Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 11036 |
| ensemblid | ENSG00000242441.8 |
| hgncid | 30727 |
| symbol | GTF2A1L |
| name | general transcription factor IIA subunit 1 like |
| refseq_nuc | NM_006872.5 |
| refseq_prot | NP_006863.2 |
| ensembl_nuc | ENST00000403751.8 |
| ensembl_prot | ENSP00000384597.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 48617856 |
| end | 48679604 |
| strand | + |
| ver | v1.2 |
| region | chr2:48617856-48679604 |
| region5000 | chr2:48612856-48684604 |
| regionname0 | GTF2A1L_chr2_48617856_48679604 |
| regionname5000 | GTF2A1L_chr2_48612856_48684604 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 478 | 265 | 79 | 49 | 94 | 10 | 31 | 67 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | MACLN others(473): Show |
chr2 | 48612856 | 48684604 |
| a0002 | 0/0 | 478 | 67 | 8 | 13 | 33 | 4 | 9 | 24 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | MACLN others(473): Show |
chr2 | 48612856 | 48684604 |
| a0003 | 0/0 | 478 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | MACLN others(473): Show |
chr2 | 48612856 | 48684604 |
| a0004 | 0/0 | 478 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | MACLN others(473): Show |
chr2 | 48612856 | 48684604 |
| a0005 | 0/0 | 478 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | MACLN others(473): Show |
chr2 | 48612856 | 48684604 |
| a0006 | 0/0 | 478 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | MACLN others(473): Show |
chr2 | 48612856 | 48684604 |
| a0007 | 0/0 | 478 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | MACLN others(473): Show |
chr2 | 48612856 | 48684604 |
| a0008 | 0/0 | 478 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | MACLN others(473): Show |
chr2 | 48612856 | 48684604 |
| a0009 | 0/0 | 478 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | MACLN others(473): Show |
chr2 | 48612856 | 48684604 |
| a0010 | 0/0 | 478 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | MACLN others(473): Show |
chr2 | 48612856 | 48684604 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1434 | 243 | 62 | 48 | 93 | 9 | 30 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | ATGGC others(1429): Show |
chr2 | 48612856 | 48684604 | ||
| a0001c0003 | 0/0 | 1434 | 18 | 17 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | ATGGC others(1429): Show |
chr2 | 48612856 | 48684604 | ||
| a0001c0005 | 1/0 | 1434 | 3 | 0 | 0 | 0 | 1 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | ATGGC others(1429): Show |
chr2 | 48612856 | 48684604 | ||
| a0001c0012 | 0/0 | 1434 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | ATGGC others(1429): Show |
chr2 | 48612856 | 48684604 | ||
| a0002c0002 | 0/0 | 1434 | 63 | 8 | 13 | 30 | 4 | 8 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | ATGGC others(1429): Show |
chr2 | 48612856 | 48684604 | ||
| a0002c0006 | 0/0 | 1434 | 3 | 0 | 0 | 3 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | ATGGC others(1429): Show |
chr2 | 48612856 | 48684604 | ||
| a0002c0014 | 0/0 | 1434 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | ATGGC others(1429): Show |
chr2 | 48612856 | 48684604 | ||
| a0003c0004 | 0/0 | 1434 | 3 | 1 | 2 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | ATGGC others(1429): Show |
chr2 | 48612856 | 48684604 | ||
| a0004c0007 | 0/0 | 1434 | 2 | 0 | 2 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | ATGGC others(1429): Show |
chr2 | 48612856 | 48684604 | ||
| a0005c0008 | 0/0 | 1434 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | ATGGC others(1429): Show |
chr2 | 48612856 | 48684604 | ||
| a0006c0009 | 0/0 | 1434 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | ATGGC others(1429): Show |
chr2 | 48612856 | 48684604 | ||
| a0007c0013 | 0/0 | 1434 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | ATGGC others(1429): Show |
chr2 | 48612856 | 48684604 | ||
| a0008c0011 | 0/0 | 1434 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | ATGGC others(1429): Show |
chr2 | 48612856 | 48684604 | ||
| a0009c0015 | 0/0 | 1434 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | ATGGC others(1429): Show |
chr2 | 48612856 | 48684604 | ||
| a0010c0010 | 0/0 | 1434 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | ATGGC others(1429): Show |
chr2 | 48612856 | 48684604 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1618 | 223 | 44 | 46 | 93 | 9 | 30 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | AGGTG others(1613): Show |
chr2 | 48612856 | 48684604 |
| a0001c0001t0002 | 0/0 | 1618 | 17 | 16 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | AGGTG others(1613): Show |
chr2 | 48612856 | 48684604 |
| a0001c0001t0004 | 0/0 | 1618 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | AGGTG others(1613): Show |
chr2 | 48612856 | 48684604 |
| a0001c0001t0005 | 0/0 | 1618 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | AGGTG others(1613): Show |
chr2 | 48612856 | 48684604 |
| a0001c0001t0006 | 0/0 | 1618 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | TGGTG others(1613): Show |
chr2 | 48612856 | 48684604 |
| a0001c0003t0001 | 0/0 | 1618 | 18 | 17 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | AGGTG others(1613): Show |
chr2 | 48612856 | 48684604 |
| a0001c0005t0003 | 1/0 | 1618 | 3 | 0 | 0 | 0 | 1 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | AGGTG others(1613): Show |
chr2 | 48612856 | 48684604 |
| a0001c0012t0001 | 0/0 | 1618 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | AGGTG others(1613): Show |
chr2 | 48612856 | 48684604 |
| a0002c0002t0001 | 0/0 | 1618 | 63 | 8 | 13 | 30 | 4 | 8 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | AGGTG others(1613): Show |
chr2 | 48612856 | 48684604 |
| a0002c0006t0001 | 0/0 | 1618 | 3 | 0 | 0 | 3 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | AGGTG others(1613): Show |
chr2 | 48612856 | 48684604 |
| a0002c0014t0001 | 0/0 | 1618 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | AGGTG others(1613): Show |
chr2 | 48612856 | 48684604 |
| a0003c0004t0001 | 0/0 | 1618 | 3 | 1 | 2 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | AGGTG others(1613): Show |
chr2 | 48612856 | 48684604 |
| a0004c0007t0001 | 0/0 | 1618 | 2 | 0 | 2 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | AGGTG others(1613): Show |
chr2 | 48612856 | 48684604 |
| a0005c0008t0002 | 0/0 | 1618 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | AGGTG others(1613): Show |
chr2 | 48612856 | 48684604 |
| a0006c0009t0001 | 0/0 | 1618 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | AGGTG others(1613): Show |
chr2 | 48612856 | 48684604 |
| a0007c0013t0001 | 0/0 | 1618 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | AGGTG others(1613): Show |
chr2 | 48612856 | 48684604 |
| a0008c0011t0001 | 0/0 | 1618 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | AGGTG others(1613): Show |
chr2 | 48612856 | 48684604 |
| a0009c0015t0001 | 0/0 | 1618 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | AGGTG others(1613): Show |
chr2 | 48612856 | 48684604 |
| a0010c0010t0001 | 0/0 | 1618 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | AGGTG others(1613): Show |
chr2 | 48612856 | 48684604 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/1 | 4 | 0 | 0 | 1 | 1 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0004g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0005g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0001t0006g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0003t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0003t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0003t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0003t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0003t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0003t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0003t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0003t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0003t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0003t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0003t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0003t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0003t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0003t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0003t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0003t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0003t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0003t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0005t0003g0083 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0005t0003g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0005t0003g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0001c0012t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0002t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0006t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0006t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0006t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0002c0014t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0003c0004t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0003c0004t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0003c0004t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0004c0007t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0004c0007t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0005c0008t0002g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0005c0008t0002g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0006c0009t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0007c0013t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0008c0011t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0009c0015t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| a0010c0010t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0033 | EUR | GBR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0134 | EUR | GBR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG00140 | hp1 | a0002 | c0002 | t0001 | g0114 | EUR | GBR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0185 | EUR | GBR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0037 | EUR | FIN | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0052 | EUR | FIN | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | CHS | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | CHS | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | CHS | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | CHS | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CHS | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0311 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG00733 | hp1 | a0004 | c0007 | t0001 | g0027 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0139 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0227 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG00741 | hp1 | a0001 | c0001 | t0005 | g0129 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0113 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01070 | hp1 | a0003 | c0004 | t0001 | g0063 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0206 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01168 | hp1 | a0002 | c0002 | t0001 | g0203 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01168 | hp2 | a0004 | c0007 | t0001 | g0028 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01243 | hp1 | a0001 | c0003 | t0001 | g0072 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0092 | AMR | PUR | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0262 | AMR | CLM | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0218 | AMR | CLM | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0221 | AMR | CLM | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0226 | AMR | CLM | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0307 | AMR | CLM | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | CLM | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01433 | hp2 | a0002 | c0002 | t0001 | g0188 | AMR | CLM | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0219 | AMR | CLM | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01496 | hp2 | a0002 | c0002 | t0001 | g0142 | AMR | CLM | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0112 | EUR | IBS | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0210 | EUR | IBS | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ACB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01891 | hp1 | a0001 | c0003 | t0001 | g0061 | AFR | ACB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01891 | hp2 | a0001 | c0001 | t0004 | g0174 | AFR | ACB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | PEL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0194 | AMR | PEL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PEL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | KHV | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0216 | EAS | KHV | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0161 | AFR | ACB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | ACB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | KHV | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02083 | hp1 | a0002 | c0002 | t0001 | g0207 | EAS | KHV | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02129 | hp2 | a0002 | c0006 | t0001 | g0093 | EAS | KHV | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0229 | EAS | KHV | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02135 | hp1 | a0002 | c0002 | t0001 | g0213 | EAS | KHV | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | ACB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | ACB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CDX | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0237 | EAS | CDX | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | ACB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02280 | hp1 | a0002 | c0002 | t0001 | g0228 | AFR | ACB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | ACB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | ACB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | ACB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02523 | hp1 | a0001 | c0012 | t0001 | g0242 | EAS | KHV | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02572 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02602 | hp2 | a0006 | c0009 | t0001 | g0152 | SAS | PJL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02615 | hp2 | a0001 | c0003 | t0001 | g0018 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0090 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02622 | hp2 | a0001 | c0003 | t0001 | g0077 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0319 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0176 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0313 | SAS | PJL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0209 | SAS | PJL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02717 | hp2 | a0007 | c0013 | t0001 | g0280 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02723 | hp2 | a0001 | c0003 | t0001 | g0069 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0225 | SAS | PJL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0268 | SAS | PJL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02738 | hp2 | a0002 | c0002 | t0001 | g0144 | SAS | PJL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02809 | hp1 | a0001 | c0003 | t0001 | g0076 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0211 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02818 | hp1 | a0001 | c0003 | t0001 | g0075 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02818 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02896 | hp1 | a0001 | c0003 | t0001 | g0079 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0320 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02897 | hp2 | a0001 | c0003 | t0001 | g0078 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02922 | hp1 | a0001 | c0003 | t0001 | g0066 | AFR | ESN | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0178 | AFR | ESN | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0321 | AFR | ESN | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0082 | AFR | ESN | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02976 | hp1 | a0005 | c0008 | t0002 | g0303 | AFR | ESN | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0172 | AFR | ESN | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0098 | SAS | PJL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0193 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG03098 | hp1 | a0005 | c0008 | t0002 | g0302 | AFR | MSL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG03098 | hp2 | a0001 | c0003 | t0001 | g0062 | AFR | MSL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG03130 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | ESN | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0260 | AFR | ESN | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0179 | AFR | ESN | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | ESN | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0102 | AFR | MSL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0182 | AFR | MSL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | MSL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0191 | SAS | PJL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0177 | AFR | MSL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | MSL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG03516 | hp1 | a0002 | c0002 | t0001 | g0208 | AFR | ESN | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0081 | AFR | ESN | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | GWD | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | MSL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | MSL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG03654 | hp2 | a0002 | c0014 | t0001 | g0195 | SAS | PJL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0304 | SAS | PJL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG03831 | hp1 | a0002 | c0002 | t0001 | g0217 | SAS | BEB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0305 | SAS | BEB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | BEB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | BEB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0312 | SAS | BEB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG04115 | hp1 | a0001 | c0005 | t0003 | g0087 | SAS | STU | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | STU | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | BEB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0141 | SAS | BEB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | STU | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | STU | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | STU | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0314 | SAS | STU | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | STU | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG04228 | hp2 | a0008 | c0011 | t0001 | g0048 | SAS | STU | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18522 | hp1 | a0001 | c0003 | t0001 | g0064 | AFR | YRI | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | YRI | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | CHB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | CHB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | CHB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0235 | EAS | CHB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18906 | hp1 | a0001 | c0003 | t0001 | g0067 | AFR | YRI | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | YRI | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18940 | hp2 | a0002 | c0006 | t0001 | g0091 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18941 | hp1 | a0002 | c0002 | t0001 | g0187 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18947 | hp1 | a0002 | c0002 | t0001 | g0171 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18950 | hp2 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18951 | hp1 | a0002 | c0002 | t0001 | g0236 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18953 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18954 | hp2 | a0002 | c0002 | t0001 | g0256 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0214 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18961 | hp1 | a0002 | c0002 | t0001 | g0200 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18968 | hp2 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18969 | hp2 | a0002 | c0002 | t0001 | g0205 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0204 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18971 | hp2 | a0002 | c0002 | t0001 | g0233 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18975 | hp2 | a0002 | c0002 | t0001 | g0189 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18982 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18998 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0192 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA19002 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA19010 | hp2 | a0009 | c0015 | t0001 | g0164 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0181 | AFR | LWK | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA19030 | hp2 | a0001 | c0003 | t0001 | g0071 | AFR | LWK | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA19043 | hp1 | a0001 | c0001 | t0006 | g0289 | AFR | LWK | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | LWK | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA19063 | hp2 | a0002 | c0002 | t0001 | g0212 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA19079 | hp1 | a0002 | c0006 | t0001 | g0094 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA19080 | hp1 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA19087 | hp1 | a0002 | c0002 | t0001 | g0232 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA19240 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | YRI | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0300 | AFR | ASW | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ASW | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA20752 | hp1 | a0001 | c0005 | t0003 | g0084 | EUR | TSI | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA20805 | hp1 | a0002 | c0002 | t0001 | g0140 | EUR | TSI | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0308 | EUR | TSI | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0111 | SAS | GIH | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | GIH | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01123 | hp1 | a0003 | c0004 | t0001 | g0080 | AMR | CLM | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0263 | AMR | CLM | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02486 | hp2 | a0001 | c0003 | t0001 | g0074 | AFR | ACB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0295 | AFR | ACB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0180 | AFR | ACB | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG03471 | hp1 | a0001 | c0003 | t0001 | g0070 | AFR | MSL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0104 | AFR | MSL | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0175 | AFR | USA | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| HG06807 | hp2 | a0001 | c0003 | t0001 | g0073 | AFR | USA | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA20300 | hp1 | a0001 | c0003 | t0001 | g0068 | AFR | USA | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA20300 | hp2 | a0010 | c0010 | t0001 | g0297 | AFR | USA | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA21309 | hp1 | a0003 | c0004 | t0001 | g0065 | AFR | LWK | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | LWK | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0001 | REF | REF | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| homoSapiens_grch38 | hp1 | a0001 | c0005 | t0003 | g0083 | REF | REF | GTF2A1L_chr2_48612856_48684604 | GTF2A1L | chr2 | 48612856 | 48684604 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:48645091 | C | T | 1 | a0009 | 1 | NA19010.hp2 | missense_variant | MODERATE | c.362C>T | p.Ala121Val | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 5/9 | 381/1618 | 362/1437 | 121/478 | chr2 | 48645091 | |||
| chr2:48646746 | G | T | 1 | a0005 | 2 | HG02976.hp1 HG03098.hp1 |
missense_variant | MODERATE | c.682G>T | p.Val228Leu | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/9 | 701/1618 | 682/1437 | 228/478 | chr2 | 48646746 | |||
| chr2:48646786 | A | G | 1 | a0003 | 3 | HG01070.hp1 HG01123.hp1 NA21309.hp1 |
missense_variant | MODERATE | c.722A>G | p.Tyr241Cys | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/9 | 741/1618 | 722/1437 | 241/478 | chr2 | 48646786 | |||
| chr2:48646839 | A | G | 1 | a0002 | 67 | HG00140.hp1 HG00609.hp2 HG00733.hp2 others(64): Show |
missense_variant | MODERATE | c.775A>G | p.Asn259Asp | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/9 | 794/1618 | 775/1437 | 259/478 | chr2 | 48646839 | |||
| chr2:48646921 | C | T | 1 | a0007 | 1 | HG02717.hp2 | missense_variant | MODERATE | c.857C>T | p.Ala286Val | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/9 | 876/1618 | 857/1437 | 286/478 | chr2 | 48646921 | |||
| chr2:48669758 | A | G | 1 | a0004 | 2 | HG00733.hp1 HG01168.hp2 |
missense_variant | MODERATE | c.1015A>G | p.Thr339Ala | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 7/9 | 1034/1618 | 1015/1437 | 339/478 | chr2 | 48669758 | |||
| chr2:48669776 | G | A | 1 | a0006 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.1033G>A | p.Glu345Lys | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 7/9 | 1052/1618 | 1033/1437 | 345/478 | chr2 | 48669776 | |||
| chr2:48669798 | G | A | 1 | a0010 | 1 | NA20300.hp2 | missense_variant | MODERATE | c.1055G>A | p.Ser352Asn | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 7/9 | 1074/1618 | 1055/1437 | 352/478 | chr2 | 48669798 | |||
| chr2:48669908 | G | A | 1 | a0008 | 1 | HG04228.hp2 | missense_variant | MODERATE | c.1165G>A | p.Asp389Asn | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 7/9 | 1184/1618 | 1165/1437 | 389/478 | chr2 | 48669908 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:48620904 | A | T | 1 | a0002c0006 | 3 | HG02129.hp2 NA18940.hp2 NA19079.hp1 |
synonymous_variant | LOW | c.75A>T | p.Leu25Leu | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 2/9 | 94/1618 | 75/1437 | 25/478 | chr2 | 48620904 | |||
| chr2:48646523 | T | C | 2 | a0001c0003 a0003c0004 |
21 | HG01070.hp1 HG01123.hp1 HG01243.hp1 others(18): Show |
