0002c0002t0001g0048 others(1): Show |
6 | HG02809.hp2 HG02896.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.1460+285C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 8/8 | chr3 | 129402238 | |||||||
| chr3:129402670 | C | A | 1 | a0001c0001t0001g0134 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1404-91G>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 7/8 | chr3 | 129402670 | |||||||
| chr3:129402845 | T | C | 1 | a0001c0001t0001g0060 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1404-266A>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 7/8 | chr3 | 129402845 | |||||||
| chr3:129402877 | G | A | 1 | a0001c0001t0001g0062 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1404-298C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 7/8 | chr3 | 129402877 | |||||||
| chr3:129402884 | C | T | 1 | a0001c0001t0001g0056 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1404-305G>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 7/8 | chr3 | 129402884 | |||||||
| chr3:129402972 | A | G | 79 | a0001c0001t0001g0019 a0001c0001t0003g0219 a0001c0007t0001g0041 others(76): Show |
134 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(131): Show |
intron_variant | MODIFIER | c.1404-393T>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 7/8 | chr3 | 129402972 | |||||||
| chr3:129403033 | G | A | 7 | a0001c0001t0001g0090 a0001c0001t0001g0151 a0001c0001t0001g0152 others(4): Show |
9 | HG02559.hp1 HG02647.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1404-454C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 7/8 | chr3 | 129403033 | |||||||
| chr3:129403038 | C | T | 1 | a0008c0009t0001g0050 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1404-459G>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 7/8 | chr3 | 129403038 | |||||||
| chr3:129403186 | C | T | 14 | a0004c0004t0001g0007 a0004c0004t0001g0022 a0004c0004t0001g0039 others(11): Show |
24 | HG00408.hp1 HG00621.hp2 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.1404-607G>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 7/8 | chr3 | 129403186 | |||||||
| chr3:129403225 | C | T | 1 | a0001c0001t0001g0062 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1404-646G>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 7/8 | chr3 | 129403225 | |||||||
| chr3:129403383 | G | A | 4 | a0009c0010t0001g0034 a0009c0010t0001g0086 a0009c0010t0001g0131 others(1): Show |
5 | HG01109.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1404-804C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 7/8 | chr3 | 129403383 | |||||||
| chr3:129403449 | A | G | 148 | a0001c0001t0001g0019 a0001c0001t0001g0035 a0001c0001t0001g0036 others(145): Show |
229 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(226): Show |
intron_variant | MODIFIER | c.1403+801T>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 7/8 | chr3 | 129403449 | |||||||
| chr3:129403484 | C | T | 9 | a0001c0001t0001g0019 a0006c0005t0001g0005 a0006c0005t0001g0083 others(6): Show |
20 | HG00738.hp2 HG01167.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.1403+766G>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 7/8 | chr3 | 129403484 | |||||||
| chr3:129403656 | C | T | 1 | a0003c0003t0002g0146 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1403+594G>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 7/8 | chr3 | 129403656 | |||||||
| chr3:129403669 | C | T | 4 | a0009c0010t0001g0034 a0009c0010t0001g0086 a0009c0010t0001g0131 others(1): Show |
5 | HG01109.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1403+581G>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 7/8 | chr3 | 129403669 | |||||||
| chr3:129403770 | G | T | 1 | a0002c0002t0001g0113 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1403+480C>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 7/8 | chr3 | 129403770 | |||||||
| chr3:129403799 | C | A | 59 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(56): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.1403+451G>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 7/8 | chr3 | 129403799 | |||||||
| chr3:129403834 | G | T | 1 | a0003c0003t0002g0149 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1403+416C>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 7/8 | chr3 | 129403834 | |||||||
| chr3:129403855 | C | T | 8 | a0005c0006t0001g0179 a0005c0006t0002g0166 a0005c0006t0002g0173 others(5): Show |
8 | HG02083.hp2 HG02135.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.1403+395G>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 7/8 | chr3 | 129403855 | |||||||
| chr3:129404208 | G | A | 3 | a0001c0001t0003g0211 a0001c0001t0003g0216 a0002c0002t0001g0116 |
3 | HG02735.hp1 NA19002.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1403+42C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 7/8 | chr3 | 129404208 | |||||||
| chr3:129404484 | G | GT | 60 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(57): Show |
96 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.1250-82dupA | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 6/8 | chr3 | 129404484 | |||||||
| chr3:129404496 | T | TTTAATTC others(2487): Show |
1 | a0005c0006t0002g0168 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1250-94_1250-93ins others(2494): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 6/8 | chr3 | 129404496 | |||||||
| chr3:129404496 | T | TTTAATTC others(2493): Show |
2 | a0005c0006t0002g0180 a0005c0015t0001g0171 |
2 | HG02083.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1250-94_1250-93ins others(2500): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 6/8 | chr3 | 129404496 | |||||||
| chr3:129404496 | T | TTTAATTC others(2494): Show |
4 | a0005c0006t0002g0172 a0005c0006t0002g0174 a0005c0006t0002g0177 others(1): Show |
4 | HG03491.hp1 HG03834.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1250-94_1250-93ins others(2501): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 6/8 | chr3 | 129404496 | |||||||
| chr3:129404496 | T | TTTAATTC others(2495): Show |
1 | a0005c0006t0001g0179 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1250-94_1250-93ins others(2502): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 6/8 | chr3 | 129404496 | |||||||
| chr3:129404496 | T | TTTAATTC others(2499): Show |
1 | a0005c0006t0002g0173 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1250-94_1250-93ins others(2506): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 6/8 | chr3 | 129404496 | |||||||
| chr3:129404496 | T | TTTAATTC others(2500): Show |
3 | a0001c0001t0002g0160 a0001c0001t0002g0161 a0005c0006t0002g0021 |
5 | HG01255.hp2 HG02615.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1250-94_1250-93ins others(2507): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 6/8 | chr3 | 129404496 | |||||||
| chr3:129404496 | T | TTTAATTC others(2502): Show |
1 | a0005c0006t0002g0178 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1250-94_1250-93ins others(2509): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 6/8 | chr3 | 129404496 | |||||||
| chr3:129404496 | T | TTTAATTC others(2501): Show |
1 | a0001c0001t0002g0159 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1250-94_1250-93ins others(2508): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 6/8 | chr3 | 129404496 | |||||||
| chr3:129404496 | T | TTTAATTC others(2511): Show |
1 | a0015c0022t0002g0169 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1250-94_1250-93ins others(2518): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 6/8 | chr3 | 129404496 | |||||||
| chr3:129404496 | T | TTTAATTC others(2520): Show |
1 | a0005c0006t0002g0175 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1250-94_1250-93ins others(2527): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 6/8 | chr3 | 129404496 | |||||||
| chr3:129404496 | T | TTTAATTC others(2498): Show |
1 | a0005c0006t0002g0166 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1250-94_1250-93ins others(2505): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 6/8 | chr3 | 129404496 | |||||||
| chr3:129404530 | C | G | 18 | a0001c0001t0002g0159 a0001c0001t0002g0160 a0001c0001t0002g0161 others(15): Show |
20 | HG01255.hp2 HG02055.hp2 HG02083.hp2 others(17): Show |
intron_variant | MODIFIER | c.1250-127G>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 6/8 | chr3 | 129404530 | |||||||
| chr3:129404675 | T | A | 1 | a0002c0002t0001g0106 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1250-272A>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 6/8 | chr3 | 129404675 | |||||||
| chr3:129404678 | C | G | 1 | a0004c0004t0001g0187 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1250-275G>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 6/8 | chr3 | 129404678 | |||||||
| chr3:129404697 | G | C | 1 | a0004c0004t0001g0187 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1250-294C>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 6/8 | chr3 | 129404697 | |||||||
| chr3:129404960 | G | A | 1 | a0001c0001t0003g0221 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1250-557C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 6/8 | chr3 | 129404960 | |||||||
| chr3:129405006 | T | G | 59 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(56): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.1250-603A>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 6/8 | chr3 | 129405006 | |||||||
| chr3:129405011 | G | T | 3 | a0001c0001t0001g0080 a0001c0001t0001g0087 a0001c0001t0001g0133 |
3 | HG02055.hp1 HG02145.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1250-608C>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 6/8 | chr3 | 129405011 | |||||||
| chr3:129405017 | A | T | 146 | a0001c0001t0001g0019 a0001c0001t0001g0035 a0001c0001t0001g0036 others(143): Show |
226 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(223): Show |
intron_variant | MODIFIER | c.1250-614T>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 6/8 | chr3 | 129405017 | |||||||
| chr3:129405111 | A | G | 91 | a0001c0001t0001g0019 a0001c0007t0001g0041 a0001c0007t0001g0184 others(88): Show |
149 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(146): Show |
intron_variant | MODIFIER | c.1250-708T>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 6/8 | chr3 | 129405111 | |||||||
| chr3:129405168 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1250-765T>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 6/8 | chr3 | 129405168 | |||||||
| chr3:129405231 | A | G | 59 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(56): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.1250-828T>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 6/8 | chr3 | 129405231 | |||||||
| chr3:129405245 | T | C | 1 | a0014c0023t0004g0209 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1250-842A>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 6/8 | chr3 | 129405245 | |||||||
| chr3:129405322 | G | C | 5 | a0001c0007t0001g0041 a0001c0007t0001g0184 a0001c0007t0001g0200 others(2): Show |
