Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9330 |
| ensemblid | ENSG00000119041.11 |
| hgncid | 4666 |
| symbol | GTF3C3 |
| name | general transcription factor IIIC subunit 3 |
| refseq_nuc | NM_012086.5 |
| refseq_prot | NP_036218.1 |
| ensembl_nuc | ENST00000263956.8 |
| ensembl_prot | ENSP00000263956.3 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 196763035 |
| end | 196799683 |
| strand | - |
| ver | v1.2 |
| region | chr2:196763035-196799683 |
| region5000 | chr2:196758035-196804683 |
| regionname0 | GTF3C3_chr2_196763035_196799683 |
| regionname5000 | GTF3C3_chr2_196758035_196804683 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 886 | 205 | 68 | 55 | 47 | 12 | 22 | 37 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | MSGFS others(881): Show |
chr2 | 196758035 | 196804683 |
| a0002 | 0/1 | 886 | 46 | 15 | 9 | 15 | 0 | 6 | 15 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | MSGFS others(881): Show |
chr2 | 196758035 | 196804683 |
| a0003 | 0/0 | 886 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | MSGFS others(881): Show |
chr2 | 196758035 | 196804683 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 2658 | 200 | 67 | 55 | 43 | 12 | 22 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | ATGTC others(2653): Show |
chr2 | 196758035 | 196804683 | ||
| a0001c0003 | 0/0 | 2658 | 3 | 0 | 0 | 3 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | ATGTC others(2653): Show |
chr2 | 196758035 | 196804683 | ||
| a0001c0005 | 0/0 | 2658 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | ATGTC others(2653): Show |
chr2 | 196758035 | 196804683 | ||
| a0001c0007 | 0/0 | 2658 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | ATGTC others(2653): Show |
chr2 | 196758035 | 196804683 | ||
| a0002c0002 | 0/1 | 2658 | 44 | 15 | 9 | 13 | 0 | 6 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | ATGTC others(2653): Show |
chr2 | 196758035 | 196804683 | ||
| a0002c0004 | 0/0 | 2658 | 2 | 0 | 0 | 2 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | ATGTC others(2653): Show |
chr2 | 196758035 | 196804683 | ||
| a0003c0006 | 0/0 | 2658 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | ATGTC others(2653): Show |
chr2 | 196758035 | 196804683 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4261 | 161 | 53 | 48 | 37 | 8 | 14 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | AGCTT others(4256): Show |
chr2 | 196758035 | 196804683 |
| a0001c0001t0002 | 0/0 | 4261 | 26 | 11 | 3 | 1 | 3 | 8 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | AGCTT others(4256): Show |
chr2 | 196758035 | 196804683 |
| a0001c0001t0004 | 0/0 | 4261 | 6 | 0 | 2 | 4 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | AGCTT others(4256): Show |
chr2 | 196758035 | 196804683 |
| a0001c0001t0005 | 0/0 | 4261 | 2 | 0 | 2 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | AGCTT others(4256): Show |
chr2 | 196758035 | 196804683 |
| a0001c0001t0006 | 0/0 | 4261 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | AGCTT others(4256): Show |
chr2 | 196758035 | 196804683 |
| a0001c0001t0008 | 0/0 | 4261 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | AGCTT others(4256): Show |
chr2 | 196758035 | 196804683 |
| a0001c0001t0009 | 0/0 | 4261 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | AGCTT others(4256): Show |
chr2 | 196758035 | 196804683 |
| a0001c0001t0011 | 0/0 | 4261 | 1 | 0 | 0 | 0 | 1 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | AGCTT others(4256): Show |
chr2 | 196758035 | 196804683 |
| a0001c0001t0012 | 0/0 | 4276 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | AGCTT others(4271): Show |
chr2 | 196758035 | 196804683 |
| a0001c0003t0001 | 0/0 | 4261 | 3 | 0 | 0 | 3 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | AGCTT others(4256): Show |
chr2 | 196758035 | 196804683 |
| a0001c0005t0002 | 0/0 | 4261 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | AGCTT others(4256): Show |
chr2 | 196758035 | 196804683 |
| a0001c0007t0010 | 0/0 | 4261 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | AGCTT others(4256): Show |
chr2 | 196758035 | 196804683 |
| a0002c0002t0001 | 0/1 | 4261 | 36 | 15 | 6 | 13 | 0 | 1 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | AGCTT others(4256): Show |
chr2 | 196758035 | 196804683 |
| a0002c0002t0003 | 0/0 | 4266 | 8 | 0 | 3 | 0 | 0 | 5 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | AGCTT others(4261): Show |
chr2 | 196758035 | 196804683 |
| a0002c0004t0007 | 0/0 | 4261 | 2 | 0 | 0 | 2 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | AGCTT others(4256): Show |
chr2 | 196758035 | 196804683 |
| a0003c0006t0006 | 0/0 | 4261 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | AGCTT others(4256): Show |
chr2 | 196758035 | 196804683 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 12 | 0 | 2 | 4 | 2 | 4 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0002 | 0/0 | 9 | 0 | 3 | 4 | 0 | 2 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0005 | 0/0 | 5 | 4 | 0 | 1 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0008 | 1/0 | 4 | 3 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0012 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0015 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0002g0004 | 0/0 | 6 | 2 | 1 | 0 | 1 | 2 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0002g0018 | 0/0 | 3 | 0 | 0 | 0 | 1 | 2 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0002g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0002g0029 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0004g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0004g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0005g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0006g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0008g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0009g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0011g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0001t0012g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0003t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0003t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0003t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0005t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0001c0007t0010g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0002c0002t0001g0003 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0002c0002t0001g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0002c0002t0001g0016 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0002c0002t0001g0017 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0002c0002t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0002c0002t0001g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0002c0002t0001g0140 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0002c0002t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0002c0002t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0002c0002t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0002c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0002c0002t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0002c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0002c0002t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0002c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0002c0002t0003g0010 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0002c0002t0003g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0002c0002t0003g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0002c0002t0003g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0002c0002t0003g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0002c0004t0007g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| a0003c0006t0006g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0035 | EUR | GBR | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG00280 | hp1 | a0001 | c0001 | t0011 | g0070 | EUR | FIN | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0038 | EUR | FIN | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | CHS | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG00621 | hp1 | a0001 | c0001 | t0008 | g0087 | EAS | CHS | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | CHS | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0027 | AMR | PUR | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG00733 | hp2 | a0002 | c0002 | t0001 | g0017 | AMR | PUR | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0161 | AMR | PUR | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01069 | hp2 | a0002 | c0002 | t0003 | g0144 | AMR | PUR | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01070 | hp1 | a0001 | c0001 | t0005 | g0020 | AMR | PUR | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01071 | hp1 | a0001 | c0001 | t0005 | g0020 | AMR | PUR | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01071 | hp2 | a0002 | c0002 | t0003 | g0010 | AMR | PUR | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01109 | hp2 | a0002 | c0002 | t0003 | g0010 | AMR | PUR | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0154 | AMR | PUR | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0016 | AMR | PUR | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01169 | hp2 | a0002 | c0002 | t0001 | g0027 | AMR | PUR | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01192 | hp2 | a0002 | c0002 | t0001 | g0153 | AMR | PUR | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0062 | EUR | IBS | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0029 | EUR | IBS | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0056 | EUR | IBS | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0055 | EUR | IBS | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01884 | hp1 | a0001 | c0001 | t0009 | g0081 | AFR | ACB | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01884 | hp2 | a0003 | c0006 | t0006 | g0136 | AFR | ACB | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01891 | hp1 | a0002 | c0002 | t0001 | g0152 | AFR | ACB | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | KHV | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0169 | AFR | ACB | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02135 | hp2 | a0001 | c0003 | t0001 | g0100 | EAS | KHV | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0096 | AFR | ACB | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02148 | hp1 | a0001 | c0001 | t0004 | g0117 | AMR | PEL | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | CDX | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | CDX | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02273 | hp1 | a0001 | c0001 | t0004 | g0079 | AMR | PEL | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | PEL | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02451 | hp2 | a0002 | c0002 | t0001 | g0151 | AFR | ACB | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02615 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | GWD | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0165 | AFR | GWD | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02622 | hp2 | a0002 | c0002 | t0001 | g0150 | AFR | GWD | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0026 | AFR | GWD | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | GWD | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0160 | SAS | PJL | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0148 | AFR | GWD | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02723 | hp1 | a0002 | c0002 | t0001 | g0147 | AFR | GWD | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0163 | SAS | PJL | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0026 | AFR | GWD | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | GWD | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ESN | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02965 | hp1 | a0001 | c0001 | t0006 | g0102 | AFR | ESN | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | ESN | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ESN | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ESN | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0003 | AFR | ESN | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | GWD | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | MSL | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | ESN | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | ESN | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0168 | AFR | ESN | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG03195 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | ESN | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | MSL | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG03225 | hp1 | a0001 | c0001 | t0012 | g0130 | AFR | MSL | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG03225 | hp2 | a0002 | c0002 | t0001 | g0141 | AFR | MSL | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG03239 | hp2 | a0002 | c0002 | t0003 | g0142 | SAS | PJL | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | MSL | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | MSL | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | MSL | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0016 | SAS | PJL | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0018 | SAS | PJL | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG03492 | hp1 | a0002 | c0002 | t0003 | g0010 | SAS | PJL | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0018 | SAS | PJL | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | MSL | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG03688 | hp2 | a0002 | c0002 | t0003 | g0143 | SAS | STU | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG03704 | hp1 | a0002 | c0002 | t0003 | g0145 | SAS | PJL | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0162 | SAS | BEB | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | BEB | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG03834 | hp1 | a0002 | c0002 | t0003 | g0010 | SAS | BEB | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0173 | SAS | BEB | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | STU | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | STU | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | STU | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | STU | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | YRI | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | YRI | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0019 | AFR | YRI | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA18939 | hp2 | a0002 | c0004 | t0007 | g0028 | EAS | JPT | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0156 | EAS | JPT | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA18946 | hp1 | a0001 | c0001 | t0004 | g0041 | EAS | JPT | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0155 | EAS | JPT | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA18970 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA18981 | hp2 | a0002 | c0004 | t0007 | g0028 | EAS | JPT | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA18982 | hp2 | a0002 | c0002 | t0001 | g0135 | EAS | JPT | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA18984 | hp2 | a0001 | c0003 | t0001 | g0174 | EAS | JPT | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA18987 | hp2 | a0001 | c0003 | t0001 | g0101 | EAS | JPT | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA18992 | hp1 | a0002 | c0002 | t0001 | g0146 | EAS | JPT | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA18995 | hp2 | a0001 | c0001 | t0004 | g0046 | EAS | JPT | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA19003 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | LWK | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | LWK | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0149 | EAS | JPT | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA19057 | hp2 | a0001 | c0001 | t0004 | g0047 | EAS | JPT | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA19065 | hp2 | a0001 | c0001 | t0004 | g0051 | EAS | JPT | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA19079 | hp2 | a0001 | c0005 | t0002 | g0164 | EAS | JPT | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA19081 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA19086 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA19240 | hp1 | a0002 | c0002 | t0001 | g0016 | AFR | YRI | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0003 | AFR | YRI | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ASW | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ASW | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0004 | EUR | TSI | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | TSI | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0018 | EUR | TSI | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | MSL | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0170 | AFR | MSL | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | USA | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0167 | AFR | USA | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | USA | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | USA | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA21309 | hp1 | a0001 | c0007 | t0010 | g0166 | AFR | LWK | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | LWK | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0140 | REF | REF | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0008 | REF | REF | GTF3C3_chr2_196758035_196804683 | GTF3C3 | chr2 | 196758035 | 196804683 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:196780641 | G | A | 1 | a0003 | 1 | HG01884.hp2 | missense_variant | MODERATE | c.1136C>T | p.Thr379Ile | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 9/18 | 1208/4261 | 1136/2661 | 379/886 | chr2 | 196780641 | |||
| chr2:196797802 | T | C | 1 | a0002 | 45 | HG00642.hp2 HG00733.hp2 HG01069.hp2 others(42): Show |
missense_variant | MODERATE | c.209A>G | p.Asn70Ser | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 2/18 | 281/4261 | 209/2661 | 70/886 | chr2 | 196797802 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:196771803 | T | C | 1 | a0001c0003 | 3 | HG02135.hp2 NA18984.hp2 NA18987.hp2 |
synonymous_variant | LOW | c.2205A>G | p.Leu735Leu | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 15/18 | 2277/4261 | 2205/2661 | 735/886 | chr2 | 196771803 | |||
| chr2:196773131 | G | A | 1 | a0001c0005 | 1 | NA19079.hp2 | synonymous_variant | LOW | c.1854C>T | p.Ser618Ser | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 14/18 | 1926/4261 | 1854/2661 | 618/886 | chr2 | 196773131 | |||
| chr2:196780580 | G | A | 1 | a0002c0004 | 2 | NA18939.hp2 NA18981.hp2 |
synonymous_variant | LOW | c.1197C>T | p.Leu399Leu | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 9/18 | 1269/4261 | 1197/2661 | 399/886 | chr2 | 196780580 | |||
| chr2:196785531 | G | A | 1 | a0001c0007 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.951C>T | p.Phe317Phe | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 7/18 | 1023/4261 | 951/2661 | 317/886 | chr2 | 196785531 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:196763239 | T | G | 2 | a0001c0001t0006 a0003c0006t0006 |
2 | HG01884.hp2 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1324A>C | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 18/18 | 1324 | chr2 | 196763239 | ||||||
| chr2:196763334 | G | T | 1 | a0001c0001t0005 | 2 | HG01070.hp1 HG01071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1229C>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 18/18 | 1229 | chr2 | 196763334 | ||||||
| chr2:196763423 | A | ATAAAG | 1 | a0002c0002t0003 | 8 | HG01069.hp2 HG01071.hp2 HG01109.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1135_*1139dupCTTT others(1): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 18/18 | 1139 | chr2 | 196763423 | ||||||
| chr2:196763491 | C | T | 3 | a0001c0001t0002 a0001c0005t0002 a0001c0007t0010 |
28 | HG00741.hp2 HG01070.hp2 HG01515.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*1072G>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 18/18 | 1072 | chr2 | 196763491 | ||||||
| chr2:196763494 | A | G | 1 | a0001c0001t0009 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1069T>C | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 18/18 | 1069 | chr2 | 196763494 | ||||||
| chr2:196763540 | C | G | 1 | a0001c0001t0008 | 1 | HG00621.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1023G>C | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 18/18 | 1023 | chr2 | 196763540 | ||||||
| chr2:196764177 | C | A | 1 | a0001c0007t0010 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*386G>T | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 18/18 | 386 | chr2 | 196764177 | ||||||
| chr2:196764190 | G | A | 1 | a0001c0001t0004 | 6 | HG02148.hp1 HG02273.hp1 NA18946.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*373C>T | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 18/18 | 373 | chr2 | 196764190 | ||||||
| chr2:196764332 | T | C | 1 | a0001c0001t0011 | 1 | HG00280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*231A>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 18/18 | 231 | chr2 | 196764332 | ||||||
| chr2:196764452 | T | TAATTCTG others(8): Show |
1 | a0001c0001t0012 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*96_*110dupGACAATT others(8): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 18/18 | 110 | chr2 | 196764452 | ||||||
| chr2:196764497 | C | A | 1 | a0002c0004t0007 | 2 | NA18939.hp2 NA18981.hp2 |
3_prime_UTR_variant | MODIFIER | c.*66G>T | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 18/18 | 66 | chr2 | 196764497 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:196764764 | A | C | 1 | a0001c0001t0002g0170 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2539-79T>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 17/17 | chr2 | 196764764 | |||||||
| chr2:196764807 | TA | T | 62 | a0001c0001t0001g0015 a0001c0001t0001g0030 a0001c0001t0001g0094 others(59): Show |
93 | HG00642.hp2 HG00733.hp2 HG00741.hp2 others(90): Show |
intron_variant | MODIFIER | c.2539-123delT | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 17/17 | chr2 | 196764807 | |||||||
| chr2:196765248 | A | G | 2 | a0001c0001t0001g0022 a0001c0001t0001g0071 |
3 | HG02109.hp1 HG02258.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2539-563T>C | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 17/17 | chr2 | 196765248 | |||||||
| chr2:196765293 | A | C | 1 | a0003c0006t0006g0136 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2539-608T>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 17/17 | chr2 | 196765293 | |||||||
| chr2:196765457 | T | C | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0174 |
3 | HG02135.hp2 NA18984.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.2539-772A>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 17/17 | chr2 | 196765457 | |||||||
| chr2:196765511 | T | C | 1 | a0001c0001t0001g0069 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2539-826A>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 17/17 | chr2 | 196765511 | |||||||
| chr2:196765614 | A | C | 1 | a0001c0001t0001g0023 | 2 | HG02615.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.2539-929T>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 17/17 | chr2 | 196765614 | |||||||
| chr2:196765614 | AATAC | A | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0012g0130 |
3 | HG02922.hp1 HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2539-933_2539-930d others(6): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 17/17 | chr2 | 196765614 | |||||||
| chr2:196765667 | A | C | 1 | a0001c0001t0002g0162 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2538+898T>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 17/17 | chr2 | 196765667 | |||||||
| chr2:196765733 | G | A | 1 | a0001c0001t0001g0015 | 3 | HG01496.hp2 HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2538+832C>T | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 17/17 | chr2 | 196765733 | |||||||
| chr2:196765769 | G | A | 1 | a0001c0001t0001g0015 | 3 | HG01496.hp2 HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2538+796C>T | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 17/17 | chr2 | 196765769 | |||||||
| chr2:196765782 | G | A | 1 | a0001c0005t0002g0164 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2538+783C>T | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 17/17 | chr2 | 196765782 | |||||||
| chr2:196765820 | T | C | 2 | a0001c0001t0001g0118 a0001c0001t0001g0127 |
2 | HG01255.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2538+745A>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 17/17 | chr2 | 196765820 | |||||||
| chr2:196765826 | T | C | 8 | a0001c0001t0001g0118 a0001c0001t0002g0161 a0002c0002t0001g0016 others(5): Show |