synonymous_variant | LOW | c.459T>C | p.His153His | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/9 | 478/1618 | 459/1437 | 153/478 | chr2 | 48646523 | |||
| chr2:48646868 | T | C | 1 | a0002c0014 | 1 | HG03654.hp2 | synonymous_variant | LOW | c.804T>C | p.Ala268Ala | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/9 | 823/1618 | 804/1437 | 268/478 | chr2 | 48646868 | |||
| chr2:48669874 | C | T | 1 | a0001c0012 | 1 | HG02523.hp1 | synonymous_variant | LOW | c.1131C>T | p.Asp377Asp | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 7/9 | 1150/1618 | 1131/1437 | 377/478 | chr2 | 48669874 | |||
| chr2:48671659 | T | A | 14 | a0001c0001 a0001c0003 a0001c0012 others(11): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
synonymous_variant | LOW | c.1308T>A | p.Val436Val | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/9 | 1327/1618 | 1308/1437 | 436/478 | chr2 | 48671659 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:48617856 | A | T | 1 | a0001c0001t0006 | 1 | NA19043.hp1 | 5_prime_UTR_variant | MODIFIER | c.-19A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/9 | 19 | chr2 | 48617856 | ||||||
| chr2:48617862 | T | C | 1 | a0001c0001t0004 | 1 | HG01891.hp2 | 5_prime_UTR_variant | MODIFIER | c.-13T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/9 | 13 | chr2 | 48617862 | ||||||
| chr2:48679459 | A | G | 1 | a0001c0001t0005 | 1 | HG00741.hp1 | 3_prime_UTR_variant | MODIFIER | c.*17A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 9/9 | 17 | chr2 | 48679459 | ||||||
| chr2:48679486 | T | C | 18 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(15): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
3_prime_UTR_variant | MODIFIER | c.*44T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 9/9 | 44 | chr2 | 48679486 | ||||||
| chr2:48679554 | G | T | 3 | a0001c0001t0002 a0001c0001t0004 a0005c0008t0002 |
20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*112G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 9/9 | 112 | chr2 | 48679554 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:48617980 | C | T | 1 | a0001c0001t0001g0321 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.21+85C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48617980 | |||||||
| chr2:48618093 | G | A | 1 | a0001c0001t0001g0017 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.21+198G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48618093 | |||||||
| chr2:48618108 | A | G | 18 | a0001c0001t0001g0016 a0001c0001t0001g0304 a0001c0001t0001g0305 others(15): Show |
19 | HG00642.hp1 HG01361.hp2 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.21+213A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48618108 | |||||||
| chr2:48618244 | C | T | 2 | a0005c0008t0002g0302 a0005c0008t0002g0303 |
2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.21+349C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48618244 | |||||||
| chr2:48618522 | C | A | 65 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(62): Show |
69 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.21+627C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48618522 | |||||||
| chr2:48618523 | C | G | 65 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(62): Show |
69 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.21+628C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48618523 | |||||||
| chr2:48618567 | C | T | 42 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(39): Show |
46 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(43): Show |
intron_variant | MODIFIER | c.21+672C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48618567 | |||||||
| chr2:48618754 | A | T | 18 | a0001c0001t0001g0016 a0001c0001t0001g0304 a0001c0001t0001g0305 others(15): Show |
19 | HG00642.hp1 HG01361.hp2 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.21+859A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48618754 | |||||||
| chr2:48618867 | C | G | 2 | a0005c0008t0002g0302 a0005c0008t0002g0303 |
2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.21+972C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48618867 | |||||||
| chr2:48618879 | C | T | 109 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(106): Show |
117 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.21+984C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48618879 | |||||||
| chr2:48618945 | G | GT | 7 | a0001c0001t0001g0015 a0001c0001t0001g0274 a0001c0001t0001g0275 others(4): Show |
8 | HG01175.hp2 HG01934.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.21+1056dupT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 48618945 | ||||||
| chr2:48618957 | G | A | 1 | a0007c0013t0001g0280 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.21+1062G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48618957 | |||||||
| chr2:48619049 | A | C | 1 | a0002c0002t0001g0014 | 2 | NA18962.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.21+1154A>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48619049 | |||||||
| chr2:48619069 | T | G | 2 | a0001c0001t0002g0081 a0001c0001t0002g0082 |
2 | HG02970.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.21+1174T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48619069 | |||||||
| chr2:48619134 | C | A | 1 | a0001c0003t0001g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.21+1239C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48619134 | |||||||
| chr2:48619224 | C | T | 315 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(312): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.21+1329C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48619224 | |||||||
| chr2:48619343 | G | A | 2 | a0005c0008t0002g0302 a0005c0008t0002g0303 |
2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.21+1448G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48619343 | |||||||
| chr2:48619360 | C | T | 1 | a0001c0001t0001g0301 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.21+1465C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48619360 | |||||||
| chr2:48619432 | C | T | 315 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(312): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.22-1419C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48619432 | |||||||
| chr2:48619469 | C | CA | 54 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(51): Show |
58 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.22-1369dupA | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 48619469 | ||||||
| chr2:48619477 | A | T | 1 | a0007c0013t0001g0280 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.22-1374A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48619477 | |||||||
| chr2:48619480 | A | T | 20 | a0001c0001t0001g0016 a0001c0001t0001g0272 a0001c0001t0001g0273 others(17): Show |
21 | HG00597.hp2 HG00642.hp1 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.22-1371A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48619480 | |||||||
| chr2:48619483 | T | A | 22 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0020 others(19): Show |
25 | HG00597.hp1 HG00738.hp2 HG01106.hp2 others(22): Show |
intron_variant | MODIFIER | c.22-1368T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48619483 | |||||||
| chr2:48619486 | T | A | 4 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(1): Show |
4 | HG02055.hp2 HG02145.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.22-1365T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48619486 | |||||||
| chr2:48619496 | A | T | 1 | a0003c0004t0001g0080 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.22-1355A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48619496 | |||||||
| chr2:48619498 | A | T | 39 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(36): Show |
43 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.22-1353A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48619498 | |||||||
| chr2:48619508 | C | T | 3 | a0001c0001t0006g0289 a0005c0008t0002g0302 a0005c0008t0002g0303 |
3 | HG02976.hp1 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.22-1343C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48619508 | |||||||
| chr2:48619551 | T | G | 1 | a0001c0001t0001g0023 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.22-1300T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48619551 | |||||||
| chr2:48619582 | G | A | 1 | a0001c0001t0001g0024 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.22-1269G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48619582 | |||||||
| chr2:48619685 | G | C | 3 | a0001c0001t0006g0289 a0005c0008t0002g0302 a0005c0008t0002g0303 |
3 | HG02976.hp1 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.22-1166G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48619685 | |||||||
| chr2:48619758 | G | A | 3 | a0001c0001t0006g0289 a0005c0008t0002g0302 a0005c0008t0002g0303 |
3 | HG02976.hp1 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.22-1093G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48619758 | |||||||
| chr2:48619833 | G | T | 1 | a0001c0001t0001g0058 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.22-1018G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48619833 | |||||||
| chr2:48619913 | A | T | 12 | a0001c0001t0001g0017 a0001c0001t0001g0290 a0001c0001t0001g0291 others(9): Show |
12 | HG01074.hp1 HG01109.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.22-938A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48619913 | |||||||
| chr2:48619929 | G | A | 7 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.22-922G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48619929 | |||||||
| chr2:48619958 | C | T | 2 | a0001c0001t0001g0270 a0001c0001t0001g0271 |
2 | HG01106.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.22-893C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48619958 | |||||||
| chr2:48620035 | G | A | 12 | a0001c0001t0001g0016 a0001c0001t0001g0304 a0001c0001t0001g0305 others(9): Show |
13 | HG00642.hp1 HG01361.hp2 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.22-816G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48620035 | |||||||
| chr2:48620218 | A | G | 3 | a0001c0001t0006g0289 a0005c0008t0002g0302 a0005c0008t0002g0303 |
3 | HG02976.hp1 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.22-633A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48620218 | |||||||
| chr2:48620394 | T | C | 2 | a0001c0001t0001g0006 a0001c0001t0001g0100 |
3 | NA18942.hp1 NA18974.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.22-457T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48620394 | |||||||
| chr2:48620487 | G | A | 3 | a0001c0001t0006g0289 a0005c0008t0002g0302 a0005c0008t0002g0303 |
3 | HG02976.hp1 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.22-364G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48620487 | |||||||
| chr2:48620593 | CA | C | 3 | a0001c0001t0006g0289 a0005c0008t0002g0302 a0005c0008t0002g0303 |
3 | HG02976.hp1 HG03098.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.22-257delA | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48620593 | |||||||
| chr2:48620729 | T | A | 47 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(44): Show |
51 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.22-122T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48620729 | |||||||
| chr2:48620731 | C | T | 2 | a0001c0001t0001g0268 a0001c0001t0001g0269 |
2 | HG02602.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.22-120C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | chr2 | 48620731 | |||||||
| chr2:48620779 | G | GAATA | 111 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(108): Show |
122 | HG00140.hp2 HG00423.hp2 HG00609.hp2 others(119): Show |
intron_variant | MODIFIER | c.22-33_22-30dupTAAA | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 48620779 | ||||||
| chr2:48620779 | G | GAATAAAT others(1): Show |
46 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0095 others(43): Show |
50 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.22-37_22-30dupTAAA others(4): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 48620779 | ||||||
| chr2:48620779 | G | GAATAAAT others(5): Show |
4 | a0001c0001t0001g0264 a0001c0001t0001g0265 a0001c0001t0001g0266 others(1): Show |
4 | HG03654.hp1 NA19000.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.22-41_22-30dupTAAA others(8): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 48620779 | ||||||
| chr2:48620779 | GAATA | G | 53 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(50): Show |
57 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.22-33_22-30delTAAA | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 48620779 | ||||||
| chr2:48620779 | GAATAAAT others(5): Show |
G | 1 | a0001c0001t0001g0101 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.22-41_22-30delTAAA others(8): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr2 | 48620779 | ||||||
| chr2:48621018 | T | C | 12 | a0001c0001t0001g0017 a0001c0001t0001g0290 a0001c0001t0001g0291 others(9): Show |
12 | HG01074.hp1 HG01109.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.123+66T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 2/8 | chr2 | 48621018 | |||||||
| chr2:48621146 | CT | C | 12 | a0001c0001t0001g0017 a0001c0001t0001g0290 a0001c0001t0001g0291 others(9): Show |
12 | HG01074.hp1 HG01109.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.124-12delT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr2 | 48621146 | ||||||
| chr2:48621156 | C | T | 47 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(44): Show |
51 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.124-11C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 2/8 | chr2 | 48621156 | |||||||
| chr2:48621376 | G | C | 66 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0086 others(63): Show |
68 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.247+86G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48621376 | |||||||
| chr2:48621409 | C | G | 2 | a0005c0008t0002g0302 a0005c0008t0002g0303 |
2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.247+119C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48621409 | |||||||
| chr2:48621501 | T | C | 208 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(205): Show |
223 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.247+211T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48621501 | |||||||
| chr2:48621657 | G | A | 2 | a0005c0008t0002g0302 a0005c0008t0002g0303 |
2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.247+367G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48621657 | |||||||
| chr2:48621695 | G | A | 4 | a0001c0003t0001g0018 a0001c0003t0001g0070 a0001c0003t0001g0071 others(1): Show |
4 | HG01243.hp1 HG02615.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.247+405G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48621695 | |||||||
| chr2:48621927 | C | G | 248 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(245): Show |
267 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(264): Show |
intron_variant | MODIFIER | c.247+637C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48621927 | |||||||
| chr2:48621985 | A | G | 47 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(44): Show |
51 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.247+695A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48621985 | |||||||
| chr2:48622014 | C | T | 5 | a0002c0002t0001g0012 a0002c0002t0001g0159 a0002c0002t0001g0235 others(2): Show |
6 | HG02027.hp2 HG02165.hp2 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.247+724C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48622014 | |||||||
| chr2:48622206 | G | T | 8 | a0001c0001t0001g0017 a0001c0001t0001g0290 a0001c0001t0001g0291 others(5): Show |
8 | HG01074.hp1 HG01884.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.247+916G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48622206 | |||||||
| chr2:48622415 | A | G | 12 | a0001c0001t0001g0016 a0001c0001t0001g0304 a0001c0001t0001g0305 others(9): Show |
13 | HG00642.hp1 HG01361.hp2 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.247+1125A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48622415 | |||||||
| chr2:48622499 | A | T | 1 | a0007c0013t0001g0280 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.247+1209A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48622499 | |||||||
| chr2:48622505 | G | GT | 6 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 others(3): Show |
6 | HG02145.hp2 HG02630.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.247+1222dupT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 48622505 | ||||||
| chr2:48622689 | C | T | 1 | a0001c0001t0001g0293 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.247+1399C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48622689 | |||||||
| chr2:48622694 | C | T | 2 | a0005c0008t0002g0302 a0005c0008t0002g0303 |
2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.247+1404C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48622694 | |||||||
| chr2:48622790 | C | T | 1 | a0001c0001t0001g0255 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.247+1500C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48622790 | |||||||
| chr2:48622809 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.247+1519G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48622809 | |||||||
| chr2:48622812 | C | T | 39 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(36): Show |
43 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.247+1522C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48622812 | |||||||
| chr2:48622833 | T | TA | 106 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(103): Show |
112 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.247+1560dupA | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 48622833 | ||||||
| chr2:48622943 | A | AAT | 315 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(312): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.247+1654_247+1655i others(4): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 48622943 | ||||||
| chr2:48623091 | T | G | 86 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(83): Show |
94 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.247+1801T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48623091 | |||||||
| chr2:48623095 | A | G | 2 | a0001c0001t0001g0085 a0001c0001t0001g0086 |
2 | NA18940.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.247+1805A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48623095 | |||||||
| chr2:48623326 | C | T | 12 | a0001c0001t0001g0017 a0001c0001t0001g0290 a0001c0001t0001g0291 others(9): Show |
12 | HG01074.hp1 HG01109.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.247+2036C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48623326 | |||||||
| chr2:48623469 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.247+2179G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48623469 | |||||||
| chr2:48623615 | T | C | 1 | a0001c0001t0001g0026 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.247+2325T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48623615 | |||||||
| chr2:48623630 | A | G | 1 | a0001c0001t0001g0184 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.247+2340A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48623630 | |||||||
| chr2:48623650 | C | G | 1 | a0001c0001t0001g0184 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.247+2360C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48623650 | |||||||
| chr2:48623675 | G | C | 207 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(204): Show |
222 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(219): Show |
intron_variant | MODIFIER | c.247+2385G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48623675 | |||||||
| chr2:48623775 | G | T | 1 | a0001c0001t0001g0158 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.247+2485G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48623775 | |||||||
| chr2:48623787 | A | G | 1 | a0007c0013t0001g0280 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.247+2497A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48623787 | |||||||
| chr2:48623872 | G | A | 2 | a0005c0008t0002g0302 a0005c0008t0002g0303 |
2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.247+2582G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48623872 | |||||||
| chr2:48623944 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.247+2654C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48623944 | |||||||
| chr2:48624024 | G | A | 2 | a0005c0008t0002g0302 a0005c0008t0002g0303 |
2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.247+2734G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48624024 | |||||||
| chr2:48624045 | C | G | 3 | a0002c0006t0001g0091 a0002c0006t0001g0093 a0002c0006t0001g0094 |
3 | HG02129.hp2 NA18940.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.247+2755C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48624045 | |||||||
| chr2:48624051 | CTAAACCC others(6755): Show |
C | 45 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(42): Show |
49 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.247+2764_247+9525d others(2): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 48624051 | ||||||
| chr2:48624233 | TAAAAC | T | 2 | a0002c0002t0001g0002 a0002c0002t0001g0188 |
5 | HG01433.hp2 HG02572.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.247+2948_247+2952d others(7): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 48624233 | ||||||
| chr2:48624378 | T | C | 41 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(38): Show |
45 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.247+3088T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48624378 | |||||||
| chr2:48624381 | C | A | 2 | a0005c0008t0002g0302 a0005c0008t0002g0303 |
2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.247+3091C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48624381 | |||||||
| chr2:48624402 | T | C | 3 | a0001c0001t0001g0190 a0002c0002t0001g0189 a0002c0002t0001g0256 |
3 | NA18953.hp1 NA18954.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.247+3112T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48624402 | |||||||
| chr2:48624457 | G | C | 1 | a0002c0002t0001g0191 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.247+3167G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48624457 | |||||||
| chr2:48624459 | T | TATAGATA others(9): Show |
1 | a0005c0008t0002g0303 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.247+3182_247+3197d others(18): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 48624459 | ||||||
| chr2:48624459 | T | TATAGATA others(13): Show |
1 | a0005c0008t0002g0302 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.247+3178_247+3197d others(22): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 48624459 | ||||||
| chr2:48624459 | TATAG | T | 205 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(202): Show |
220 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.247+3194_247+3197d others(6): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 48624459 | ||||||
| chr2:48624467 | G | T | 3 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0234 |
3 | HG03710.hp1 HG04199.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.247+3177G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48624467 | |||||||
| chr2:48624681 | G | T | 267 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(264): Show |
286 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.247+3391G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48624681 | |||||||
| chr2:48624762 | GTT | G | 267 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(264): Show |
286 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.247+3483_247+3484d others(4): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 48624762 | ||||||
| chr2:48624999 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.247+3709G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48624999 | |||||||
| chr2:48625331 | G | C | 1 | a0002c0002t0001g0193 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.247+4041G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48625331 | |||||||
| chr2:48625393 | T | A | 1 | a0001c0001t0001g0096 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.247+4103T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48625393 | |||||||
| chr2:48625421 | T | C | 1 | a0001c0001t0001g0238 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.247+4131T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48625421 | |||||||
| chr2:48625604 | G | A | 2 | a0005c0008t0002g0302 a0005c0008t0002g0303 |
2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.247+4314G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48625604 | |||||||
| chr2:48625639 | G | A | 3 | a0001c0001t0001g0017 a0001c0001t0001g0290 a0001c0001t0001g0291 |
3 | HG01884.hp1 HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.247+4349G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48625639 | |||||||
| chr2:48625696 | C | A | 1 | a0001c0001t0001g0273 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.247+4406C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48625696 | |||||||
| chr2:48625713 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.247+4423A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48625713 | |||||||
| chr2:48625788 | G | A | 2 | a0001c0003t0001g0073 a0001c0003t0001g0074 |
2 | HG02486.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.247+4498G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48625788 | |||||||
| chr2:48625845 | A | T | 3 | a0002c0002t0001g0011 a0002c0002t0001g0232 a0002c0002t0001g0233 |
4 | NA18971.hp2 NA18998.hp1 NA19085.hp1 others(1): Show |
intron_variant | MODIFIER | c.247+4555A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48625845 | |||||||
| chr2:48625869 | G | A | 6 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 others(3): Show |
6 | HG02145.hp2 HG02630.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.247+4579G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48625869 | |||||||
| chr2:48625893 | C | T | 7 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.247+4603C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48625893 | |||||||
| chr2:48625906 | C | T | 2 | a0005c0008t0002g0302 a0005c0008t0002g0303 |
2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.247+4616C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48625906 | |||||||
