Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 220108 |
| ensemblid | ENSG00000150510.17 |
| hgncid | 26413 |
| symbol | FAM124A |
| name | family with sequence similarity 124 member A |
| refseq_nuc | NM_001242312.2 |
| refseq_prot | NP_001229241.1 |
| ensembl_nuc | ENST00000322475.13 |
| ensembl_prot | ENSP00000324625.8 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 51222398 |
| end | 51284239 |
| strand | + |
| ver | v1.2 |
| region | chr13:51222398-51284239 |
| region5000 | chr13:51217398-51289239 |
| regionname0 | FAM124A_chr13_51222398_51284239 |
| regionname5000 | FAM124A_chr13_51217398_51289239 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 546 | 336 | 61 | 56 | 167 | 12 | 38 | 122 | FAM124A_chr13_51217398_51289239 | FAM124A | MDPKA others(541): Show |
chr13 | 51217398 | 51289239 |
| a0002 | 0/0 | 546 | 43 | 15 | 7 | 16 | 3 | 2 | 15 | FAM124A_chr13_51217398_51289239 | FAM124A | MDPKA others(541): Show |
chr13 | 51217398 | 51289239 |
| a0003 | 0/0 | 546 | 12 | 11 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | MDPKA others(541): Show |
chr13 | 51217398 | 51289239 |
| a0004 | 0/0 | 546 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | MDPKA others(541): Show |
chr13 | 51217398 | 51289239 |
| a0005 | 0/0 | 546 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | FAM124A_chr13_51217398_51289239 | FAM124A | MDPKA others(541): Show |
chr13 | 51217398 | 51289239 |
| a0006 | 0/0 | 546 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | MDPKA others(541): Show |
chr13 | 51217398 | 51289239 |
| a0007 | 0/0 | 546 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | MDPKA others(541): Show |
chr13 | 51217398 | 51289239 |
| a0008 | 0/0 | 546 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | MDPKA others(541): Show |
chr13 | 51217398 | 51289239 |
| a0009 | 0/0 | 546 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | MDPKA others(541): Show |
chr13 | 51217398 | 51289239 |
| a0010 | 0/0 | 546 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | MDPKA others(541): Show |
chr13 | 51217398 | 51289239 |
| a0011 | 0/0 | 546 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | MDPKA others(541): Show |
chr13 | 51217398 | 51289239 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1638 | 325 | 54 | 56 | 163 | 12 | 38 | FAM124A_chr13_51217398_51289239 | FAM124A | ATGGA others(1633): Show |
chr13 | 51217398 | 51289239 | ||
| a0001c0006 | 0/0 | 1638 | 4 | 1 | 0 | 3 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | ATGGA others(1633): Show |
chr13 | 51217398 | 51289239 | ||
| a0001c0007 | 0/0 | 1638 | 3 | 3 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | ATGGA others(1633): Show |
chr13 | 51217398 | 51289239 | ||
| a0001c0009 | 0/0 | 1638 | 2 | 2 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | ATGGA others(1633): Show |
chr13 | 51217398 | 51289239 | ||
| a0001c0016 | 0/0 | 1638 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | ATGGA others(1633): Show |
chr13 | 51217398 | 51289239 | ||
| a0001c0017 | 0/0 | 1638 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | ATGGA others(1633): Show |
chr13 | 51217398 | 51289239 | ||
| a0002c0002 | 0/0 | 1638 | 36 | 13 | 7 | 11 | 3 | 2 | FAM124A_chr13_51217398_51289239 | FAM124A | ATGGA others(1633): Show |
chr13 | 51217398 | 51289239 | ||
| a0002c0004 | 0/0 | 1638 | 7 | 2 | 0 | 5 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | ATGGA others(1633): Show |
chr13 | 51217398 | 51289239 | ||
| a0003c0003 | 0/0 | 1638 | 12 | 11 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | ATGGA others(1633): Show |
chr13 | 51217398 | 51289239 | ||
| a0004c0005 | 0/0 | 1638 | 6 | 6 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | ATGGA others(1633): Show |
chr13 | 51217398 | 51289239 | ||
| a0004c0011 | 0/0 | 1638 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | ATGGA others(1633): Show |
chr13 | 51217398 | 51289239 | ||
| a0005c0008 | 0/0 | 1638 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | ATGGA others(1633): Show |
chr13 | 51217398 | 51289239 | ||
| a0006c0012 | 0/0 | 1638 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | ATGGA others(1633): Show |
chr13 | 51217398 | 51289239 | ||
| a0007c0015 | 0/0 | 1638 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | ATGGA others(1633): Show |
chr13 | 51217398 | 51289239 | ||
| a0008c0010 | 0/0 | 1638 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | ATGGA others(1633): Show |
chr13 | 51217398 | 51289239 | ||
| a0009c0013 | 0/0 | 1638 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | ATGGA others(1633): Show |
chr13 | 51217398 | 51289239 | ||
| a0010c0014 | 0/0 | 1638 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | ATGGA others(1633): Show |
chr13 | 51217398 | 51289239 | ||
| a0011c0018 | 0/0 | 1638 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | ATGGA others(1633): Show |
chr13 | 51217398 | 51289239 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4729 | 86 | 7 | 22 | 41 | 5 | 11 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4724): Show |
chr13 | 51217398 | 51289239 |
| a0001c0001t0002 | 1/1 | 4728 | 83 | 10 | 15 | 43 | 6 | 7 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4723): Show |
chr13 | 51217398 | 51289239 |
| a0001c0001t0003 | 0/0 | 4730 | 35 | 1 | 1 | 32 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4725): Show |
chr13 | 51217398 | 51289239 |
| a0001c0001t0004 | 0/0 | 4730 | 29 | 4 | 7 | 11 | 0 | 7 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4725): Show |
chr13 | 51217398 | 51289239 |
| a0001c0001t0005 | 0/0 | 4731 | 19 | 1 | 1 | 16 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4726): Show |
chr13 | 51217398 | 51289239 |
| a0001c0001t0006 | 0/0 | 4733 | 16 | 1 | 2 | 6 | 1 | 6 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4728): Show |
chr13 | 51217398 | 51289239 |
| a0001c0001t0007 | 0/0 | 4727 | 7 | 4 | 3 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4722): Show |
chr13 | 51217398 | 51289239 |
| a0001c0001t0009 | 0/0 | 4728 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4723): Show |
chr13 | 51217398 | 51289239 |
| a0001c0001t0011 | 0/0 | 4734 | 6 | 0 | 2 | 1 | 0 | 3 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4729): Show |
chr13 | 51217398 | 51289239 |
| a0001c0001t0012 | 0/0 | 4730 | 7 | 7 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4725): Show |
chr13 | 51217398 | 51289239 |
| a0001c0001t0013 | 0/0 | 4732 | 2 | 2 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4727): Show |
chr13 | 51217398 | 51289239 |
| a0001c0001t0014 | 0/0 | 4731 | 4 | 4 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4726): Show |
chr13 | 51217398 | 51289239 |
| a0001c0001t0015 | 0/0 | 4729 | 4 | 0 | 0 | 4 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4724): Show |
chr13 | 51217398 | 51289239 |
| a0001c0001t0017 | 0/0 | 4731 | 3 | 3 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4726): Show |
chr13 | 51217398 | 51289239 |
| a0001c0001t0018 | 0/0 | 4731 | 2 | 2 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4726): Show |
chr13 | 51217398 | 51289239 |
| a0001c0001t0019 | 0/0 | 4730 | 2 | 2 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4725): Show |
chr13 | 51217398 | 51289239 |
| a0001c0001t0021 | 0/0 | 4729 | 2 | 0 | 2 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4724): Show |
chr13 | 51217398 | 51289239 |
| a0001c0001t0022 | 0/0 | 4733 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4728): Show |
chr13 | 51217398 | 51289239 |
| a0001c0001t0023 | 0/0 | 4730 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4725): Show |
chr13 | 51217398 | 51289239 |
| a0001c0001t0025 | 0/0 | 4730 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4725): Show |
chr13 | 51217398 | 51289239 |
| a0001c0001t0026 | 0/0 | 4732 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4727): Show |
chr13 | 51217398 | 51289239 |
| a0001c0001t0028 | 0/0 | 4731 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4726): Show |
chr13 | 51217398 | 51289239 |
| a0001c0001t0029 | 0/0 | 4731 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4726): Show |
chr13 | 51217398 | 51289239 |
| a0001c0001t0030 | 0/0 | 4727 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4722): Show |
chr13 | 51217398 | 51289239 |
| a0001c0001t0034 | 0/0 | 4730 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4725): Show |
chr13 | 51217398 | 51289239 |
| a0001c0001t0035 | 0/0 | 4730 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4725): Show |
chr13 | 51217398 | 51289239 |
| a0001c0001t0036 | 0/0 | 4728 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4723): Show |
chr13 | 51217398 | 51289239 |
| a0001c0001t0037 | 0/0 | 4729 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4724): Show |
chr13 | 51217398 | 51289239 |
| a0001c0001t0038 | 0/0 | 4733 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4728): Show |
chr13 | 51217398 | 51289239 |
| a0001c0001t0041 | 0/0 | 4730 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4725): Show |
chr13 | 51217398 | 51289239 |
| a0001c0001t0042 | 0/0 | 4731 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4726): Show |
chr13 | 51217398 | 51289239 |
| a0001c0001t0043 | 0/0 | 4728 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4723): Show |
chr13 | 51217398 | 51289239 |
| a0001c0001t0044 | 0/0 | 4732 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4727): Show |
chr13 | 51217398 | 51289239 |
| a0001c0006t0010 | 0/0 | 4731 | 3 | 0 | 0 | 3 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4726): Show |
chr13 | 51217398 | 51289239 |
| a0001c0006t0016 | 0/0 | 4732 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4727): Show |
chr13 | 51217398 | 51289239 |
| a0001c0007t0001 | 0/0 | 4729 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4724): Show |
chr13 | 51217398 | 51289239 |
| a0001c0007t0013 | 0/0 | 4732 | 2 | 2 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4727): Show |
chr13 | 51217398 | 51289239 |
| a0001c0009t0020 | 0/0 | 4740 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4735): Show |
chr13 | 51217398 | 51289239 |
| a0001c0009t0033 | 0/0 | 4720 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4715): Show |
chr13 | 51217398 | 51289239 |
| a0001c0016t0002 | 0/0 | 4728 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4723): Show |
chr13 | 51217398 | 51289239 |
| a0001c0017t0001 | 0/0 | 4729 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4724): Show |
chr13 | 51217398 | 51289239 |
| a0002c0002t0001 | 0/0 | 4729 | 6 | 2 | 1 | 3 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4724): Show |
chr13 | 51217398 | 51289239 |
| a0002c0002t0002 | 0/0 | 4728 | 6 | 1 | 0 | 4 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4723): Show |
chr13 | 51217398 | 51289239 |
| a0002c0002t0004 | 0/0 | 4730 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4725): Show |
chr13 | 51217398 | 51289239 |
| a0002c0002t0007 | 0/0 | 4727 | 9 | 6 | 1 | 2 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4722): Show |
chr13 | 51217398 | 51289239 |
| a0002c0002t0009 | 0/0 | 4728 | 8 | 1 | 4 | 0 | 1 | 2 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4723): Show |
chr13 | 51217398 | 51289239 |
| a0002c0002t0011 | 0/0 | 4734 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4729): Show |
chr13 | 51217398 | 51289239 |
| a0002c0002t0018 | 0/0 | 4731 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4726): Show |
chr13 | 51217398 | 51289239 |
| a0002c0002t0019 | 0/0 | 4730 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4725): Show |
chr13 | 51217398 | 51289239 |
| a0002c0002t0031 | 0/0 | 4726 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4721): Show |
chr13 | 51217398 | 51289239 |
| a0002c0002t0032 | 0/0 | 4727 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4722): Show |
chr13 | 51217398 | 51289239 |
| a0002c0002t0040 | 0/0 | 4728 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4723): Show |
chr13 | 51217398 | 51289239 |
| a0002c0004t0010 | 0/0 | 4731 | 5 | 2 | 0 | 3 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4726): Show |
chr13 | 51217398 | 51289239 |
| a0002c0004t0016 | 0/0 | 4732 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4727): Show |
chr13 | 51217398 | 51289239 |
| a0003c0003t0008 | 0/0 | 4721 | 9 | 8 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4716): Show |
chr13 | 51217398 | 51289239 |
| a0003c0003t0024 | 0/0 | 4721 | 2 | 2 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4716): Show |
chr13 | 51217398 | 51289239 |
| a0003c0003t0039 | 0/0 | 4730 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4725): Show |
chr13 | 51217398 | 51289239 |
| a0004c0005t0013 | 0/0 | 4732 | 2 | 2 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4727): Show |
chr13 | 51217398 | 51289239 |
| a0004c0005t0022 | 0/0 | 4733 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4728): Show |
chr13 | 51217398 | 51289239 |
| a0004c0005t0023 | 0/0 | 4730 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4725): Show |
chr13 | 51217398 | 51289239 |
| a0004c0005t0027 | 0/0 | 4733 | 2 | 2 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4728): Show |
chr13 | 51217398 | 51289239 |
| a0004c0011t0002 | 0/0 | 4728 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4723): Show |
chr13 | 51217398 | 51289239 |
| a0005c0008t0003 | 0/0 | 4730 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4725): Show |
chr13 | 51217398 | 51289239 |
| a0005c0008t0005 | 0/0 | 4731 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4726): Show |
chr13 | 51217398 | 51289239 |
| a0006c0012t0006 | 0/0 | 4733 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4728): Show |
chr13 | 51217398 | 51289239 |
| a0007c0015t0004 | 0/0 | 4730 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4725): Show |
chr13 | 51217398 | 51289239 |
| a0008c0010t0020 | 0/0 | 4740 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4735): Show |
chr13 | 51217398 | 51289239 |
| a0009c0013t0008 | 0/0 | 4721 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4716): Show |
chr13 | 51217398 | 51289239 |
| a0010c0014t0026 | 0/0 | 4732 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4727): Show |
chr13 | 51217398 | 51289239 |
| a0011c0018t0002 | 0/0 | 4728 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | AGACG others(4723): Show |
chr13 | 51217398 | 51289239 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0045 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0136 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0229 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0003g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0003g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0003g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0003g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0003g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0003g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0003g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0004g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0004g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0004g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0004g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0004g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0004g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0004g0046 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0004g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0004g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0004g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0004g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0004g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0004g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0004g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0004g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0004g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0004g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0004g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0004g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0005g0012 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0005g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0005g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0005g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0005g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0005g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0005g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0005g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0005g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0005g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0005g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0005g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0005g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0005g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0005g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0005g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0005g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0006g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0006g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0006g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0006g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0006g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0006g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0006g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0006g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0006g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0006g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0006g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0006g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0006g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0007g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0007g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0007g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0007g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0007g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0009g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0011g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0011g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0011g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0011g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0011g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0011g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0012g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0012g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0012g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0012g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0012g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0012g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0013g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0013g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0014g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0014g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0014g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0015g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0015g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0015g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0015g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0017g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0017g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0017g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0018g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0018g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0019g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0019g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0021g0054 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0022g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0023g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0025g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0025g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0026g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0028g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0029g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0030g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0034g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0035g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0036g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0037g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0038g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0041g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0042g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0043g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0001t0044g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0006t0010g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0006t0010g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0006t0010g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0006t0016g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0007t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0007t0013g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0007t0013g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0009t0020g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0009t0033g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0016t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0001c0017t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0002c0002t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0002c0002t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0002c0002t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0002c0002t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0002c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0002c0002t0002g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0002c0002t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0002c0002t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0002c0002t0007g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0002c0002t0007g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0002c0002t0007g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0002c0002t0007g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0002c0002t0007g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0002c0002t0007g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0002c0002t0007g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0002c0002t0007g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0002c0002t0009g0018 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0002c0002t0009g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0002c0002t0009g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0002c0002t0009g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0002c0002t0009g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0002c0002t0009g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0002c0002t0011g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0002c0002t0018g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0002c0002t0019g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0002c0002t0031g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0002c0002t0032g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0002c0002t0040g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0002c0004t0010g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0002c0004t0010g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0002c0004t0010g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0002c0004t0010g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0002c0004t0016g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0002c0004t0016g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0003c0003t0008g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0003c0003t0008g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0003c0003t0008g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0003c0003t0008g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0003c0003t0008g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0003c0003t0008g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0003c0003t0008g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0003c0003t0008g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0003c0003t0024g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0003c0003t0024g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0003c0003t0039g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0004c0005t0013g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0004c0005t0013g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0004c0005t0022g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0004c0005t0023g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0004c0005t0027g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0004c0011t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0005c0008t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0005c0008t0005g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0006c0012t0006g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0007c0015t0004g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0008c0010t0020g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0009c0013t0008g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0010c0014t0026g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| a0011c0018t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0303 | EUR | GBR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0167 | EUR | GBR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG00140 | hp1 | a0002 | c0002 | t0002 | g0048 | EUR | GBR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG00140 | hp2 | a0006 | c0012 | t0006 | g0126 | EUR | GBR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0045 | EUR | FIN | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | FIN | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0251 | EUR | FIN | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG00323 | hp2 | a0002 | c0002 | t0031 | g0216 | EUR | FIN | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0078 | EAS | CHS | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG00408 | hp2 | a0001 | c0016 | t0002 | g0001 | EAS | CHS | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG00423 | hp1 | a0001 | c0006 | t0010 | g0265 | EAS | CHS | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | CHS | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | CHS | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | CHS | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG00544 | hp1 | a0001 | c0001 | t0006 | g0274 | EAS | CHS | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | CHS | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG00558 | hp2 | a0001 | c0001 | t0036 | g0001 | EAS | CHS | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG00597 | hp1 | a0001 | c0001 | t0005 | g0076 | EAS | CHS | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | CHS | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | CHS | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG00621 | hp1 | a0001 | c0001 | t0004 | g0079 | EAS | CHS | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0239 | EAS | CHS | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0266 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0181 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | CHS | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | CHS | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0215 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG00738 | hp1 | a0001 | c0001 | t0004 | g0211 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG00738 | hp2 | a0001 | c0001 | t0007 | g0025 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01069 | hp2 | a0001 | c0001 | t0011 | g0227 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01070 | hp1 | a0001 | c0001 | t0007 | g0026 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01074 | hp2 | a0002 | c0002 | t0007 | g0021 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0305 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0223 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01106 | hp2 | a0001 | c0001 | t0004 | g0135 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01109 | hp1 | a0001 | c0001 | t0004 | g0017 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01109 | hp2 | a0001 | c0001 | t0023 | g0288 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0298 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01167 | hp2 | a0002 | c0002 | t0009 | g0018 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01168 | hp1 | a0001 | c0001 | t0021 | g0054 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01168 | hp2 | a0001 | c0001 | t0007 | g0025 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01169 | hp1 | a0002 | c0002 | t0009 | g0018 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01169 | hp2 | a0001 | c0001 | t0021 | g0054 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01175 | hp1 | a0002 | c0002 | t0009 | g0230 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01175 | hp2 | a0007 | c0015 | t0004 | g0006 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0051 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01192 | hp2 | a0003 | c0003 | t0008 | g0199 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01243 | hp1 | a0002 | c0002 | t0019 | g0242 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0306 | AMR | PUR | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01255 | hp1 | a0001 | c0001 | t0005 | g0034 | AMR | CLM | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01255 | hp2 | a0002 | c0002 | t0009 | g0286 | AMR | CLM | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0212 | AMR | CLM | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01346 | hp1 | a0001 | c0001 | t0011 | g0208 | AMR | CLM | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0033 | AMR | CLM | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0160 | AMR | CLM | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0045 | AMR | CLM | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | CLM | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0252 | EUR | IBS | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0203 | EUR | IBS | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0144 | EUR | IBS | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01884 | hp1 | a0003 | c0003 | t0008 | g0201 | AFR | ACB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01884 | hp2 | a0008 | c0010 | t0020 | g0073 | AFR | ACB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01891 | hp1 | a0004 | c0005 | t0022 | g0289 | AFR | ACB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01891 | hp2 | a0001 | c0007 | t0013 | g0092 | AFR | ACB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | PEL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01934 | hp1 | a0001 | c0001 | t0006 | g0173 | AMR | PEL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01934 | hp2 | a0001 | c0001 | t0004 | g0017 | AMR | PEL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01943 | hp1 | a0001 | c0001 | t0006 | g0150 | AMR | PEL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01975 | hp1 | a0009 | c0013 | t0008 | g0224 | AMR | PEL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | PEL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01981 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | PEL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0267 | AMR | PEL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02027 | hp1 | a0001 | c0001 | t0011 | g0084 | EAS | KHV | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0238 | EAS | KHV | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0221 | AFR | ACB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0005 | AFR | ACB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | KHV | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02056 | hp2 | a0001 | c0001 | t0004 | g0226 | EAS | KHV | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | KHV | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0106 | EAS | KHV | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02074 | hp1 | a0001 | c0001 | t0005 | g0101 | EAS | KHV | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02074 | hp2 | a0001 | c0001 | t0015 | g0297 | EAS | KHV | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02080 | hp1 | a0001 | c0001 | t0005 | g0085 | EAS | KHV | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0019 | EAS | KHV | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | KHV | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02083 | hp2 | a0001 | c0001 | t0006 | g0152 | EAS | KHV | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02129 | hp1 | a0001 | c0001 | t0004 | g0022 | EAS | KHV | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0176 | EAS | KHV | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | KHV | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02132 | hp2 | a0002 | c0004 | t0016 | g0243 | EAS | KHV | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02135 | hp1 | a0001 | c0001 | t0005 | g0107 | EAS | KHV | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | KHV | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02145 | hp1 | a0001 | c0001 | t0014 | g0003 | AFR | ACB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02145 | hp2 | a0001 | c0001 | t0018 | g0128 | AFR | ACB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | CDX | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | CDX | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CDX | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02257 | hp1 | a0001 | c0001 | t0012 | g0003 | AFR | ACB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02258 | hp1 | a0001 | c0001 | t0030 | g0117 | AFR | ACB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02258 | hp2 | a0002 | c0002 | t0007 | g0282 | AFR | ACB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02280 | hp1 | a0001 | c0006 | t0016 | g0313 | AFR | ACB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0196 | AFR | ACB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0042 | AMR | PEL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0011 | AMR | PEL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02451 | hp1 | a0001 | c0001 | t0019 | g0310 | AFR | ACB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0241 | AFR | ACB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | KHV | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | KHV | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0189 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02572 | hp2 | a0004 | c0005 | t0023 | g0233 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0304 | SAS | PJL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02602 | hp2 | a0001 | c0001 | t0006 | g0257 | SAS | PJL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0314 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0222 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02622 | hp1 | a0001 | c0001 | t0017 | g0044 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02622 | hp2 | a0002 | c0002 | t0007 | g0246 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02630 | hp1 | a0001 | c0001 | t0013 | g0044 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02630 | hp2 | a0002 | c0002 | t0002 | g0278 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02647 | hp1 | a0001 | c0017 | t0001 | g0170 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02647 | hp2 | a0001 | c0007 | t0001 | g0030 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02683 | hp2 | a0001 | c0001 | t0006 | g0146 | SAS | PJL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02717 | hp1 | a0001 | c0001 | t0012 | g0250 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02717 | hp2 | a0002 | c0002 | t0007 | g0279 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02723 | hp1 | a0001 | c0001 | t0017 | g0194 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02723 | hp2 | a0001 | c0001 | t0043 | g0003 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02735 | hp2 | a0001 | c0001 | t0004 | g0270 | SAS | PJL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02738 | hp1 | a0001 | c0001 | t0004 | g0091 | SAS | PJL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0177 | SAS | PJL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02818 | hp1 | a0001 | c0007 | t0013 | g0030 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0190 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02886 | hp1 | a0001 | c0001 | t0009 | g0047 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02886 | hp2 | a0003 | c0003 | t0008 | g0200 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02895 | hp1 | a0002 | c0002 | t0009 | g0018 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02895 | hp2 | a0001 | c0001 | t0012 | g0311 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02896 | hp1 | a0003 | c0003 | t0039 | g0007 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02897 | hp1 | a0001 | c0001 | t0012 | g0307 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02897 | hp2 | a0003 | c0003 | t0024 | g0007 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0231 | AFR | ESN | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02922 | hp2 | a0003 | c0003 | t0008 | g0206 | AFR | ESN | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02965 | hp1 | a0004 | c0005 | t0013 | g0281 | AFR | ESN | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02965 | hp2 | a0003 | c0003 | t0008 | g0129 | AFR | ESN | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02970 | hp1 | a0001 | c0001 | t0013 | g0191 | AFR | ESN | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ESN | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02976 | hp1 | a0001 | c0001 | t0012 | g0309 | AFR | ESN | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0142 | SAS | PJL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG03041 | hp1 | a0001 | c0001 | t0007 | g0047 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG03041 | hp2 | a0001 | c0001 | t0012 | g0003 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG03098 | hp1 | a0001 | c0001 | t0038 | g0293 | AFR | MSL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0312 | AFR | MSL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0188 | AFR | ESN | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG03130 | hp2 | a0002 | c0002 | t0007 | g0285 | AFR | ESN | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG03139 | hp1 | a0004 | c0005 | t0013 | g0290 | AFR | ESN | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG03139 | hp2 | a0002 | c0002 | t0007 | g0021 | AFR | ESN | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG03195 | hp1 | a0001 | c0001 | t0017 | g0192 | AFR | ESN | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0280 | AFR | ESN | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG03209 | hp1 | a0004 | c0005 | t0027 | g0052 | AFR | MSL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG03209 | hp2 | a0001 | c0009 | t0033 | g0213 | AFR | MSL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG03453 | hp1 | a0002 | c0002 | t0004 | g0234 | AFR | MSL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG03453 | hp2 | a0003 | c0003 | t0008 | g0198 | AFR | MSL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG03486 | hp1 | a0003 | c0003 | t0008 | g0195 | AFR | MSL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0131 | AFR | MSL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0161 | SAS | PJL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG03490 | hp2 | a0001 | c0001 | t0006 | g0040 | SAS | PJL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0292 | SAS | PJL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG03492 | hp1 | a0001 | c0001 | t0006 | g0039 | SAS | PJL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0046 | AFR | ESN | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG03516 | hp2 | a0002 | c0002 | t0018 | g0301 | AFR | ESN | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG03540 | hp1 | a0003 | c0003 | t0008 | g0007 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG03540 | hp2 | a0001 | c0001 | t0014 | g0294 | AFR | GWD | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG03579 | hp1 | a0001 | c0001 | t0014 | g0240 | AFR | MSL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG03579 | hp2 | a0010 | c0014 | t0026 | g0249 | AFR | MSL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG03669 | hp2 | a0001 | c0001 | t0006 | g0039 | SAS | PJL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG03704 | hp1 | a0001 | c0001 | t0004 | g0232 | SAS | PJL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG03704 | hp2 | a0001 | c0001 | t0004 | g0268 | SAS | PJL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG03710 | hp2 | a0001 | c0001 | t0006 | g0040 | SAS | PJL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG03831 | hp1 | a0001 | c0001 | t0034 | g0001 | SAS | BEB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG03831 | hp2 | a0002 | c0002 | t0009 | g0244 | SAS | BEB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0184 | SAS | BEB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0109 | SAS | BEB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0263 | SAS | BEB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | BEB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG03942 | hp1 | a0002 | c0002 | t0009 | g0225 | SAS | BEB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG03942 | hp2 | a0001 | c0001 | t0005 | g0087 | SAS | BEB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG04115 | hp1 | a0001 | c0001 | t0011 | g0156 | SAS | STU | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG04115 | hp2 | a0001 | c0001 | t0004 | g0187 | SAS | STU | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0291 | SAS | BEB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | BEB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0037 | SAS | STU | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG04199 | hp2 | a0001 | c0001 | t0011 | g0276 | SAS | STU | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG04204 | hp1 | a0001 | c0001 | t0004 | g0155 | SAS | STU | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG04204 | hp2 | a0001 | c0001 | t0004 | g0259 | SAS | STU | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18522 | hp1 | a0001 | c0001 | t0012 | g0093 | AFR | YRI | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18522 | hp2 | a0003 | c0003 | t0008 | g0007 | AFR | YRI | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | CHB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18612 | hp2 | a0001 | c0001 | t0044 | g0137 | EAS | CHB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | CHB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | CHB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18906 | hp1 | a0002 | c0004 | t0010 | g0284 | AFR | YRI | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18906 | hp2 | a0004 | c0005 | t0027 | g0052 | AFR | YRI | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18939 | hp1 | a0002 | c0002 | t0002 | g0299 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18940 | hp2 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18941 | hp1 | a0001 | c0001 | t0005 | g0077 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0100 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18942 | hp2 | a0001 | c0001 | t0006 | g0038 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18945 | hp1 | a0001 | c0001 | t0005 | g0031 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18947 | hp2 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18949 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18950 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18951 | hp1 | a0002 | c0002 | t0040 | g0302 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18952 | hp1 | a0001 | c0006 | t0010 | g0001 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18952 | hp2 | a0002 | c0004 | t0010 | g0050 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18954 | hp2 | a0001 | c0001 | t0025 | g0002 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18956 | hp1 | a0002 | c0002 | t0001 | g0245 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18956 | hp2 | a0001 | c0001 | t0025 | g0296 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18959 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18959 | hp2 | a0001 | c0001 | t0006 | g0038 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18960 | hp2 | a0002 | c0004 | t0010 | g0050 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18961 | hp2 | a0005 | c0008 | t0003 | g0058 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18963 | hp1 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18965 | hp2 | a0001 | c0001 | t0005 | g0012 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18967 | hp1 | a0001 | c0001 | t0041 | g0053 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18967 | hp2 | a0001 | c0001 | t0005 | g0081 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18969 | hp2 | a0005 | c0008 | t0005 | g0059 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18971 | hp2 | a0002 | c0004 | t0010 | g0277 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18978 | hp2 | a0001 | c0001 | t0005 | g0097 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18986 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18988 | hp1 | a0001 | c0001 | t0028 | g0271 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0095 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18993 | hp2 | a0001 | c0001 | t0006 | g0258 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18995 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18997 | hp1 | a0001 | c0001 | t0029 | g0147 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18997 | hp2 | a0001 | c0001 | t0004 | g0124 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18999 | hp1 | a0002 | c0002 | t0011 | g0120 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19000 | hp1 | a0001 | c0001 | t0004 | g0235 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19003 | hp1 | a0001 | c0001 | t0005 | g0031 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19003 | hp2 | a0001 | c0006 | t0010 | g0264 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19004 | hp1 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19004 | hp2 | a0001 | c0001 | t0026 | g0082 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19010 | hp1 | a0001 | c0001 | t0015 | g0053 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19011 | hp1 | a0001 | c0001 | t0005 | g0083 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19012 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19030 | hp1 | a0001 | c0001 | t0019 | g0162 | AFR | LWK | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | LWK | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0308 | AFR | LWK | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19043 | hp2 | a0001 | c0001 | t0007 | g0205 | AFR | LWK | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19054 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19058 | hp2 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19060 | hp1 | a0001 | c0001 | t0003 | g0098 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19066 | hp2 | a0001 | c0001 | t0004 | g0028 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19068 | hp2 | a0001 | c0001 | t0005 | g0148 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19072 | hp1 | a0002 | c0004 | t0016 | g0255 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19072 | hp2 | a0002 | c0002 | t0002 | g0119 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19074 | hp1 | a0001 | c0001 | t0005 | g0236 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19081 | hp1 | a0002 | c0002 | t0007 | g0247 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19081 | hp2 | a0001 | c0001 | t0015 | g0154 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19082 | hp1 | a0002 | c0002 | t0007 | g0295 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19082 | hp2 | a0001 | c0001 | t0004 | g0111 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19083 | hp1 | a0001 | c0001 | t0005 | g0175 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0096 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19084 | hp2 | a0001 | c0001 | t0006 | g0149 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19085 | hp1 | a0001 | c0001 | t0015 | g0005 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0300 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19088 | hp1 | a0011 | c0018 | t0002 | g0001 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19089 | hp1 | a0001 | c0001 | t0005 | g0062 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19089 | hp2 | a0001 | c0001 | t0042 | g0088 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19090 | hp1 | a0001 | c0001 | t0005 | g0075 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19240 | hp1 | a0001 | c0001 | t0022 | g0287 | AFR | YRI | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA19240 | hp2 | a0003 | c0003 | t0024 | g0197 | AFR | YRI | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA20129 | hp1 | a0001 | c0001 | t0005 | g0012 | AFR | ASW | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA20129 | hp2 | a0001 | c0001 | t0035 | g0166 | AFR | ASW | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0171 | EUR | TSI | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA20752 | hp2 | a0001 | c0001 | t0006 | g0217 | EUR | TSI | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA20805 | hp1 | a0002 | c0002 | t0009 | g0048 | EUR | TSI | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0143 | EUR | TSI | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA20905 | hp1 | a0001 | c0001 | t0037 | g0145 | SAS | GIH | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA20905 | hp2 | a0001 | c0001 | t0011 | g0256 | SAS | GIH | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02109 | hp1 | a0001 | c0001 | t0014 | g0003 | AFR | ACB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02109 | hp2 | a0001 | c0001 | t0007 | g0193 | AFR | ACB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0228 | AFR | ACB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02559 | hp1 | a0004 | c0011 | t0002 | g0122 | AFR | ACB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG02559 | hp2 | a0001 | c0001 | t0004 | g0046 | AFR | ACB | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG03471 | hp1 | a0002 | c0002 | t0032 | g0021 | AFR | MSL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG03471 | hp2 | a0002 | c0002 | t0007 | g0134 | AFR | MSL | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG06807 | hp1 | a0002 | c0004 | t0010 | g0283 | AFR | USA | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | USA | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA20300 | hp1 | a0001 | c0001 | t0018 | g0130 | AFR | USA | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA20300 | hp2 | a0001 | c0009 | t0020 | g0110 | AFR | USA | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA21309 | hp1 | a0001 | c0001 | t0007 | g0026 | AFR | LWK | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| NA21309 | hp2 | a0001 | c0001 | t0006 | g0180 | AFR | LWK | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0136 | REF | REF | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0229 | REF | REF | FAM124A_chr13_51217398_51289239 | FAM124A | chr13 | 51217398 | 51289239 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:51251545 | C | A | 1 | a0008 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.178C>A | p.Pro60Thr | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/4 | 282/4728 | 178/1641 | 60/546 | chr13 | 51251545 | |||