13 | HG00642.hp2 HG00733.hp2 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.2538+739A>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 17/17 | chr2 | 196765826 | |||||||
| chr2:196765879 | A | G | 64 | a0001c0001t0001g0015 a0001c0001t0001g0030 a0001c0001t0001g0094 others(61): Show |
95 | HG00642.hp2 HG00733.hp2 HG00741.hp2 others(92): Show |
intron_variant | MODIFIER | c.2538+686T>C | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 17/17 | chr2 | 196765879 | |||||||
| chr2:196765883 | A | G | 5 | a0001c0001t0002g0018 a0001c0001t0002g0029 a0001c0001t0002g0161 others(2): Show |
8 | HG00741.hp2 HG01515.hp2 HG02293.hp2 others(5): Show |
intron_variant | MODIFIER | c.2538+682T>C | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 17/17 | chr2 | 196765883 | |||||||
| chr2:196765965 | G | C | 2 | a0001c0001t0001g0094 a0001c0001t0009g0081 |
2 | HG01884.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2538+600C>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 17/17 | chr2 | 196765965 | |||||||
| chr2:196765966 | T | C | 2 | a0001c0001t0001g0094 a0001c0001t0009g0081 |
2 | HG01884.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.2538+599A>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 17/17 | chr2 | 196765966 | |||||||
| chr2:196765989 | C | G | 3 | a0001c0001t0001g0030 a0001c0001t0001g0103 a0001c0001t0001g0104 |
3 | HG03453.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2538+576G>C | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 17/17 | chr2 | 196765989 | |||||||
| chr2:196766001 | C | T | 1 | a0002c0002t0001g0026 | 2 | HG02630.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.2538+564G>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 17/17 | chr2 | 196766001 | |||||||
| chr2:196766010 | C | CA | 62 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(59): Show |
87 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.2538+554dupT | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 17/17 | chr2 | 196766010 | |||||||
| chr2:196766010 | C | CAA | 18 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0014 others(15): Show |
24 | HG00642.hp1 HG01099.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.2538+553_2538+554d others(4): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 17/17 | chr2 | 196766010 | |||||||
| chr2:196766010 | CA | C | 38 | a0001c0001t0001g0015 a0001c0001t0001g0068 a0001c0001t0001g0127 others(35): Show |
53 | HG00733.hp2 HG00741.hp2 HG01070.hp2 others(50): Show |
intron_variant | MODIFIER | c.2538+554delT | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 17/17 | chr2 | 196766010 | |||||||
| chr2:196766010 | CAA | C | 15 | a0002c0002t0001g0003 a0002c0002t0001g0006 a0002c0002t0001g0016 others(12): Show |
31 | HG00642.hp2 HG01071.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.2538+553_2538+554d others(4): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 17/17 | chr2 | 196766010 | |||||||
| chr2:196766042 | G | T | 3 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0077 |
3 | HG00099.hp1 HG01099.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.2538+523C>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 17/17 | chr2 | 196766042 | |||||||
| chr2:196766296 | T | C | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0174 |
3 | HG02135.hp2 NA18984.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.2538+269A>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 17/17 | chr2 | 196766296 | |||||||
| chr2:196766433 | T | C | 1 | a0001c0001t0001g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2538+132A>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 17/17 | chr2 | 196766433 | |||||||
| chr2:196766855 | TATTACAG others(2): Show |
T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0103 a0001c0001t0001g0104 |
3 | HG03453.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2386-147_2386-139d others(11): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 16/17 | chr2 | 196766855 | |||||||
| chr2:196766860 | C | A | 1 | a0001c0001t0011g0070 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.2386-143G>T | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 16/17 | chr2 | 196766860 | |||||||
| chr2:196766883 | A | C | 1 | a0001c0003t0001g0100 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.2386-166T>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 16/17 | chr2 | 196766883 | |||||||
| chr2:196766887 | C | T | 2 | a0001c0001t0001g0038 a0001c0001t0001g0076 |
2 | HG00280.hp2 HG00733.hp1 |
intron_variant | MODIFIER | c.2386-170G>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 16/17 | chr2 | 196766887 | |||||||
| chr2:196766894 | G | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0061 |
4 | HG01257.hp1 HG01258.hp1 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.2386-177C>T | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 16/17 | chr2 | 196766894 | |||||||
| chr2:196767100 | A | T | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0174 |
3 | HG02135.hp2 NA18984.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.2386-383T>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 16/17 | chr2 | 196767100 | |||||||
| chr2:196767292 | C | T | 1 | a0001c0001t0002g0160 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2386-575G>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 16/17 | chr2 | 196767292 | |||||||
| chr2:196767296 | G | T | 1 | a0001c0001t0001g0090 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2386-579C>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 16/17 | chr2 | 196767296 | |||||||
| chr2:196767412 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2386-695T>C | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 16/17 | chr2 | 196767412 | |||||||
| chr2:196767481 | T | C | 1 | a0002c0002t0003g0145 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2386-764A>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 16/17 | chr2 | 196767481 | |||||||
| chr2:196767648 | A | C | 23 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0171 others(20): Show |
33 | HG00741.hp2 HG01070.hp2 HG01358.hp1 others(30): Show |
intron_variant | MODIFIER | c.2386-931T>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 16/17 | chr2 | 196767648 | |||||||
| chr2:196767705 | G | A | 2 | a0001c0001t0001g0129 a0001c0001t0012g0130 |
2 | HG02922.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2386-988C>T | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 16/17 | chr2 | 196767705 | |||||||
| chr2:196767831 | C | A | 19 | a0001c0001t0001g0159 a0001c0001t0002g0004 a0001c0001t0002g0018 others(16): Show |
29 | HG00741.hp2 HG01070.hp2 HG01358.hp1 others(26): Show |
intron_variant | MODIFIER | c.2386-1114G>T | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 16/17 | chr2 | 196767831 | |||||||
| chr2:196768086 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2386-1369G>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 16/17 | chr2 | 196768086 | |||||||
| chr2:196768089 | C | T | 1 | a0002c0002t0003g0142 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2386-1372G>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 16/17 | chr2 | 196768089 | |||||||
| chr2:196768155 | T | C | 1 | a0001c0001t0001g0056 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.2386-1438A>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 16/17 | chr2 | 196768155 | |||||||
| chr2:196768164 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2386-1447G>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 16/17 | chr2 | 196768164 | |||||||
| chr2:196768165 | A | G | 1 | a0001c0001t0001g0071 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2386-1448T>C | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 16/17 | chr2 | 196768165 | |||||||
| chr2:196768166 | C | T | 1 | a0001c0001t0001g0074 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2386-1449G>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 16/17 | chr2 | 196768166 | |||||||
| chr2:196768245 | GAC | G | 74 | a0001c0001t0001g0015 a0001c0001t0001g0030 a0001c0001t0001g0059 others(71): Show |
105 | HG00642.hp2 HG00733.hp2 HG00741.hp2 others(102): Show |
intron_variant | MODIFIER | c.2386-1530_2386-152 others(6): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 16/17 | chr2 | 196768245 | |||||||
| chr2:196768315 | C | G | 91 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0015 others(88): Show |
129 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(126): Show |
intron_variant | MODIFIER | c.2386-1598G>C | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 16/17 | chr2 | 196768315 | |||||||
| chr2:196768430 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2385+1485G>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 16/17 | chr2 | 196768430 | |||||||
| chr2:196768940 | C | T | 25 | a0002c0002t0001g0003 a0002c0002t0001g0006 a0002c0002t0001g0016 others(22): Show |
44 | HG00642.hp2 HG00733.hp2 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.2385+975G>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 16/17 | chr2 | 196768940 | |||||||
| chr2:196768966 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2385+949G>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 16/17 | chr2 | 196768966 | |||||||
| chr2:196769008 | T | C | 2 | a0001c0001t0001g0044 a0001c0001t0001g0054 |
2 | NA18989.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.2385+907A>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 16/17 | chr2 | 196769008 | |||||||
| chr2:196769225 | T | C | 13 | a0002c0002t0001g0003 a0002c0002t0001g0016 a0002c0002t0001g0017 others(10): Show |
24 | HG00642.hp2 HG00733.hp2 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.2385+690A>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 16/17 | chr2 | 196769225 | |||||||
| chr2:196769845 | A | T | 2 | a0001c0001t0001g0031 a0001c0001t0001g0082 |
2 | HG03239.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.2385+70T>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 16/17 | chr2 | 196769845 | |||||||
| chr2:196770917 | G | C | 1 | a0001c0001t0002g0169 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2260+831C>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 15/17 | chr2 | 196770917 | |||||||
| chr2:196770951 | C | A | 1 | a0002c0002t0001g0151 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2260+797G>T | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 15/17 | chr2 | 196770951 | |||||||
| chr2:196770956 | T | C | 171 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(168): Show |
245 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.2260+792A>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 15/17 | chr2 | 196770956 | |||||||
| chr2:196771084 | T | C | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0174 |
3 | HG02135.hp2 NA18984.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.2260+664A>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 15/17 | chr2 | 196771084 | |||||||
| chr2:196771134 | G | C | 1 | a0002c0002t0001g0151 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2260+614C>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 15/17 | chr2 | 196771134 | |||||||
| chr2:196771272 | T | C | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0012g0130 |
3 | HG02922.hp1 HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2260+476A>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 15/17 | chr2 | 196771272 | |||||||
| chr2:196771368 | AAAAT | A | 7 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0031 others(4): Show |
11 | HG00639.hp1 HG01069.hp1 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.2260+376_2260+379d others(6): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 15/17 | chr2 | 196771368 | |||||||
| chr2:196771487 | T | A | 1 | a0001c0001t0002g0170 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2260+261A>T | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 15/17 | chr2 | 196771487 | |||||||
| chr2:196771553 | C | G | 1 | a0001c0001t0005g0020 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.2260+195G>C | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 15/17 | chr2 | 196771553 | |||||||
| chr2:196771566 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2260+182G>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 15/17 | chr2 | 196771566 | |||||||
| chr2:196771655 | A | G | 67 | a0001c0001t0001g0015 a0001c0001t0001g0030 a0001c0001t0001g0094 others(64): Show |
98 | HG00642.hp2 HG00733.hp2 HG00741.hp2 others(95): Show |