| chr2:48626218 | C | A | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG00558.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.247+4928C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48626218 | |||||||
| chr2:48626221 | C | T | 19 | a0001c0001t0001g0006 a0001c0001t0001g0096 a0001c0001t0001g0097 others(16): Show |
20 | HG00423.hp1 HG02015.hp1 HG02056.hp2 others(17): Show |
intron_variant | MODIFIER | c.247+4931C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48626221 | |||||||
| chr2:48626251 | A | G | 1 | a0002c0002t0001g0229 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.247+4961A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48626251 | |||||||
| chr2:48626388 | C | A | 269 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(266): Show |
288 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.247+5098C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48626388 | |||||||
| chr2:48626388 | C | T | 1 | a0001c0001t0001g0276 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.247+5098C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48626388 | |||||||
| chr2:48626469 | A | G | 39 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(36): Show |
43 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.247+5179A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48626469 | |||||||
| chr2:48626474 | C | G | 3 | a0002c0006t0001g0091 a0002c0006t0001g0093 a0002c0006t0001g0094 |
3 | HG02129.hp2 NA18940.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.247+5184C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48626474 | |||||||
| chr2:48626492 | T | C | 1 | a0001c0001t0001g0160 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.247+5202T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48626492 | |||||||
| chr2:48626657 | C | A | 1 | a0002c0002t0001g0194 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.247+5367C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48626657 | |||||||
| chr2:48626690 | G | A | 1 | a0002c0014t0001g0195 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.247+5400G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48626690 | |||||||
| chr2:48626758 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.247+5468G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48626758 | |||||||
| chr2:48626782 | C | T | 1 | a0007c0013t0001g0280 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.247+5492C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48626782 | |||||||
| chr2:48626922 | T | C | 18 | a0001c0001t0001g0016 a0001c0001t0001g0304 a0001c0001t0001g0305 others(15): Show |
19 | HG00642.hp1 HG01361.hp2 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.247+5632T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48626922 | |||||||
| chr2:48626959 | C | G | 270 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(267): Show |
289 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(286): Show |
intron_variant | MODIFIER | c.247+5669C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48626959 | |||||||
| chr2:48627094 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.247+5804C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48627094 | |||||||
| chr2:48627108 | T | C | 2 | a0005c0008t0002g0302 a0005c0008t0002g0303 |
2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.247+5818T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48627108 | |||||||
| chr2:48627114 | T | A | 1 | a0001c0001t0001g0310 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.247+5824T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48627114 | |||||||
| chr2:48627154 | T | A | 1 | a0002c0002t0001g0189 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.247+5864T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48627154 | |||||||
| chr2:48627372 | A | T | 1 | a0001c0001t0001g0281 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.247+6082A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48627372 | |||||||
| chr2:48627490 | C | A | 4 | a0002c0002t0001g0111 a0002c0002t0001g0112 a0002c0002t0001g0113 others(1): Show |
4 | HG00140.hp1 HG00741.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.247+6200C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48627490 | |||||||
| chr2:48627502 | T | G | 3 | a0001c0001t0001g0006 a0001c0001t0001g0100 a0001c0001t0001g0145 |
4 | NA18942.hp1 NA18974.hp2 NA19007.hp1 others(1): Show |
intron_variant | MODIFIER | c.247+6212T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48627502 | |||||||
| chr2:48627503 | G | C | 8 | a0001c0001t0001g0013 a0001c0001t0001g0196 a0001c0001t0001g0197 others(5): Show |
9 | HG02451.hp2 HG02886.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.247+6213G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48627503 | |||||||
| chr2:48627538 | C | A | 20 | a0001c0003t0001g0018 a0001c0003t0001g0062 a0001c0003t0001g0064 others(17): Show |
20 | HG01070.hp1 HG01123.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.247+6248C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48627538 | |||||||
| chr2:48627546 | G | C | 267 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(264): Show |
286 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.247+6256G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48627546 | |||||||
| chr2:48627616 | T | A | 20 | a0001c0003t0001g0018 a0001c0003t0001g0062 a0001c0003t0001g0064 others(17): Show |
20 | HG01070.hp1 HG01123.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.247+6326T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48627616 | |||||||
| chr2:48627641 | A | C | 1 | a0001c0001t0001g0272 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.247+6351A>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48627641 | |||||||
| chr2:48627652 | C | G | 3 | a0002c0006t0001g0091 a0002c0006t0001g0093 a0002c0006t0001g0094 |
3 | HG02129.hp2 NA18940.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.247+6362C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48627652 | |||||||
| chr2:48627761 | A | G | 3 | a0002c0006t0001g0091 a0002c0006t0001g0093 a0002c0006t0001g0094 |
3 | HG02129.hp2 NA18940.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.247+6471A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48627761 | |||||||
| chr2:48627772 | A | G | 2 | a0005c0008t0002g0302 a0005c0008t0002g0303 |
2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.247+6482A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48627772 | |||||||
| chr2:48627930 | T | C | 21 | a0001c0003t0001g0018 a0001c0003t0001g0061 a0001c0003t0001g0062 others(18): Show |
21 | HG01070.hp1 HG01123.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.247+6640T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48627930 | |||||||
| chr2:48628061 | G | T | 2 | a0001c0001t0001g0089 a0001c0001t0001g0095 |
2 | HG00597.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.247+6771G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48628061 | |||||||
| chr2:48628075 | C | G | 2 | a0001c0003t0001g0078 a0001c0003t0001g0079 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.247+6785C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48628075 | |||||||
| chr2:48628150 | A | C | 1 | a0001c0001t0001g0281 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.247+6860A>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48628150 | |||||||
| chr2:48628156 | T | C | 2 | a0001c0001t0001g0003 a0001c0001t0001g0288 |
5 | HG01884.hp2 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.247+6866T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48628156 | |||||||
| chr2:48628183 | A | C | 19 | a0001c0001t0001g0006 a0001c0001t0001g0096 a0001c0001t0001g0097 others(16): Show |
20 | HG00423.hp1 HG02015.hp1 HG02056.hp2 others(17): Show |
intron_variant | MODIFIER | c.247+6893A>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48628183 | |||||||
| chr2:48628406 | A | G | 1 | a0007c0013t0001g0280 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.247+7116A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48628406 | |||||||
| chr2:48628477 | G | A | 246 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(243): Show |
265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.247+7187G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48628477 | |||||||
| chr2:48628507 | C | T | 2 | a0001c0001t0001g0003 a0001c0001t0001g0288 |
5 | HG01884.hp2 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.247+7217C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48628507 | |||||||
| chr2:48628515 | T | C | 1 | a0001c0001t0002g0092 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.247+7225T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48628515 | |||||||
| chr2:48628540 | C | A | 2 | a0001c0001t0002g0090 a0001c0001t0002g0102 |
2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.247+7250C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48628540 | |||||||
| chr2:48628627 | A | G | 18 | a0001c0003t0001g0018 a0001c0003t0001g0061 a0001c0003t0001g0064 others(15): Show |
18 | HG01243.hp1 HG01891.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.247+7337A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48628627 | |||||||
| chr2:48628631 | G | A | 2 | a0005c0008t0002g0302 a0005c0008t0002g0303 |
2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.247+7341G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48628631 | |||||||
| chr2:48628638 | G | A | 27 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0282 others(24): Show |
31 | HG00642.hp1 HG01361.hp2 HG01515.hp2 others(28): Show |
intron_variant | MODIFIER | c.247+7348G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48628638 | |||||||
| chr2:48628674 | A | G | 1 | a0001c0003t0001g0069 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.247+7384A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48628674 | |||||||
| chr2:48628897 | G | C | 1 | a0007c0013t0001g0280 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.247+7607G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48628897 | |||||||
| chr2:48629000 | T | C | 2 | a0005c0008t0002g0302 a0005c0008t0002g0303 |
2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.247+7710T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48629000 | |||||||
| chr2:48629030 | A | T | 2 | a0005c0008t0002g0302 a0005c0008t0002g0303 |
2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.247+7740A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48629030 | |||||||
| chr2:48629045 | C | G | 2 | a0005c0008t0002g0302 a0005c0008t0002g0303 |
2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.247+7755C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48629045 | |||||||
| chr2:48629079 | A | G | 3 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0088 |
3 | HG04115.hp2 NA18940.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.247+7789A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48629079 | |||||||
| chr2:48629317 | T | A | 1 | a0001c0001t0001g0115 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.247+8027T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48629317 | |||||||
| chr2:48629372 | C | T | 1 | a0002c0002t0001g0228 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.247+8082C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48629372 | |||||||
| chr2:48629434 | C | T | 27 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0282 others(24): Show |
31 | HG00642.hp1 HG01361.hp2 HG01515.hp2 others(28): Show |
intron_variant | MODIFIER | c.247+8144C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48629434 | |||||||
| chr2:48629440 | A | T | 27 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0282 others(24): Show |
31 | HG00642.hp1 HG01361.hp2 HG01515.hp2 others(28): Show |
intron_variant | MODIFIER | c.247+8150A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48629440 | |||||||
| chr2:48629479 | G | A | 12 | a0001c0001t0001g0017 a0001c0001t0001g0290 a0001c0001t0001g0291 others(9): Show |
12 | HG01074.hp1 HG01109.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.247+8189G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48629479 | |||||||
| chr2:48629610 | A | G | 2 | a0005c0008t0002g0302 a0005c0008t0002g0303 |
2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.247+8320A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48629610 | |||||||
| chr2:48629631 | G | A | 246 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(243): Show |
265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.247+8341G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48629631 | |||||||
| chr2:48629707 | G | C | 1 | a0007c0013t0001g0280 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.247+8417G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48629707 | |||||||
| chr2:48629709 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.247+8419C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48629709 | |||||||
| chr2:48629867 | C | A | 2 | a0005c0008t0002g0302 a0005c0008t0002g0303 |
2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.247+8577C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48629867 | |||||||
| chr2:48629885 | G | A | 1 | a0001c0001t0002g0161 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.247+8595G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48629885 | |||||||
| chr2:48629925 | G | T | 3 | a0002c0002t0001g0227 a0002c0002t0001g0262 a0002c0002t0001g0263 |
3 | HG00735.hp2 HG01123.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.247+8635G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48629925 | |||||||
| chr2:48629996 | G | T | 1 | a0001c0001t0001g0183 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.247+8706G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48629996 | |||||||
| chr2:48629997 | C | G | 2 | a0005c0008t0002g0302 a0005c0008t0002g0303 |
2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.247+8707C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48629997 | |||||||
| chr2:48630099 | G | C | 6 | a0001c0003t0001g0064 a0001c0003t0001g0075 a0001c0003t0001g0076 others(3): Show |
6 | HG02622.hp2 HG02809.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.247+8809G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48630099 | |||||||
| chr2:48630188 | A | G | 15 | a0001c0003t0001g0018 a0001c0003t0001g0064 a0001c0003t0001g0066 others(12): Show |
15 | HG01243.hp1 HG02486.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.247+8898A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48630188 | |||||||
| chr2:48630199 | T | G | 271 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(268): Show |
290 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(287): Show |
intron_variant | MODIFIER | c.247+8909T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48630199 | |||||||
| chr2:48630254 | G | A | 2 | a0001c0001t0001g0270 a0001c0001t0001g0271 |
2 | HG01106.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.247+8964G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48630254 | |||||||
| chr2:48630330 | C | G | 21 | a0001c0003t0001g0018 a0001c0003t0001g0061 a0001c0003t0001g0062 others(18): Show |
21 | HG01070.hp1 HG01123.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.247+9040C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48630330 | |||||||
| chr2:48630352 | C | G | 1 | a0001c0001t0001g0096 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.247+9062C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48630352 | |||||||
| chr2:48630581 | G | C | 2 | a0005c0008t0002g0302 a0005c0008t0002g0303 |
2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.247+9291G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48630581 | |||||||
| chr2:48630700 | G | A | 2 | a0005c0008t0002g0302 a0005c0008t0002g0303 |
2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.247+9410G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48630700 | |||||||
| chr2:48631001 | A | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(83): Show |
94 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.247+9711A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48631001 | |||||||
| chr2:48631053 | C | G | 2 | a0002c0002t0001g0225 a0002c0002t0001g0226 |
2 | HG01361.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.247+9763C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48631053 | |||||||
| chr2:48631080 | T | G | 2 | a0005c0008t0002g0302 a0005c0008t0002g0303 |
2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.247+9790T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48631080 | |||||||
| chr2:48631121 | C | T | 1 | a0001c0001t0001g0270 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.247+9831C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48631121 | |||||||
| chr2:48631188 | T | G | 1 | a0001c0001t0001g0281 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.247+9898T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48631188 | |||||||
| chr2:48631306 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.247+10016G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48631306 | |||||||
| chr2:48631421 | C | G | 6 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(3): Show |
6 | HG01099.hp2 HG01175.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.247+10131C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48631421 | |||||||
| chr2:48631797 | C | T | 6 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 others(3): Show |
6 | HG02145.hp2 HG02630.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.247+10507C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48631797 | |||||||
| chr2:48631985 | C | G | 291 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(288): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.248-10417C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48631985 | |||||||
| chr2:48632098 | G | A | 1 | a0001c0001t0001g0162 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.248-10304G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48632098 | |||||||
| chr2:48632135 | G | A | 2 | a0005c0008t0002g0302 a0005c0008t0002g0303 |
2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.248-10267G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48632135 | |||||||
| chr2:48632306 | A | G | 7 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.248-10096A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48632306 | |||||||
| chr2:48632391 | G | GT | 8 | a0001c0001t0001g0053 a0001c0001t0001g0143 a0001c0001t0001g0238 others(5): Show |
8 | HG00738.hp1 HG01175.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.248-9999dupT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 48632391 | ||||||
| chr2:48632532 | A | T | 1 | a0002c0006t0001g0091 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.248-9870A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48632532 | |||||||
| chr2:48632672 | C | T | 1 | a0001c0001t0001g0183 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.248-9730C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48632672 | |||||||
| chr2:48632743 | G | T | 1 | a0001c0001t0001g0281 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.248-9659G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48632743 | |||||||
| chr2:48632808 | A | C | 1 | a0001c0003t0001g0068 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.248-9594A>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48632808 | |||||||
| chr2:48632832 | C | A | 1 | a0002c0002t0001g0191 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.248-9570C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48632832 | |||||||
| chr2:48632992 | C | T | 9 | a0001c0001t0001g0003 a0001c0001t0001g0282 a0001c0001t0001g0283 others(6): Show |
12 | HG01884.hp2 HG02055.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.248-9410C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48632992 | |||||||
| chr2:48633240 | A | G | 1 | a0001c0001t0001g0287 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.248-9162A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48633240 | |||||||
| chr2:48633257 | C | A | 1 | a0001c0001t0001g0286 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.248-9145C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48633257 | |||||||
| chr2:48633259 | C | T | 1 | a0001c0001t0001g0234 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.248-9143C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48633259 | |||||||
| chr2:48633372 | G | C | 4 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(1): Show |
4 | HG00621.hp2 HG02040.hp2 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.248-9030G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48633372 | |||||||
| chr2:48633378 | C | T | 1 | a0001c0001t0001g0053 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.248-9024C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48633378 | |||||||
| chr2:48633379 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.248-9023G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48633379 | |||||||
| chr2:48633477 | C | G | 39 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(36): Show |
43 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.248-8925C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48633477 | |||||||
| chr2:48633699 | C | T | 1 | a0007c0013t0001g0280 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.248-8703C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48633699 | |||||||
| chr2:48633729 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.248-8673C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48633729 | |||||||
| chr2:48633731 | A | T | 1 | a0001c0001t0001g0058 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.248-8671A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48633731 | |||||||
| chr2:48633756 | C | T | 2 | a0001c0001t0001g0105 a0001c0001t0001g0106 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.248-8646C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48633756 | |||||||
| chr2:48633759 | A | G | 65 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(62): Show |
69 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.248-8643A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48633759 | |||||||
| chr2:48633773 | G | A | 1 | a0001c0001t0001g0287 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.248-8629G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48633773 | |||||||
| chr2:48633784 | C | G | 6 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(3): Show |
6 | HG01099.hp2 HG01175.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.248-8618C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48633784 | |||||||
| chr2:48633812 | G | A | 2 | a0004c0007t0001g0027 a0004c0007t0001g0028 |
2 | HG00733.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.248-8590G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48633812 | |||||||
| chr2:48633897 | G | GTCT | 295 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(292): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.248-8504_248-8503i others(5): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 48633897 | ||||||
| chr2:48633914 | T | G | 39 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(36): Show |
43 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.248-8488T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48633914 | |||||||
| chr2:48633979 | G | C | 18 | a0001c0001t0001g0016 a0001c0001t0001g0304 a0001c0001t0001g0305 others(15): Show |
19 | HG00642.hp1 HG01361.hp2 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.248-8423G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48633979 | |||||||
| chr2:48634012 | A | T | 1 | a0001c0001t0001g0058 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.248-8390A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48634012 | |||||||
| chr2:48634143 | T | C | 1 | a0001c0001t0001g0287 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.248-8259T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48634143 | |||||||
| chr2:48634151 | C | T | 20 | a0001c0001t0001g0173 a0001c0001t0002g0081 a0001c0001t0002g0082 others(17): Show |
20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.248-8251C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48634151 | |||||||
| chr2:48634199 | G | A | 1 | a0001c0001t0001g0301 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.248-8203G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48634199 | |||||||
| chr2:48634201 | C | T | 1 | a0001c0003t0001g0068 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.248-8201C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48634201 | |||||||
| chr2:48634204 | C | T | 45 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(42): Show |
49 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.248-8198C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48634204 | |||||||
| chr2:48634265 | C | A | 1 | a0001c0001t0001g0120 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.248-8137C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48634265 | |||||||
| chr2:48634300 | C | T | 1 | a0001c0001t0002g0182 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.248-8102C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48634300 | |||||||
| chr2:48634376 | G | T | 1 | a0001c0001t0001g0003 | 4 | HG01884.hp2 HG03195.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.248-8026G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48634376 | |||||||
| chr2:48634578 | A | G | 12 | a0001c0001t0001g0017 a0001c0001t0001g0290 a0001c0001t0001g0291 others(9): Show |
12 | HG01074.hp1 HG01109.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.248-7824A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48634578 | |||||||
| chr2:48634621 | C | G | 1 | a0001c0001t0001g0288 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.248-7781C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48634621 | |||||||
| chr2:48634765 | C | T | 44 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(41): Show |
48 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.248-7637C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48634765 | |||||||
| chr2:48634780 | G | T | 2 | a0005c0008t0002g0302 a0005c0008t0002g0303 |
2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.248-7622G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48634780 | |||||||
| chr2:48635034 | A | G | 3 | a0001c0003t0001g0061 a0001c0003t0001g0069 a0003c0004t0001g0065 |
3 | HG01891.hp1 HG02723.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.248-7368A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48635034 | |||||||
| chr2:48635070 | A | G | 6 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 others(3): Show |