| chr13:51251614 | G | A | 1 | a0006 | 1 | HG00140.hp2 | missense_variant | MODERATE | c.247G>A | p.Glu83Lys | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/4 | 351/4728 | 247/1641 | 83/546 | chr13 | 51251614 | |||
| chr13:51251656 | G | A | 1 | a0005 | 2 | NA18961.hp2 NA18969.hp2 |
missense_variant | MODERATE | c.289G>A | p.Ala97Thr | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/4 | 393/4728 | 289/1641 | 97/546 | chr13 | 51251656 | |||
| chr13:51251903 | G | T | 1 | a0008 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.536G>T | p.Arg179Leu | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/4 | 640/4728 | 536/1641 | 179/546 | chr13 | 51251903 | |||
| chr13:51251908 | G | C | 2 | a0002 a0009 |
44 | HG00140.hp1 HG00323.hp2 HG01074.hp2 others(41): Show |
missense_variant | MODERATE | c.541G>C | p.Asp181His | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/4 | 645/4728 | 541/1641 | 181/546 | chr13 | 51251908 | |||
| chr13:51280514 | G | A | 1 | a0010 | 1 | HG03579.hp2 | missense_variant | MODERATE | c.899G>A | p.Arg300His | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 1003/4728 | 899/1641 | 300/546 | chr13 | 51280514 | |||
| chr13:51280532 | C | T | 1 | a0011 | 1 | NA19088.hp1 | missense_variant | MODERATE | c.917C>T | p.Pro306Leu | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 1021/4728 | 917/1641 | 306/546 | chr13 | 51280532 | |||
| chr13:51280648 | G | A | 1 | a0007 | 1 | HG01175.hp2 | missense_variant | MODERATE | c.1033G>A | p.Gly345Arg | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 1137/4728 | 1033/1641 | 345/546 | chr13 | 51280648 | |||
| chr13:51280907 | A | G | 2 | a0003 a0009 |
13 | HG01192.hp2 HG01884.hp1 HG01975.hp1 others(10): Show |
missense_variant | MODERATE | c.1292A>G | p.Tyr431Cys | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 1396/4728 | 1292/1641 | 431/546 | chr13 | 51280907 | |||
| chr13:51280978 | G | T | 1 | a0004 | 7 | HG01891.hp1 HG02559.hp1 HG02572.hp2 others(4): Show |
missense_variant | MODERATE | c.1363G>T | p.Ala455Ser | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 1467/4728 | 1363/1641 | 455/546 | chr13 | 51280978 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:51251598 | G | A | 3 | a0001c0007 a0004c0011 a0008c0010 |
5 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(2): Show |
synonymous_variant | LOW | c.231G>A | p.Pro77Pro | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/4 | 335/4728 | 231/1641 | 77/546 | chr13 | 51251598 | |||
| chr13:51280503 | C | T | 2 | a0001c0009 a0008c0010 |
3 | HG01884.hp2 HG03209.hp2 NA20300.hp2 |
synonymous_variant | LOW | c.888C>T | p.Ser296Ser | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 992/4728 | 888/1641 | 296/546 | chr13 | 51280503 | |||
| chr13:51280815 | C | T | 1 | a0001c0017 | 1 | HG02647.hp1 | synonymous_variant | LOW | c.1200C>T | p.Leu400Leu | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 1304/4728 | 1200/1641 | 400/546 | chr13 | 51280815 | |||
| chr13:51280824 | C | T | 1 | a0010c0014 | 1 | HG03579.hp2 | synonymous_variant | LOW | c.1209C>T | p.Ile403Ile | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 1313/4728 | 1209/1641 | 403/546 | chr13 | 51280824 | |||
| chr13:51280950 | C | T | 1 | a0001c0016 | 1 | HG00408.hp2 | synonymous_variant | LOW | c.1335C>T | p.Leu445Leu | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 1439/4728 | 1335/1641 | 445/546 | chr13 | 51280950 | |||
| chr13:51280956 | C | T | 2 | a0001c0006 a0002c0004 |
11 | HG00423.hp1 HG02132.hp2 HG02280.hp1 others(8): Show |
synonymous_variant | LOW | c.1341C>T | p.Ser447Ser | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 1445/4728 | 1341/1641 | 447/546 | chr13 | 51280956 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:51222416 | C | T | 1 | a0001c0001t0044 | 1 | NA18612.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-86C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/4 | chr13 | 51222416 | |||||||
| chr13:51281343 | A | G | 1 | a0001c0001t0043 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*87A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 87 | chr13 | 51281343 | ||||||
| chr13:51281403 | T | TG | 6 | a0001c0001t0006 a0001c0001t0011 a0001c0001t0028 others(3): Show |
26 | HG00140.hp2 HG00544.hp1 HG01069.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*153dupG | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 154 | INFO_REALIGN_3_PRIME | chr13 | 51281403 | |||||
| chr13:51281570 | AAAG | A | 7 | a0001c0001t0007 a0001c0001t0009 a0001c0001t0030 others(4): Show |
28 | HG00323.hp2 HG00738.hp2 HG01070.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*317_*319delGAA | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 317 | INFO_REALIGN_3_PRIME | chr13 | 51281570 | |||||
| chr13:51281812 | G | T | 1 | a0004c0005t0027 | 2 | HG03209.hp1 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*556G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 556 | chr13 | 51281812 | ||||||
| chr13:51281871 | T | G | 3 | a0001c0009t0020 a0001c0009t0033 a0008c0010t0020 |
3 | HG01884.hp2 HG03209.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*615T>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 615 | chr13 | 51281871 | ||||||
| chr13:51281874 | A | C | 11 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0015 others(8): Show |
67 | HG00408.hp1 HG00597.hp1 HG00621.hp2 others(64): Show |
3_prime_UTR_variant | MODIFIER | c.*618A>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 618 | chr13 | 51281874 | ||||||
| chr13:51282167 | C | T | 1 | a0002c0002t0032 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*911C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 911 | chr13 | 51282167 | ||||||
| chr13:51282197 | G | A | 1 | a0001c0001t0025 | 2 | NA18954.hp2 NA18956.hp2 |
3_prime_UTR_variant | MODIFIER | c.*941G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 941 | chr13 | 51282197 | ||||||
| chr13:51282263 | A | T | 1 | a0001c0001t0042 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1007A>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 1007 | chr13 | 51282263 | ||||||
| chr13:51282303 | C | T | 1 | a0002c0002t0040 | 1 | NA18951.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1047C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 1047 | chr13 | 51282303 | ||||||
| chr13:51282304 | G | A | 1 | a0001c0009t0033 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1048G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 1048 | chr13 | 51282304 | ||||||
| chr13:51282323 | G | A | 3 | a0001c0009t0020 a0001c0009t0033 a0008c0010t0020 |
3 | HG01884.hp2 HG03209.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1067G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 1067 | chr13 | 51282323 | ||||||
| chr13:51282349 | T | G | 1 | a0001c0001t0021 | 2 | HG01168.hp1 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1093T>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 1093 | chr13 | 51282349 | ||||||
| chr13:51282711 | C | G | 2 | a0001c0001t0012 a0001c0001t0014 |
11 | HG02109.hp1 HG02145.hp1 HG02257.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1455C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 1455 | chr13 | 51282711 | ||||||
| chr13:51282954 | C | CTT | 40 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0006 others(37): Show |
145 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(142): Show |
3_prime_UTR_variant | MODIFIER | c.*1699_*1700dupTT | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 1701 | INFO_REALIGN_3_PRIME | chr13 | 51282954 | |||||
| chr13:51283045 | A | C | 2 | a0003c0003t0024 a0003c0003t0039 |
3 | HG02896.hp1 HG02897.hp2 NA19240.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1789A>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 1789 | chr13 | 51283045 | ||||||
| chr13:51283065 | G | A | 1 | a0001c0001t0034 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1809G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 1809 | chr13 | 51283065 | ||||||
| chr13:51283098 | A | G | 6 | a0001c0001t0012 a0001c0001t0014 a0001c0001t0018 others(3): Show |
17 | HG01243.hp1 HG02109.hp1 HG02145.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1842A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 1842 | chr13 | 51283098 | ||||||
| chr13:51283336 | C | T | 1 | a0001c0001t0037 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2080C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 2080 | chr13 | 51283336 | ||||||
| chr13:51283446 | C | T | 1 | a0001c0001t0038 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2190C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 2190 | chr13 | 51283446 | ||||||
| chr13:51283511 | A | G | 15 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0026 others(12): Show |
76 | HG00408.hp1 HG00597.hp1 HG00621.hp2 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*2255A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 2255 | chr13 | 51283511 | ||||||
| chr13:51283589 | C | G | 4 | a0003c0003t0008 a0003c0003t0024 a0003c0003t0039 others(1): Show |
13 | HG01192.hp2 HG01884.hp1 HG01975.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2333C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 2333 | chr13 | 51283589 | ||||||
| chr13:51283705 | G | T | 3 | a0001c0009t0020 a0001c0009t0033 a0008c0010t0020 |
3 | HG01884.hp2 HG03209.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2449G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 2449 | chr13 | 51283705 | ||||||
| chr13:51283767 | C | CA | 17 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0014 others(14): Show |
141 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*2539dupA | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 2540 | INFO_REALIGN_3_PRIME | chr13 | 51283767 | |||||
| chr13:51283767 | C | CAA | 22 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(19): Show |
84 | HG00140.hp2 HG00544.hp1 HG00621.hp1 others(81): Show |
3_prime_UTR_variant | MODIFIER | c.*2538_*2539dupAA | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 2540 | INFO_REALIGN_3_PRIME | chr13 | 51283767 | |||||
| chr13:51283767 | C | CAAA | 8 | a0001c0001t0009 a0001c0001t0011 a0001c0001t0022 others(5): Show |
21 | HG01069.hp2 HG01167.hp2 HG01169.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2537_*2539dupAAA | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 2540 | INFO_REALIGN_3_PRIME | chr13 | 51283767 | |||||
| chr13:51283767 | C | CAAAAAAA others(3): Show |
2 | a0001c0009t0020 a0008c0010t0020 |
2 | HG01884.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2530_*2539dupAAAA others(6): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 2540 | INFO_REALIGN_3_PRIME | chr13 | 51283767 | |||||
| chr13:51283767 | CAAAAAAA others(2): Show |
C | 3 | a0003c0003t0008 a0003c0003t0024 a0009c0013t0008 |
12 | HG01192.hp2 HG01884.hp1 HG01975.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2531_*2539delAAAA others(5): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 2531 | INFO_REALIGN_3_PRIME | chr13 | 51283767 | |||||
| chr13:51283767 | CAAAAAAA others(3): Show |
C | 1 | a0001c0009t0033 | 1 | HG03209.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2530_*2539delAAAA others(6): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 2530 | INFO_REALIGN_3_PRIME | chr13 | 51283767 | |||||
| chr13:51283887 | A | G | 1 | a0001c0001t0036 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2631A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 2631 | chr13 | 51283887 | ||||||
| chr13:51284030 | A | C | 1 | a0001c0001t0028 | 1 | NA18988.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2774A>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 2774 | chr13 | 51284030 | ||||||
| chr13:51284171 | T | C | 2 | a0001c0001t0030 a0001c0001t0035 |
2 | HG02258.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2915T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 2915 | chr13 | 51284171 | ||||||
| chr13:51284208 | T | C | 4 | a0001c0006t0010 a0001c0006t0016 a0002c0004t0010 others(1): Show |
11 | HG00423.hp1 HG02132.hp2 HG02280.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2952T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 4/4 | 2952 | chr13 | 51284208 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:51222707 | T | C | 209 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(206): Show |
240 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.68+138T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51222707 | |||||||
| chr13:51222838 | C | G | 209 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(206): Show |
240 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.68+269C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51222838 | |||||||
| chr13:51222958 | A | G | 211 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(208): Show |
242 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.68+389A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51222958 | |||||||
| chr13:51223018 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.68+449C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51223018 | |||||||
| chr13:51223195 | CT | C | 196 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(193): Show |
226 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.68+639delT | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 51223195 | ||||||
| chr13:51223257 | G | C | 36 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0022 others(33): Show |
44 | HG00438.hp1 HG00738.hp2 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.68+688G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51223257 | |||||||
| chr13:51223296 | C | A | 1 | a0008c0010t0020g0073 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.68+727C>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51223296 | |||||||
| chr13:51223301 | G | C | 225 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(222): Show |
257 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.68+732G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51223301 | |||||||
| chr13:51223344 | G | C | 1 | a0001c0001t0003g0074 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.68+775G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51223344 | |||||||
| chr13:51223414 | C | G | 7 | a0001c0001t0001g0306 a0001c0001t0002g0308 a0001c0001t0002g0312 others(4): Show |
7 | HG01243.hp2 HG02451.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.68+845C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51223414 | |||||||
| chr13:51223597 | C | G | 1 | a0001c0001t0001g0220 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.68+1028C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51223597 | |||||||
| chr13:51223684 | C | T | 2 | a0001c0001t0003g0314 a0001c0006t0016g0313 |
2 | HG02280.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.68+1115C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51223684 | |||||||
| chr13:51223829 | C | CTG | 198 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(195): Show |
228 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.68+1260_68+1261ins others(2): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51223829 | |||||||
| chr13:51223979 | T | C | 3 | a0001c0001t0005g0075 a0001c0001t0005g0076 a0001c0001t0005g0077 |
3 | HG00597.hp1 NA18941.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.68+1410T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51223979 | |||||||
| chr13:51224079 | G | C | 3 | a0001c0001t0002g0222 a0001c0001t0004g0046 a0001c0001t0004g0221 |
4 | HG02055.hp1 HG02559.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.68+1510G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51224079 | |||||||
| chr13:51224194 | T | C | 211 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(208): Show |
242 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.68+1625T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51224194 | |||||||
| chr13:51224230 | T | A | 198 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(195): Show |
228 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.68+1661T>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51224230 | |||||||
| chr13:51224331 | T | C | 198 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(195): Show |
228 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(225): Show |
intron_variant | MODIFIER | c.68+1762T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51224331 | |||||||
| chr13:51224339 | C | T | 1 | a0001c0001t0001g0219 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.68+1770C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51224339 | |||||||
| chr13:51224433 | T | G | 68 | a0001c0001t0001g0014 a0001c0001t0001g0080 a0001c0001t0001g0086 others(65): Show |
80 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.68+1864T>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51224433 | |||||||
| chr13:51224459 | A | G | 197 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(194): Show |
227 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.68+1890A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51224459 | |||||||
| chr13:51224464 | T | A | 115 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0014 others(112): Show |
135 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.68+1895T>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51224464 | |||||||
| chr13:51224465 | C | A | 115 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0014 others(112): Show |
135 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.68+1896C>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51224465 | |||||||
| chr13:51224472 | C | CA | 91 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0015 others(88): Show |
101 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.68+1912dupA | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 51224472 | ||||||
| chr13:51224802 | C | T | 1 | a0001c0001t0002g0127 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.68+2233C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51224802 | |||||||
| chr13:51224884 | C | T | 1 | a0006c0012t0006g0126 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.68+2315C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51224884 | |||||||
| chr13:51224893 | T | C | 1 | a0003c0003t0008g0129 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.68+2324T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51224893 | |||||||
| chr13:51225056 | A | C | 87 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0015 others(84): Show |
97 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.68+2487A>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51225056 | |||||||
| chr13:51225131 | T | C | 2 | a0002c0002t0001g0223 a0009c0013t0008g0224 |
2 | HG01106.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.68+2562T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51225131 | |||||||
| chr13:51225138 | T | C | 3 | a0001c0001t0007g0047 a0001c0001t0007g0205 a0001c0001t0009g0047 |
3 | HG02886.hp1 HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.68+2569T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51225138 | |||||||
| chr13:51225311 | C | T | 13 | a0001c0001t0002g0196 a0001c0001t0013g0044 a0001c0001t0017g0044 others(10): Show |
14 | HG01192.hp2 HG01884.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.68+2742C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51225311 | |||||||
| chr13:51225361 | T | C | 85 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0015 others(82): Show |
95 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.68+2792T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51225361 | |||||||
| chr13:51225444 | A | G | 3 | a0001c0001t0002g0188 a0001c0001t0002g0189 a0001c0001t0002g0190 |
3 | HG02572.hp1 HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.68+2875A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51225444 | |||||||
| chr13:51225466 | T | C | 199 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(196): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.68+2897T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51225466 | |||||||
| chr13:51225499 | C | T | 84 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0015 others(81): Show |
94 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.68+2930C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51225499 | |||||||
| chr13:51225666 | A | G | 4 | a0001c0001t0001g0218 a0001c0001t0004g0135 a0001c0001t0006g0217 others(1): Show |
4 | HG00323.hp2 HG01070.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.68+3097A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51225666 | |||||||
| chr13:51225770 | G | A | 1 | a0002c0002t0009g0225 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.68+3201G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51225770 | |||||||
| chr13:51225968 | CTTGCTTT others(6): Show |
C | 1 | a0001c0001t0004g0187 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.68+3402_68+3414del others(13): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 51225968 | ||||||
| chr13:51225968 | CTTGCTTT others(7): Show |
C | 15 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0182 others(12): Show |
17 | HG00099.hp1 HG00642.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.68+3402_68+3415del others(14): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 51225968 | ||||||
| chr13:51225968 | CTTGCTTT others(8): Show |
C | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | HG00639.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.68+3402_68+3416del others(15): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 51225968 | ||||||
| chr13:51225975 | T | G | 3 | a0001c0001t0007g0047 a0001c0001t0009g0047 a0003c0003t0008g0198 |
3 | HG02886.hp1 HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.68+3406T>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51225975 | |||||||
| chr13:51225976 | C | CT | 37 | a0001c0001t0001g0020 a0001c0001t0001g0254 a0001c0001t0001g0260 others(34): Show |
38 | HG00558.hp2 HG01106.hp1 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.68+3442dupT | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 51225976 | ||||||
| chr13:51225976 | C | CTT | 17 | a0001c0001t0001g0306 a0001c0001t0002g0251 a0001c0001t0002g0253 others(14): Show |
17 | HG00140.hp1 HG00323.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.68+3441_68+3442dup others(2): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 51225976 | ||||||
| chr13:51225976 | C | CTTTTTTT others(4): Show |
1 | a0001c0006t0016g0313 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.68+3432_68+3442dup others(11): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 51225976 | ||||||
| chr13:51225976 | CT | C | 17 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0051 others(14): Show |
18 | HG00733.hp1 HG01168.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.68+3442delT | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 51225976 | ||||||
| chr13:51225976 | CTTTTTT | C | 7 | a0001c0001t0001g0024 a0001c0001t0002g0070 a0001c0001t0003g0036 others(4): Show |
7 | HG00140.hp2 NA18942.hp1 NA18950.hp2 others(4): Show |
intron_variant | MODIFIER | c.68+3437_68+3442del others(6): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 51225976 | ||||||
| chr13:51225976 | CTTTTTTT | C | 90 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0014 others(87): Show |
106 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(103): Show |
intron_variant | MODIFIER | c.68+3436_68+3442del others(7): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 51225976 | ||||||
| chr13:51225976 | CTTTTTTT others(1): Show |
C | 8 | a0001c0001t0001g0022 a0001c0001t0002g0002 a0001c0001t0002g0011 others(5): Show |
8 | HG01975.hp2 HG02165.hp2 NA18954.hp2 others(5): Show |
intron_variant | MODIFIER | c.68+3435_68+3442del others(8): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 51225976 | ||||||
| chr13:51225976 | CTTTTTTT others(3): Show |
C | 62 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0037 others(59): Show |
68 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.68+3433_68+3442del others(10): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 51225976 | ||||||
