Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79843 |
| ensemblid | ENSG00000124019.10 |
| hgncid | 26224 |
| symbol | FAM124B |
| name | family with sequence similarity 124 member B |
| refseq_nuc | NM_001122779.2 |
| refseq_prot | NP_001116251.1 |
| ensembl_nuc | ENST00000409685.4 |
| ensembl_prot | ENSP00000386895.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 224378698 |
| end | 224402107 |
| strand | - |
| ver | v1.2 |
| region | chr2:224378698-224402107 |
| region5000 | chr2:224373698-224407107 |
| regionname0 | FAM124B_chr2_224378698_224402107 |
| regionname5000 | FAM124B_chr2_224373698_224407107 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/0 | 455 | 348 | 86 | 68 | 151 | 9 | 34 | 120 | FAM124B_chr2_224373698_224407107 | FAM124B | MDETQ others(450): Show |
chr2 | 224373698 | 224407107 |
| a0002 | 0/0 | 455 | 80 | 5 | 11 | 51 | 3 | 10 | 39 | FAM124B_chr2_224373698_224407107 | FAM124B | MDETQ others(450): Show |
chr2 | 224373698 | 224407107 |
| a0003 | 0/0 | 455 | 9 | 5 | 1 | 1 | 2 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | MDETQ others(450): Show |
chr2 | 224373698 | 224407107 |
| a0004 | 0/0 | 455 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | MDETQ others(450): Show |
chr2 | 224373698 | 224407107 |
| a0005 | 0/0 | 80 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM124B_chr2_224373698_224407107 | FAM124B | MDETQ others(75): Show |
chr2 | 224373698 | 224407107 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1365 | 312 | 64 | 67 | 139 | 9 | 33 | FAM124B_chr2_224373698_224407107 | FAM124B | ATGGA others(1360): Show |
chr2 | 224373698 | 224407107 | ||
| a0001c0003 | 0/0 | 1365 | 16 | 9 | 0 | 6 | 0 | 1 | FAM124B_chr2_224373698_224407107 | FAM124B | ATGGA others(1360): Show |
chr2 | 224373698 | 224407107 | ||
| a0001c0005 | 0/0 | 1365 | 8 | 7 | 1 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | ATGGA others(1360): Show |
chr2 | 224373698 | 224407107 | ||
| a0001c0006 | 0/0 | 1365 | 6 | 6 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | ATGGA others(1360): Show |
chr2 | 224373698 | 224407107 | ||
| a0001c0007 | 0/0 | 1365 | 5 | 0 | 0 | 5 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | ATGGA others(1360): Show |
chr2 | 224373698 | 224407107 | ||
| a0001c0012 | 0/0 | 1365 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | ATGGA others(1360): Show |
chr2 | 224373698 | 224407107 | ||
| a0002c0002 | 0/0 | 1365 | 78 | 5 | 11 | 50 | 3 | 9 | FAM124B_chr2_224373698_224407107 | FAM124B | ATGGA others(1360): Show |
chr2 | 224373698 | 224407107 | ||
| a0002c0010 | 0/0 | 1365 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | ATGGA others(1360): Show |
chr2 | 224373698 | 224407107 | ||
| a0002c0011 | 0/0 | 1365 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124B_chr2_224373698_224407107 | FAM124B | ATGGA others(1360): Show |
chr2 | 224373698 | 224407107 | ||
| a0003c0004 | 0/0 | 1365 | 9 | 5 | 1 | 1 | 2 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | ATGGA others(1360): Show |
chr2 | 224373698 | 224407107 | ||
| a0004c0008 | 0/0 | 1365 | 2 | 2 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | ATGGA others(1360): Show |
chr2 | 224373698 | 224407107 | ||
| a0005c0009 | 0/0 | 1366 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | ATGGA others(1361): Show |
chr2 | 224373698 | 224407107 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2582 | 221 | 36 | 58 | 94 | 7 | 26 | FAM124B_chr2_224373698_224407107 | FAM124B | AGGAT others(2577): Show |
chr2 | 224373698 | 224407107 |
| a0001c0001t0003 | 0/0 | 2582 | 47 | 1 | 3 | 43 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | AGGAT others(2577): Show |
chr2 | 224373698 | 224407107 |
| a0001c0001t0004 | 0/0 | 2582 | 40 | 25 | 6 | 0 | 2 | 7 | FAM124B_chr2_224373698_224407107 | FAM124B | AGGAT others(2577): Show |
chr2 | 224373698 | 224407107 |
| a0001c0001t0008 | 0/0 | 2582 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | AGGAT others(2577): Show |
chr2 | 224373698 | 224407107 |
| a0001c0001t0011 | 0/0 | 2582 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | AGGAT others(2577): Show |
chr2 | 224373698 | 224407107 |
| a0001c0001t0012 | 0/0 | 2582 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | AGGAT others(2577): Show |
chr2 | 224373698 | 224407107 |
| a0001c0001t0013 | 0/0 | 2582 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | AGGAT others(2577): Show |
chr2 | 224373698 | 224407107 |
| a0001c0003t0001 | 0/0 | 2582 | 15 | 8 | 0 | 6 | 0 | 1 | FAM124B_chr2_224373698_224407107 | FAM124B | AGGAT others(2577): Show |
chr2 | 224373698 | 224407107 |
| a0001c0003t0010 | 0/0 | 2582 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | AGGAT others(2577): Show |
chr2 | 224373698 | 224407107 |
| a0001c0005t0001 | 0/0 | 2582 | 7 | 6 | 1 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | AGGAT others(2577): Show |
chr2 | 224373698 | 224407107 |
| a0001c0005t0004 | 0/0 | 2582 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | AGGAT others(2577): Show |
chr2 | 224373698 | 224407107 |
| a0001c0006t0001 | 0/0 | 2582 | 4 | 4 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | AGGAT others(2577): Show |
chr2 | 224373698 | 224407107 |
| a0001c0006t0006 | 0/0 | 2582 | 2 | 2 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | AGGAT others(2577): Show |
chr2 | 224373698 | 224407107 |
| a0001c0007t0003 | 0/0 | 2582 | 5 | 0 | 0 | 5 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | AGGAT others(2577): Show |
chr2 | 224373698 | 224407107 |
| a0001c0012t0001 | 0/0 | 2582 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | AGGAT others(2577): Show |
chr2 | 224373698 | 224407107 |
| a0002c0002t0002 | 0/0 | 2582 | 77 | 4 | 11 | 50 | 3 | 9 | FAM124B_chr2_224373698_224407107 | FAM124B | AGGAT others(2577): Show |
chr2 | 224373698 | 224407107 |
| a0002c0002t0007 | 0/0 | 2582 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | AGGAT others(2577): Show |
chr2 | 224373698 | 224407107 |
| a0002c0010t0002 | 0/0 | 2582 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | AGGAT others(2577): Show |
chr2 | 224373698 | 224407107 |
| a0002c0011t0002 | 0/0 | 2582 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124B_chr2_224373698_224407107 | FAM124B | AGGAT others(2577): Show |
chr2 | 224373698 | 224407107 |
| a0003c0004t0005 | 0/0 | 2582 | 8 | 4 | 1 | 1 | 2 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | AGGAT others(2577): Show |
chr2 | 224373698 | 224407107 |
| a0003c0004t0009 | 0/0 | 2582 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | AGGAT others(2577): Show |
chr2 | 224373698 | 224407107 |
| a0004c0008t0001 | 0/0 | 2582 | 2 | 2 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | AGGAT others(2577): Show |
chr2 | 224373698 | 224407107 |
| a0005c0009t0003 | 0/0 | 2583 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | AGGAT others(2578): Show |
chr2 | 224373698 | 224407107 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 16 | 1 | 4 | 8 | 1 | 2 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0007 | 0/0 | 6 | 0 | 5 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0009 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0010 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0017 | 0/0 | 4 | 1 | 1 | 0 | 0 | 2 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0019 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0027 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0028 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0042 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0050 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0052 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0057 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0059 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0060 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0003g0005 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0003g0006 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0003g0012 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0003g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0003g0061 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0003g0064 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0003g0065 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0003g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0004g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0004g0014 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0004g0015 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0004g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0004g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0004g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0004g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0004g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0004g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0004g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0004g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0004g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0004g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0004g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0004g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0004g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0004g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0004g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0004g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0004g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0008g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0011g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0012g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0001t0013g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0003t0001g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0003t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0003t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0003t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0003t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0003t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0003t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0003t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0003t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0003t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0003t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0003t0010g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0005t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0005t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0005t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0005t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0005t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0005t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0006t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0006t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0006t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0006t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0006t0006g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0006t0006g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0007t0003g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0007t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0007t0003g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0007t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0007t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0001c0012t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0002c0002t0002g0002 | 0/0 | 10 | 0 | 4 | 3 | 1 | 2 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0002c0002t0002g0003 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0002c0002t0002g0004 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0002c0002t0002g0018 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0002c0002t0002g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0002c0002t0002g0025 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0002c0002t0002g0056 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0002c0002t0002g0058 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0002c0002t0002g0062 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0002c0002t0002g0063 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0002c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0002c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0002c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0002c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0002c0002t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0002c0002t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0002c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0002c0002t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0002c0002t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0002c0002t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0002c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0002c0002t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0002c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0002c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0002c0002t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0002c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0002c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0002c0002t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0002c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0002c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0002c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0002c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0002c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0002c0002t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0002c0002t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0002c0002t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0002c0002t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0002c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0002c0002t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0002c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0002c0002t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0002c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0002c0002t0007g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0002c0010t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0002c0011t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0003c0004t0005g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0003c0004t0005g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0003c0004t0005g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0003c0004t0005g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0003c0004t0005g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0003c0004t0005g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0003c0004t0009g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0004c0008t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| a0005c0009t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0004 | g0014 | EUR | GBR | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG00140 | hp2 | a0003 | c0004 | t0005 | g0168 | EUR | GBR | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG00280 | hp1 | a0001 | c0001 | t0004 | g0073 | EUR | FIN | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG00280 | hp2 | a0002 | c0002 | t0002 | g0139 | EUR | FIN | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0175 | EUR | FIN | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG00323 | hp2 | a0003 | c0004 | t0005 | g0156 | EUR | FIN | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG00408 | hp2 | a0002 | c0002 | t0002 | g0225 | EAS | CHS | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG00423 | hp1 | a0002 | c0002 | t0002 | g0022 | EAS | CHS | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG00423 | hp2 | a0002 | c0002 | t0002 | g0018 | EAS | CHS | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0177 | EAS | CHS | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG00438 | hp2 | a0002 | c0002 | t0002 | g0222 | EAS | CHS | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG00544 | hp1 | a0002 | c0002 | t0002 | g0100 | EAS | CHS | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG00558 | hp2 | a0002 | c0002 | t0002 | g0018 | EAS | CHS | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | CHS | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG00609 | hp2 | a0002 | c0002 | t0002 | g0002 | EAS | CHS | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG00673 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | CHS | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG00738 | hp2 | a0002 | c0002 | t0002 | g0197 | AMR | PUR | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG00741 | hp1 | a0001 | c0001 | t0004 | g0029 | AMR | PUR | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0065 | AMR | PUR | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01070 | hp2 | a0001 | c0001 | t0004 | g0085 | AMR | PUR | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01071 | hp1 | a0001 | c0001 | t0004 | g0084 | AMR | PUR | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01074 | hp1 | a0001 | c0001 | t0004 | g0081 | AMR | PUR | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01081 | hp1 | a0001 | c0001 | t0004 | g0015 | AMR | PUR | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01167 | hp1 | a0003 | c0004 | t0005 | g0215 | AMR | PUR | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01168 | hp2 | a0002 | c0002 | t0002 | g0056 | AMR | PUR | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01169 | hp1 | a0002 | c0002 | t0002 | g0056 | AMR | PUR | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01175 | hp2 | a0001 | c0001 | t0003 | g0285 | AMR | PUR | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01192 | hp2 | a0001 | c0001 | t0004 | g0015 | AMR | PUR | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01243 | hp2 | a0001 | c0005 | t0001 | g0120 | AMR | PUR | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | CLM | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01256 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01258 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01358 | hp1 | a0002 | c0002 | t0002 | g0182 | AMR | CLM | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | CLM | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01496 | hp1 | a0002 | c0002 | t0002 | g0062 | AMR | CLM | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0021 | EUR | IBS | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0048 | EUR | IBS | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0122 | EUR | IBS | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01884 | hp1 | a0003 | c0004 | t0005 | g0053 | AFR | ACB | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01891 | hp1 | a0002 | c0002 | t0002 | g0269 | AFR | ACB | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01891 | hp2 | a0001 | c0005 | t0001 | g0035 | AFR | ACB | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01934 | hp1 | a0002 | c0002 | t0002 | g0174 | AMR | PEL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0012 | AMR | PEL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01975 | hp2 | a0002 | c0002 | t0002 | g0270 | AMR | PEL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01978 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | KHV | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02040 | hp2 | a0003 | c0004 | t0005 | g0209 | EAS | KHV | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02055 | hp2 | a0001 | c0006 | t0006 | g0294 | AFR | ACB | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02056 | hp1 | a0002 | c0002 | t0002 | g0018 | EAS | KHV | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02071 | hp1 | a0002 | c0002 | t0002 | g0282 | EAS | KHV | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02074 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0025 | EAS | KHV | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | KHV | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02145 | hp2 | a0001 | c0003 | t0001 | g0026 | AFR | ACB | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0231 | EAS | CDX | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | CDX | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02257 | hp1 | a0002 | c0002 | t0002 | g0058 | AFR | ACB | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02257 | hp2 | a0001 | c0005 | t0004 | g0066 | AFR | ACB | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02258 | hp2 | a0003 | c0004 | t0005 | g0053 | AFR | ACB | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02273 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0030 | AFR | ACB | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | PEL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | ACB | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02451 | hp2 | a0001 | c0003 | t0001 | g0026 | AFR | ACB | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02572 | hp2 | a0001 | c0003 | t0001 | g0227 | AFR | GWD | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0092 | AFR | GWD | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02622 | hp2 | a0001 | c0001 | t0004 | g0083 | AFR | GWD | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02698 | hp2 | a0002 | c0002 | t0002 | g0261 | SAS | PJL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0077 | AFR | GWD | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02723 | hp2 | a0001 | c0001 | t0011 | g0112 | AFR | GWD | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02735 | hp2 | a0002 | c0002 | t0002 | g0063 | SAS | PJL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0076 | AFR | GWD | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02809 | hp2 | a0001 | c0003 | t0001 | g0277 | AFR | GWD | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0088 | AFR | GWD | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0089 | AFR | GWD | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02886 | hp1 | a0001 | c0005 | t0001 | g0035 | AFR | GWD | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0078 | AFR | GWD | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02896 | hp1 | a0003 | c0004 | t0005 | g0033 | AFR | GWD | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02896 | hp2 | a0001 | c0005 | t0001 | g0036 | AFR | GWD | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0079 | AFR | GWD | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02897 | hp2 | a0001 | c0005 | t0001 | g0118 | AFR | GWD | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0075 | AFR | ESN | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02922 | hp2 | a0002 | c0002 | t0007 | g0090 | AFR | ESN | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02965 | hp1 | a0001 | c0005 | t0001 | g0036 | AFR | ESN | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ESN | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | ESN | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02976 | hp1 | a0001 | c0001 | t0008 | g0070 | AFR | ESN | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02976 | hp2 | a0001 | c0006 | t0001 | g0138 | AFR | ESN | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0260 | SAS | PJL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG03098 | hp1 | a0001 | c0006 | t0001 | g0105 | AFR | MSL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0094 | AFR | MSL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG03130 | hp2 | a0001 | c0003 | t0001 | g0253 | AFR | ESN | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | ESN | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0068 | AFR | ESN | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0013 | AFR | ESN | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG03209 | hp1 | a0003 | c0004 | t0009 | g0071 | AFR | MSL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG03209 | hp2 | a0004 | c0008 | t0001 | g0037 | AFR | MSL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG03225 | hp1 | a0001 | c0003 | t0001 | g0026 | AFR | MSL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | MSL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG03453 | hp2 | a0001 | c0001 | t0004 | g0086 | AFR | MSL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG03486 | hp1 | a0004 | c0008 | t0001 | g0037 | AFR | MSL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0030 | AFR | MSL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG03490 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0249 | SAS | PJL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0087 | AFR | ESN | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG03540 | hp1 | a0001 | c0003 | t0001 | g0195 | AFR | GWD | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG03540 | hp2 | a0003 | c0004 | t0005 | g0033 | AFR | GWD | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG03579 | hp1 | a0001 | c0003 | t0010 | g0147 | AFR | MSL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG03579 | hp2 | a0002 | c0002 | t0002 | g0228 | AFR | MSL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG03654 | hp1 | a0001 | c0001 | t0004 | g0072 | SAS | PJL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0015 | SAS | PJL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0014 | SAS | STU | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | STU | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG03704 | hp1 | a0001 | c0001 | t0004 | g0015 | SAS | PJL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG03704 | hp2 | a0002 | c0002 | t0002 | g0248 | SAS | PJL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG03710 | hp1 | a0001 | c0001 | t0004 | g0082 | SAS | PJL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG03710 | hp2 | a0001 | c0001 | t0004 | g0014 | SAS | PJL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG03831 | hp1 | a0002 | c0002 | t0002 | g0063 | SAS | BEB | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG03831 | hp2 | a0002 | c0002 | t0002 | g0025 | SAS | BEB | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG03834 | hp1 | a0002 | c0002 | t0002 | g0004 | SAS | BEB | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | BEB | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0263 | SAS | BEB | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG03942 | hp2 | a0001 | c0001 | t0004 | g0080 | SAS | BEB | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0290 | SAS | STU | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | STU | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG04184 | hp1 | a0001 | c0003 | t0001 | g0125 | SAS | BEB | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0189 | SAS | BEB | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | STU | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG04199 | hp2 | a0002 | c0011 | t0002 | g0097 | SAS | STU | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | STU | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0254 | SAS | STU | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18522 | hp1 | a0001 | c0003 | t0001 | g0276 | AFR | YRI | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | YRI | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | CHB | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | CHB | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHB | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | CHB | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | YRI | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | YRI | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18943 | hp2 | a0002 | c0002 | t0002 | g0273 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18944 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18944 | hp2 | a0002 | c0002 | t0002 | g0255 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18945 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18946 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18948 | hp1 | a0001 | c0007 | t0003 | g0143 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18948 | hp2 | a0002 | c0002 | t0002 | g0275 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18950 | hp1 | a0001 | c0003 | t0001 | g0126 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18951 | hp1 | a0002 | c0002 | t0002 | g0288 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18952 | hp1 | a0002 | c0002 | t0002 | g0183 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18952 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18956 | hp2 | a0001 | c0012 | t0001 | g0153 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18960 | hp1 | a0002 | c0002 | t0002 | g0022 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18960 | hp2 | a0001 | c0001 | t0003 | g0047 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18961 | hp1 | a0002 | c0002 | t0002 | g0207 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0284 