intron_variant | MODIFIER | c.2260+93T>C | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 15/17 | chr2 | 196771655 | |||||||
| chr2:196772280 | G | A | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0174 |
3 | HG02135.hp2 NA18984.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.2070-342C>T | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 14/17 | chr2 | 196772280 | |||||||
| chr2:196772335 | G | C | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0174 |
3 | HG02135.hp2 NA18984.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.2070-397C>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 14/17 | chr2 | 196772335 | |||||||
| chr2:196772339 | G | A | 1 | a0001c0001t0002g0163 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2070-401C>T | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 14/17 | chr2 | 196772339 | |||||||
| chr2:196772420 | C | T | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0174 |
3 | HG02135.hp2 NA18984.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.2070-482G>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 14/17 | chr2 | 196772420 | |||||||
| chr2:196772463 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2069+453C>T | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 14/17 | chr2 | 196772463 | |||||||
| chr2:196772467 | G | A | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0174 |
3 | HG02135.hp2 NA18984.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.2069+449C>T | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 14/17 | chr2 | 196772467 | |||||||
| chr2:196772549 | AAAT | A | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0174 |
3 | HG02135.hp2 NA18984.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.2069+364_2069+366d others(5): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 14/17 | chr2 | 196772549 | |||||||
| chr2:196772788 | C | G | 1 | a0001c0001t0001g0067 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2069+128G>C | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 14/17 | chr2 | 196772788 | |||||||
| chr2:196773290 | G | T | 1 | a0002c0002t0001g0149 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1832-137C>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 13/17 | chr2 | 196773290 | |||||||
| chr2:196773559 | C | T | 1 | a0001c0001t0001g0059 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1832-406G>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 13/17 | chr2 | 196773559 | |||||||
| chr2:196773576 | G | A | 3 | a0001c0001t0001g0024 a0001c0001t0001g0088 a0001c0001t0001g0090 |
4 | HG02109.hp2 HG02145.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1832-423C>T | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 13/17 | chr2 | 196773576 | |||||||
| chr2:196773583 | G | C | 1 | a0001c0001t0001g0080 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1832-430C>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 13/17 | chr2 | 196773583 | |||||||
| chr2:196773649 | G | T | 1 | a0001c0001t0001g0122 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1832-496C>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 13/17 | chr2 | 196773649 | |||||||
| chr2:196773958 | G | T | 1 | a0002c0002t0001g0148 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1832-805C>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 13/17 | chr2 | 196773958 | |||||||
| chr2:196774024 | T | G | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0174 |
3 | HG02135.hp2 NA18984.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.1832-871A>C | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 13/17 | chr2 | 196774024 | |||||||
| chr2:196774235 | T | G | 24 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(21): Show |
34 | HG00741.hp2 HG01070.hp2 HG01358.hp1 others(31): Show |
intron_variant | MODIFIER | c.1831+881A>C | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 13/17 | chr2 | 196774235 | |||||||
| chr2:196774255 | C | G | 20 | a0001c0001t0001g0157 a0001c0001t0001g0159 a0001c0001t0002g0004 others(17): Show |
30 | HG00741.hp2 HG01070.hp2 HG01358.hp1 others(27): Show |
intron_variant | MODIFIER | c.1831+861G>C | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 13/17 | chr2 | 196774255 | |||||||
| chr2:196774758 | T | C | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0174 |
3 | HG02135.hp2 NA18984.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.1831+358A>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 13/17 | chr2 | 196774758 | |||||||
| chr2:196774904 | C | T | 1 | a0001c0001t0001g0066 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1831+212G>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 13/17 | chr2 | 196774904 | |||||||
| chr2:196775072 | A | G | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0174 |
3 | HG02135.hp2 NA18984.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.1831+44T>C | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 13/17 | chr2 | 196775072 | |||||||
| chr2:196775612 | G | A | 2 | a0001c0001t0006g0102 a0003c0006t0006g0136 |
2 | HG01884.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1696-361C>T | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 12/17 | chr2 | 196775612 | |||||||
| chr2:196775616 | A | C | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0174 |
3 | HG02135.hp2 NA18984.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.1696-365T>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 12/17 | chr2 | 196775616 | |||||||
| chr2:196775776 | A | C | 20 | a0001c0001t0001g0157 a0001c0001t0001g0159 a0001c0001t0002g0004 others(17): Show |
30 | HG00741.hp2 HG01070.hp2 HG01358.hp1 others(27): Show |
intron_variant | MODIFIER | c.1695+234T>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 12/17 | chr2 | 196775776 | |||||||
| chr2:196775778 | C | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0093 |
2 | HG02258.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1695+232G>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 12/17 | chr2 | 196775778 | |||||||
| chr2:196775782 | G | T | 1 | a0002c0002t0001g0147 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1695+228C>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 12/17 | chr2 | 196775782 | |||||||
| chr2:196775800 | A | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0093 |
2 | HG02258.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1695+210T>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 12/17 | chr2 | 196775800 | |||||||
| chr2:196776190 | TA | T | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0174 |
3 | HG02135.hp2 NA18984.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.1594-80delT | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 11/17 | chr2 | 196776190 | |||||||
| chr2:196776191 | A | T | 1 | a0001c0001t0001g0015 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1594-80T>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 11/17 | chr2 | 196776191 | |||||||
| chr2:196776254 | A | G | 4 | a0001c0001t0001g0015 a0001c0001t0001g0030 a0001c0001t0001g0103 others(1): Show |
6 | HG01496.hp2 HG03453.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1594-143T>C | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 11/17 | chr2 | 196776254 | |||||||
| chr2:196776274 | T | C | 28 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0002c0002t0001g0003 others(25): Show |
47 | HG00642.hp2 HG00733.hp2 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.1593+153A>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 11/17 | chr2 | 196776274 | |||||||
| chr2:196776288 | T | A | 28 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0002c0002t0001g0003 others(25): Show |
47 | HG00642.hp2 HG00733.hp2 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.1593+139A>T | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 11/17 | chr2 | 196776288 | |||||||
| chr2:196776668 | A | G | 2 | a0001c0001t0001g0094 a0001c0001t0009g0081 |
2 | HG01884.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1391-39T>C | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 10/17 | chr2 | 196776668 | |||||||
| chr2:196776894 | T | C | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0174 |
3 | HG02135.hp2 NA18984.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.1391-265A>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 10/17 | chr2 | 196776894 | |||||||
| chr2:196777458 | C | A | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0174 |
3 | HG02135.hp2 NA18984.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.1391-829G>T | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 10/17 | chr2 | 196777458 | |||||||
| chr2:196777493 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1391-864G>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 10/17 | chr2 | 196777493 | |||||||
| chr2:196777573 | G | A | 1 | a0001c0001t0001g0015 | 3 | HG01496.hp2 HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1391-944C>T | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 10/17 | chr2 | 196777573 | |||||||
| chr2:196777612 | T | G | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0174 |
3 | HG02135.hp2 NA18984.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.1391-983A>C | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 10/17 | chr2 | 196777612 | |||||||
| chr2:196778188 | G | A | 2 | a0001c0001t0001g0158 a0001c0001t0001g0171 |
2 | HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1390+708C>T | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 10/17 | chr2 | 196778188 | |||||||
| chr2:196778247 | T | C | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0174 |
3 | HG02135.hp2 NA18984.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.1390+649A>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 10/17 | chr2 | 196778247 | |||||||
| chr2:196778447 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1390+449A>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 10/17 | chr2 | 196778447 | |||||||
| chr2:196778525 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1390+371A>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 10/17 | chr2 | 196778525 | |||||||
| chr2:196778698 | T | A | 1 | a0001c0007t0010g0166 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1390+198A>T | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 10/17 | chr2 | 196778698 | |||||||
| chr2:196779380 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1219-313C>T | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 9/17 | chr2 | 196779380 | |||||||
| chr2:196779602 | G | C | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0174 |
3 | HG02135.hp2 NA18984.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.1219-535C>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 9/17 | chr2 | 196779602 | |||||||
| chr2:196779828 | G | A | 2 | a0002c0002t0001g0155 a0002c0002t0001g0172 |
2 | NA18946.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.1218+731C>T | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 9/17 | chr2 | 196779828 | |||||||
| chr2:196779868 | G | A | 1 | a0001c0001t0001g0033 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1218+691C>T | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 9/17 | chr2 | 196779868 | |||||||
| chr2:196779911 | G | A | 3 | a0001c0001t0001g0030 a0001c0001t0001g0103 a0001c0001t0001g0104 |
3 | HG03453.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1218+648C>T | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 9/17 | chr2 | 196779911 | |||||||
| chr2:196779928 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1218+631C>T | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 9/17 | chr2 | 196779928 | |||||||
| chr2:196779979 | C | T | 1 | a0001c0001t0001g0011 | 3 | HG02559.hp1 HG03041.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1218+580G>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 9/17 | chr2 | 196779979 | |||||||
| chr2:196780076 | C | T | 1 | a0002c0002t0001g0146 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1218+483G>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 9/17 | chr2 | 196780076 | |||||||
| chr2:196780151 | G | T | 1 | a0001c0001t0002g0165 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1218+408C>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 9/17 | chr2 | 196780151 | |||||||
| chr2:196780215 | C | CT | 63 | a0001c0001t0001g0015 a0001c0001t0001g0030 a0001c0001t0001g0103 others(60): Show |
94 | HG00642.hp2 HG00733.hp2 HG00741.hp2 others(91): Show |