| chr13:51225976 | CTTTTTTT others(4): Show |
C | 11 | a0001c0001t0001g0016 a0001c0001t0001g0132 a0001c0001t0001g0202 others(8): Show |
11 | HG02109.hp2 HG02970.hp1 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.68+3432_68+3442del others(11): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 51225976 | ||||||
| chr13:51225976 | CTTTTTTT others(5): Show |
C | 13 | a0001c0001t0002g0141 a0001c0001t0002g0196 a0001c0001t0013g0044 others(10): Show |
14 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.68+3431_68+3442del others(12): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 51225976 | ||||||
| chr13:51225976 | CTTTTTTT others(6): Show |
C | 15 | a0001c0001t0001g0207 a0001c0001t0001g0209 a0001c0001t0001g0210 others(12): Show |
16 | HG00280.hp1 HG00733.hp2 HG00735.hp1 others(13): Show |
intron_variant | MODIFIER | c.68+3430_68+3442del others(13): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 51225976 | ||||||
| chr13:51225976 | CTTTTTTT others(7): Show |
C | 3 | a0001c0001t0001g0218 a0002c0002t0031g0216 a0003c0003t0008g0206 |
3 | HG00323.hp2 HG01070.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.68+3429_68+3442del others(14): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 51225976 | ||||||
| chr13:51225976 | CTTTTTTT others(9): Show |
C | 7 | a0001c0001t0001g0275 a0001c0001t0002g0273 a0001c0001t0004g0235 others(4): Show |
7 | HG00544.hp1 HG00558.hp1 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.68+3427_68+3442del others(16): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 51225976 | ||||||
| chr13:51225976 | CTTTTTTT others(10): Show |
C | 1 | a0001c0001t0005g0236 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.68+3426_68+3442del others(17): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 51225976 | ||||||
| chr13:51225985 | T | C | 1 | a0001c0001t0004g0187 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.68+3416T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51225985 | |||||||
| chr13:51225986 | T | C | 15 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0182 others(12): Show |
17 | HG00099.hp1 HG00642.hp2 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.68+3417T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51225986 | |||||||
| chr13:51225987 | T | C | 2 | a0001c0001t0001g0178 a0001c0001t0001g0179 |
2 | HG00639.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.68+3418T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51225987 | |||||||
| chr13:51226061 | T | C | 2 | a0001c0001t0007g0205 a0003c0003t0008g0129 |
2 | HG02965.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.68+3492T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51226061 | |||||||
| chr13:51226198 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.68+3629A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51226198 | |||||||
| chr13:51226318 | A | G | 2 | a0001c0001t0001g0133 a0002c0002t0007g0134 |
2 | HG02257.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.68+3749A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51226318 | |||||||
| chr13:51226419 | G | T | 1 | a0002c0002t0040g0302 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.68+3850G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51226419 | |||||||
| chr13:51226912 | A | G | 122 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0014 others(119): Show |
143 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(140): Show |
intron_variant | MODIFIER | c.68+4343A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51226912 | |||||||
| chr13:51226921 | G | T | 105 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0014 others(102): Show |
125 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.68+4352G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51226921 | |||||||
| chr13:51226980 | G | A | 1 | a0001c0001t0007g0205 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.69-4368G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51226980 | |||||||
| chr13:51227222 | C | G | 229 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(226): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.69-4126C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51227222 | |||||||
| chr13:51227280 | C | T | 1 | a0001c0001t0001g0219 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.69-4068C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51227280 | |||||||
| chr13:51227569 | G | A | 1 | a0001c0001t0004g0226 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.69-3779G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51227569 | |||||||
| chr13:51227885 | T | G | 7 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0139 others(4): Show |
9 | HG02523.hp2 NA18951.hp2 NA18966.hp1 others(6): Show |
intron_variant | MODIFIER | c.69-3463T>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51227885 | |||||||
| chr13:51227965 | A | G | 184 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(181): Show |
213 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.69-3383A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51227965 | |||||||
| chr13:51228222 | GTAT | G | 2 | a0001c0001t0001g0298 a0001c0001t0021g0054 |
3 | HG01167.hp1 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.69-3124_69-3122del others(3): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 51228222 | ||||||
| chr13:51228271 | A | T | 1 | a0003c0003t0008g0129 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.69-3077A>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51228271 | |||||||
| chr13:51228311 | C | G | 70 | a0001c0001t0001g0080 a0001c0001t0001g0086 a0001c0001t0001g0094 others(67): Show |
80 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.69-3037C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51228311 | |||||||
| chr13:51228425 | G | A | 1 | a0002c0002t0001g0231 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.69-2923G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51228425 | |||||||
| chr13:51228461 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.69-2887C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51228461 | |||||||
| chr13:51228668 | G | T | 1 | a0004c0011t0002g0122 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.69-2680G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51228668 | |||||||
| chr13:51228769 | AG | A | 4 | a0001c0001t0015g0053 a0001c0001t0015g0297 a0001c0001t0025g0296 others(1): Show |
4 | HG02074.hp2 NA18956.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.69-2577delG | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 51228769 | ||||||
| chr13:51229390 | G | A | 5 | a0001c0001t0003g0300 a0001c0001t0007g0047 a0001c0001t0007g0205 others(2): Show |
5 | HG01884.hp2 HG02886.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.69-1958G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51229390 | |||||||
| chr13:51229477 | T | C | 2 | a0001c0001t0003g0314 a0001c0006t0016g0313 |
2 | HG02280.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.69-1871T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51229477 | |||||||
| chr13:51229504 | T | G | 1 | a0001c0001t0004g0232 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.69-1844T>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51229504 | |||||||
| chr13:51229657 | A | C | 1 | a0002c0002t0007g0295 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.69-1691A>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51229657 | |||||||
| chr13:51229929 | T | C | 14 | a0001c0001t0001g0080 a0001c0001t0001g0086 a0001c0001t0002g0011 others(11): Show |
17 | HG00597.hp1 HG00621.hp1 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.69-1419T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51229929 | |||||||
| chr13:51230075 | T | TTA | 70 | a0001c0001t0001g0080 a0001c0001t0001g0086 a0001c0001t0001g0094 others(67): Show |
80 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.69-1259_69-1258dup others(2): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 51230075 | ||||||
| chr13:51230075 | T | TTATATAT others(1): Show |
3 | a0001c0001t0001g0133 a0001c0001t0004g0232 a0002c0002t0007g0134 |
3 | HG02257.hp2 HG03471.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.69-1265_69-1258dup others(8): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 51230075 | ||||||
| chr13:51230075 | T | TTATATAT others(3): Show |
1 | a0004c0005t0023g0233 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.69-1267_69-1258dup others(10): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 51230075 | ||||||
| chr13:51230075 | T | TTATATAT others(5): Show |
1 | a0003c0003t0008g0206 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.69-1269_69-1258dup others(12): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr13 | 51230075 | ||||||
| chr13:51230077 | A | T | 13 | a0001c0001t0002g0196 a0001c0001t0013g0044 a0001c0001t0017g0044 others(10): Show |
14 | HG01192.hp2 HG01884.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.69-1271A>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51230077 | |||||||
| chr13:51230083 | A | T | 1 | a0001c0001t0014g0294 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.69-1265A>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51230083 | |||||||
| chr13:51230108 | T | G | 1 | a0001c0001t0001g0133 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.69-1240T>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51230108 | |||||||
| chr13:51230131 | G | C | 1 | a0001c0001t0042g0088 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.69-1217G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51230131 | |||||||
| chr13:51230138 | T | C | 3 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0002g0303 |
3 | HG00099.hp1 HG01081.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.69-1210T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51230138 | |||||||
| chr13:51230315 | T | A | 3 | a0001c0001t0001g0133 a0002c0002t0001g0231 a0002c0002t0004g0234 |
3 | HG02257.hp2 HG02922.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.69-1033T>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51230315 | |||||||
| chr13:51230460 | A | T | 1 | a0001c0001t0038g0293 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.69-888A>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51230460 | |||||||
| chr13:51230496 | C | G | 2 | a0001c0001t0001g0292 a0001c0001t0002g0291 |
2 | HG03491.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.69-852C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51230496 | |||||||
| chr13:51230529 | G | A | 70 | a0001c0001t0001g0080 a0001c0001t0001g0086 a0001c0001t0001g0094 others(67): Show |
80 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.69-819G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51230529 | |||||||
| chr13:51230569 | C | T | 1 | a0001c0001t0002g0177 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.69-779C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51230569 | |||||||
| chr13:51230707 | A | G | 6 | a0001c0001t0001g0133 a0001c0001t0004g0232 a0001c0009t0033g0213 others(3): Show |
6 | HG02257.hp2 HG02572.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.69-641A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51230707 | |||||||
| chr13:51230855 | G | C | 5 | a0001c0001t0001g0133 a0001c0001t0004g0232 a0002c0002t0007g0134 others(2): Show |
5 | HG02257.hp2 HG02572.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.69-493G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51230855 | |||||||
| chr13:51230889 | G | A | 68 | a0001c0001t0001g0080 a0001c0001t0001g0086 a0001c0001t0001g0094 others(65): Show |
78 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.69-459G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51230889 | |||||||
| chr13:51231192 | C | G | 2 | a0002c0002t0001g0223 a0009c0013t0008g0224 |
2 | HG01106.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.69-156C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51231192 | |||||||
| chr13:51231196 | A | G | 5 | a0001c0001t0001g0043 a0001c0001t0001g0174 a0001c0001t0002g0043 others(2): Show |
5 | HG02129.hp2 HG03927.hp2 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.69-152A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51231196 | |||||||
| chr13:51231234 | T | C | 1 | a0001c0001t0001g0306 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.69-114T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 1/3 | chr13 | 51231234 | |||||||
| chr13:51231666 | C | T | 16 | a0001c0001t0022g0287 a0001c0001t0023g0288 a0002c0002t0001g0280 others(13): Show |
18 | HG01074.hp2 HG01109.hp2 HG01255.hp2 others(15): Show |
intron_variant | MODIFIER | c.100+287C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51231666 | |||||||
| chr13:51231945 | T | C | 1 | a0001c0001t0004g0187 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.100+566T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51231945 | |||||||
| chr13:51232173 | A | G | 1 | a0002c0002t0002g0299 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.100+794A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51232173 | |||||||
| chr13:51232254 | T | C | 1 | a0001c0001t0003g0089 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.100+875T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51232254 | |||||||
| chr13:51232304 | C | CTTAT | 161 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(158): Show |
186 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(183): Show |
intron_variant | MODIFIER | c.100+928_100+931dup others(4): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 51232304 | ||||||
| chr13:51232328 | T | C | 1 | a0001c0001t0001g0133 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.100+949T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51232328 | |||||||
| chr13:51232378 | T | C | 1 | a0001c0001t0001g0178 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.100+999T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51232378 | |||||||
| chr13:51232458 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.100+1079A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51232458 | |||||||
| chr13:51232562 | A | G | 1 | a0001c0001t0001g0178 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.100+1183A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51232562 | |||||||
| chr13:51232744 | C | T | 1 | a0001c0001t0003g0314 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.100+1365C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51232744 | |||||||
| chr13:51232795 | A | G | 1 | a0002c0002t0009g0230 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.100+1416A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51232795 | |||||||
| chr13:51232830 | A | G | 1 | a0001c0001t0001g0292 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.100+1451A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51232830 | |||||||
| chr13:51232861 | C | T | 2 | a0001c0001t0001g0125 a0001c0001t0001g0172 |
2 | HG00544.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.100+1482C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51232861 | |||||||
| chr13:51232957 | T | C | 87 | a0001c0001t0001g0005 a0001c0001t0001g0043 a0001c0001t0001g0080 others(84): Show |
100 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.100+1578T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51232957 | |||||||
| chr13:51233052 | G | A | 154 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(151): Show |
179 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(176): Show |
intron_variant | MODIFIER | c.100+1673G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51233052 | |||||||
| chr13:51233109 | G | A | 1 | a0001c0001t0002g0068 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.100+1730G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51233109 | |||||||
| chr13:51233163 | G | A | 158 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(155): Show |
183 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.100+1784G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51233163 | |||||||
| chr13:51233262 | G | A | 7 | a0001c0001t0001g0028 a0001c0001t0001g0072 a0001c0001t0002g0049 others(4): Show |
8 | HG00597.hp2 NA18945.hp2 NA18961.hp1 others(5): Show |
intron_variant | MODIFIER | c.100+1883G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51233262 | |||||||
| chr13:51233389 | T | C | 5 | a0001c0001t0001g0133 a0001c0001t0004g0232 a0002c0002t0007g0134 others(2): Show |
5 | HG02257.hp2 HG02572.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.100+2010T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51233389 | |||||||
| chr13:51233493 | A | T | 1 | a0001c0001t0005g0087 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.100+2114A>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51233493 | |||||||
| chr13:51233652 | C | T | 66 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0015 others(63): Show |
78 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.100+2273C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51233652 | |||||||
| chr13:51233912 | A | G | 155 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(152): Show |
180 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(177): Show |
intron_variant | MODIFIER | c.100+2533A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51233912 | |||||||
| chr13:51233935 | T | C | 350 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(347): Show |
402 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(399): Show |
intron_variant | MODIFIER | c.100+2556T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51233935 | |||||||
| chr13:51234008 | G | A | 2 | a0001c0001t0007g0047 a0001c0001t0009g0047 |
2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.100+2629G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51234008 | |||||||
| chr13:51234076 | C | G | 1 | a0002c0004t0010g0277 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.100+2697C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51234076 | |||||||
| chr13:51234106 | G | A | 156 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0010 others(153): Show |
181 | HG00099.hp2 HG00140.hp2 HG00438.hp1 others(178): Show |
intron_variant | MODIFIER | c.100+2727G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51234106 | |||||||
| chr13:51234224 | T | C | 92 | a0001c0001t0001g0005 a0001c0001t0001g0043 a0001c0001t0001g0080 others(89): Show |
105 | HG00140.hp2 HG00408.hp1 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.100+2845T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51234224 | |||||||
| chr13:51234488 | T | C | 103 | a0001c0001t0001g0005 a0001c0001t0001g0043 a0001c0001t0001g0080 others(100): Show |
117 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.100+3109T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51234488 | |||||||
| chr13:51234501 | G | A | 103 | a0001c0001t0001g0005 a0001c0001t0001g0043 a0001c0001t0001g0080 others(100): Show |
117 | HG00140.hp2 HG00597.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.100+3122G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51234501 | |||||||
| chr13:51234674 | A | T | 1 | a0002c0002t0011g0120 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.100+3295A>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51234674 | |||||||
| chr13:51234751 | G | C | 1 | a0002c0002t0011g0120 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.100+3372G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51234751 | |||||||
| chr13:51234780 | T | C | 37 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0023 others(34): Show |
46 | HG00438.hp1 HG00438.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.100+3401T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51234780 | |||||||
| chr13:51234846 | A | G | 287 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(284): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(324): Show |
intron_variant | MODIFIER | c.100+3467A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51234846 | |||||||
| chr13:51235065 | G | A | 1 | a0001c0001t0003g0090 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.100+3686G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51235065 | |||||||
| chr13:51235090 | A | AT | 70 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0086 others(67): Show |
75 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(72): Show |
intron_variant | MODIFIER | c.100+3717dupT | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 51235090 | ||||||
| chr13:51235110 | G | T | 1 | a0001c0001t0003g0116 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.100+3731G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51235110 | |||||||
| chr13:51235131 | C | T | 1 | a0001c0001t0006g0149 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.100+3752C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51235131 | |||||||
| chr13:51235303 | T | C | 4 | a0001c0001t0001g0121 a0001c0001t0002g0131 a0001c0001t0003g0314 others(1): Show |
4 | HG02258.hp1 HG02615.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+3924T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51235303 | |||||||
| chr13:51235322 | T | C | 1 | a0001c0001t0004g0091 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.100+3943T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51235322 | |||||||
| chr13:51235346 | ATTAT | A | 6 | a0001c0001t0001g0306 a0001c0001t0002g0241 a0001c0001t0002g0308 others(3): Show |
6 | HG01243.hp2 HG02451.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.100+3972_100+3975d others(6): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 51235346 | ||||||
| chr13:51235389 | G | GA | 7 | a0001c0001t0012g0093 a0001c0001t0030g0117 a0001c0006t0016g0313 others(4): Show |
7 | HG01891.hp2 HG02258.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.100+4017dupA | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 51235389 | ||||||
| chr13:51235420 | C | T | 32 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0023 others(29): Show |
41 | HG00438.hp1 HG00438.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.100+4041C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51235420 | |||||||
| chr13:51235441 | TTGAA | T | 4 | a0001c0001t0001g0121 a0001c0001t0002g0131 a0001c0001t0003g0314 others(1): Show |
4 | HG02258.hp1 HG02615.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.100+4064_100+4067d others(6): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 51235441 | ||||||
| chr13:51235516 | A | G | 2 | a0001c0001t0001g0132 a0001c0001t0018g0130 |
2 | HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.100+4137A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51235516 | |||||||
| chr13:51235598 | TA | T | 72 | a0001c0001t0001g0005 a0001c0001t0001g0043 a0001c0001t0001g0102 others(69): Show |
81 | HG00140.hp2 HG00408.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.100+4220delA | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51235598 | |||||||
| chr13:51235788 | A | T | 1 | a0001c0001t0004g0232 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.100+4409A>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51235788 | |||||||
| chr13:51235821 | G | T | 1 | a0001c0001t0001g0171 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.100+4442G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51235821 | |||||||
| chr13:51235929 | A | T | 1 | a0001c0001t0001g0272 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.100+4550A>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51235929 | |||||||
| chr13:51236201 | G | A | 2 | a0002c0002t0001g0280 a0004c0005t0013g0281 |
2 | HG02965.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.100+4822G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51236201 | |||||||
| chr13:51236376 | T | G | 36 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0023 others(33): Show |
45 | HG00438.hp1 HG00438.hp2 HG00738.hp2 others(42): Show |
intron_variant | MODIFIER | c.100+4997T>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51236376 | |||||||
| chr13:51236526 | A | C | 77 | a0001c0001t0001g0005 a0001c0001t0001g0043 a0001c0001t0001g0094 others(74): Show |
87 | HG00140.hp2 HG00408.hp1 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.100+5147A>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51236526 | |||||||
| chr13:51236580 | C | T | 72 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0015 others(69): Show |
84 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.100+5201C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51236580 | |||||||
| chr13:51236671 | G | T | 1 | a0001c0001t0007g0205 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.100+5292G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51236671 | |||||||
| chr13:51236817 | A | G | 33 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0023 others(30): Show |
42 | HG00438.hp1 HG00438.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.100+5438A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51236817 | |||||||
| chr13:51236839 | TAG | T | 37 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0037 others(34): Show |
40 | HG00099.hp2 HG00639.hp2 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.100+5463_100+5464d others(4): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 51236839 | ||||||
| chr13:51237015 | C | A | 13 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0032 others(10): Show |