6 | HG02145.hp2 HG02630.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.248-7332A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48635070 | |||||||
| chr2:48635073 | G | C | 2 | a0001c0001t0001g0059 a0001c0001t0001g0060 |
2 | HG00544.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.248-7329G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48635073 | |||||||
| chr2:48635090 | G | A | 1 | a0001c0003t0001g0068 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.248-7312G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48635090 | |||||||
| chr2:48635171 | G | C | 65 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(62): Show |
69 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.248-7231G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48635171 | |||||||
| chr2:48635359 | A | G | 45 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(42): Show |
49 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.248-7043A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48635359 | |||||||
| chr2:48635498 | C | T | 2 | a0003c0004t0001g0063 a0003c0004t0001g0080 |
2 | HG01070.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.248-6904C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48635498 | |||||||
| chr2:48635691 | C | T | 1 | a0002c0002t0001g0219 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.248-6711C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48635691 | |||||||
| chr2:48635744 | T | C | 18 | a0001c0001t0001g0173 a0001c0001t0002g0081 a0001c0001t0002g0082 others(15): Show |
18 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.248-6658T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48635744 | |||||||
| chr2:48635763 | C | T | 45 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(42): Show |
49 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.248-6639C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48635763 | |||||||
| chr2:48636095 | C | T | 1 | a0007c0013t0001g0280 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.248-6307C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48636095 | |||||||
| chr2:48636135 | C | G | 1 | a0001c0001t0001g0301 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.248-6267C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48636135 | |||||||
| chr2:48636272 | T | G | 1 | a0001c0001t0001g0270 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.248-6130T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48636272 | |||||||
| chr2:48636308 | C | G | 1 | a0007c0013t0001g0280 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.248-6094C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48636308 | |||||||
| chr2:48636643 | A | G | 1 | a0001c0001t0002g0181 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.248-5759A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48636643 | |||||||
| chr2:48636722 | G | A | 1 | a0001c0001t0006g0289 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.248-5680G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48636722 | |||||||
| chr2:48636731 | T | C | 12 | a0001c0001t0001g0017 a0001c0001t0001g0290 a0001c0001t0001g0291 others(9): Show |
12 | HG01074.hp1 HG01109.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.248-5671T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48636731 | |||||||
| chr2:48636770 | G | A | 294 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(291): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.248-5632G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48636770 | |||||||
| chr2:48636917 | A | T | 294 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(291): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.248-5485A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48636917 | |||||||
| chr2:48636925 | A | G | 2 | a0001c0001t0001g0298 a0001c0001t0001g0299 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.248-5477A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48636925 | |||||||
| chr2:48636957 | G | A | 45 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(42): Show |
49 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.248-5445G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48636957 | |||||||
| chr2:48637041 | A | G | 2 | a0001c0001t0001g0270 a0001c0001t0001g0271 |
2 | HG01106.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.248-5361A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48637041 | |||||||
| chr2:48637080 | G | T | 39 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(36): Show |
43 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.248-5322G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48637080 | |||||||
| chr2:48637152 | C | T | 1 | a0001c0001t0001g0254 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.248-5250C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48637152 | |||||||
| chr2:48637177 | T | A | 45 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(42): Show |
49 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.248-5225T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48637177 | |||||||
| chr2:48637265 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.248-5137C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48637265 | |||||||
| chr2:48637377 | G | A | 294 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(291): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.248-5025G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48637377 | |||||||
| chr2:48637392 | T | A | 1 | a0001c0001t0001g0185 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.248-5010T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48637392 | |||||||
| chr2:48637425 | A | G | 6 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 others(3): Show |
6 | HG02145.hp2 HG02630.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.248-4977A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48637425 | |||||||
| chr2:48637448 | C | G | 1 | a0002c0002t0001g0228 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.248-4954C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48637448 | |||||||
| chr2:48637461 | A | G | 1 | a0007c0013t0001g0280 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.248-4941A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48637461 | |||||||
| chr2:48637565 | T | A | 1 | a0001c0001t0001g0281 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.248-4837T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48637565 | |||||||
| chr2:48637574 | C | A | 1 | a0002c0002t0001g0192 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.248-4828C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48637574 | |||||||
| chr2:48637610 | G | A | 1 | a0001c0001t0001g0315 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.248-4792G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48637610 | |||||||
| chr2:48637625 | A | G | 39 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(36): Show |
43 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.248-4777A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48637625 | |||||||
| chr2:48637687 | T | C | 2 | a0005c0008t0002g0302 a0005c0008t0002g0303 |
2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.248-4715T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48637687 | |||||||
| chr2:48637690 | G | C | 2 | a0005c0008t0002g0302 a0005c0008t0002g0303 |
2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.248-4712G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48637690 | |||||||
| chr2:48637731 | A | G | 39 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(36): Show |
43 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.248-4671A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48637731 | |||||||
| chr2:48637780 | T | C | 3 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0234 |
3 | HG03710.hp1 HG04199.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.248-4622T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48637780 | |||||||
| chr2:48638153 | G | A | 47 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(44): Show |
51 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.248-4249G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48638153 | |||||||
| chr2:48638289 | G | A | 268 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(265): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.248-4113G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48638289 | |||||||
| chr2:48638344 | C | T | 1 | a0001c0001t0001g0296 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.248-4058C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48638344 | |||||||
| chr2:48638480 | C | T | 1 | a0002c0002t0001g0228 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.248-3922C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48638480 | |||||||
| chr2:48638707 | T | A | 3 | a0005c0008t0002g0302 a0005c0008t0002g0303 a0007c0013t0001g0280 |
3 | HG02717.hp2 HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.248-3695T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48638707 | |||||||
| chr2:48638792 | T | G | 5 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(2): Show |
5 | HG02129.hp1 NA18951.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.248-3610T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48638792 | |||||||
| chr2:48638834 | G | A | 9 | a0001c0001t0001g0016 a0001c0001t0001g0304 a0001c0001t0001g0305 others(6): Show |
10 | HG00642.hp1 HG01361.hp2 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.248-3568G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48638834 | |||||||
| chr2:48638885 | A | G | 6 | a0001c0003t0001g0064 a0001c0003t0001g0075 a0001c0003t0001g0076 others(3): Show |
6 | HG02622.hp2 HG02809.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.248-3517A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48638885 | |||||||
| chr2:48638969 | A | G | 45 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(42): Show |
49 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.248-3433A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48638969 | |||||||
| chr2:48639143 | G | T | 309 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(306): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.248-3259G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48639143 | |||||||
| chr2:48639208 | C | T | 48 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(45): Show |
52 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.248-3194C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48639208 | |||||||
| chr2:48639328 | G | T | 45 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(42): Show |
49 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.248-3074G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48639328 | |||||||
| chr2:48639342 | C | G | 7 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.248-3060C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48639342 | |||||||
| chr2:48639347 | A | G | 39 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(36): Show |
43 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.248-3055A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48639347 | |||||||
| chr2:48639407 | C | T | 1 | a0002c0002t0001g0218 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.248-2995C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48639407 | |||||||
| chr2:48639421 | C | G | 5 | a0001c0001t0001g0238 a0001c0001t0001g0252 a0001c0001t0001g0253 others(2): Show |
5 | NA18960.hp2 NA19000.hp1 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.248-2981C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48639421 | |||||||
| chr2:48639499 | C | T | 5 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(2): Show |
5 | HG02055.hp2 HG02145.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.248-2903C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48639499 | |||||||
| chr2:48639636 | A | G | 1 | a0001c0001t0001g0026 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.248-2766A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48639636 | |||||||
| chr2:48639765 | C | A | 201 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(198): Show |
216 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.248-2637C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48639765 | |||||||
| chr2:48640010 | C | T | 58 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0011 others(55): Show |
66 | HG00140.hp1 HG00609.hp2 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.248-2392C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48640010 | |||||||
| chr2:48640269 | T | C | 8 | a0001c0001t0001g0017 a0001c0001t0001g0290 a0001c0001t0001g0291 others(5): Show |
8 | HG01074.hp1 HG01884.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.248-2133T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48640269 | |||||||
| chr2:48640290 | C | G | 18 | a0001c0001t0001g0173 a0001c0001t0002g0081 a0001c0001t0002g0082 others(15): Show |
18 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.248-2112C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48640290 | |||||||
| chr2:48640309 | T | A | 289 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(286): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.248-2093T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48640309 | |||||||
| chr2:48640378 | A | G | 2 | a0001c0001t0001g0105 a0001c0001t0001g0106 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.248-2024A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48640378 | |||||||
| chr2:48640378 | A | T | 39 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(36): Show |
43 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.248-2024A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48640378 | |||||||
| chr2:48640641 | C | G | 1 | a0001c0001t0001g0054 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.248-1761C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48640641 | |||||||
| chr2:48640703 | A | T | 39 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(36): Show |
43 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.248-1699A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48640703 | |||||||
| chr2:48640725 | C | T | 20 | a0001c0001t0001g0173 a0001c0001t0002g0081 a0001c0001t0002g0082 others(17): Show |
20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.248-1677C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48640725 | |||||||
| chr2:48640770 | T | C | 104 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(101): Show |
112 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.248-1632T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48640770 | |||||||
| chr2:48640779 | T | C | 1 | a0001c0001t0001g0033 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.248-1623T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48640779 | |||||||
| chr2:48640900 | CTTGTTAG others(1): Show |
C | 45 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(42): Show |
49 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.248-1499_248-1492d others(10): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 48640900 | ||||||
| chr2:48640980 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.248-1422C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48640980 | |||||||
| chr2:48641060 | C | T | 1 | a0001c0001t0001g0254 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.248-1342C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48641060 | |||||||
| chr2:48641101 | A | C | 8 | a0002c0002t0001g0004 a0002c0002t0001g0171 a0002c0002t0001g0212 others(5): Show |
10 | HG00609.hp2 HG02040.hp1 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.248-1301A>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48641101 | |||||||
| chr2:48641303 | G | C | 20 | a0001c0001t0001g0173 a0001c0001t0002g0081 a0001c0001t0002g0082 others(17): Show |
20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.248-1099G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48641303 | |||||||
| chr2:48641372 | G | C | 39 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(36): Show |
43 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.248-1030G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48641372 | |||||||
| chr2:48641649 | C | A | 1 | a0001c0001t0001g0097 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.248-753C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48641649 | |||||||
| chr2:48641668 | T | G | 1 | a0001c0001t0001g0199 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.248-734T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48641668 | |||||||
| chr2:48641674 | C | T | 1 | a0007c0013t0001g0280 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.248-728C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48641674 | |||||||
| chr2:48641846 | T | C | 1 | a0002c0002t0001g0111 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.248-556T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48641846 | |||||||
| chr2:48641850 | A | G | 1 | a0002c0002t0001g0211 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.248-552A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48641850 | |||||||
| chr2:48642056 | T | C | 1 | a0001c0001t0002g0172 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.248-346T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48642056 | |||||||
| chr2:48642059 | A | G | 201 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(198): Show |
216 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.248-343A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48642059 | |||||||
| chr2:48642258 | C | T | 2 | a0001c0001t0001g0319 a0001c0001t0001g0320 |
2 | HG02630.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.248-144C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48642258 | |||||||
| chr2:48642262 | CTTGGAAT others(8): Show |
C | 1 | a0001c0001t0001g0292 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.248-137_248-123del others(15): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr2 | 48642262 | ||||||
| chr2:48642278 | T | A | 1 | a0001c0001t0001g0292 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.248-124T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48642278 | |||||||
| chr2:48642324 | T | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0103 a0001c0001t0001g0105 others(1): Show |
5 | HG01070.hp2 HG01071.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.248-78T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48642324 | |||||||
| chr2:48642361 | T | C | 8 | a0001c0001t0001g0017 a0001c0001t0001g0290 a0001c0001t0001g0291 others(5): Show |
8 | HG01074.hp1 HG01884.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.248-41T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 3/8 | chr2 | 48642361 | |||||||
| chr2:48642583 | G | A | 1 | a0001c0001t0001g0146 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.303+126G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48642583 | |||||||
| chr2:48642592 | C | T | 2 | a0001c0001t0001g0268 a0001c0001t0001g0269 |
2 | HG02602.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.303+135C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48642592 | |||||||
| chr2:48642731 | T | C | 4 | a0003c0004t0001g0063 a0003c0004t0001g0065 a0003c0004t0001g0080 others(1): Show |
4 | HG01070.hp1 HG01123.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.303+274T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48642731 | |||||||
| chr2:48642856 | C | G | 39 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(36): Show |
43 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.303+399C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48642856 | |||||||
| chr2:48642858 | A | G | 2 | a0005c0008t0002g0302 a0005c0008t0002g0303 |
2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.303+401A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48642858 | |||||||
| chr2:48642860 | GA | G | 208 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(205): Show |
226 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.303+416delA | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 48642860 | ||||||
| chr2:48642876 | TGTG | T | 39 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(36): Show |
43 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.303+422_303+424del others(3): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 48642876 | ||||||
| chr2:48642978 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.303+521A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48642978 | |||||||
| chr2:48643063 | T | C | 2 | a0001c0001t0001g0268 a0001c0001t0001g0269 |
2 | HG02602.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.303+606T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48643063 | |||||||
| chr2:48643067 | A | G | 45 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(42): Show |
49 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.303+610A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48643067 | |||||||
| chr2:48643226 | C | T | 45 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(42): Show |
49 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.303+769C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48643226 | |||||||
| chr2:48643228 | C | G | 1 | a0001c0001t0001g0315 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.303+771C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48643228 | |||||||
| chr2:48643470 | T | G | 1 | a0001c0001t0001g0160 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.303+1013T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48643470 | |||||||
| chr2:48643568 | A | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(83): Show |
94 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.303+1111A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48643568 | |||||||
| chr2:48643693 | A | AT | 60 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(57): Show |
64 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.303+1259dupT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 48643693 | ||||||
| chr2:48643693 | A | ATT | 7 | a0001c0001t0001g0032 a0001c0001t0001g0049 a0001c0001t0001g0057 others(4): Show |
7 | HG01978.hp1 HG02055.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.303+1258_303+1259d others(4): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 48643693 | ||||||
| chr2:48643693 | AT | A | 10 | a0001c0001t0001g0145 a0001c0001t0001g0147 a0001c0001t0001g0163 others(7): Show |
10 | HG00733.hp2 HG02523.hp2 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.303+1259delT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 48643693 | ||||||
| chr2:48643693 | ATTTTTTT others(6): Show |
A | 39 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(36): Show |
43 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.303+1247_303+1259d others(15): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr2 | 48643693 | ||||||
| chr2:48643741 | C | G | 1 | a0001c0001t0001g0138 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.303+1284C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48643741 | |||||||
| chr2:48643749 | G | T | 39 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(36): Show |
43 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.304-1284G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48643749 | |||||||
| chr2:48643843 | C | T | 18 | a0001c0003t0001g0018 a0001c0003t0001g0061 a0001c0003t0001g0062 others(15): Show |
18 | HG01243.hp1 HG01891.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.304-1190C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48643843 | |||||||
| chr2:48643844 | G | A | 7 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.304-1189G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48643844 | |||||||
| chr2:48643929 | C | T | 8 | a0001c0001t0001g0013 a0001c0001t0001g0196 a0001c0001t0001g0197 others(5): Show |
9 | HG02451.hp2 HG02886.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.304-1104C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48643929 | |||||||
| chr2:48644013 | T | A | 20 | a0001c0001t0001g0173 a0001c0001t0002g0081 a0001c0001t0002g0082 others(17): Show |
20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.304-1020T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48644013 | |||||||
| chr2:48644014 | T | A | 20 | a0001c0001t0001g0173 a0001c0001t0002g0081 a0001c0001t0002g0082 others(17): Show |
20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.304-1019T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48644014 | |||||||
| chr2:48644015 | A | T | 5 | a0002c0002t0001g0012 a0002c0002t0001g0159 a0002c0002t0001g0235 others(2): Show |
6 | HG02027.hp2 HG02165.hp2 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.304-1018A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48644015 | |||||||
| chr2:48644093 | C | T | 1 | a0002c0014t0001g0195 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.304-940C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48644093 | |||||||
| chr2:48644094 | C | A | 1 | a0002c0014t0001g0195 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.304-939C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48644094 | |||||||
| chr2:48644095 | T | C | 1 | a0002c0014t0001g0195 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.304-938T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48644095 | |||||||
| chr2:48644096 | C | A | 1 | a0002c0014t0001g0195 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.304-937C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48644096 | |||||||
| chr2:48644151 | A | G | 1 | a0001c0001t0001g0101 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.304-882A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48644151 | |||||||
| chr2:48644404 | C | A | 1 | a0001c0001t0001g0036 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.304-629C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48644404 | |||||||
| chr2:48644445 | G | C | 2 | a0005c0008t0002g0302 a0005c0008t0002g0303 |
2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.304-588G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48644445 | |||||||
| chr2:48644694 | C | T | 18 | a0001c0001t0001g0006 a0001c0001t0001g0096 a0001c0001t0001g0097 others(15): Show |
19 | HG00423.hp1 HG02015.hp1 HG02056.hp2 others(16): Show |
intron_variant | MODIFIER | c.304-339C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48644694 | |||||||
| chr2:48644730 | C | G | 2 | a0001c0001t0001g0085 a0001c0001t0001g0086 |