6 | HG00140.hp1 HG00738.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.1250-919C>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 6/8 | chr3 | 129405322 | |||||||
| chr3:129405535 | AC | A | 32 | a0001c0001t0001g0019 a0001c0007t0001g0041 a0001c0007t0001g0184 others(29): Show |
54 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.1250-1133delG | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 6/8 | chr3 | 129405535 | |||||||
| chr3:129405783 | T | C | 1 | a0001c0001t0003g0217 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1250-1380A>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 6/8 | chr3 | 129405783 | |||||||
| chr3:129405849 | G | A | 4 | a0002c0002t0001g0103 a0002c0002t0001g0154 a0002c0002t0001g0191 others(1): Show |
4 | HG01123.hp2 HG02486.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1250-1446C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 6/8 | chr3 | 129405849 | |||||||
| chr3:129406006 | A | T | 3 | a0002c0002t0001g0040 a0002c0002t0001g0194 a0002c0002t0001g0196 |
4 | HG02015.hp1 NA18950.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.1250-1603T>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 6/8 | chr3 | 129406006 | |||||||
| chr3:129406048 | T | TA | 10 | a0001c0001t0001g0064 a0001c0001t0001g0133 a0001c0020t0001g0206 others(7): Show |
13 | HG02055.hp1 HG02109.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1250-1646dupT | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 6/8 | chr3 | 129406048 | |||||||
| chr3:129406048 | T | TAAAA | 12 | a0002c0002t0001g0040 a0002c0002t0001g0095 a0002c0002t0001g0112 others(9): Show |
13 | HG00544.hp2 HG01070.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1250-1649_1250-164 others(8): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 6/8 | chr3 | 129406048 | |||||||
| chr3:129406048 | T | TAAAAA | 43 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(40): Show |
76 | HG00544.hp1 HG00597.hp1 HG00673.hp2 others(73): Show |
intron_variant | MODIFIER | c.1250-1650_1250-164 others(9): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 6/8 | chr3 | 129406048 | |||||||
| chr3:129406048 | T | TAAAAAA | 4 | a0002c0002t0001g0018 a0002c0002t0001g0110 a0002c0002t0001g0119 others(1): Show |
6 | HG00558.hp1 HG01255.hp1 HG02027.hp1 others(3): Show |
intron_variant | MODIFIER | c.1250-1651_1250-164 others(10): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 6/8 | chr3 | 129406048 | |||||||
| chr3:129406048 | TA | T | 20 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0062 others(17): Show |
23 | HG01069.hp1 HG01071.hp2 HG01515.hp1 others(20): Show |
intron_variant | MODIFIER | c.1250-1646delT | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 6/8 | chr3 | 129406048 | |||||||
| chr3:129406141 | A | G | 1 | a0001c0001t0001g0029 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1250-1738T>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 6/8 | chr3 | 129406141 | |||||||
| chr3:129406254 | G | A | 13 | a0002c0002t0001g0023 a0002c0002t0001g0024 a0002c0002t0001g0040 others(10): Show |
16 | HG00544.hp2 HG01884.hp2 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.1250-1851C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 6/8 | chr3 | 129406254 | |||||||
| chr3:129406388 | C | A | 32 | a0001c0001t0001g0019 a0001c0007t0001g0041 a0001c0007t0001g0184 others(29): Show |
54 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(51): Show |
intron_variant | MODIFIER | c.1250-1985G>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 6/8 | chr3 | 129406388 | |||||||
| chr3:129406818 | G | A | 59 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(56): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.1249+1827C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 6/8 | chr3 | 129406818 | |||||||
| chr3:129406819 | A | G | 59 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(56): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.1249+1826T>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 6/8 | chr3 | 129406819 | |||||||
| chr3:129406866 | GT | G | 132 | a0001c0001t0001g0019 a0001c0001t0001g0036 a0001c0001t0001g0065 others(129): Show |
212 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(209): Show |
intron_variant | MODIFIER | c.1249+1778delA | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 6/8 | chr3 | 129406866 | |||||||
| chr3:129406913 | T | G | 2 | a0011c0014t0001g0081 a0011c0014t0001g0100 |
2 | HG02280.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1249+1732A>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 6/8 | chr3 | 129406913 | |||||||
| chr3:129407140 | C | T | 1 | a0014c0023t0004g0209 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1249+1505G>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 6/8 | chr3 | 129407140 | |||||||
| chr3:129407381 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1249+1264C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 6/8 | chr3 | 129407381 | |||||||
| chr3:129407983 | C | T | 2 | a0001c0001t0001g0060 a0001c0001t0001g0066 |
2 | HG02074.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.1249+662G>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 6/8 | chr3 | 129407983 | |||||||
| chr3:129408024 | C | A | 1 | a0004c0004t0001g0045 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1249+621G>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 6/8 | chr3 | 129408024 | |||||||
| chr3:129408030 | G | C | 155 | a0001c0001t0001g0019 a0001c0001t0001g0035 a0001c0001t0001g0036 others(152): Show |
237 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.1249+615C>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 6/8 | chr3 | 129408030 | |||||||
| chr3:129408101 | G | A | 3 | a0008c0009t0001g0009 a0008c0009t0001g0049 a0008c0009t0001g0050 |
6 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1249+544C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 6/8 | chr3 | 129408101 | |||||||
| chr3:129408132 | T | C | 59 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(56): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.1249+513A>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 6/8 | chr3 | 129408132 | |||||||
| chr3:129408188 | C | T | 14 | a0004c0004t0001g0007 a0004c0004t0001g0022 a0004c0004t0001g0039 others(11): Show |
24 | HG00408.hp1 HG00621.hp2 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.1249+457G>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 6/8 | chr3 | 129408188 | |||||||
| chr3:129408323 | C | T | 12 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0136 others(9): Show |
14 | HG01069.hp1 HG01071.hp2 HG01515.hp1 others(11): Show |
intron_variant | MODIFIER | c.1249+322G>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 6/8 | chr3 | 129408323 | |||||||
| chr3:129408326 | G | A | 10 | a0001c0001t0001g0019 a0001c0007t0001g0091 a0006c0005t0001g0005 others(7): Show |
21 | HG00738.hp2 HG01167.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.1249+319C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 6/8 | chr3 | 129408326 | |||||||
| chr3:129408523 | A | G | 1 | a0005c0006t0002g0172 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1249+122T>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 6/8 | chr3 | 129408523 | |||||||
| chr3:129408863 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG03098.hp2 | splice_region_variant&intron_variant | LOW | c.1036-5C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 5/8 | chr3 | 129408863 | |||||||
| chr3:129408904 | C | T | 1 | a0001c0001t0001g0061 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1036-46G>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 5/8 | chr3 | 129408904 | |||||||
| chr3:129409113 | T | C | 59 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(56): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.1036-255A>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 5/8 | chr3 | 129409113 | |||||||
| chr3:129409144 | G | A | 59 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(56): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.1036-286C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 5/8 | chr3 | 129409144 | |||||||
| chr3:129409179 | A | G | 59 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(56): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.1036-321T>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 5/8 | chr3 | 129409179 | |||||||
| chr3:129409248 | G | A | 1 | a0003c0003t0002g0147 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1036-390C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 5/8 | chr3 | 129409248 | |||||||
| chr3:129409266 | A | G | 1 | a0001c0001t0003g0213 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1036-408T>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 5/8 | chr3 | 129409266 | |||||||
| chr3:129409315 | C | T | 1 | a0014c0023t0004g0209 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1036-457G>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 5/8 | chr3 | 129409315 | |||||||
| chr3:129409687 | T | TATAA | 58 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(55): Show |
94 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.1036-833_1036-830d others(6): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 5/8 | chr3 | 129409687 | |||||||
| chr3:129409788 | C | T | 59 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(56): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.1036-930G>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 5/8 | chr3 | 129409788 | |||||||
| chr3:129409904 | T | C | 2 | a0012c0012t0001g0155 a0012c0012t0001g0156 |
2 | HG02257.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1036-1046A>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 5/8 | chr3 | 129409904 | |||||||
| chr3:129410009 | T | A | 58 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(55): Show |
94 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.1035+1149A>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 5/8 | chr3 | 129410009 | |||||||
| chr3:129410010 | A | AT | 56 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(53): Show |
92 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.1035+1147dupA | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 5/8 | chr3 | 129410010 | |||||||
| chr3:129410010 | A | T | 1 | a0002c0002t0001g0112 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1035+1148T>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 5/8 | chr3 | 129410010 | |||||||
| chr3:129410014 | A | T | 59 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(56): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.1035+1144T>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 5/8 | chr3 | 129410014 | |||||||
| chr3:129410018 | T | A | 7 | a0001c0001t0001g0152 a0001c0007t0001g0199 a0001c0007t0001g0203 others(4): Show |
10 | HG01496.hp1 HG01884.hp1 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.1035+1140A>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 5/8 | chr3 | 129410018 | |||||||
| chr3:129410072 | G | A | 59 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(56): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.1035+1086C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 5/8 | chr3 | 129410072 | |||||||