17 | HG02074.hp1 NA18941.hp2 NA18965.hp2 others(14): Show |
intron_variant | MODIFIER | c.100+5636C>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51237015 | |||||||
| chr13:51237115 | A | C | 1 | a0008c0010t0020g0073 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.100+5736A>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51237115 | |||||||
| chr13:51237235 | A | C | 67 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0086 others(64): Show |
71 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(68): Show |
intron_variant | MODIFIER | c.100+5856A>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51237235 | |||||||
| chr13:51237307 | T | C | 1 | a0001c0001t0004g0232 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.100+5928T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51237307 | |||||||
| chr13:51237348 | G | C | 6 | a0001c0001t0001g0204 a0001c0001t0002g0049 a0001c0001t0002g0071 others(3): Show |
7 | HG00423.hp2 HG00597.hp2 NA18945.hp2 others(4): Show |
intron_variant | MODIFIER | c.100+5969G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51237348 | |||||||
| chr13:51237364 | A | G | 64 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0086 others(61): Show |
68 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.100+5985A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51237364 | |||||||
| chr13:51237573 | G | A | 1 | a0003c0003t0008g0206 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.100+6194G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51237573 | |||||||
| chr13:51237669 | T | G | 221 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(218): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.100+6290T>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51237669 | |||||||
| chr13:51237765 | T | C | 1 | a0001c0009t0033g0213 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.100+6386T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51237765 | |||||||
| chr13:51237789 | TG | T | 44 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0086 others(41): Show |
47 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.100+6411delG | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51237789 | |||||||
| chr13:51238219 | G | A | 3 | a0001c0001t0001g0102 a0001c0001t0004g0091 a0001c0001t0004g0232 |
3 | HG02738.hp1 HG03017.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.100+6840G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51238219 | |||||||
| chr13:51238285 | CA | C | 3 | a0001c0001t0002g0131 a0001c0001t0003g0314 a0001c0001t0030g0117 |
3 | HG02258.hp1 HG02615.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.100+6907delA | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51238285 | |||||||
| chr13:51238286 | A | T | 1 | a0008c0010t0020g0073 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.100+6907A>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51238286 | |||||||
| chr13:51238396 | C | T | 1 | a0003c0003t0008g0201 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.100+7017C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51238396 | |||||||
| chr13:51238397 | G | A | 1 | a0001c0001t0001g0055 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.100+7018G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51238397 | |||||||
| chr13:51238489 | A | C | 1 | a0001c0001t0002g0158 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.100+7110A>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51238489 | |||||||
| chr13:51239000 | A | T | 13 | a0001c0001t0003g0012 a0001c0001t0003g0013 a0001c0001t0003g0032 others(10): Show |
17 | HG02074.hp1 NA18941.hp2 NA18965.hp2 others(14): Show |
intron_variant | MODIFIER | c.100+7621A>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51239000 | |||||||
| chr13:51239019 | G | A | 1 | a0004c0011t0002g0122 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.100+7640G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51239019 | |||||||
| chr13:51239059 | C | T | 1 | a0001c0001t0003g0115 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.100+7680C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51239059 | |||||||
| chr13:51239253 | A | G | 1 | a0001c0001t0005g0085 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.100+7874A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51239253 | |||||||
| chr13:51239305 | G | A | 1 | a0001c0009t0033g0213 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.100+7926G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51239305 | |||||||
| chr13:51239642 | A | G | 1 | a0004c0005t0027g0052 | 2 | HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.100+8263A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51239642 | |||||||
| chr13:51239774 | G | A | 3 | a0001c0001t0001g0023 a0001c0001t0002g0023 a0001c0001t0002g0056 |
3 | NA18940.hp1 NA18969.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.100+8395G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51239774 | |||||||
| chr13:51239778 | G | T | 1 | a0001c0001t0007g0205 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.100+8399G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51239778 | |||||||
| chr13:51239832 | GTAGA | G | 34 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0023 others(31): Show |
43 | HG00438.hp1 HG00438.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.100+8461_100+8464d others(6): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 51239832 | ||||||
| chr13:51239867 | G | A | 1 | a0001c0001t0002g0009 | 3 | HG01433.hp1 HG01952.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.100+8488G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51239867 | |||||||
| chr13:51239895 | T | C | 16 | a0001c0001t0002g0196 a0001c0001t0004g0232 a0001c0001t0013g0044 others(13): Show |
17 | HG01192.hp2 HG01884.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.100+8516T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51239895 | |||||||
| chr13:51240022 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.100+8643T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51240022 | |||||||
| chr13:51240198 | G | A | 2 | a0001c0001t0001g0254 a0002c0004t0010g0050 |
3 | NA18952.hp2 NA18960.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.100+8819G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51240198 | |||||||
| chr13:51240228 | C | T | 16 | a0001c0001t0002g0196 a0001c0001t0004g0232 a0001c0001t0013g0044 others(13): Show |
17 | HG01192.hp2 HG01884.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.100+8849C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51240228 | |||||||
| chr13:51240295 | C | T | 4 | a0001c0001t0005g0148 a0001c0001t0006g0038 a0001c0001t0006g0149 others(1): Show |
5 | NA18942.hp2 NA18959.hp2 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.100+8916C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51240295 | |||||||
| chr13:51240391 | T | G | 158 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0015 others(155): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.100+9012T>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51240391 | |||||||
| chr13:51240596 | G | T | 1 | a0004c0011t0002g0122 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.100+9217G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51240596 | |||||||
| chr13:51240605 | A | G | 14 | a0001c0001t0001g0275 a0001c0001t0001g0304 a0001c0001t0001g0305 others(11): Show |
15 | HG00544.hp1 HG00558.hp1 HG01081.hp1 others(12): Show |
intron_variant | MODIFIER | c.100+9226A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51240605 | |||||||
| chr13:51240629 | G | A | 1 | a0001c0001t0002g0303 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.100+9250G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51240629 | |||||||
| chr13:51240650 | C | T | 2 | a0002c0002t0001g0223 a0009c0013t0008g0224 |
2 | HG01106.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.100+9271C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51240650 | |||||||
| chr13:51240845 | C | T | 1 | a0001c0001t0007g0205 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.100+9466C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51240845 | |||||||
| chr13:51240917 | A | G | 5 | a0001c0001t0012g0093 a0001c0006t0016g0313 a0001c0007t0001g0030 others(2): Show |
5 | HG01891.hp2 HG02280.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.100+9538A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51240917 | |||||||
| chr13:51241143 | TA | T | 2 | a0001c0001t0001g0133 a0004c0005t0027g0052 |
3 | HG02257.hp2 HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.100+9768delA | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 51241143 | ||||||
| chr13:51241217 | A | G | 1 | a0001c0001t0030g0117 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.100+9838A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51241217 | |||||||
| chr13:51241287 | C | A | 1 | a0001c0001t0002g0181 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.100+9908C>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51241287 | |||||||
| chr13:51241303 | T | TC | 5 | a0001c0001t0012g0093 a0001c0006t0016g0313 a0001c0007t0001g0030 others(2): Show |
5 | HG01891.hp2 HG02280.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.100+9925dupC | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 51241303 | ||||||
| chr13:51241305 | A | G | 98 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(95): Show |
118 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.100+9926A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51241305 | |||||||
| chr13:51241416 | C | T | 3 | a0001c0001t0003g0112 a0001c0001t0003g0113 a0001c0001t0003g0116 |
3 | NA18970.hp2 NA18973.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.100+10037C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51241416 | |||||||
| chr13:51241702 | A | C | 1 | a0001c0001t0004g0111 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.101-9766A>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51241702 | |||||||
| chr13:51241741 | CA | C | 211 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(208): Show |
243 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.101-9714delA | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 51241741 | ||||||
| chr13:51241741 | CAA | C | 44 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0086 others(41): Show |
47 | HG00099.hp1 HG00544.hp1 HG00558.hp1 others(44): Show |
intron_variant | MODIFIER | c.101-9715_101-9714d others(4): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 51241741 | ||||||
| chr13:51241787 | G | T | 1 | a0001c0001t0007g0205 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.101-9681G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51241787 | |||||||
| chr13:51241986 | G | T | 34 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0037 others(31): Show |
37 | HG00099.hp2 HG00639.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.101-9482G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51241986 | |||||||
| chr13:51241997 | C | T | 2 | a0001c0001t0004g0270 a0001c0001t0006g0173 |
2 | HG01934.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.101-9471C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51241997 | |||||||
| chr13:51242098 | T | C | 1 | a0001c0001t0001g0057 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.101-9370T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51242098 | |||||||
| chr13:51242183 | G | A | 1 | a0001c0001t0002g0131 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.101-9285G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51242183 | |||||||
| chr13:51242209 | G | A | 1 | a0002c0002t0007g0282 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.101-9259G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51242209 | |||||||
| chr13:51242259 | TG | T | 14 | a0001c0001t0001g0014 a0001c0001t0001g0019 a0001c0001t0001g0028 others(11): Show |
18 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(15): Show |
intron_variant | MODIFIER | c.101-9207delG | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 51242259 | ||||||
| chr13:51242268 | G | C | 1 | a0001c0006t0016g0313 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.101-9200G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51242268 | |||||||
| chr13:51242315 | A | G | 1 | a0001c0001t0006g0152 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.101-9153A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51242315 | |||||||
| chr13:51242322 | C | A | 1 | a0006c0012t0006g0126 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.101-9146C>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51242322 | |||||||
| chr13:51242361 | A | G | 17 | a0001c0001t0002g0196 a0001c0001t0004g0232 a0001c0001t0013g0044 others(14): Show |
18 | HG01192.hp2 HG01884.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.101-9107A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51242361 | |||||||
| chr13:51242478 | A | C | 5 | a0001c0001t0012g0093 a0001c0006t0016g0313 a0001c0007t0001g0030 others(2): Show |
5 | HG01891.hp2 HG02280.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.101-8990A>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51242478 | |||||||
| chr13:51242509 | A | G | 1 | a0001c0001t0002g0312 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.101-8959A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51242509 | |||||||
| chr13:51242529 | T | C | 310 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(307): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(353): Show |
intron_variant | MODIFIER | c.101-8939T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51242529 | |||||||
| chr13:51242724 | C | T | 1 | a0001c0001t0005g0101 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.101-8744C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51242724 | |||||||
| chr13:51242752 | C | T | 1 | a0002c0002t0009g0286 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.101-8716C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51242752 | |||||||
| chr13:51242826 | C | T | 1 | a0001c0001t0030g0117 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.101-8642C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51242826 | |||||||
| chr13:51242835 | T | A | 2 | a0002c0002t0002g0278 a0002c0002t0007g0279 |
2 | HG02630.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.101-8633T>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51242835 | |||||||
| chr13:51242899 | C | G | 1 | a0001c0001t0030g0117 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.101-8569C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51242899 | |||||||
| chr13:51243007 | G | A | 82 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0016 others(79): Show |
88 | HG00099.hp1 HG00099.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.101-8461G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51243007 | |||||||
| chr13:51243081 | T | G | 1 | a0001c0001t0042g0088 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.101-8387T>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51243081 | |||||||
| chr13:51243208 | C | G | 1 | a0001c0001t0002g0066 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.101-8260C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51243208 | |||||||
| chr13:51243359 | C | T | 53 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0020 others(50): Show |
65 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.101-8109C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51243359 | |||||||
| chr13:51243456 | C | G | 1 | a0001c0001t0005g0077 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.101-8012C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51243456 | |||||||
| chr13:51243514 | C | T | 181 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(178): Show |
207 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.101-7954C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51243514 | |||||||
| chr13:51243584 | G | A | 181 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(178): Show |
207 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.101-7884G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51243584 | |||||||
| chr13:51243698 | T | G | 1 | a0001c0001t0007g0205 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.101-7770T>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51243698 | |||||||
| chr13:51243723 | A | G | 2 | a0001c0001t0003g0013 a0001c0001t0003g0100 |
4 | NA18941.hp2 NA19007.hp1 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.101-7745A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51243723 | |||||||
| chr13:51243787 | C | T | 30 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0023 others(27): Show |
39 | HG00438.hp1 HG00438.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.101-7681C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51243787 | |||||||
| chr13:51243952 | G | T | 1 | a0001c0001t0014g0240 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.101-7516G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51243952 | |||||||
| chr13:51243986 | G | T | 1 | a0001c0001t0002g0269 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.101-7482G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51243986 | |||||||
| chr13:51244348 | G | A | 111 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0015 others(108): Show |
124 | HG00099.hp1 HG00099.hp2 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.101-7120G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51244348 | |||||||
| chr13:51244392 | A | G | 1 | a0001c0009t0033g0213 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.101-7076A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51244392 | |||||||
| chr13:51244642 | C | G | 1 | a0001c0001t0001g0157 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.101-6826C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51244642 | |||||||
| chr13:51244805 | C | T | 282 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(279): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(319): Show |
intron_variant | MODIFIER | c.101-6663C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51244805 | |||||||
| chr13:51244836 | C | T | 1 | a0001c0001t0011g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.101-6632C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51244836 | |||||||
| chr13:51244950 | A | G | 3 | a0001c0001t0002g0131 a0001c0001t0003g0314 a0001c0001t0007g0205 |
3 | HG02615.hp1 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.101-6518A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51244950 | |||||||
| chr13:51244965 | G | A | 1 | a0001c0001t0004g0160 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.101-6503G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51244965 | |||||||
| chr13:51245099 | G | A | 2 | a0001c0001t0002g0131 a0001c0001t0003g0314 |
2 | HG02615.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.101-6369G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51245099 | |||||||
| chr13:51245131 | A | G | 15 | a0001c0001t0002g0196 a0001c0001t0013g0044 a0001c0001t0017g0044 others(12): Show |
16 | HG01192.hp2 HG01884.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.101-6337A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51245131 | |||||||
| chr13:51245211 | G | A | 2 | a0001c0001t0013g0044 a0001c0001t0017g0044 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.101-6257G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51245211 | |||||||
| chr13:51245303 | A | G | 2 | a0001c0001t0001g0023 a0001c0001t0002g0023 |
2 | NA18940.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.101-6165A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51245303 | |||||||
| chr13:51245330 | G | A | 6 | a0001c0001t0001g0023 a0001c0001t0002g0023 a0001c0001t0002g0056 others(3): Show |
6 | HG03209.hp2 NA18940.hp1 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.101-6138G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51245330 | |||||||
| chr13:51245398 | G | A | 1 | a0002c0002t0002g0278 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.101-6070G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51245398 | |||||||
| chr13:51245830 | G | A | 1 | a0001c0001t0004g0232 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.101-5638G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51245830 | |||||||
| chr13:51246026 | T | C | 1 | a0001c0001t0001g0159 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.101-5442T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51246026 | |||||||
| chr13:51246208 | C | T | 105 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0016 others(102): Show |
113 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.101-5260C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51246208 | |||||||
| chr13:51246382 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.101-5086C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51246382 | |||||||
| chr13:51246399 | T | TG | 28 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0037 others(25): Show |
30 | HG01069.hp1 HG01070.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.101-5065dupG | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 51246399 | ||||||
| chr13:51246399 | T | TGG | 7 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0220 others(4): Show |
7 | HG00099.hp1 HG00733.hp2 HG00735.hp1 others(4): Show |
intron_variant | MODIFIER | c.101-5066_101-5065d others(4): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 51246399 | ||||||
| chr13:51246399 | T | TGGG | 12 | a0001c0001t0001g0207 a0001c0001t0001g0275 a0001c0001t0004g0135 others(9): Show |
13 | HG00140.hp2 HG00544.hp1 HG00558.hp1 others(10): Show |
intron_variant | MODIFIER | c.101-5067_101-5065d others(5): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 51246399 | ||||||
| chr13:51246399 | T | TGGGC | 32 | a0001c0001t0001g0072 a0001c0001t0001g0153 a0001c0001t0001g0157 others(29): Show |
34 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.101-5066_101-5065i others(6): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 51246399 | ||||||
| chr13:51246399 | T | TGGGCG | 9 | a0001c0001t0001g0005 a0001c0001t0001g0102 a0001c0001t0002g0033 others(6): Show |
10 | HG01346.hp2 HG01433.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.101-5066_101-5065i others(7): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 51246399 | ||||||
| chr13:51246400 | G | GGGC | 33 | a0001c0001t0001g0043 a0001c0001t0001g0094 a0001c0001t0002g0043 others(30): Show |
40 | HG00621.hp2 HG00735.hp2 HG02165.hp1 others(37): Show |
intron_variant | MODIFIER | c.101-5066_101-5065i others(5): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 51246400 | ||||||
| chr13:51246401 | GGGT | G | 61 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(58): Show |
76 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.101-5064_101-5062d others(5): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 51246401 | ||||||
| chr13:51246402 | G | C | 1 | a0008c0010t0020g0073 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.101-5066G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51246402 | |||||||
| chr13:51246402 | GGT | G | 24 | a0001c0001t0001g0014 a0001c0001t0001g0019 a0001c0001t0001g0028 others(21): Show |
28 | HG00280.hp1 HG00323.hp1 HG00438.hp1 others(25): Show |
intron_variant | MODIFIER | c.101-5064_101-5063d others(4): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr13 | 51246402 | ||||||
| chr13:51246403 | GT | G | 40 | a0001c0001t0001g0019 a0001c0001t0001g0132 a0001c0001t0001g0167 others(37): Show |
42 | HG00099.hp2 HG01168.hp1 HG01358.hp2 others(39): Show |
intron_variant | MODIFIER | c.101-5064delT | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51246403 | |||||||
| chr13:51246404 | T | C | 5 | a0001c0001t0001g0163 a0001c0001t0007g0193 a0001c0001t0013g0191 others(2): Show |
5 | HG02109.hp2 HG02970.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.101-5064T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51246404 | |||||||
| chr13:51246404 | T | G | 159 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0015 others(156): Show |
174 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.101-5064T>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51246404 | |||||||
| chr13:51246405 | G | C | 2 | a0001c0001t0001g0172 a0001c0001t0035g0166 |
2 | HG02486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.101-5063G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51246405 | |||||||
| chr13:51246406 | G | T | 1 | a0001c0017t0001g0170 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.101-5062G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51246406 | |||||||
| chr13:51246407 | G | C | 1 | a0001c0001t0007g0205 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.101-5061G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51246407 | |||||||
| chr13:51246410 | G | A | 1 | a0001c0001t0004g0232 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.101-5058G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51246410 | |||||||
| chr13:51246758 | C | T | 1 | a0001c0001t0004g0155 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.101-4710C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51246758 | |||||||
| chr13:51246766 | C | T | 16 | a0001c0001t0004g0270 a0001c0001t0005g0148 a0001c0001t0006g0038 others(13): Show |