2 | NA18940.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.304-303C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48644730 | |||||||
| chr2:48644769 | G | A | 2 | a0001c0001t0001g0121 a0001c0001t0001g0272 |
2 | HG00544.hp1 HG00597.hp2 |
intron_variant | MODIFIER | c.304-264G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48644769 | |||||||
| chr2:48644893 | A | G | 7 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(4): Show |
7 | HG00738.hp2 HG01106.hp2 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.304-140A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48644893 | |||||||
| chr2:48644974 | A | G | 22 | a0001c0001t0001g0016 a0001c0001t0001g0294 a0001c0001t0001g0295 others(19): Show |
23 | HG00642.hp1 HG01109.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.304-59A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48644974 | |||||||
| chr2:48644996 | C | G | 1 | a0001c0001t0001g0168 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.304-37C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 4/8 | chr2 | 48644996 | |||||||
| chr2:48645192 | T | A | 1 | a0007c0013t0001g0280 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.388+75T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 5/8 | chr2 | 48645192 | |||||||
| chr2:48645310 | G | C | 1 | a0001c0001t0001g0122 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.388+193G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 5/8 | chr2 | 48645310 | |||||||
| chr2:48645326 | A | T | 1 | a0001c0001t0001g0137 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.388+209A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 5/8 | chr2 | 48645326 | |||||||
| chr2:48645369 | T | C | 2 | a0004c0007t0001g0027 a0004c0007t0001g0028 |
2 | HG00733.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.388+252T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 5/8 | chr2 | 48645369 | |||||||
| chr2:48645472 | A | T | 309 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(306): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.388+355A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 5/8 | chr2 | 48645472 | |||||||
| chr2:48645646 | C | G | 21 | a0001c0003t0001g0018 a0001c0003t0001g0061 a0001c0003t0001g0062 others(18): Show |
21 | HG01070.hp1 HG01123.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.388+529C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 5/8 | chr2 | 48645646 | |||||||
| chr2:48645677 | C | G | 2 | a0005c0008t0002g0302 a0005c0008t0002g0303 |
2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.388+560C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 5/8 | chr2 | 48645677 | |||||||
| chr2:48645937 | C | T | 1 | a0001c0001t0001g0153 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.389-516C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 5/8 | chr2 | 48645937 | |||||||
| chr2:48645939 | C | T | 1 | a0001c0003t0001g0069 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.389-514C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 5/8 | chr2 | 48645939 | |||||||
| chr2:48645947 | C | CT | 48 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(45): Show |
52 | HG00099.hp1 HG00544.hp2 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.389-493dupT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 48645947 | ||||||
| chr2:48645947 | CT | C | 8 | a0001c0001t0001g0017 a0001c0001t0001g0290 a0001c0001t0001g0291 others(5): Show |
8 | HG01074.hp1 HG01884.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.389-493delT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 48645947 | ||||||
| chr2:48646018 | C | A | 1 | a0001c0001t0001g0321 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.389-435C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 5/8 | chr2 | 48646018 | |||||||
| chr2:48646118 | C | T | 44 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(41): Show |
48 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.389-335C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 5/8 | chr2 | 48646118 | |||||||
| chr2:48646179 | A | T | 2 | a0001c0001t0001g0085 a0001c0001t0001g0086 |
2 | NA18940.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.389-274A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 5/8 | chr2 | 48646179 | |||||||
| chr2:48646204 | G | A | 2 | a0001c0001t0001g0183 a0009c0015t0001g0164 |
2 | NA18942.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.389-249G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 5/8 | chr2 | 48646204 | |||||||
| chr2:48646373 | A | AT | 6 | a0001c0001t0001g0047 a0001c0001t0001g0136 a0001c0001t0001g0163 others(3): Show |
6 | HG01099.hp1 HG02145.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.389-65dupT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 48646373 | ||||||
| chr2:48646373 | AT | A | 6 | a0001c0001t0001g0173 a0001c0001t0001g0198 a0001c0001t0001g0301 others(3): Show |
6 | HG01358.hp1 HG02451.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.389-65delT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 5/8 | INFO_REALIGN_3_PRIME | chr2 | 48646373 | ||||||
| chr2:48646387 | T | G | 1 | a0001c0003t0001g0062 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.389-66T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 5/8 | chr2 | 48646387 | |||||||
| chr2:48646443 | C | T | 39 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(36): Show |
43 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.389-10C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 5/8 | chr2 | 48646443 | |||||||
| chr2:48647155 | T | G | 2 | a0001c0001t0001g0089 a0001c0001t0001g0095 |
2 | HG00597.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.978+113T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48647155 | |||||||
| chr2:48647218 | A | G | 1 | a0001c0001t0001g0168 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.978+176A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48647218 | |||||||
| chr2:48647297 | A | T | 39 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(36): Show |
43 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.978+255A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48647297 | |||||||
| chr2:48647391 | A | G | 9 | a0001c0001t0001g0173 a0001c0001t0002g0081 a0001c0001t0002g0082 others(6): Show |
9 | HG01243.hp2 HG01891.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.978+349A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48647391 | |||||||
| chr2:48647517 | C | T | 1 | a0001c0001t0001g0026 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.978+475C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48647517 | |||||||
| chr2:48647527 | G | A | 318 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(315): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.978+485G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48647527 | |||||||
| chr2:48647563 | T | C | 1 | a0007c0013t0001g0280 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.978+521T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48647563 | |||||||
| chr2:48647565 | T | C | 2 | a0001c0001t0001g0123 a0001c0001t0001g0124 |
2 | NA18954.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.978+523T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48647565 | |||||||
| chr2:48647643 | C | T | 2 | a0005c0008t0002g0302 a0005c0008t0002g0303 |
2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.978+601C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48647643 | |||||||
| chr2:48647682 | C | A | 184 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(181): Show |
199 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.978+640C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48647682 | |||||||
| chr2:48647880 | A | G | 44 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(41): Show |
48 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.978+838A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48647880 | |||||||
| chr2:48647923 | A | C | 11 | a0001c0003t0001g0064 a0001c0003t0001g0066 a0001c0003t0001g0067 others(8): Show |
11 | HG02486.hp2 HG02622.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.978+881A>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48647923 | |||||||
| chr2:48647969 | G | A | 1 | a0002c0002t0001g0142 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.978+927G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48647969 | |||||||
| chr2:48648011 | C | T | 1 | a0002c0002t0001g0111 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.978+969C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48648011 | |||||||
| chr2:48648222 | G | GT | 19 | a0001c0001t0001g0016 a0001c0001t0001g0135 a0001c0001t0001g0304 others(16): Show |
20 | HG00642.hp1 HG01361.hp2 HG01515.hp2 others(17): Show |
intron_variant | MODIFIER | c.978+1188dupT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48648222 | ||||||
| chr2:48648286 | A | T | 1 | a0002c0002t0001g0139 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.978+1244A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48648286 | |||||||
| chr2:48648326 | T | G | 18 | a0001c0001t0001g0016 a0001c0001t0001g0304 a0001c0001t0001g0305 others(15): Show |
19 | HG00642.hp1 HG01361.hp2 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.978+1284T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48648326 | |||||||
| chr2:48648523 | G | A | 20 | a0001c0003t0001g0018 a0001c0003t0001g0062 a0001c0003t0001g0064 others(17): Show |
20 | HG01070.hp1 HG01123.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.978+1481G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48648523 | |||||||
| chr2:48648703 | C | T | 1 | a0002c0002t0001g0229 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.978+1661C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48648703 | |||||||
| chr2:48648799 | G | A | 56 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0011 others(53): Show |
63 | HG00140.hp1 HG00609.hp2 HG00733.hp2 others(60): Show |
intron_variant | MODIFIER | c.978+1757G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48648799 | |||||||
| chr2:48648840 | T | C | 45 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(42): Show |
49 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.978+1798T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48648840 | |||||||
| chr2:48648851 | T | G | 1 | a0007c0013t0001g0280 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.978+1809T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48648851 | |||||||
| chr2:48648995 | C | G | 2 | a0001c0001t0001g0270 a0001c0001t0001g0271 |
2 | HG01106.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.978+1953C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48648995 | |||||||
| chr2:48649060 | T | A | 1 | a0001c0001t0006g0289 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.978+2018T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48649060 | |||||||
| chr2:48649100 | A | G | 309 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(306): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(329): Show |
intron_variant | MODIFIER | c.978+2058A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48649100 | |||||||
| chr2:48649131 | T | C | 20 | a0001c0001t0001g0173 a0001c0001t0002g0081 a0001c0001t0002g0082 others(17): Show |
20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.978+2089T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48649131 | |||||||
| chr2:48649230 | A | G | 20 | a0001c0001t0001g0173 a0001c0001t0002g0081 a0001c0001t0002g0082 others(17): Show |
20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.978+2188A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48649230 | |||||||
| chr2:48649238 | C | T | 18 | a0001c0001t0001g0016 a0001c0001t0001g0304 a0001c0001t0001g0305 others(15): Show |
19 | HG00642.hp1 HG01361.hp2 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.978+2196C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48649238 | |||||||
| chr2:48649277 | G | A | 3 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0012t0001g0242 |
3 | HG02523.hp1 NA18941.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.978+2235G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48649277 | |||||||
| chr2:48649326 | G | C | 39 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(36): Show |
43 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.978+2284G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48649326 | |||||||
| chr2:48649374 | C | T | 20 | a0001c0003t0001g0018 a0001c0003t0001g0062 a0001c0003t0001g0064 others(17): Show |
20 | HG01070.hp1 HG01123.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.978+2332C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48649374 | |||||||
| chr2:48649405 | A | G | 1 | a0001c0001t0001g0168 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.978+2363A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48649405 | |||||||
| chr2:48649435 | C | G | 20 | a0001c0001t0001g0173 a0001c0001t0002g0081 a0001c0001t0002g0082 others(17): Show |
20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.978+2393C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48649435 | |||||||
| chr2:48649486 | A | T | 1 | a0001c0003t0001g0062 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.978+2444A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48649486 | |||||||
| chr2:48649655 | A | T | 4 | a0001c0001t0001g0294 a0001c0001t0001g0295 a0001c0001t0001g0296 others(1): Show |
4 | HG01109.hp2 HG02559.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.978+2613A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48649655 | |||||||
| chr2:48649744 | C | G | 5 | a0001c0001t0001g0304 a0001c0001t0001g0305 a0001c0001t0001g0306 others(2): Show |
5 | HG02280.hp2 HG02683.hp1 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.978+2702C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48649744 | |||||||
| chr2:48649993 | G | A | 20 | a0001c0001t0001g0173 a0001c0001t0002g0081 a0001c0001t0002g0082 others(17): Show |
20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.978+2951G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48649993 | |||||||
| chr2:48650117 | G | A | 1 | a0001c0001t0001g0055 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.978+3075G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48650117 | |||||||
| chr2:48650131 | C | T | 20 | a0001c0001t0001g0173 a0001c0001t0002g0081 a0001c0001t0002g0082 others(17): Show |
20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.978+3089C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48650131 | |||||||
| chr2:48650221 | A | G | 1 | a0001c0001t0001g0293 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.978+3179A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48650221 | |||||||
| chr2:48650297 | C | T | 1 | a0004c0007t0001g0028 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.978+3255C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48650297 | |||||||
| chr2:48650332 | A | G | 9 | a0001c0001t0001g0003 a0001c0001t0001g0282 a0001c0001t0001g0283 others(6): Show |
12 | HG01884.hp2 HG02055.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.978+3290A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48650332 | |||||||
| chr2:48650361 | A | G | 64 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(61): Show |
68 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.978+3319A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48650361 | |||||||
| chr2:48650518 | C | G | 3 | a0002c0002t0001g0011 a0002c0002t0001g0232 a0002c0002t0001g0233 |
4 | NA18971.hp2 NA18998.hp1 NA19085.hp1 others(1): Show |
intron_variant | MODIFIER | c.978+3476C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48650518 | |||||||
| chr2:48650563 | A | G | 20 | a0001c0001t0001g0173 a0001c0001t0002g0081 a0001c0001t0002g0082 others(17): Show |
20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.978+3521A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48650563 | |||||||
| chr2:48650741 | A | C | 2 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
2 | HG01099.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.978+3699A>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48650741 | |||||||
| chr2:48650850 | A | G | 12 | a0001c0001t0001g0016 a0001c0001t0001g0304 a0001c0001t0001g0305 others(9): Show |
13 | HG00642.hp1 HG01361.hp2 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.978+3808A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48650850 | |||||||
| chr2:48651084 | C | G | 6 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 others(3): Show |
6 | HG02145.hp2 HG02630.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.978+4042C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48651084 | |||||||
| chr2:48651115 | A | G | 2 | a0001c0001t0001g0089 a0001c0001t0001g0095 |
2 | HG00597.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.978+4073A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48651115 | |||||||
| chr2:48651144 | A | G | 1 | a0002c0002t0001g0219 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.978+4102A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48651144 | |||||||
| chr2:48651162 | G | A | 1 | a0002c0002t0001g0112 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.978+4120G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48651162 | |||||||
| chr2:48651307 | T | A | 44 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(41): Show |
48 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.978+4265T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48651307 | |||||||
| chr2:48651409 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.978+4367C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48651409 | |||||||
| chr2:48651416 | G | T | 1 | a0001c0001t0001g0261 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.978+4374G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48651416 | |||||||
| chr2:48651422 | T | C | 2 | a0001c0001t0001g0274 a0001c0001t0001g0276 |
2 | NA18975.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.978+4380T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48651422 | |||||||
| chr2:48651436 | C | CT | 51 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(48): Show |
55 | HG00621.hp2 HG01074.hp1 HG01109.hp2 others(52): Show |
intron_variant | MODIFIER | c.978+4412dupT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48651436 | ||||||
| chr2:48651436 | CT | C | 52 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(49): Show |
56 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.978+4412delT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48651436 | ||||||
| chr2:48651436 | CTTTT | C | 20 | a0001c0001t0001g0173 a0001c0001t0002g0081 a0001c0001t0002g0082 others(17): Show |
20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.978+4409_978+4412d others(6): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48651436 | ||||||
| chr2:48651455 | A | T | 3 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0012t0001g0242 |
3 | HG02523.hp1 NA18941.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.978+4413A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48651455 | |||||||
| chr2:48651576 | G | A | 20 | a0001c0001t0001g0173 a0001c0001t0002g0081 a0001c0001t0002g0082 others(17): Show |
20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.978+4534G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48651576 | |||||||
| chr2:48651586 | A | C | 20 | a0001c0001t0001g0173 a0001c0001t0002g0081 a0001c0001t0002g0082 others(17): Show |
20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.978+4544A>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48651586 | |||||||
| chr2:48651588 | T | A | 191 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(188): Show |
206 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.978+4546T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48651588 | |||||||
| chr2:48651605 | A | G | 20 | a0001c0001t0001g0173 a0001c0001t0002g0081 a0001c0001t0002g0082 others(17): Show |
20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.978+4563A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48651605 | |||||||
| chr2:48651681 | C | T | 1 | a0002c0002t0001g0210 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.978+4639C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48651681 | |||||||
| chr2:48651696 | G | C | 1 | a0007c0013t0001g0280 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.978+4654G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48651696 | |||||||
| chr2:48651786 | AGCCCTTG others(6): Show |
A | 1 | a0002c0002t0001g0212 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.978+4745_978+4757d others(15): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48651786 | |||||||
| chr2:48652064 | A | G | 6 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 others(3): Show |
6 | HG02145.hp2 HG02630.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.978+5022A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48652064 | |||||||
| chr2:48652228 | C | G | 20 | a0001c0001t0001g0173 a0001c0001t0002g0081 a0001c0001t0002g0082 others(17): Show |
20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.978+5186C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48652228 | |||||||
| chr2:48652234 | C | T | 1 | a0001c0001t0001g0008 | 2 | HG01261.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.978+5192C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48652234 | |||||||
| chr2:48652279 | G | A | 64 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(61): Show |
68 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.978+5237G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48652279 | |||||||
| chr2:48652380 | C | T | 44 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(41): Show |
48 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(45): Show |
intron_variant | MODIFIER | c.978+5338C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48652380 | |||||||
| chr2:48652402 | G | A | 20 | a0001c0001t0001g0173 a0001c0001t0002g0081 a0001c0001t0002g0082 others(17): Show |
20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.978+5360G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48652402 | |||||||
| chr2:48652418 | C | G | 1 | a0001c0001t0002g0179 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.978+5376C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48652418 | |||||||
| chr2:48652431 | C | T | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | HG03710.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.978+5389C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48652431 | |||||||
| chr2:48652445 | G | A | 20 | a0001c0001t0001g0173 a0001c0001t0002g0081 a0001c0001t0002g0082 others(17): Show |
20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.978+5403G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48652445 | |||||||
| chr2:48652475 | G | A | 2 | a0001c0001t0002g0090 a0001c0001t0002g0102 |
2 | HG02622.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.978+5433G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48652475 | |||||||
| chr2:48652508 | C | T | 2 | a0001c0001t0001g0308 a0001c0001t0001g0311 |
2 | HG00642.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.978+5466C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48652508 | |||||||
| chr2:48652520 | C | T | 1 | a0002c0002t0001g0144 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.978+5478C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48652520 | |||||||
| chr2:48652560 | A | C | 6 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(3): Show |
6 | HG01099.hp2 HG01175.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.978+5518A>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48652560 | |||||||
| chr2:48652576 | C | T | 2 | a0001c0003t0001g0062 a0001c0003t0001g0069 |
2 | HG02723.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.978+5534C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48652576 | |||||||
| chr2:48652577 | T | G | 2 | a0001c0003t0001g0062 a0001c0003t0001g0069 |
2 | HG02723.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.978+5535T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48652577 | |||||||
| chr2:48652763 | C | T | 43 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(40): Show |
47 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.978+5721C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48652763 | |||||||
| chr2:48652776 | C | A | 8 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 others(5): Show |
8 | HG00738.hp2 HG01106.hp2 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.978+5734C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48652776 | |||||||
| chr2:48652780 | T | C | 20 | a0001c0001t0001g0173 a0001c0001t0002g0081 a0001c0001t0002g0082 others(17): Show |
20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.978+5738T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48652780 | |||||||
| chr2:48652815 | G | C | 315 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(312): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.978+5773G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48652815 | |||||||
| chr2:48652951 | C | G | 4 | a0001c0001t0001g0294 a0001c0001t0001g0295 a0001c0001t0001g0296 others(1): Show |
4 | HG01109.hp2 HG02559.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.978+5909C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48652951 | |||||||
| chr2:48653089 | C | A | 12 | a0001c0001t0001g0017 a0001c0001t0001g0290 a0001c0001t0001g0291 others(9): Show |
12 | HG01074.hp1 HG01109.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.978+6047C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48653089 | |||||||
| chr2:48653095 | G | C | 315 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(312): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.978+6053G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48653095 | |||||||
| chr2:48653189 | C | G | 1 | a0001c0001t0001g0170 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.978+6147C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48653189 | |||||||
| chr2:48653211 | A | G | 1 | a0001c0001t0001g0292 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.978+6169A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48653211 | |||||||
| chr2:48653220 | C | CA | 59 | a0001c0001t0001g0003 a0001c0001t0001g0169 a0001c0001t0001g0170 others(56): Show |
66 | HG00597.hp2 HG00609.hp2 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.978+6198dupA | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48653220 | ||||||
| chr2:48653220 | CA | C | 11 | a0001c0001t0001g0024 a0001c0001t0001g0058 a0001c0001t0001g0122 others(8): Show |