| chr3:129410115 | T | C | 59 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(56): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.1035+1043A>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 5/8 | chr3 | 129410115 | |||||||
| chr3:129410180 | A | T | 1 | a0002c0002t0001g0031 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1035+978T>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 5/8 | chr3 | 129410180 | |||||||
| chr3:129410273 | T | G | 97 | a0001c0001t0001g0019 a0001c0007t0001g0041 a0001c0007t0001g0091 others(94): Show |
158 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(155): Show |
intron_variant | MODIFIER | c.1035+885A>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 5/8 | chr3 | 129410273 | |||||||
| chr3:129410318 | A | AT | 50 | a0001c0001t0001g0015 a0001c0001t0001g0025 a0001c0001t0001g0060 others(47): Show |
86 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.1035+839dupA | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 5/8 | chr3 | 129410318 | |||||||
| chr3:129410318 | A | ATT | 16 | a0001c0001t0001g0028 a0002c0002t0001g0023 a0002c0002t0001g0024 others(13): Show |
20 | HG00544.hp2 HG00558.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1035+838_1035+839d others(4): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 5/8 | chr3 | 129410318 | |||||||
| chr3:129410318 | AT | A | 71 | a0001c0001t0001g0019 a0001c0001t0001g0207 a0001c0001t0001g0208 others(68): Show |
114 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(111): Show |
intron_variant | MODIFIER | c.1035+839delA | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 5/8 | chr3 | 129410318 | |||||||
| chr3:129410387 | G | A | 15 | a0002c0002t0001g0023 a0002c0002t0001g0024 a0002c0002t0001g0040 others(12): Show |
18 | HG00544.hp2 HG01884.hp2 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.1035+771C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 5/8 | chr3 | 129410387 | |||||||
| chr3:129410507 | A | G | 18 | a0001c0007t0001g0091 a0003c0003t0002g0003 a0003c0003t0002g0037 others(15): Show |
33 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.1035+651T>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 5/8 | chr3 | 129410507 | |||||||
| chr3:129410526 | T | C | 59 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(56): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.1035+632A>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 5/8 | chr3 | 129410526 | |||||||
| chr3:129411045 | C | T | 2 | a0001c0001t0001g0207 a0001c0001t0001g0208 |
2 | HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1035+113G>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 5/8 | chr3 | 129411045 | |||||||
| chr3:129411094 | G | A | 1 | a0004c0004t0001g0007 | 7 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.1035+64C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 5/8 | chr3 | 129411094 | |||||||
| chr3:129411585 | T | C | 59 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(56): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.839-231A>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129411585 | |||||||
| chr3:129411645 | T | C | 1 | a0001c0001t0003g0218 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.839-291A>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129411645 | |||||||
| chr3:129411660 | C | T | 1 | a0014c0023t0004g0209 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.839-306G>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129411660 | |||||||
| chr3:129411879 | C | T | 59 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(56): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.839-525G>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129411879 | |||||||
| chr3:129411886 | G | A | 14 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0066 others(11): Show |
16 | HG01069.hp1 HG01071.hp2 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.839-532C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129411886 | |||||||
| chr3:129411914 | C | T | 1 | a0001c0001t0003g0212 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.839-560G>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129411914 | |||||||
| chr3:129411932 | A | AAAAC | 132 | a0001c0001t0001g0019 a0001c0001t0001g0207 a0001c0001t0001g0208 others(129): Show |
210 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(207): Show |
intron_variant | MODIFIER | c.839-582_839-579dup others(4): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129411932 | |||||||
| chr3:129412177 | A | T | 59 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(56): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.839-823T>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129412177 | |||||||
| chr3:129412188 | G | A | 94 | a0001c0001t0001g0019 a0001c0007t0001g0041 a0001c0007t0001g0184 others(91): Show |
155 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(152): Show |
intron_variant | MODIFIER | c.839-834C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129412188 | |||||||
| chr3:129412218 | T | A | 59 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(56): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.839-864A>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129412218 | |||||||
| chr3:129412289 | G | A | 59 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(56): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.839-935C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129412289 | |||||||
| chr3:129412418 | GTAGA | G | 19 | a0001c0001t0002g0159 a0001c0001t0002g0160 a0001c0001t0003g0043 others(16): Show |
23 | HG00544.hp1 HG01123.hp1 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.839-1068_839-1065d others(6): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129412418 | |||||||
| chr3:129412418 | GTAGATGG others(1): Show |
G | 7 | a0002c0002t0001g0006 a0002c0002t0001g0031 a0002c0002t0001g0075 others(4): Show |
14 | HG02132.hp2 HG03490.hp1 HG03492.hp1 others(11): Show |
intron_variant | MODIFIER | c.839-1072_839-1065d others(10): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129412418 | |||||||
| chr3:129412420 | A | AGATG | 10 | a0001c0001t0001g0207 a0003c0003t0002g0003 a0003c0003t0002g0037 others(7): Show |
12 | HG00639.hp2 HG02071.hp1 HG02132.hp1 others(9): Show |
intron_variant | MODIFIER | c.839-1070_839-1067d others(6): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129412420 | |||||||
| chr3:129412420 | A | G | 55 | a0001c0001t0002g0161 a0001c0001t0003g0013 a0002c0002t0001g0002 others(52): Show |
86 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.839-1066T>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129412420 | |||||||
| chr3:129412424 | GGATGGAT others(9): Show |
G | 1 | a0002c0002t0001g0103 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.839-1086_839-1071d others(18): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129412424 | |||||||
| chr3:129412428 | G | A | 50 | a0002c0002t0001g0002 a0002c0002t0001g0012 a0002c0002t0001g0017 others(47): Show |
78 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.839-1074C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129412428 | |||||||
| chr3:129412428 | G | GGATGGAT others(1): Show |
3 | a0003c0003t0002g0003 a0003c0003t0002g0037 a0003c0003t0002g0149 |
5 | HG00621.hp1 HG03669.hp1 NA18612.hp2 others(2): Show |
intron_variant | MODIFIER | c.839-1075_839-1074i others(10): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129412428 | |||||||
| chr3:129412428 | G | GGATGGAT others(5): Show |
1 | a0003c0003t0002g0162 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.839-1075_839-1074i others(14): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129412428 | |||||||
| chr3:129412428 | GGATA | G | 67 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(64): Show |
120 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.839-1078_839-1075d others(6): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129412428 | |||||||
| chr3:129412428 | GGATAGAT others(1): Show |
G | 39 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0014 others(36): Show |
65 | HG00140.hp1 HG00423.hp1 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.839-1082_839-1075d others(10): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129412428 | |||||||
| chr3:129412428 | GGATAGAT others(5): Show |
G | 7 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0008c0009t0001g0009 others(4): Show |
10 | HG01167.hp1 HG02109.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.839-1086_839-1075d others(14): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129412428 | |||||||
| chr3:129412428 | GGATAGAT others(9): Show |
G | 1 | a0004c0004t0001g0198 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.839-1090_839-1075d others(18): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129412428 | |||||||
| chr3:129412428 | GGATAGAT others(17): Show |
G | 8 | a0001c0001t0001g0080 a0001c0001t0001g0087 a0001c0001t0001g0133 others(5): Show |
9 | HG01109.hp2 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.839-1098_839-1075d others(26): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129412428 | |||||||
| chr3:129412431 | T | C | 6 | a0004c0004t0001g0039 a0004c0004t0001g0187 a0004c0004t0001g0190 others(3): Show |
6 | HG01891.hp1 HG02809.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.839-1077A>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129412431 | |||||||
| chr3:129412432 | A | G | 33 | a0001c0001t0002g0159 a0001c0001t0002g0160 a0001c0001t0003g0043 others(30): Show |
49 | HG01123.hp1 HG01255.hp2 HG01943.hp1 others(46): Show |
intron_variant | MODIFIER | c.839-1078T>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129412432 | |||||||
| chr3:129412435 | T | C | 7 | a0004c0004t0001g0007 a0004c0004t0001g0022 a0004c0004t0001g0039 others(4): Show |
14 | HG00408.hp1 HG00621.hp2 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.839-1081A>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129412435 | |||||||
| chr3:129412436 | A | G | 3 | a0001c0001t0001g0011 a0001c0001t0001g0151 a0001c0001t0001g0208 |
3 | HG03098.hp2 HG03486.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.839-1082T>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129412436 | |||||||
| chr3:129412439 | T | C | 1 | a0004c0004t0001g0022 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.839-1085A>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129412439 | |||||||
| chr3:129412440 | A | G | 1 | a0003c0003t0002g0003 | 2 | HG00423.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.839-1086T>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129412440 | |||||||
| chr3:129412447 | T | C | 1 | a0004c0004t0001g0198 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.839-1093A>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129412447 | |||||||
| chr3:129412471 | T | C | 24 | a0002c0002t0001g0006 a0002c0002t0001g0017 a0002c0002t0001g0023 others(21): Show |
36 | HG00544.hp1 HG00558.hp1 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.839-1117A>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129412471 | |||||||