17 | HG00140.hp2 HG01069.hp2 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.101-4702C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51246766 | |||||||
| chr13:51246780 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.101-4688G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51246780 | |||||||
| chr13:51246913 | G | A | 2 | a0001c0001t0002g0131 a0001c0001t0003g0314 |
2 | HG02615.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.101-4555G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51246913 | |||||||
| chr13:51246917 | T | C | 2 | a0004c0011t0002g0122 a0008c0010t0020g0073 |
2 | HG01884.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.101-4551T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51246917 | |||||||
| chr13:51247106 | G | A | 1 | a0002c0002t0009g0225 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.101-4362G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51247106 | |||||||
| chr13:51247176 | G | T | 1 | a0001c0001t0004g0232 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.101-4292G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51247176 | |||||||
| chr13:51247315 | C | T | 1 | a0001c0001t0006g0257 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.101-4153C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51247315 | |||||||
| chr13:51247343 | G | C | 2 | a0001c0001t0001g0144 a0001c0001t0001g0203 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.101-4125G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51247343 | |||||||
| chr13:51247589 | G | A | 1 | a0001c0001t0042g0088 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.101-3879G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51247589 | |||||||
| chr13:51247672 | G | A | 1 | a0001c0001t0001g0153 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.101-3796G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51247672 | |||||||
| chr13:51247733 | G | A | 2 | a0001c0001t0001g0016 a0001c0001t0002g0016 |
3 | NA18970.hp1 NA18990.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.101-3735G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51247733 | |||||||
| chr13:51247746 | G | C | 1 | a0001c0001t0001g0132 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.101-3722G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51247746 | |||||||
| chr13:51247781 | C | T | 101 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0016 others(98): Show |
108 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.101-3687C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51247781 | |||||||
| chr13:51247826 | C | G | 289 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(286): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(327): Show |
intron_variant | MODIFIER | c.101-3642C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51247826 | |||||||
| chr13:51247865 | G | A | 1 | a0001c0001t0002g0131 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.101-3603G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51247865 | |||||||
| chr13:51247872 | G | C | 2 | a0004c0011t0002g0122 a0008c0010t0020g0073 |
2 | HG01884.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.101-3596G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51247872 | |||||||
| chr13:51248034 | C | T | 2 | a0001c0001t0001g0292 a0001c0001t0002g0291 |
2 | HG03491.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.101-3434C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51248034 | |||||||
| chr13:51248053 | C | A | 280 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(277): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(317): Show |
intron_variant | MODIFIER | c.101-3415C>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51248053 | |||||||
| chr13:51248210 | A | G | 286 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(283): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(323): Show |
intron_variant | MODIFIER | c.101-3258A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51248210 | |||||||
| chr13:51248222 | C | T | 2 | a0004c0005t0023g0233 a0004c0005t0027g0052 |
3 | HG02572.hp2 HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.101-3246C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51248222 | |||||||
| chr13:51248337 | G | A | 1 | a0001c0001t0007g0205 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.101-3131G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51248337 | |||||||
| chr13:51248382 | G | A | 2 | a0001c0001t0001g0121 a0001c0001t0002g0131 |
2 | HG03486.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.101-3086G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51248382 | |||||||
| chr13:51248430 | T | C | 108 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0016 others(105): Show |
116 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.101-3038T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51248430 | |||||||
| chr13:51248634 | C | T | 1 | a0001c0006t0016g0313 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.101-2834C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51248634 | |||||||
| chr13:51249049 | T | C | 78 | a0001c0001t0001g0005 a0001c0001t0001g0043 a0001c0001t0001g0094 others(75): Show |
88 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.101-2419T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51249049 | |||||||
| chr13:51249073 | C | T | 285 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(282): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(322): Show |
intron_variant | MODIFIER | c.101-2395C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51249073 | |||||||
| chr13:51249086 | C | T | 1 | a0001c0001t0002g0131 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.101-2382C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51249086 | |||||||
| chr13:51249125 | A | G | 28 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0001g0024 others(25): Show |
34 | HG00438.hp2 HG00642.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.101-2343A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51249125 | |||||||
| chr13:51249239 | C | G | 1 | a0001c0001t0002g0131 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.101-2229C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51249239 | |||||||
| chr13:51249270 | T | C | 1 | a0001c0001t0022g0287 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.101-2198T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51249270 | |||||||
| chr13:51249310 | T | C | 1 | a0008c0010t0020g0073 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.101-2158T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51249310 | |||||||
| chr13:51249561 | C | T | 1 | a0001c0001t0005g0087 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.101-1907C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51249561 | |||||||
| chr13:51249842 | G | T | 70 | a0001c0001t0001g0005 a0001c0001t0001g0043 a0001c0001t0001g0102 others(67): Show |
80 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.101-1626G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51249842 | |||||||
| chr13:51250096 | C | T | 3 | a0001c0001t0003g0314 a0001c0001t0014g0240 a0001c0001t0018g0130 |
3 | HG02615.hp1 HG03579.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.101-1372C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51250096 | |||||||
| chr13:51250192 | A | G | 37 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0086 others(34): Show |
40 | HG00099.hp1 HG00639.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.101-1276A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51250192 | |||||||
| chr13:51250200 | AT | A | 3 | a0001c0001t0001g0164 a0001c0001t0001g0168 a0001c0001t0004g0160 |
3 | HG01069.hp1 HG01074.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.101-1267delT | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51250200 | |||||||
| chr13:51250565 | C | T | 313 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(310): Show |
359 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(356): Show |
intron_variant | MODIFIER | c.101-903C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51250565 | |||||||
| chr13:51250600 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.101-868G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51250600 | |||||||
| chr13:51250647 | A | C | 1 | a0010c0014t0026g0249 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.101-821A>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51250647 | |||||||
| chr13:51250655 | A | G | 189 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0015 others(186): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.101-813A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51250655 | |||||||
| chr13:51250657 | A | T | 1 | a0001c0001t0001g0151 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.101-811A>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51250657 | |||||||
| chr13:51250811 | A | G | 11 | a0001c0001t0001g0163 a0001c0001t0007g0047 a0001c0001t0007g0205 others(8): Show |
11 | HG01884.hp2 HG01891.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.101-657A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51250811 | |||||||
| chr13:51250943 | G | A | 1 | a0002c0002t0004g0234 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.101-525G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51250943 | |||||||
| chr13:51250950 | G | A | 1 | a0002c0004t0010g0050 | 2 | NA18952.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.101-518G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51250950 | |||||||
| chr13:51251016 | C | T | 1 | a0004c0011t0002g0122 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.101-452C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51251016 | |||||||
| chr13:51251163 | G | A | 1 | a0001c0001t0001g0121 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.101-305G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51251163 | |||||||
| chr13:51251279 | T | C | 2 | a0001c0001t0001g0102 a0001c0001t0004g0091 |
2 | HG02738.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.101-189T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51251279 | |||||||
| chr13:51251290 | G | C | 5 | a0001c0001t0001g0163 a0001c0001t0007g0047 a0001c0001t0009g0047 others(2): Show |
5 | HG02145.hp2 HG02886.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.101-178G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51251290 | |||||||
| chr13:51251386 | C | G | 1 | a0001c0001t0004g0268 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.101-82C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51251386 | |||||||
| chr13:51251412 | T | C | 82 | a0001c0001t0001g0005 a0001c0001t0001g0043 a0001c0001t0001g0102 others(79): Show |
92 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(89): Show |
intron_variant | MODIFIER | c.101-56T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 2/3 | chr13 | 51251412 | |||||||
| chr13:51252258 | G | C | 1 | a0001c0001t0003g0314 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.834+57G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51252258 | |||||||
| chr13:51252402 | C | T | 1 | a0004c0011t0002g0122 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.834+201C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51252402 | |||||||
| chr13:51252507 | A | G | 60 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(57): Show |
75 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.834+306A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51252507 | |||||||
| chr13:51253190 | G | A | 2 | a0001c0001t0001g0172 a0001c0001t0035g0166 |
2 | HG02486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.834+989G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51253190 | |||||||
| chr13:51253470 | G | A | 230 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(227): Show |
274 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.834+1269G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51253470 | |||||||
| chr13:51253774 | T | G | 1 | a0001c0001t0002g0131 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.834+1573T>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51253774 | |||||||
| chr13:51253783 | G | T | 1 | a0001c0001t0005g0087 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.834+1582G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51253783 | |||||||
| chr13:51253804 | G | A | 1 | a0002c0002t0040g0302 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.834+1603G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51253804 | |||||||
| chr13:51253945 | C | G | 73 | a0001c0001t0001g0005 a0001c0001t0001g0043 a0001c0001t0001g0094 others(70): Show |
83 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.834+1744C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51253945 | |||||||
| chr13:51253946 | T | C | 246 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(243): Show |
290 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(287): Show |
intron_variant | MODIFIER | c.834+1745T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51253946 | |||||||
| chr13:51253948 | C | A | 1 | a0001c0001t0030g0117 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.834+1747C>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51253948 | |||||||
| chr13:51254104 | G | T | 33 | a0002c0002t0001g0008 a0002c0002t0001g0231 a0002c0002t0001g0245 others(30): Show |
39 | HG00140.hp1 HG00323.hp2 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.834+1903G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51254104 | |||||||
| chr13:51254396 | C | CT | 12 | a0001c0001t0001g0163 a0001c0001t0002g0212 a0001c0001t0007g0205 others(9): Show |
12 | HG01261.hp1 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.834+2204dupT | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 51254396 | ||||||
| chr13:51254563 | C | T | 1 | a0001c0001t0001g0185 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.834+2362C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51254563 | |||||||
| chr13:51254824 | T | C | 247 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(244): Show |
291 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(288): Show |
intron_variant | MODIFIER | c.834+2623T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51254824 | |||||||
| chr13:51254863 | T | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(133): Show |
165 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.834+2662T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51254863 | |||||||
| chr13:51254900 | G | A | 1 | a0001c0009t0033g0213 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.834+2699G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51254900 | |||||||
| chr13:51254920 | T | C | 8 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0061 others(5): Show |
8 | HG02083.hp1 NA18940.hp1 NA18969.hp1 others(5): Show |
intron_variant | MODIFIER | c.834+2719T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51254920 | |||||||
| chr13:51255062 | G | A | 1 | a0002c0002t0001g0280 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.834+2861G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51255062 | |||||||
| chr13:51255202 | G | A | 241 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(238): Show |
285 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(282): Show |
intron_variant | MODIFIER | c.834+3001G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51255202 | |||||||
| chr13:51255305 | A | G | 1 | a0003c0003t0008g0199 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.834+3104A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51255305 | |||||||
| chr13:51255343 | G | A | 1 | a0001c0001t0005g0085 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.834+3142G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51255343 | |||||||
| chr13:51255349 | A | T | 1 | a0001c0001t0003g0099 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.834+3148A>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51255349 | |||||||
| chr13:51255355 | T | A | 4 | a0001c0001t0002g0131 a0001c0001t0014g0240 a0001c0001t0018g0128 others(1): Show |
4 | HG02145.hp2 HG03486.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.834+3154T>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51255355 | |||||||
| chr13:51255357 | A | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(133): Show |
165 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.834+3156A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51255357 | |||||||
| chr13:51255444 | G | A | 3 | a0001c0001t0002g0188 a0001c0001t0002g0189 a0001c0001t0002g0190 |
3 | HG02572.hp1 HG02818.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.834+3243G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51255444 | |||||||
| chr13:51255524 | A | C | 1 | a0001c0001t0019g0162 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.834+3323A>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51255524 | |||||||
| chr13:51255575 | A | G | 2 | a0001c0001t0001g0051 a0001c0001t0002g0051 |
2 | HG00733.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.834+3374A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51255575 | |||||||
| chr13:51255682 | C | G | 231 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(228): Show |
275 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(272): Show |
intron_variant | MODIFIER | c.834+3481C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51255682 | |||||||
| chr13:51255738 | AG | A | 34 | a0001c0001t0007g0193 a0002c0002t0001g0008 a0002c0002t0001g0231 others(31): Show |
40 | HG00140.hp1 HG00323.hp2 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.834+3539delG | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 51255738 | ||||||
| chr13:51255749 | G | GT | 104 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(101): Show |
127 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.834+3548_834+3549i others(3): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51255749 | |||||||
| chr13:51255978 | G | A | 1 | a0001c0001t0002g0104 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.834+3777G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51255978 | |||||||
| chr13:51256337 | C | T | 101 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0024 others(98): Show |
116 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(113): Show |
intron_variant | MODIFIER | c.834+4136C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51256337 | |||||||
| chr13:51256395 | C | A | 1 | a0001c0001t0019g0162 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.834+4194C>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51256395 | |||||||
| chr13:51256434 | T | C | 3 | a0001c0001t0003g0032 a0001c0001t0003g0090 a0001c0001t0003g0095 |
4 | NA18983.hp1 NA18990.hp1 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.834+4233T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51256434 | |||||||
| chr13:51256509 | A | T | 2 | a0001c0001t0001g0132 a0002c0002t0007g0285 |
2 | HG02976.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.834+4308A>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51256509 | |||||||
| chr13:51256531 | T | C | 1 | a0001c0001t0002g0228 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.834+4330T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51256531 | |||||||
| chr13:51256577 | G | C | 108 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0024 others(105): Show |
123 | HG00408.hp1 HG00438.hp2 HG00597.hp1 others(120): Show |
intron_variant | MODIFIER | c.834+4376G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51256577 | |||||||
| chr13:51256675 | A | G | 5 | a0001c0007t0001g0030 a0001c0007t0013g0030 a0001c0007t0013g0092 others(2): Show |
5 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.834+4474A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51256675 | |||||||
| chr13:51256770 | C | A | 72 | a0001c0001t0001g0005 a0001c0001t0001g0043 a0001c0001t0001g0102 others(69): Show |
82 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(79): Show |
intron_variant | MODIFIER | c.834+4569C>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51256770 | |||||||
| chr13:51256856 | G | A | 4 | a0001c0001t0014g0240 a0001c0001t0018g0128 a0001c0001t0018g0130 others(1): Show |
4 | HG01243.hp1 HG02145.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.834+4655G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51256856 | |||||||
| chr13:51256884 | C | G | 1 | a0001c0001t0005g0148 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.834+4683C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51256884 | |||||||
| chr13:51256992 | A | G | 2 | a0001c0001t0004g0232 a0001c0009t0033g0213 |
2 | HG03209.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.834+4791A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51256992 | |||||||
| chr13:51256997 | T | C | 14 | a0001c0001t0001g0163 a0001c0001t0007g0047 a0001c0001t0007g0205 others(11): Show |
14 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.834+4796T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51256997 | |||||||
| chr13:51257017 | C | T | 2 | a0001c0001t0001g0172 a0001c0001t0035g0166 |
2 | HG02486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.834+4816C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51257017 | |||||||
| chr13:51257150 | G | A | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(214): Show |
256 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.834+4949G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51257150 | |||||||
| chr13:51257161 | T | C | 1 | a0002c0002t0019g0242 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.834+4960T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51257161 | |||||||
| chr13:51257256 | C | G | 1 | a0004c0005t0027g0052 | 2 | HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.834+5055C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51257256 | |||||||
| chr13:51257383 | C | T | 22 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0061 others(19): Show |
27 | HG00438.hp2 HG00642.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.834+5182C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51257383 | |||||||
| chr13:51257703 | A | G | 249 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(246): Show |
293 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(290): Show |
intron_variant | MODIFIER | c.834+5502A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51257703 | |||||||
| chr13:51257868 | C | T | 1 | a0001c0001t0002g0131 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.834+5667C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51257868 | |||||||
| chr13:51257919 | A | C | 6 | a0002c0002t0002g0048 a0002c0002t0007g0246 a0002c0002t0009g0048 others(3): Show |
6 | HG00140.hp1 HG00323.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.834+5718A>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51257919 | |||||||
| chr13:51257924 | C | T | 1 | a0001c0001t0006g0257 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.834+5723C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51257924 | |||||||
| chr13:51258026 | A | G | 4 | a0001c0001t0001g0163 a0001c0001t0007g0047 a0001c0001t0009g0047 others(1): Show |
4 | HG02886.hp1 HG02970.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.834+5825A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51258026 | |||||||
| chr13:51258041 | T | G | 129 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0019 others(126): Show |
148 | HG00280.hp1 HG00323.hp1 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.834+5840T>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51258041 | |||||||
| chr13:51258074 | T | C | 75 | a0001c0001t0001g0005 a0001c0001t0001g0043 a0001c0001t0001g0102 others(72): Show |
85 | HG00408.hp1 HG00597.hp1 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.834+5873T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51258074 | |||||||
| chr13:51258132 | C | T | 22 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0061 others(19): Show |
27 | HG00438.hp2 HG00642.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.834+5931C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51258132 | |||||||
| chr13:51258169 | T | C | 1 | a0001c0001t0001g0132 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.834+5968T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51258169 | |||||||
| chr13:51258184 | G | C | 1 | a0001c0001t0001g0186 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.834+5983G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51258184 | |||||||
| chr13:51258194 | A | G | 6 | a0001c0001t0002g0266 a0001c0001t0002g0267 a0001c0001t0004g0268 others(3): Show |
6 | HG00642.hp1 HG01346.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.834+5993A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51258194 | |||||||
| chr13:51258214 | C | T | 1 | a0004c0011t0002g0122 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.834+6013C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51258214 | |||||||
| chr13:51258218 | A | G | 1 | a0001c0001t0015g0154 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.834+6017A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51258218 | |||||||
| chr13:51258543 | G | A | 9 | a0001c0001t0014g0240 a0001c0001t0018g0128 a0001c0001t0018g0130 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.834+6342G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51258543 | |||||||
