Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 2645 |
| ensemblid | ENSG00000106633.18 |
| hgncid | 4195 |
| symbol | GCK |
| name | glucokinase |
| refseq_nuc | NM_000162.5 |
| refseq_prot | NP_000153.1 |
| ensembl_nuc | ENST00000403799.8 |
| ensembl_prot | ENSP00000384247.3 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 44144275 |
| end | 44189439 |
| strand | - |
| ver | v1.2 |
| region | chr7:44144275-44189439 |
| region5000 | chr7:44139275-44194439 |
| regionname0 | GCK_chr7_44144275_44189439 |
| regionname5000 | GCK_chr7_44139275_44194439 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 465 | 389 | 87 | 64 | 180 | 18 | 38 | 146 | GCK_chr7_44139275_44194439 | GCK | MLDDR others(460): Show |
chr7 | 44139275 | 44194439 |
| a0002 | 0/0 | 465 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | MLDDR others(460): Show |
chr7 | 44139275 | 44194439 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1395 | 384 | 84 | 62 | 180 | 18 | 38 | GCK_chr7_44139275_44194439 | GCK | ATGCT others(1390): Show |
chr7 | 44139275 | 44194439 | ||
| a0001c0003 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | ATGCT others(1390): Show |
chr7 | 44139275 | 44194439 | ||
| a0001c0004 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | ATGCT others(1390): Show |
chr7 | 44139275 | 44194439 | ||
| a0001c0005 | 0/0 | 1395 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | ATGCT others(1390): Show |
chr7 | 44139275 | 44194439 | ||
| a0001c0006 | 0/0 | 1395 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | ATGCT others(1390): Show |
chr7 | 44139275 | 44194439 | ||
| a0001c0007 | 0/0 | 1395 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | ATGCT others(1390): Show |
chr7 | 44139275 | 44194439 | ||
| a0002c0002 | 0/0 | 1395 | 3 | 3 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | ATGCT others(1390): Show |
chr7 | 44139275 | 44194439 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2745 | 136 | 16 | 20 | 69 | 7 | 23 | GCK_chr7_44139275_44194439 | GCK | ACTCC others(2740): Show |
chr7 | 44139275 | 44194439 |
| a0001c0001t0002 | 0/0 | 2744 | 131 | 38 | 14 | 64 | 4 | 11 | GCK_chr7_44139275_44194439 | GCK | ACTCC others(2739): Show |
chr7 | 44139275 | 44194439 |
| a0001c0001t0003 | 0/1 | 2745 | 51 | 1 | 22 | 19 | 5 | 3 | GCK_chr7_44139275_44194439 | GCK | ACTCC others(2740): Show |
chr7 | 44139275 | 44194439 |
| a0001c0001t0004 | 0/0 | 2744 | 16 | 15 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | ACTCC others(2739): Show |
chr7 | 44139275 | 44194439 |
| a0001c0001t0005 | 0/0 | 2744 | 11 | 9 | 2 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | ACTCC others(2739): Show |
chr7 | 44139275 | 44194439 |
| a0001c0001t0006 | 0/0 | 2744 | 6 | 0 | 0 | 6 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | ACTCC others(2739): Show |
chr7 | 44139275 | 44194439 |
| a0001c0001t0007 | 0/0 | 2745 | 6 | 0 | 2 | 4 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | ACTCC others(2740): Show |
chr7 | 44139275 | 44194439 |
| a0001c0001t0008 | 0/0 | 2745 | 6 | 0 | 1 | 5 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | ACTCC others(2740): Show |
chr7 | 44139275 | 44194439 |
| a0001c0001t0009 | 0/0 | 2745 | 4 | 0 | 0 | 4 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | ACTCC others(2740): Show |
chr7 | 44139275 | 44194439 |
| a0001c0001t0010 | 0/0 | 2744 | 3 | 0 | 0 | 3 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | ACTCC others(2739): Show |
chr7 | 44139275 | 44194439 |
| a0001c0001t0011 | 0/0 | 2744 | 3 | 0 | 0 | 3 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | ACTCC others(2739): Show |
chr7 | 44139275 | 44194439 |
| a0001c0001t0012 | 0/0 | 2745 | 3 | 3 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | ACTCC others(2740): Show |
chr7 | 44139275 | 44194439 |
| a0001c0001t0013 | 0/0 | 2744 | 2 | 2 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | ACTCC others(2739): Show |
chr7 | 44139275 | 44194439 |
| a0001c0001t0014 | 0/0 | 2745 | 2 | 0 | 0 | 0 | 2 | 0 | GCK_chr7_44139275_44194439 | GCK | ACTCC others(2740): Show |
chr7 | 44139275 | 44194439 |
| a0001c0001t0015 | 0/0 | 2745 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | ACTCC others(2740): Show |
chr7 | 44139275 | 44194439 |
| a0001c0001t0017 | 0/0 | 2745 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | ACTCC others(2740): Show |
chr7 | 44139275 | 44194439 |
| a0001c0001t0018 | 0/0 | 2745 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | ACTCC others(2740): Show |
chr7 | 44139275 | 44194439 |
| a0001c0001t0019 | 0/0 | 2744 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | ACTCC others(2739): Show |
chr7 | 44139275 | 44194439 |
| a0001c0003t0002 | 0/0 | 2744 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | ACTCC others(2739): Show |
chr7 | 44139275 | 44194439 |
| a0001c0004t0004 | 0/0 | 2744 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | ACTCC others(2739): Show |
chr7 | 44139275 | 44194439 |
| a0001c0005t0001 | 0/0 | 2745 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | ACTCC others(2740): Show |
chr7 | 44139275 | 44194439 |
| a0001c0006t0002 | 0/0 | 2744 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | ACTCC others(2739): Show |
chr7 | 44139275 | 44194439 |
| a0001c0007t0016 | 0/0 | 2744 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | ACTCC others(2739): Show |
chr7 | 44139275 | 44194439 |
| a0002c0002t0002 | 0/0 | 2744 | 3 | 3 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | ACTCC others(2739): Show |
chr7 | 44139275 | 44194439 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0296 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0003g0004 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0003g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0003g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0003g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0003g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0003g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0003g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0003g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0003g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0003g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0003g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0003g0328 