Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 84455 |
| ensemblid | ENSG00000203965.13 |
| hgncid | 29379 |
| symbol | EFCAB7 |
| name | EF-hand calcium binding domain 7 |
| refseq_nuc | NM_032437.4 |
| refseq_prot | NP_115813.2 |
| ensembl_nuc | ENST00000371088.5 |
| ensembl_prot | ENSP00000360129.4 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 63523525 |
| end | 63572693 |
| strand | + |
| ver | v1.2 |
| region | chr1:63523525-63572693 |
| region5000 | chr1:63518525-63577693 |
| regionname0 | EFCAB7_chr1_63523525_63572693 |
| regionname5000 | EFCAB7_chr1_63518525_63577693 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 629 | 234 | 27 | 54 | 121 | 5 | 25 | 91 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | MAISP others(624): Show |
chr1 | 63518525 | 63577693 |
| a0002 | 0/0 | 629 | 66 | 5 | 15 | 38 | 1 | 7 | 33 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | MAISP others(624): Show |
chr1 | 63518525 | 63577693 |
| a0003 | 0/0 | 629 | 39 | 30 | 3 | 3 | 0 | 3 | 3 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | MAISP others(624): Show |
chr1 | 63518525 | 63577693 |
| a0004 | 0/0 | 629 | 9 | 7 | 2 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | MAISP others(624): Show |
chr1 | 63518525 | 63577693 |
| a0005 | 0/0 | 629 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | MAISP others(624): Show |
chr1 | 63518525 | 63577693 |
| a0006 | 0/0 | 629 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | MAISP others(624): Show |
chr1 | 63518525 | 63577693 |
| a0007 | 0/0 | 629 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | MAISP others(624): Show |
chr1 | 63518525 | 63577693 |
| a0008 | 0/0 | 629 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | MAISP others(624): Show |
chr1 | 63518525 | 63577693 |
| a0009 | 0/0 | 629 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | MAISP others(624): Show |
chr1 | 63518525 | 63577693 |
| a0010 | 0/0 | 629 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | MAISP others(624): Show |
chr1 | 63518525 | 63577693 |
| a0011 | 0/0 | 629 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | MAISP others(624): Show |
chr1 | 63518525 | 63577693 |
| a0012 | 0/0 | 629 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | MAISP others(624): Show |
chr1 | 63518525 | 63577693 |
| a0013 | 0/0 | 629 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | MAISP others(624): Show |
chr1 | 63518525 | 63577693 |
| a0014 | 0/0 | 629 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | MAISP others(624): Show |
chr1 | 63518525 | 63577693 |
| a0015 | 0/0 | 629 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | MAISP others(624): Show |
chr1 | 63518525 | 63577693 |
| a0016 | 0/0 | 629 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | MAISP others(624): Show |
chr1 | 63518525 | 63577693 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1887 | 119 | 11 | 23 | 71 | 3 | 9 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | ATGGC others(1882): Show |
chr1 | 63518525 | 63577693 | ||
| a0001c0002 | 0/0 | 1887 | 111 | 16 | 31 | 46 | 2 | 16 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | ATGGC others(1882): Show |
chr1 | 63518525 | 63577693 | ||
| a0001c0009 | 0/0 | 1887 | 4 | 0 | 0 | 4 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | ATGGC others(1882): Show |
chr1 | 63518525 | 63577693 | ||
| a0002c0003 | 0/0 | 1887 | 66 | 5 | 15 | 38 | 1 | 7 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | ATGGC others(1882): Show |
chr1 | 63518525 | 63577693 | ||
| a0003c0004 | 0/0 | 1887 | 26 | 23 | 3 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | ATGGC others(1882): Show |
chr1 | 63518525 | 63577693 | ||
| a0003c0005 | 0/0 | 1887 | 13 | 7 | 0 | 3 | 0 | 3 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | ATGGC others(1882): Show |
chr1 | 63518525 | 63577693 | ||
| a0004c0006 | 0/0 | 1887 | 9 | 7 | 2 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | ATGGC others(1882): Show |
chr1 | 63518525 | 63577693 | ||
| a0005c0007 | 0/0 | 1887 | 6 | 5 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | ATGGC others(1882): Show |
chr1 | 63518525 | 63577693 | ||
| a0006c0008 | 0/0 | 1887 | 5 | 5 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | ATGGC others(1882): Show |
chr1 | 63518525 | 63577693 | ||
| a0007c0010 | 0/0 | 1887 | 4 | 4 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | ATGGC others(1882): Show |
chr1 | 63518525 | 63577693 | ||
| a0008c0011 | 0/0 | 1887 | 3 | 0 | 0 | 3 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | ATGGC others(1882): Show |
chr1 | 63518525 | 63577693 | ||
| a0009c0016 | 0/0 | 1887 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | ATGGC others(1882): Show |
chr1 | 63518525 | 63577693 | ||
| a0010c0017 | 0/0 | 1887 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | ATGGC others(1882): Show |
chr1 | 63518525 | 63577693 | ||
| a0011c0014 | 0/0 | 1887 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | ATGGC others(1882): Show |
chr1 | 63518525 | 63577693 | ||
| a0012c0012 | 0/0 | 1887 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | ATGGC others(1882): Show |
chr1 | 63518525 | 63577693 | ||
| a0013c0013 | 0/0 | 1887 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | ATGGC others(1882): Show |
chr1 | 63518525 | 63577693 | ||
| a0014c0019 | 0/0 | 1887 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | ATGGC others(1882): Show |
chr1 | 63518525 | 63577693 | ||
| a0015c0018 | 0/0 | 1887 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | ATGGC others(1882): Show |
chr1 | 63518525 | 63577693 | ||
| a0016c0015 | 0/0 | 1887 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | ATGGC others(1882): Show |
chr1 | 63518525 | 63577693 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2177 | 114 | 9 | 23 | 68 | 3 | 9 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | AGTTG others(2172): Show |
chr1 | 63518525 | 63577693 |
| a0001c0001t0002 | 0/0 | 2177 | 3 | 0 | 0 | 3 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | AGTTG others(2172): Show |
chr1 | 63518525 | 63577693 |
| a0001c0001t0003 | 0/0 | 2177 | 2 | 2 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | AGTTG others(2172): Show |
chr1 | 63518525 | 63577693 |
| a0001c0002t0001 | 0/0 | 2177 | 111 | 16 | 31 | 46 | 2 | 16 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | AGTTG others(2172): Show |
chr1 | 63518525 | 63577693 |
| a0001c0009t0001 | 0/0 | 2177 | 4 | 0 | 0 | 4 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | AGTTG others(2172): Show |
chr1 | 63518525 | 63577693 |
| a0002c0003t0001 | 0/0 | 2177 | 66 | 5 | 15 | 38 | 1 | 7 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | AGTTG others(2172): Show |
chr1 | 63518525 | 63577693 |
| a0003c0004t0001 | 0/0 | 2177 | 26 | 23 | 3 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | AGTTG others(2172): Show |
chr1 | 63518525 | 63577693 |
| a0003c0005t0001 | 0/0 | 2177 | 13 | 7 | 0 | 3 | 0 | 3 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | AGTTG others(2172): Show |
chr1 | 63518525 | 63577693 |
| a0004c0006t0001 | 0/0 | 2177 | 9 | 7 | 2 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | AGTTG others(2172): Show |
chr1 | 63518525 | 63577693 |
| a0005c0007t0001 | 0/0 | 2177 | 6 | 5 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | AGTTG others(2172): Show |
chr1 | 63518525 | 63577693 |
| a0006c0008t0001 | 0/0 | 2177 | 5 | 5 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | AGTTG others(2172): Show |
chr1 | 63518525 | 63577693 |
| a0007c0010t0001 | 0/0 | 2177 | 4 | 4 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | AGTTG others(2172): Show |
chr1 | 63518525 | 63577693 |
| a0008c0011t0001 | 0/0 | 2177 | 3 | 0 | 0 | 3 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | AGTTG others(2172): Show |
chr1 | 63518525 | 63577693 |
| a0009c0016t0001 | 0/0 | 2177 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | AGTTG others(2172): Show |
chr1 | 63518525 | 63577693 |
| a0010c0017t0001 | 0/0 | 2177 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | AGTTG others(2172): Show |
chr1 | 63518525 | 63577693 |
| a0011c0014t0001 | 0/0 | 2177 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | AGTTG others(2172): Show |
chr1 | 63518525 | 63577693 |
| a0012c0012t0001 | 0/0 | 2177 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | AGTTG others(2172): Show |
chr1 | 63518525 | 63577693 |
| a0013c0013t0001 | 0/0 | 2177 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | AGTTG others(2172): Show |
chr1 | 63518525 | 63577693 |
| a0014c0019t0001 | 0/0 | 2177 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | AGTTG others(2172): Show |
chr1 | 63518525 | 63577693 |
| a0015c0018t0001 | 0/0 | 2177 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | AGTTG others(2172): Show |
chr1 | 63518525 | 63577693 |
| a0016c0015t0001 | 0/0 | 2177 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | AGTTG others(2172): Show |
chr1 | 63518525 | 63577693 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 15 | 0 | 0 | 13 | 1 | 1 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0003 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 3 | 0 | 2 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0025 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0172 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0001g0229 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0001t0003g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0004 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0005 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0008 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0010 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0011 | 0/0 | 3 | 0 | 0 | 1 | 2 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0012 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0022 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0009t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0009t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0009t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0001c0009t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0002c0003t0001g0002 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0002c0003t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0002c0003t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0002c0003t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0002c0003t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0002c0003t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0002c0003t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0002c0003t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0002c0003t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0002c0003t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0002c0003t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0002c0003t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0002c0003t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0002c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0002c0003t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0002c0003t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0002c0003t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0002c0003t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0002c0003t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0002c0003t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0002c0003t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0002c0003t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0002c0003t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0002c0003t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0002c0003t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0002c0003t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0002c0003t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0002c0003t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0002c0003t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0002c0003t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0002c0003t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0002c0003t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0002c0003t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0002c0003t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0002c0003t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0002c0003t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0002c0003t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0002c0003t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0002c0003t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0002c0003t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0002c0003t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0002c0003t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0002c0003t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0002c0003t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0002c0003t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0002c0003t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0002c0003t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0002c0003t0001g0277 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0003c0004t0001g0006 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0003c0004t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0003c0004t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0003c0004t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0003c0004t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0003c0004t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0003c0004t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0003c0004t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0003c0004t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0003c0004t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0003c0004t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0003c0004t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0003c0004t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0003c0004t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0003c0004t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0003c0004t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0003c0004t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0003c0004t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0003c0004t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0003c0004t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0003c0004t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0003c0004t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0003c0005t0001g0029 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0003c0005t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0003c0005t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0003c0005t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0003c0005t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0003c0005t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0003c0005t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0003c0005t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0003c0005t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0003c0005t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0003c0005t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0003c0005t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0004c0006t0001g0009 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0004c0006t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0004c0006t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0004c0006t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0004c0006t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0004c0006t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0004c0006t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0005c0007t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0005c0007t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0005c0007t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0005c0007t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0005c0007t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0006c0008t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0006c0008t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0006c0008t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0006c0008t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0006c0008t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0007c0010t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0007c0010t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0007c0010t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0008c0011t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0008c0011t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0008c0011t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0009c0016t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0010c0017t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0011c0014t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0012c0012t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0013c0013t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0014c0019t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0015c0018t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| a0016c0015t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0141 | EAS | CHS | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0075 | EAS | CHS | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG00438 | hp2 | a0009 | c0016 | t0001 | g0016 | EAS | CHS | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG00558 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | CHS | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | CHS | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0069 | AMR | PUR | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | CHS | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG00673 | hp2 | a0001 | c0009 | t0001 | g0082 | EAS | CHS | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG00733 | hp1 | a0002 | c0003 | t0001 | g0253 | AMR | PUR | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0122 | AMR | PUR | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG00735 | hp1 | a0001 | c0002 | t0001 | g0104 | AMR | PUR | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG00735 | hp2 | a0001 | c0002 | t0001 | g0078 | AMR | PUR | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG00738 | hp2 | a0004 | c0006 | t0001 | g0174 | AMR | PUR | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG00741 | hp2 | a0002 | c0003 | t0001 | g0234 | AMR | PUR | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01069 | hp1 | a0002 | c0003 | t0001 | g0254 | AMR | PUR | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0080 | AMR | PUR | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01071 | hp1 | a0002 | c0003 | t0001 | g0252 | AMR | PUR | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01074 | hp1 | a0001 | c0002 | t0001 | g0022 | AMR | PUR | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01074 | hp2 | a0002 | c0003 | t0001 | g0040 | AMR | PUR | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01081 | hp1 | a0002 | c0003 | t0001 | g0040 | AMR | PUR | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01081 | hp2 | a0003 | c0004 | t0001 | g0183 | AMR | PUR | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0137 | AMR | PUR | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0119 | AMR | PUR | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01109 | hp2 | a0003 | c0004 | t0001 | g0182 | AMR | PUR | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01167 | hp2 | a0003 | c0004 | t0001 | g0006 | AMR | PUR | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01168 | hp2 | a0002 | c0003 | t0001 | g0271 | AMR | PUR | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01169 | hp1 | a0002 | c0003 | t0001 | g0270 | AMR | PUR | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01175 | hp1 | a0002 | c0003 | t0001 | g0269 | AMR | PUR | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01192 | hp1 | a0005 | c0007 | t0001 | g0191 | AMR | PUR | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01192 | hp2 | a0001 | c0002 | t0001 | g0129 | AMR | PUR | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01243 | hp2 | a0010 | c0017 | t0001 | g0274 | AMR | PUR | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0140 | AMR | CLM | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01256 | hp1 | a0002 | c0003 | t0001 | g0236 | AMR | CLM | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0135 | AMR | CLM | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0136 | AMR | CLM | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01261 | hp1 | a0001 | c0002 | t0001 | g0051 | AMR | CLM | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01358 | hp1 | a0002 | c0003 | t0001 | g0265 | AMR | CLM | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01358 | hp2 | a0001 | c0002 | t0001 | g0021 | AMR | CLM | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0099 | AMR | CLM | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0068 | AMR | CLM | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | CLM | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0011 | EUR | IBS | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0011 | EUR | IBS | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01884 | hp1 | a0002 | c0003 | t0001 | g0276 | AFR | ACB | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0079 | AFR | ACB | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01891 | hp1 | a0007 | c0010 | t0001 | g0228 | AFR | ACB | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0067 | AFR | ACB | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | PEL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01928 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | PEL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01934 | hp1 | a0004 | c0006 | t0001 | g0009 | AMR | PEL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0101 | AMR | PEL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | PEL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01943 | hp2 | a0001 | c0002 | t0001 | g0102 | AMR | PEL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | PEL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01978 | hp1 | a0002 | c0003 | t0001 | g0267 | AMR | PEL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0113 | AMR | PEL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0086 | AMR | PEL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01981 | hp2 | a0002 | c0003 | t0001 | g0264 | AMR | PEL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01993 | hp2 | a0001 | c0002 | t0001 | g0021 | AMR | PEL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0124 | AMR | PEL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02015 | hp1 | a0002 | c0003 | t0001 | g0258 | EAS | KHV | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0012 | EAS | KHV | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0111 | EAS | KHV | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02055 | hp1 | a0003 | c0004 | t0001 | g0180 | AFR | ACB | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0093 | EAS | KHV | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02071 | hp1 | a0001 | c0009 | t0001 | g0084 | EAS | KHV | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02071 | hp2 | a0002 | c0003 | t0001 | g0257 | EAS | KHV | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02080 | hp1 | a0001 | c0002 | t0001 | g0090 | EAS | KHV | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0095 | EAS | KHV | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0116 | EAS | KHV | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02145 | hp1 | a0002 | c0003 | t0001 | g0235 | AFR | ACB | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02145 | hp2 | a0003 | c0004 | t0001 | g0058 | AFR | ACB | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02155 | hp2 | a0001 | c0002 | t0001 | g0185 | EAS | CDX | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02165 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | CDX | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | CDX | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02257 | hp1 | a0002 | c0003 | t0001 | g0244 | AFR | ACB | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02257 | hp2 | a0004 | c0006 | t0001 | g0044 | AFR | ACB | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02258 | hp1 | a0003 | c0004 | t0001 | g0176 | AFR | ACB | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02258 | hp2 | a0001 | c0002 | t0001 | g0070 | AFR | ACB | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02280 | hp1 | a0006 | c0008 | t0001 | g0187 | AFR | ACB | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02293 | hp1 | a0002 | c0003 | t0001 | g0263 | AMR | PEL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02293 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | PEL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02300 | hp1 | a0002 | c0003 | t0001 | g0266 | AMR | PEL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02300 | hp2 | a0001 | c0002 | t0001 | g0117 | AMR | PEL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0004 | AFR | ACB | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02451 | hp2 | a0004 | c0006 | t0001 | g0041 | AFR | ACB | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02523 | hp1 | a0002 | c0003 | t0001 | g0259 | EAS | KHV | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | KHV | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02572 | hp1 | a0006 | c0008 | t0001 | g0045 | AFR | GWD | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02572 | hp2 | a0003 | c0005 | t0001 | g0193 | AFR | GWD | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02602 | hp1 | a0012 | c0012 | t0001 | g0106 | SAS | PJL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0120 | SAS | PJL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02615 | hp1 | a0003 | c0004 | t0001 | g0006 | AFR | GWD | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02615 | hp2 | a0007 | c0010 | t0001 | g0034 | AFR | GWD | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02622 | hp1 | a0003 | c0005 | t0001 | g0052 | AFR | GWD | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02622 | hp2 | a0005 | c0007 | t0001 | g0030 | AFR | GWD | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02647 | hp1 | a0003 | c0004 | t0001 | g0064 | AFR | GWD | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02647 | hp2 | a0005 | c0007 | t0001 | g0190 | AFR | GWD | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02683 | hp1 | a0001 | c0002 | t0001 | g0123 | SAS | PJL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0133 | SAS | PJL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02698 | hp1 | a0001 | c0002 | t0001 | g0131 | SAS | PJL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02698 | hp2 | a0001 | c0002 | t0001 | g0275 | SAS | PJL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02717 | hp2 | a0005 | c0007 | t0001 | g0188 | AFR | GWD | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02723 | hp1 | a0001 | c0002 | t0001 | g0004 | AFR | GWD | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02723 | hp2 | a0003 | c0004 | t0001 | g0179 | AFR | GWD | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02738 | hp1 | a0002 | c0003 | t0001 | g0268 | SAS | PJL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0128 | AFR | GWD | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02809 | hp2 | a0013 | c0013 | t0001 | g0256 | AFR | GWD | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02886 | hp1 | a0006 | c0008 | t0001 | g0047 | AFR | GWD | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02886 | hp2 | a0003 | c0005 | t0001 | g0194 | AFR | GWD | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0050 | AFR | GWD | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02895 | hp2 | a0003 | c0004 | t0001 | g0056 | AFR | GWD | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02896 | hp1 | a0003 | c0004 | t0001 | g0175 | AFR | GWD | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02896 | hp2 | a0003 | c0004 | t0001 | g0059 | AFR | GWD | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02897 | hp1 | a0003 | c0004 | t0001 | g0061 | AFR | GWD | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02897 | hp2 | a0003 | c0004 | t0001 | g0055 | AFR | GWD | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | ESN | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02922 | hp2 | a0003 | c0004 | t0001 | g0062 | AFR | ESN | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0004 | AFR | ESN | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02965 | hp2 | a0007 | c0010 | t0001 | g0230 | AFR | ESN | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0004 | AFR | ESN | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02970 | hp2 | a0004 | c0006 | t0001 | g0009 | AFR | ESN | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02976 | hp1 | a0003 | c0004 | t0001 | g0006 | AFR | ESN | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02976 | hp2 | a0003 | c0005 | t0001 | g0186 | AFR | ESN | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0012 | SAS | PJL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG03017 | hp2 | a0001 | c0002 | t0001 | g0091 | SAS | PJL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG03041 | hp1 | a0004 | c0006 | t0001 | g0173 | AFR | GWD | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0004 | AFR | GWD | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG03098 | hp1 | a0004 | c0006 | t0001 | g0043 | AFR | MSL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG03098 | hp2 | a0014 | c0019 | t0001 | g0066 | AFR | MSL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0004 | AFR | ESN | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG03130 | hp2 | a0006 | c0008 | t0001 | g0048 | AFR | ESN | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG03139 | hp1 | a0015 | c0018 | t0001 | g0273 | AFR | ESN | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG03139 | hp2 | a0001 | c0002 | t0001 | g0004 | AFR | ESN | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG03195 | hp1 | a0003 | c0004 | t0001 | g0057 | AFR | ESN | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | ESN | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG03209 | hp1 | a0006 | c0008 | t0001 | g0046 | AFR | MSL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG03209 | hp2 | a0003 | c0005 | t0001 | g0054 | AFR | MSL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG03225 | hp1 | a0003 | c0004 | t0001 | g0006 | AFR | MSL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG03225 | hp2 | a0003 | c0004 | t0001 | g0181 | AFR | MSL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG03453 | hp1 | a0003 | c0005 | t0001 | g0053 | AFR | MSL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG03453 | hp2 | a0003 | c0004 | t0001 | g0060 | AFR | MSL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG03486 | hp1 | a0003 | c0004 | t0001 | g0177 | AFR | MSL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG03486 | hp2 | a0003 | c0004 | t0001 | g0063 | AFR | MSL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG03490 | hp2 | a0001 | c0002 | t0001 | g0024 | SAS | PJL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG03491 | hp1 | a0002 | c0003 | t0001 | g0035 | SAS | PJL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG03492 | hp1 | a0002 | c0003 | t0001 | g0035 | SAS | PJL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0024 | SAS | PJL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0134 | AFR | ESN | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG03540 | hp1 | a0002 | c0003 | t0001 | g0272 | AFR | GWD | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG03540 | hp2 | a0004 | c0006 | t0001 | g0009 | AFR | GWD | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG03579 | hp1 | a0003 | c0004 | t0001 | g0178 | AFR | MSL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG03579 | hp2 | a0007 | c0010 | t0001 | g0034 | AFR | MSL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG03669 | hp1 | a0002 | c0003 | t0001 | g0251 | SAS | PJL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG03669 | hp2 | a0003 | c0005 | t0001 | g0168 | SAS | PJL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG03688 | hp1 | a0003 | c0005 | t0001 | g0170 | SAS | STU | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | STU | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG03704 | hp1 | a0002 | c0003 | t0001 | g0246 | SAS | PJL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0098 | SAS | PJL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG03710 | hp2 | a0001 | c0002 | t0001 | g0010 | SAS | PJL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0094 | SAS | BEB | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | BEB | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0115 | SAS | BEB | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG03834 | hp2 | a0002 | c0003 | t0001 | g0237 | SAS | BEB | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG03927 | hp1 | a0003 | c0005 | t0001 | g0029 | SAS | BEB | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0022 | SAS | BEB | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | STU | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | STU | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG04199 | hp1 | a0002 | c0003 | t0001 | g0243 | SAS | STU | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0008 | SAS | STU | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0023 | AFR | YRI | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | YRI | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CHB | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHB | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18747 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | CHB | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0130 | AFR | YRI | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | YRI | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18939 | hp1 | a0002 | c0003 | t0001 | g0261 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18940 | hp2 | a0002 | c0003 | t0001 | g0241 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18941 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0231 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0105 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18948 | hp2 | a0001 | c0009 | t0001 | g0008 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18951 | hp2 | a0002 | c0003 | t0001 | g0245 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18952 | hp2 | a0002 | c0003 | t0001 | g0039 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18957 | hp1 | a0002 | c0003 | t0001 | g0260 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18959 | hp1 | a0002 | c0003 | t0001 | g0250 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18959 | hp2 | a0001 | c0002 | t0001 | g0109 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18961 | hp1 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18963 | hp1 | a0002 | c0003 | t0001 | g0039 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18964 | hp1 | a0002 | c0003 | t0001 | g0248 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18964 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18966 | hp2 | a0002 | c0003 | t0001 | g0255 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18969 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18971 | hp1 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18973 | hp1 | a0002 | c0003 | t0001 | g0036 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0127 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18979 | hp1 | a0002 | c0003 | t0001 | g0038 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18980 | hp2 | a0002 | c0003 | t0001 | g0018 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18981 | hp1 | a0002 | c0003 | t0001 | g0240 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18981 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18983 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18984 | hp2 | a0001 | c0002 | t0001 | g0087 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0126 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18989 | hp1 | a0002 | c0003 | t0001 | g0238 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18989 | hp2 | a0003 | c0005 | t0001 | g0029 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18990 | hp1 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18990 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18991 | hp1 | a0002 | c0003 | t0001 | g0018 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18995 | hp2 | a0002 | c0003 | t0001 | g0247 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18997 | hp1 | a0002 | c0003 | t0001 | g0239 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA18997 | hp2 | a0003 | c0005 | t0001 | g0195 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19000 | hp2 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19001 | hp1 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19002 | hp1 | a0001 | c0009 | t0001 | g0103 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19002 | hp2 | a0002 | c0003 | t0001 | g0036 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19003 | hp1 | a0008 | c0011 | t0001 | g0085 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19004 | hp1 | a0003 | c0005 | t0001 | g0169 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19006 | hp1 | a0008 | c0011 | t0001 | g0108 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0089 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19007 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19010 | hp2 | a0008 | c0011 | t0001 | g0100 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19011 | hp1 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19012 | hp2 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19043 | hp1 | a0003 | c0004 | t0001 | g0184 | AFR | LWK | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19043 | hp2 | a0005 | c0007 | t0001 | g0030 | AFR | LWK | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19056 | hp1 | a0002 | c0003 | t0001 | g0249 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19057 | hp1 | a0002 | c0003 | t0001 | g0262 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19058 | hp2 | a0001 | c0002 | t0001 | g0020 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19063 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19065 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19072 | hp2 | a0001 | c0002 | t0001 | g0121 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19074 | hp1 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19076 | hp1 | a0002 | c0003 | t0001 | g0038 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19076 | hp2 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19077 | hp1 | a0002 | c0003 | t0001 | g0018 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19080 | hp1 | a0002 | c0003 | t0001 | g0037 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19082 | hp2 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19086 | hp1 | a0001 | c0002 | t0001 | g0139 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19086 | hp2 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19087 | hp1 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19088 | hp2 | a0001 | c0002 | t0001 | g0232 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19090 | hp2 | a0002 | c0003 | t0001 | g0037 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19091 | hp1 | a0002 | c0003 | t0001 | g0002 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA19091 | hp2 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0072 | AFR | ASW | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ASW | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA20805 | hp1 | a0002 | c0003 | t0001 | g0277 | EUR | TSI | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | TSI | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA20905 | hp1 | a0001 | c0002 | t0001 | g0132 | SAS | GIH | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | GIH | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0071 | AMR | CLM | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0112 | AMR | CLM | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0081 | AFR | ACB | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02109 | hp2 | a0011 | c0014 | t0001 | g0027 | AFR | ACB | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02559 | hp1 | a0004 | c0006 | t0001 | g0042 | AFR | ACB | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG02559 | hp2 | a0003 | c0004 | t0001 | g0065 | AFR | ACB | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG03471 | hp1 | a0003 | c0004 | t0001 | g0006 | AFR | MSL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | MSL | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG06807 | hp1 | a0003 | c0005 | t0001 | g0192 | AFR | USA | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| HG06807 | hp2 | a0002 | c0003 | t0001 | g0242 | AFR | USA | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA20300 | hp1 | a0005 | c0007 | t0001 | g0189 | AFR | USA | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| NA20300 | hp2 | a0016 | c0015 | t0001 | g0152 | AFR | USA | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0172 | REF | REF | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0229 | REF | REF | EFCAB7_chr1_63518525_63577693 | EFCAB7 | chr1 | 63518525 | 63577693 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:63525651 | T | A | 1 | a0006 | 5 | HG02280.hp1 HG02572.hp1 HG02886.hp1 others(2): Show |
missense_variant | MODERATE | c.79T>A | p.Phe27Ile | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/14 | 190/2178 | 79/1890 | 27/629 | chr1 | 63525651 | |||
| chr1:63525708 | G | A | 1 | a0013 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.136G>A | p.Val46Ile | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/14 | 247/2178 | 136/1890 | 46/629 | chr1 | 63525708 | |||
| chr1:63532692 | A | T | 1 | a0009 | 1 | HG00438.hp2 | missense_variant | MODERATE | c.422A>T | p.Glu141Val | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 4/14 | 533/2178 | 422/1890 | 141/629 | chr1 | 63532692 | |||
| chr1:63533523 | A | G | 1 | a0007 | 4 | HG01891.hp1 HG02615.hp2 HG02965.hp2 others(1): Show |
missense_variant | MODERATE | c.556A>G | p.Ser186Gly | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 5/14 | 667/2178 | 556/1890 | 186/629 | chr1 | 63533523 | |||
| chr1:63533587 | C | T | 1 | a0014 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.620C>T | p.Pro207Leu | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 5/14 | 731/2178 | 620/1890 | 207/629 | chr1 | 63533587 | |||
| chr1:63534155 | C | T | 4 | a0002 a0010 a0013 others(1): Show |
69 | HG00558.hp1 HG00733.hp1 HG00741.hp2 others(66): Show |
missense_variant | MODERATE | c.743C>T | p.Thr248Ile | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/14 | 854/2178 | 743/1890 | 248/629 | chr1 | 63534155 | |||
| chr1:63534197 | T | C | 10 | a0002 a0003 a0004 others(7): Show |
133 | HG00558.hp1 HG00733.hp1 HG00738.hp2 others(130): Show |
missense_variant | MODERATE | c.785T>C | p.Met262Thr | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/14 | 896/2178 | 785/1890 | 262/629 | chr1 | 63534197 | |||
| chr1:63545922 | C | A | 1 | a0008 | 3 | NA19003.hp1 NA19006.hp1 NA19010.hp2 |
missense_variant | MODERATE | c.811C>A | p.Gln271Lys | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/14 | 922/2178 | 811/1890 | 271/629 | chr1 | 63545922 | |||
| chr1:63545986 | A | G | 1 | a0016 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.875A>G | p.Tyr292Cys | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/14 | 986/2178 | 875/1890 | 292/629 | chr1 | 63545986 | |||
| chr1:63551748 | G | A | 1 | a0011 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.970G>A | p.Val324Ile | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 8/14 | 1081/2178 | 970/1890 | 324/629 | chr1 | 63551748 | |||
| chr1:63551757 | G | T | 1 | a0012 | 1 | HG02602.hp1 | missense_variant | MODERATE | c.979G>T | p.Ala327Ser | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 8/14 | 1090/2178 | 979/1890 | 327/629 | chr1 | 63551757 | |||
| chr1:63555425 | G | A | 2 | a0002 a0013 |
67 | HG00558.hp1 HG00733.hp1 HG00741.hp2 others(64): Show |
missense_variant | MODERATE | c.1124G>A | p.Arg375Lys | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 9/14 | 1235/2178 | 1124/1890 | 375/629 | chr1 | 63555425 | |||
| chr1:63568388 | G | A | 1 | a0004 | 9 | HG00738.hp2 HG01934.hp1 HG02257.hp2 others(6): Show |
missense_variant | MODERATE | c.1576G>A | p.Gly526Arg | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 12/14 | 1687/2178 | 1576/1890 | 526/629 | chr1 | 63568388 | |||
| chr1:63568469 | G | A | 1 | a0010 | 1 | HG01243.hp2 | missense_variant | MODERATE | c.1657G>A | p.Val553Met | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 12/14 | 1768/2178 | 1657/1890 | 553/629 | chr1 | 63568469 | |||
| chr1:63571026 | T | G | 1 | a0005 | 6 | HG01192.hp1 HG02622.hp2 HG02647.hp2 others(3): Show |
missense_variant | MODERATE | c.1713T>G | p.Asp571Glu | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 13/14 | 1824/2178 | 1713/1890 | 571/629 | chr1 | 63571026 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:63525596 | T | C | 4 | a0001c0002 a0001c0009 a0008c0011 others(1): Show |
119 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(116): Show |
synonymous_variant | LOW | c.24T>C | p.Asp8Asp | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/14 | 135/2178 | 24/1890 | 8/629 | chr1 | 63525596 | |||