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18966 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18967 | hp2 | a0002 | c0002 | t0002 | g0152 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18968 | hp2 | a0002 | c0002 | t0002 | g0025 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18969 | hp1 | a0002 | c0002 | t0002 | g0271 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0129 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18970 | hp1 | a0002 | c0002 | t0002 | g0204 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18971 | hp2 | a0001 | c0007 | t0003 | g0238 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18975 | hp1 | a0002 | c0002 | t0002 | g0135 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18978 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18978 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18979 | hp2 | a0002 | c0002 | t0002 | g0099 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18982 | hp2 | a0002 | c0002 | t0002 | g0018 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0283 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18984 | hp1 | a0001 | c0003 | t0001 | g0163 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18985 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18985 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18986 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18988 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18988 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18989 | hp2 | a0002 | c0002 | t0002 | g0117 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0280 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18990 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0239 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18992 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18992 | hp2 | a0001 | c0001 | t0003 | g0281 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0291 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18993 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18995 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18998 | hp1 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA18998 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19000 | hp1 | a0001 | c0003 | t0001 | g0038 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19002 | hp1 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19003 | hp1 | a0002 | c0010 | t0002 | g0096 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19004 | hp2 | a0001 | c0007 | t0003 | g0145 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19007 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19009 | hp1 | a0002 | c0002 | t0002 | g0235 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19009 | hp2 | a0002 | c0002 | t0002 | g0279 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19012 | hp1 | a0002 | c0002 | t0002 | g0229 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19012 | hp2 | a0001 | c0007 | t0003 | g0127 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0013 | AFR | LWK | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0137 | AFR | LWK | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | LWK | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0029 | AFR | LWK | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0289 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19056 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19057 | hp1 | a0002 | c0002 | t0002 | g0200 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19058 | hp2 | a0002 | c0002 | t0002 | g0287 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0265 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19063 | hp2 | a0005 | c0009 | t0003 | g0095 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19064 | hp1 | a0002 | c0002 | t0002 | g0267 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19064 | hp2 | a0001 | c0003 | t0001 | g0038 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19066 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19067 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19068 | hp1 | a0002 | c0002 | t0002 | g0136 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19070 | hp1 | a0001 | c0007 | t0003 | g0144 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19074 | hp1 | a0002 | c0002 | t0002 | g0268 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19077 | hp1 | a0001 | c0001 | t0013 | g0292 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19078 | hp1 | a0001 | c0003 | t0001 | g0166 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19083 | hp1 | a0001 | c0001 | t0012 | g0149 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0226 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19085 | hp2 | a0002 | c0002 | t0002 | g0022 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19087 | hp2 | a0001 | c0003 | t0001 | g0128 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19090 | hp2 | a0002 | c0002 | t0002 | g0194 | EAS | JPT | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19240 | hp1 | a0002 | c0002 | t0002 | g0058 | AFR | YRI | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | YRI | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA20129 | hp1 | a0001 | c0001 | t0004 | g0067 | AFR | ASW | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ASW | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | TSI | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA20752 | hp2 | a0002 | c0002 | t0002 | g0002 | EUR | TSI | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0218 | EUR | TSI | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA20805 | hp2 | a0002 | c0002 | t0002 | g0062 | EUR | TSI | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA20905 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | GIH | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | GIH | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0093 | AFR | ACB | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02486 | hp2 | a0001 | c0006 | t0001 | g0146 | AFR | ACB | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02559 | hp1 | a0001 | c0006 | t0001 | g0241 | AFR | ACB | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0013 | AFR | ACB | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG03471 | hp1 | a0001 | c0005 | t0001 | g0158 | AFR | MSL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG06807 | hp1 | a0001 | c0001 | t0004 | g0074 | AFR | USA | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | USA | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA20300 | hp1 | a0001 | c0006 | t0006 | g0293 | AFR | USA | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA20300 | hp2 | a0001 | c0001 | t0004 | g0013 | AFR | USA | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA21309 | hp1 | a0001 | c0001 | t0004 | g0069 | AFR | LWK | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| NA21309 | hp2 | a0001 | c0001 | t0004 | g0091 | AFR | LWK | FAM124B_chr2_224373698_224407107 | FAM124B | chr2 | 224373698 | 224407107 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:224379635 | G | A | 1 | a0003 | 9 | HG00140.hp2 HG00323.hp2 HG01167.hp1 others(6): Show |
missense_variant | MODERATE | c.1306C>T | p.Leu436Phe | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 2/2 | 1645/2582 | 1306/1368 | 436/455 | chr2 | 224379635 | |||
| chr2:224379731 | T | C | 1 | a0004 | 2 | HG03209.hp2 HG03486.hp1 |
missense_variant | MODERATE | c.1210A>G | p.Thr404Ala | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 2/2 | 1549/2582 | 1210/1368 | 404/455 | chr2 | 224379731 | |||
| chr2:224380171 | A | G | 1 | a0002 | 80 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(77): Show |
missense_variant | MODERATE | c.770T>C | p.Ile257Thr | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 2/2 | 1109/2582 | 770/1368 | 257/455 | chr2 | 224380171 | |||
| chr2:224401585 | A | AC | 1 | a0005 | 1 | NA19063.hp2 | frameshift_variant | HIGH | c.183dupG | p.Ser62fs | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/2 | 522/2582 | 183/1368 | 61/455 | chr2 | 224401585 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:224379846 | G | A | 1 | a0001c0012 | 1 | NA18956.hp2 | synonymous_variant | LOW | c.1095C>T | p.Thr365Thr | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 2/2 | 1434/2582 | 1095/1368 | 365/455 | chr2 | 224379846 | |||
| chr2:224379918 | G | A | 1 | a0001c0006 | 6 | HG02055.hp2 HG02486.hp2 HG02559.hp1 others(3): Show |
synonymous_variant | LOW | c.1023C>T | p.Ser341Ser | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 2/2 | 1362/2582 | 1023/1368 | 341/455 | chr2 | 224379918 | |||
| chr2:224379933 | A | C | 2 | a0001c0007 a0005c0009 |
6 | NA18948.hp1 NA18971.hp2 NA19004.hp2 others(3): Show |
synonymous_variant | LOW | c.1008T>G | p.Ser336Ser | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 2/2 | 1347/2582 | 1008/1368 | 336/455 | chr2 | 224379933 | |||
| chr2:224380185 | A | G | 1 | a0001c0005 | 8 | HG01243.hp2 HG01891.hp2 HG02257.hp2 others(5): Show |
synonymous_variant | LOW | c.756T>C | p.Gly252Gly | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 2/2 | 1095/2582 | 756/1368 | 252/455 | chr2 | 224380185 | |||
| chr2:224380206 | A | G | 5 | a0001c0003 a0001c0005 a0002c0002 others(2): Show |
104 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(101): Show |
splice_region_variant&synonymous_variant | LOW | c.735T>C | p.Val245Val | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 2/2 | 1074/2582 | 735/1368 | 245/455 | chr2 | 224380206 | |||
| chr2:224401055 | G | T | 1 | a0002c0011 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.714C>A | p.Gly238Gly | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/2 | 1053/2582 | 714/1368 | 238/455 | chr2 | 224401055 | |||
| chr2:224401217 | C | T | 1 | a0002c0010 | 1 | NA19003.hp1 | synonymous_variant | LOW | c.552G>A | p.Leu184Leu | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/2 | 891/2582 | 552/1368 | 184/455 | chr2 | 224401217 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:224379066 | A | G | 2 | a0003c0004t0005 a0003c0004t0009 |
9 | HG00140.hp2 HG00323.hp2 HG01167.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*507T>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 2/2 | 507 | chr2 | 224379066 | ||||||
| chr2:224379288 | T | G | 1 | a0001c0001t0012 | 1 | NA19083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*285A>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 2/2 | 285 | chr2 | 224379288 | ||||||
| chr2:224379326 | G | A | 1 | a0001c0001t0013 | 1 | NA19077.hp1 | 3_prime_UTR_variant | MODIFIER | c.*247C>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 2/2 | 247 | chr2 | 224379326 | ||||||
| chr2:224379326 | G | C | 3 | a0001c0001t0003 a0001c0007t0003 a0005c0009t0003 |
53 | HG00438.hp1 HG00597.hp2 HG01069.hp1 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*247C>G | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 2/2 | 247 | chr2 | 224379326 | ||||||
| chr2:224379340 | C | T | 1 | a0001c0001t0008 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*233G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 2/2 | 233 | chr2 | 224379340 | ||||||
| chr2:224379385 | C | T | 4 | a0002c0002t0002 a0002c0002t0007 a0002c0010t0002 others(1): Show |
80 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*188G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 2/2 | 188 | chr2 | 224379385 | ||||||
| chr2:224379395 | A | G | 1 | a0001c0001t0011 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*178T>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 2/2 | 178 | chr2 | 224379395 | ||||||
| chr2:224379399 | T | C | 4 | a0002c0002t0002 a0002c0002t0007 a0002c0010t0002 others(1): Show |
80 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*174A>G | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 2/2 | 174 | chr2 | 224379399 | ||||||
| chr2:224379497 | C | T | 1 | a0001c0003t0010 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*76G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 2/2 | 76 | chr2 | 224379497 | ||||||
| chr2:224379518 | A | C | 4 | a0002c0002t0002 a0002c0002t0007 a0002c0010t0002 others(1): Show |
80 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*55T>G | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 2/2 | 55 | chr2 | 224379518 | ||||||
| chr2:224401848 | G | A | 1 | a0001c0001t0013 | 1 | NA19077.hp1 | 5_prime_UTR_variant | MODIFIER | c.-80C>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/2 | 80 | chr2 | 224401848 | ||||||
| chr2:224401950 | G | A | 5 | a0001c0001t0004 a0001c0001t0008 a0001c0005t0004 others(2): Show |
45 | HG00140.hp1 HG00280.hp1 HG00741.hp1 others(42): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-182C>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/2 | chr2 | 224401950 | |||||||
| chr2:224402008 | C | T | 5 | a0001c0001t0004 a0001c0001t0008 a0001c0005t0004 others(2): Show |
45 | HG00140.hp1 HG00280.hp1 HG00741.hp1 others(42): Show |
5_prime_UTR_variant | MODIFIER | c.-240G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/2 | 240 | chr2 | 224402008 | ||||||
| chr2:224402064 | G | A | 1 | a0001c0006t0006 | 2 | HG02055.hp2 NA20300.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-296C>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/2 | chr2 | 224402064 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:224380241 | A | G | 1 | a0001c0001t0001g0167 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.733-33T>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224380241 | |||||||
| chr2:224380302 | T | C | 3 | a0003c0004t0005g0033 a0003c0004t0005g0053 a0003c0004t0009g0071 |
5 | HG01884.hp1 HG02258.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.733-94A>G | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224380302 | |||||||
| chr2:224380434 | A | G | 7 | a0003c0004t0005g0033 a0003c0004t0005g0053 a0003c0004t0005g0156 others(4): Show |
9 | HG00140.hp2 HG00323.hp2 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.733-226T>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224380434 | |||||||
| chr2:224380444 | T | C | 48 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(45): Show |
80 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.733-236A>G | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224380444 | |||||||
| chr2:224380466 | G | T | 3 | a0003c0004t0005g0033 a0003c0004t0005g0053 a0003c0004t0009g0071 |