intron_variant | MODIFIER | c.1218+343dupA | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 9/17 | chr2 | 196780215 | |||||||
| chr2:196780456 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1218+103T>C | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 9/17 | chr2 | 196780456 | |||||||
| chr2:196780673 | C | T | 10 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0023 others(7): Show |
16 | HG00639.hp1 HG01069.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.1115-11G>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196780673 | |||||||
| chr2:196780849 | C | T | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0174 |
3 | HG02135.hp2 NA18984.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.1115-187G>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196780849 | |||||||
| chr2:196780908 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1115-246G>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196780908 | |||||||
| chr2:196781139 | A | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0061 |
4 | HG01257.hp1 HG01258.hp1 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.1115-477T>C | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781139 | |||||||
| chr2:196781157 | G | C | 2 | a0001c0001t0006g0102 a0003c0006t0006g0136 |
2 | HG01884.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1115-495C>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781157 | |||||||
| chr2:196781222 | A | AC | 29 | a0001c0001t0001g0015 a0001c0001t0001g0030 a0001c0001t0001g0103 others(26): Show |
41 | HG00741.hp2 HG01070.hp2 HG01358.hp1 others(38): Show |
intron_variant | MODIFIER | c.1115-561_1115-560i others(3): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781222 | |||||||
| chr2:196781228 | G | GT | 4 | a0001c0001t0001g0015 a0001c0001t0001g0030 a0001c0001t0001g0103 others(1): Show |
6 | HG01496.hp2 HG03453.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1115-567_1115-566i others(3): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781228 | |||||||
| chr2:196781314 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1115-652T>C | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781314 | |||||||
| chr2:196781342 | G | GA | 6 | a0002c0002t0001g0006 a0002c0002t0001g0027 a0002c0002t0001g0135 others(3): Show |
12 | HG00642.hp2 HG01169.hp2 NA18939.hp2 others(9): Show |
intron_variant | MODIFIER | c.1115-681dupT | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781342 | |||||||
| chr2:196781342 | G | GAAAAAAA others(1): Show |
3 | a0001c0001t0001g0015 a0001c0001t0001g0103 a0003c0006t0006g0136 |
5 | HG01496.hp2 HG01884.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1115-688_1115-681d others(10): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781342 | |||||||
| chr2:196781342 | G | GAAAAAAA others(5): Show |
1 | a0001c0001t0002g0096 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1115-692_1115-681d others(14): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781342 | |||||||
| chr2:196781342 | G | GAAAAAAA others(9): Show |
1 | a0001c0001t0001g0132 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1115-696_1115-681d others(18): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781342 | |||||||
| chr2:196781342 | G | GAAAAAAA others(11): Show |
1 | a0001c0001t0002g0019 | 3 | HG02970.hp1 HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1115-681_1115-680i others(20): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781342 | |||||||
| chr2:196781342 | G | GAAAAAAA others(12): Show |
2 | a0001c0001t0002g0018 a0001c0001t0002g0169 |
4 | HG02055.hp1 HG03491.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.1115-681_1115-680i others(21): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781342 | |||||||
| chr2:196781342 | G | GAAAAAAA others(14): Show |
1 | a0001c0001t0002g0165 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1115-681_1115-680i others(23): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781342 | |||||||
| chr2:196781349 | A | ATATATAT others(8): Show |
1 | a0001c0001t0004g0046 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1115-688_1115-687i others(17): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781349 | |||||||
| chr2:196781349 | A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0045 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1115-688_1115-687i others(21): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781349 | |||||||
| chr2:196781351 | A | AATATATA others(7): Show |
1 | a0001c0001t0001g0052 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1115-690_1115-689i others(16): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781351 | |||||||
| chr2:196781351 | A | ATATATAT others(6): Show |
2 | a0001c0001t0001g0050 a0001c0001t0004g0051 |
2 | HG02970.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.1115-690_1115-689i others(15): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781351 | |||||||
| chr2:196781351 | A | ATATATAT others(8): Show |
1 | a0001c0001t0004g0047 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1115-690_1115-689i others(17): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781351 | |||||||
| chr2:196781351 | A | T | 2 | a0001c0001t0001g0045 a0001c0001t0004g0046 |
2 | HG01123.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.1115-689T>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781351 | |||||||
| chr2:196781353 | A | AATATATA others(3): Show |
2 | a0001c0001t0001g0059 a0001c0001t0001g0060 |
2 | HG04204.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.1115-692_1115-691i others(12): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781353 | |||||||
| chr2:196781353 | A | AATATATA others(7): Show |
2 | a0001c0001t0001g0037 a0001c0001t0001g0057 |
2 | HG00639.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.1115-692_1115-691i others(16): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781353 | |||||||
| chr2:196781353 | A | AATATATA others(11): Show |
1 | a0001c0001t0001g0049 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1115-692_1115-691i others(20): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781353 | |||||||
| chr2:196781353 | A | AATATATA others(19): Show |
2 | a0001c0001t0001g0032 a0001c0001t0001g0044 |
2 | NA18989.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.1115-692_1115-691i others(28): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781353 | |||||||
| chr2:196781353 | A | ATATATAT others(4): Show |
3 | a0001c0001t0001g0058 a0001c0001t0001g0110 a0001c0001t0001g0113 |
3 | HG02698.hp1 NA18981.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.1115-692_1115-691i others(13): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781353 | |||||||
| chr2:196781353 | A | ATATATAT others(6): Show |
2 | a0001c0001t0001g0055 a0001c0001t0001g0056 |
2 | HG01516.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.1115-692_1115-691i others(15): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781353 | |||||||
| chr2:196781353 | A | ATATATAT others(8): Show |
3 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0112 |
3 | HG00408.hp1 HG00408.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.1115-692_1115-691i others(17): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781353 | |||||||
| chr2:196781353 | A | ATATATAT others(10): Show |
2 | a0001c0001t0001g0048 a0001c0001t0001g0097 |
2 | HG03654.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.1115-692_1115-691i others(19): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781353 | |||||||
| chr2:196781353 | A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0111 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1115-692_1115-691i others(23): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781353 | |||||||
| chr2:196781353 | A | T | 6 | a0001c0001t0001g0045 a0001c0001t0001g0050 a0001c0001t0001g0052 others(3): Show |
6 | HG01123.hp2 HG01361.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1115-691T>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781353 | |||||||
| chr2:196781354 | AAAAATAT others(4): Show |
A | 1 | a0001c0001t0001g0080 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1115-703_1115-693d others(13): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781354 | |||||||
| chr2:196781355 | A | AATATATA others(3): Show |
4 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0014 others(1): Show |
5 | HG01167.hp1 HG01169.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.1115-694_1115-693i others(12): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781355 | |||||||
| chr2:196781355 | A | AATATATA others(7): Show |
3 | a0001c0001t0001g0009 a0001c0001t0001g0042 a0001c0001t0001g0121 |
3 | HG00639.hp1 HG01952.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.1115-694_1115-693i others(16): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781355 | |||||||
| chr2:196781355 | A | AATATATA others(9): Show |
1 | a0001c0001t0001g0120 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1115-694_1115-693i others(18): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781355 | |||||||
| chr2:196781355 | A | AATATATA others(11): Show |
1 | a0001c0001t0001g0005 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1115-694_1115-693i others(20): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781355 | |||||||
| chr2:196781355 | A | AATATATA others(13): Show |
1 | a0001c0001t0001g0001 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1115-694_1115-693i others(22): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781355 | |||||||
| chr2:196781355 | A | ATATATAT others(2): Show |
3 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0086 |
3 | HG03704.hp2 NA20129.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1115-694_1115-693i others(11): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781355 | |||||||
| chr2:196781355 | A | ATATATAT others(4): Show |
8 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0021 others(5): Show |
9 | HG01099.hp1 HG01099.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.1115-694_1115-693i others(13): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781355 | |||||||
| chr2:196781355 | A | ATATATAT others(6): Show |
6 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0034 others(3): Show |
7 | HG00741.hp1 HG01109.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.1115-694_1115-693i others(15): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781355 | |||||||
| chr2:196781355 | A | ATATATAT others(8): Show |
7 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(4): Show |
8 | HG01257.hp1 HG01258.hp1 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.1115-694_1115-693i others(17): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781355 | |||||||
| chr2:196781355 | A | ATATATAT others(10): Show |
4 | a0001c0001t0001g0013 a0001c0001t0001g0065 a0001c0001t0001g0105 others(1): Show |
4 | HG01433.hp1 HG02148.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.1115-694_1115-693i others(19): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781355 | |||||||
| chr2:196781355 | A | ATATATAT others(12): Show |
2 | a0001c0001t0001g0001 a0001c0001t0008g0087 |
2 | HG00621.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1115-694_1115-693i others(21): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781355 | |||||||
| chr2:196781355 | A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0005 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1115-694_1115-693i others(23): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781355 | |||||||
| chr2:196781355 | A | ATATATAT others(11): Show |
3 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0036 |
3 | HG00099.hp1 HG00099.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.1115-694_1115-693i others(20): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781355 | |||||||
| chr2:196781355 | A | T | 26 | a0001c0001t0001g0001 a0001c0001t0001g0032 a0001c0001t0001g0037 others(23): Show |
27 | HG00408.hp1 HG00408.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.1115-693T>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781355 | |||||||
| chr2:196781357 | A | AAAAAAAA others(14): Show |
1 | a0001c0001t0002g0160 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1115-696_1115-695i others(23): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781357 | |||||||
| chr2:196781357 | A | AAAAAAAA others(13): Show |
2 | a0001c0001t0002g0004 a0001c0001t0002g0161 |