| chr1:63531962 | A | T | 6 | a0002c0003 a0003c0004 a0010c0017 others(3): Show |
96 | HG00558.hp1 HG00733.hp1 HG00741.hp2 others(93): Show |
synonymous_variant | LOW | c.330A>T | p.Ser110Ser | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 3/14 | 441/2178 | 330/1890 | 110/629 | chr1 | 63531962 | |||
| chr1:63533552 | C | T | 1 | a0001c0009 | 4 | HG00673.hp2 HG02071.hp1 NA18948.hp2 others(1): Show |
synonymous_variant | LOW | c.585C>T | p.Asn195Asn | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 5/14 | 696/2178 | 585/1890 | 195/629 | chr1 | 63533552 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:63523625 | C | T | 1 | a0001c0001t0003 | 2 | HG03195.hp2 NA18522.hp1 |
5_prime_UTR_variant | MODIFIER | c.-11C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 1/14 | 1948 | chr1 | 63523625 | ||||||
| chr1:63572603 | G | A | 1 | a0001c0001t0002 | 3 | NA19010.hp1 NA19070.hp2 NA19074.hp2 |
3_prime_UTR_variant | MODIFIER | c.*87G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 14/14 | 87 | chr1 | 63572603 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:63523658 | G | A | 9 | a0004c0006t0001g0009 a0004c0006t0001g0041 a0004c0006t0001g0042 others(6): Show |
11 | HG01934.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-2+24G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 1/13 | chr1 | 63523658 | |||||||
| chr1:63523814 | C | T | 52 | a0001c0002t0001g0275 a0002c0003t0001g0002 a0002c0003t0001g0018 others(49): Show |
70 | HG00558.hp1 HG00733.hp1 HG00741.hp2 others(67): Show |
intron_variant | MODIFIER | c.-2+180C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 1/13 | chr1 | 63523814 | |||||||
| chr1:63523829 | G | C | 1 | a0002c0003t0001g0234 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-2+195G>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 1/13 | chr1 | 63523829 | |||||||
| chr1:63523954 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-2+320G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 1/13 | chr1 | 63523954 | |||||||
| chr1:63523956 | C | T | 2 | a0002c0003t0001g0276 a0002c0003t0001g0277 |
2 | HG01884.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-2+322C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 1/13 | chr1 | 63523956 | |||||||
| chr1:63524040 | G | T | 3 | a0001c0002t0001g0231 a0001c0002t0001g0232 a0001c0002t0001g0233 |
3 | NA18942.hp1 NA18990.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.-2+406G>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 1/13 | chr1 | 63524040 | |||||||
| chr1:63524560 | T | C | 277 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(274): Show |
368 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(365): Show |
intron_variant | MODIFIER | c.-2+926T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 1/13 | chr1 | 63524560 | |||||||
| chr1:63524640 | T | C | 2 | a0001c0002t0001g0050 a0001c0002t0001g0051 |
2 | HG01261.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.-1-932T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 1/13 | chr1 | 63524640 | |||||||
| chr1:63524730 | G | A | 3 | a0003c0005t0001g0052 a0003c0005t0001g0053 a0003c0005t0001g0054 |
3 | HG02622.hp1 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-1-842G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 1/13 | chr1 | 63524730 | |||||||
| chr1:63525047 | A | G | 38 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(35): Show |
51 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.-1-525A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 1/13 | chr1 | 63525047 | |||||||
| chr1:63525127 | C | T | 2 | a0001c0001t0001g0226 a0001c0001t0001g0227 |
2 | HG01243.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.-1-445C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 1/13 | chr1 | 63525127 | |||||||
| chr1:63525156 | C | G | 3 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0198 |
3 | HG00642.hp1 HG01069.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.-1-416C>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 1/13 | chr1 | 63525156 | |||||||
| chr1:63525327 | AAAATTAG others(26): Show |
A | 1 | a0003c0005t0001g0195 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.-1-244_-1-212delAA others(31): Show |
EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 1/13 | chr1 | 63525327 | |||||||
| chr1:63525469 | T | C | 260 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(257): Show |
350 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(347): Show |
intron_variant | MODIFIER | c.-1-103T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 1/13 | chr1 | 63525469 | |||||||
| chr1:63525546 | C | A | 2 | a0003c0004t0001g0055 a0003c0004t0001g0056 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-1-26C>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 1/13 | chr1 | 63525546 | |||||||
| chr1:63525568 | A | G | 1 | a0001c0002t0001g0185 | 1 | HG02155.hp2 | splice_region_variant&intron_variant | LOW | c.-1-4A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 1/13 | chr1 | 63525568 | |||||||
| chr1:63525819 | G | A | 48 | a0002c0003t0001g0002 a0002c0003t0001g0018 a0002c0003t0001g0035 others(45): Show |
66 | HG00558.hp1 HG00733.hp1 HG00741.hp2 others(63): Show |
intron_variant | MODIFIER | c.187+60G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63525819 | |||||||
| chr1:63525882 | G | T | 1 | a0003c0005t0001g0195 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.187+123G>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63525882 | |||||||
| chr1:63526003 | G | A | 6 | a0002c0003t0001g0272 a0004c0006t0001g0009 a0004c0006t0001g0041 others(3): Show |
8 | HG01934.hp1 HG02257.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.187+244G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63526003 | |||||||
| chr1:63526037 | T | A | 1 | a0003c0005t0001g0195 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.187+278T>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63526037 | |||||||
| chr1:63526039 | A | G | 1 | a0003c0005t0001g0195 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.187+280A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63526039 | |||||||
| chr1:63526040 | G | A | 1 | a0003c0005t0001g0195 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.187+281G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63526040 | |||||||
| chr1:63526088 | C | A | 1 | a0003c0004t0001g0057 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.187+329C>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63526088 | |||||||
| chr1:63526274 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.187+515C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63526274 | |||||||
| chr1:63526323 | A | G | 1 | a0003c0004t0001g0184 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.187+564A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63526323 | |||||||
| chr1:63526425 | A | G | 1 | a0001c0001t0001g0224 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.187+666A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63526425 | |||||||
| chr1:63526467 | T | C | 1 | a0003c0005t0001g0195 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.187+708T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63526467 | |||||||
| chr1:63526490 | A | G | 6 | a0003c0005t0001g0052 a0003c0005t0001g0053 a0003c0005t0001g0054 others(3): Show |
6 | HG02572.hp2 HG02622.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.187+731A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63526490 | |||||||
| chr1:63526787 | C | T | 9 | a0003c0004t0001g0175 a0003c0004t0001g0176 a0003c0004t0001g0177 others(6): Show |
9 | HG01081.hp2 HG01109.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.187+1028C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63526787 | |||||||
| chr1:63526796 | G | T | 1 | a0007c0010t0001g0230 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.187+1037G>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63526796 | |||||||
| chr1:63526826 | G | A | 252 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(249): Show |
340 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(337): Show |
intron_variant | MODIFIER | c.187+1067G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63526826 | |||||||
| chr1:63526957 | G | A | 1 | a0001c0001t0001g0019 | 2 | HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.187+1198G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63526957 | |||||||
| chr1:63527095 | T | A | 74 | a0002c0003t0001g0002 a0002c0003t0001g0018 a0002c0003t0001g0035 others(71): Show |
96 | HG00558.hp1 HG00733.hp1 HG00741.hp2 others(93): Show |
intron_variant | MODIFIER | c.187+1336T>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63527095 | |||||||
| chr1:63527111 | C | T | 1 | a0003c0004t0001g0184 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.187+1352C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63527111 | |||||||
| chr1:63527440 | T | TATAAC | 176 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0008 others(173): Show |
222 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(219): Show |
intron_variant | MODIFIER | c.187+1683_187+1684i others(7): Show |
EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 63527440 | ||||||
| chr1:63527442 | T | TAAC | 57 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(54): Show |
75 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(72): Show |
intron_variant | MODIFIER | c.187+1683_187+1684i others(5): Show |
EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63527442 | |||||||
| chr1:63527573 | T | A | 1 | a0003c0005t0001g0186 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.187+1814T>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63527573 | |||||||
| chr1:63527599 | T | C | 101 | a0002c0003t0001g0002 a0002c0003t0001g0018 a0002c0003t0001g0035 others(98): Show |
127 | HG00558.hp1 HG00733.hp1 HG00738.hp2 others(124): Show |
intron_variant | MODIFIER | c.187+1840T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63527599 | |||||||
| chr1:63527679 | T | A | 1 | a0001c0002t0001g0067 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.187+1920T>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63527679 | |||||||
| chr1:63527779 | G | T | 101 | a0002c0003t0001g0002 a0002c0003t0001g0018 a0002c0003t0001g0035 others(98): Show |
127 | HG00558.hp1 HG00733.hp1 HG00738.hp2 others(124): Show |
intron_variant | MODIFIER | c.187+2020G>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63527779 | |||||||
| chr1:63527836 | C | A | 1 | a0004c0006t0001g0041 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.187+2077C>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63527836 | |||||||
| chr1:63528113 | T | G | 1 | a0001c0001t0001g0199 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.187+2354T>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63528113 | |||||||
| chr1:63528173 | TA | T | 4 | a0002c0003t0001g0040 a0002c0003t0001g0269 a0002c0003t0001g0270 others(1): Show |
5 | HG01074.hp2 HG01081.hp1 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.187+2416delA | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 63528173 | ||||||
| chr1:63528213 | G | A | 1 | a0001c0002t0001g0068 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.187+2454G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63528213 | |||||||
| chr1:63528234 | G | C | 13 | a0003c0004t0001g0006 a0003c0004t0001g0055 a0003c0004t0001g0056 others(10): Show |
17 | HG01167.hp2 HG02145.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.187+2475G>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63528234 | |||||||
| chr1:63528237 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.187+2478C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63528237 | |||||||
| chr1:63528281 | T | C | 101 | a0002c0003t0001g0002 a0002c0003t0001g0018 a0002c0003t0001g0035 others(98): Show |
127 | HG00558.hp1 HG00733.hp1 HG00738.hp2 others(124): Show |
intron_variant | MODIFIER | c.187+2522T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63528281 | |||||||
| chr1:63528626 | C | T | 63 | a0002c0003t0001g0002 a0002c0003t0001g0018 a0002c0003t0001g0035 others(60): Show |
85 | HG00558.hp1 HG00733.hp1 HG00741.hp2 others(82): Show |
intron_variant | MODIFIER | c.187+2867C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63528626 | |||||||
| chr1:63528695 | A | T | 1 | a0003c0005t0001g0195 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.187+2936A>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63528695 | |||||||
| chr1:63528697 | T | A | 1 | a0003c0005t0001g0195 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.187+2938T>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63528697 | |||||||
| chr1:63528789 | G | T | 1 | a0001c0001t0003g0023 | 2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.187+3030G>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63528789 | |||||||
| chr1:63528821 | T | C | 234 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(231): Show |
299 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(296): Show |
intron_variant | MODIFIER | c.188-2999T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63528821 | |||||||
| chr1:63528838 | A | G | 1 | a0001c0002t0001g0141 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.188-2982A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63528838 | |||||||
| chr1:63528963 | C | CA | 39 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(36): Show |
53 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.188-2847dupA | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 63528963 | ||||||
| chr1:63528978 | A | C | 1 | a0001c0001t0003g0023 | 2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.188-2842A>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63528978 | |||||||
| chr1:63528983 | C | T | 4 | a0001c0001t0001g0033 a0001c0001t0001g0220 a0001c0001t0001g0221 others(1): Show |
5 | NA18940.hp1 NA18944.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.188-2837C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63528983 | |||||||
| chr1:63528984 | A | T | 4 | a0001c0001t0001g0033 a0001c0001t0001g0220 a0001c0001t0001g0221 others(1): Show |
5 | NA18940.hp1 NA18944.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.188-2836A>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63528984 | |||||||
| chr1:63529018 | G | C | 6 | a0003c0005t0001g0052 a0003c0005t0001g0053 a0003c0005t0001g0054 others(3): Show |
6 | HG02572.hp2 HG02622.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.188-2802G>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63529018 | |||||||
| chr1:63529029 | C | G | 1 | a0003c0005t0001g0195 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.188-2791C>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63529029 | |||||||
| chr1:63529030 | T | C | 1 | a0003c0005t0001g0195 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.188-2790T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63529030 | |||||||
| chr1:63529031 | G | T | 1 | a0003c0005t0001g0195 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.188-2789G>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63529031 | |||||||
| chr1:63529048 | A | G | 2 | a0003c0004t0001g0065 a0003c0004t0001g0184 |
2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.188-2772A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63529048 | |||||||
| chr1:63529055 | T | C | 1 | a0002c0003t0001g0035 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.188-2765T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63529055 | |||||||
| chr1:63529155 | A | T | 1 | a0003c0005t0001g0195 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.188-2665A>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63529155 | |||||||
| chr1:63529180 | A | G | 1 | a0005c0007t0001g0191 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.188-2640A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63529180 | |||||||
| chr1:63529256 | G | A | 2 | a0001c0002t0001g0069 a0001c0002t0001g0070 |
2 | HG00639.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.188-2564G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63529256 | |||||||
| chr1:63529439 | C | T | 93 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0008 others(90): Show |
118 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.188-2381C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63529439 | |||||||
| chr1:63529503 | C | T | 1 | a0003c0005t0001g0186 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.188-2317C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63529503 | |||||||
| chr1:63529504 | A | G | 234 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(231): Show |
299 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(296): Show |
intron_variant | MODIFIER | c.188-2316A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63529504 | |||||||
| chr1:63529605 | C | T | 2 | a0004c0006t0001g0173 a0004c0006t0001g0174 |
2 | HG00738.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.188-2215C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63529605 | |||||||
| chr1:63529628 | A | G | 195 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0008 others(192): Show |
246 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(243): Show |
intron_variant | MODIFIER | c.188-2192A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63529628 | |||||||
| chr1:63529639 | G | T | 94 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0008 others(91): Show |
119 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.188-2181G>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63529639 | |||||||
| chr1:63529671 | C | T | 5 | a0004c0006t0001g0009 a0004c0006t0001g0041 a0004c0006t0001g0042 others(2): Show |
7 | HG01934.hp1 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.188-2149C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63529671 | |||||||
| chr1:63529677 | C | T | 7 | a0004c0006t0001g0009 a0004c0006t0001g0041 a0004c0006t0001g0042 others(4): Show |
9 | HG00738.hp2 HG01934.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.188-2143C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63529677 | |||||||
| chr1:63529832 | T | A | 1 | a0003c0005t0001g0195 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.188-1988T>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63529832 | |||||||
| chr1:63530002 | A | T | 1 | a0003c0005t0001g0195 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.188-1818A>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63530002 | |||||||
| chr1:63530052 | A | G | 1 | a0001c0001t0001g0219 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.188-1768A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63530052 | |||||||
| chr1:63530106 | T | C | 8 | a0006c0008t0001g0045 a0006c0008t0001g0046 a0006c0008t0001g0047 others(5): Show |
9 | HG01891.hp1 HG02280.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.188-1714T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63530106 | |||||||
| chr1:63530290 | A | G | 1 | a0014c0019t0001g0066 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.188-1530A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63530290 | |||||||
| chr1:63530446 | T | C | 14 | a0003c0005t0001g0186 a0005c0007t0001g0030 a0005c0007t0001g0188 others(11): Show |
16 | HG01192.hp1 HG01891.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.188-1374T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63530446 | |||||||
| chr1:63530610 | G | A | 13 | a0003c0004t0001g0006 a0003c0004t0001g0055 a0003c0004t0001g0056 others(10): Show |
17 | HG01167.hp2 HG02145.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.188-1210G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63530610 | |||||||
| chr1:63530921 | A | G | 1 | a0006c0008t0001g0187 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.188-899A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63530921 | |||||||
| chr1:63530938 | A | T | 1 | a0003c0005t0001g0195 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.188-882A>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63530938 | |||||||
| chr1:63530939 | T | A | 1 | a0003c0005t0001g0195 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.188-881T>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63530939 | |||||||
| chr1:63530940 | A | T | 1 | a0003c0005t0001g0195 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.188-880A>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63530940 | |||||||
| chr1:63531022 | C | T | 1 | a0001c0002t0001g0233 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.188-798C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63531022 | |||||||
| chr1:63531063 | A | G | 39 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(36): Show |
53 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.188-757A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63531063 | |||||||
| chr1:63531210 | A | C | 1 | a0003c0005t0001g0195 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.188-610A>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63531210 | |||||||
| chr1:63531232 | C | T | 10 | a0003c0004t0001g0175 a0003c0004t0001g0176 a0003c0004t0001g0177 others(7): Show |
10 | HG01081.hp2 HG01109.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.188-588C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63531232 | |||||||
| chr1:63531310 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.188-510C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63531310 | |||||||
| chr1:63531316 | ATGT | A | 74 | a0002c0003t0001g0002 a0002c0003t0001g0018 a0002c0003t0001g0035 others(71): Show |
96 | HG00558.hp1 HG00733.hp1 HG00741.hp2 others(93): Show |
intron_variant | MODIFIER | c.188-500_188-498del others(3): Show |
EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr1 | 63531316 | ||||||
| chr1:63531439 | T | A | 1 | a0003c0005t0001g0195 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.188-381T>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63531439 | |||||||
| chr1:63531448 | C | A | 1 | a0003c0004t0001g0184 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.188-372C>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63531448 | |||||||
| chr1:63531478 | T | C | 1 | a0003c0005t0001g0195 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.188-342T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63531478 | |||||||
| chr1:63531549 | G | A | 1 | a0002c0003t0001g0235 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.188-271G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63531549 | |||||||
| chr1:63531568 | G | A | 5 | a0004c0006t0001g0009 a0004c0006t0001g0041 a0004c0006t0001g0042 others(2): Show |
7 | HG01934.hp1 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.188-252G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63531568 | |||||||