5 | HG01884.hp1 HG02258.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.733-258C>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224380466 | |||||||
| chr2:224380560 | A | G | 16 | a0001c0003t0001g0038 a0001c0003t0001g0125 a0001c0003t0001g0126 others(13): Show |
19 | HG01243.hp2 HG01891.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.733-352T>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224380560 | |||||||
| chr2:224380613 | G | A | 1 | a0002c0002t0002g0204 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.733-405C>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224380613 | |||||||
| chr2:224380697 | A | G | 48 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(45): Show |
80 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.733-489T>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224380697 | |||||||
| chr2:224380734 | A | G | 48 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(45): Show |
80 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.733-526T>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224380734 | |||||||
| chr2:224380735 | C | T | 18 | a0001c0003t0001g0026 a0001c0003t0001g0038 a0001c0003t0001g0125 others(15): Show |
23 | HG01243.hp2 HG01891.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.733-527G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224380735 | |||||||
| chr2:224380789 | G | T | 1 | a0001c0001t0001g0236 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.733-581C>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224380789 | |||||||
| chr2:224380830 | A | G | 48 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(45): Show |
80 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.733-622T>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224380830 | |||||||
| chr2:224380858 | C | A | 48 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(45): Show |
80 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.733-650G>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224380858 | |||||||
| chr2:224380884 | C | G | 126 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0019 others(123): Show |
172 | HG00140.hp2 HG00323.hp2 HG00438.hp1 others(169): Show |
intron_variant | MODIFIER | c.733-676G>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224380884 | |||||||
| chr2:224380935 | T | G | 1 | a0001c0001t0003g0283 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.733-727A>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224380935 | |||||||
| chr2:224380980 | C | G | 48 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(45): Show |
80 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.733-772G>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224380980 | |||||||
| chr2:224380984 | C | T | 1 | a0002c0002t0002g0063 | 2 | HG02735.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.733-776G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224380984 | |||||||
| chr2:224381083 | T | G | 48 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(45): Show |
80 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.733-875A>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224381083 | |||||||
| chr2:224381144 | G | A | 1 | a0001c0001t0001g0264 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.733-936C>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224381144 | |||||||
| chr2:224381273 | C | G | 1 | a0001c0001t0001g0052 | 2 | HG00735.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.733-1065G>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224381273 | |||||||
| chr2:224381309 | C | T | 66 | a0001c0003t0001g0026 a0001c0003t0001g0038 a0001c0003t0001g0125 others(63): Show |
103 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.733-1101G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224381309 | |||||||
| chr2:224381331 | A | G | 192 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0019 others(189): Show |
275 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(272): Show |
intron_variant | MODIFIER | c.733-1123T>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224381331 | |||||||
| chr2:224381528 | G | T | 12 | a0001c0001t0001g0060 a0001c0001t0001g0119 a0001c0001t0004g0067 others(9): Show |
13 | HG02055.hp2 HG02486.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.733-1320C>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224381528 | |||||||
| chr2:224381617 | T | G | 4 | a0001c0001t0001g0108 a0001c0001t0004g0074 a0001c0001t0004g0075 others(1): Show |
4 | HG02615.hp1 HG02809.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.733-1409A>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224381617 | |||||||
| chr2:224381775 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.733-1567G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224381775 | |||||||
| chr2:224381967 | T | TAC | 5 | a0001c0001t0001g0008 a0001c0001t0001g0049 a0001c0001t0001g0142 others(2): Show |
10 | HG00609.hp1 HG00621.hp1 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.733-1761_733-1760d others(4): Show |
FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224381967 | |||||||
| chr2:224382290 | A | G | 3 | a0001c0001t0004g0092 a0001c0001t0004g0093 a0001c0001t0004g0094 |
3 | HG02486.hp1 HG02622.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.733-2082T>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224382290 | |||||||
| chr2:224382328 | C | A | 7 | a0003c0004t0005g0033 a0003c0004t0005g0053 a0003c0004t0005g0156 others(4): Show |
9 | HG00140.hp2 HG00323.hp2 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.733-2120G>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224382328 | |||||||
| chr2:224382405 | C | CT | 8 | a0001c0001t0001g0048 a0001c0001t0001g0106 a0001c0001t0001g0111 others(5): Show |
9 | HG00642.hp1 HG00642.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.733-2198dupA | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224382405 | |||||||
| chr2:224382405 | CT | C | 79 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0019 others(76): Show |
105 | HG00280.hp2 HG00544.hp2 HG00621.hp2 others(102): Show |
intron_variant | MODIFIER | c.733-2198delA | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224382405 | |||||||
| chr2:224382405 | CTT | C | 107 | a0001c0001t0001g0119 a0001c0001t0001g0122 a0001c0001t0001g0236 others(104): Show |
162 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.733-2199_733-2198d others(4): Show |
FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224382405 | |||||||
| chr2:224382405 | CTTT | C | 7 | a0001c0001t0003g0281 a0001c0003t0001g0026 a0001c0003t0001g0227 others(4): Show |
9 | HG01975.hp2 HG02145.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.733-2200_733-2198d others(5): Show |
FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224382405 | |||||||
| chr2:224382476 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.733-2268G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224382476 | |||||||
| chr2:224382478 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.733-2270G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224382478 | |||||||
| chr2:224382573 | C | A | 1 | a0001c0001t0004g0089 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.733-2365G>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224382573 | |||||||
| chr2:224382726 | C | T | 18 | a0001c0003t0001g0026 a0001c0003t0001g0038 a0001c0003t0001g0125 others(15): Show |
23 | HG01243.hp2 HG01891.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.733-2518G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224382726 | |||||||
| chr2:224382770 | C | A | 192 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0019 others(189): Show |
275 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(272): Show |
intron_variant | MODIFIER | c.733-2562G>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224382770 | |||||||
| chr2:224382810 | G | A | 1 | a0003c0004t0009g0071 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.733-2602C>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224382810 | |||||||
| chr2:224382907 | T | C | 3 | a0001c0001t0001g0188 a0001c0001t0004g0015 a0001c0001t0004g0082 |
6 | HG01081.hp1 HG01192.hp2 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.733-2699A>G | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224382907 | |||||||
| chr2:224382972 | T | C | 4 | a0001c0001t0001g0060 a0001c0001t0004g0067 a0001c0001t0004g0068 others(1): Show |
5 | HG02647.hp2 HG02818.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.733-2764A>G | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224382972 | |||||||
| chr2:224382994 | A | C | 1 | a0001c0001t0001g0263 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.733-2786T>G | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224382994 | |||||||
| chr2:224383014 | A | G | 1 | a0001c0001t0001g0272 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.733-2806T>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224383014 | |||||||
| chr2:224383029 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.733-2821C>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224383029 | |||||||
| chr2:224383032 | A | G | 2 | a0001c0003t0001g0163 a0001c0003t0001g0166 |
2 | NA18984.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.733-2824T>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224383032 | |||||||
| chr2:224383270 | T | C | 1 | a0002c0002t0002g0271 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.733-3062A>G | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224383270 | |||||||
| chr2:224383505 | T | C | 1 | a0002c0002t0002g0229 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.733-3297A>G | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224383505 | |||||||
| chr2:224383586 | T | C | 4 | a0001c0001t0001g0060 a0001c0001t0004g0067 a0001c0001t0004g0068 others(1): Show |
5 | HG02647.hp2 HG02818.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.733-3378A>G | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224383586 | |||||||
| chr2:224383608 | C | G | 5 | a0001c0001t0001g0057 a0001c0001t0001g0123 a0001c0001t0001g0232 others(2): Show |
6 | HG02723.hp1 HG02965.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.733-3400G>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224383608 | |||||||
| chr2:224383888 | T | C | 1 | a0001c0003t0001g0195 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.733-3680A>G | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224383888 | |||||||
| chr2:224384084 | G | A | 1 | a0001c0001t0008g0070 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.733-3876C>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224384084 | |||||||
| chr2:224384394 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.733-4186T>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224384394 | |||||||
| chr2:224384555 | G | A | 7 | a0003c0004t0005g0033 a0003c0004t0005g0053 a0003c0004t0005g0156 others(4): Show |
9 | HG00140.hp2 HG00323.hp2 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.733-4347C>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224384555 | |||||||
| chr2:224384557 | C | T | 44 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(41): Show |
75 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.733-4349G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224384557 | |||||||
| chr2:224384666 | C | G | 18 | a0001c0003t0001g0026 a0001c0003t0001g0038 a0001c0003t0001g0125 others(15): Show |
23 | HG01243.hp2 HG01891.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.733-4458G>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224384666 | |||||||
| chr2:224384714 | G | A | 2 | a0001c0001t0001g0245 a0001c0001t0004g0077 |
2 | HG02572.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.733-4506C>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224384714 | |||||||
| chr2:224384732 | A | C | 1 | a0001c0003t0010g0147 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.733-4524T>G | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224384732 | |||||||
| chr2:224384916 | T | C | 1 | a0003c0004t0005g0215 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.733-4708A>G | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224384916 | |||||||
| chr2:224384964 | T | C | 1 | a0002c0002t0002g0197 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.733-4756A>G | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224384964 | |||||||
| chr2:224385062 | T | G | 6 | a0001c0001t0001g0057 a0001c0001t0001g0060 a0001c0001t0001g0123 others(3): Show |
8 | HG02647.hp2 HG02723.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.733-4854A>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224385062 | |||||||
| chr2:224385196 | C | A | 1 | a0001c0001t0001g0122 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.733-4988G>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224385196 | |||||||
| chr2:224385212 | A | G | 1 | a0001c0001t0004g0092 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.733-5004T>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224385212 | |||||||
| chr2:224385366 | C | A | 34 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0012 others(31): Show |
53 | HG00438.hp1 HG00597.hp2 HG01069.hp1 others(50): Show |
intron_variant | MODIFIER | c.733-5158G>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224385366 | |||||||
| chr2:224385533 | G | T | 1 | a0001c0001t0001g0205 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.733-5325C>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224385533 | |||||||
| chr2:224385559 | C | T | 3 | a0001c0001t0001g0185 a0001c0001t0001g0191 a0001c0001t0001g0219 |
3 | NA18963.hp2 NA18986.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.733-5351G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224385559 | |||||||
| chr2:224385656 | C | T | 6 | a0001c0001t0001g0108 a0001c0001t0001g0151 a0001c0001t0001g0278 others(3): Show |
6 | HG02055.hp1 HG02615.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.733-5448G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224385656 | |||||||
| chr2:224385670 | A | C | 45 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0019 others(42): Show |
62 | HG00408.hp1 HG00544.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.733-5462T>G | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224385670 | |||||||
| chr2:224385795 | C | T | 1 | a0001c0003t0010g0147 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.733-5587G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224385795 | |||||||