| chr3:129412471 | T | TAGAC | 27 | a0002c0002t0001g0002 a0002c0002t0001g0012 a0002c0002t0001g0018 others(24): Show |
50 | HG00597.hp1 HG00673.hp2 HG01070.hp2 others(47): Show |
intron_variant | MODIFIER | c.839-1118_839-1117i others(6): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129412471 | |||||||
| chr3:129412475 | T | C | 58 | a0001c0001t0001g0067 a0001c0007t0001g0203 a0002c0002t0001g0002 others(55): Show |
96 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.839-1121A>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129412475 | |||||||
| chr3:129412475 | T | TAGACAGA others(1): Show |
5 | a0002c0002t0001g0118 a0002c0002t0001g0119 a0002c0002t0001g0194 others(2): Show |
5 | HG00544.hp2 HG01257.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.839-1129_839-1122d others(10): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129412475 | |||||||
| chr3:129412475 | T | TAGATAGA others(5): Show |
2 | a0002c0002t0001g0030 a0002c0002t0001g0196 |
3 | NA18995.hp1 NA18999.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.839-1122_839-1121i others(14): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129412475 | |||||||
| chr3:129412478 | A | G | 1 | a0001c0001t0001g0059 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.839-1124T>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129412478 | |||||||
| chr3:129412501 | C | T | 59 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(56): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.839-1147G>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129412501 | |||||||
| chr3:129412576 | G | A | 59 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(56): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.839-1222C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129412576 | |||||||
| chr3:129412617 | A | C | 1 | a0001c0001t0001g0058 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.839-1263T>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129412617 | |||||||
| chr3:129412635 | C | A | 8 | a0002c0002t0001g0040 a0002c0002t0001g0125 a0002c0002t0001g0126 others(5): Show |
9 | HG00544.hp2 HG01884.hp2 HG02015.hp1 others(6): Show |
intron_variant | MODIFIER | c.839-1281G>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129412635 | |||||||
| chr3:129412755 | T | C | 8 | a0001c0001t0001g0080 a0001c0001t0001g0087 a0001c0001t0001g0133 others(5): Show |
9 | HG01109.hp2 HG02055.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.839-1401A>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129412755 | |||||||
| chr3:129412939 | C | T | 31 | a0001c0007t0001g0041 a0001c0007t0001g0184 a0001c0007t0001g0199 others(28): Show |
51 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.839-1585G>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129412939 | |||||||
| chr3:129413109 | T | C | 1 | a0001c0001t0003g0224 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.839-1755A>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129413109 | |||||||
| chr3:129413214 | G | A | 59 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(56): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.839-1860C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129413214 | |||||||
| chr3:129413233 | T | G | 1 | a0002c0002t0001g0120 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.839-1879A>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129413233 | |||||||
| chr3:129413250 | C | T | 1 | a0001c0001t0001g0051 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.839-1896G>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129413250 | |||||||
| chr3:129413270 | C | A | 2 | a0005c0006t0002g0021 a0005c0006t0002g0178 |
4 | HG01255.hp2 HG02055.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.839-1916G>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129413270 | |||||||
| chr3:129413455 | A | G | 1 | a0001c0018t0001g0137 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.838+1790T>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129413455 | |||||||
| chr3:129413483 | TA | T | 12 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0136 others(9): Show |
14 | HG01069.hp1 HG01071.hp2 HG01515.hp1 others(11): Show |
intron_variant | MODIFIER | c.838+1761delT | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129413483 | |||||||
| chr3:129413581 | A | G | 58 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(55): Show |
94 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.838+1664T>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129413581 | |||||||
| chr3:129413583 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.838+1662T>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129413583 | |||||||
| chr3:129413747 | T | TC | 59 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(56): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.838+1497dupG | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129413747 | |||||||
| chr3:129413833 | G | A | 59 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(56): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.838+1412C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129413833 | |||||||
| chr3:129413910 | A | C | 59 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(56): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.838+1335T>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129413910 | |||||||
| chr3:129413990 | T | C | 59 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(56): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.838+1255A>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129413990 | |||||||
| chr3:129414043 | C | A | 3 | a0008c0009t0001g0009 a0008c0009t0001g0049 a0008c0009t0001g0050 |
6 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.838+1202G>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129414043 | |||||||
| chr3:129414620 | T | G | 59 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(56): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.838+625A>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129414620 | |||||||
| chr3:129414714 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.838+531T>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129414714 | |||||||
| chr3:129414944 | A | G | 1 | a0002c0002t0001g0104 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.838+301T>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 4/8 | chr3 | 129414944 | |||||||
| chr3:129415467 | G | T | 3 | a0001c0007t0001g0041 a0001c0007t0001g0200 a0001c0007t0001g0201 |
4 | HG00140.hp1 HG00738.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.682-66C>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129415467 | |||||||
| chr3:129415493 | T | C | 3 | a0008c0009t0001g0009 a0008c0009t0001g0049 a0008c0009t0001g0050 |
6 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.682-92A>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129415493 | |||||||
| chr3:129415567 | G | A | 59 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(56): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.682-166C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129415567 | |||||||
| chr3:129415592 | G | C | 59 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(56): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.682-191C>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129415592 | |||||||
| chr3:129415625 | C | T | 59 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(56): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.682-224G>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129415625 | |||||||
| chr3:129415757 | G | A | 29 | a0001c0007t0001g0041 a0001c0007t0001g0184 a0001c0007t0001g0199 others(26): Show |
49 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.682-356C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129415757 | |||||||
| chr3:129415849 | T | C | 1 | a0001c0007t0001g0199 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.682-448A>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129415849 | |||||||
| chr3:129416043 | A | G | 59 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(56): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.682-642T>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129416043 | |||||||
| chr3:129416050 | T | C | 96 | a0001c0007t0001g0041 a0001c0007t0001g0091 a0001c0007t0001g0184 others(93): Show |
155 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(152): Show |
intron_variant | MODIFIER | c.682-649A>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129416050 | |||||||
| chr3:129416074 | T | C | 57 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(54): Show |
93 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.682-673A>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129416074 | |||||||
| chr3:129416162 | T | C | 12 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0136 others(9): Show |
14 | HG01069.hp1 HG01071.hp2 HG01515.hp1 others(11): Show |
intron_variant | MODIFIER | c.682-761A>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129416162 | |||||||
| chr3:129416165 | A | T | 59 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(56): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.682-764T>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129416165 | |||||||
| chr3:129416413 | G | A | 1 | a0010c0011t0001g0182 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.682-1012C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129416413 | |||||||
| chr3:129416418 | A | AAAAC | 9 | a0001c0001t0001g0056 a0001c0001t0001g0069 a0001c0001t0001g0140 others(6): Show |
17 | HG00423.hp2 HG00642.hp1 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.682-1021_682-1018d others(6): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129416418 | |||||||
| chr3:129416418 | A | AAAACAAA others(1): Show |
3 | a0008c0009t0001g0009 a0008c0009t0001g0049 a0008c0009t0001g0050 |
6 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.682-1025_682-1018d others(10): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129416418 | |||||||
| chr3:129416418 | A | AAAACAAA others(5): Show |
2 | a0004c0004t0001g0045 a0004c0004t0001g0047 |
2 | HG01891.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.682-1029_682-1018d others(14): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129416418 | |||||||
| chr3:129416418 | AAAAC | A | 24 | a0001c0001t0001g0019 a0001c0001t0001g0090 a0001c0001t0001g0151 others(21): Show |
37 | HG00738.hp2 HG01167.hp2 HG01169.hp2 others(34): Show |
intron_variant | MODIFIER | c.682-1021_682-1018d others(6): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129416418 | |||||||
| chr3:129416442 | C | T | 59 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(56): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.682-1041G>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129416442 | |||||||
| chr3:129416446 | C | A | 3 | a0010c0011t0001g0038 a0010c0011t0001g0181 a0010c0011t0001g0182 |
4 | HG01891.hp1 HG02451.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.682-1045G>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129416446 | |||||||