| chr1:63531629 | G | A | 3 | a0003c0005t0001g0052 a0003c0005t0001g0053 a0003c0005t0001g0054 |
3 | HG02622.hp1 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.188-191G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 2/13 | chr1 | 63531629 | |||||||
| chr1:63532193 | A | G | 20 | a0003c0005t0001g0052 a0003c0005t0001g0053 a0003c0005t0001g0054 others(17): Show |
22 | HG01192.hp1 HG01891.hp1 HG02280.hp1 others(19): Show |
intron_variant | MODIFIER | c.399+162A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 3/13 | chr1 | 63532193 | |||||||
| chr1:63533073 | G | C | 9 | a0003c0004t0001g0175 a0003c0004t0001g0176 a0003c0004t0001g0177 others(6): Show |
9 | HG01081.hp2 HG01109.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.486+317G>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 4/13 | chr1 | 63533073 | |||||||
| chr1:63533106 | T | C | 3 | a0007c0010t0001g0034 a0007c0010t0001g0228 a0007c0010t0001g0230 |
4 | HG01891.hp1 HG02615.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.487-348T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 4/13 | chr1 | 63533106 | |||||||
| chr1:63533161 | T | C | 1 | a0015c0018t0001g0273 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.487-293T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 4/13 | chr1 | 63533161 | |||||||
| chr1:63533199 | T | A | 1 | a0003c0005t0001g0195 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.487-255T>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 4/13 | chr1 | 63533199 | |||||||
| chr1:63533200 | A | T | 1 | a0003c0005t0001g0195 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.487-254A>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 4/13 | chr1 | 63533200 | |||||||
| chr1:63533316 | A | C | 1 | a0002c0003t0001g0268 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.487-138A>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 4/13 | chr1 | 63533316 | |||||||
| chr1:63533416 | T | C | 94 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0008 others(91): Show |
119 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.487-38T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 4/13 | chr1 | 63533416 | |||||||
| chr1:63533426 | T | C | 1 | a0002c0003t0001g0236 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.487-28T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 4/13 | chr1 | 63533426 | |||||||
| chr1:63533432 | C | T | 3 | a0001c0002t0001g0069 a0001c0002t0001g0070 a0001c0002t0001g0140 |
3 | HG00639.hp2 HG01255.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.487-22C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 4/13 | chr1 | 63533432 | |||||||
| chr1:63533803 | T | G | 94 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0008 others(91): Show |
119 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.682+154T>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 5/13 | chr1 | 63533803 | |||||||
| chr1:63533843 | G | A | 3 | a0003c0005t0001g0052 a0003c0005t0001g0053 a0003c0005t0001g0054 |
3 | HG02622.hp1 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.682+194G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 5/13 | chr1 | 63533843 | |||||||
| chr1:63533860 | A | C | 10 | a0003c0005t0001g0029 a0003c0005t0001g0168 a0003c0005t0001g0169 others(7): Show |
13 | HG01934.hp1 HG02257.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.682+211A>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 5/13 | chr1 | 63533860 | |||||||
| chr1:63533889 | A | G | 2 | a0001c0002t0001g0013 a0001c0002t0001g0139 |
4 | NA18979.hp2 NA18981.hp2 NA19074.hp1 others(1): Show |
intron_variant | MODIFIER | c.683-206A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 5/13 | chr1 | 63533889 | |||||||
| chr1:63534220 | T | C | 49 | a0002c0003t0001g0002 a0002c0003t0001g0018 a0002c0003t0001g0035 others(46): Show |
67 | HG00558.hp1 HG00733.hp1 HG00741.hp2 others(64): Show |
splice_region_variant&intron_variant | LOW | c.804+4T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63534220 | |||||||
| chr1:63534363 | G | T | 1 | a0001c0002t0001g0138 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.804+147G>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63534363 | |||||||
| chr1:63534586 | T | C | 2 | a0002c0003t0001g0237 a0002c0003t0001g0268 |
2 | HG02738.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.804+370T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63534586 | |||||||
| chr1:63534739 | C | T | 9 | a0003c0004t0001g0175 a0003c0004t0001g0176 a0003c0004t0001g0177 others(6): Show |
9 | HG01081.hp2 HG01109.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.804+523C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63534739 | |||||||
| chr1:63534859 | T | C | 5 | a0004c0006t0001g0009 a0004c0006t0001g0041 a0004c0006t0001g0042 others(2): Show |
7 | HG01934.hp1 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.804+643T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63534859 | |||||||
| chr1:63534922 | TA | T | 4 | a0002c0003t0001g0264 a0002c0003t0001g0265 a0002c0003t0001g0266 others(1): Show |
4 | HG01358.hp1 HG01978.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.804+710delA | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr1 | 63534922 | ||||||
| chr1:63534936 | A | G | 9 | a0003c0004t0001g0175 a0003c0004t0001g0176 a0003c0004t0001g0177 others(6): Show |
9 | HG01081.hp2 HG01109.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.804+720A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63534936 | |||||||
| chr1:63534976 | A | G | 13 | a0003c0004t0001g0006 a0003c0004t0001g0055 a0003c0004t0001g0056 others(10): Show |
17 | HG01167.hp2 HG02145.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.804+760A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63534976 | |||||||
| chr1:63535037 | A | T | 3 | a0007c0010t0001g0034 a0007c0010t0001g0228 a0007c0010t0001g0230 |
4 | HG01891.hp1 HG02615.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.804+821A>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63535037 | |||||||
| chr1:63535138 | A | G | 5 | a0001c0001t0001g0015 a0001c0001t0001g0164 a0001c0001t0001g0165 others(2): Show |
7 | NA18973.hp2 NA18991.hp2 NA19006.hp2 others(4): Show |
intron_variant | MODIFIER | c.804+922A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63535138 | |||||||
| chr1:63535467 | A | T | 5 | a0002c0003t0001g0237 a0002c0003t0001g0263 a0002c0003t0001g0268 others(2): Show |
5 | HG01884.hp1 HG02293.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.804+1251A>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63535467 | |||||||
| chr1:63535551 | C | T | 2 | a0003c0004t0001g0057 a0003c0004t0001g0064 |
2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.804+1335C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63535551 | |||||||
| chr1:63535739 | G | GT | 94 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0008 others(91): Show |
119 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.804+1525dupT | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr1 | 63535739 | ||||||
| chr1:63536100 | G | T | 1 | a0001c0002t0001g0137 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.804+1884G>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63536100 | |||||||
| chr1:63536118 | T | A | 74 | a0002c0003t0001g0002 a0002c0003t0001g0018 a0002c0003t0001g0035 others(71): Show |
96 | HG00558.hp1 HG00733.hp1 HG00741.hp2 others(93): Show |
intron_variant | MODIFIER | c.804+1902T>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63536118 | |||||||
| chr1:63536167 | T | C | 2 | a0002c0003t0001g0238 a0002c0003t0001g0239 |
2 | NA18989.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.804+1951T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63536167 | |||||||
| chr1:63536202 | G | A | 14 | a0003c0005t0001g0186 a0005c0007t0001g0030 a0005c0007t0001g0188 others(11): Show |
16 | HG01192.hp1 HG01891.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.804+1986G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63536202 | |||||||
| chr1:63536359 | T | C | 1 | a0001c0002t0001g0072 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.804+2143T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63536359 | |||||||
| chr1:63536420 | T | A | 1 | a0010c0017t0001g0274 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.804+2204T>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63536420 | |||||||
| chr1:63536464 | T | G | 1 | a0001c0001t0001g0142 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.804+2248T>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63536464 | |||||||
| chr1:63536761 | T | A | 74 | a0002c0003t0001g0002 a0002c0003t0001g0018 a0002c0003t0001g0035 others(71): Show |
96 | HG00558.hp1 HG00733.hp1 HG00741.hp2 others(93): Show |
intron_variant | MODIFIER | c.804+2545T>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63536761 | |||||||
| chr1:63537027 | G | T | 1 | a0001c0001t0001g0171 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.804+2811G>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63537027 | |||||||
| chr1:63537104 | C | T | 64 | a0002c0003t0001g0002 a0002c0003t0001g0018 a0002c0003t0001g0035 others(61): Show |
86 | HG00558.hp1 HG00733.hp1 HG00741.hp2 others(83): Show |
intron_variant | MODIFIER | c.804+2888C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63537104 | |||||||
| chr1:63537126 | A | G | 2 | a0003c0004t0001g0182 a0003c0004t0001g0183 |
2 | HG01081.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.804+2910A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63537126 | |||||||
| chr1:63537185 | G | A | 56 | a0001c0002t0001g0008 a0001c0002t0001g0010 a0001c0002t0001g0013 others(53): Show |
63 | HG00408.hp2 HG00423.hp1 HG00673.hp2 others(60): Show |
intron_variant | MODIFIER | c.804+2969G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63537185 | |||||||
| chr1:63537445 | C | T | 3 | a0001c0002t0001g0109 a0001c0002t0001g0110 a0001c0002t0001g0111 |
3 | HG02027.hp1 NA18959.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.804+3229C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63537445 | |||||||
| chr1:63537456 | T | C | 6 | a0001c0002t0001g0020 a0001c0002t0001g0073 a0001c0002t0001g0074 others(3): Show |
7 | HG00423.hp1 NA18963.hp2 NA18983.hp2 others(4): Show |
intron_variant | MODIFIER | c.804+3240T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63537456 | |||||||
| chr1:63537535 | C | G | 1 | a0005c0007t0001g0191 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.804+3319C>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63537535 | |||||||
| chr1:63537554 | C | T | 9 | a0003c0004t0001g0175 a0003c0004t0001g0176 a0003c0004t0001g0177 others(6): Show |
9 | HG01081.hp2 HG01109.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.804+3338C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63537554 | |||||||
| chr1:63537754 | A | G | 1 | a0015c0018t0001g0273 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.804+3538A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63537754 | |||||||
| chr1:63537853 | A | G | 2 | a0001c0002t0001g0110 a0001c0002t0001g0111 |
2 | HG02027.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.804+3637A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63537853 | |||||||
| chr1:63537878 | C | A | 38 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(35): Show |
51 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.804+3662C>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63537878 | |||||||
| chr1:63537951 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.804+3735C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63537951 | |||||||
| chr1:63537962 | G | T | 195 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0008 others(192): Show |
246 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(243): Show |
intron_variant | MODIFIER | c.804+3746G>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63537962 | |||||||
| chr1:63538111 | T | TA | 7 | a0004c0006t0001g0009 a0004c0006t0001g0041 a0004c0006t0001g0042 others(4): Show |
9 | HG00738.hp2 HG01934.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.804+3896dupA | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr1 | 63538111 | ||||||
| chr1:63538445 | A | AT | 52 | a0002c0003t0001g0002 a0002c0003t0001g0018 a0002c0003t0001g0035 others(49): Show |
70 | HG00558.hp1 HG00733.hp1 HG00741.hp2 others(67): Show |
intron_variant | MODIFIER | c.804+4238dupT | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr1 | 63538445 | ||||||
| chr1:63538445 | A | ATT | 13 | a0003c0004t0001g0006 a0003c0004t0001g0055 a0003c0004t0001g0056 others(10): Show |
17 | HG01167.hp2 HG02145.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.804+4237_804+4238d others(4): Show |
EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr1 | 63538445 | ||||||
| chr1:63538461 | C | T | 3 | a0003c0005t0001g0052 a0003c0005t0001g0053 a0003c0005t0001g0054 |
3 | HG02622.hp1 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.804+4245C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63538461 | |||||||
| chr1:63538465 | T | C | 1 | a0001c0002t0001g0109 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.804+4249T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63538465 | |||||||
| chr1:63538490 | A | G | 2 | a0003c0004t0001g0065 a0003c0004t0001g0184 |
2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.804+4274A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63538490 | |||||||
| chr1:63538717 | T | C | 5 | a0004c0006t0001g0009 a0004c0006t0001g0041 a0004c0006t0001g0042 others(2): Show |
7 | HG01934.hp1 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.804+4501T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63538717 | |||||||
| chr1:63538740 | C | T | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | HG03491.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.804+4524C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63538740 | |||||||
| chr1:63538741 | G | T | 31 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0014 others(28): Show |
56 | HG00642.hp1 HG00642.hp2 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.804+4525G>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63538741 | |||||||
| chr1:63538809 | A | G | 1 | a0003c0004t0001g0184 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.804+4593A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63538809 | |||||||
| chr1:63538904 | G | A | 2 | a0001c0002t0001g0068 a0001c0002t0001g0071 |
2 | HG01123.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.804+4688G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63538904 | |||||||
| chr1:63539188 | G | A | 74 | a0002c0003t0001g0002 a0002c0003t0001g0018 a0002c0003t0001g0035 others(71): Show |
96 | HG00558.hp1 HG00733.hp1 HG00741.hp2 others(93): Show |
intron_variant | MODIFIER | c.804+4972G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63539188 | |||||||
| chr1:63539299 | G | A | 6 | a0003c0005t0001g0052 a0003c0005t0001g0053 a0003c0005t0001g0054 others(3): Show |
6 | HG02572.hp2 HG02622.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.804+5083G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63539299 | |||||||
| chr1:63539395 | C | G | 3 | a0001c0002t0001g0022 a0001c0002t0001g0135 a0001c0002t0001g0136 |
4 | HG01074.hp1 HG01256.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.804+5179C>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63539395 | |||||||
| chr1:63539596 | A | G | 74 | a0002c0003t0001g0002 a0002c0003t0001g0018 a0002c0003t0001g0035 others(71): Show |
96 | HG00558.hp1 HG00733.hp1 HG00741.hp2 others(93): Show |
intron_variant | MODIFIER | c.804+5380A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63539596 | |||||||
| chr1:63539641 | T | G | 1 | a0003c0005t0001g0186 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.804+5425T>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63539641 | |||||||
| chr1:63539955 | AG | A | 74 | a0002c0003t0001g0002 a0002c0003t0001g0018 a0002c0003t0001g0035 others(71): Show |
96 | HG00558.hp1 HG00733.hp1 HG00741.hp2 others(93): Show |
intron_variant | MODIFIER | c.804+5742delG | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr1 | 63539955 | ||||||
| chr1:63540058 | C | T | 9 | a0003c0004t0001g0175 a0003c0004t0001g0176 a0003c0004t0001g0177 others(6): Show |
9 | HG01081.hp2 HG01109.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.804+5842C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63540058 | |||||||
| chr1:63540129 | G | A | 20 | a0003c0005t0001g0052 a0003c0005t0001g0053 a0003c0005t0001g0054 others(17): Show |
22 | HG01192.hp1 HG01891.hp1 HG02280.hp1 others(19): Show |
intron_variant | MODIFIER | c.805-5787G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63540129 | |||||||
| chr1:63540137 | C | T | 52 | a0001c0002t0001g0008 a0001c0002t0001g0010 a0001c0002t0001g0013 others(49): Show |
59 | HG00408.hp2 HG00423.hp1 HG00673.hp2 others(56): Show |
intron_variant | MODIFIER | c.805-5779C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63540137 | |||||||
| chr1:63540165 | C | T | 6 | a0003c0005t0001g0052 a0003c0005t0001g0053 a0003c0005t0001g0054 others(3): Show |
6 | HG02572.hp2 HG02622.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.805-5751C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63540165 | |||||||
| chr1:63540228 | G | A | 1 | a0014c0019t0001g0066 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.805-5688G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63540228 | |||||||
| chr1:63540363 | C | CA | 34 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0151 others(31): Show |
36 | HG00673.hp2 HG00735.hp2 HG01123.hp2 others(33): Show |
intron_variant | MODIFIER | c.805-5530dupA | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr1 | 63540363 | ||||||
| chr1:63540363 | CA | C | 13 | a0001c0001t0001g0150 a0001c0001t0001g0216 a0001c0002t0001g0107 others(10): Show |
13 | HG00639.hp1 HG01081.hp2 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.805-5530delA | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr1 | 63540363 | ||||||
| chr1:63540492 | G | T | 94 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0008 others(91): Show |
119 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.805-5424G>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63540492 | |||||||
| chr1:63540557 | C | G | 9 | a0003c0004t0001g0175 a0003c0004t0001g0176 a0003c0004t0001g0177 others(6): Show |
9 | HG01081.hp2 HG01109.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.805-5359C>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63540557 | |||||||
| chr1:63540564 | C | T | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | HG00741.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.805-5352C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63540564 | |||||||
| chr1:63540618 | A | G | 1 | a0002c0003t0001g0258 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.805-5298A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63540618 | |||||||
| chr1:63540653 | G | T | 5 | a0005c0007t0001g0030 a0005c0007t0001g0188 a0005c0007t0001g0189 others(2): Show |
6 | HG01192.hp1 HG02622.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.805-5263G>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63540653 | |||||||
| chr1:63540654 | A | T | 5 | a0005c0007t0001g0030 a0005c0007t0001g0188 a0005c0007t0001g0189 others(2): Show |
6 | HG01192.hp1 HG02622.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.805-5262A>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63540654 | |||||||
| chr1:63540685 | T | C | 8 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(5): Show |
9 | HG02280.hp2 HG02717.hp1 HG03471.hp2 others(6): Show |
intron_variant | MODIFIER | c.805-5231T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63540685 | |||||||
| chr1:63540856 | C | A | 74 | a0002c0003t0001g0002 a0002c0003t0001g0018 a0002c0003t0001g0035 others(71): Show |
96 | HG00558.hp1 HG00733.hp1 HG00741.hp2 others(93): Show |
intron_variant | MODIFIER | c.805-5060C>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63540856 | |||||||
| chr1:63540858 | GT | G | 94 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0008 others(91): Show |
119 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.805-5055delT | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr1 | 63540858 | ||||||
| chr1:63541209 | T | C | 1 | a0003c0005t0001g0168 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.805-4707T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63541209 | |||||||
| chr1:63541227 | G | A | 3 | a0001c0001t0001g0196 a0001c0001t0001g0197 a0001c0001t0001g0198 |
3 | HG00642.hp1 HG01069.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.805-4689G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63541227 | |||||||
| chr1:63541251 | A | G | 4 | a0002c0003t0001g0237 a0002c0003t0001g0268 a0002c0003t0001g0276 others(1): Show |
4 | HG01884.hp1 HG02738.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.805-4665A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63541251 | |||||||
| chr1:63541386 | G | A | 1 | a0001c0002t0001g0112 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.805-4530G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63541386 | |||||||
| chr1:63541417 | T | G | 2 | a0001c0001t0001g0217 a0001c0001t0001g0218 |
2 | HG03491.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.805-4499T>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63541417 | |||||||
| chr1:63541435 | G | T | 2 | a0003c0004t0001g0055 a0003c0004t0001g0056 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.805-4481G>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63541435 | |||||||
| chr1:63541478 | C | T | 8 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(5): Show |
9 | HG02280.hp2 HG02717.hp1 HG03471.hp2 others(6): Show |
intron_variant | MODIFIER | c.805-4438C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63541478 | |||||||
| chr1:63541572 | G | GT | 6 | a0001c0001t0001g0167 a0001c0002t0001g0114 a0002c0003t0001g0257 others(3): Show |
6 | HG02071.hp2 HG02602.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.805-4334dupT | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr1 | 63541572 | ||||||
| chr1:63541628 | G | A | 51 | a0002c0003t0001g0002 a0002c0003t0001g0018 a0002c0003t0001g0035 others(48): Show |
69 | HG00558.hp1 HG00733.hp1 HG00741.hp2 others(66): Show |
intron_variant | MODIFIER | c.805-4288G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63541628 | |||||||
| chr1:63541666 | G | A | 5 | a0004c0006t0001g0009 a0004c0006t0001g0041 a0004c0006t0001g0042 others(2): Show |
7 | HG01934.hp1 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.805-4250G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63541666 | |||||||
| chr1:63541724 | G | A | 1 | a0003c0004t0001g0181 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.805-4192G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63541724 | |||||||