| chr2:224385848 | C | T | 18 | a0001c0003t0001g0026 a0001c0003t0001g0038 a0001c0003t0001g0125 others(15): Show |
23 | HG01243.hp2 HG01891.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.733-5640G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224385848 | |||||||
| chr2:224386006 | C | G | 1 | a0001c0001t0001g0252 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.733-5798G>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224386006 | |||||||
| chr2:224386009 | C | T | 1 | a0001c0003t0010g0147 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.733-5801G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224386009 | |||||||
| chr2:224386044 | T | A | 3 | a0001c0001t0004g0067 a0001c0001t0004g0068 a0001c0001t0004g0089 |
3 | HG02818.hp2 HG03195.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.733-5836A>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224386044 | |||||||
| chr2:224386180 | C | T | 2 | a0001c0001t0001g0057 a0001c0001t0001g0123 |
3 | HG02965.hp2 HG03471.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.733-5972G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224386180 | |||||||
| chr2:224386248 | A | T | 6 | a0001c0001t0001g0057 a0001c0001t0001g0060 a0001c0001t0001g0123 others(3): Show |
8 | HG02647.hp2 HG02723.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.733-6040T>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224386248 | |||||||
| chr2:224386259 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.733-6051G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224386259 | |||||||
| chr2:224386345 | C | T | 1 | a0002c0002t0002g0204 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.733-6137G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224386345 | |||||||
| chr2:224386455 | C | T | 6 | a0001c0006t0001g0105 a0001c0006t0001g0138 a0001c0006t0001g0146 others(3): Show |
6 | HG02055.hp2 HG02486.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.733-6247G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224386455 | |||||||
| chr2:224386505 | C | T | 1 | a0001c0001t0011g0112 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.733-6297G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224386505 | |||||||
| chr2:224386540 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.733-6332G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224386540 | |||||||
| chr2:224386542 | T | A | 1 | a0001c0003t0010g0147 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.733-6334A>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224386542 | |||||||
| chr2:224386630 | T | C | 111 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0012 others(108): Show |
167 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.733-6422A>G | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224386630 | |||||||
| chr2:224386739 | C | A | 7 | a0003c0004t0005g0033 a0003c0004t0005g0053 a0003c0004t0005g0156 others(4): Show |
9 | HG00140.hp2 HG00323.hp2 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.733-6531G>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224386739 | |||||||
| chr2:224386764 | A | G | 1 | a0002c0002t0002g0200 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.733-6556T>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224386764 | |||||||
| chr2:224386782 | TATAA | T | 9 | a0001c0001t0001g0192 a0001c0001t0001g0196 a0001c0006t0001g0105 others(6): Show |
9 | HG00438.hp2 HG02055.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.733-6578_733-6575d others(6): Show |
FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224386782 | |||||||
| chr2:224386953 | A | T | 1 | a0001c0003t0010g0147 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.733-6745T>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224386953 | |||||||
| chr2:224386961 | TAAGAG | T | 2 | a0001c0001t0004g0015 a0001c0001t0004g0082 |
5 | HG01081.hp1 HG01192.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.733-6758_733-6754d others(7): Show |
FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224386961 | |||||||
| chr2:224386978 | C | T | 2 | a0002c0002t0002g0062 a0002c0002t0002g0182 |
3 | HG01358.hp1 HG01496.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.733-6770G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224386978 | |||||||
| chr2:224387037 | T | G | 1 | a0001c0003t0010g0147 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.733-6829A>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224387037 | |||||||
| chr2:224387050 | A | G | 1 | a0001c0001t0001g0175 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.733-6842T>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224387050 | |||||||
| chr2:224387225 | T | C | 19 | a0001c0003t0001g0026 a0001c0003t0001g0038 a0001c0003t0001g0125 others(16): Show |
24 | HG01243.hp2 HG01891.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.733-7017A>G | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224387225 | |||||||
| chr2:224387332 | T | G | 1 | a0001c0001t0001g0250 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.733-7124A>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224387332 | |||||||
| chr2:224387455 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.733-7247T>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224387455 | |||||||
| chr2:224387485 | G | A | 1 | a0001c0001t0001g0210 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.733-7277C>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224387485 | |||||||
| chr2:224387545 | T | G | 2 | a0002c0002t0002g0100 a0002c0002t0002g0204 |
2 | HG00544.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.733-7337A>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224387545 | |||||||
| chr2:224387549 | A | G | 34 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0019 others(31): Show |
48 | HG00544.hp2 HG00621.hp2 HG01123.hp1 others(45): Show |
intron_variant | MODIFIER | c.733-7341T>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224387549 | |||||||
| chr2:224387727 | G | A | 82 | a0001c0001t0003g0005 a0001c0001t0003g0006 a0001c0001t0003g0012 others(79): Show |
133 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.733-7519C>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224387727 | |||||||
| chr2:224387938 | T | C | 3 | a0001c0001t0001g0020 a0001c0001t0001g0192 a0001c0001t0001g0196 |
5 | NA18939.hp2 NA18975.hp2 NA19054.hp2 others(2): Show |
intron_variant | MODIFIER | c.733-7730A>G | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224387938 | |||||||
| chr2:224387971 | T | C | 1 | a0001c0003t0010g0147 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.733-7763A>G | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224387971 | |||||||
| chr2:224388006 | G | C | 1 | a0001c0001t0001g0236 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.733-7798C>G | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224388006 | |||||||
| chr2:224388029 | G | A | 118 | a0001c0001t0001g0057 a0001c0001t0001g0109 a0001c0001t0001g0119 others(115): Show |
178 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.733-7821C>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224388029 | |||||||
| chr2:224388094 | CAT | C | 4 | a0001c0001t0001g0236 a0001c0001t0004g0067 a0001c0001t0004g0068 others(1): Show |
4 | HG02818.hp2 HG02886.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.733-7888_733-7887d others(4): Show |
FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224388094 | |||||||
| chr2:224388123 | C | G | 1 | a0001c0003t0010g0147 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.733-7915G>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224388123 | |||||||
| chr2:224388337 | A | G | 24 | a0001c0001t0001g0057 a0001c0001t0001g0109 a0001c0001t0001g0119 others(21): Show |
31 | HG01243.hp2 HG01891.hp2 HG02145.hp2 others(28): Show |
intron_variant | MODIFIER | c.733-8129T>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224388337 | |||||||
| chr2:224388356 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.733-8148C>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224388356 | |||||||
| chr2:224388417 | A | G | 1 | a0001c0001t0011g0112 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.733-8209T>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224388417 | |||||||
| chr2:224388536 | GA | G | 47 | a0002c0002t0002g0002 a0002c0002t0002g0003 a0002c0002t0002g0004 others(44): Show |
79 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.733-8329delT | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224388536 | |||||||
| chr2:224388572 | C | T | 5 | a0001c0001t0001g0109 a0001c0003t0001g0026 a0001c0003t0001g0227 others(2): Show |
8 | HG02145.hp2 HG02451.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.733-8364G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224388572 | |||||||
| chr2:224388737 | A | G | 1 | a0001c0001t0001g0259 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.733-8529T>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224388737 | |||||||
| chr2:224388873 | G | A | 11 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0059 others(8): Show |
17 | HG01346.hp1 HG02280.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.733-8665C>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224388873 | |||||||
| chr2:224388987 | C | G | 1 | a0001c0001t0001g0211 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.733-8779G>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224388987 | |||||||
| chr2:224389057 | G | A | 2 | a0001c0001t0001g0246 a0001c0001t0001g0247 |
2 | HG02451.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.733-8849C>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224389057 | |||||||
| chr2:224389184 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.733-8976C>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224389184 | |||||||
| chr2:224389198 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.733-8990G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224389198 | |||||||
| chr2:224389211 | C | A | 8 | a0001c0001t0012g0149 a0003c0004t0005g0033 a0003c0004t0005g0053 others(5): Show |
10 | HG00140.hp2 HG00323.hp2 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.733-9003G>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224389211 | |||||||
| chr2:224389252 | G | A | 1 | a0001c0001t0001g0210 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.733-9044C>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224389252 | |||||||
| chr2:224389697 | C | T | 1 | a0001c0003t0010g0147 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.733-9489G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224389697 | |||||||
| chr2:224389796 | A | G | 4 | a0001c0001t0001g0108 a0001c0001t0004g0074 a0001c0001t0004g0075 others(1): Show |
4 | HG02615.hp1 HG02809.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.733-9588T>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224389796 | |||||||
| chr2:224389923 | G | A | 4 | a0001c0001t0001g0108 a0001c0001t0004g0074 a0001c0001t0004g0075 others(1): Show |
4 | HG02615.hp1 HG02809.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.733-9715C>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224389923 | |||||||
| chr2:224389955 | C | G | 45 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(42): Show |
63 | HG00140.hp1 HG00280.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.733-9747G>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224389955 | |||||||
| chr2:224389970 | T | C | 1 | a0001c0001t0001g0211 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.733-9762A>G | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224389970 | |||||||
| chr2:224390087 | G | C | 1 | a0001c0001t0001g0057 | 2 | HG02965.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.733-9879C>G | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224390087 | |||||||
| chr2:224390114 | T | TAC | 26 | a0001c0001t0001g0009 a0001c0001t0001g0040 a0001c0001t0001g0057 others(23): Show |
34 | HG00280.hp2 HG00738.hp1 HG00741.hp1 others(31): Show |
intron_variant | MODIFIER | c.733-9908_733-9907d others(4): Show |
FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224390114 | |||||||
| chr2:224390114 | T | TACAC | 49 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0017 others(46): Show |
78 | HG00408.hp1 HG00423.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.733-9910_733-9907d others(6): Show |
FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224390114 | |||||||
| chr2:224390114 | T | TACACAC | 38 | a0001c0001t0001g0020 a0001c0001t0001g0024 a0001c0001t0001g0045 others(35): Show |
52 | HG00140.hp2 HG00544.hp1 HG01175.hp2 others(49): Show |
intron_variant | MODIFIER | c.733-9912_733-9907d others(8): Show |
FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224390114 | |||||||
| chr2:224390114 | T | TACACACA others(1): Show |
21 | a0001c0001t0001g0016 a0001c0001t0001g0051 a0001c0001t0001g0101 others(18): Show |
26 | HG02015.hp2 HG02040.hp2 HG02257.hp2 others(23): Show |
intron_variant | MODIFIER | c.733-9914_733-9907d others(10): Show |
FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224390114 | |||||||
| chr2:224390114 | T | TACACACA others(3): Show |
7 | a0001c0001t0001g0034 a0001c0001t0001g0052 a0001c0001t0001g0164 others(4): Show |
10 | HG00735.hp2 HG01069.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.733-9916_733-9907d others(12): Show |
FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224390114 | |||||||
| chr2:224390114 | T | TACACACA others(5): Show |
3 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0003c0004t0005g0156 |
3 | HG00323.hp2 HG00544.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.733-9918_733-9907d others(14): Show |
FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224390114 | |||||||
| chr2:224390114 | T | TACACACA others(7): Show |
3 | a0001c0001t0004g0068 a0001c0001t0004g0092 a0001c0001t0004g0094 |
3 | HG02622.hp1 HG03098.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.733-9920_733-9907d others(16): Show |
FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224390114 | |||||||
| chr2:224390114 | T | TACACACA others(9): Show |
2 | a0001c0001t0001g0106 a0001c0006t0001g0138 |
2 | HG01109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.733-9922_733-9907d others(18): Show |
FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224390114 | |||||||