| chr3:129416477 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.682-1076A>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129416477 | |||||||
| chr3:129416529 | C | T | 1 | a0001c0001t0001g0055 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.682-1128G>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129416529 | |||||||
| chr3:129416787 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.682-1386G>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129416787 | |||||||
| chr3:129416788 | G | T | 95 | a0001c0007t0001g0041 a0001c0007t0001g0184 a0001c0007t0001g0199 others(92): Show |
154 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(151): Show |
intron_variant | MODIFIER | c.682-1387C>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129416788 | |||||||
| chr3:129417217 | C | A | 21 | a0001c0007t0001g0041 a0001c0007t0001g0184 a0001c0007t0001g0199 others(18): Show |
32 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.681+1037G>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129417217 | |||||||
| chr3:129417218 | G | A | 59 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(56): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.681+1036C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129417218 | |||||||
| chr3:129417307 | G | C | 1 | a0001c0001t0003g0221 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.681+947C>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129417307 | |||||||
| chr3:129417323 | C | CA | 40 | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0069 others(37): Show |
60 | HG00423.hp1 HG00423.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.681+930dupT | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129417323 | |||||||
| chr3:129417323 | C | CAA | 6 | a0001c0007t0001g0184 a0003c0003t0002g0078 a0003c0003t0002g0089 others(3): Show |
6 | HG01175.hp1 HG02135.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.681+929_681+930dup others(2): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129417323 | |||||||
| chr3:129417323 | CA | C | 57 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(54): Show |
93 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.681+930delT | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129417323 | |||||||
| chr3:129417329 | A | C | 1 | a0001c0020t0001g0206 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.681+925T>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129417329 | |||||||
| chr3:129417330 | A | C | 2 | a0002c0002t0001g0075 a0002c0002t0001g0121 |
2 | NA18979.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.681+924T>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129417330 | |||||||
| chr3:129417331 | A | C | 57 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(54): Show |
93 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.681+923T>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129417331 | |||||||
| chr3:129417333 | A | C | 3 | a0008c0009t0001g0009 a0008c0009t0001g0049 a0008c0009t0001g0050 |
6 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.681+921T>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129417333 | |||||||
| chr3:129417334 | A | C | 7 | a0001c0007t0001g0205 a0001c0020t0001g0206 a0004c0004t0001g0045 others(4): Show |
8 | HG00735.hp1 HG01891.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.681+920T>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129417334 | |||||||
| chr3:129417335 | A | C | 2 | a0002c0002t0001g0075 a0002c0002t0001g0121 |
2 | NA18979.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.681+919T>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129417335 | |||||||
| chr3:129417336 | A | C | 57 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(54): Show |
93 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.681+918T>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129417336 | |||||||
| chr3:129417339 | A | C | 4 | a0001c0007t0001g0205 a0001c0020t0001g0206 a0002c0002t0001g0075 others(1): Show |
4 | HG00735.hp1 HG03471.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.681+915T>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129417339 | |||||||
| chr3:129417339 | AC | A | 26 | a0001c0001t0001g0019 a0001c0001t0001g0035 a0001c0001t0001g0036 others(23): Show |
35 | HG01069.hp1 HG01071.hp2 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.681+914delG | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129417339 | |||||||
| chr3:129417340 | C | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(83): Show |
178 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.681+914G>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129417340 | |||||||
| chr3:129417341 | C | A | 118 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0076 others(115): Show |
177 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(174): Show |
intron_variant | MODIFIER | c.681+913G>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129417341 | |||||||
| chr3:129417343 | A | C | 2 | a0002c0002t0001g0075 a0002c0002t0001g0121 |
2 | NA18979.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.681+911T>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129417343 | |||||||
| chr3:129417344 | A | C | 45 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(42): Show |
78 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.681+910T>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129417344 | |||||||
| chr3:129417346 | A | G | 1 | a0001c0007t0001g0200 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.681+908T>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129417346 | |||||||
| chr3:129417362 | CA | C | 40 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0054 others(37): Show |
60 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.681+891delT | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129417362 | |||||||
| chr3:129417362 | CAA | C | 44 | a0001c0007t0001g0041 a0001c0007t0001g0184 a0001c0007t0001g0199 others(41): Show |
66 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.681+890_681+891del others(2): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129417362 | |||||||
| chr3:129417362 | CAAA | C | 59 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(56): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.681+889_681+891del others(3): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129417362 | |||||||
| chr3:129417508 | G | T | 2 | a0001c0001t0001g0027 a0001c0001t0001g0073 |
3 | HG02293.hp2 NA18955.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.681+746C>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129417508 | |||||||
| chr3:129417807 | T | TAGAAATA others(323): Show |
1 | a0001c0001t0001g0143 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.681+446_681+447ins others(330): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129417807 | |||||||
| chr3:129417807 | T | TAGAAATA others(328): Show |
1 | a0016c0019t0001g0129 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.681+446_681+447ins others(335): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129417807 | |||||||
| chr3:129417807 | T | TAGAAATA others(329): Show |
2 | a0001c0001t0001g0140 a0001c0001t0001g0141 |
2 | NA18952.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.681+446_681+447ins others(336): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129417807 | |||||||
| chr3:129417807 | T | TAGAAATA others(330): Show |
1 | a0001c0001t0001g0136 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.681+446_681+447ins others(337): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129417807 | |||||||
| chr3:129417807 | T | TAGAAATA others(344): Show |
1 | a0012c0012t0001g0155 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.681+446_681+447ins others(351): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129417807 | |||||||
| chr3:129417807 | T | TAGAAATA others(345): Show |
2 | a0001c0001t0001g0035 a0001c0001t0001g0138 |
3 | HG01069.hp1 HG01071.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.681+446_681+447ins others(352): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129417807 | |||||||
| chr3:129417807 | T | TAGAAATA others(346): Show |
2 | a0001c0001t0001g0036 a0001c0001t0001g0139 |
3 | HG02698.hp1 HG02735.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.681+446_681+447ins others(353): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129417807 | |||||||
| chr3:129417807 | T | TAGAAATA others(347): Show |
1 | a0012c0012t0001g0156 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.681+446_681+447ins others(354): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129417807 | |||||||
| chr3:129417807 | T | TAGAAATA others(348): Show |
1 | a0001c0001t0001g0142 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.681+446_681+447ins others(355): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129417807 | |||||||
| chr3:129417807 | T | TAGAAATA others(355): Show |
1 | a0001c0018t0001g0137 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.681+446_681+447ins others(362): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129417807 | |||||||
| chr3:129417863 | C | T | 1 | a0001c0001t0001g0016 | 3 | HG00323.hp1 HG03704.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.681+391G>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129417863 | |||||||
| chr3:129417902 | G | A | 12 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0136 others(9): Show |
14 | HG01069.hp1 HG01071.hp2 HG01515.hp1 others(11): Show |
intron_variant | MODIFIER | c.681+352C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129417902 | |||||||
| chr3:129417931 | T | C | 59 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(56): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.681+323A>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129417931 | |||||||
| chr3:129417944 | T | C | 13 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0136 others(10): Show |
15 | HG01069.hp1 HG01071.hp2 HG01515.hp1 others(12): Show |
intron_variant | MODIFIER | c.681+310A>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129417944 | |||||||
| chr3:129417965 | T | C | 59 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(56): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.681+289A>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129417965 | |||||||
| chr3:129417990 | G | T | 1 | a0001c0001t0003g0223 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.681+264C>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129417990 | |||||||
| chr3:129418093 | T | C | 59 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(56): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.681+161A>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129418093 | |||||||
| chr3:129418180 | C | T | 2 | a0001c0001t0001g0027 a0001c0001t0001g0073 |
3 | HG02293.hp2 NA18955.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.681+74G>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129418180 | |||||||