| chr1:63541790 | T | C | 27 | a0003c0005t0001g0052 a0003c0005t0001g0053 a0003c0005t0001g0054 others(24): Show |
31 | HG00738.hp2 HG01192.hp1 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.805-4126T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63541790 | |||||||
| chr1:63541866 | A | G | 3 | a0003c0005t0001g0192 a0003c0005t0001g0193 a0003c0005t0001g0194 |
3 | HG02572.hp2 HG02886.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.805-4050A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63541866 | |||||||
| chr1:63541876 | T | A | 1 | a0001c0001t0001g0146 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.805-4040T>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63541876 | |||||||
| chr1:63541905 | T | C | 1 | a0001c0001t0001g0019 | 2 | HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.805-4011T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63541905 | |||||||
| chr1:63542073 | C | T | 1 | a0015c0018t0001g0273 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.805-3843C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63542073 | |||||||
| chr1:63542332 | G | A | 13 | a0005c0007t0001g0030 a0005c0007t0001g0188 a0005c0007t0001g0189 others(10): Show |
15 | HG01192.hp1 HG01891.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.805-3584G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63542332 | |||||||
| chr1:63542556 | A | T | 1 | a0001c0001t0001g0224 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.805-3360A>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63542556 | |||||||
| chr1:63542617 | T | C | 7 | a0004c0006t0001g0009 a0004c0006t0001g0041 a0004c0006t0001g0042 others(4): Show |
9 | HG00738.hp2 HG01934.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.805-3299T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63542617 | |||||||
| chr1:63542815 | T | C | 1 | a0004c0006t0001g0173 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.805-3101T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63542815 | |||||||
| chr1:63542848 | C | G | 8 | a0006c0008t0001g0045 a0006c0008t0001g0046 a0006c0008t0001g0047 others(5): Show |
9 | HG01891.hp1 HG02280.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.805-3068C>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63542848 | |||||||
| chr1:63542852 | A | G | 1 | a0001c0001t0001g0215 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.805-3064A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63542852 | |||||||
| chr1:63543088 | G | C | 1 | a0003c0005t0001g0186 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.805-2828G>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63543088 | |||||||
| chr1:63543276 | C | A | 1 | a0001c0002t0001g0275 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.805-2640C>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63543276 | |||||||
| chr1:63543392 | G | A | 93 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0008 others(90): Show |
118 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.805-2524G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63543392 | |||||||
| chr1:63543414 | G | A | 1 | a0002c0003t0001g0258 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.805-2502G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63543414 | |||||||
| chr1:63543416 | A | T | 1 | a0001c0002t0001g0081 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.805-2500A>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63543416 | |||||||
| chr1:63543560 | T | A | 1 | a0003c0005t0001g0186 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.805-2356T>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63543560 | |||||||
| chr1:63543594 | A | G | 8 | a0006c0008t0001g0045 a0006c0008t0001g0046 a0006c0008t0001g0047 others(5): Show |
9 | HG01891.hp1 HG02280.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.805-2322A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63543594 | |||||||
| chr1:63543608 | G | A | 25 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0031 others(22): Show |
35 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.805-2308G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63543608 | |||||||
| chr1:63543647 | C | T | 3 | a0001c0001t0001g0028 a0001c0001t0001g0160 a0001c0001t0001g0161 |
4 | NA18941.hp2 NA18951.hp1 NA19072.hp1 others(1): Show |
intron_variant | MODIFIER | c.805-2269C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63543647 | |||||||
| chr1:63543679 | G | A | 1 | a0001c0002t0001g0134 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.805-2237G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63543679 | |||||||
| chr1:63543745 | A | G | 13 | a0003c0004t0001g0006 a0003c0004t0001g0055 a0003c0004t0001g0056 others(10): Show |
17 | HG01167.hp2 HG02145.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.805-2171A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63543745 | |||||||
| chr1:63543803 | G | T | 234 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(231): Show |
299 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(296): Show |
intron_variant | MODIFIER | c.805-2113G>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63543803 | |||||||
| chr1:63543858 | A | C | 7 | a0004c0006t0001g0009 a0004c0006t0001g0041 a0004c0006t0001g0042 others(4): Show |
9 | HG00738.hp2 HG01934.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.805-2058A>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63543858 | |||||||
| chr1:63543970 | T | C | 1 | a0001c0002t0001g0114 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.805-1946T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63543970 | |||||||
| chr1:63543971 | C | CT | 14 | a0001c0001t0001g0007 a0001c0001t0001g0027 a0001c0001t0001g0149 others(11): Show |
20 | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.805-1929dupT | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr1 | 63543971 | ||||||
| chr1:63543971 | C | T | 1 | a0001c0002t0001g0114 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.805-1945C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63543971 | |||||||
| chr1:63543971 | CT | C | 55 | a0001c0002t0001g0050 a0001c0002t0001g0051 a0001c0002t0001g0087 others(52): Show |
73 | HG00558.hp1 HG00733.hp1 HG00741.hp2 others(70): Show |
intron_variant | MODIFIER | c.805-1929delT | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr1 | 63543971 | ||||||
| chr1:63544038 | T | C | 195 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0008 others(192): Show |
246 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(243): Show |
intron_variant | MODIFIER | c.805-1878T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63544038 | |||||||
| chr1:63544119 | G | A | 1 | a0015c0018t0001g0273 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.805-1797G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63544119 | |||||||
| chr1:63544203 | C | T | 1 | a0001c0002t0001g0134 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.805-1713C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63544203 | |||||||
| chr1:63544217 | G | C | 1 | a0001c0002t0001g0114 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.805-1699G>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63544217 | |||||||
| chr1:63544218 | C | G | 1 | a0001c0002t0001g0114 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.805-1698C>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63544218 | |||||||
| chr1:63544235 | G | T | 1 | a0001c0001t0001g0214 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.805-1681G>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63544235 | |||||||
| chr1:63544285 | C | T | 27 | a0003c0005t0001g0052 a0003c0005t0001g0053 a0003c0005t0001g0054 others(24): Show |
31 | HG00738.hp2 HG01192.hp1 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.805-1631C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63544285 | |||||||
| chr1:63544558 | G | A | 5 | a0004c0006t0001g0009 a0004c0006t0001g0041 a0004c0006t0001g0042 others(2): Show |
7 | HG01934.hp1 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.805-1358G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63544558 | |||||||
| chr1:63544574 | G | A | 49 | a0002c0003t0001g0002 a0002c0003t0001g0018 a0002c0003t0001g0035 others(46): Show |
67 | HG00558.hp1 HG00733.hp1 HG00741.hp2 others(64): Show |
intron_variant | MODIFIER | c.805-1342G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63544574 | |||||||
| chr1:63544602 | G | A | 1 | a0003c0005t0001g0186 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.805-1314G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63544602 | |||||||
| chr1:63544786 | C | T | 39 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(36): Show |
53 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.805-1130C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63544786 | |||||||
| chr1:63544808 | C | G | 2 | a0001c0002t0001g0132 a0001c0002t0001g0133 |
2 | HG02683.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.805-1108C>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63544808 | |||||||
| chr1:63544921 | C | CT | 12 | a0001c0001t0001g0145 a0001c0001t0001g0159 a0001c0001t0001g0166 others(9): Show |
12 | HG02145.hp1 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.805-980dupT | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr1 | 63544921 | ||||||
| chr1:63545092 | T | C | 2 | a0003c0005t0001g0193 a0003c0005t0001g0194 |
2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.805-824T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63545092 | |||||||
| chr1:63545108 | AG | A | 3 | a0003c0005t0001g0192 a0003c0005t0001g0193 a0003c0005t0001g0194 |
3 | HG02572.hp2 HG02886.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.805-805delG | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr1 | 63545108 | ||||||
| chr1:63545149 | T | C | 234 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(231): Show |
299 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(296): Show |
intron_variant | MODIFIER | c.805-767T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63545149 | |||||||
| chr1:63545162 | C | G | 1 | a0014c0019t0001g0066 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.805-754C>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63545162 | |||||||
| chr1:63545164 | A | G | 1 | a0004c0006t0001g0044 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.805-752A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63545164 | |||||||
| chr1:63545215 | C | A | 27 | a0003c0005t0001g0052 a0003c0005t0001g0053 a0003c0005t0001g0054 others(24): Show |
31 | HG00738.hp2 HG01192.hp1 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.805-701C>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63545215 | |||||||
| chr1:63545245 | C | G | 1 | a0002c0003t0001g0255 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.805-671C>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63545245 | |||||||
| chr1:63545345 | A | G | 7 | a0004c0006t0001g0009 a0004c0006t0001g0041 a0004c0006t0001g0042 others(4): Show |
9 | HG00738.hp2 HG01934.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.805-571A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63545345 | |||||||
| chr1:63545401 | T | G | 7 | a0004c0006t0001g0009 a0004c0006t0001g0041 a0004c0006t0001g0042 others(4): Show |
9 | HG00738.hp2 HG01934.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.805-515T>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63545401 | |||||||
| chr1:63545490 | G | A | 52 | a0002c0003t0001g0002 a0002c0003t0001g0018 a0002c0003t0001g0035 others(49): Show |
70 | HG00558.hp1 HG00733.hp1 HG00741.hp2 others(67): Show |
intron_variant | MODIFIER | c.805-426G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63545490 | |||||||
| chr1:63545500 | T | C | 1 | a0001c0009t0001g0082 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.805-416T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63545500 | |||||||
| chr1:63545590 | C | T | 2 | a0001c0002t0001g0050 a0001c0002t0001g0051 |
2 | HG01261.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.805-326C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63545590 | |||||||
| chr1:63545662 | C | T | 7 | a0004c0006t0001g0009 a0004c0006t0001g0041 a0004c0006t0001g0042 others(4): Show |
9 | HG00738.hp2 HG01934.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.805-254C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63545662 | |||||||
| chr1:63545787 | G | A | 27 | a0003c0005t0001g0052 a0003c0005t0001g0053 a0003c0005t0001g0054 others(24): Show |
31 | HG00738.hp2 HG01192.hp1 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.805-129G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 6/13 | chr1 | 63545787 | |||||||
| chr1:63546522 | C | T | 1 | a0003c0005t0001g0186 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.946+465C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63546522 | |||||||
| chr1:63546590 | A | T | 14 | a0003c0005t0001g0186 a0005c0007t0001g0030 a0005c0007t0001g0188 others(11): Show |
16 | HG01192.hp1 HG01891.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.946+533A>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63546590 | |||||||
| chr1:63546610 | C | T | 4 | a0002c0003t0001g0234 a0002c0003t0001g0252 a0002c0003t0001g0253 others(1): Show |
4 | HG00733.hp1 HG00741.hp2 HG01069.hp1 others(1): Show |
intron_variant | MODIFIER | c.946+553C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63546610 | |||||||
| chr1:63546614 | C | T | 6 | a0003c0005t0001g0052 a0003c0005t0001g0053 a0003c0005t0001g0054 others(3): Show |
6 | HG02572.hp2 HG02622.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.946+557C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63546614 | |||||||
| chr1:63546615 | G | A | 93 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0008 others(90): Show |
118 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.946+558G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63546615 | |||||||
| chr1:63546620 | G | A | 3 | a0003c0005t0001g0192 a0003c0005t0001g0193 a0003c0005t0001g0194 |
3 | HG02572.hp2 HG02886.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.946+563G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63546620 | |||||||
| chr1:63546635 | T | G | 1 | a0001c0002t0001g0083 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.946+578T>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63546635 | |||||||
| chr1:63546658 | A | G | 195 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0008 others(192): Show |
246 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(243): Show |
intron_variant | MODIFIER | c.946+601A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63546658 | |||||||
| chr1:63546689 | A | C | 1 | a0003c0005t0001g0186 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.946+632A>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63546689 | |||||||
| chr1:63546717 | A | G | 7 | a0003c0004t0001g0006 a0003c0004t0001g0058 a0003c0004t0001g0059 others(4): Show |
11 | HG01167.hp2 HG02145.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.946+660A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63546717 | |||||||
| chr1:63546830 | T | A | 1 | a0001c0002t0001g0112 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.946+773T>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63546830 | |||||||
| chr1:63546925 | T | G | 1 | a0014c0019t0001g0066 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.946+868T>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63546925 | |||||||
| chr1:63547008 | G | A | 7 | a0004c0006t0001g0009 a0004c0006t0001g0041 a0004c0006t0001g0042 others(4): Show |
9 | HG00738.hp2 HG01934.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.946+951G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63547008 | |||||||
| chr1:63547113 | G | A | 94 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0008 others(91): Show |
119 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.946+1056G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63547113 | |||||||
| chr1:63547186 | G | A | 94 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0008 others(91): Show |
119 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.946+1129G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63547186 | |||||||
| chr1:63547294 | G | A | 101 | a0002c0003t0001g0002 a0002c0003t0001g0018 a0002c0003t0001g0035 others(98): Show |
127 | HG00558.hp1 HG00733.hp1 HG00738.hp2 others(124): Show |
intron_variant | MODIFIER | c.946+1237G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63547294 | |||||||
| chr1:63547510 | A | G | 14 | a0003c0005t0001g0186 a0005c0007t0001g0030 a0005c0007t0001g0188 others(11): Show |
16 | HG01192.hp1 HG01891.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.946+1453A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63547510 | |||||||
| chr1:63547660 | T | C | 1 | a0001c0002t0001g0115 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.946+1603T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63547660 | |||||||
| chr1:63547697 | G | C | 1 | a0001c0001t0001g0202 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.946+1640G>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63547697 | |||||||
| chr1:63547757 | G | A | 94 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0008 others(91): Show |
119 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.946+1700G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63547757 | |||||||
| chr1:63547828 | C | A | 1 | a0001c0001t0001g0019 | 2 | HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.946+1771C>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63547828 | |||||||
| chr1:63547851 | C | T | 1 | a0001c0001t0001g0201 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.946+1794C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63547851 | |||||||
| chr1:63547886 | C | T | 31 | a0001c0002t0001g0008 a0001c0002t0001g0013 a0001c0002t0001g0020 others(28): Show |
36 | HG00408.hp2 HG00423.hp1 HG00673.hp2 others(33): Show |
intron_variant | MODIFIER | c.946+1829C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63547886 | |||||||
| chr1:63547977 | A | T | 2 | a0001c0002t0001g0094 a0001c0002t0001g0095 |
2 | HG02083.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.946+1920A>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63547977 | |||||||
| chr1:63548026 | C | T | 1 | a0005c0007t0001g0190 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.946+1969C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63548026 | |||||||
| chr1:63548117 | G | A | 1 | a0001c0002t0001g0050 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.946+2060G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63548117 | |||||||
| chr1:63548384 | T | A | 1 | a0004c0006t0001g0044 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.946+2327T>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63548384 | |||||||
| chr1:63548607 | T | G | 1 | a0002c0003t0001g0265 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.946+2550T>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63548607 | |||||||
| chr1:63548695 | T | C | 2 | a0004c0006t0001g0173 a0004c0006t0001g0174 |
2 | HG00738.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.946+2638T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63548695 | |||||||
| chr1:63548822 | T | C | 6 | a0003c0005t0001g0052 a0003c0005t0001g0053 a0003c0005t0001g0054 others(3): Show |
6 | HG02572.hp2 HG02622.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.946+2765T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63548822 | |||||||
| chr1:63548967 | A | C | 7 | a0004c0006t0001g0009 a0004c0006t0001g0041 a0004c0006t0001g0042 others(4): Show |
9 | HG00738.hp2 HG01934.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.947-2758A>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63548967 | |||||||
| chr1:63549034 | C | G | 94 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0008 others(91): Show |
119 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.947-2691C>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63549034 | |||||||
| chr1:63549047 | C | T | 1 | a0006c0008t0001g0187 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.947-2678C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63549047 | |||||||
| chr1:63549431 | T | C | 5 | a0004c0006t0001g0009 a0004c0006t0001g0041 a0004c0006t0001g0042 others(2): Show |
7 | HG01934.hp1 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.947-2294T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63549431 | |||||||
| chr1:63549546 | G | A | 195 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0008 others(192): Show |
246 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(243): Show |
intron_variant | MODIFIER | c.947-2179G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63549546 | |||||||
| chr1:63549671 | T | C | 13 | a0003c0004t0001g0006 a0003c0004t0001g0055 a0003c0004t0001g0056 others(10): Show |
17 | HG01167.hp2 HG02145.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.947-2054T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63549671 | |||||||
| chr1:63549728 | T | C | 1 | a0003c0004t0001g0065 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.947-1997T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63549728 | |||||||
| chr1:63549902 | G | A | 3 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 |
3 | HG02280.hp2 HG02717.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.947-1823G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63549902 | |||||||
| chr1:63549905 | A | G | 1 | a0001c0002t0001g0105 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.947-1820A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63549905 | |||||||
| chr1:63550051 | T | C | 1 | a0001c0001t0001g0007 | 5 | HG01070.hp1 HG01071.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.947-1674T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63550051 | |||||||
| chr1:63550106 | A | C | 13 | a0005c0007t0001g0030 a0005c0007t0001g0188 a0005c0007t0001g0189 others(10): Show |
15 | HG01192.hp1 HG01891.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.947-1619A>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63550106 | |||||||
| chr1:63550186 | T | G | 2 | a0001c0001t0001g0019 a0001c0001t0001g0147 |
3 | HG03516.hp1 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.947-1539T>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63550186 | |||||||
| chr1:63550193 | G | A | 1 | a0003c0004t0001g0184 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.947-1532G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63550193 | |||||||
| chr1:63550281 | T | C | 49 | a0002c0003t0001g0002 a0002c0003t0001g0018 a0002c0003t0001g0035 others(46): Show |