| chr2:224390114 | T | TACACACA others(11): Show |
3 | a0001c0001t0001g0213 a0001c0001t0004g0084 a0001c0001t0004g0085 |
3 | HG01070.hp2 HG01071.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.733-9924_733-9907d others(20): Show |
FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224390114 | |||||||
| chr2:224390114 | T | TACACACA others(15): Show |
1 | a0001c0001t0004g0093 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.733-9928_733-9907d others(24): Show |
FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224390114 | |||||||
| chr2:224390114 | TAC | T | 17 | a0001c0001t0001g0007 a0001c0001t0001g0042 a0001c0001t0001g0148 others(14): Show |
27 | HG00639.hp2 HG01069.hp2 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.733-9908_733-9907d others(4): Show |
FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224390114 | |||||||
| chr2:224390114 | TACAC | T | 11 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(8): Show |
17 | HG00408.hp2 HG00639.hp1 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.733-9910_733-9907d others(6): Show |
FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224390114 | |||||||
| chr2:224390114 | TACACAC | T | 28 | a0001c0001t0001g0019 a0001c0001t0001g0028 a0001c0001t0001g0046 others(25): Show |
56 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(53): Show |
intron_variant | MODIFIER | c.733-9912_733-9907d others(8): Show |
FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224390114 | |||||||
| chr2:224390114 | TACACACA others(1): Show |
T | 15 | a0001c0001t0001g0060 a0001c0001t0001g0109 a0001c0001t0001g0123 others(12): Show |
19 | HG02055.hp1 HG02083.hp1 HG02572.hp2 others(16): Show |
intron_variant | MODIFIER | c.733-9914_733-9907d others(10): Show |
FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224390114 | |||||||
| chr2:224390114 | TACACACA others(3): Show |
T | 4 | a0001c0001t0001g0059 a0001c0001t0001g0232 a0001c0001t0001g0233 others(1): Show |
5 | HG02280.hp1 HG02615.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.733-9916_733-9907d others(12): Show |
FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224390114 | |||||||
| chr2:224390154 | C | G | 1 | a0001c0003t0010g0147 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.733-9946G>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224390154 | |||||||
| chr2:224390156 | C | G | 1 | a0001c0003t0010g0147 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.733-9948G>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224390156 | |||||||
| chr2:224390158 | C | CACACACA others(5): Show |
1 | a0001c0006t0006g0293 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.733-9951_733-9950i others(14): Show |
FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224390158 | |||||||
| chr2:224390158 | C | G | 1 | a0001c0003t0010g0147 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.733-9950G>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224390158 | |||||||
| chr2:224390258 | G | A | 1 | a0001c0003t0010g0147 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.733-10050C>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224390258 | |||||||
| chr2:224390291 | C | A | 1 | a0001c0003t0010g0147 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.733-10083G>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224390291 | |||||||
| chr2:224390297 | T | C | 52 | a0001c0001t0001g0010 a0001c0001t0001g0016 a0001c0001t0001g0021 others(49): Show |
65 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.733-10089A>G | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224390297 | |||||||
| chr2:224390424 | C | T | 4 | a0001c0001t0001g0176 a0001c0001t0001g0178 a0001c0001t0001g0258 others(1): Show |
4 | HG00438.hp1 NA18994.hp2 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.733-10216G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224390424 | |||||||
| chr2:224390426 | T | C | 2 | a0001c0001t0001g0024 a0001c0001t0001g0217 |
4 | NA18945.hp2 NA18951.hp2 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.733-10218A>G | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224390426 | |||||||
| chr2:224390507 | G | A | 1 | a0001c0001t0003g0265 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.733-10299C>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224390507 | |||||||
| chr2:224390657 | C | G | 155 | a0001c0001t0001g0019 a0001c0001t0001g0028 a0001c0001t0001g0032 others(152): Show |
233 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.732+10380G>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224390657 | |||||||
| chr2:224390700 | T | G | 18 | a0001c0001t0001g0101 a0001c0001t0001g0104 a0001c0001t0001g0111 others(15): Show |
22 | HG01123.hp2 HG01433.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.732+10337A>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224390700 | |||||||
| chr2:224390700 | TTTTG | T | 11 | a0001c0001t0001g0108 a0001c0001t0001g0110 a0001c0001t0001g0165 others(8): Show |
12 | HG01081.hp2 HG02615.hp1 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.732+10333_732+1033 others(8): Show |
FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224390700 | |||||||
| chr2:224390701 | TTTG | T | 41 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(38): Show |
61 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.732+10333_732+1033 others(7): Show |
FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224390701 | |||||||
| chr2:224390703 | TG | T | 47 | a0001c0001t0001g0019 a0001c0001t0001g0028 a0001c0001t0001g0057 others(44): Show |
84 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.732+10333delC | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224390703 | |||||||
| chr2:224390703 | TGTTTG | T | 5 | a0001c0001t0001g0109 a0001c0001t0001g0123 a0001c0001t0001g0124 others(2): Show |
6 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.732+10329_732+1033 others(9): Show |
FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224390703 | |||||||
| chr2:224390704 | G | T | 23 | a0001c0001t0001g0286 a0001c0001t0003g0005 a0001c0001t0003g0012 others(20): Show |
36 | HG01069.hp1 HG01175.hp2 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.732+10333C>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224390704 | |||||||
| chr2:224390706 | T | G | 2 | a0001c0001t0003g0231 a0002c0002t0007g0090 |
2 | HG02165.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.732+10331A>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224390706 | |||||||
| chr2:224390708 | G | T | 120 | a0001c0001t0001g0019 a0001c0001t0001g0028 a0001c0001t0001g0032 others(117): Show |
191 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.732+10329C>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224390708 | |||||||
| chr2:224390709 | T | G | 1 | a0001c0001t0003g0231 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.732+10328A>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224390709 | |||||||
| chr2:224390712 | G | T | 63 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(60): Show |
85 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.732+10325C>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224390712 | |||||||
| chr2:224390722 | A | C | 9 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0123 others(6): Show |
10 | HG02055.hp1 HG02615.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.732+10315T>G | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224390722 | |||||||
| chr2:224390773 | C | T | 1 | a0001c0003t0010g0147 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.732+10264G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224390773 | |||||||
| chr2:224390779 | C | A | 1 | a0001c0003t0010g0147 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.732+10258G>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224390779 | |||||||
| chr2:224390782 | C | G | 1 | a0001c0003t0010g0147 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.732+10255G>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224390782 | |||||||
| chr2:224390786 | C | T | 1 | a0001c0003t0010g0147 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.732+10251G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224390786 | |||||||
| chr2:224390787 | A | G | 293 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(290): Show |
440 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(437): Show |
intron_variant | MODIFIER | c.732+10250T>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224390787 | |||||||
| chr2:224390790 | T | C | 1 | a0001c0003t0010g0147 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.732+10247A>G | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224390790 | |||||||
| chr2:224390793 | C | T | 1 | a0001c0003t0010g0147 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.732+10244G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224390793 | |||||||
| chr2:224390850 | A | G | 5 | a0001c0001t0001g0150 a0001c0001t0001g0219 a0002c0002t0002g0003 others(2): Show |
11 | HG02015.hp2 NA18944.hp1 NA18946.hp1 others(8): Show |
intron_variant | MODIFIER | c.732+10187T>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224390850 | |||||||
| chr2:224390855 | C | T | 4 | a0001c0001t0001g0150 a0002c0002t0002g0003 a0002c0002t0002g0267 others(1): Show |
10 | HG02015.hp2 NA18944.hp1 NA18946.hp1 others(7): Show |
intron_variant | MODIFIER | c.732+10182G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224390855 | |||||||
| chr2:224390856 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.732+10181T>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224390856 | |||||||
| chr2:224390857 | C | G | 1 | a0001c0003t0010g0147 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.732+10180G>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224390857 | |||||||
| chr2:224390889 | G | C | 1 | a0001c0003t0010g0147 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.732+10148C>G | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224390889 | |||||||
| chr2:224390904 | C | T | 5 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0232 others(2): Show |
7 | HG02280.hp1 HG02615.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.732+10133G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224390904 | |||||||
| chr2:224390925 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.732+10112C>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224390925 | |||||||
| chr2:224390955 | G | A | 1 | a0001c0001t0001g0252 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.732+10082C>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224390955 | |||||||
| chr2:224391130 | C | G | 8 | a0001c0001t0001g0111 a0001c0001t0001g0121 a0001c0001t0004g0013 others(5): Show |
11 | HG01884.hp2 HG02559.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.732+9907G>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224391130 | |||||||
| chr2:224391144 | G | T | 4 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0001g0173 others(1): Show |
6 | HG01167.hp2 HG01169.hp2 HG01928.hp2 others(3): Show |
intron_variant | MODIFIER | c.732+9893C>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224391144 | |||||||
| chr2:224391223 | T | C | 1 | a0001c0003t0010g0147 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.732+9814A>G | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224391223 | |||||||
| chr2:224391254 | T | C | 5 | a0001c0001t0001g0109 a0001c0001t0001g0123 a0001c0001t0001g0124 others(2): Show |
6 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.732+9783A>G | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224391254 | |||||||
| chr2:224391273 | G | A | 2 | a0001c0001t0001g0055 a0001c0001t0001g0251 |
3 | HG00408.hp1 HG02056.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.732+9764C>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224391273 | |||||||
| chr2:224391275 | A | G | 1 | a0001c0003t0010g0147 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.732+9762T>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224391275 | |||||||
| chr2:224391341 | C | CA | 12 | a0001c0001t0001g0102 a0001c0001t0001g0111 a0001c0001t0001g0167 others(9): Show |
12 | HG01167.hp1 HG01884.hp2 HG01934.hp2 others(9): Show |
intron_variant | MODIFIER | c.732+9695dupT | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224391341 | |||||||
| chr2:224391341 | CA | C | 15 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0123 others(12): Show |
16 | HG00140.hp2 HG02055.hp1 HG02165.hp2 others(13): Show |
intron_variant | MODIFIER | c.732+9695delT | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224391341 | |||||||
| chr2:224391356 | A | G | 4 | a0001c0001t0001g0170 a0001c0001t0004g0077 a0001c0001t0004g0078 others(1): Show |
4 | HG01099.hp1 HG02717.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.732+9681T>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224391356 | |||||||
| chr2:224391519 | G | A | 4 | a0001c0001t0001g0031 a0001c0001t0001g0103 a0001c0001t0001g0104 others(1): Show |
5 | HG00735.hp1 HG01123.hp2 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.732+9518C>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224391519 | |||||||
| chr2:224391536 | G | A | 1 | a0001c0003t0010g0147 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.732+9501C>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224391536 | |||||||
| chr2:224391594 | T | A | 1 | a0002c0002t0002g0228 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.732+9443A>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224391594 | |||||||
| chr2:224392162 | C | T | 4 | a0001c0001t0001g0169 a0001c0001t0001g0278 a0002c0002t0002g0058 others(1): Show |
5 | HG01070.hp1 HG02257.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.732+8875G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224392162 | |||||||
| chr2:224392163 | G | C | 1 | a0001c0003t0010g0147 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.732+8874C>G | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224392163 | |||||||
| chr2:224392170 | C | T | 19 | a0001c0001t0001g0111 a0001c0001t0001g0121 a0001c0001t0001g0246 others(16): Show |
23 | HG00280.hp2 HG01884.hp2 HG02257.hp1 others(20): Show |
intron_variant | MODIFIER | c.732+8867G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224392170 | |||||||
| chr2:224392171 | G | A | 1 | a0001c0001t0001g0023 | 3 | HG01261.hp1 HG01358.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.732+8866C>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224392171 | |||||||