| chr3:129418181 | G | A | 1 | a0002c0002t0001g0122 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.681+73C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129418181 | |||||||
| chr3:129418182 | G | A | 29 | a0001c0007t0001g0041 a0001c0007t0001g0184 a0001c0007t0001g0199 others(26): Show |
49 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.681+72C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 3/8 | chr3 | 129418182 | |||||||
| chr3:129418504 | C | T | 4 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0138 others(1): Show |
6 | HG01069.hp1 HG01071.hp2 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.487-56G>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 2/8 | chr3 | 129418504 | |||||||
| chr3:129418787 | G | C | 1 | a0016c0019t0001g0129 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.487-339C>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 2/8 | chr3 | 129418787 | |||||||
| chr3:129418813 | G | T | 15 | a0005c0006t0001g0179 a0005c0006t0002g0021 a0005c0006t0002g0166 others(12): Show |
17 | HG01255.hp2 HG02055.hp2 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.487-365C>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 2/8 | chr3 | 129418813 | |||||||
| chr3:129418894 | C | G | 4 | a0002c0002t0001g0103 a0002c0002t0001g0154 a0002c0002t0001g0191 others(1): Show |
4 | HG01123.hp2 HG02486.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.487-446G>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 2/8 | chr3 | 129418894 | |||||||
| chr3:129418903 | A | G | 59 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(56): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.487-455T>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 2/8 | chr3 | 129418903 | |||||||
| chr3:129418921 | G | T | 1 | a0001c0001t0001g0133 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.487-473C>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 2/8 | chr3 | 129418921 | |||||||
| chr3:129418959 | G | A | 59 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(56): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.487-511C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 2/8 | chr3 | 129418959 | |||||||
| chr3:129419015 | A | C | 2 | a0004c0004t0001g0045 a0004c0004t0001g0047 |
2 | HG01891.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.487-567T>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 2/8 | chr3 | 129419015 | |||||||
| chr3:129419015 | A | G | 93 | a0001c0007t0001g0041 a0001c0007t0001g0184 a0001c0007t0001g0199 others(90): Show |
152 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(149): Show |
intron_variant | MODIFIER | c.487-567T>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 2/8 | chr3 | 129419015 | |||||||
| chr3:129419279 | T | C | 5 | a0004c0004t0001g0045 a0004c0004t0001g0047 a0008c0009t0001g0009 others(2): Show |
8 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.487-831A>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 2/8 | chr3 | 129419279 | |||||||
| chr3:129419441 | A | G | 5 | a0004c0004t0001g0045 a0004c0004t0001g0047 a0008c0009t0001g0009 others(2): Show |
8 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.487-993T>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 2/8 | chr3 | 129419441 | |||||||
| chr3:129419461 | G | A | 1 | a0001c0001t0001g0016 | 3 | HG00323.hp1 HG03704.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.487-1013C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 2/8 | chr3 | 129419461 | |||||||
| chr3:129419465 | G | A | 31 | a0001c0007t0001g0041 a0001c0007t0001g0184 a0001c0007t0001g0199 others(28): Show |
51 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.487-1017C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 2/8 | chr3 | 129419465 | |||||||
| chr3:129419642 | G | A | 12 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0136 others(9): Show |
14 | HG01069.hp1 HG01071.hp2 HG01515.hp1 others(11): Show |
intron_variant | MODIFIER | c.487-1194C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 2/8 | chr3 | 129419642 | |||||||
| chr3:129419756 | A | C | 1 | a0004c0004t0001g0186 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.487-1308T>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 2/8 | chr3 | 129419756 | |||||||
| chr3:129419810 | G | A | 59 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(56): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.487-1362C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 2/8 | chr3 | 129419810 | |||||||
| chr3:129419918 | T | C | 59 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(56): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.486+1449A>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 2/8 | chr3 | 129419918 | |||||||
| chr3:129419960 | G | C | 1 | a0004c0004t0001g0190 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.486+1407C>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 2/8 | chr3 | 129419960 | |||||||
| chr3:129420168 | C | T | 1 | a0001c0001t0001g0026 | 2 | HG00609.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.486+1199G>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 2/8 | chr3 | 129420168 | |||||||
| chr3:129420186 | G | T | 5 | a0004c0004t0001g0045 a0004c0004t0001g0047 a0008c0009t0001g0009 others(2): Show |
8 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.486+1181C>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 2/8 | chr3 | 129420186 | |||||||
| chr3:129420256 | C | T | 2 | a0002c0002t0001g0101 a0002c0002t0001g0102 |
2 | HG02165.hp2 NA18951.hp1 |
intron_variant | MODIFIER | c.486+1111G>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 2/8 | chr3 | 129420256 | |||||||
| chr3:129420338 | A | G | 1 | a0008c0009t0001g0049 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.486+1029T>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 2/8 | chr3 | 129420338 | |||||||
| chr3:129420423 | A | G | 2 | a0001c0007t0001g0205 a0001c0020t0001g0206 |
2 | HG00735.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.486+944T>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 2/8 | chr3 | 129420423 | |||||||
| chr3:129420444 | A | G | 1 | a0001c0001t0003g0210 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.486+923T>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 2/8 | chr3 | 129420444 | |||||||
| chr3:129420474 | A | G | 1 | a0001c0020t0001g0206 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.486+893T>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 2/8 | chr3 | 129420474 | |||||||
| chr3:129420477 | A | G | 153 | a0001c0001t0001g0019 a0001c0001t0001g0035 a0001c0001t0001g0036 others(150): Show |
235 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.486+890T>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 2/8 | chr3 | 129420477 | |||||||
| chr3:129420579 | A | G | 1 | a0001c0001t0001g0025 | 2 | HG01934.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.486+788T>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 2/8 | chr3 | 129420579 | |||||||
| chr3:129420729 | CCTTT | C | 6 | a0001c0001t0001g0090 a0001c0001t0001g0158 a0001c0001t0002g0020 others(3): Show |
8 | HG02559.hp1 HG02647.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.486+634_486+637del others(4): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 2/8 | chr3 | 129420729 | |||||||
| chr3:129420870 | C | G | 2 | a0011c0014t0001g0081 a0011c0014t0001g0100 |
2 | HG02280.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.486+497G>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 2/8 | chr3 | 129420870 | |||||||
| chr3:129421225 | T | G | 3 | a0002c0002t0001g0023 a0002c0002t0001g0024 a0002c0002t0002g0046 |
5 | HG02622.hp1 HG02896.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.486+142A>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 2/8 | chr3 | 129421225 | |||||||
| chr3:129421325 | C | T | 1 | a0002c0002t0001g0030 | 2 | NA18995.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.486+42G>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 2/8 | chr3 | 129421325 | |||||||
| chr3:129421358 | G | A | 1 | a0002c0002t0001g0048 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.486+9C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 2/8 | chr3 | 129421358 | |||||||
| chr3:129421895 | A | T | 124 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0136 others(121): Show |
187 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(184): Show |
intron_variant | MODIFIER | c.50-92T>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129421895 | |||||||
| chr3:129421925 | T | C | 1 | a0004c0004t0001g0190 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.50-122A>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129421925 | |||||||
| chr3:129421944 | G | A | 1 | a0002c0002t0001g0123 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.50-141C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129421944 | |||||||
| chr3:129421952 | A | G | 1 | a0014c0023t0004g0209 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.50-149T>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129421952 | |||||||
| chr3:129421999 | A | G | 9 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0136 others(6): Show |
11 | HG01069.hp1 HG01071.hp2 HG01515.hp1 others(8): Show |
intron_variant | MODIFIER | c.50-196T>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129421999 | |||||||
| chr3:129422060 | T | C | 23 | a0001c0007t0001g0041 a0001c0007t0001g0184 a0001c0007t0001g0199 others(20): Show |
34 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(31): Show |
intron_variant | MODIFIER | c.50-257A>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129422060 | |||||||
| chr3:129422156 | G | A | 1 | a0014c0023t0004g0209 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.50-353C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129422156 | |||||||
| chr3:129422183 | C | T | 1 | a0001c0001t0001g0053 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.50-380G>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129422183 | |||||||
| chr3:129422579 | C | T | 3 | a0008c0009t0001g0009 a0008c0009t0001g0049 a0008c0009t0001g0050 |
6 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.50-776G>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129422579 | |||||||
| chr3:129422617 | T | A | 1 | a0001c0001t0001g0073 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.50-814A>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129422617 | |||||||
| chr3:129422816 | T | A | 59 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(56): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.50-1013A>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129422816 | |||||||
| chr3:129422886 | T | C | 59 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(56): Show |
94 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.50-1083A>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129422886 | |||||||
| chr3:129422928 | A | G | 15 | a0005c0006t0001g0179 a0005c0006t0002g0021 a0005c0006t0002g0166 others(12): Show |
17 | HG01255.hp2 HG02055.hp2 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.50-1125T>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129422928 | |||||||