67 | HG00558.hp1 HG00733.hp1 HG00741.hp2 others(64): Show |
intron_variant | MODIFIER | c.947-1444T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63550281 | |||||||
| chr1:63550636 | T | TA | 22 | a0003c0005t0001g0052 a0003c0005t0001g0053 a0003c0005t0001g0054 others(19): Show |
24 | HG00738.hp2 HG01192.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.947-1076dupA | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 63550636 | ||||||
| chr1:63550636 | TA | T | 17 | a0001c0001t0001g0209 a0001c0001t0001g0222 a0001c0002t0001g0004 others(14): Show |
24 | HG00639.hp2 HG01106.hp1 HG01123.hp2 others(21): Show |
intron_variant | MODIFIER | c.947-1076delA | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 63550636 | ||||||
| chr1:63550667 | T | A | 1 | a0001c0002t0001g0096 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.947-1058T>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63550667 | |||||||
| chr1:63550864 | GA | G | 38 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(35): Show |
51 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.947-860delA | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63550864 | |||||||
| chr1:63550889 | G | T | 1 | a0001c0001t0001g0032 | 2 | HG00423.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.947-836G>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63550889 | |||||||
| chr1:63550915 | G | T | 1 | a0002c0003t0001g0251 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.947-810G>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63550915 | |||||||
| chr1:63551216 | G | A | 1 | a0001c0001t0001g0146 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.947-509G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63551216 | |||||||
| chr1:63551284 | C | T | 1 | a0002c0003t0001g0250 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.947-441C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63551284 | |||||||
| chr1:63551314 | C | T | 1 | a0001c0002t0001g0077 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.947-411C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63551314 | |||||||
| chr1:63551497 | A | G | 50 | a0002c0003t0001g0002 a0002c0003t0001g0018 a0002c0003t0001g0035 others(47): Show |
68 | HG00558.hp1 HG00733.hp1 HG00741.hp2 others(65): Show |
intron_variant | MODIFIER | c.947-228A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63551497 | |||||||
| chr1:63551563 | G | C | 195 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0008 others(192): Show |
246 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(243): Show |
intron_variant | MODIFIER | c.947-162G>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63551563 | |||||||
| chr1:63551590 | T | TG | 13 | a0005c0007t0001g0030 a0005c0007t0001g0188 a0005c0007t0001g0189 others(10): Show |
15 | HG01192.hp1 HG01891.hp1 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.947-134dupG | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 63551590 | ||||||
| chr1:63551591 | GA | G | 93 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0008 others(90): Show |
118 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.947-123delA | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr1 | 63551591 | ||||||
| chr1:63551713 | T | G | 5 | a0004c0006t0001g0009 a0004c0006t0001g0041 a0004c0006t0001g0042 others(2): Show |
7 | HG01934.hp1 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.947-12T>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 7/13 | chr1 | 63551713 | |||||||
| chr1:63551882 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1056+48C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 8/13 | chr1 | 63551882 | |||||||
| chr1:63551999 | TATTAA | T | 14 | a0003c0005t0001g0186 a0005c0007t0001g0030 a0005c0007t0001g0188 others(11): Show |
16 | HG01192.hp1 HG01891.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1056+178_1056+182d others(7): Show |
EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 63551999 | ||||||
| chr1:63552159 | A | G | 234 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(231): Show |
299 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(296): Show |
intron_variant | MODIFIER | c.1056+325A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 8/13 | chr1 | 63552159 | |||||||
| chr1:63552175 | T | G | 195 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0008 others(192): Show |
246 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(243): Show |
intron_variant | MODIFIER | c.1056+341T>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 8/13 | chr1 | 63552175 | |||||||
| chr1:63552447 | T | A | 1 | a0001c0002t0001g0132 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1056+613T>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 8/13 | chr1 | 63552447 | |||||||
| chr1:63552475 | T | C | 64 | a0002c0003t0001g0002 a0002c0003t0001g0018 a0002c0003t0001g0035 others(61): Show |
86 | HG00558.hp1 HG00733.hp1 HG00741.hp2 others(83): Show |
intron_variant | MODIFIER | c.1056+641T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 8/13 | chr1 | 63552475 | |||||||
| chr1:63552660 | T | C | 1 | a0001c0002t0001g0107 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1056+826T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 8/13 | chr1 | 63552660 | |||||||
| chr1:63552734 | G | A | 101 | a0002c0003t0001g0002 a0002c0003t0001g0018 a0002c0003t0001g0035 others(98): Show |
127 | HG00558.hp1 HG00733.hp1 HG00738.hp2 others(124): Show |
intron_variant | MODIFIER | c.1056+900G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 8/13 | chr1 | 63552734 | |||||||
| chr1:63552773 | A | G | 1 | a0010c0017t0001g0274 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1056+939A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 8/13 | chr1 | 63552773 | |||||||
| chr1:63552855 | T | C | 1 | a0001c0002t0001g0116 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1056+1021T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 8/13 | chr1 | 63552855 | |||||||
| chr1:63552973 | CTCTTA | C | 13 | a0003c0004t0001g0006 a0003c0004t0001g0055 a0003c0004t0001g0056 others(10): Show |
17 | HG01167.hp2 HG02145.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.1056+1141_1056+114 others(9): Show |
EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 63552973 | ||||||
| chr1:63553023 | T | C | 14 | a0003c0005t0001g0186 a0005c0007t0001g0030 a0005c0007t0001g0188 others(11): Show |
16 | HG01192.hp1 HG01891.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1056+1189T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 8/13 | chr1 | 63553023 | |||||||
| chr1:63553029 | T | G | 1 | a0001c0002t0001g0128 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1056+1195T>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 8/13 | chr1 | 63553029 | |||||||
| chr1:63553043 | A | G | 1 | a0014c0019t0001g0066 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1056+1209A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 8/13 | chr1 | 63553043 | |||||||
| chr1:63553154 | A | G | 1 | a0003c0004t0001g0065 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1056+1320A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 8/13 | chr1 | 63553154 | |||||||
| chr1:63553241 | G | A | 1 | a0001c0001t0003g0023 | 2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1056+1407G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 8/13 | chr1 | 63553241 | |||||||
| chr1:63553287 | A | G | 8 | a0006c0008t0001g0045 a0006c0008t0001g0046 a0006c0008t0001g0047 others(5): Show |
9 | HG01891.hp1 HG02280.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1056+1453A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 8/13 | chr1 | 63553287 | |||||||
| chr1:63553327 | C | T | 13 | a0003c0004t0001g0006 a0003c0004t0001g0055 a0003c0004t0001g0056 others(10): Show |
17 | HG01167.hp2 HG02145.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.1056+1493C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 8/13 | chr1 | 63553327 | |||||||
| chr1:63553420 | A | G | 1 | a0003c0004t0001g0063 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1056+1586A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 8/13 | chr1 | 63553420 | |||||||
| chr1:63553422 | C | G | 39 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(36): Show |
53 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.1056+1588C>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 8/13 | chr1 | 63553422 | |||||||
| chr1:63553525 | A | G | 1 | a0003c0004t0001g0064 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1056+1691A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 8/13 | chr1 | 63553525 | |||||||
| chr1:63553760 | C | T | 2 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
2 | HG02280.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1057-1598C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 8/13 | chr1 | 63553760 | |||||||
| chr1:63553905 | A | G | 1 | a0001c0002t0001g0131 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1057-1453A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 8/13 | chr1 | 63553905 | |||||||
| chr1:63554020 | G | A | 2 | a0003c0004t0001g0065 a0003c0004t0001g0184 |
2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1057-1338G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 8/13 | chr1 | 63554020 | |||||||
| chr1:63554319 | T | C | 6 | a0003c0005t0001g0052 a0003c0005t0001g0053 a0003c0005t0001g0054 others(3): Show |
6 | HG02572.hp2 HG02622.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1057-1039T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 8/13 | chr1 | 63554319 | |||||||
| chr1:63554377 | A | G | 5 | a0002c0003t0001g0238 a0002c0003t0001g0239 a0002c0003t0001g0248 others(2): Show |
5 | HG02071.hp2 NA18964.hp1 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.1057-981A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 8/13 | chr1 | 63554377 | |||||||
| chr1:63554433 | G | A | 49 | a0002c0003t0001g0002 a0002c0003t0001g0018 a0002c0003t0001g0035 others(46): Show |
67 | HG00558.hp1 HG00733.hp1 HG00741.hp2 others(64): Show |
intron_variant | MODIFIER | c.1057-925G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 8/13 | chr1 | 63554433 | |||||||
| chr1:63554449 | C | G | 1 | a0014c0019t0001g0066 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1057-909C>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 8/13 | chr1 | 63554449 | |||||||
| chr1:63554485 | G | A | 1 | a0002c0003t0001g0242 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1057-873G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 8/13 | chr1 | 63554485 | |||||||
| chr1:63554611 | A | G | 1 | a0003c0004t0001g0184 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1057-747A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 8/13 | chr1 | 63554611 | |||||||
| chr1:63554678 | G | A | 275 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(272): Show |
367 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(364): Show |
intron_variant | MODIFIER | c.1057-680G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 8/13 | chr1 | 63554678 | |||||||
| chr1:63554732 | T | C | 3 | a0003c0005t0001g0052 a0003c0005t0001g0053 a0003c0005t0001g0054 |
3 | HG02622.hp1 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1057-626T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 8/13 | chr1 | 63554732 | |||||||
| chr1:63554789 | A | T | 2 | a0003c0005t0001g0193 a0003c0005t0001g0194 |
2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1057-569A>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 8/13 | chr1 | 63554789 | |||||||
| chr1:63554948 | A | T | 3 | a0007c0010t0001g0034 a0007c0010t0001g0228 a0007c0010t0001g0230 |
4 | HG01891.hp1 HG02615.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1057-410A>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 8/13 | chr1 | 63554948 | |||||||
| chr1:63554967 | A | G | 7 | a0003c0004t0001g0006 a0003c0004t0001g0058 a0003c0004t0001g0059 others(4): Show |
11 | HG01167.hp2 HG02145.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1057-391A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 8/13 | chr1 | 63554967 | |||||||
| chr1:63554971 | CT | C | 33 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0014 others(30): Show |
59 | HG00642.hp1 HG00642.hp2 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.1057-380delT | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr1 | 63554971 | ||||||
| chr1:63555016 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1057-342C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 8/13 | chr1 | 63555016 | |||||||
| chr1:63555567 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1214+52T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 9/13 | chr1 | 63555567 | |||||||
| chr1:63555733 | G | A | 1 | a0014c0019t0001g0066 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1214+218G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 9/13 | chr1 | 63555733 | |||||||
| chr1:63556112 | T | C | 2 | a0003c0004t0001g0065 a0003c0004t0001g0184 |
2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1214+597T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 9/13 | chr1 | 63556112 | |||||||
| chr1:63556193 | A | G | 5 | a0001c0001t0001g0049 a0001c0001t0001g0149 a0001c0001t0001g0150 others(2): Show |
5 | HG00639.hp1 HG00642.hp2 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.1214+678A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 9/13 | chr1 | 63556193 | |||||||
| chr1:63556372 | A | G | 5 | a0001c0002t0001g0114 a0001c0002t0001g0116 a0001c0002t0001g0125 others(2): Show |
5 | HG02132.hp2 NA18974.hp2 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.1215-742A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 9/13 | chr1 | 63556372 | |||||||
| chr1:63556443 | T | C | 7 | a0004c0006t0001g0009 a0004c0006t0001g0041 a0004c0006t0001g0042 others(4): Show |
9 | HG00738.hp2 HG01934.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1215-671T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 9/13 | chr1 | 63556443 | |||||||
| chr1:63556568 | A | C | 2 | a0002c0003t0001g0237 a0002c0003t0001g0268 |
2 | HG02738.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1215-546A>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 9/13 | chr1 | 63556568 | |||||||
| chr1:63556586 | G | A | 1 | a0014c0019t0001g0066 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1215-528G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 9/13 | chr1 | 63556586 | |||||||
| chr1:63556613 | CT | C | 26 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0031 others(23): Show |
36 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(33): Show |
intron_variant | MODIFIER | c.1215-495delT | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr1 | 63556613 | ||||||
| chr1:63556747 | G | C | 1 | a0001c0002t0001g0129 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1215-367G>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 9/13 | chr1 | 63556747 | |||||||
| chr1:63556793 | C | T | 1 | a0010c0017t0001g0274 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1215-321C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 9/13 | chr1 | 63556793 | |||||||
| chr1:63556831 | G | C | 3 | a0007c0010t0001g0034 a0007c0010t0001g0228 a0007c0010t0001g0230 |
4 | HG01891.hp1 HG02615.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1215-283G>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 9/13 | chr1 | 63556831 | |||||||
| chr1:63556871 | T | C | 9 | a0003c0004t0001g0175 a0003c0004t0001g0176 a0003c0004t0001g0177 others(6): Show |
9 | HG01081.hp2 HG01109.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1215-243T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 9/13 | chr1 | 63556871 | |||||||
| chr1:63556873 | C | CA | 44 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0016 others(41): Show |
60 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(57): Show |
intron_variant | MODIFIER | c.1215-226dupA | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr1 | 63556873 | ||||||
| chr1:63556873 | CA | C | 49 | a0001c0002t0001g0093 a0002c0003t0001g0002 a0002c0003t0001g0018 others(46): Show |
67 | HG00558.hp1 HG00733.hp1 HG00741.hp2 others(64): Show |
intron_variant | MODIFIER | c.1215-226delA | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr1 | 63556873 | ||||||
| chr1:63556875 | A | C | 9 | a0003c0004t0001g0175 a0003c0004t0001g0176 a0003c0004t0001g0177 others(6): Show |
9 | HG01081.hp2 HG01109.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1215-239A>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 9/13 | chr1 | 63556875 | |||||||
| chr1:63556877 | A | C | 6 | a0003c0004t0001g0175 a0003c0004t0001g0178 a0003c0004t0001g0179 others(3): Show |
6 | HG01081.hp2 HG01109.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.1215-237A>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 9/13 | chr1 | 63556877 | |||||||
| chr1:63556879 | A | C | 1 | a0003c0004t0001g0180 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1215-235A>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 9/13 | chr1 | 63556879 | |||||||
| chr1:63556910 | C | T | 51 | a0002c0003t0001g0002 a0002c0003t0001g0018 a0002c0003t0001g0035 others(48): Show |
69 | HG00558.hp1 HG00733.hp1 HG00741.hp2 others(66): Show |
intron_variant | MODIFIER | c.1215-204C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 9/13 | chr1 | 63556910 | |||||||
| chr1:63557037 | C | CA | 88 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0143 others(85): Show |
111 | HG00558.hp1 HG00642.hp1 HG00733.hp1 others(108): Show |
intron_variant | MODIFIER | c.1215-61dupA | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr1 | 63557037 | ||||||
| chr1:63557037 | C | CAA | 16 | a0002c0003t0001g0036 a0002c0003t0001g0236 a0002c0003t0001g0238 others(13): Show |
17 | HG01071.hp1 HG01169.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.1215-62_1215-61dup others(2): Show |
EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr1 | 63557037 | ||||||
| chr1:63557050 | A | C | 1 | a0003c0005t0001g0186 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1215-64A>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 9/13 | chr1 | 63557050 | |||||||
| chr1:63557066 | G | A | 7 | a0004c0006t0001g0009 a0004c0006t0001g0041 a0004c0006t0001g0042 others(4): Show |
9 | HG00738.hp2 HG01934.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1215-48G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 9/13 | chr1 | 63557066 | |||||||
| chr1:63557374 | A | C | 1 | a0015c0018t0001g0273 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1348+127A>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 10/13 | chr1 | 63557374 | |||||||
| chr1:63557532 | G | A | 9 | a0003c0004t0001g0175 a0003c0004t0001g0176 a0003c0004t0001g0177 others(6): Show |
9 | HG01081.hp2 HG01109.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1348+285G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 10/13 | chr1 | 63557532 | |||||||
| chr1:63557692 | G | A | 3 | a0001c0002t0001g0022 a0001c0002t0001g0135 a0001c0002t0001g0136 |
4 | HG01074.hp1 HG01256.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1348+445G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 10/13 | chr1 | 63557692 | |||||||
| chr1:63557830 | A | G | 1 | a0001c0002t0001g0104 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1348+583A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 10/13 | chr1 | 63557830 | |||||||
| chr1:63558272 | G | A | 7 | a0003c0005t0001g0052 a0003c0005t0001g0053 a0003c0005t0001g0054 others(4): Show |
7 | HG02572.hp2 HG02622.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1348+1025G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 10/13 | chr1 | 63558272 | |||||||
| chr1:63558360 | C | G | 1 | a0001c0001t0001g0157 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1348+1113C>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 10/13 | chr1 | 63558360 | |||||||
| chr1:63558430 | T | TC | 6 | a0003c0005t0001g0052 a0003c0005t0001g0053 a0003c0005t0001g0054 others(3): Show |
6 | HG02572.hp2 HG02622.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1348+1184dupC | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 63558430 | ||||||
| chr1:63558558 | T | A | 2 | a0001c0002t0001g0125 a0001c0002t0001g0126 |
2 | NA18986.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.1348+1311T>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 10/13 | chr1 | 63558558 | |||||||
| chr1:63558560 | G | T | 2 | a0001c0002t0001g0125 a0001c0002t0001g0126 |
2 | NA18986.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.1348+1313G>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 10/13 | chr1 | 63558560 | |||||||
| chr1:63558699 | C | CT | 4 | a0001c0001t0001g0016 a0001c0001t0001g0208 a0001c0001t0001g0210 others(1): Show |
5 | HG00438.hp1 HG00438.hp2 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.1348+1459dupT | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 63558699 | ||||||
| chr1:63558719 | G | A | 1 | a0014c0019t0001g0066 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1348+1472G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 10/13 | chr1 | 63558719 | |||||||
| chr1:63558836 | C | T | 5 | a0005c0007t0001g0030 a0005c0007t0001g0188 a0005c0007t0001g0189 others(2): Show |
6 | HG01192.hp1 HG02622.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1348+1589C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 10/13 | chr1 | 63558836 | |||||||
| chr1:63558851 | C | T | 3 | a0002c0003t0001g0234 a0002c0003t0001g0252 a0002c0003t0001g0254 |
3 | HG00741.hp2 HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.1348+1604C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 10/13 | chr1 | 63558851 | |||||||
| chr1:63558911 | T | A | 1 | a0002c0003t0001g0259 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1348+1664T>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 10/13 | chr1 | 63558911 | |||||||
| chr1:63558939 | C | A | 1 | a0002c0003t0001g0255 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1348+1692C>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 10/13 | chr1 | 63558939 | |||||||
| chr1:63559021 | GA | G | 7 | a0001c0001t0001g0197 a0001c0001t0001g0219 a0001c0002t0001g0080 others(4): Show |
7 | HG01069.hp2 HG01070.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1348+1789delA | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 63559021 | ||||||
| chr1:63559093 | T | G | 234 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(231): Show |
299 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(296): Show |
intron_variant | MODIFIER | c.1348+1846T>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 10/13 | chr1 | 63559093 | |||||||
| chr1:63559157 | C | T | 6 | a0003c0005t0001g0052 a0003c0005t0001g0053 a0003c0005t0001g0054 others(3): Show |
6 | HG02572.hp2 HG02622.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1348+1910C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 10/13 | chr1 | 63559157 | |||||||