11 | HG00738.hp1 HG01934.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.978+6198delA | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48653220 | ||||||
| chr2:48653220 | CAA | C | 61 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(58): Show |
65 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.978+6197_978+6198d others(4): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48653220 | ||||||
| chr2:48653320 | A | G | 1 | a0001c0003t0001g0064 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.978+6278A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48653320 | |||||||
| chr2:48653447 | A | G | 1 | a0001c0003t0001g0061 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.978+6405A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48653447 | |||||||
| chr2:48653533 | C | G | 6 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(3): Show |
6 | HG01099.hp2 HG01175.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.978+6491C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48653533 | |||||||
| chr2:48653920 | C | CA | 38 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0162 others(35): Show |
38 | HG01070.hp2 HG01243.hp1 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.978+6901dupA | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48653920 | ||||||
| chr2:48653920 | C | CAA | 112 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(109): Show |
123 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.978+6900_978+6901d others(4): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48653920 | ||||||
| chr2:48653920 | C | CAAA | 19 | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(16): Show |
19 | HG00735.hp1 HG00738.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.978+6899_978+6901d others(5): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48653920 | ||||||
| chr2:48653920 | CAAAAAA | C | 7 | a0001c0001t0001g0013 a0001c0001t0001g0127 a0001c0001t0001g0128 others(4): Show |
8 | HG02523.hp2 HG02886.hp2 HG03516.hp1 others(5): Show |
intron_variant | MODIFIER | c.978+6896_978+6901d others(8): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48653920 | ||||||
| chr2:48653920 | CAAAAAAA | C | 133 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(130): Show |
144 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(141): Show |
intron_variant | MODIFIER | c.978+6895_978+6901d others(9): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48653920 | ||||||
| chr2:48653954 | C | G | 1 | a0001c0001t0001g0170 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.978+6912C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48653954 | |||||||
| chr2:48653995 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.978+6953G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48653995 | |||||||
| chr2:48654024 | C | T | 20 | a0001c0001t0001g0173 a0001c0001t0002g0081 a0001c0001t0002g0082 others(17): Show |
20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.978+6982C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48654024 | |||||||
| chr2:48654195 | G | C | 1 | a0001c0001t0001g0281 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.978+7153G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48654195 | |||||||
| chr2:48654222 | C | T | 20 | a0001c0001t0001g0173 a0001c0001t0002g0081 a0001c0001t0002g0082 others(17): Show |
20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.978+7180C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48654222 | |||||||
| chr2:48654242 | T | C | 20 | a0001c0001t0001g0173 a0001c0001t0002g0081 a0001c0001t0002g0082 others(17): Show |
20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.978+7200T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48654242 | |||||||
| chr2:48654249 | C | A | 315 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(312): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.978+7207C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48654249 | |||||||
| chr2:48654472 | C | T | 46 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(43): Show |
51 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.978+7430C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48654472 | |||||||
| chr2:48654606 | C | T | 2 | a0001c0001t0001g0268 a0001c0001t0001g0269 |
2 | HG02602.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.978+7564C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48654606 | |||||||
| chr2:48654870 | C | G | 1 | a0001c0001t0001g0168 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.978+7828C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48654870 | |||||||
| chr2:48654904 | T | C | 8 | a0001c0001t0001g0017 a0001c0001t0001g0290 a0001c0001t0001g0291 others(5): Show |
8 | HG01074.hp1 HG01884.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.978+7862T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48654904 | |||||||
| chr2:48655014 | G | T | 1 | a0007c0013t0001g0280 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.978+7972G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48655014 | |||||||
| chr2:48655044 | A | G | 1 | a0001c0001t0001g0126 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.978+8002A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48655044 | |||||||
| chr2:48655117 | C | T | 1 | a0001c0001t0002g0161 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.978+8075C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48655117 | |||||||
| chr2:48655126 | G | T | 19 | a0001c0001t0002g0081 a0001c0001t0002g0082 a0001c0001t0002g0090 others(16): Show |
19 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.978+8084G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48655126 | |||||||
| chr2:48655201 | A | G | 315 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(312): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.978+8159A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48655201 | |||||||
| chr2:48655223 | AT | A | 5 | a0001c0001t0002g0104 a0001c0001t0002g0172 a0001c0001t0002g0175 others(2): Show |
5 | HG01891.hp2 HG02647.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.978+8182delT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48655223 | |||||||
| chr2:48655225 | C | G | 1 | a0001c0001t0002g0161 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.978+8183C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48655225 | |||||||
| chr2:48655385 | C | G | 186 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(183): Show |
200 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.978+8343C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48655385 | |||||||
| chr2:48655430 | C | G | 19 | a0001c0001t0002g0081 a0001c0001t0002g0082 a0001c0001t0002g0090 others(16): Show |
19 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.978+8388C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48655430 | |||||||
| chr2:48655609 | T | A | 40 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(37): Show |
44 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.978+8567T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48655609 | |||||||
| chr2:48655666 | T | C | 1 | a0001c0001t0001g0266 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.978+8624T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48655666 | |||||||
| chr2:48655667 | C | T | 1 | a0001c0001t0001g0266 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.978+8625C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48655667 | |||||||
| chr2:48655718 | T | C | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG00558.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.978+8676T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48655718 | |||||||
| chr2:48655739 | A | G | 67 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(64): Show |
72 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.978+8697A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48655739 | |||||||
| chr2:48656105 | C | T | 8 | a0001c0001t0002g0081 a0001c0001t0002g0082 a0001c0001t0002g0092 others(5): Show |
8 | HG01243.hp2 HG01891.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.978+9063C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48656105 | |||||||
| chr2:48656126 | A | G | 40 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(37): Show |
44 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.978+9084A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48656126 | |||||||
| chr2:48656165 | T | A | 40 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(37): Show |
44 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.978+9123T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48656165 | |||||||
| chr2:48656255 | A | G | 1 | a0001c0001t0001g0168 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.978+9213A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48656255 | |||||||
| chr2:48656339 | T | A | 140 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(137): Show |
152 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.978+9297T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48656339 | |||||||
| chr2:48656348 | G | GT | 12 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0085 others(9): Show |
15 | HG01884.hp1 HG01884.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.978+9335dupT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48656348 | ||||||
| chr2:48656348 | G | GTT | 7 | a0001c0001t0001g0086 a0001c0001t0001g0292 a0001c0001t0001g0294 others(4): Show |
7 | HG01074.hp1 HG01109.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.978+9334_978+9335d others(4): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48656348 | ||||||
| chr2:48656348 | GT | G | 191 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(188): Show |
205 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(202): Show |
intron_variant | MODIFIER | c.978+9335delT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48656348 | ||||||
| chr2:48656348 | GTT | G | 50 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(47): Show |
55 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.978+9334_978+9335d others(4): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48656348 | ||||||
| chr2:48656348 | GTTTTTTT others(1): Show |
G | 19 | a0001c0001t0002g0081 a0001c0001t0002g0082 a0001c0001t0002g0090 others(16): Show |
19 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.978+9328_978+9335d others(10): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48656348 | ||||||
| chr2:48656359 | T | G | 3 | a0001c0001t0001g0133 a0001c0001t0001g0240 a0002c0014t0001g0195 |
3 | HG03654.hp2 NA19012.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.978+9317T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48656359 | |||||||
| chr2:48656360 | T | G | 183 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(180): Show |
197 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.978+9318T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48656360 | |||||||
| chr2:48656361 | T | G | 47 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(44): Show |
52 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.978+9319T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48656361 | |||||||
| chr2:48656362 | T | G | 1 | a0004c0007t0001g0028 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.978+9320T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48656362 | |||||||
| chr2:48656367 | T | G | 3 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0234 |
3 | HG03710.hp1 HG04199.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.978+9325T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48656367 | |||||||
| chr2:48656368 | T | G | 19 | a0001c0001t0002g0081 a0001c0001t0002g0082 a0001c0001t0002g0090 others(16): Show |
19 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.978+9326T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48656368 | |||||||
| chr2:48656391 | C | A | 1 | a0001c0001t0001g0201 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.978+9349C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48656391 | |||||||
| chr2:48656517 | C | T | 60 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(57): Show |
67 | HG00140.hp1 HG00609.hp2 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.978+9475C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48656517 | |||||||
| chr2:48656828 | G | T | 19 | a0001c0001t0001g0006 a0001c0001t0001g0096 a0001c0001t0001g0097 others(16): Show |
20 | HG00423.hp1 HG02015.hp1 HG02056.hp2 others(17): Show |
intron_variant | MODIFIER | c.978+9786G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48656828 | |||||||
| chr2:48656870 | G | A | 2 | a0001c0001t0001g0003 a0001c0001t0001g0288 |
5 | HG01884.hp2 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.978+9828G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48656870 | |||||||
| chr2:48657032 | T | C | 315 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(312): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.978+9990T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48657032 | |||||||
| chr2:48657086 | A | G | 1 | a0001c0001t0001g0279 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.978+10044A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48657086 | |||||||
| chr2:48657092 | A | G | 49 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0054 others(46): Show |
51 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.978+10050A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48657092 | |||||||
| chr2:48657251 | C | T | 12 | a0001c0001t0001g0017 a0001c0001t0001g0290 a0001c0001t0001g0291 others(9): Show |
12 | HG01074.hp1 HG01109.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.978+10209C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48657251 | |||||||
| chr2:48657280 | A | G | 49 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0054 others(46): Show |
51 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.978+10238A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48657280 | |||||||
| chr2:48657308 | C | T | 1 | a0001c0001t0001g0020 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.978+10266C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48657308 | |||||||
| chr2:48657367 | G | A | 10 | a0001c0003t0001g0064 a0001c0003t0001g0066 a0001c0003t0001g0068 others(7): Show |
10 | HG02486.hp2 HG02622.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.978+10325G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48657367 | |||||||
| chr2:48657409 | T | G | 47 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(44): Show |
52 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.978+10367T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48657409 | |||||||
| chr2:48657672 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.978+10630A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48657672 | |||||||
| chr2:48657763 | GT | G | 279 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(276): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.978+10733delT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48657763 | ||||||
| chr2:48658235 | A | G | 296 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(293): Show |
319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.978+11193A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48658235 | |||||||
| chr2:48658303 | T | G | 2 | a0001c0001t0001g0085 a0001c0001t0001g0086 |
2 | NA18940.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.978+11261T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48658303 | |||||||
| chr2:48658318 | A | G | 48 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(45): Show |
53 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.978+11276A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48658318 | |||||||
| chr2:48658345 | T | A | 18 | a0001c0003t0001g0018 a0001c0003t0001g0062 a0001c0003t0001g0064 others(15): Show |
18 | HG01243.hp1 HG02486.hp2 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.978+11303T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48658345 | |||||||
| chr2:48658358 | A | G | 2 | a0001c0001t0001g0003 a0001c0001t0001g0288 |
5 | HG01884.hp2 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.978+11316A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48658358 | |||||||
| chr2:48658407 | G | A | 1 | a0001c0001t0001g0167 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.979-11315G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48658407 | |||||||
| chr2:48658501 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.979-11221G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48658501 | |||||||
| chr2:48658561 | T | C | 19 | a0001c0001t0002g0081 a0001c0001t0002g0082 a0001c0001t0002g0090 others(16): Show |
19 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.979-11161T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48658561 | |||||||
| chr2:48658714 | A | G | 315 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(312): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.979-11008A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48658714 | |||||||
| chr2:48658816 | T | C | 21 | a0001c0001t0001g0003 a0001c0001t0001g0288 a0001c0001t0002g0081 others(18): Show |
24 | HG01243.hp2 HG01884.hp2 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.979-10906T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48658816 | |||||||
| chr2:48658847 | T | G | 1 | a0001c0003t0001g0064 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.979-10875T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48658847 | |||||||
| chr2:48658850 | T | TC | 107 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(104): Show |
116 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.979-10872_979-1087 others(5): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48658850 | |||||||
| chr2:48659090 | C | T | 315 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(312): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.979-10632C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48659090 | |||||||
| chr2:48659134 | T | A | 315 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(312): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.979-10588T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48659134 | |||||||
| chr2:48659289 | G | T | 1 | a0007c0013t0001g0280 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.979-10433G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48659289 | |||||||
| chr2:48659318 | T | G | 1 | a0006c0009t0001g0152 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.979-10404T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48659318 | |||||||
| chr2:48659456 | G | C | 1 | a0001c0001t0002g0161 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.979-10266G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48659456 | |||||||
| chr2:48659636 | A | C | 2 | a0002c0002t0001g0216 a0002c0002t0001g0217 |
2 | HG02040.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.979-10086A>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48659636 | |||||||
| chr2:48659726 | G | A | 66 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(63): Show |
71 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.979-9996G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48659726 | |||||||
| chr2:48659743 | A | T | 18 | a0001c0003t0001g0018 a0001c0003t0001g0062 a0001c0003t0001g0064 others(15): Show |
18 | HG01243.hp1 HG02486.hp2 HG02615.hp2 others(15): Show |
intron_variant | MODIFIER | c.979-9979A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48659743 | |||||||
| chr2:48659904 | A | G | 2 | a0001c0001t0001g0309 a0001c0001t0001g0310 |
2 | HG02258.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.979-9818A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48659904 | |||||||
| chr2:48659908 | A | G | 1 | a0001c0001t0001g0122 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.979-9814A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48659908 | |||||||
| chr2:48659912 | G | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0307 a0001c0001t0001g0308 others(1): Show |
5 | HG00642.hp1 HG01361.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.979-9810G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48659912 | |||||||
| chr2:48660093 | A | AC | 32 | a0001c0001t0001g0006 a0001c0001t0001g0096 a0001c0001t0001g0097 others(29): Show |
33 | HG00423.hp1 HG00741.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.979-9629_979-9628i others(3): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48660093 | |||||||
| chr2:48660095 | T | G | 32 | a0001c0001t0001g0006 a0001c0001t0001g0096 a0001c0001t0001g0097 others(29): Show |
33 | HG00423.hp1 HG00741.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.979-9627T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48660095 | |||||||
| chr2:48660095 | T | TG | 286 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(283): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.979-9627_979-9626i others(3): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48660095 | |||||||
| chr2:48660311 | T | C | 1 | a0001c0001t0001g0276 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.979-9411T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48660311 | |||||||
| chr2:48660312 | T | C | 1 | a0001c0001t0001g0276 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.979-9410T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48660312 | |||||||
| chr2:48660397 | G | T | 4 | a0001c0001t0001g0097 a0001c0001t0001g0150 a0001c0001t0001g0151 others(1): Show |
4 | HG02015.hp1 HG02056.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.979-9325G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48660397 | |||||||
| chr2:48660454 | G | A | 4 | a0001c0001t0001g0097 a0001c0001t0001g0150 a0001c0001t0001g0151 others(1): Show |
4 | HG02015.hp1 HG02056.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.979-9268G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48660454 | |||||||
| chr2:48660506 | G | A | 1 | a0001c0003t0001g0069 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.979-9216G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48660506 | |||||||
| chr2:48660560 | T | G | 1 | a0001c0001t0004g0174 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.979-9162T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48660560 | |||||||
| chr2:48660650 | T | C | 1 | a0001c0001t0001g0274 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.979-9072T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48660650 | |||||||
| chr2:48660659 | T | C | 3 | a0001c0001t0001g0025 a0001c0001t0001g0052 a0001c0001t0001g0056 |
3 | HG00323.hp2 HG01074.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.979-9063T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48660659 | |||||||
| chr2:48660677 | C | T | 47 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(44): Show |
52 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.979-9045C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48660677 | |||||||
| chr2:48660917 | A | C | 1 | a0007c0013t0001g0280 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.979-8805A>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48660917 | |||||||
| chr2:48660918 | G | C | 1 | a0007c0013t0001g0280 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.979-8804G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48660918 | |||||||
| chr2:48660952 | T | G | 1 | a0001c0001t0001g0038 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.979-8770T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48660952 | |||||||
| chr2:48661247 | C | CT | 104 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0013 others(101): Show |
112 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.979-8447dupT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48661247 | ||||||
| chr2:48661247 | C | CTT | 92 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(89): Show |
98 | HG00099.hp2 HG00423.hp1 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.979-8448_979-8447d others(4): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48661247 | ||||||
| chr2:48661247 | C | CTTT | 11 | a0001c0001t0001g0100 a0001c0001t0001g0119 a0001c0001t0001g0125 others(8): Show |
11 | HG00621.hp2 HG01069.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.979-8449_979-8447d others(5): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48661247 | ||||||
| chr2:48661247 | C | CTTTT | 8 | a0001c0001t0001g0003 a0001c0001t0001g0282 a0001c0001t0001g0283 others(5): Show |
11 | HG01109.hp2 HG01884.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.979-8450_979-8447d others(6): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48661247 | ||||||
| chr2:48661247 | C | CTTTTT | 7 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0295 others(4): Show |
7 | HG02145.hp1 HG02145.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.979-8451_979-8447d others(7): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48661247 | ||||||
| chr2:48661247 | CT | C | 38 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(35): Show |
43 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(40): Show |
intron_variant | MODIFIER | c.979-8447delT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48661247 | ||||||
| chr2:48661247 | CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0001g0085 a0001c0001t0001g0086 |
2 | NA18940.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.979-8456_979-8447d others(12): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48661247 | ||||||
| chr2:48661247 | CTTTTTTT others(4): Show |
C | 13 | a0001c0001t0001g0016 a0001c0001t0001g0273 a0001c0001t0001g0304 others(10): Show |
14 | HG00642.hp1 HG01361.hp2 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.979-8457_979-8447d others(13): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48661247 | ||||||
| chr2:48661394 | T | C | 65 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(62): Show |
70 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.979-8328T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48661394 | |||||||
| chr2:48661414 | T | C | 1 | a0002c0002t0001g0213 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.979-8308T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48661414 | |||||||
| chr2:48661696 | A | AT | 47 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(44): Show |
52 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.979-8018dupT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48661696 | ||||||