| chr3:129422957 | T | G | 2 | a0004c0004t0001g0185 a0004c0004t0001g0198 |
2 | HG00621.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.50-1154A>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129422957 | |||||||
| chr3:129423040 | T | C | 3 | a0008c0009t0001g0009 a0008c0009t0001g0049 a0008c0009t0001g0050 |
6 | HG02109.hp1 HG02280.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.50-1237A>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129423040 | |||||||
| chr3:129423043 | ACAGACCT others(32): Show |
A | 1 | a0001c0001t0001g0077 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.50-1279_50-1241del others(39): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129423043 | |||||||
| chr3:129423051 | A | G | 59 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(56): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.50-1248T>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129423051 | |||||||
| chr3:129423053 | G | A | 59 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(56): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.50-1250C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129423053 | |||||||
| chr3:129423321 | G | A | 59 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(56): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.50-1518C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129423321 | |||||||
| chr3:129423428 | G | A | 59 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(56): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.50-1625C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129423428 | |||||||
| chr3:129423428 | G | T | 31 | a0001c0007t0001g0041 a0001c0007t0001g0184 a0001c0007t0001g0199 others(28): Show |
51 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.50-1625C>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129423428 | |||||||
| chr3:129423456 | A | G | 2 | a0004c0004t0001g0045 a0004c0004t0001g0047 |
2 | HG01891.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.50-1653T>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129423456 | |||||||
| chr3:129423461 | T | C | 59 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(56): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.50-1658A>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129423461 | |||||||
| chr3:129423511 | G | A | 59 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(56): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.50-1708C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129423511 | |||||||
| chr3:129423535 | G | A | 1 | a0007c0008t0001g0008 | 6 | HG00280.hp1 HG00642.hp2 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.50-1732C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129423535 | |||||||
| chr3:129423568 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.50-1765G>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129423568 | |||||||
| chr3:129423587 | G | A | 2 | a0001c0007t0001g0205 a0001c0020t0001g0206 |
2 | HG00735.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.50-1784C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129423587 | |||||||
| chr3:129423610 | C | G | 1 | a0014c0023t0004g0209 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.50-1807G>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129423610 | |||||||
| chr3:129423633 | T | A | 59 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(56): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.50-1830A>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129423633 | |||||||
| chr3:129423634 | T | A | 59 | a0002c0002t0001g0002 a0002c0002t0001g0006 a0002c0002t0001g0012 others(56): Show |
95 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.50-1831A>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129423634 | |||||||
| chr3:129423806 | C | A | 13 | a0002c0002t0001g0023 a0002c0002t0001g0024 a0002c0002t0001g0040 others(10): Show |
16 | HG00544.hp2 HG01884.hp2 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.50-2003G>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129423806 | |||||||
| chr3:129423867 | C | A | 1 | a0001c0001t0001g0074 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.50-2064G>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129423867 | |||||||
| chr3:129423898 | T | C | 116 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0136 others(113): Show |
178 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(175): Show |
intron_variant | MODIFIER | c.50-2095A>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129423898 | |||||||
| chr3:129424046 | C | G | 4 | a0009c0010t0001g0034 a0009c0010t0001g0086 a0009c0010t0001g0131 others(1): Show |
5 | HG01109.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.50-2243G>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129424046 | |||||||
| chr3:129424108 | C | G | 28 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0136 others(25): Show |
32 | HG01069.hp1 HG01071.hp2 HG01255.hp2 others(29): Show |
intron_variant | MODIFIER | c.50-2305G>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129424108 | |||||||
| chr3:129424132 | A | ACTGTGTC others(15): Show |
4 | a0009c0010t0001g0034 a0009c0010t0001g0086 a0009c0010t0001g0131 others(1): Show |
5 | HG01109.hp2 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.50-2351_50-2330dup others(22): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129424132 | |||||||
| chr3:129424234 | G | T | 85 | a0001c0007t0001g0041 a0001c0007t0001g0184 a0001c0007t0001g0199 others(82): Show |
135 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(132): Show |
intron_variant | MODIFIER | c.50-2431C>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129424234 | |||||||
| chr3:129424248 | G | T | 120 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0136 others(117): Show |
183 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(180): Show |
intron_variant | MODIFIER | c.50-2445C>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129424248 | |||||||
| chr3:129424260 | T | C | 15 | a0005c0006t0001g0179 a0005c0006t0002g0021 a0005c0006t0002g0166 others(12): Show |
17 | HG01255.hp2 HG02055.hp2 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.50-2457A>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129424260 | |||||||
| chr3:129424309 | A | G | 27 | a0001c0001t0001g0165 a0001c0007t0001g0041 a0001c0007t0001g0184 others(24): Show |
41 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.50-2506T>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129424309 | |||||||
| chr3:129424466 | T | C | 19 | a0002c0002t0001g0023 a0002c0002t0001g0024 a0002c0002t0002g0046 others(16): Show |
23 | HG01255.hp2 HG02055.hp2 HG02083.hp2 others(20): Show |
intron_variant | MODIFIER | c.50-2663A>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129424466 | |||||||
| chr3:129424496 | A | G | 1 | a0005c0006t0002g0168 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.50-2693T>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129424496 | |||||||
| chr3:129424535 | C | T | 2 | a0002c0002t0001g0094 a0002c0002t0001g0095 |
2 | HG01070.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.50-2732G>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129424535 | |||||||
| chr3:129424653 | C | T | 1 | a0006c0005t0001g0167 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.50-2850G>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129424653 | |||||||
| chr3:129424674 | T | A | 62 | a0001c0001t0001g0011 a0001c0001t0001g0076 a0002c0002t0001g0002 others(59): Show |
108 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(105): Show |
intron_variant | MODIFIER | c.50-2871A>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129424674 | |||||||
| chr3:129424716 | G | A | 63 | a0001c0001t0001g0011 a0001c0001t0001g0076 a0002c0002t0001g0002 others(60): Show |
109 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(106): Show |
intron_variant | MODIFIER | c.50-2913C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129424716 | |||||||
| chr3:129424753 | T | C | 21 | a0001c0007t0001g0041 a0001c0007t0001g0184 a0001c0007t0001g0200 others(18): Show |
32 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.50-2950A>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129424753 | |||||||
| chr3:129424758 | G | A | 9 | a0002c0002t0001g0023 a0002c0002t0001g0024 a0002c0002t0001g0048 others(6): Show |
14 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.50-2955C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129424758 | |||||||
| chr3:129424760 | G | A | 9 | a0002c0002t0001g0023 a0002c0002t0001g0024 a0002c0002t0001g0048 others(6): Show |
14 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.50-2957C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129424760 | |||||||
| chr3:129424819 | G | A | 39 | a0001c0007t0001g0041 a0001c0007t0001g0184 a0001c0007t0001g0199 others(36): Show |
52 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.50-3016C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129424819 | |||||||
| chr3:129424865 | C | T | 21 | a0001c0007t0001g0041 a0001c0007t0001g0184 a0001c0007t0001g0199 others(18): Show |
32 | HG00140.hp1 HG00408.hp1 HG00621.hp2 others(29): Show |
intron_variant | MODIFIER | c.50-3062G>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129424865 | |||||||
| chr3:129424894 | G | T | 1 | a0014c0023t0004g0209 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.50-3091C>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129424894 | |||||||
| chr3:129424896 | G | T | 35 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0136 others(32): Show |
52 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.50-3093C>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129424896 | |||||||
| chr3:129425163 | C | T | 3 | a0009c0010t0001g0034 a0009c0010t0001g0086 a0009c0010t0001g0131 |
4 | HG01109.hp2 HG03209.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+3277G>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129425163 | |||||||
| chr3:129425238 | G | A | 6 | a0001c0001t0001g0090 a0001c0001t0001g0158 a0001c0001t0002g0020 others(3): Show |
8 | HG02559.hp1 HG02647.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.49+3202C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129425238 | |||||||
| chr3:129425348 | A | G | 9 | a0002c0002t0001g0023 a0002c0002t0001g0024 a0002c0002t0001g0048 others(6): Show |
14 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.49+3092T>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129425348 | |||||||
| chr3:129425377 | C | T | 6 | a0002c0002t0001g0023 a0002c0002t0001g0024 a0002c0002t0001g0048 others(3): Show |
8 | HG01891.hp2 HG02622.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.49+3063G>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129425377 | |||||||
| chr3:129425480 | G | A | 18 | a0001c0007t0001g0205 a0001c0020t0001g0206 a0005c0006t0001g0179 others(15): Show |
20 | HG00735.hp1 HG01255.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.49+2960C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129425480 | |||||||
| chr3:129425518 | G | GCACTGCA others(30): Show |