2 | HG00741.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.1115-696_1115-695i others(22): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781357 | |||||||
| chr2:196781357 | A | AAAAAAAA others(25): Show |
1 | a0001c0001t0002g0004 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1115-696_1115-695i others(34): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781357 | |||||||
| chr2:196781357 | A | AAAAAAAA others(12): Show |
1 | a0001c0001t0002g0004 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1115-696_1115-695i others(21): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781357 | |||||||
| chr2:196781357 | A | AAAAAAAA others(14): Show |
1 | a0001c0001t0002g0167 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1115-696_1115-695i others(23): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781357 | |||||||
| chr2:196781357 | A | AAAAAAAA others(16): Show |
1 | a0001c0001t0002g0162 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1115-696_1115-695i others(25): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781357 | |||||||
| chr2:196781357 | A | AAAAAAAA others(11): Show |
2 | a0001c0001t0001g0131 a0001c0001t0002g0168 |
2 | HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1115-696_1115-695i others(20): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781357 | |||||||
| chr2:196781357 | A | AAAAAAAA others(13): Show |
1 | a0001c0001t0002g0163 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1115-696_1115-695i others(22): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781357 | |||||||
| chr2:196781357 | A | AAAAAAAA others(15): Show |
2 | a0001c0001t0002g0170 a0001c0001t0002g0173 |
2 | HG03471.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1115-696_1115-695i others(24): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781357 | |||||||
| chr2:196781357 | A | AAAAAAAA others(19): Show |
1 | a0001c0001t0002g0004 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1115-696_1115-695i others(28): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781357 | |||||||
| chr2:196781357 | A | AAAAAAAA others(12): Show |
1 | a0001c0001t0002g0029 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1115-696_1115-695i others(21): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781357 | |||||||
| chr2:196781357 | A | AAAAAAAA others(14): Show |
2 | a0001c0001t0001g0159 a0001c0001t0002g0004 |
2 | HG01358.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1115-696_1115-695i others(23): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781357 | |||||||
| chr2:196781357 | A | AAAAAAAA others(11): Show |
1 | a0001c0007t0010g0166 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1115-696_1115-695i others(20): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781357 | |||||||
| chr2:196781357 | A | AAAAAAAA others(13): Show |
1 | a0001c0001t0002g0029 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1115-696_1115-695i others(22): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781357 | |||||||
| chr2:196781357 | A | AAAAAAAA others(19): Show |
1 | a0001c0001t0002g0095 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1115-696_1115-695i others(28): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781357 | |||||||
| chr2:196781357 | A | AAAAAAAA others(14): Show |
1 | a0001c0001t0001g0133 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1115-696_1115-695i others(23): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781357 | |||||||
| chr2:196781357 | A | AAAAAAAA others(18): Show |
1 | a0001c0001t0002g0004 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1115-696_1115-695i others(27): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781357 | |||||||
| chr2:196781357 | A | AAAAAAAA others(7): Show |
1 | a0001c0001t0012g0130 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1115-696_1115-695i others(16): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781357 | |||||||
| chr2:196781357 | A | AAAAAAAA others(6): Show |
1 | a0001c0001t0009g0081 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1115-696_1115-695i others(15): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781357 | |||||||
| chr2:196781357 | A | AAAAAAAA others(8): Show |
1 | a0001c0001t0001g0128 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1115-696_1115-695i others(17): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781357 | |||||||
| chr2:196781357 | A | AAAAAAAA others(12): Show |
1 | a0001c0005t0002g0164 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1115-696_1115-695i others(21): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781357 | |||||||
| chr2:196781357 | A | AAAAAAAA others(7): Show |
1 | a0001c0001t0001g0129 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1115-696_1115-695i others(16): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781357 | |||||||
| chr2:196781357 | A | AAAAAAAA others(8): Show |
1 | a0001c0001t0001g0158 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1115-696_1115-695i others(17): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781357 | |||||||
| chr2:196781357 | A | AAAAAATA others(5): Show |
2 | a0001c0001t0001g0123 a0001c0001t0001g0125 |
2 | HG03041.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1115-696_1115-695i others(14): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781357 | |||||||
| chr2:196781357 | A | AAAAATAT others(8): Show |
2 | a0001c0001t0001g0002 a0001c0001t0001g0127 |
2 | HG02897.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.1115-696_1115-695i others(17): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781357 | |||||||
| chr2:196781357 | A | AAAATATA others(5): Show |
1 | a0001c0001t0001g0089 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1115-696_1115-695i others(14): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781357 | |||||||
| chr2:196781357 | A | AAAATATA others(9): Show |
1 | a0001c0001t0001g0083 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1115-696_1115-695i others(18): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781357 | |||||||
| chr2:196781357 | A | AAAATATA others(15): Show |
1 | a0001c0001t0001g0001 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1115-696_1115-695i others(24): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781357 | |||||||
| chr2:196781357 | A | AAATATAT others(4): Show |
4 | a0001c0001t0001g0007 a0001c0001t0001g0033 a0001c0001t0001g0109 others(1): Show |
4 | NA19002.hp2 NA19060.hp1 NA19085.hp1 others(1): Show |
intron_variant | MODIFIER | c.1115-696_1115-695i others(13): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781357 | |||||||
| chr2:196781357 | A | AAATATAT others(6): Show |
1 | a0001c0001t0001g0011 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1115-696_1115-695i others(15): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781357 | |||||||
| chr2:196781357 | A | AAATATAT others(8): Show |
1 | a0001c0001t0001g0023 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1115-696_1115-695i others(17): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781357 | |||||||
| chr2:196781357 | A | AAATATAT others(10): Show |
2 | a0001c0001t0001g0001 a0001c0001t0001g0012 |
2 | HG00642.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.1115-696_1115-695i others(19): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781357 | |||||||
| chr2:196781357 | A | AATATATA others(3): Show |
2 | a0001c0001t0001g0082 a0001c0001t0001g0085 |
2 | HG01433.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.1115-705_1115-696d others(12): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781357 | |||||||
| chr2:196781357 | A | AATATATA others(7): Show |
4 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0090 others(1): Show |
5 | HG01070.hp1 HG01071.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.1115-709_1115-696d others(16): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781357 | |||||||
| chr2:196781357 | A | AATATATA others(11): Show |
1 | a0001c0001t0001g0076 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1115-713_1115-696d others(20): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781357 | |||||||
| chr2:196781357 | A | AATATATA others(13): Show |
1 | a0001c0001t0001g0074 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1115-715_1115-696d others(22): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781357 | |||||||
| chr2:196781357 | A | AATATATA others(15): Show |
2 | a0001c0001t0001g0038 a0001c0001t0001g0122 |
2 | HG00280.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1115-717_1115-696d others(24): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781357 | |||||||
| chr2:196781357 | A | AATATATA others(19): Show |
1 | a0001c0001t0001g0005 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1115-721_1115-696d others(28): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781357 | |||||||
| chr2:196781357 | A | ATATATAT | 4 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0072 others(1): Show |
4 | HG01243.hp1 HG01243.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1115-696_1115-695i others(9): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781357 | |||||||
| chr2:196781357 | A | ATATATAT others(2): Show |
5 | a0001c0001t0001g0007 a0001c0001t0001g0024 a0001c0001t0001g0107 others(2): Show |
6 | HG01255.hp2 HG01358.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1115-696_1115-695i others(11): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781357 | |||||||
| chr2:196781357 | A | ATATATAT others(4): Show |
9 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0062 others(6): Show |
10 | HG01255.hp1 HG01515.hp1 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.1115-696_1115-695i others(13): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781357 | |||||||
| chr2:196781357 | A | ATATATAT others(6): Show |
6 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(3): Show |
6 | HG01261.hp2 HG01891.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.1115-696_1115-695i others(15): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781357 | |||||||
| chr2:196781357 | A | ATATATAT others(8): Show |
4 | a0001c0001t0001g0002 a0001c0001t0001g0043 a0001c0001t0001g0091 others(1): Show |
4 | HG02273.hp1 HG03942.hp2 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.1115-696_1115-695i others(17): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781357 | |||||||
| chr2:196781357 | A | ATATATAT others(10): Show |
3 | a0001c0001t0001g0002 a0001c0001t0001g0066 a0001c0001t0011g0070 |
3 | HG00280.hp1 HG01993.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1115-696_1115-695i others(19): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781357 | |||||||
| chr2:196781357 | A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0108 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1115-696_1115-695i others(25): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781357 | |||||||
| chr2:196781357 | A | T | 70 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(67): Show |
99 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.1115-695T>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781357 | |||||||
| chr2:196781357 | AATATATA others(3): Show |
A | 1 | a0001c0001t0001g0064 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1115-705_1115-696d others(12): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781357 | |||||||
| chr2:196781359 | T | A | 27 | a0001c0001t0001g0015 a0001c0001t0001g0103 a0001c0001t0002g0096 others(24): Show |
45 | HG00642.hp2 HG00733.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.1115-697A>T | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781359 | |||||||
| chr2:196781361 | T | A | 18 | a0001c0001t0002g0096 a0001c0001t0006g0102 a0002c0002t0001g0003 others(15): Show |
29 | HG00642.hp2 HG00733.hp2 HG01168.hp2 others(26): Show |
intron_variant | MODIFIER | c.1115-699A>T | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781361 | |||||||
| chr2:196781363 | T | A | 16 | a0001c0001t0002g0096 a0001c0001t0006g0102 a0002c0002t0001g0003 others(13): Show |
25 | HG00642.hp2 HG00733.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.1115-701A>T | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781363 | |||||||
| chr2:196781365 | T | A | 7 | a0001c0001t0002g0096 a0001c0001t0006g0102 a0002c0002t0001g0003 others(4): Show |
11 | HG00642.hp2 HG01891.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1115-703A>T | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781365 | |||||||