| chr2:224392201 | T | C | 1 | a0001c0003t0010g0147 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.732+8836A>G | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224392201 | |||||||
| chr2:224392316 | C | T | 1 | a0003c0004t0005g0168 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.732+8721G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224392316 | |||||||
| chr2:224392565 | G | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0217 |
4 | NA18945.hp2 NA18951.hp2 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.732+8472C>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224392565 | |||||||
| chr2:224392616 | A | C | 1 | a0001c0003t0010g0147 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.732+8421T>G | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224392616 | |||||||
| chr2:224392754 | C | CA | 9 | a0001c0001t0001g0150 a0001c0001t0001g0246 a0001c0001t0001g0247 others(6): Show |
9 | HG02015.hp2 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.732+8282dupT | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224392754 | |||||||
| chr2:224392800 | C | A | 9 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0123 others(6): Show |
10 | HG02055.hp1 HG02615.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.732+8237G>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224392800 | |||||||
| chr2:224392808 | CTA | C | 78 | a0001c0001t0001g0019 a0001c0001t0001g0028 a0001c0001t0001g0057 others(75): Show |
130 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.732+8227_732+8228d others(4): Show |
FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224392808 | |||||||
| chr2:224392945 | G | T | 1 | a0001c0001t0001g0236 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.732+8092C>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224392945 | |||||||
| chr2:224393072 | G | A | 1 | a0001c0001t0004g0094 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.732+7965C>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224393072 | |||||||
| chr2:224393108 | A | C | 58 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(55): Show |
80 | HG00140.hp1 HG00280.hp1 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.732+7929T>G | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224393108 | |||||||
| chr2:224393170 | T | G | 4 | a0001c0001t0001g0108 a0001c0001t0004g0074 a0001c0001t0004g0075 others(1): Show |
4 | HG02615.hp1 HG02809.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.732+7867A>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224393170 | |||||||
| chr2:224393226 | G | T | 1 | a0002c0002t0002g0267 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.732+7811C>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224393226 | |||||||
| chr2:224393276 | T | C | 1 | a0002c0002t0007g0090 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.732+7761A>G | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224393276 | |||||||
| chr2:224393299 | G | A | 1 | a0002c0002t0007g0090 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.732+7738C>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224393299 | |||||||
| chr2:224393301 | C | A | 1 | a0002c0002t0007g0090 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.732+7736G>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224393301 | |||||||
| chr2:224393392 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.732+7645A>G | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224393392 | |||||||
| chr2:224393398 | G | T | 5 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0232 others(2): Show |
7 | HG02280.hp1 HG02615.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.732+7639C>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224393398 | |||||||
| chr2:224393464 | C | T | 1 | a0001c0001t0003g0137 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.732+7573G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224393464 | |||||||
| chr2:224393557 | C | G | 6 | a0001c0001t0001g0236 a0001c0006t0001g0105 a0001c0006t0001g0146 others(3): Show |
6 | HG02055.hp2 HG02486.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.732+7480G>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224393557 | |||||||
| chr2:224393666 | T | C | 2 | a0001c0001t0001g0218 a0001c0003t0010g0147 |
2 | HG03579.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.732+7371A>G | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224393666 | |||||||
| chr2:224393736 | T | C | 1 | a0001c0001t0001g0236 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.732+7301A>G | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224393736 | |||||||
| chr2:224393740 | G | A | 1 | a0001c0003t0010g0147 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.732+7297C>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224393740 | |||||||
| chr2:224393856 | C | T | 38 | a0001c0001t0001g0019 a0001c0001t0001g0028 a0001c0001t0001g0220 others(35): Show |
72 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.732+7181G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224393856 | |||||||
| chr2:224393868 | G | C | 2 | a0002c0002t0002g0099 a0002c0002t0002g0136 |
2 | NA18979.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.732+7169C>G | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224393868 | |||||||
| chr2:224393873 | G | A | 9 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0123 others(6): Show |
10 | HG02055.hp1 HG02615.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.732+7164C>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224393873 | |||||||
| chr2:224394100 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.732+6937G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224394100 | |||||||
| chr2:224394110 | G | C | 15 | a0001c0001t0001g0111 a0001c0001t0001g0121 a0001c0001t0001g0246 others(12): Show |
19 | HG00280.hp2 HG01884.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.732+6927C>G | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224394110 | |||||||
| chr2:224394174 | C | T | 6 | a0001c0006t0001g0105 a0001c0006t0001g0146 a0001c0006t0001g0241 others(3): Show |
6 | HG02055.hp2 HG02486.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.732+6863G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224394174 | |||||||
| chr2:224394596 | A | T | 22 | a0001c0001t0001g0286 a0001c0001t0003g0005 a0001c0001t0003g0012 others(19): Show |
35 | HG01069.hp1 HG01175.hp2 HG01952.hp1 others(32): Show |
intron_variant | MODIFIER | c.732+6441T>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224394596 | |||||||
| chr2:224394613 | G | A | 1 | a0001c0001t0001g0219 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.732+6424C>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224394613 | |||||||
| chr2:224394615 | A | G | 1 | a0001c0001t0003g0137 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.732+6422T>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224394615 | |||||||
| chr2:224394639 | G | A | 155 | a0001c0001t0001g0019 a0001c0001t0001g0028 a0001c0001t0001g0032 others(152): Show |
233 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.732+6398C>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224394639 | |||||||
| chr2:224394724 | C | T | 47 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(44): Show |
68 | HG00140.hp1 HG00280.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.732+6313G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224394724 | |||||||
| chr2:224394742 | T | G | 3 | a0001c0001t0003g0280 a0002c0002t0002g0229 a0002c0002t0002g0279 |
3 | NA18990.hp1 NA19009.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.732+6295A>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224394742 | |||||||
| chr2:224394832 | A | G | 1 | a0001c0003t0010g0147 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.732+6205T>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224394832 | |||||||
| chr2:224394940 | A | C | 1 | a0001c0003t0010g0147 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.732+6097T>G | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224394940 | |||||||
| chr2:224394973 | A | G | 1 | a0001c0003t0010g0147 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.732+6064T>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224394973 | |||||||
| chr2:224395054 | A | G | 1 | a0001c0001t0001g0257 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.732+5983T>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224395054 | |||||||
| chr2:224395069 | T | A | 1 | a0001c0003t0010g0147 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.732+5968A>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224395069 | |||||||
| chr2:224395302 | C | T | 9 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0123 others(6): Show |
10 | HG02055.hp1 HG02615.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.732+5735G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224395302 | |||||||
| chr2:224395432 | G | A | 1 | a0001c0003t0010g0147 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.732+5605C>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224395432 | |||||||
| chr2:224395521 | G | A | 1 | a0002c0002t0002g0100 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.732+5516C>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224395521 | |||||||
| chr2:224395574 | C | T | 5 | a0001c0006t0001g0105 a0001c0006t0001g0146 a0001c0006t0001g0241 others(2): Show |
5 | HG02055.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.732+5463G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224395574 | |||||||
| chr2:224395655 | G | A | 27 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0232 others(24): Show |
42 | HG01069.hp1 HG01175.hp2 HG01952.hp1 others(39): Show |
intron_variant | MODIFIER | c.732+5382C>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224395655 | |||||||
| chr2:224395699 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.732+5338G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224395699 | |||||||
| chr2:224395709 | A | G | 1 | a0001c0003t0010g0147 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.732+5328T>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224395709 | |||||||
| chr2:224395732 | C | T | 1 | a0001c0003t0010g0147 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.732+5305G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224395732 | |||||||
| chr2:224395734 | C | T | 5 | a0001c0006t0001g0105 a0001c0006t0001g0146 a0001c0006t0001g0241 others(2): Show |
5 | HG02055.hp2 HG02486.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.732+5303G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224395734 | |||||||
| chr2:224395778 | T | G | 1 | a0001c0003t0010g0147 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.732+5259A>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224395778 | |||||||
| chr2:224395782 | T | C | 1 | a0002c0002t0002g0235 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.732+5255A>G | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224395782 | |||||||
| chr2:224395797 | T | C | 1 | a0002c0002t0007g0090 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.732+5240A>G | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224395797 | |||||||
| chr2:224395809 | C | T | 1 | a0001c0003t0001g0026 | 3 | HG02145.hp2 HG02451.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.732+5228G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224395809 | |||||||
| chr2:224395810 | G | T | 5 | a0001c0001t0001g0109 a0001c0001t0001g0123 a0001c0001t0001g0124 others(2): Show |
6 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.732+5227C>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224395810 | |||||||
| chr2:224395828 | G | T | 47 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(44): Show |
68 | HG00140.hp1 HG00280.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.732+5209C>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224395828 | |||||||
| chr2:224395879 | G | T | 47 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(44): Show |
68 | HG00140.hp1 HG00280.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.732+5158C>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224395879 | |||||||
| chr2:224395901 | C | T | 47 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0042 others(44): Show |
68 | HG00140.hp1 HG00280.hp1 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.732+5136G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224395901 | |||||||
| chr2:224395960 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.732+5077T>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224395960 | |||||||
| chr2:224395975 | C | G | 5 | a0001c0001t0001g0109 a0001c0001t0001g0123 a0001c0001t0001g0124 others(2): Show |
6 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.732+5062G>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224395975 | |||||||
| chr2:224395991 | C | A | 1 | a0001c0001t0001g0236 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.732+5046G>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224395991 | |||||||
| chr2:224396029 | A | G | 1 | a0002c0002t0007g0090 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.732+5008T>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224396029 | |||||||
| chr2:224396119 | A | G | 1 | a0001c0001t0004g0074 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.732+4918T>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224396119 | |||||||
| chr2:224396131 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.732+4906C>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224396131 | |||||||
| chr2:224396163 | C | T | 1 | a0001c0003t0010g0147 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.732+4874G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224396163 | |||||||
| chr2:224396302 | C | T | 11 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0123 others(8): Show |
12 | HG02055.hp1 HG02615.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.732+4735G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224396302 | |||||||
| chr2:224396321 | C | T | 1 | a0001c0003t0010g0147 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.732+4716G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224396321 | |||||||
| chr2:224396335 | T | C | 2 | a0002c0002t0002g0287 a0002c0002t0002g0288 |
2 | NA18951.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.732+4702A>G | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224396335 | |||||||