1 | a0001c0001t0001g0136 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.49+2885_49+2921dup others(37): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129425518 | |||||||
| chr3:129425621 | C | A | 1 | a0002c0002t0001g0128 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.49+2819G>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129425621 | |||||||
| chr3:129425684 | T | C | 1 | a0001c0001t0003g0222 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.49+2756A>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129425684 | |||||||
| chr3:129425804 | G | A | 1 | a0001c0001t0001g0016 | 3 | HG00323.hp1 HG03704.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.49+2636C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129425804 | |||||||
| chr3:129425862 | T | A | 18 | a0001c0007t0001g0205 a0001c0020t0001g0206 a0005c0006t0001g0179 others(15): Show |
20 | HG00735.hp1 HG01255.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.49+2578A>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129425862 | |||||||
| chr3:129425984 | C | T | 18 | a0001c0007t0001g0205 a0001c0020t0001g0206 a0005c0006t0001g0179 others(15): Show |
20 | HG00735.hp1 HG01255.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.49+2456G>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129425984 | |||||||
| chr3:129426349 | G | GT | 5 | a0001c0001t0001g0136 a0002c0002t0001g0023 a0002c0002t0002g0046 others(2): Show |
6 | HG02622.hp1 HG02922.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.49+2090dupA | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129426349 | |||||||
| chr3:129426358 | T | G | 1 | a0001c0001t0001g0001 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.49+2082A>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129426358 | |||||||
| chr3:129426359 | G | GT | 32 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0011 others(29): Show |
68 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.49+2080dupA | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129426359 | |||||||
| chr3:129426359 | G | GTT | 11 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0027 others(8): Show |
15 | HG02056.hp1 HG02109.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.49+2079_49+2080dup others(2): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129426359 | |||||||
| chr3:129426359 | G | T | 26 | a0001c0001t0001g0001 a0001c0001t0001g0051 a0001c0007t0001g0205 others(23): Show |
30 | HG00735.hp1 HG01109.hp1 HG01255.hp2 others(27): Show |
intron_variant | MODIFIER | c.49+2081C>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129426359 | |||||||
| chr3:129426359 | GT | G | 7 | a0001c0001t0001g0011 a0001c0007t0001g0184 a0003c0003t0002g0162 others(4): Show |
7 | HG01175.hp1 HG01891.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.49+2080delA | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129426359 | |||||||
| chr3:129426359 | GTT | G | 25 | a0001c0007t0001g0041 a0001c0007t0001g0199 a0001c0007t0001g0200 others(22): Show |
33 | HG00140.hp1 HG00408.hp1 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.49+2079_49+2080del others(2): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129426359 | |||||||
| chr3:129426360 | T | G | 18 | a0001c0007t0001g0205 a0001c0020t0001g0206 a0005c0006t0001g0179 others(15): Show |
20 | HG00735.hp1 HG01255.hp2 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.49+2080A>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129426360 | |||||||
| chr3:129426363 | T | G | 40 | a0001c0001t0001g0019 a0001c0001t0001g0035 a0001c0001t0001g0036 others(37): Show |
61 | HG00423.hp1 HG00621.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.49+2077A>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129426363 | |||||||
| chr3:129426364 | T | G | 1 | a0003c0003t0002g0162 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.49+2076A>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129426364 | |||||||
| chr3:129426366 | T | G | 19 | a0001c0001t0001g0165 a0001c0007t0001g0205 a0001c0020t0001g0206 others(16): Show |
21 | HG00735.hp1 HG01255.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.49+2074A>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129426366 | |||||||
| chr3:129426367 | T | G | 2 | a0003c0003t0002g0163 a0003c0003t0002g0164 |
2 | NA18962.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.49+2073A>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129426367 | |||||||
| chr3:129426368 | T | G | 4 | a0001c0001t0003g0013 a0001c0001t0003g0043 a0001c0001t0003g0223 others(1): Show |
8 | HG01123.hp1 HG01934.hp1 HG01943.hp1 others(5): Show |
intron_variant | MODIFIER | c.49+2072A>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129426368 | |||||||
| chr3:129426370 | T | TG | 53 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0007t0001g0091 others(50): Show |
95 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.49+2069_49+2070ins others(1): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129426370 | |||||||
| chr3:129426372 | T | G | 2 | a0001c0007t0001g0205 a0001c0020t0001g0206 |
2 | HG00735.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.49+2068A>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129426372 | |||||||
| chr3:129426434 | G | A | 1 | a0001c0001t0001g0051 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.49+2006C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129426434 | |||||||
| chr3:129426460 | G | T | 1 | a0006c0005t0001g0085 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.49+1980C>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129426460 | |||||||
| chr3:129426508 | G | C | 1 | a0016c0019t0001g0129 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.49+1932C>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129426508 | |||||||
| chr3:129426643 | C | T | 1 | a0002c0002t0001g0084 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.49+1797G>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129426643 | |||||||
| chr3:129426655 | C | A | 1 | a0001c0020t0001g0206 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.49+1785G>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129426655 | |||||||
| chr3:129426689 | T | TTAATTGA others(32): Show |
1 | a0001c0001t0001g0077 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.49+1712_49+1750dup others(39): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129426689 | |||||||
| chr3:129426696 | A | C | 6 | a0002c0002t0001g0023 a0002c0002t0001g0024 a0002c0002t0001g0048 others(3): Show |
8 | HG01891.hp2 HG02622.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.49+1744T>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129426696 | |||||||
| chr3:129426770 | G | A | 164 | a0001c0001t0001g0019 a0001c0001t0001g0035 a0001c0001t0001g0036 others(161): Show |
247 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(244): Show |
intron_variant | MODIFIER | c.49+1670C>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129426770 | |||||||
| chr3:129426774 | T | C | 1 | a0004c0004t0001g0198 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.49+1666A>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129426774 | |||||||
| chr3:129426845 | C | CT | 92 | a0001c0001t0001g0014 a0001c0001t0001g0051 a0001c0001t0001g0087 others(89): Show |
152 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(149): Show |
intron_variant | MODIFIER | c.49+1594dupA | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129426845 | |||||||
| chr3:129426845 | C | CTT | 7 | a0001c0001t0001g0080 a0002c0002t0001g0082 a0004c0004t0001g0183 others(4): Show |
7 | HG02145.hp1 HG02486.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.49+1593_49+1594dup others(2): Show |
EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129426845 | |||||||
| chr3:129426961 | C | A | 1 | a0001c0001t0003g0044 | 2 | HG00639.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.49+1479G>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129426961 | |||||||
| chr3:129427037 | C | T | 1 | a0003c0003t0002g0079 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.49+1403G>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129427037 | |||||||
| chr3:129427248 | C | G | 1 | a0003c0003t0002g0078 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.49+1192G>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129427248 | |||||||
| chr3:129427274 | G | T | 1 | a0001c0007t0001g0205 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.49+1166C>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129427274 | |||||||
| chr3:129427304 | T | G | 1 | a0001c0001t0001g0165 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.49+1136A>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129427304 | |||||||
| chr3:129427365 | C | G | 29 | a0001c0007t0001g0041 a0001c0007t0001g0184 a0001c0007t0001g0199 others(26): Show |
41 | HG00140.hp1 HG00408.hp1 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.49+1075G>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129427365 | |||||||
| chr3:129427372 | C | T | 16 | a0005c0006t0001g0179 a0005c0006t0002g0021 a0005c0006t0002g0166 others(13): Show |
18 | HG01255.hp2 HG02055.hp2 HG02083.hp2 others(15): Show |
intron_variant | MODIFIER | c.49+1068G>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129427372 | |||||||
| chr3:129427378 | CT | C | 164 | a0001c0001t0001g0019 a0001c0001t0001g0035 a0001c0001t0001g0036 others(161): Show |
247 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(244): Show |
intron_variant | MODIFIER | c.49+1061delA | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129427378 | |||||||
| chr3:129427401 | C | T | 9 | a0002c0002t0001g0023 a0002c0002t0001g0024 a0002c0002t0001g0048 others(6): Show |
14 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.49+1039G>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129427401 | |||||||
| chr3:129427448 | C | T | 1 | a0005c0006t0002g0166 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.49+992G>A | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129427448 | |||||||
| chr3:129427610 | C | A | 47 | a0001c0007t0001g0041 a0001c0007t0001g0184 a0001c0007t0001g0199 others(44): Show |
61 | HG00140.hp1 HG00408.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.49+830G>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129427610 | |||||||
| chr3:129427803 | T | G | 47 | a0001c0007t0001g0041 a0001c0007t0001g0184 a0001c0007t0001g0199 others(44): Show |
61 | HG00140.hp1 HG00408.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.49+637A>C | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129427803 | |||||||
| chr3:129428044 | T | C | 47 | a0001c0007t0001g0041 a0001c0007t0001g0184 a0001c0007t0001g0199 others(44): Show |
61 | HG00140.hp1 HG00408.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.49+396A>G | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129428044 | |||||||
| chr3:129428347 | C | A | 2 | a0001c0001t0001g0207 a0001c0001t0001g0208 |
2 | HG02572.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.49+93G>T | EFCAB12 | ENSG00000172771.13 | transcript | ENST00000505956.6 | protein_coding | 1/8 | chr3 | 129428347 |