| chr2:196781367 | T | A | 1 | a0002c0002t0001g0152 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1115-705A>T | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781367 | |||||||
| chr2:196781389 | A | T | 4 | a0001c0001t0001g0040 a0001c0001t0001g0122 a0001c0001t0006g0102 others(1): Show |
4 | HG01884.hp2 HG02155.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1115-727T>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781389 | |||||||
| chr2:196781689 | C | T | 1 | a0002c0002t0001g0172 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1115-1027G>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781689 | |||||||
| chr2:196781808 | A | G | 28 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0002c0002t0001g0003 others(25): Show |
47 | HG00642.hp2 HG00733.hp2 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.1115-1146T>C | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196781808 | |||||||
| chr2:196782146 | G | T | 1 | a0001c0001t0001g0092 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1115-1484C>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196782146 | |||||||
| chr2:196782166 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1115-1504A>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196782166 | |||||||
| chr2:196782343 | G | C | 3 | a0001c0001t0001g0030 a0001c0001t0001g0103 a0001c0001t0001g0104 |
3 | HG03453.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1115-1681C>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196782343 | |||||||
| chr2:196782356 | G | GA | 66 | a0001c0001t0001g0015 a0001c0001t0001g0030 a0001c0001t0001g0103 others(63): Show |
97 | HG00642.hp2 HG00733.hp2 HG00741.hp2 others(94): Show |
intron_variant | MODIFIER | c.1115-1695dupT | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196782356 | |||||||
| chr2:196782450 | C | T | 1 | a0001c0001t0001g0043 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1115-1788G>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196782450 | |||||||
| chr2:196782470 | T | C | 1 | a0001c0001t0006g0102 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1115-1808A>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196782470 | |||||||
| chr2:196782508 | A | G | 1 | a0002c0002t0003g0142 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1115-1846T>C | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196782508 | |||||||
| chr2:196782624 | CA | C | 9 | a0001c0001t0001g0040 a0001c0001t0001g0042 a0001c0001t0001g0171 others(6): Show |
12 | HG01069.hp2 HG01071.hp2 HG01109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1115-1963delT | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196782624 | |||||||
| chr2:196783372 | A | G | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG02976.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1114+1485T>C | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196783372 | |||||||
| chr2:196783596 | C | T | 3 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0012g0130 |
3 | HG02922.hp1 HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1114+1261G>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196783596 | |||||||
| chr2:196783708 | A | G | 2 | a0001c0001t0001g0024 a0001c0001t0001g0088 |
3 | HG02109.hp2 HG02559.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1114+1149T>C | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196783708 | |||||||
| chr2:196783770 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1114+1087T>C | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196783770 | |||||||
| chr2:196783818 | G | A | 1 | a0001c0001t0001g0125 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1114+1039C>T | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196783818 | |||||||
| chr2:196784042 | T | C | 28 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0002c0002t0001g0003 others(25): Show |
47 | HG00642.hp2 HG00733.hp2 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.1114+815A>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196784042 | |||||||
| chr2:196784080 | A | C | 1 | a0001c0001t0001g0039 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1114+777T>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196784080 | |||||||
| chr2:196784138 | C | A | 18 | a0001c0001t0002g0004 a0001c0001t0002g0018 a0001c0001t0002g0019 others(15): Show |
28 | HG00741.hp2 HG01070.hp2 HG01515.hp2 others(25): Show |
intron_variant | MODIFIER | c.1114+719G>T | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196784138 | |||||||
| chr2:196784141 | G | A | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0174 |
3 | HG02135.hp2 NA18984.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.1114+716C>T | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196784141 | |||||||
| chr2:196784257 | C | G | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0174 |
3 | HG02135.hp2 NA18984.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.1114+600G>C | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196784257 | |||||||
| chr2:196784321 | GAATGTT | G | 2 | a0001c0001t0001g0158 a0001c0001t0001g0171 |
2 | HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1114+530_1114+535d others(8): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196784321 | |||||||
| chr2:196784668 | T | A | 1 | a0001c0001t0001g0078 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1114+189A>T | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196784668 | |||||||
| chr2:196784772 | G | A | 1 | a0001c0001t0004g0079 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1114+85C>T | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 8/17 | chr2 | 196784772 | |||||||
| chr2:196785034 | G | C | 1 | a0001c0001t0001g0080 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1042-105C>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 7/17 | chr2 | 196785034 | |||||||
| chr2:196785147 | A | C | 1 | a0001c0001t0001g0039 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1042-218T>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 7/17 | chr2 | 196785147 | |||||||
| chr2:196785222 | T | TACAG | 68 | a0001c0001t0001g0015 a0001c0001t0001g0030 a0001c0001t0001g0094 others(65): Show |
99 | HG00642.hp2 HG00733.hp2 HG00741.hp2 others(96): Show |
intron_variant | MODIFIER | c.1041+218_1041+219i others(6): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 7/17 | chr2 | 196785222 | |||||||
| chr2:196785225 | A | C | 1 | a0001c0001t0001g0039 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1041+216T>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 7/17 | chr2 | 196785225 | |||||||
| chr2:196785394 | CAGAAACA others(17): Show |
C | 26 | a0002c0002t0001g0003 a0002c0002t0001g0006 a0002c0002t0001g0016 others(23): Show |
45 | HG00642.hp2 HG00733.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.1041+23_1041+46del others(24): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 7/17 | chr2 | 196785394 | |||||||
| chr2:196785941 | C | T | 2 | a0001c0001t0001g0025 a0001c0001t0001g0126 |
3 | HG01099.hp1 HG01257.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.894-353G>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 6/17 | chr2 | 196785941 | |||||||
| chr2:196786239 | G | A | 7 | a0001c0001t0001g0009 a0001c0001t0001g0023 a0001c0001t0001g0031 others(4): Show |
11 | HG00639.hp1 HG01069.hp1 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.894-651C>T | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 6/17 | chr2 | 196786239 | |||||||
| chr2:196786472 | C | G | 1 | a0001c0001t0001g0038 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.894-884G>C | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 6/17 | chr2 | 196786472 | |||||||
| chr2:196786562 | C | T | 1 | a0002c0002t0001g0141 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.894-974G>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 6/17 | chr2 | 196786562 | |||||||
| chr2:196786628 | C | T | 2 | a0001c0001t0001g0138 a0001c0001t0001g0139 |
2 | HG02630.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.894-1040G>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 6/17 | chr2 | 196786628 | |||||||
| chr2:196786711 | C | CA | 21 | a0001c0001t0001g0127 a0001c0001t0001g0157 a0001c0001t0001g0159 others(18): Show |
31 | HG00741.hp2 HG01070.hp2 HG01358.hp1 others(28): Show |
intron_variant | MODIFIER | c.894-1124dupT | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 6/17 | chr2 | 196786711 | |||||||
| chr2:196787290 | A | G | 3 | a0001c0001t0001g0030 a0001c0001t0001g0103 a0001c0001t0001g0104 |
3 | HG03453.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.894-1702T>C | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 6/17 | chr2 | 196787290 | |||||||
| chr2:196787330 | A | G | 1 | a0001c0001t0001g0037 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.894-1742T>C | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 6/17 | chr2 | 196787330 | |||||||
| chr2:196787349 | T | G | 1 | a0001c0001t0001g0086 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.894-1761A>C | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 6/17 | chr2 | 196787349 | |||||||
| chr2:196787471 | C | A | 1 | a0001c0001t0001g0127 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.893+1733G>T | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 6/17 | chr2 | 196787471 | |||||||
| chr2:196787814 | C | T | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0174 |
3 | HG02135.hp2 NA18984.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.893+1390G>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 6/17 | chr2 | 196787814 | |||||||
| chr2:196788536 | A | G | 2 | a0001c0001t0001g0035 a0001c0001t0001g0036 |
2 | HG00099.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.893+668T>C | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 6/17 | chr2 | 196788536 | |||||||
| chr2:196788561 | C | T | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0174 |
3 | HG02135.hp2 NA18984.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.893+643G>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 6/17 | chr2 | 196788561 | |||||||
| chr2:196788612 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.893+592G>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 6/17 | chr2 | 196788612 | |||||||
| chr2:196788819 | T | C | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0174 |
3 | HG02135.hp2 NA18984.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.893+385A>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 6/17 | chr2 | 196788819 | |||||||
| chr2:196788871 | C | A | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0174 |
3 | HG02135.hp2 NA18984.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.893+333G>T | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 6/17 | chr2 | 196788871 | |||||||
| chr2:196788924 | G | A | 7 | a0002c0002t0001g0006 a0002c0002t0001g0135 a0002c0002t0001g0153 others(4): Show |
12 | HG01167.hp2 HG01192.hp2 NA18939.hp2 others(9): Show |
intron_variant | MODIFIER | c.893+280C>T | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 6/17 | chr2 | 196788924 | |||||||
| chr2:196789854 | GA | G | 8 | a0001c0001t0001g0110 a0001c0001t0001g0128 a0001c0001t0001g0129 others(5): Show |
10 | HG02055.hp1 HG02145.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.727+24delT | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 5/17 | chr2 | 196789854 | |||||||
| chr2:196790111 | A | G | 1 | a0001c0001t0002g0167 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.536-41T>C | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 4/17 | chr2 | 196790111 | |||||||
| chr2:196790188 | C | G | 1 | a0001c0001t0001g0103 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.536-118G>C | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 4/17 | chr2 | 196790188 | |||||||
| chr2:196790209 | C | G | 1 | a0001c0001t0001g0103 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.536-139G>C | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 4/17 | chr2 | 196790209 | |||||||
| chr2:196790498 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.536-428G>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 4/17 | chr2 | 196790498 | |||||||
| chr2:196790505 | C | T | 5 | a0001c0001t0001g0007 a0001c0001t0001g0032 a0001c0001t0001g0033 others(2): Show |
8 | NA18945.hp1 NA18986.hp1 NA18989.hp1 others(5): Show |
intron_variant | MODIFIER | c.536-435G>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 4/17 | chr2 | 196790505 | |||||||