| chr13:51258544 | C | A | 9 | a0001c0001t0014g0240 a0001c0001t0018g0128 a0001c0001t0018g0130 others(6): Show |
9 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.834+6343C>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51258544 | |||||||
| chr13:51258763 | C | G | 1 | a0001c0001t0002g0143 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.834+6562C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51258763 | |||||||
| chr13:51258783 | G | A | 1 | a0004c0011t0002g0122 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.834+6582G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51258783 | |||||||
| chr13:51258928 | T | G | 1 | a0001c0001t0002g0266 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.834+6727T>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51258928 | |||||||
| chr13:51258963 | G | C | 1 | a0001c0001t0013g0191 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.834+6762G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51258963 | |||||||
| chr13:51258990 | G | A | 16 | a0001c0001t0002g0196 a0001c0001t0003g0096 a0001c0001t0013g0044 others(13): Show |
17 | HG01192.hp2 HG01884.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.834+6789G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51258990 | |||||||
| chr13:51258999 | G | A | 1 | a0001c0001t0007g0205 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.834+6798G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51258999 | |||||||
| chr13:51259054 | C | G | 15 | a0001c0001t0001g0014 a0001c0001t0001g0019 a0001c0001t0001g0028 others(12): Show |
19 | HG00280.hp1 HG00323.hp1 HG00544.hp2 others(16): Show |
intron_variant | MODIFIER | c.834+6853C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51259054 | |||||||
| chr13:51259111 | C | T | 33 | a0001c0001t0007g0193 a0002c0002t0001g0008 a0002c0002t0001g0231 others(30): Show |
39 | HG00140.hp1 HG00323.hp2 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.834+6910C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51259111 | |||||||
| chr13:51259146 | C | T | 15 | a0001c0001t0002g0196 a0001c0001t0013g0044 a0001c0001t0017g0044 others(12): Show |
16 | HG01192.hp2 HG01884.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.834+6945C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51259146 | |||||||
| chr13:51259396 | C | T | 15 | a0001c0001t0002g0196 a0001c0001t0013g0044 a0001c0001t0017g0044 others(12): Show |
16 | HG01192.hp2 HG01884.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.834+7195C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51259396 | |||||||
| chr13:51259402 | C | CCT | 22 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0061 others(19): Show |
27 | HG00438.hp2 HG00642.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.834+7205_834+7206d others(4): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 51259402 | ||||||
| chr13:51259452 | C | T | 1 | a0001c0001t0011g0208 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.834+7251C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51259452 | |||||||
| chr13:51259465 | C | T | 70 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0086 others(67): Show |
75 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.834+7264C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51259465 | |||||||
| chr13:51259521 | C | G | 1 | a0002c0002t0001g0245 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.834+7320C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51259521 | |||||||
| chr13:51259521 | C | T | 1 | a0001c0001t0002g0312 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.834+7320C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51259521 | |||||||
| chr13:51259523 | G | C | 1 | a0002c0002t0001g0245 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.834+7322G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51259523 | |||||||
| chr13:51259582 | G | A | 53 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0086 others(50): Show |
57 | HG00099.hp1 HG00140.hp2 HG00544.hp1 others(54): Show |
intron_variant | MODIFIER | c.834+7381G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51259582 | |||||||
| chr13:51259601 | G | A | 1 | a0001c0001t0030g0117 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.834+7400G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51259601 | |||||||
| chr13:51259740 | C | A | 1 | a0002c0002t0001g0245 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.834+7539C>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51259740 | |||||||
| chr13:51259808 | A | C | 84 | a0001c0001t0001g0005 a0001c0001t0001g0043 a0001c0001t0001g0102 others(81): Show |
94 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.834+7607A>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51259808 | |||||||
| chr13:51259893 | G | A | 4 | a0001c0001t0001g0163 a0001c0001t0007g0047 a0001c0001t0009g0047 others(1): Show |
4 | HG02258.hp1 HG02886.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.834+7692G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51259893 | |||||||
| chr13:51259919 | T | G | 1 | a0001c0001t0002g0188 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.834+7718T>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51259919 | |||||||
| chr13:51259937 | G | T | 21 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0061 others(18): Show |
27 | HG00438.hp2 HG00642.hp2 HG01070.hp1 others(24): Show |
intron_variant | MODIFIER | c.834+7736G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51259937 | |||||||
| chr13:51259994 | G | C | 11 | a0001c0001t0005g0031 a0001c0001t0005g0075 a0001c0001t0005g0076 others(8): Show |
12 | HG00597.hp1 HG02080.hp1 HG03942.hp2 others(9): Show |
intron_variant | MODIFIER | c.834+7793G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51259994 | |||||||
| chr13:51260192 | C | T | 1 | a0001c0006t0010g0265 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.834+7991C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51260192 | |||||||
| chr13:51260227 | C | T | 70 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0017 others(67): Show |
79 | HG00099.hp1 HG00544.hp2 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.834+8026C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51260227 | |||||||
| chr13:51260292 | T | C | 6 | a0001c0001t0001g0163 a0001c0001t0007g0047 a0001c0001t0009g0047 others(3): Show |
7 | HG02258.hp1 HG02572.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.834+8091T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51260292 | |||||||
| chr13:51260565 | C | T | 1 | a0001c0001t0002g0131 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.834+8364C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51260565 | |||||||
| chr13:51260581 | G | T | 6 | a0001c0001t0001g0163 a0001c0001t0007g0047 a0001c0001t0009g0047 others(3): Show |
7 | HG02258.hp1 HG02572.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.834+8380G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51260581 | |||||||
| chr13:51260634 | C | T | 1 | a0001c0001t0004g0232 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.834+8433C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51260634 | |||||||
| chr13:51260748 | G | T | 67 | a0001c0001t0001g0005 a0001c0001t0001g0094 a0001c0001t0001g0102 others(64): Show |
77 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.834+8547G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51260748 | |||||||
| chr13:51260790 | G | C | 23 | a0001c0001t0001g0207 a0001c0001t0003g0314 a0001c0001t0004g0270 others(20): Show |
24 | HG00140.hp2 HG00544.hp1 HG01069.hp2 others(21): Show |
intron_variant | MODIFIER | c.834+8589G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51260790 | |||||||
| chr13:51260919 | G | A | 1 | a0001c0001t0018g0130 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.834+8718G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51260919 | |||||||
| chr13:51261011 | T | C | 1 | a0004c0011t0002g0122 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.834+8810T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51261011 | |||||||
| chr13:51261013 | A | T | 54 | a0001c0001t0002g0045 a0001c0001t0002g0196 a0001c0001t0002g0251 others(51): Show |
64 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.834+8812A>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51261013 | |||||||
| chr13:51261098 | C | A | 1 | a0001c0001t0002g0060 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.834+8897C>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51261098 | |||||||
| chr13:51261163 | C | T | 18 | a0001c0001t0001g0207 a0001c0001t0004g0270 a0001c0001t0005g0148 others(15): Show |
19 | HG00140.hp2 HG00544.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.834+8962C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51261163 | |||||||
| chr13:51261312 | T | A | 1 | a0002c0002t0001g0245 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.834+9111T>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51261312 | |||||||
| chr13:51261349 | G | A | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(135): Show |
162 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(159): Show |
intron_variant | MODIFIER | c.834+9148G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51261349 | |||||||
| chr13:51261471 | A | G | 12 | a0001c0001t0014g0240 a0001c0001t0018g0128 a0001c0001t0018g0130 others(9): Show |
13 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.834+9270A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51261471 | |||||||
| chr13:51261506 | C | T | 8 | a0001c0001t0001g0010 a0001c0001t0001g0027 a0001c0001t0001g0055 others(5): Show |
9 | NA18747.hp1 NA18939.hp2 NA18957.hp1 others(6): Show |
intron_variant | MODIFIER | c.834+9305C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51261506 | |||||||
| chr13:51261518 | G | A | 3 | a0001c0001t0013g0044 a0001c0001t0017g0044 a0001c0001t0017g0194 |
3 | HG02622.hp1 HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.834+9317G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51261518 | |||||||
| chr13:51261565 | T | TCCATAGT others(13): Show |
58 | a0001c0001t0001g0163 a0001c0001t0002g0045 a0001c0001t0002g0196 others(55): Show |
68 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(65): Show |
intron_variant | MODIFIER | c.834+9364_834+9365i others(22): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51261565 | |||||||
| chr13:51261918 | G | T | 1 | a0001c0001t0007g0205 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.834+9717G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51261918 | |||||||
| chr13:51261984 | C | T | 1 | a0001c0001t0004g0232 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.834+9783C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51261984 | |||||||
| chr13:51262177 | C | T | 2 | a0004c0011t0002g0122 a0008c0010t0020g0073 |
2 | HG01884.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.834+9976C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51262177 | |||||||
| chr13:51262266 | G | C | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(249): Show |
290 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.834+10065G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51262266 | |||||||
| chr13:51262483 | G | A | 262 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(259): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(298): Show |
intron_variant | MODIFIER | c.834+10282G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51262483 | |||||||
| chr13:51262484 | T | A | 2 | a0001c0001t0001g0304 a0001c0001t0001g0305 |
2 | HG01081.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.834+10283T>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51262484 | |||||||
| chr13:51262710 | T | C | 321 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(318): Show |
370 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(367): Show |
intron_variant | MODIFIER | c.834+10509T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51262710 | |||||||
| chr13:51262713 | C | G | 1 | a0001c0001t0019g0162 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.834+10512C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51262713 | |||||||
| chr13:51262766 | T | C | 1 | a0001c0001t0001g0272 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.834+10565T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51262766 | |||||||
| chr13:51262797 | C | T | 12 | a0001c0001t0012g0003 a0001c0001t0012g0093 a0001c0001t0012g0250 others(9): Show |
14 | HG01891.hp1 HG02109.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.834+10596C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51262797 | |||||||
| chr13:51262854 | C | T | 2 | a0001c0001t0003g0013 a0001c0001t0003g0100 |
4 | NA18941.hp2 NA19007.hp1 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.834+10653C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51262854 | |||||||
| chr13:51262998 | C | A | 1 | a0009c0013t0008g0224 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.834+10797C>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51262998 | |||||||
| chr13:51263016 | C | T | 20 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0061 others(17): Show |
23 | HG00438.hp2 HG00642.hp2 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.834+10815C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51263016 | |||||||
| chr13:51263163 | A | G | 57 | a0001c0001t0002g0045 a0001c0001t0002g0196 a0001c0001t0002g0251 others(54): Show |
67 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.834+10962A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51263163 | |||||||
| chr13:51263170 | C | T | 1 | a0001c0001t0004g0232 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.834+10969C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51263170 | |||||||
| chr13:51263217 | C | T | 1 | a0001c0001t0002g0070 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.834+11016C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51263217 | |||||||
| chr13:51263318 | A | G | 6 | a0001c0001t0002g0033 a0001c0001t0003g0033 a0001c0001t0003g0034 others(3): Show |
6 | HG01255.hp1 HG01346.hp2 HG01928.hp1 others(3): Show |
intron_variant | MODIFIER | c.834+11117A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51263318 | |||||||
| chr13:51263706 | T | C | 1 | a0001c0001t0004g0232 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.834+11505T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51263706 | |||||||
| chr13:51264009 | A | G | 2 | a0001c0001t0002g0263 a0001c0001t0002g0269 |
2 | HG02056.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.834+11808A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51264009 | |||||||
| chr13:51264473 | C | T | 2 | a0001c0001t0004g0232 a0001c0001t0007g0205 |
2 | HG03704.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.834+12272C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51264473 | |||||||
| chr13:51264475 | C | A | 1 | a0001c0001t0001g0121 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.834+12274C>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51264475 | |||||||
| chr13:51264501 | G | C | 93 | a0001c0001t0001g0005 a0001c0001t0001g0102 a0001c0001t0001g0132 others(90): Show |
104 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.834+12300G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51264501 | |||||||
| chr13:51264544 | C | G | 6 | a0001c0007t0001g0030 a0001c0007t0013g0030 a0001c0007t0013g0092 others(3): Show |
6 | HG01884.hp2 HG01891.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.834+12343C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51264544 | |||||||
| chr13:51264545 | G | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(131): Show |
158 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.834+12344G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51264545 | |||||||
| chr13:51264650 | A | T | 1 | a0001c0001t0004g0232 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.834+12449A>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51264650 | |||||||
| chr13:51264774 | C | T | 2 | a0001c0001t0015g0053 a0001c0001t0041g0053 |
2 | NA18967.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.834+12573C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51264774 | |||||||
| chr13:51264861 | G | A | 351 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(348): Show |
403 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(400): Show |
intron_variant | MODIFIER | c.834+12660G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51264861 | |||||||
| chr13:51264922 | C | T | 1 | a0001c0001t0001g0254 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.834+12721C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51264922 | |||||||
| chr13:51265074 | C | T | 319 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(316): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
intron_variant | MODIFIER | c.834+12873C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51265074 | |||||||
| chr13:51265200 | G | A | 66 | a0001c0001t0001g0005 a0001c0001t0001g0102 a0001c0001t0001g0153 others(63): Show |
76 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.834+12999G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51265200 | |||||||
| chr13:51265280 | C | T | 11 | a0001c0001t0007g0193 a0002c0002t0001g0231 a0002c0002t0001g0280 others(8): Show |
14 | HG01074.hp2 HG01167.hp2 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.834+13079C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51265280 | |||||||
| chr13:51265414 | T | C | 1 | a0002c0002t0007g0282 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.834+13213T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51265414 | |||||||
| chr13:51265426 | C | T | 1 | a0001c0009t0020g0110 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.834+13225C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51265426 | |||||||
| chr13:51265545 | C | T | 1 | a0001c0001t0002g0161 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.834+13344C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51265545 | |||||||
| chr13:51265829 | C | A | 1 | a0001c0001t0002g0042 | 2 | HG01978.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.834+13628C>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51265829 | |||||||
| chr13:51265970 | T | C | 58 | a0001c0001t0001g0014 a0001c0001t0001g0019 a0001c0001t0001g0023 others(55): Show |
67 | HG00438.hp2 HG00544.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.834+13769T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51265970 | |||||||
| chr13:51266054 | T | A | 2 | a0001c0001t0007g0025 a0001c0001t0007g0026 |
4 | HG00738.hp2 HG01070.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.834+13853T>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51266054 | |||||||
| chr13:51266077 | GTGT | G | 23 | a0001c0001t0001g0207 a0001c0001t0003g0314 a0001c0001t0004g0270 others(20): Show |
26 | HG00140.hp2 HG00544.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.834+13881_834+1388 others(7): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 51266077 | ||||||
| chr13:51266113 | T | G | 2 | a0001c0001t0007g0047 a0001c0001t0009g0047 |
2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.834+13912T>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51266113 | |||||||
| chr13:51266357 | T | C | 1 | a0001c0001t0011g0276 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.835-14093T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51266357 | |||||||
| chr13:51266434 | G | T | 20 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0061 others(17): Show |
23 | HG00438.hp2 HG00642.hp2 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.835-14016G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51266434 | |||||||
| chr13:51266594 | T | G | 1 | a0001c0001t0005g0085 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.835-13856T>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51266594 | |||||||
| chr13:51267021 | C | T | 47 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0061 others(44): Show |
53 | HG00438.hp2 HG00642.hp2 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.835-13429C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51267021 | |||||||
| chr13:51267155 | G | A | 12 | a0001c0001t0002g0042 a0001c0001t0002g0045 a0001c0001t0002g0131 others(9): Show |
14 | HG00280.hp1 HG00323.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.835-13295G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51267155 | |||||||
| chr13:51267678 | T | G | 1 | a0001c0001t0001g0132 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.835-12772T>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51267678 | |||||||
| chr13:51267713 | C | T | 1 | a0001c0001t0002g0141 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.835-12737C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51267713 | |||||||
| chr13:51267852 | G | A | 4 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0220 others(1): Show |
4 | HG00733.hp2 HG00735.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.835-12598G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51267852 | |||||||
| chr13:51267911 | G | T | 2 | a0001c0001t0006g0217 a0001c0001t0011g0208 |
2 | HG01346.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.835-12539G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51267911 | |||||||
| chr13:51267943 | A | G | 1 | a0001c0001t0007g0205 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.835-12507A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51267943 | |||||||
| chr13:51268101 | T | A | 1 | a0001c0001t0018g0130 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.835-12349T>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51268101 | |||||||
| chr13:51268330 | G | A | 14 | a0001c0001t0001g0132 a0001c0001t0002g0196 a0003c0003t0008g0007 others(11): Show |
15 | HG01192.hp2 HG01884.hp1 HG01975.hp1 others(12): Show |
intron_variant | MODIFIER | c.835-12120G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51268330 | |||||||
| chr13:51268377 | A | G | 98 | a0001c0001t0001g0005 a0001c0001t0001g0102 a0001c0001t0001g0157 others(95): Show |
112 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.835-12073A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51268377 | |||||||
| chr13:51268399 | A | T | 1 | a0001c0001t0019g0162 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.835-12051A>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51268399 | |||||||
| chr13:51268414 | A | G | 1 | a0001c0001t0001g0262 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.835-12036A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51268414 | |||||||
| chr13:51268814 | G | A | 183 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0024 others(180): Show |
207 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.835-11636G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51268814 | |||||||
| chr13:51269566 | T | A | 1 | a0001c0001t0004g0259 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.835-10884T>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51269566 | |||||||
| chr13:51269635 | A | C | 1 | a0001c0001t0003g0098 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.835-10815A>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51269635 | |||||||
| chr13:51269636 | G | C | 1 | a0001c0017t0001g0170 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.835-10814G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51269636 | |||||||
| chr13:51269642 | A | G | 1 | a0001c0001t0011g0084 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.835-10808A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51269642 | |||||||
| chr13:51269742 | A | G | 9 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0061 others(6): Show |
9 | HG02083.hp1 NA18940.hp1 NA18969.hp1 others(6): Show |
intron_variant | MODIFIER | c.835-10708A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51269742 | |||||||
| chr13:51269999 | A | G | 39 | a0001c0001t0001g0014 a0001c0001t0001g0019 a0001c0001t0001g0028 others(36): Show |
45 | HG00544.hp2 HG00621.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.835-10451A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51269999 | |||||||
| chr13:51270040 | A | C | 4 | a0001c0009t0020g0110 a0001c0009t0033g0213 a0004c0011t0002g0122 others(1): Show |
4 | HG01884.hp2 HG02559.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.835-10410A>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51270040 | |||||||
| chr13:51270057 | T | C | 1 | a0001c0001t0003g0112 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.835-10393T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51270057 | |||||||
| chr13:51270115 | G | A | 12 | a0001c0001t0002g0042 a0001c0001t0002g0045 a0001c0001t0002g0131 others(9): Show |
14 | HG00280.hp1 HG00323.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.835-10335G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51270115 | |||||||
| chr13:51270158 | C | G | 20 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0061 others(17): Show |
23 | HG00438.hp2 HG00642.hp2 HG01433.hp1 others(20): Show |
intron_variant | MODIFIER | c.835-10292C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51270158 | |||||||
| chr13:51270169 | G | A | 95 | a0001c0001t0001g0005 a0001c0001t0001g0102 a0001c0001t0001g0157 others(92): Show |