| chr1:63559301 | C | CA | 45 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(42): Show |
59 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(56): Show |
intron_variant | MODIFIER | c.1348+2078dupA | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 63559301 | ||||||
| chr1:63559301 | C | CAA | 76 | a0001c0001t0001g0031 a0001c0001t0001g0166 a0001c0001t0001g0203 others(73): Show |
97 | HG00408.hp2 HG00558.hp2 HG00639.hp2 others(94): Show |
intron_variant | MODIFIER | c.1348+2077_1348+207 others(6): Show |
EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 63559301 | ||||||
| chr1:63559301 | C | CAAA | 25 | a0001c0002t0001g0011 a0001c0002t0001g0021 a0001c0002t0001g0022 others(22): Show |
30 | HG00423.hp1 HG00673.hp1 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.1348+2076_1348+207 others(7): Show |
EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 63559301 | ||||||
| chr1:63559301 | C | CAAAA | 6 | a0001c0002t0001g0113 a0001c0002t0001g0120 a0003c0005t0001g0186 others(3): Show |
6 | HG01978.hp2 HG02572.hp1 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.1348+2075_1348+207 others(8): Show |
EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 63559301 | ||||||
| chr1:63559301 | CA | C | 63 | a0002c0003t0001g0002 a0002c0003t0001g0018 a0002c0003t0001g0035 others(60): Show |
86 | HG00558.hp1 HG00733.hp1 HG00741.hp2 others(83): Show |
intron_variant | MODIFIER | c.1348+2078delA | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 63559301 | ||||||
| chr1:63559301 | CAAAAAAA others(3): Show |
C | 1 | a0001c0009t0001g0103 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1348+2069_1348+207 others(14): Show |
EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 63559301 | ||||||
| chr1:63559326 | T | A | 1 | a0003c0005t0001g0168 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1348+2079T>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 10/13 | chr1 | 63559326 | |||||||
| chr1:63559348 | C | T | 2 | a0003c0004t0001g0057 a0003c0004t0001g0064 |
2 | HG02647.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1348+2101C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 10/13 | chr1 | 63559348 | |||||||
| chr1:63559478 | G | A | 1 | a0001c0001t0003g0023 | 2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1348+2231G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 10/13 | chr1 | 63559478 | |||||||
| chr1:63559564 | C | T | 2 | a0003c0004t0001g0059 a0003c0004t0001g0061 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1349-2145C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 10/13 | chr1 | 63559564 | |||||||
| chr1:63559835 | A | G | 1 | a0005c0007t0001g0188 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1349-1874A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 10/13 | chr1 | 63559835 | |||||||
| chr1:63559960 | AT | A | 191 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0008 others(188): Show |
242 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(239): Show |
intron_variant | MODIFIER | c.1349-1736delT | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 63559960 | ||||||
| chr1:63559995 | G | A | 1 | a0002c0003t0001g0018 | 3 | NA18980.hp2 NA18991.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.1349-1714G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 10/13 | chr1 | 63559995 | |||||||
| chr1:63560099 | C | T | 38 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(35): Show |
51 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.1349-1610C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 10/13 | chr1 | 63560099 | |||||||
| chr1:63560165 | G | A | 13 | a0003c0004t0001g0006 a0003c0004t0001g0055 a0003c0004t0001g0056 others(10): Show |
17 | HG01167.hp2 HG02145.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.1349-1544G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 10/13 | chr1 | 63560165 | |||||||
| chr1:63560182 | G | C | 1 | a0010c0017t0001g0274 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1349-1527G>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 10/13 | chr1 | 63560182 | |||||||
| chr1:63560188 | A | G | 101 | a0002c0003t0001g0002 a0002c0003t0001g0018 a0002c0003t0001g0035 others(98): Show |
127 | HG00558.hp1 HG00733.hp1 HG00738.hp2 others(124): Show |
intron_variant | MODIFIER | c.1349-1521A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 10/13 | chr1 | 63560188 | |||||||
| chr1:63560243 | C | T | 7 | a0004c0006t0001g0009 a0004c0006t0001g0041 a0004c0006t0001g0042 others(4): Show |
9 | HG00738.hp2 HG01934.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1349-1466C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 10/13 | chr1 | 63560243 | |||||||
| chr1:63560313 | C | T | 64 | a0002c0003t0001g0002 a0002c0003t0001g0018 a0002c0003t0001g0035 others(61): Show |
84 | HG00558.hp1 HG00733.hp1 HG00741.hp2 others(81): Show |
intron_variant | MODIFIER | c.1349-1396C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 10/13 | chr1 | 63560313 | |||||||
| chr1:63560418 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1349-1291C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 10/13 | chr1 | 63560418 | |||||||
| chr1:63560512 | CT | C | 183 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(180): Show |
244 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(241): Show |
intron_variant | MODIFIER | c.1349-1175delT | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 63560512 | ||||||
| chr1:63560512 | CTT | C | 33 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0218 others(30): Show |
37 | HG01168.hp2 HG01192.hp1 HG01256.hp1 others(34): Show |
intron_variant | MODIFIER | c.1349-1176_1349-117 others(6): Show |
EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 63560512 | ||||||
| chr1:63560512 | CTTT | C | 7 | a0003c0005t0001g0193 a0004c0006t0001g0173 a0004c0006t0001g0174 others(4): Show |
7 | HG00738.hp2 HG02572.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1349-1177_1349-117 others(7): Show |
EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr1 | 63560512 | ||||||
| chr1:63560548 | A | G | 175 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0008 others(172): Show |
224 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(221): Show |
intron_variant | MODIFIER | c.1349-1161A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 10/13 | chr1 | 63560548 | |||||||
| chr1:63560669 | G | A | 6 | a0003c0005t0001g0052 a0003c0005t0001g0053 a0003c0005t0001g0054 others(3): Show |
6 | HG02572.hp2 HG02622.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1349-1040G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 10/13 | chr1 | 63560669 | |||||||
| chr1:63560745 | C | A | 1 | a0003c0005t0001g0186 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1349-964C>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 10/13 | chr1 | 63560745 | |||||||
| chr1:63561262 | C | T | 9 | a0001c0002t0001g0123 a0006c0008t0001g0045 a0006c0008t0001g0046 others(6): Show |
10 | HG01891.hp1 HG02280.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1349-447C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 10/13 | chr1 | 63561262 | |||||||
| chr1:63561263 | G | A | 1 | a0001c0001t0001g0202 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.1349-446G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 10/13 | chr1 | 63561263 | |||||||
| chr1:63561302 | A | C | 1 | a0001c0009t0001g0082 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1349-407A>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 10/13 | chr1 | 63561302 | |||||||
| chr1:63561422 | A | T | 9 | a0003c0004t0001g0175 a0003c0004t0001g0176 a0003c0004t0001g0177 others(6): Show |
9 | HG01081.hp2 HG01109.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1349-287A>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 10/13 | chr1 | 63561422 | |||||||
| chr1:63561687 | A | C | 9 | a0003c0004t0001g0175 a0003c0004t0001g0176 a0003c0004t0001g0177 others(6): Show |
9 | HG01081.hp2 HG01109.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1349-22A>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 10/13 | chr1 | 63561687 | |||||||
| chr1:63562000 | T | C | 1 | a0001c0002t0001g0122 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1497+143T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63562000 | |||||||
| chr1:63562056 | C | T | 3 | a0003c0005t0001g0052 a0003c0005t0001g0053 a0003c0005t0001g0054 |
3 | HG02622.hp1 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1497+199C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63562056 | |||||||
| chr1:63562211 | A | G | 14 | a0003c0005t0001g0186 a0005c0007t0001g0030 a0005c0007t0001g0188 others(11): Show |
16 | HG01192.hp1 HG01891.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1497+354A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63562211 | |||||||
| chr1:63562223 | C | A | 195 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0008 others(192): Show |
246 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(243): Show |
intron_variant | MODIFIER | c.1497+366C>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63562223 | |||||||
| chr1:63562270 | C | T | 10 | a0003c0004t0001g0175 a0003c0004t0001g0176 a0003c0004t0001g0177 others(7): Show |
10 | HG01081.hp2 HG01109.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1497+413C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63562270 | |||||||
| chr1:63562395 | C | G | 1 | a0001c0001t0001g0158 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1497+538C>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63562395 | |||||||
| chr1:63562424 | T | A | 21 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0031 others(18): Show |
31 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.1497+567T>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63562424 | |||||||
| chr1:63562442 | AATTT | A | 12 | a0001c0001t0001g0206 a0001c0001t0001g0220 a0001c0002t0001g0051 others(9): Show |
12 | HG00639.hp2 HG01261.hp1 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.1497+592_1497+595d others(6): Show |
EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 63562442 | ||||||
| chr1:63562445 | T | TTA | 4 | a0001c0002t0001g0068 a0001c0002t0001g0086 a0003c0005t0001g0052 others(1): Show |
4 | HG01433.hp2 HG01981.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1497+590_1497+591d others(4): Show |
EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 63562445 | ||||||
| chr1:63562445 | TTATTTA | T | 15 | a0001c0001t0001g0221 a0001c0002t0001g0010 a0001c0002t0001g0013 others(12): Show |
16 | HG00738.hp2 HG01891.hp1 HG02083.hp1 others(13): Show |
intron_variant | MODIFIER | c.1497+592_1497+597d others(8): Show |
EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 63562445 | ||||||
| chr1:63562445 | TTATTTAT others(1): Show |
T | 26 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0207 others(23): Show |
30 | HG00408.hp2 HG00673.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.1497+592_1497+599d others(10): Show |
EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 63562445 | ||||||
| chr1:63562445 | TTATTTAT others(3): Show |
T | 19 | a0001c0001t0001g0213 a0001c0002t0001g0005 a0001c0002t0001g0021 others(16): Show |
23 | HG00423.hp1 HG00735.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.1497+592_1497+601d others(12): Show |
EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 63562445 | ||||||
| chr1:63562445 | TTATTTAT others(5): Show |
T | 26 | a0001c0001t0001g0212 a0001c0001t0001g0223 a0001c0001t0001g0225 others(23): Show |
29 | HG00558.hp2 HG00673.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.1497+592_1497+603d others(14): Show |
EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 63562445 | ||||||
| chr1:63562445 | TTATTTAT others(7): Show |
T | 18 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0199 others(15): Show |
25 | HG00733.hp2 HG01106.hp2 HG01192.hp2 others(22): Show |
intron_variant | MODIFIER | c.1497+592_1497+605d others(16): Show |
EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 63562445 | ||||||
| chr1:63562445 | TTATTTAT others(9): Show |
T | 9 | a0001c0001t0001g0017 a0001c0001t0001g0033 a0001c0001t0001g0214 others(6): Show |
11 | HG01243.hp1 HG01433.hp1 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.1497+592_1497+607d others(18): Show |
EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 63562445 | ||||||
| chr1:63562445 | TTATTTAT others(11): Show |
T | 15 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0031 others(12): Show |
20 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(17): Show |
intron_variant | MODIFIER | c.1497+592_1497+609d others(20): Show |
EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 63562445 | ||||||
| chr1:63562445 | TTATTTAT others(13): Show |
T | 1 | a0001c0001t0001g0204 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1497+592_1497+611d others(22): Show |
EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 63562445 | ||||||
| chr1:63562445 | TTATTTAT others(17): Show |
T | 5 | a0001c0002t0001g0275 a0002c0003t0001g0238 a0002c0003t0001g0239 others(2): Show |
5 | HG02280.hp1 HG02698.hp2 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.1497+592_1497+615d others(26): Show |
EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 63562445 | ||||||
| chr1:63562445 | TTATTTAT others(19): Show |
T | 47 | a0002c0003t0001g0002 a0002c0003t0001g0018 a0002c0003t0001g0035 others(44): Show |
65 | HG00558.hp1 HG00733.hp1 HG00741.hp2 others(62): Show |
intron_variant | MODIFIER | c.1497+592_1497+617d others(28): Show |
EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 63562445 | ||||||
| chr1:63562445 | TTATTTAT others(21): Show |
T | 24 | a0003c0004t0001g0006 a0003c0004t0001g0055 a0003c0004t0001g0056 others(21): Show |
28 | HG01081.hp2 HG01109.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.1497+592_1497+619d others(30): Show |
EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 63562445 | ||||||
| chr1:63562445 | TTATTTAT others(23): Show |
T | 1 | a0003c0005t0001g0186 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1497+592_1497+621d others(32): Show |
EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 63562445 | ||||||
| chr1:63562447 | ATT | A | 13 | a0001c0002t0001g0071 a0001c0002t0001g0088 a0001c0002t0001g0105 others(10): Show |
13 | HG01123.hp1 HG01192.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.1497+592_1497+593d others(4): Show |
EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 63562447 | ||||||
| chr1:63562449 | T | A | 18 | a0001c0001t0001g0166 a0001c0002t0001g0012 a0001c0002t0001g0068 others(15): Show |
21 | HG01433.hp2 HG01934.hp1 HG01981.hp1 others(18): Show |
intron_variant | MODIFIER | c.1497+592T>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63562449 | |||||||
| chr1:63562449 | T | TTA | 6 | a0001c0001t0001g0049 a0001c0001t0001g0142 a0001c0001t0001g0162 others(3): Show |
6 | HG00642.hp2 HG00741.hp1 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.1497+637_1497+638d others(4): Show |
EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 63562449 | ||||||
| chr1:63562449 | T | TTATA | 12 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0014 others(9): Show |
14 | HG00642.hp1 HG01167.hp1 HG01169.hp2 others(11): Show |
intron_variant | MODIFIER | c.1497+635_1497+638d others(6): Show |
EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 63562449 | ||||||
| chr1:63562449 | T | TTATATA | 9 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0019 others(6): Show |
9 | HG01168.hp1 HG01255.hp2 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.1497+633_1497+638d others(8): Show |
EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 63562449 | ||||||
| chr1:63562449 | T | TTATATAT others(1): Show |
4 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0158 others(1): Show |
4 | HG01517.hp1 HG02129.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.1497+631_1497+638d others(10): Show |
EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 63562449 | ||||||
| chr1:63562449 | T | TTATATAT others(3): Show |
11 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0014 others(8): Show |
13 | HG00738.hp1 HG01258.hp1 HG03669.hp2 others(10): Show |
intron_variant | MODIFIER | c.1497+629_1497+638d others(12): Show |
EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 63562449 | ||||||
| chr1:63562449 | T | TTATATAT others(5): Show |
1 | a0001c0001t0001g0007 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1497+627_1497+638d others(14): Show |
EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 63562449 | ||||||
| chr1:63562449 | T | TTATATAT others(7): Show |
2 | a0001c0001t0001g0001 a0003c0005t0001g0029 |
2 | HG03927.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.1497+625_1497+638d others(16): Show |
EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 63562449 | ||||||
| chr1:63562449 | T | TTATATAT others(9): Show |
1 | a0001c0001t0001g0161 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1497+623_1497+638d others(18): Show |
EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 63562449 | ||||||
| chr1:63562449 | T | TTATATAT others(29): Show |
1 | a0001c0001t0001g0001 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1497+603_1497+638d others(38): Show |
EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 63562449 | ||||||
| chr1:63562449 | TTATATAT others(15): Show |
T | 4 | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0027 others(1): Show |
8 | NA18944.hp2 NA18945.hp1 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.1497+617_1497+638d others(24): Show |
EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 63562449 | ||||||
| chr1:63562449 | TTATATAT others(23): Show |
T | 1 | a0001c0001t0001g0146 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1497+609_1497+638d others(32): Show |
EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 63562449 | ||||||
| chr1:63562471 | A | T | 3 | a0002c0003t0001g0238 a0002c0003t0001g0239 a0002c0003t0001g0249 |
3 | NA18989.hp1 NA18997.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1497+614A>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63562471 | |||||||
| chr1:63562473 | A | T | 46 | a0002c0003t0001g0002 a0002c0003t0001g0018 a0002c0003t0001g0035 others(43): Show |
64 | HG00558.hp1 HG00733.hp1 HG00741.hp2 others(61): Show |
intron_variant | MODIFIER | c.1497+616A>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63562473 | |||||||
| chr1:63562475 | A | T | 24 | a0003c0004t0001g0006 a0003c0004t0001g0055 a0003c0004t0001g0056 others(21): Show |
28 | HG01081.hp2 HG01109.hp2 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.1497+618A>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63562475 | |||||||
| chr1:63562476 | TATATATA others(12): Show |
T | 1 | a0004c0006t0001g0044 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1497+621_1497+639d others(21): Show |
EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 63562476 | ||||||
| chr1:63562482 | TATATATA others(6): Show |
T | 1 | a0001c0002t0001g0012 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1497+627_1497+639d others(15): Show |
EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 63562482 | ||||||
| chr1:63562484 | TATATATA others(4): Show |
T | 1 | a0004c0006t0001g0041 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1497+629_1497+639d others(13): Show |
EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 63562484 | ||||||
| chr1:63562494 | T | A | 14 | a0003c0004t0001g0175 a0003c0004t0001g0176 a0003c0004t0001g0177 others(11): Show |
14 | HG01081.hp2 HG01109.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.1497+637T>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63562494 | |||||||
| chr1:63562496 | A | T | 2 | a0001c0001t0001g0196 a0004c0006t0001g0043 |
2 | HG00642.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1497+639A>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63562496 | |||||||
| chr1:63562498 | A | C | 4 | a0004c0006t0001g0009 a0004c0006t0001g0041 a0004c0006t0001g0042 others(1): Show |
6 | HG01934.hp1 HG02257.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1497+641A>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63562498 | |||||||
| chr1:63562499 | C | CT | 83 | a0001c0001t0001g0220 a0002c0003t0001g0002 a0002c0003t0001g0018 others(80): Show |
105 | HG00558.hp1 HG00733.hp1 HG00738.hp2 others(102): Show |
intron_variant | MODIFIER | c.1497+655dupT | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 63562499 | ||||||
| chr1:63562499 | C | CTT | 14 | a0003c0005t0001g0186 a0005c0007t0001g0030 a0005c0007t0001g0188 others(11): Show |
16 | HG01192.hp1 HG01891.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1497+654_1497+655d others(4): Show |
EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 63562499 | ||||||
| chr1:63562499 | C | T | 4 | a0004c0006t0001g0009 a0004c0006t0001g0041 a0004c0006t0001g0042 others(1): Show |
6 | HG01934.hp1 HG02257.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1497+642C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63562499 | |||||||
| chr1:63562656 | C | T | 27 | a0003c0005t0001g0052 a0003c0005t0001g0053 a0003c0005t0001g0054 others(24): Show |
31 | HG00738.hp2 HG01192.hp1 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.1497+799C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63562656 | |||||||
| chr1:63562754 | T | C | 1 | a0015c0018t0001g0273 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1497+897T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63562754 | |||||||
| chr1:63562839 | C | G | 7 | a0004c0006t0001g0009 a0004c0006t0001g0041 a0004c0006t0001g0042 others(4): Show |
9 | HG00738.hp2 HG01934.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1497+982C>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63562839 | |||||||
| chr1:63563424 | C | T | 1 | a0001c0002t0001g0071 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1497+1567C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63563424 | |||||||
| chr1:63563818 | C | T | 1 | a0001c0001t0001g0015 | 3 | NA18973.hp2 NA19054.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.1497+1961C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63563818 | |||||||
| chr1:63563920 | C | T | 3 | a0001c0002t0001g0088 a0001c0002t0001g0090 a0001c0002t0001g0092 |
3 | HG02080.hp1 NA18971.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.1497+2063C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63563920 | |||||||
| chr1:63563935 | G | A | 195 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0008 others(192): Show |
246 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(243): Show |
intron_variant | MODIFIER | c.1497+2078G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63563935 | |||||||
| chr1:63563949 | T | C | 6 | a0003c0005t0001g0052 a0003c0005t0001g0053 a0003c0005t0001g0054 others(3): Show |