| chr2:48661740 | A | G | 2 | a0001c0001t0001g0265 a0001c0003t0001g0075 |
2 | HG02818.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.979-7982A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48661740 | |||||||
| chr2:48661758 | A | C | 48 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(45): Show |
53 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.979-7964A>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48661758 | |||||||
| chr2:48661868 | T | G | 3 | a0001c0001t0001g0169 a0001c0001t0001g0251 a0001c0001t0001g0255 |
3 | HG01928.hp1 HG01978.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.979-7854T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48661868 | |||||||
| chr2:48661892 | C | T | 1 | a0002c0002t0001g0140 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.979-7830C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48661892 | |||||||
| chr2:48661909 | G | A | 46 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(43): Show |
51 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.979-7813G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48661909 | |||||||
| chr2:48661932 | C | T | 1 | a0001c0001t0001g0287 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.979-7790C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48661932 | |||||||
| chr2:48661990 | C | T | 2 | a0001c0001t0001g0003 a0001c0001t0001g0288 |
5 | HG01884.hp2 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.979-7732C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48661990 | |||||||
| chr2:48662111 | T | G | 19 | a0001c0001t0002g0081 a0001c0001t0002g0082 a0001c0001t0002g0090 others(16): Show |
19 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.979-7611T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48662111 | |||||||
| chr2:48662114 | A | C | 1 | a0001c0001t0001g0255 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.979-7608A>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48662114 | |||||||
| chr2:48662204 | T | A | 1 | a0001c0001t0001g0266 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.979-7518T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48662204 | |||||||
| chr2:48662307 | A | T | 188 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(185): Show |
202 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.979-7415A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48662307 | |||||||
| chr2:48662445 | C | T | 320 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(317): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.979-7277C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48662445 | |||||||
| chr2:48662594 | G | C | 47 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(44): Show |
52 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.979-7128G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48662594 | |||||||
| chr2:48662652 | C | CT | 36 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0089 others(33): Show |
39 | HG00544.hp1 HG00558.hp1 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.979-7050dupT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48662652 | ||||||
| chr2:48662652 | CT | C | 41 | a0001c0001t0001g0005 a0001c0001t0001g0016 a0001c0001t0001g0017 others(38): Show |
43 | HG00323.hp1 HG00642.hp1 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.979-7050delT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48662652 | ||||||
| chr2:48662652 | CTT | C | 70 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0019 others(67): Show |
77 | HG00099.hp1 HG00323.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.979-7051_979-7050d others(4): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48662652 | ||||||
| chr2:48662799 | T | C | 6 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 others(3): Show |
6 | HG02145.hp2 HG02630.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.979-6923T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48662799 | |||||||
| chr2:48662828 | A | G | 37 | a0001c0001t0001g0006 a0001c0001t0001g0096 a0001c0001t0001g0097 others(34): Show |
38 | HG00423.hp1 HG00741.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.979-6894A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48662828 | |||||||
| chr2:48662869 | C | G | 1 | a0001c0001t0001g0054 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.979-6853C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48662869 | |||||||
| chr2:48662898 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.979-6824C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48662898 | |||||||
| chr2:48662915 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.979-6807G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48662915 | |||||||
| chr2:48662955 | C | T | 48 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(45): Show |
53 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.979-6767C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48662955 | |||||||
| chr2:48662959 | G | A | 21 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0282 others(18): Show |
24 | HG01074.hp1 HG01109.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.979-6763G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48662959 | |||||||
| chr2:48663037 | C | T | 19 | a0001c0003t0001g0018 a0001c0003t0001g0061 a0001c0003t0001g0062 others(16): Show |
19 | HG01243.hp1 HG01891.hp1 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.979-6685C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48663037 | |||||||
| chr2:48663118 | A | G | 19 | a0001c0001t0001g0016 a0001c0001t0001g0273 a0001c0001t0001g0304 others(16): Show |
20 | HG00642.hp1 HG01361.hp2 HG01515.hp2 others(17): Show |
intron_variant | MODIFIER | c.979-6604A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48663118 | |||||||
| chr2:48663191 | T | C | 13 | a0001c0001t0001g0016 a0001c0001t0001g0273 a0001c0001t0001g0304 others(10): Show |
14 | HG00642.hp1 HG01361.hp2 HG01515.hp2 others(11): Show |
intron_variant | MODIFIER | c.979-6531T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48663191 | |||||||
| chr2:48663328 | C | T | 1 | a0001c0001t0001g0183 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.979-6394C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48663328 | |||||||
| chr2:48663393 | A | G | 315 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(312): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.979-6329A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48663393 | |||||||
| chr2:48663611 | A | C | 1 | a0001c0001t0001g0021 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.979-6111A>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48663611 | |||||||
| chr2:48663637 | A | T | 1 | a0001c0001t0001g0155 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.979-6085A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48663637 | |||||||
| chr2:48663774 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.979-5948G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48663774 | |||||||
| chr2:48663824 | G | T | 1 | a0001c0001t0001g0035 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.979-5898G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48663824 | |||||||
| chr2:48664019 | C | T | 21 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0282 others(18): Show |
24 | HG01074.hp1 HG01109.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.979-5703C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48664019 | |||||||
| chr2:48664079 | A | G | 21 | a0001c0003t0001g0018 a0001c0003t0001g0061 a0001c0003t0001g0062 others(18): Show |
21 | HG01070.hp1 HG01123.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.979-5643A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48664079 | |||||||
| chr2:48664095 | A | T | 1 | a0002c0002t0001g0210 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.979-5627A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48664095 | |||||||
| chr2:48664145 | T | C | 19 | a0001c0001t0001g0016 a0001c0001t0001g0273 a0001c0001t0001g0304 others(16): Show |
20 | HG00642.hp1 HG01361.hp2 HG01515.hp2 others(17): Show |
intron_variant | MODIFIER | c.979-5577T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48664145 | |||||||
| chr2:48664148 | C | T | 47 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(44): Show |
52 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.979-5574C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48664148 | |||||||
| chr2:48664228 | C | A | 12 | a0001c0001t0001g0017 a0001c0001t0001g0290 a0001c0001t0001g0291 others(9): Show |
12 | HG01074.hp1 HG01109.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.979-5494C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48664228 | |||||||
| chr2:48664265 | T | G | 1 | a0001c0001t0001g0301 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.979-5457T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48664265 | |||||||
| chr2:48664298 | C | A | 86 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(83): Show |
94 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.979-5424C>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48664298 | |||||||
| chr2:48664318 | T | G | 19 | a0001c0001t0002g0081 a0001c0001t0002g0082 a0001c0001t0002g0090 others(16): Show |
19 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.979-5404T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48664318 | |||||||
| chr2:48664415 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0134 a0001c0001t0001g0158 |
4 | HG00099.hp2 HG01192.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.979-5307C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48664415 | |||||||
| chr2:48664590 | G | A | 4 | a0001c0001t0001g0294 a0001c0001t0001g0295 a0001c0001t0001g0296 others(1): Show |
4 | HG01109.hp2 HG02559.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.979-5132G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48664590 | |||||||
| chr2:48664689 | G | A | 1 | a0001c0001t0001g0281 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.979-5033G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48664689 | |||||||
| chr2:48664952 | ACT | A | 4 | a0001c0001t0001g0316 a0001c0001t0001g0318 a0001c0001t0001g0319 others(1): Show |
4 | HG02145.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.979-4767_979-4766d others(4): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48664952 | ||||||
| chr2:48665022 | C | T | 6 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(3): Show |
6 | HG02055.hp2 HG02145.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.979-4700C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48665022 | |||||||
| chr2:48665032 | G | C | 1 | a0002c0002t0001g0014 | 2 | NA18962.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.979-4690G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48665032 | |||||||
| chr2:48665046 | C | T | 1 | a0001c0001t0001g0287 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.979-4676C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48665046 | |||||||
| chr2:48665055 | G | A | 19 | a0001c0001t0002g0081 a0001c0001t0002g0082 a0001c0001t0002g0090 others(16): Show |
19 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.979-4667G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48665055 | |||||||
| chr2:48665203 | C | T | 12 | a0001c0001t0001g0017 a0001c0001t0001g0290 a0001c0001t0001g0291 others(9): Show |
12 | HG01074.hp1 HG01109.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.979-4519C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48665203 | |||||||
| chr2:48665257 | G | A | 315 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(312): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.979-4465G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48665257 | |||||||
| chr2:48665276 | TTC | T | 5 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 others(2): Show |
5 | HG02145.hp2 HG02630.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.979-4436_979-4435d others(4): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48665276 | ||||||
| chr2:48665286 | C | CT | 67 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(64): Show |
72 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.979-4421dupT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48665286 | ||||||
| chr2:48665286 | CT | C | 25 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0085 others(22): Show |
28 | HG01074.hp1 HG01109.hp2 HG01257.hp2 others(25): Show |
intron_variant | MODIFIER | c.979-4421delT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48665286 | ||||||
| chr2:48665349 | T | TTCCTCCT others(22): Show |
1 | a0001c0001t0001g0100 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.979-4372_979-4344d others(31): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48665349 | ||||||
| chr2:48665550 | A | T | 1 | a0001c0001t0001g0050 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.979-4172A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48665550 | |||||||
| chr2:48665623 | A | G | 49 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(46): Show |
54 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.979-4099A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48665623 | |||||||
| chr2:48665626 | T | C | 1 | a0001c0001t0001g0039 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.979-4096T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48665626 | |||||||
| chr2:48665632 | A | G | 19 | a0001c0001t0002g0081 a0001c0001t0002g0082 a0001c0001t0002g0090 others(16): Show |
19 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.979-4090A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48665632 | |||||||
| chr2:48665668 | T | C | 6 | a0001c0001t0001g0238 a0001c0001t0001g0252 a0001c0001t0001g0253 others(3): Show |
6 | NA18960.hp2 NA19000.hp1 NA19003.hp2 others(3): Show |
intron_variant | MODIFIER | c.979-4054T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48665668 | |||||||
| chr2:48665762 | C | T | 1 | a0001c0001t0001g0307 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.979-3960C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48665762 | |||||||
| chr2:48665974 | A | G | 2 | a0005c0008t0002g0302 a0005c0008t0002g0303 |
2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.979-3748A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48665974 | |||||||
| chr2:48666168 | T | C | 69 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(66): Show |
74 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.979-3554T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48666168 | |||||||
| chr2:48666193 | G | T | 12 | a0001c0001t0001g0016 a0001c0001t0001g0304 a0001c0001t0001g0305 others(9): Show |
13 | HG00642.hp1 HG01361.hp2 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.979-3529G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48666193 | |||||||
| chr2:48666211 | CT | C | 12 | a0001c0003t0001g0018 a0001c0003t0001g0061 a0001c0003t0001g0062 others(9): Show |
12 | HG01243.hp1 HG01891.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.979-3499delT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48666211 | ||||||
| chr2:48666348 | G | C | 12 | a0001c0001t0001g0017 a0001c0001t0001g0290 a0001c0001t0001g0291 others(9): Show |
12 | HG01074.hp1 HG01109.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.979-3374G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48666348 | |||||||
| chr2:48666505 | C | T | 68 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(65): Show |
73 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.979-3217C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48666505 | |||||||
| chr2:48666523 | A | G | 1 | a0001c0001t0001g0023 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.979-3199A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48666523 | |||||||
| chr2:48666584 | G | GGT | 142 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(139): Show |
155 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(152): Show |
intron_variant | MODIFIER | c.979-3111_979-3110d others(4): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48666584 | ||||||
| chr2:48666584 | G | GGTGT | 43 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0015 others(40): Show |
47 | HG00099.hp2 HG00544.hp1 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.979-3113_979-3110d others(6): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48666584 | ||||||
| chr2:48666584 | G | GGTGTGT | 4 | a0001c0001t0001g0127 a0001c0001t0001g0272 a0001c0001t0001g0278 others(1): Show |
4 | HG00597.hp2 HG01934.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.979-3115_979-3110d others(8): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48666584 | ||||||
| chr2:48666584 | G | GTGT | 5 | a0001c0001t0001g0222 a0001c0001t0001g0269 a0001c0001t0001g0316 others(2): Show |
5 | HG01175.hp1 HG02165.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.979-3138_979-3137i others(5): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48666584 | |||||||
| chr2:48666584 | GGTGT | G | 7 | a0001c0001t0001g0003 a0001c0001t0001g0288 a0001c0001t0001g0294 others(4): Show |
10 | HG01109.hp2 HG01884.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.979-3113_979-3110d others(6): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48666584 | ||||||
| chr2:48666584 | GGTGTGT | G | 15 | a0001c0001t0001g0017 a0001c0001t0001g0282 a0001c0001t0001g0283 others(12): Show |
15 | HG01074.hp1 HG01884.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.979-3115_979-3110d others(8): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48666584 | ||||||
| chr2:48666613 | T | G | 1 | a0002c0002t0001g0204 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.979-3109T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48666613 | |||||||
| chr2:48666691 | T | C | 1 | a0001c0001t0001g0042 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.979-3031T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48666691 | |||||||
| chr2:48666874 | T | C | 1 | a0001c0001t0005g0129 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.979-2848T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48666874 | |||||||
| chr2:48667115 | A | AT | 203 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(200): Show |
217 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.979-2592dupT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48667115 | ||||||
| chr2:48667115 | A | ATT | 8 | a0001c0001t0001g0170 a0001c0001t0001g0238 a0001c0001t0001g0252 others(5): Show |
8 | HG04184.hp2 NA18941.hp1 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.979-2593_979-2592d others(4): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48667115 | ||||||
| chr2:48667115 | AT | A | 44 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0043 others(41): Show |
47 | HG00544.hp2 HG01074.hp1 HG01109.hp2 others(44): Show |
intron_variant | MODIFIER | c.979-2592delT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48667115 | ||||||
| chr2:48667166 | C | T | 17 | a0001c0001t0002g0081 a0001c0001t0002g0082 a0001c0001t0002g0090 others(14): Show |
17 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.979-2556C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48667166 | |||||||
| chr2:48667202 | G | T | 12 | a0001c0001t0001g0017 a0001c0001t0001g0290 a0001c0001t0001g0291 others(9): Show |
12 | HG01074.hp1 HG01109.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.979-2520G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48667202 | |||||||
| chr2:48667343 | C | G | 1 | a0001c0001t0001g0275 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.979-2379C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48667343 | |||||||
| chr2:48667465 | A | G | 71 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(68): Show |
77 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.979-2257A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48667465 | |||||||
| chr2:48667682 | A | T | 1 | a0001c0001t0001g0292 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.979-2040A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48667682 | |||||||
| chr2:48667996 | C | G | 18 | a0001c0001t0002g0081 a0001c0001t0002g0082 a0001c0001t0002g0090 others(15): Show |
18 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.979-1726C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48667996 | |||||||
| chr2:48668017 | C | T | 9 | a0001c0001t0001g0003 a0001c0001t0001g0282 a0001c0001t0001g0283 others(6): Show |
12 | HG01884.hp2 HG02055.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.979-1705C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48668017 | |||||||
| chr2:48668018 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.979-1704G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48668018 | |||||||
| chr2:48668109 | C | T | 1 | a0007c0013t0001g0280 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.979-1613C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48668109 | |||||||
| chr2:48668115 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.979-1607C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48668115 | |||||||
| chr2:48668299 | A | G | 1 | a0001c0001t0001g0199 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.979-1423A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48668299 | |||||||
| chr2:48668661 | C | G | 1 | a0001c0001t0001g0281 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.979-1061C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48668661 | |||||||
| chr2:48668696 | A | G | 49 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(46): Show |
54 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.979-1026A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48668696 | |||||||
| chr2:48668837 | A | AAAAT | 7 | a0001c0001t0001g0088 a0001c0001t0001g0150 a0002c0002t0001g0004 others(4): Show |
9 | HG00609.hp2 HG02015.hp1 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.979-859_979-856dup others(4): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48668837 | ||||||
| chr2:48668837 | A | AAAATAAA others(5): Show |
3 | a0001c0001t0002g0092 a0001c0001t0002g0176 a0005c0008t0002g0303 |
3 | HG01243.hp2 HG02647.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.979-867_979-856dup others(12): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48668837 | ||||||
| chr2:48668837 | A | AAAATAAA others(9): Show |
13 | a0001c0001t0002g0081 a0001c0001t0002g0082 a0001c0001t0002g0090 others(10): Show |
13 | HG01891.hp2 HG02055.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.979-871_979-856dup others(16): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48668837 | ||||||
| chr2:48668837 | A | AAAATAAA others(13): Show |
3 | a0001c0001t0002g0177 a0001c0001t0002g0179 a0001c0001t0002g0182 |
3 | HG03139.hp2 HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.979-875_979-856dup others(20): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48668837 | ||||||
| chr2:48668837 | AAAAT | A | 50 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0019 others(47): Show |
55 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.979-859_979-856del others(4): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr2 | 48668837 | ||||||
| chr2:48669069 | A | G | 1 | a0001c0001t0001g0281 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.979-653A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48669069 | |||||||
| chr2:48669310 | T | A | 46 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0089 others(43): Show |
48 | HG00140.hp2 HG00423.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.979-412T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48669310 | |||||||
| chr2:48669679 | C | T | 1 | a0002c0002t0001g0215 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.979-43C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 6/8 | chr2 | 48669679 | |||||||
| chr2:48670120 | C | T | 1 | a0001c0001t0001g0183 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1239+138C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 7/8 | chr2 | 48670120 | |||||||
| chr2:48670133 | A | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(109): Show |
122 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.1239+151A>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 7/8 | chr2 | 48670133 | |||||||
| chr2:48670248 | G | A | 7 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1239+266G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 7/8 | chr2 | 48670248 | |||||||
| chr2:48670256 | TG | T | 20 | a0001c0001t0002g0081 a0001c0001t0002g0082 a0001c0001t0002g0090 others(17): Show |
20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1239+276delG | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr2 | 48670256 | ||||||
| chr2:48670379 | T | TA | 56 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(53): Show |
62 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.1239+409dupA | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr2 | 48670379 | ||||||
| chr2:48670398 | T | A | 12 | a0001c0001t0001g0017 a0001c0001t0001g0290 a0001c0001t0001g0291 others(9): Show |
12 | HG01074.hp1 HG01109.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1239+416T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 7/8 | chr2 | 48670398 | |||||||
| chr2:48670786 | G | T | 1 | a0001c0003t0001g0064 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1239+804G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 7/8 | chr2 | 48670786 | |||||||
| chr2:48670802 | A | G | 40 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(37): Show |
44 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.1240-789A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 7/8 | chr2 | 48670802 | |||||||
| chr2:48670816 | C | CA | 73 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(70): Show |
79 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.1240-775_1240-774i others(3): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 7/8 | chr2 | 48670816 | |||||||
| chr2:48670914 | C | T | 1 | a0001c0001t0006g0289 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1240-677C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 7/8 | chr2 | 48670914 | |||||||
| chr2:48670918 | G | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(70): Show |
79 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.1240-673G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 7/8 | chr2 | 48670918 | |||||||
| chr2:48670926 | T | C | 73 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(70): Show |
79 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.1240-665T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 7/8 | chr2 | 48670926 | |||||||