109 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.835-10281G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51270169 | |||||||
| chr13:51270230 | G | C | 6 | a0001c0001t0004g0270 a0001c0001t0006g0173 a0001c0001t0006g0180 others(3): Show |
6 | HG01069.hp2 HG01934.hp1 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.835-10220G>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51270230 | |||||||
| chr13:51270293 | C | T | 6 | a0001c0001t0002g0042 a0001c0001t0002g0045 a0001c0001t0002g0251 others(3): Show |
8 | HG00280.hp1 HG00323.hp1 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.835-10157C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51270293 | |||||||
| chr13:51270472 | C | T | 1 | a0001c0001t0002g0177 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.835-9978C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51270472 | |||||||
| chr13:51270593 | G | A | 2 | a0001c0001t0001g0027 a0001c0001t0002g0027 |
2 | NA18939.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.835-9857G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51270593 | |||||||
| chr13:51270734 | C | T | 1 | a0002c0002t0009g0244 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.835-9716C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51270734 | |||||||
| chr13:51270798 | C | T | 1 | a0001c0001t0004g0232 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.835-9652C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51270798 | |||||||
| chr13:51270933 | G | A | 1 | a0001c0001t0004g0232 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.835-9517G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51270933 | |||||||
| chr13:51271027 | ATGTGGCA others(18): Show |
A | 1 | a0001c0001t0001g0139 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.835-9422_835-9398d others(27): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51271027 | |||||||
| chr13:51271104 | A | G | 19 | a0001c0001t0001g0014 a0001c0001t0001g0019 a0001c0001t0001g0028 others(16): Show |
22 | HG00544.hp2 HG00621.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.835-9346A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51271104 | |||||||
| chr13:51271112 | A | G | 1 | a0001c0001t0019g0162 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.835-9338A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51271112 | |||||||
| chr13:51271188 | C | T | 23 | a0001c0001t0001g0207 a0001c0001t0004g0270 a0001c0001t0005g0148 others(20): Show |
26 | HG00140.hp2 HG00544.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.835-9262C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51271188 | |||||||
| chr13:51271206 | C | A | 1 | a0001c0001t0001g0171 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.835-9244C>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51271206 | |||||||
| chr13:51271261 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.835-9189C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51271261 | |||||||
| chr13:51271515 | G | A | 4 | a0001c0001t0002g0131 a0001c0001t0013g0044 a0001c0001t0017g0044 others(1): Show |
4 | HG02622.hp1 HG02630.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.835-8935G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51271515 | |||||||
| chr13:51271884 | G | A | 2 | a0001c0001t0012g0307 a0001c0001t0012g0311 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.835-8566G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51271884 | |||||||
| chr13:51271930 | T | C | 27 | a0001c0001t0007g0025 a0001c0001t0007g0026 a0001c0001t0007g0193 others(24): Show |
32 | HG00140.hp1 HG00323.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.835-8520T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51271930 | |||||||
| chr13:51272126 | G | A | 26 | a0001c0001t0001g0207 a0001c0001t0001g0304 a0001c0001t0001g0305 others(23): Show |
29 | HG00140.hp2 HG00544.hp1 HG01069.hp2 others(26): Show |
intron_variant | MODIFIER | c.835-8324G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51272126 | |||||||
| chr13:51272191 | C | G | 1 | a0002c0002t0018g0301 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.835-8259C>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51272191 | |||||||
| chr13:51272233 | G | A | 1 | a0001c0007t0013g0092 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.835-8217G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51272233 | |||||||
| chr13:51272249 | T | C | 1 | a0001c0001t0007g0025 | 2 | HG00738.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.835-8201T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51272249 | |||||||
| chr13:51272443 | C | A | 1 | a0001c0001t0002g0131 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.835-8007C>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51272443 | |||||||
| chr13:51272469 | T | C | 209 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0019 others(206): Show |
236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.835-7981T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51272469 | |||||||
| chr13:51272566 | T | TAC | 16 | a0001c0001t0001g0014 a0001c0001t0001g0019 a0001c0001t0001g0028 others(13): Show |
20 | HG00544.hp2 HG00621.hp1 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.835-7857_835-7856d others(4): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 51272566 | ||||||
| chr13:51272566 | T | TACAC | 161 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0024 others(158): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.835-7859_835-7856d others(6): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 51272566 | ||||||
| chr13:51272566 | T | TACACAC | 13 | a0001c0001t0003g0300 a0001c0001t0005g0085 a0001c0001t0006g0274 others(10): Show |
13 | HG00544.hp1 HG01884.hp2 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.835-7861_835-7856d others(8): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 51272566 | ||||||
| chr13:51272566 | T | TACACACA others(1): Show |
16 | a0001c0001t0001g0132 a0001c0001t0002g0104 a0001c0001t0002g0196 others(13): Show |
17 | HG00673.hp2 HG01109.hp2 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.835-7863_835-7856d others(10): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 51272566 | ||||||
| chr13:51272566 | T | TACACACA others(3): Show |
4 | a0001c0001t0013g0044 a0001c0001t0017g0044 a0001c0001t0017g0194 others(1): Show |
4 | HG02622.hp1 HG02630.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.835-7865_835-7856d others(12): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 51272566 | ||||||
| chr13:51272566 | T | TACACACA others(5): Show |
1 | a0001c0001t0002g0131 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.835-7867_835-7856d others(14): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 51272566 | ||||||
| chr13:51272566 | T | TACACACA others(15): Show |
1 | a0001c0001t0004g0232 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.835-7877_835-7856d others(24): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 51272566 | ||||||
| chr13:51272566 | TAC | T | 35 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0086 others(32): Show |
38 | HG00639.hp1 HG00639.hp2 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.835-7857_835-7856d others(4): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 51272566 | ||||||
| chr13:51272593 | A | C | 1 | a0001c0001t0002g0303 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.835-7857A>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51272593 | |||||||
| chr13:51272709 | A | AGGAGTGC others(32): Show |
2 | a0002c0004t0010g0283 a0002c0004t0010g0284 |
2 | HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.835-7733_835-7695d others(41): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 51272709 | ||||||
| chr13:51272972 | G | A | 13 | a0001c0001t0007g0025 a0001c0001t0007g0026 a0001c0001t0030g0117 others(10): Show |
15 | HG00140.hp1 HG00323.hp2 HG00738.hp2 others(12): Show |
intron_variant | MODIFIER | c.835-7478G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51272972 | |||||||
| chr13:51272990 | C | A | 2 | a0001c0001t0022g0287 a0001c0001t0023g0288 |
2 | HG01109.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.835-7460C>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51272990 | |||||||
| chr13:51273300 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.835-7150C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51273300 | |||||||
| chr13:51273486 | C | T | 72 | a0001c0001t0001g0005 a0001c0001t0001g0043 a0001c0001t0001g0102 others(69): Show |
81 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.835-6964C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51273486 | |||||||
| chr13:51273494 | A | G | 1 | a0004c0005t0027g0052 | 2 | HG03209.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.835-6956A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51273494 | |||||||
| chr13:51273574 | A | AT | 31 | a0001c0001t0001g0207 a0001c0001t0003g0314 a0001c0001t0004g0270 others(28): Show |
35 | HG00140.hp2 HG00544.hp1 HG01069.hp2 others(32): Show |
intron_variant | MODIFIER | c.835-6867dupT | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 51273574 | ||||||
| chr13:51273574 | A | T | 15 | a0001c0001t0002g0237 a0001c0001t0003g0035 a0001c0001t0003g0036 others(12): Show |
17 | HG00597.hp1 HG02071.hp2 HG02129.hp2 others(14): Show |
intron_variant | MODIFIER | c.835-6876A>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51273574 | |||||||
| chr13:51273583 | T | A | 2 | a0001c0001t0003g0108 a0001c0001t0005g0175 |
2 | NA18999.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.835-6867T>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51273583 | |||||||
| chr13:51274015 | A | G | 2 | a0001c0001t0001g0004 a0001c0001t0004g0004 |
5 | NA18949.hp1 NA18950.hp1 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.835-6435A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51274015 | |||||||
| chr13:51274029 | A | G | 1 | a0001c0001t0002g0303 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.835-6421A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51274029 | |||||||
| chr13:51274030 | G | T | 1 | a0001c0001t0002g0303 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.835-6420G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51274030 | |||||||
| chr13:51274034 | T | A | 1 | a0001c0001t0002g0303 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.835-6416T>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51274034 | |||||||
| chr13:51274168 | C | A | 1 | a0001c0001t0002g0104 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.835-6282C>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51274168 | |||||||
| chr13:51274241 | A | G | 208 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0019 others(205): Show |
235 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(232): Show |
intron_variant | MODIFIER | c.835-6209A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51274241 | |||||||
| chr13:51274261 | A | G | 36 | a0001c0001t0001g0014 a0001c0001t0001g0019 a0001c0001t0001g0028 others(33): Show |
42 | HG00544.hp2 HG00621.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.835-6189A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51274261 | |||||||
| chr13:51274367 | A | G | 16 | a0001c0001t0001g0014 a0001c0001t0001g0019 a0001c0001t0001g0028 others(13): Show |
19 | HG00544.hp2 HG00621.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.835-6083A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51274367 | |||||||
| chr13:51274398 | G | T | 1 | a0001c0001t0001g0139 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.835-6052G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51274398 | |||||||
| chr13:51274530 | A | T | 1 | a0001c0001t0001g0139 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.835-5920A>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51274530 | |||||||
| chr13:51274542 | A | C | 1 | a0001c0001t0001g0139 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.835-5908A>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51274542 | |||||||
| chr13:51274624 | G | T | 35 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0061 others(32): Show |
39 | HG00438.hp2 HG00642.hp2 HG01192.hp2 others(36): Show |
intron_variant | MODIFIER | c.835-5826G>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51274624 | |||||||
| chr13:51274745 | A | T | 7 | a0001c0001t0001g0179 a0001c0001t0001g0182 a0001c0001t0001g0185 others(4): Show |
8 | HG00639.hp1 HG01167.hp1 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.835-5705A>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51274745 | |||||||
| chr13:51274852 | C | T | 2 | a0001c0001t0002g0123 a0001c0001t0002g0273 |
2 | NA18747.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.835-5598C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51274852 | |||||||
| chr13:51274860 | AGTGAAGA others(9): Show |
A | 1 | a0001c0001t0004g0124 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.835-5589_835-5574d others(18): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51274860 | |||||||
| chr13:51274928 | G | A | 14 | a0001c0001t0001g0132 a0001c0001t0002g0196 a0003c0003t0008g0007 others(11): Show |
15 | HG01192.hp2 HG01884.hp1 HG01975.hp1 others(12): Show |
intron_variant | MODIFIER | c.835-5522G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51274928 | |||||||
| chr13:51274944 | C | T | 1 | a0001c0001t0002g0161 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.835-5506C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51274944 | |||||||
| chr13:51275205 | T | A | 7 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0139 others(4): Show |
9 | HG02523.hp2 NA18951.hp2 NA18966.hp1 others(6): Show |
intron_variant | MODIFIER | c.835-5245T>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51275205 | |||||||
| chr13:51275209 | C | CA | 92 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(89): Show |
110 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.835-5222dupA | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 51275209 | ||||||
| chr13:51275209 | CA | C | 55 | a0001c0001t0001g0207 a0001c0001t0001g0210 a0001c0001t0001g0218 others(52): Show |
61 | HG00140.hp2 HG00544.hp1 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.835-5222delA | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 51275209 | ||||||
| chr13:51275345 | G | A | 24 | a0001c0001t0012g0003 a0001c0001t0012g0093 a0001c0001t0012g0250 others(21): Show |
27 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.835-5105G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51275345 | |||||||
| chr13:51275606 | GC | G | 29 | a0001c0001t0001g0207 a0001c0001t0003g0314 a0001c0001t0004g0232 others(26): Show |
32 | HG00140.hp2 HG00544.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.835-4841delC | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 51275606 | ||||||
| chr13:51275612 | A | T | 29 | a0001c0001t0001g0207 a0001c0001t0003g0314 a0001c0001t0004g0232 others(26): Show |
32 | HG00140.hp2 HG00544.hp1 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.835-4838A>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51275612 | |||||||
| chr13:51275774 | A | G | 62 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0061 others(59): Show |
71 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.835-4676A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51275774 | |||||||
| chr13:51275976 | T | A | 1 | a0003c0003t0008g0200 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.835-4474T>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51275976 | |||||||
| chr13:51276059 | G | A | 132 | a0001c0001t0001g0005 a0001c0001t0001g0043 a0001c0001t0001g0102 others(129): Show |
147 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(144): Show |
intron_variant | MODIFIER | c.835-4391G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51276059 | |||||||
| chr13:51276071 | C | T | 71 | a0001c0001t0001g0005 a0001c0001t0001g0043 a0001c0001t0001g0102 others(68): Show |
80 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.835-4379C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51276071 | |||||||
| chr13:51276072 | G | A | 1 | a0001c0001t0004g0232 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.835-4378G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51276072 | |||||||
| chr13:51276209 | G | A | 2 | a0002c0002t0007g0247 a0002c0002t0007g0295 |
2 | NA19081.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.835-4241G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51276209 | |||||||
| chr13:51276373 | G | A | 1 | a0005c0008t0003g0058 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.835-4077G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51276373 | |||||||
| chr13:51276422 | T | G | 1 | a0001c0001t0001g0260 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.835-4028T>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51276422 | |||||||
| chr13:51276607 | CA | C | 2 | a0001c0001t0001g0020 a0001c0001t0001g0261 |
4 | NA18960.hp1 NA18978.hp1 NA18988.hp2 others(1): Show |
intron_variant | MODIFIER | c.835-3842delA | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51276607 | |||||||
| chr13:51276744 | T | C | 24 | a0001c0001t0001g0207 a0001c0001t0004g0270 a0001c0001t0005g0148 others(21): Show |
27 | HG00140.hp2 HG00544.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.835-3706T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51276744 | |||||||
| chr13:51276752 | T | C | 23 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0086 others(20): Show |
26 | HG00099.hp1 HG00639.hp1 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.835-3698T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51276752 | |||||||
| chr13:51276786 | CT | C | 14 | a0001c0001t0001g0043 a0001c0001t0001g0174 a0001c0001t0002g0043 others(11): Show |
14 | HG00609.hp2 HG02080.hp1 HG03927.hp2 others(11): Show |
intron_variant | MODIFIER | c.835-3663delT | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51276786 | |||||||
| chr13:51276789 | TG | T | 13 | a0001c0001t0001g0043 a0001c0001t0001g0174 a0001c0001t0002g0043 others(10): Show |
13 | HG00609.hp2 HG02080.hp1 HG03927.hp2 others(10): Show |
intron_variant | MODIFIER | c.835-3660delG | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51276789 | |||||||
| chr13:51276975 | C | T | 2 | a0002c0002t0007g0285 a0002c0002t0009g0286 |
2 | HG01255.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.835-3475C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51276975 | |||||||
| chr13:51276986 | G | A | 79 | a0001c0001t0001g0005 a0001c0001t0001g0043 a0001c0001t0001g0102 others(76): Show |
88 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.835-3464G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51276986 | |||||||
| chr13:51277042 | A | G | 3 | a0001c0009t0020g0110 a0001c0009t0033g0213 a0008c0010t0020g0073 |
3 | HG01884.hp2 HG03209.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.835-3408A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51277042 | |||||||
| chr13:51277048 | G | A | 194 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0024 others(191): Show |
218 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.835-3402G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51277048 | |||||||
| chr13:51277051 | C | T | 72 | a0001c0001t0001g0005 a0001c0001t0001g0043 a0001c0001t0001g0102 others(69): Show |
81 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.835-3399C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51277051 | |||||||
| chr13:51277094 | G | A | 1 | a0001c0001t0025g0296 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.835-3356G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51277094 | |||||||
| chr13:51277103 | G | GA | 25 | a0001c0001t0011g0208 a0001c0001t0012g0003 a0001c0001t0012g0093 others(22): Show |
28 | HG01243.hp1 HG01346.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.835-3338dupA | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr13 | 51277103 | ||||||
| chr13:51277116 | G | A | 2 | a0001c0001t0019g0310 a0002c0002t0019g0242 |
2 | HG01243.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.835-3334G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51277116 | |||||||
| chr13:51277154 | G | A | 1 | a0004c0005t0022g0289 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.835-3296G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51277154 | |||||||
| chr13:51277261 | G | A | 3 | a0001c0007t0001g0030 a0001c0007t0013g0030 a0001c0007t0013g0092 |
3 | HG01891.hp2 HG02647.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.835-3189G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51277261 | |||||||
| chr13:51277337 | G | A | 36 | a0001c0001t0001g0006 a0001c0001t0001g0017 a0001c0001t0001g0086 others(33): Show |
39 | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.835-3113G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51277337 | |||||||
| chr13:51277414 | A | G | 2 | a0001c0001t0007g0047 a0001c0001t0009g0047 |
2 | HG02886.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.835-3036A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51277414 | |||||||
| chr13:51277650 | C | T | 47 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0061 others(44): Show |
55 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.835-2800C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51277650 | |||||||
| chr13:51277665 | G | A | 4 | a0001c0001t0013g0191 a0001c0001t0017g0192 a0003c0003t0008g0199 others(1): Show |
4 | HG01192.hp2 HG01975.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.835-2785G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51277665 | |||||||
| chr13:51277771 | CGACAGAG others(79): Show |
C | 62 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0061 others(59): Show |
71 | HG00140.hp1 HG00323.hp2 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.835-2678_835-2593d others(88): Show |
FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51277771 | |||||||
| chr13:51277780 | G | A | 1 | a0004c0011t0002g0122 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.835-2670G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51277780 | |||||||
| chr13:51277884 | G | A | 24 | a0001c0001t0012g0003 a0001c0001t0012g0093 a0001c0001t0012g0250 others(21): Show |
27 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.835-2566G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51277884 | |||||||
| chr13:51277899 | G | A | 79 | a0001c0001t0001g0005 a0001c0001t0001g0043 a0001c0001t0001g0102 others(76): Show |
88 | HG00099.hp2 HG00408.hp1 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.835-2551G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51277899 | |||||||
| chr13:51278119 | T | C | 1 | a0001c0001t0003g0314 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.835-2331T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51278119 | |||||||
| chr13:51278140 | G | A | 2 | a0002c0002t0007g0285 a0002c0002t0009g0286 |
2 | HG01255.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.835-2310G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51278140 | |||||||
| chr13:51278149 | G | A | 1 | a0001c0001t0001g0261 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.835-2301G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51278149 | |||||||
| chr13:51278318 | G | A | 20 | a0001c0001t0012g0003 a0001c0001t0012g0093 a0001c0001t0012g0250 others(17): Show |
23 | HG01243.hp1 HG01891.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.835-2132G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51278318 | |||||||
| chr13:51278404 | C | T | 1 | a0004c0011t0002g0122 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.835-2046C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51278404 | |||||||
| chr13:51278601 | A | G | 1 | a0003c0003t0024g0197 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.835-1849A>G | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51278601 | |||||||
| chr13:51278619 | A | T | 1 | a0001c0001t0001g0061 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.835-1831A>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51278619 | |||||||
| chr13:51278981 | C | T | 190 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0024 others(187): Show |
214 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.835-1469C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51278981 | |||||||
| chr13:51279180 | T | C | 1 | a0001c0001t0002g0196 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.835-1270T>C | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51279180 | |||||||
| chr13:51279609 | A | T | 23 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0061 others(20): Show |
26 | HG00438.hp2 HG00642.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.835-841A>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51279609 | |||||||
| chr13:51279760 | C | T | 3 | a0001c0001t0002g0049 a0001c0001t0002g0127 a0001c0001t0002g0237 |
4 | HG00597.hp2 NA18945.hp2 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.835-690C>T | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51279760 | |||||||
| chr13:51280168 | G | A | 1 | a0001c0001t0005g0077 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.835-282G>A | FAM124A | ENSG00000150510.17 | transcript | ENST00000322475.13 | protein_coding | 3/3 | chr13 | 51280168 |