| chr2:196790567 | G | A | 1 | a0001c0001t0008g0087 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.536-497C>T | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 4/17 | chr2 | 196790567 | |||||||
| chr2:196791023 | G | C | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0174 |
3 | HG02135.hp2 NA18984.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.535+314C>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 4/17 | chr2 | 196791023 | |||||||
| chr2:196791059 | CATAAT | C | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0174 |
3 | HG02135.hp2 NA18984.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.535+273_535+277del others(5): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 4/17 | chr2 | 196791059 | |||||||
| chr2:196791126 | A | AG | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0174 |
3 | HG02135.hp2 NA18984.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.535+210dupC | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 4/17 | chr2 | 196791126 | |||||||
| chr2:196791272 | T | A | 1 | a0001c0001t0001g0108 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.535+65A>T | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 4/17 | chr2 | 196791272 | |||||||
| chr2:196791591 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.412-131G>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 3/17 | chr2 | 196791591 | |||||||
| chr2:196791601 | T | A | 1 | a0001c0001t0001g0121 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.412-141A>T | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 3/17 | chr2 | 196791601 | |||||||
| chr2:196791642 | G | A | 8 | a0001c0001t0001g0024 a0001c0001t0001g0088 a0001c0001t0001g0089 others(5): Show |
9 | HG01261.hp2 HG02109.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.412-182C>T | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 3/17 | chr2 | 196791642 | |||||||
| chr2:196791689 | A | C | 4 | a0001c0001t0002g0019 a0001c0001t0002g0096 a0001c0001t0002g0168 others(1): Show |
6 | HG02055.hp1 HG02145.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.412-229T>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 3/17 | chr2 | 196791689 | |||||||
| chr2:196791767 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.412-307A>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 3/17 | chr2 | 196791767 | |||||||
| chr2:196791938 | T | A | 1 | a0002c0002t0001g0135 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.412-478A>T | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 3/17 | chr2 | 196791938 | |||||||
| chr2:196792599 | T | C | 1 | a0001c0001t0002g0167 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.411+357A>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 3/17 | chr2 | 196792599 | |||||||
| chr2:196792640 | C | T | 8 | a0001c0001t0001g0030 a0001c0001t0001g0103 a0001c0001t0001g0104 others(5): Show |
8 | HG02135.hp2 HG02717.hp2 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.411+316G>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 3/17 | chr2 | 196792640 | |||||||
| chr2:196792664 | G | T | 4 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(1): Show |
4 | HG01255.hp2 HG02148.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.411+292C>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 3/17 | chr2 | 196792664 | |||||||
| chr2:196792677 | A | T | 1 | a0001c0001t0001g0127 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.411+279T>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 3/17 | chr2 | 196792677 | |||||||
| chr2:196792680 | T | C | 4 | a0001c0001t0001g0015 a0001c0001t0001g0131 a0001c0001t0001g0132 others(1): Show |
6 | HG01496.hp2 HG02647.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.411+276A>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 3/17 | chr2 | 196792680 | |||||||
| chr2:196793381 | C | T | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0174 |
3 | HG02135.hp2 NA18984.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.215-229G>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 2/17 | chr2 | 196793381 | |||||||
| chr2:196793435 | A | T | 1 | a0001c0001t0001g0031 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.215-283T>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 2/17 | chr2 | 196793435 | |||||||
| chr2:196793696 | A | G | 2 | a0001c0001t0001g0158 a0001c0001t0001g0171 |
2 | HG02717.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.215-544T>C | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 2/17 | chr2 | 196793696 | |||||||
| chr2:196794099 | T | C | 2 | a0001c0001t0001g0025 a0001c0001t0001g0126 |
3 | HG01099.hp1 HG01257.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.215-947A>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 2/17 | chr2 | 196794099 | |||||||
| chr2:196794155 | CCATGTGA others(7): Show |
C | 4 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(1): Show |
4 | HG01255.hp2 HG02148.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.215-1017_215-1004d others(16): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 2/17 | chr2 | 196794155 | |||||||
| chr2:196794316 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.215-1164G>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 2/17 | chr2 | 196794316 | |||||||
| chr2:196794391 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.215-1239A>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 2/17 | chr2 | 196794391 | |||||||
| chr2:196794399 | T | G | 1 | a0001c0001t0001g0092 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.215-1247A>C | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 2/17 | chr2 | 196794399 | |||||||
| chr2:196794587 | C | T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0103 a0001c0001t0001g0104 |
3 | HG03453.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.215-1435G>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 2/17 | chr2 | 196794587 | |||||||
| chr2:196794724 | T | G | 1 | a0001c0001t0001g0097 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.215-1572A>C | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 2/17 | chr2 | 196794724 | |||||||
| chr2:196794854 | G | A | 4 | a0001c0001t0002g0019 a0001c0001t0002g0096 a0001c0001t0002g0168 others(1): Show |
6 | HG02055.hp1 HG02145.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.215-1702C>T | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 2/17 | chr2 | 196794854 | |||||||
| chr2:196795318 | T | G | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0174 |
3 | HG02135.hp2 NA18984.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.215-2166A>C | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 2/17 | chr2 | 196795318 | |||||||
| chr2:196795357 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.215-2205C>T | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 2/17 | chr2 | 196795357 | |||||||
| chr2:196795529 | GAGGAACA others(9): Show |
G | 27 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0002c0002t0001g0003 others(24): Show |
46 | HG00642.hp2 HG00733.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.214+2252_214+2267d others(18): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 2/17 | chr2 | 196795529 | |||||||
| chr2:196795567 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.214+2230C>T | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 2/17 | chr2 | 196795567 | |||||||
| chr2:196796053 | G | A | 3 | a0001c0001t0001g0030 a0001c0001t0001g0103 a0001c0001t0001g0104 |
3 | HG03453.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.214+1744C>T | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 2/17 | chr2 | 196796053 | |||||||
| chr2:196796192 | T | C | 1 | a0001c0001t0002g0170 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.214+1605A>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 2/17 | chr2 | 196796192 | |||||||
| chr2:196796242 | T | G | 65 | a0001c0001t0001g0015 a0001c0001t0001g0030 a0001c0001t0001g0103 others(62): Show |
96 | HG00642.hp2 HG00733.hp2 HG00741.hp2 others(93): Show |
intron_variant | MODIFIER | c.214+1555A>C | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 2/17 | chr2 | 196796242 | |||||||
| chr2:196796317 | C | T | 6 | a0001c0001t0001g0030 a0001c0001t0001g0103 a0001c0001t0001g0104 others(3): Show |
6 | HG02135.hp2 HG03453.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.214+1480G>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 2/17 | chr2 | 196796317 | |||||||
| chr2:196796691 | T | G | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0174 |
3 | HG02135.hp2 NA18984.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.214+1106A>C | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 2/17 | chr2 | 196796691 | |||||||
| chr2:196796712 | C | T | 1 | a0003c0006t0006g0136 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.214+1085G>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 2/17 | chr2 | 196796712 | |||||||
| chr2:196796992 | G | C | 1 | a0001c0001t0001g0134 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.214+805C>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 2/17 | chr2 | 196796992 | |||||||
| chr2:196797215 | C | T | 3 | a0001c0001t0001g0030 a0001c0001t0001g0103 a0001c0001t0001g0104 |
3 | HG03453.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.214+582G>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 2/17 | chr2 | 196797215 | |||||||
| chr2:196797461 | T | C | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0174 |
3 | HG02135.hp2 NA18984.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.214+336A>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 2/17 | chr2 | 196797461 | |||||||
| chr2:196797580 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.214+217A>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 2/17 | chr2 | 196797580 | |||||||
| chr2:196797705 | G | C | 1 | a0001c0001t0001g0097 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.214+92C>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 2/17 | chr2 | 196797705 | |||||||
| chr2:196798041 | T | C | 1 | a0001c0001t0002g0173 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.103-133A>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 1/17 | chr2 | 196798041 | |||||||
| chr2:196798143 | C | T | 2 | a0001c0001t0006g0102 a0003c0006t0006g0136 |
2 | HG01884.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.103-235G>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 1/17 | chr2 | 196798143 | |||||||
| chr2:196798272 | C | T | 2 | a0001c0001t0006g0102 a0003c0006t0006g0136 |
2 | HG01884.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.103-364G>A | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 1/17 | chr2 | 196798272 | |||||||
| chr2:196798359 | T | C | 2 | a0001c0001t0001g0098 a0001c0001t0001g0099 |
2 | HG02922.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.103-451A>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 1/17 | chr2 | 196798359 | |||||||
| chr2:196798428 | G | A | 3 | a0001c0003t0001g0100 a0001c0003t0001g0101 a0001c0003t0001g0174 |
3 | HG02135.hp2 NA18984.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.103-520C>T | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 1/17 | chr2 | 196798428 | |||||||
| chr2:196798835 | C | G | 1 | a0002c0002t0001g0135 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.102+675G>C | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 1/17 | chr2 | 196798835 | |||||||
| chr2:196798862 | C | CA | 37 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(34): Show |
51 | HG00408.hp2 HG01192.hp1 HG01255.hp1 others(48): Show |
intron_variant | MODIFIER | c.102+647dupT | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 1/17 | chr2 | 196798862 | |||||||
| chr2:196798862 | C | CAA | 29 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(26): Show |
48 | HG00642.hp2 HG00733.hp2 HG01069.hp2 others(45): Show |
intron_variant | MODIFIER | c.102+646_102+647dup others(2): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 1/17 | chr2 | 196798862 | |||||||
| chr2:196798862 | C | CAAA | 22 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(19): Show |
32 | HG00741.hp2 HG01070.hp2 HG01358.hp1 others(29): Show |
intron_variant | MODIFIER | c.102+645_102+647dup others(3): Show |
GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 1/17 | chr2 | 196798862 | |||||||
| chr2:196799118 | T | C | 1 | a0001c0001t0001g0175 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.102+392A>G | GTF3C3 | ENSG00000119041.11 | transcript | ENST00000263956.8 | protein_coding | 1/17 | chr2 | 196799118 |