6 | HG02572.hp2 HG02622.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1497+2092T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63563949 | |||||||
| chr1:63564087 | T | C | 4 | a0006c0008t0001g0045 a0006c0008t0001g0046 a0006c0008t0001g0047 others(1): Show |
4 | HG02572.hp1 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1497+2230T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63564087 | |||||||
| chr1:63564092 | A | G | 195 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0008 others(192): Show |
246 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(243): Show |
intron_variant | MODIFIER | c.1497+2235A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63564092 | |||||||
| chr1:63564093 | T | G | 195 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0008 others(192): Show |
246 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(243): Show |
intron_variant | MODIFIER | c.1497+2236T>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63564093 | |||||||
| chr1:63564177 | G | A | 277 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(274): Show |
369 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(366): Show |
intron_variant | MODIFIER | c.1497+2320G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63564177 | |||||||
| chr1:63564279 | A | C | 7 | a0004c0006t0001g0009 a0004c0006t0001g0041 a0004c0006t0001g0042 others(4): Show |
9 | HG00738.hp2 HG01934.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1497+2422A>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63564279 | |||||||
| chr1:63564347 | G | T | 1 | a0002c0003t0001g0268 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1497+2490G>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63564347 | |||||||
| chr1:63564441 | G | A | 20 | a0003c0005t0001g0052 a0003c0005t0001g0053 a0003c0005t0001g0054 others(17): Show |
22 | HG01192.hp1 HG01891.hp1 HG02280.hp1 others(19): Show |
intron_variant | MODIFIER | c.1497+2584G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63564441 | |||||||
| chr1:63564543 | G | A | 10 | a0003c0004t0001g0175 a0003c0004t0001g0176 a0003c0004t0001g0177 others(7): Show |
10 | HG01081.hp2 HG01109.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1497+2686G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63564543 | |||||||
| chr1:63564593 | C | A | 1 | a0001c0001t0003g0023 | 2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1497+2736C>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63564593 | |||||||
| chr1:63564596 | G | T | 1 | a0001c0001t0003g0023 | 2 | HG03195.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1497+2739G>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63564596 | |||||||
| chr1:63564708 | A | T | 7 | a0004c0006t0001g0009 a0004c0006t0001g0041 a0004c0006t0001g0042 others(4): Show |
9 | HG00738.hp2 HG01934.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1497+2851A>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63564708 | |||||||
| chr1:63564729 | CA | C | 234 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(231): Show |
299 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(296): Show |
intron_variant | MODIFIER | c.1497+2880delA | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 63564729 | ||||||
| chr1:63564765 | G | A | 2 | a0004c0006t0001g0173 a0004c0006t0001g0174 |
2 | HG00738.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1497+2908G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63564765 | |||||||
| chr1:63564841 | A | C | 13 | a0003c0004t0001g0006 a0003c0004t0001g0055 a0003c0004t0001g0056 others(10): Show |
17 | HG01167.hp2 HG02145.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.1497+2984A>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63564841 | |||||||
| chr1:63565031 | C | T | 7 | a0004c0006t0001g0009 a0004c0006t0001g0041 a0004c0006t0001g0042 others(4): Show |
9 | HG00738.hp2 HG01934.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1497+3174C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63565031 | |||||||
| chr1:63565084 | C | T | 74 | a0002c0003t0001g0002 a0002c0003t0001g0018 a0002c0003t0001g0035 others(71): Show |
96 | HG00558.hp1 HG00733.hp1 HG00741.hp2 others(93): Show |
intron_variant | MODIFIER | c.1498-3226C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63565084 | |||||||
| chr1:63565131 | G | C | 3 | a0003c0005t0001g0052 a0003c0005t0001g0053 a0003c0005t0001g0054 |
3 | HG02622.hp1 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1498-3179G>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63565131 | |||||||
| chr1:63565191 | G | T | 94 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0008 others(91): Show |
119 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.1498-3119G>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63565191 | |||||||
| chr1:63565202 | A | G | 2 | a0004c0006t0001g0173 a0004c0006t0001g0174 |
2 | HG00738.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1498-3108A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63565202 | |||||||
| chr1:63565231 | T | C | 195 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0008 others(192): Show |
246 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(243): Show |
intron_variant | MODIFIER | c.1498-3079T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63565231 | |||||||
| chr1:63565256 | G | A | 64 | a0002c0003t0001g0002 a0002c0003t0001g0018 a0002c0003t0001g0035 others(61): Show |
86 | HG00558.hp1 HG00733.hp1 HG00741.hp2 others(83): Show |
intron_variant | MODIFIER | c.1498-3054G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63565256 | |||||||
| chr1:63565291 | A | G | 100 | a0002c0003t0001g0002 a0002c0003t0001g0018 a0002c0003t0001g0035 others(97): Show |
126 | HG00558.hp1 HG00733.hp1 HG00738.hp2 others(123): Show |
intron_variant | MODIFIER | c.1498-3019A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63565291 | |||||||
| chr1:63565337 | C | T | 1 | a0001c0002t0001g0134 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1498-2973C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63565337 | |||||||
| chr1:63565358 | C | CA | 47 | a0001c0002t0001g0074 a0002c0003t0001g0002 a0002c0003t0001g0018 others(44): Show |
65 | HG00558.hp1 HG00741.hp2 HG01069.hp1 others(62): Show |
intron_variant | MODIFIER | c.1498-2941dupA | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 63565358 | ||||||
| chr1:63565367 | A | AC | 3 | a0002c0003t0001g0260 a0002c0003t0001g0261 a0002c0003t0001g0262 |
3 | NA18939.hp1 NA18957.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.1498-2943_1498-294 others(5): Show |
EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63565367 | |||||||
| chr1:63565367 | A | C | 3 | a0001c0002t0001g0072 a0001c0002t0001g0093 a0006c0008t0001g0187 |
3 | HG02056.hp1 HG02280.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1498-2943A>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63565367 | |||||||
| chr1:63565370 | C | A | 6 | a0003c0005t0001g0052 a0003c0005t0001g0053 a0003c0005t0001g0054 others(3): Show |
6 | HG02572.hp2 HG02622.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1498-2940C>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63565370 | |||||||
| chr1:63565376 | C | A | 2 | a0007c0010t0001g0034 a0007c0010t0001g0228 |
3 | HG01891.hp1 HG02615.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1498-2934C>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63565376 | |||||||
| chr1:63565379 | C | A | 226 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(223): Show |
290 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(287): Show |
intron_variant | MODIFIER | c.1498-2931C>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63565379 | |||||||
| chr1:63565382 | A | C | 1 | a0001c0001t0001g0161 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1498-2928A>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63565382 | |||||||
| chr1:63565510 | G | A | 1 | a0002c0003t0001g0276 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1498-2800G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63565510 | |||||||
| chr1:63565530 | T | C | 277 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(274): Show |
369 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(366): Show |
intron_variant | MODIFIER | c.1498-2780T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63565530 | |||||||
| chr1:63565694 | T | TA | 195 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0008 others(192): Show |
246 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(243): Show |
intron_variant | MODIFIER | c.1498-2611dupA | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 63565694 | ||||||
| chr1:63565947 | T | A | 1 | a0001c0009t0001g0084 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1498-2363T>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63565947 | |||||||
| chr1:63566120 | G | C | 1 | a0001c0002t0001g0131 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1498-2190G>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63566120 | |||||||
| chr1:63566220 | A | T | 1 | a0003c0005t0001g0193 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1498-2090A>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63566220 | |||||||
| chr1:63566283 | G | A | 2 | a0001c0002t0001g0050 a0001c0002t0001g0051 |
2 | HG01261.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1498-2027G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63566283 | |||||||
| chr1:63566520 | T | A | 1 | a0003c0005t0001g0170 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1498-1790T>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63566520 | |||||||
| chr1:63566612 | A | G | 195 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0008 others(192): Show |
246 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(243): Show |
intron_variant | MODIFIER | c.1498-1698A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63566612 | |||||||
| chr1:63566613 | T | C | 190 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0008 others(187): Show |
239 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(236): Show |
intron_variant | MODIFIER | c.1498-1697T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63566613 | |||||||
| chr1:63567171 | G | A | 2 | a0001c0001t0001g0204 a0001c0001t0001g0219 |
2 | NA18957.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.1498-1139G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63567171 | |||||||
| chr1:63567323 | G | T | 1 | a0006c0008t0001g0047 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1498-987G>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63567323 | |||||||
| chr1:63567377 | C | T | 52 | a0001c0002t0001g0008 a0001c0002t0001g0010 a0001c0002t0001g0013 others(49): Show |
59 | HG00408.hp2 HG00423.hp1 HG00673.hp2 others(56): Show |
intron_variant | MODIFIER | c.1498-933C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63567377 | |||||||
| chr1:63567461 | A | T | 1 | a0001c0001t0001g0153 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1498-849A>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63567461 | |||||||
| chr1:63567525 | G | A | 9 | a0003c0004t0001g0175 a0003c0004t0001g0176 a0003c0004t0001g0177 others(6): Show |
9 | HG01081.hp2 HG01109.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1498-785G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63567525 | |||||||
| chr1:63567829 | C | A | 2 | a0004c0006t0001g0173 a0004c0006t0001g0174 |
2 | HG00738.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1498-481C>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63567829 | |||||||
| chr1:63567854 | C | A | 2 | a0004c0006t0001g0173 a0004c0006t0001g0174 |
2 | HG00738.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1498-456C>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63567854 | |||||||
| chr1:63567877 | G | A | 5 | a0002c0003t0001g0237 a0002c0003t0001g0263 a0002c0003t0001g0268 others(2): Show |
5 | HG01884.hp1 HG02293.hp1 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.1498-433G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63567877 | |||||||
| chr1:63568051 | AAAG | A | 4 | a0004c0006t0001g0009 a0004c0006t0001g0042 a0004c0006t0001g0043 others(1): Show |
6 | HG01934.hp1 HG02257.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.1498-255_1498-253d others(5): Show |
EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr1 | 63568051 | ||||||
| chr1:63568147 | T | C | 2 | a0004c0006t0001g0173 a0004c0006t0001g0174 |
2 | HG00738.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.1498-163T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 11/13 | chr1 | 63568147 | |||||||
| chr1:63568637 | A | G | 6 | a0003c0005t0001g0052 a0003c0005t0001g0053 a0003c0005t0001g0054 others(3): Show |
6 | HG02572.hp2 HG02622.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1707+118A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 12/13 | chr1 | 63568637 | |||||||
| chr1:63568702 | AT | A | 74 | a0002c0003t0001g0002 a0002c0003t0001g0018 a0002c0003t0001g0035 others(71): Show |
96 | HG00558.hp1 HG00733.hp1 HG00741.hp2 others(93): Show |
intron_variant | MODIFIER | c.1707+188delT | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr1 | 63568702 | ||||||
| chr1:63568716 | C | A | 1 | a0001c0002t0001g0134 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1707+197C>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 12/13 | chr1 | 63568716 | |||||||
| chr1:63568797 | T | A | 94 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0008 others(91): Show |
119 | HG00408.hp2 HG00423.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.1707+278T>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 12/13 | chr1 | 63568797 | |||||||
| chr1:63568851 | G | T | 74 | a0002c0003t0001g0002 a0002c0003t0001g0018 a0002c0003t0001g0035 others(71): Show |
96 | HG00558.hp1 HG00733.hp1 HG00741.hp2 others(93): Show |
intron_variant | MODIFIER | c.1707+332G>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 12/13 | chr1 | 63568851 | |||||||
| chr1:63568964 | T | C | 1 | a0001c0002t0001g0088 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1707+445T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 12/13 | chr1 | 63568964 | |||||||
| chr1:63569062 | C | T | 14 | a0003c0005t0001g0186 a0005c0007t0001g0030 a0005c0007t0001g0188 others(11): Show |
16 | HG01192.hp1 HG01891.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1707+543C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 12/13 | chr1 | 63569062 | |||||||
| chr1:63569115 | C | T | 9 | a0003c0004t0001g0175 a0003c0004t0001g0176 a0003c0004t0001g0177 others(6): Show |
9 | HG01081.hp2 HG01109.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.1707+596C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 12/13 | chr1 | 63569115 | |||||||
| chr1:63569392 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1707+873C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 12/13 | chr1 | 63569392 | |||||||
| chr1:63569476 | G | A | 195 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0008 others(192): Show |
246 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(243): Show |
intron_variant | MODIFIER | c.1707+957G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 12/13 | chr1 | 63569476 | |||||||
| chr1:63569505 | AGGGAACT others(7): Show |
A | 1 | a0001c0001t0001g0156 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1707+991_1707+1004 others(17): Show |
EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr1 | 63569505 | ||||||
| chr1:63569527 | G | A | 50 | a0002c0003t0001g0002 a0002c0003t0001g0018 a0002c0003t0001g0035 others(47): Show |
68 | HG00558.hp1 HG00733.hp1 HG00741.hp2 others(65): Show |
intron_variant | MODIFIER | c.1707+1008G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 12/13 | chr1 | 63569527 | |||||||
| chr1:63569593 | G | GT | 21 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0031 others(18): Show |
31 | HG00408.hp1 HG00423.hp2 HG00438.hp2 others(28): Show |
intron_variant | MODIFIER | c.1707+1075dupT | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr1 | 63569593 | ||||||
| chr1:63569798 | T | A | 14 | a0003c0005t0001g0186 a0005c0007t0001g0030 a0005c0007t0001g0188 others(11): Show |
16 | HG01192.hp1 HG01891.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1708-1223T>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 12/13 | chr1 | 63569798 | |||||||
| chr1:63569841 | T | C | 5 | a0005c0007t0001g0030 a0005c0007t0001g0188 a0005c0007t0001g0189 others(2): Show |
6 | HG01192.hp1 HG02622.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1708-1180T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 12/13 | chr1 | 63569841 | |||||||
| chr1:63569921 | A | G | 4 | a0006c0008t0001g0045 a0006c0008t0001g0046 a0006c0008t0001g0047 others(1): Show |
4 | HG02572.hp1 HG02886.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1708-1100A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 12/13 | chr1 | 63569921 | |||||||
| chr1:63569934 | G | A | 1 | a0003c0004t0001g0184 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1708-1087G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 12/13 | chr1 | 63569934 | |||||||
| chr1:63570401 | C | T | 5 | a0001c0002t0001g0005 a0001c0002t0001g0024 a0001c0002t0001g0117 others(2): Show |
11 | HG01109.hp1 HG01496.hp2 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.1708-620C>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 12/13 | chr1 | 63570401 | |||||||
| chr1:63570548 | G | T | 1 | a0015c0018t0001g0273 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1708-473G>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 12/13 | chr1 | 63570548 | |||||||
| chr1:63570646 | A | G | 1 | a0001c0001t0001g0221 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1708-375A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 12/13 | chr1 | 63570646 | |||||||
| chr1:63570715 | C | G | 2 | a0005c0007t0001g0189 a0005c0007t0001g0191 |
2 | HG01192.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1708-306C>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 12/13 | chr1 | 63570715 | |||||||
| chr1:63570800 | G | A | 16 | a0003c0004t0001g0175 a0003c0004t0001g0176 a0003c0004t0001g0177 others(13): Show |
16 | HG01081.hp2 HG01109.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.1708-221G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 12/13 | chr1 | 63570800 | |||||||
| chr1:63571167 | G | A | 51 | a0002c0003t0001g0002 a0002c0003t0001g0018 a0002c0003t0001g0035 others(48): Show |
69 | HG00558.hp1 HG00733.hp1 HG00741.hp2 others(66): Show |
intron_variant | MODIFIER | c.1815+39G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 13/13 | chr1 | 63571167 | |||||||
| chr1:63571193 | G | C | 1 | a0001c0001t0001g0227 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1815+65G>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 13/13 | chr1 | 63571193 | |||||||
| chr1:63571201 | T | C | 2 | a0010c0017t0001g0274 a0015c0018t0001g0273 |
2 | HG01243.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1815+73T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 13/13 | chr1 | 63571201 | |||||||
| chr1:63571378 | A | G | 51 | a0002c0003t0001g0002 a0002c0003t0001g0018 a0002c0003t0001g0035 others(48): Show |
69 | HG00558.hp1 HG00733.hp1 HG00741.hp2 others(66): Show |
intron_variant | MODIFIER | c.1815+250A>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 13/13 | chr1 | 63571378 | |||||||
| chr1:63571386 | T | G | 25 | a0002c0003t0001g0040 a0002c0003t0001g0234 a0002c0003t0001g0236 others(22): Show |
28 | HG00733.hp1 HG00741.hp2 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.1815+258T>G | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 13/13 | chr1 | 63571386 | |||||||
| chr1:63571495 | GAAACCCC others(16): Show |
G | 1 | a0006c0008t0001g0187 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1815+371_1815+393d others(25): Show |
EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 63571495 | ||||||
| chr1:63571555 | T | C | 195 | a0001c0002t0001g0004 a0001c0002t0001g0005 a0001c0002t0001g0008 others(192): Show |
246 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(243): Show |
intron_variant | MODIFIER | c.1815+427T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 13/13 | chr1 | 63571555 | |||||||
| chr1:63571670 | C | CA | 17 | a0001c0001t0001g0142 a0001c0001t0001g0167 a0002c0003t0001g0038 others(14): Show |
20 | HG01175.hp1 HG01934.hp1 HG01981.hp2 others(17): Show |
intron_variant | MODIFIER | c.1815+567dupA | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 63571670 | ||||||
| chr1:63571670 | CA | C | 38 | a0001c0001t0001g0017 a0001c0001t0001g0033 a0001c0001t0001g0153 others(35): Show |
43 | HG00438.hp1 HG01069.hp1 HG01106.hp2 others(40): Show |
intron_variant | MODIFIER | c.1815+567delA | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 63571670 | ||||||
| chr1:63571670 | CAA | C | 112 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0031 others(109): Show |
147 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.1815+566_1815+567d others(4): Show |
EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 63571670 | ||||||
| chr1:63571670 | CAAA | C | 6 | a0001c0001t0001g0208 a0001c0001t0001g0217 a0001c0002t0001g0080 others(3): Show |
6 | HG01070.hp2 HG01943.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1815+565_1815+567d others(5): Show |
EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 63571670 | ||||||
| chr1:63571724 | CAAAGTT | C | 3 | a0003c0005t0001g0192 a0003c0005t0001g0193 a0003c0005t0001g0194 |
3 | HG02572.hp2 HG02886.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1815+602_1815+607d others(8): Show |
EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr1 | 63571724 | ||||||
| chr1:63571756 | G | A | 2 | a0001c0002t0001g0135 a0001c0002t0001g0136 |
2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1815+628G>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 13/13 | chr1 | 63571756 | |||||||
| chr1:63572067 | C | A | 7 | a0004c0006t0001g0009 a0004c0006t0001g0041 a0004c0006t0001g0042 others(4): Show |
9 | HG00738.hp2 HG01934.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1816-375C>A | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 13/13 | chr1 | 63572067 | |||||||
| chr1:63572293 | T | C | 7 | a0004c0006t0001g0009 a0004c0006t0001g0041 a0004c0006t0001g0042 others(4): Show |
9 | HG00738.hp2 HG01934.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1816-149T>C | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 13/13 | chr1 | 63572293 | |||||||
| chr1:63572436 | G | T | 74 | a0002c0003t0001g0002 a0002c0003t0001g0018 a0002c0003t0001g0035 others(71): Show |
96 | HG00558.hp1 HG00733.hp1 HG00741.hp2 others(93): Show |
splice_region_variant&intron_variant | LOW | c.1816-6G>T | EFCAB7 | ENSG00000203965.13 | transcript | ENST00000371088.5 | protein_coding | 13/13 | chr1 | 63572436 |