| chr2:48670970 | C | T | 1 | a0001c0001t0006g0289 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1240-621C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 7/8 | chr2 | 48670970 | |||||||
| chr2:48671075 | G | A | 2 | a0001c0001t0001g0105 a0001c0001t0001g0106 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1240-516G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 7/8 | chr2 | 48671075 | |||||||
| chr2:48671078 | T | A | 1 | a0005c0008t0002g0303 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1240-513T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 7/8 | chr2 | 48671078 | |||||||
| chr2:48671261 | G | C | 53 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(50): Show |
59 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(56): Show |
intron_variant | MODIFIER | c.1240-330G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 7/8 | chr2 | 48671261 | |||||||
| chr2:48671400 | C | T | 73 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(70): Show |
79 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.1240-191C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 7/8 | chr2 | 48671400 | |||||||
| chr2:48671479 | T | C | 1 | a0001c0001t0001g0275 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1240-112T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 7/8 | chr2 | 48671479 | |||||||
| chr2:48671582 | C | T | 2 | a0005c0008t0002g0302 a0005c0008t0002g0303 |
2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1240-9C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 7/8 | chr2 | 48671582 | |||||||
| chr2:48671710 | T | G | 1 | a0001c0001t0001g0036 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1329+30T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48671710 | |||||||
| chr2:48672011 | G | A | 181 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(178): Show |
194 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.1329+331G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48672011 | |||||||
| chr2:48672052 | A | G | 20 | a0001c0001t0002g0081 a0001c0001t0002g0082 a0001c0001t0002g0090 others(17): Show |
20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1329+372A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48672052 | |||||||
| chr2:48672147 | G | A | 21 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0282 others(18): Show |
24 | HG01074.hp1 HG01109.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.1329+467G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48672147 | |||||||
| chr2:48672377 | C | G | 51 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(48): Show |
57 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(54): Show |
intron_variant | MODIFIER | c.1329+697C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48672377 | |||||||
| chr2:48672563 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1329+883G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48672563 | |||||||
| chr2:48672668 | C | T | 35 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0015 others(32): Show |
38 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(35): Show |
intron_variant | MODIFIER | c.1329+988C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48672668 | |||||||
| chr2:48672722 | T | C | 70 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(67): Show |
76 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.1329+1042T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48672722 | |||||||
| chr2:48672727 | G | A | 1 | a0001c0001t0001g0269 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1329+1047G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48672727 | |||||||
| chr2:48672728 | T | A | 21 | a0001c0003t0001g0018 a0001c0003t0001g0061 a0001c0003t0001g0062 others(18): Show |
21 | HG01070.hp1 HG01123.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1329+1048T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48672728 | |||||||
| chr2:48672783 | G | T | 2 | a0001c0001t0001g0003 a0001c0001t0001g0288 |
5 | HG01884.hp2 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1329+1103G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48672783 | |||||||
| chr2:48672867 | C | T | 18 | a0001c0001t0001g0016 a0001c0001t0001g0304 a0001c0001t0001g0305 others(15): Show |
19 | HG00642.hp1 HG01361.hp2 HG01515.hp2 others(16): Show |
intron_variant | MODIFIER | c.1329+1187C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48672867 | |||||||
| chr2:48672917 | T | C | 1 | a0001c0001t0001g0245 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1329+1237T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48672917 | |||||||
| chr2:48673000 | A | G | 72 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(69): Show |
78 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.1329+1320A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48673000 | |||||||
| chr2:48673038 | T | C | 2 | a0002c0002t0001g0200 a0002c0002t0001g0205 |
2 | NA18961.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.1329+1358T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48673038 | |||||||
| chr2:48673084 | G | T | 2 | a0002c0002t0001g0140 a0002c0002t0001g0142 |
2 | HG01496.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1329+1404G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48673084 | |||||||
| chr2:48673104 | T | C | 1 | a0001c0001t0001g0294 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1329+1424T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48673104 | |||||||
| chr2:48673189 | C | T | 20 | a0001c0001t0002g0081 a0001c0001t0002g0082 a0001c0001t0002g0090 others(17): Show |
20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1329+1509C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48673189 | |||||||
| chr2:48673310 | A | G | 1 | a0001c0001t0001g0109 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1329+1630A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48673310 | |||||||
| chr2:48673359 | C | CT | 169 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(166): Show |
181 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(178): Show |
intron_variant | MODIFIER | c.1329+1700dupT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 48673359 | ||||||
| chr2:48673359 | C | CTT | 7 | a0001c0001t0001g0119 a0001c0001t0001g0122 a0001c0001t0001g0123 others(4): Show |
7 | HG00140.hp2 HG00621.hp2 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.1329+1699_1329+170 others(6): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 48673359 | ||||||
| chr2:48673359 | CT | C | 49 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0290 others(46): Show |
50 | HG00642.hp1 HG01070.hp1 HG01074.hp1 others(47): Show |
intron_variant | MODIFIER | c.1329+1700delT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 48673359 | ||||||
| chr2:48673359 | CTT | C | 19 | a0001c0001t0001g0100 a0001c0001t0002g0082 a0001c0001t0002g0090 others(16): Show |
19 | HG01243.hp2 HG01891.hp2 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.1329+1699_1329+170 others(6): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 48673359 | ||||||
| chr2:48673359 | CTTT | C | 52 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(49): Show |
58 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.1329+1698_1329+170 others(7): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 48673359 | ||||||
| chr2:48673507 | C | T | 39 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0017 others(36): Show |
43 | HG00642.hp1 HG01074.hp1 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.1329+1827C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48673507 | |||||||
| chr2:48673592 | T | C | 73 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(70): Show |
79 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.1329+1912T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48673592 | |||||||
| chr2:48673663 | A | C | 73 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(70): Show |
79 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.1329+1983A>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48673663 | |||||||
| chr2:48673720 | G | A | 6 | a0002c0002t0001g0004 a0002c0002t0001g0171 a0002c0002t0001g0212 others(3): Show |
8 | HG00609.hp2 HG02135.hp1 NA18947.hp1 others(5): Show |
intron_variant | MODIFIER | c.1329+2040G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48673720 | |||||||
| chr2:48673850 | A | G | 20 | a0001c0001t0002g0081 a0001c0001t0002g0082 a0001c0001t0002g0090 others(17): Show |
20 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1329+2170A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48673850 | |||||||
| chr2:48673912 | C | T | 180 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(177): Show |
193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.1329+2232C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48673912 | |||||||
| chr2:48674125 | T | C | 1 | a0001c0001t0001g0266 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1329+2445T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48674125 | |||||||
| chr2:48674173 | A | C | 1 | a0001c0001t0001g0165 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1329+2493A>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48674173 | |||||||
| chr2:48674174 | T | A | 1 | a0001c0001t0001g0165 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1329+2494T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48674174 | |||||||
| chr2:48674174 | T | C | 73 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(70): Show |
79 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.1329+2494T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48674174 | |||||||
| chr2:48674175 | T | C | 1 | a0001c0001t0001g0165 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1329+2495T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48674175 | |||||||
| chr2:48674177 | G | C | 1 | a0001c0001t0001g0165 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1329+2497G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48674177 | |||||||
| chr2:48674178 | A | G | 1 | a0001c0001t0001g0165 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1329+2498A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48674178 | |||||||
| chr2:48674183 | T | A | 1 | a0001c0001t0001g0165 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1329+2503T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48674183 | |||||||
| chr2:48674346 | A | G | 1 | a0001c0001t0006g0289 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1329+2666A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48674346 | |||||||
| chr2:48674356 | C | G | 1 | a0001c0001t0006g0289 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1329+2676C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48674356 | |||||||
| chr2:48674379 | T | G | 3 | a0001c0001t0001g0282 a0001c0001t0001g0284 a0001c0001t0001g0285 |
3 | HG02055.hp2 HG02145.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1329+2699T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48674379 | |||||||
| chr2:48674500 | C | T | 2 | a0003c0004t0001g0063 a0003c0004t0001g0080 |
2 | HG01070.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.1329+2820C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48674500 | |||||||
| chr2:48674529 | A | T | 1 | a0001c0003t0001g0061 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1329+2849A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48674529 | |||||||
| chr2:48674758 | G | A | 1 | a0001c0003t0001g0067 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1329+3078G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48674758 | |||||||
| chr2:48674833 | G | A | 21 | a0001c0003t0001g0018 a0001c0003t0001g0061 a0001c0003t0001g0062 others(18): Show |
21 | HG01070.hp1 HG01123.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1329+3153G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48674833 | |||||||
| chr2:48675309 | G | C | 1 | a0001c0001t0006g0289 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1329+3629G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48675309 | |||||||
| chr2:48675322 | A | G | 1 | a0001c0001t0006g0289 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1329+3642A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48675322 | |||||||
| chr2:48675387 | A | G | 1 | a0001c0001t0001g0221 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1329+3707A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48675387 | |||||||
| chr2:48675428 | A | C | 3 | a0001c0001t0001g0169 a0001c0001t0001g0251 a0001c0001t0001g0255 |
3 | HG01928.hp1 HG01978.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.1329+3748A>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48675428 | |||||||
| chr2:48675439 | A | G | 59 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(56): Show |
65 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(62): Show |
intron_variant | MODIFIER | c.1329+3759A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48675439 | |||||||
| chr2:48675451 | G | C | 1 | a0001c0001t0001g0126 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1329+3771G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48675451 | |||||||
| chr2:48675487 | A | G | 12 | a0001c0001t0001g0017 a0001c0001t0001g0290 a0001c0001t0001g0291 others(9): Show |
12 | HG01074.hp1 HG01109.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1329+3807A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48675487 | |||||||
| chr2:48675617 | C | T | 4 | a0001c0001t0001g0316 a0001c0001t0001g0318 a0001c0001t0001g0319 others(1): Show |
4 | HG02145.hp2 HG02630.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1330-3718C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48675617 | |||||||
| chr2:48675618 | G | A | 18 | a0001c0001t0002g0081 a0001c0001t0002g0082 a0001c0001t0002g0090 others(15): Show |
18 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1330-3717G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48675618 | |||||||
| chr2:48675728 | G | A | 1 | a0001c0001t0001g0146 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1330-3607G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48675728 | |||||||
| chr2:48675729 | T | C | 5 | a0001c0003t0001g0075 a0001c0003t0001g0076 a0001c0003t0001g0077 others(2): Show |
5 | HG02622.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1330-3606T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48675729 | |||||||
| chr2:48675870 | G | A | 316 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(313): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.1330-3465G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48675870 | |||||||
| chr2:48675932 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1330-3403G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48675932 | |||||||
| chr2:48676248 | C | G | 12 | a0001c0001t0001g0017 a0001c0001t0001g0290 a0001c0001t0001g0291 others(9): Show |
12 | HG01074.hp1 HG01109.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1330-3087C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48676248 | |||||||
| chr2:48676536 | C | G | 1 | a0001c0012t0001g0242 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1330-2799C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48676536 | |||||||
| chr2:48676833 | C | CATCTAT | 3 | a0001c0001t0001g0238 a0001c0001t0001g0274 a0001c0001t0001g0276 |
3 | NA18975.hp1 NA19075.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.1330-2481_1330-247 others(10): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 48676833 | ||||||
| chr2:48676925 | AT | A | 58 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(55): Show |
64 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.1330-2399delT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 48676925 | ||||||
| chr2:48676930 | T | A | 1 | a0001c0001t0001g0246 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1330-2405T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48676930 | |||||||
| chr2:48676931 | T | A | 4 | a0001c0001t0001g0003 a0001c0001t0001g0281 a0001c0001t0001g0288 others(1): Show |
7 | HG00738.hp1 HG01884.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.1330-2404T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48676931 | |||||||
| chr2:48677050 | T | C | 1 | a0001c0001t0001g0148 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1330-2285T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48677050 | |||||||
| chr2:48677128 | G | A | 315 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(312): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.1330-2207G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48677128 | |||||||
| chr2:48677223 | T | C | 3 | a0001c0001t0001g0197 a0001c0001t0001g0258 a0001c0001t0001g0261 |
3 | HG03486.hp2 HG03579.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1330-2112T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48677223 | |||||||
| chr2:48677231 | A | T | 79 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(76): Show |
85 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.1330-2104A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48677231 | |||||||
| chr2:48677262 | C | T | 2 | a0001c0001t0001g0173 a0001c0001t0001g0321 |
2 | HG02970.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1330-2073C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48677262 | |||||||
| chr2:48677311 | G | C | 1 | a0001c0001t0001g0126 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1330-2024G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48677311 | |||||||
| chr2:48677338 | G | A | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG00558.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.1330-1997G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48677338 | |||||||
| chr2:48677411 | T | C | 81 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(78): Show |
87 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.1330-1924T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48677411 | |||||||
| chr2:48677423 | G | A | 7 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 others(4): Show |
7 | HG02145.hp2 HG02630.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1330-1912G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48677423 | |||||||
| chr2:48677470 | C | T | 58 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(55): Show |
64 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.1330-1865C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48677470 | |||||||
| chr2:48677520 | A | G | 60 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(57): Show |
66 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.1330-1815A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48677520 | |||||||
| chr2:48677571 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1330-1764T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48677571 | |||||||
| chr2:48677671 | C | G | 12 | a0001c0001t0001g0016 a0001c0001t0001g0304 a0001c0001t0001g0305 others(9): Show |
13 | HG00642.hp1 HG01361.hp2 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.1330-1664C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48677671 | |||||||
| chr2:48677697 | G | T | 1 | a0001c0001t0001g0312 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1330-1638G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48677697 | |||||||
| chr2:48677699 | G | C | 1 | a0001c0001t0001g0148 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1330-1636G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48677699 | |||||||
| chr2:48677700 | G | C | 12 | a0001c0001t0001g0016 a0001c0001t0001g0304 a0001c0001t0001g0305 others(9): Show |
13 | HG00642.hp1 HG01361.hp2 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.1330-1635G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48677700 | |||||||
| chr2:48677703 | A | G | 286 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(283): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.1330-1632A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48677703 | |||||||
| chr2:48677892 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1330-1443A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48677892 | |||||||
| chr2:48677896 | G | A | 7 | a0001c0001t0001g0282 a0001c0001t0001g0283 a0001c0001t0001g0284 others(4): Show |
7 | HG02055.hp2 HG02145.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.1330-1439G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48677896 | |||||||
| chr2:48677978 | G | GGT | 30 | a0001c0001t0001g0259 a0001c0001t0001g0270 a0001c0001t0001g0271 others(27): Show |
30 | HG00738.hp1 HG01070.hp1 HG01106.hp1 others(27): Show |
intron_variant | MODIFIER | c.1330-1326_1330-132 others(6): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 48677978 | ||||||
| chr2:48677978 | GGT | G | 178 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(175): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.1330-1326_1330-132 others(6): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 48677978 | ||||||
| chr2:48677978 | GGTGT | G | 84 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(81): Show |
97 | HG00323.hp2 HG00544.hp2 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.1330-1328_1330-132 others(8): Show |
GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 48677978 | ||||||
| chr2:48678009 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1330-1326G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48678009 | |||||||
| chr2:48678129 | A | C | 1 | a0001c0001t0001g0250 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1330-1206A>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48678129 | |||||||
| chr2:48678150 | G | C | 2 | a0001c0001t0001g0003 a0001c0001t0001g0288 |
5 | HG01884.hp2 HG02723.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1330-1185G>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48678150 | |||||||
| chr2:48678172 | T | C | 5 | a0002c0002t0001g0012 a0002c0002t0001g0159 a0002c0002t0001g0235 others(2): Show |
6 | HG02027.hp2 HG02165.hp2 NA18747.hp2 others(3): Show |
intron_variant | MODIFIER | c.1330-1163T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48678172 | |||||||
| chr2:48678191 | T | C | 2 | a0001c0001t0002g0161 a0001c0001t0002g0181 |
2 | HG02055.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1330-1144T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48678191 | |||||||
| chr2:48678266 | G | T | 1 | a0001c0001t0001g0281 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1330-1069G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48678266 | |||||||
| chr2:48678290 | T | A | 1 | a0001c0001t0001g0287 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1330-1045T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48678290 | |||||||
| chr2:48678543 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1330-792G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48678543 | |||||||
| chr2:48678659 | A | G | 1 | a0001c0005t0003g0087 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1330-676A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48678659 | |||||||
| chr2:48678803 | T | C | 1 | a0001c0001t0001g0055 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1330-532T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48678803 | |||||||
| chr2:48678805 | T | C | 1 | a0001c0001t0001g0055 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1330-530T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48678805 | |||||||
| chr2:48678806 | T | A | 1 | a0001c0001t0001g0055 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1330-529T>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48678806 | |||||||
| chr2:48678808 | C | G | 1 | a0001c0001t0001g0055 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1330-527C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48678808 | |||||||
| chr2:48678809 | T | C | 1 | a0001c0001t0001g0055 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1330-526T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48678809 | |||||||
| chr2:48678810 | T | G | 1 | a0001c0001t0001g0055 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1330-525T>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48678810 | |||||||
| chr2:48678811 | T | C | 1 | a0001c0001t0001g0055 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1330-524T>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48678811 | |||||||
| chr2:48678815 | G | T | 1 | a0001c0001t0001g0055 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1330-520G>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48678815 | |||||||
| chr2:48678817 | C | T | 224 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(221): Show |
241 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.1330-518C>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48678817 | |||||||
| chr2:48678818 | A | T | 1 | a0001c0001t0001g0055 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1330-517A>T | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48678818 | |||||||
| chr2:48678856 | G | A | 1 | a0001c0001t0001g0258 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1330-479G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48678856 | |||||||
| chr2:48678910 | A | C | 317 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(314): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.1330-425A>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48678910 | |||||||
| chr2:48679003 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1330-332G>A | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48679003 | |||||||
| chr2:48679055 | A | AT | 275 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(272): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.1330-272dupT | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr2 | 48679055 | ||||||
| chr2:48679095 | A | G | 1 | a0001c0001t0001g0301 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1330-240A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48679095 | |||||||
| chr2:48679179 | C | G | 1 | a0001c0001t0001g0089 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1330-156C>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48679179 | |||||||
| chr2:48679220 | A | C | 1 | a0001c0001t0001g0103 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1330-115A>C | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48679220 | |||||||
| chr2:48679221 | A | G | 295 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(292): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.1330-114A>G | GTF2A1L | ENSG00000242441.8 | transcript | ENST00000403751.8 | protein_coding | 8/8 | chr2 | 48679221 |