| chr2:224396371 | C | T | 5 | a0001c0001t0001g0109 a0001c0001t0001g0123 a0001c0001t0001g0124 others(2): Show |
6 | HG02055.hp1 HG02630.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.732+4666G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224396371 | |||||||
| chr2:224396385 | T | C | 1 | a0001c0001t0001g0237 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.732+4652A>G | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224396385 | |||||||
| chr2:224396420 | C | T | 1 | a0003c0004t0005g0156 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.732+4617G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224396420 | |||||||
| chr2:224396421 | G | A | 1 | a0001c0003t0010g0147 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.732+4616C>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224396421 | |||||||
| chr2:224396552 | C | T | 1 | a0001c0003t0010g0147 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.732+4485G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224396552 | |||||||
| chr2:224396594 | C | T | 6 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0154 others(3): Show |
8 | HG02015.hp1 NA18956.hp2 NA18967.hp2 others(5): Show |
intron_variant | MODIFIER | c.732+4443G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224396594 | |||||||
| chr2:224396632 | A | G | 10 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0123 others(7): Show |
11 | HG02055.hp1 HG02615.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.732+4405T>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224396632 | |||||||
| chr2:224396671 | C | G | 1 | a0001c0003t0010g0147 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.732+4366G>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224396671 | |||||||
| chr2:224396687 | G | A | 1 | a0001c0001t0004g0088 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.732+4350C>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224396687 | |||||||
| chr2:224396745 | G | C | 1 | a0001c0001t0008g0070 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.732+4292C>G | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224396745 | |||||||
| chr2:224396797 | T | C | 1 | a0001c0003t0010g0147 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.732+4240A>G | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224396797 | |||||||
| chr2:224396865 | G | A | 4 | a0001c0001t0004g0067 a0001c0001t0004g0068 a0001c0001t0004g0089 others(1): Show |
4 | HG02257.hp2 HG02818.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.732+4172C>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224396865 | |||||||
| chr2:224396873 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.732+4164G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224396873 | |||||||
| chr2:224396874 | G | A | 1 | a0001c0001t0004g0073 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.732+4163C>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224396874 | |||||||
| chr2:224396893 | G | A | 4 | a0001c0001t0001g0108 a0001c0001t0004g0074 a0001c0001t0004g0075 others(1): Show |
4 | HG02615.hp1 HG02809.hp1 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.732+4144C>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224396893 | |||||||
| chr2:224396920 | G | T | 1 | a0001c0001t0012g0149 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.732+4117C>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224396920 | |||||||
| chr2:224397030 | T | G | 9 | a0001c0001t0003g0061 a0001c0001t0003g0239 a0001c0001t0003g0240 others(6): Show |
10 | NA18948.hp1 NA18962.hp2 NA18971.hp2 others(7): Show |
intron_variant | MODIFIER | c.732+4007A>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224397030 | |||||||
| chr2:224397037 | T | TTCTTC | 9 | a0001c0001t0001g0108 a0001c0001t0004g0074 a0001c0001t0004g0075 others(6): Show |
9 | HG02055.hp2 HG02559.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.732+3995_732+3999d others(7): Show |
FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224397037 | |||||||
| chr2:224397142 | T | G | 1 | a0001c0001t0001g0290 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.732+3895A>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224397142 | |||||||
| chr2:224397146 | G | A | 2 | a0001c0001t0001g0242 a0001c0001t0003g0137 |
2 | NA19030.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.732+3891C>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224397146 | |||||||
| chr2:224397154 | A | C | 1 | a0001c0001t0001g0148 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.732+3883T>G | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224397154 | |||||||
| chr2:224397215 | A | T | 8 | a0001c0001t0001g0108 a0001c0001t0001g0252 a0001c0001t0004g0074 others(5): Show |
8 | HG02486.hp2 HG02615.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.732+3822T>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224397215 | |||||||
| chr2:224397261 | T | C | 4 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0002c0002t0007g0090 others(1): Show |
7 | HG01346.hp1 HG02896.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.732+3776A>G | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224397261 | |||||||
| chr2:224397279 | G | A | 1 | a0001c0001t0003g0291 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.732+3758C>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224397279 | |||||||
| chr2:224397307 | G | T | 8 | a0001c0001t0001g0008 a0001c0001t0001g0140 a0001c0001t0001g0141 others(5): Show |
12 | HG00597.hp1 HG00621.hp1 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.732+3730C>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224397307 | |||||||
| chr2:224397328 | C | T | 1 | a0002c0002t0002g0139 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.732+3709G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224397328 | |||||||
| chr2:224397455 | G | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0243 a0001c0001t0001g0244 |
7 | NA18939.hp1 NA18950.hp2 NA18963.hp1 others(4): Show |
intron_variant | MODIFIER | c.732+3582C>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224397455 | |||||||
| chr2:224397641 | T | C | 3 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 |
3 | HG02451.hp1 HG02572.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.732+3396A>G | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224397641 | |||||||
| chr2:224397746 | C | T | 1 | a0002c0002t0002g0254 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.732+3291G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224397746 | |||||||
| chr2:224398028 | C | G | 30 | a0001c0001t0004g0013 a0001c0001t0004g0014 a0001c0001t0004g0015 others(27): Show |
41 | HG00140.hp1 HG00280.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.732+3009G>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224398028 | |||||||
| chr2:224398116 | TAC | T | 26 | a0001c0001t0001g0039 a0001c0001t0001g0119 a0001c0001t0001g0121 others(23): Show |
36 | HG00597.hp2 HG00673.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.732+2919_732+2920d others(4): Show |
FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224398116 | |||||||
| chr2:224398138 | T | A | 1 | a0002c0002t0002g0248 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.732+2899A>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224398138 | |||||||
| chr2:224398200 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.732+2837G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224398200 | |||||||
| chr2:224398217 | C | T | 6 | a0001c0001t0001g0119 a0001c0001t0001g0121 a0001c0005t0001g0035 others(3): Show |
8 | HG01243.hp2 HG01891.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.732+2820G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224398217 | |||||||
| chr2:224398289 | G | T | 1 | a0002c0002t0002g0117 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.732+2748C>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224398289 | |||||||
| chr2:224398389 | C | T | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.732+2648G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224398389 | |||||||
| chr2:224398453 | T | G | 35 | a0001c0001t0001g0249 a0001c0001t0004g0013 a0001c0001t0004g0014 others(32): Show |
46 | HG00140.hp1 HG00280.hp1 HG00741.hp1 others(43): Show |
intron_variant | MODIFIER | c.732+2584A>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224398453 | |||||||
| chr2:224398536 | T | C | 34 | a0001c0001t0004g0013 a0001c0001t0004g0014 a0001c0001t0004g0015 others(31): Show |
45 | HG00140.hp1 HG00280.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.732+2501A>G | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224398536 | |||||||
| chr2:224398592 | A | T | 1 | a0001c0003t0001g0253 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.732+2445T>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224398592 | |||||||
| chr2:224398604 | A | G | 7 | a0001c0001t0004g0013 a0001c0001t0004g0069 a0001c0001t0004g0074 others(4): Show |
10 | HG02559.hp2 HG02809.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.732+2433T>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224398604 | |||||||
| chr2:224398810 | C | T | 34 | a0001c0001t0004g0013 a0001c0001t0004g0014 a0001c0001t0004g0015 others(31): Show |
45 | HG00140.hp1 HG00280.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.732+2227G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224398810 | |||||||
| chr2:224398901 | C | T | 3 | a0001c0001t0004g0074 a0001c0001t0004g0075 a0001c0001t0004g0076 |
3 | HG02809.hp1 HG02922.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.732+2136G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224398901 | |||||||
| chr2:224399071 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.732+1966G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224399071 | |||||||
| chr2:224399089 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.732+1948A>G | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224399089 | |||||||
| chr2:224399112 | C | G | 2 | a0001c0001t0004g0072 a0001c0001t0004g0073 |
2 | HG00280.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.732+1925G>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224399112 | |||||||
| chr2:224399283 | C | T | 4 | a0001c0001t0004g0013 a0001c0001t0004g0069 a0001c0001t0008g0070 others(1): Show |
7 | HG02559.hp2 HG02976.hp1 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.732+1754G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224399283 | |||||||
| chr2:224399385 | G | T | 1 | a0001c0001t0001g0113 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.732+1652C>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224399385 | |||||||
| chr2:224399408 | A | G | 9 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0108 others(6): Show |
12 | HG01346.hp1 HG01884.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.732+1629T>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224399408 | |||||||
| chr2:224399653 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.732+1384T>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224399653 | |||||||
| chr2:224399830 | T | C | 53 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0256 others(50): Show |
94 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(91): Show |
intron_variant | MODIFIER | c.732+1207A>G | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224399830 | |||||||
| chr2:224399881 | G | A | 34 | a0001c0001t0004g0013 a0001c0001t0004g0014 a0001c0001t0004g0015 others(31): Show |
45 | HG00140.hp1 HG00280.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.732+1156C>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224399881 | |||||||
| chr2:224399902 | G | A | 34 | a0001c0001t0004g0013 a0001c0001t0004g0014 a0001c0001t0004g0015 others(31): Show |
45 | HG00140.hp1 HG00280.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.732+1135C>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224399902 | |||||||
| chr2:224400061 | A | T | 1 | a0001c0001t0001g0252 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.732+976T>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224400061 | |||||||
| chr2:224400173 | G | A | 1 | a0001c0001t0001g0250 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.732+864C>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224400173 | |||||||
| chr2:224400239 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.732+798G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224400239 | |||||||
| chr2:224400288 | C | T | 3 | a0001c0001t0004g0067 a0001c0001t0004g0068 a0001c0005t0004g0066 |
3 | HG02257.hp2 HG03195.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.732+749G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224400288 | |||||||
| chr2:224400570 | C | T | 1 | a0001c0006t0001g0105 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.732+467G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224400570 | |||||||
| chr2:224400654 | C | T | 4 | a0001c0001t0001g0031 a0001c0001t0001g0102 a0001c0001t0001g0103 others(1): Show |
5 | HG00735.hp1 HG01123.hp2 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.732+383G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224400654 | |||||||
| chr2:224400714 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0101 |
5 | NA18949.hp1 NA18964.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.732+323G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224400714 | |||||||
| chr2:224400872 | G | A | 1 | a0001c0001t0001g0251 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.732+165C>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224400872 | |||||||
| chr2:224400883 | T | G | 1 | a0001c0001t0001g0252 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.732+154A>C | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224400883 | |||||||
| chr2:224400928 | G | A | 53 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0256 others(50): Show |
94 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(91): Show |
intron_variant | MODIFIER | c.732+109C>T | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224400928 | |||||||
| chr2:224400999 | C | T | 3 | a0001c0001t0001g0098 a0002c0002t0002g0099 a0002c0002t0002g0100 |
3 | HG00544.hp1 HG02132.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.732+38G>A | FAM124B | ENSG00000124019.10 | transcript | ENST00000409685.4 | protein_coding | 1/1 | chr2 | 224400999 |