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0004g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0004g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0004g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0004g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0004g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0004g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0004g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0004g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0004g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0004g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0004g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0005g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0005g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0005g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0005g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0005g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0005g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0005g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0005g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0005g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0005g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0005g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0006g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0006g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0006g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0006g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0006g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0006g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0007g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0007g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0007g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0007g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0007g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0008g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0008g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0008g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0008g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0008g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0008g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0009g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0009g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0009g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0010g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0010g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0010g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0011g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0011g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0011g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0012g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0012g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0012g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0013g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0013g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0014g0025 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0015g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0017g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0018g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0001t0019g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0003t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0004t0004g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0005t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0006t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0001c0007t0016g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| a0002c0002t0002g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0234 | EUR | GBR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0027 | EUR | GBR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0061 | EUR | GBR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG00140 | hp2 | a0001 | c0001 | t0003 | g0292 | EUR | GBR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0171 | EUR | FIN | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0208 | EUR | FIN | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0222 | EUR | FIN | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0004 | EUR | FIN | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG00423 | hp1 | a0001 | c0001 | t0007 | g0023 | EAS | CHS | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | CHS | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | CHS | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | CHS | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0287 | EAS | CHS | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | CHS | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | CHS | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG00597 | hp1 | a0001 | c0001 | t0008 | g0341 | EAS | CHS | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0115 | EAS | CHS | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | CHS | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | CHS | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | CHS | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG00639 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG00639 | hp2 | a0001 | c0006 | t0002 | g0067 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | CHS | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG00733 | hp1 | a0001 | c0001 | t0007 | g0336 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0211 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0324 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0207 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG00741 | hp2 | a0001 | c0001 | t0005 | g0236 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0271 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0170 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0301 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01081 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0307 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0298 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0157 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0146 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0331 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01169 | hp2 | a0001 | c0001 | t0008 | g0338 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0110 | AMR | PUR | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0334 | AMR | CLM | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0108 | AMR | CLM | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0259 | AMR | CLM | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01257 | hp2 | a0001 | c0001 | t0003 | g0216 | AMR | CLM | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | CLM | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0151 | AMR | CLM | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0332 | AMR | CLM | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0325 | AMR | CLM | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0043 | AMR | CLM | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0101 | AMR | CLM | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01433 | hp2 | a0001 | c0001 | t0004 | g0021 | AMR | CLM | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01496 | hp1 | a0001 | c0001 | t0003 | g0149 | AMR | CLM | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0014 | EUR | IBS | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0290 | EUR | IBS | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01516 | hp1 | a0001 | c0001 | t0014 | g0025 | EUR | IBS | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0326 | EUR | IBS | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01517 | hp1 | a0001 | c0001 | t0014 | g0025 | EUR | IBS | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0014 | EUR | IBS | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | ACB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0322 | AFR | ACB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | ACB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0135 | AMR | PEL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0253 | AMR | PEL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0150 | AMR | PEL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0265 | AMR | PEL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PEL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0012 | AMR | PEL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0147 | AMR | PEL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0133 | AMR | PEL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0109 | AMR | PEL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0255 | AMR | PEL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0198 | AMR | PEL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0267 | AMR | PEL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | KHV | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | KHV | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02055 | hp1 | a0001 | c0001 | t0002 | g0309 | AFR | ACB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0182 | EAS | KHV | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | KHV | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | KHV | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | KHV | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | KHV | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | KHV | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02145 | hp1 | a0001 | c0001 | t0002 | g0047 | AFR | ACB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0320 | AFR | ACB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0269 | AMR | PEL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0217 | AMR | PEL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02257 | hp1 | a0002 | c0002 | t0002 | g0003 | AFR | ACB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0021 | AFR | ACB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0064 | AFR | ACB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0316 | AFR | ACB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | ACB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0179 | AMR | PEL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02293 | hp2 | a0001 | c0005 | t0001 | g0227 | AMR | PEL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02451 | hp1 | a0001 | c0001 | t0004 | g0220 | AFR | ACB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0084 | AFR | ACB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | KHV | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | KHV | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0144 | AFR | GWD | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0071 | AFR | GWD | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0091 | SAS | PJL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0323 | AFR | GWD | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | GWD | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02622 | hp1 | a0001 | c0001 | t0005 | g0112 | AFR | GWD | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0167 | AFR | GWD | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0214 | AFR | GWD | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0066 | AFR | GWD | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0166 | AFR | GWD | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0299 | SAS | PJL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | PJL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02717 | hp1 | a0001 | c0003 | t0002 | g0286 | AFR | GWD | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0114 | AFR | GWD | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02735 | hp2 | a0001 | c0001 | t0003 | g0169 | SAS | PJL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0315 | AFR | GWD | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02809 | hp2 | a0001 | c0001 | t0004 | g0046 | AFR | GWD | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | GWD | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0020 | AFR | GWD | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02886 | hp1 | a0001 | c0001 | t0005 | g0134 | AFR | GWD | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0288 | AFR | GWD | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0272 | AFR | GWD | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0317 | AFR | GWD | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0218 | AFR | GWD | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0107 | AFR | GWD | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02922 | hp1 | a0001 | c0001 | t0013 | g0360 | AFR | ESN | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0124 | AFR | ESN | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0103 | AFR | ESN | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0142 | AFR | ESN | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0312 | AFR | ESN | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02970 | hp2 | a0001 | c0001 | t0005 | g0274 | AFR | ESN | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0139 | AFR | ESN | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02976 | hp2 | a0001 | c0001 | t0004 | g0314 | AFR | ESN | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0020 | AFR | GWD | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG03041 | hp2 | a0001 | c0004 | t0004 | g0261 | AFR | GWD | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0106 | AFR | MSL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | MSL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | ESN | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG03130 | hp2 | a0001 | c0001 | t0012 | g0357 | AFR | ESN | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0127 | AFR | ESN | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG03139 | hp2 | a0002 | c0002 | t0002 | g0003 | AFR | ESN | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0123 | AFR | ESN | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG03195 | hp2 | a0001 | c0001 | t0004 | g0273 | AFR | ESN | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0065 | AFR | MSL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | MSL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0300 | SAS | PJL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0327 | SAS | PJL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG03486 | hp1 | a0001 | c0001 | t0004 | g0050 | AFR | MSL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG03486 | hp2 | a0001 | c0001 | t0005 | g0113 | AFR | MSL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ESN | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | GWD | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG03540 | hp2 | a0001 | c0001 | t0005 | g0145 | AFR | GWD | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG03579 | hp1 | a0001 | c0001 | t0013 | g0359 | AFR | MSL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | MSL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0201 | SAS | PJL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0225 | SAS | PJL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0306 | SAS | STU | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | STU | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | PJL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0105 | SAS | PJL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0160 | SAS | PJL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0295 | SAS | PJL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0204 | SAS | BEB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG03831 | hp2 | a0001 | c0001 | t0017 | g0072 | SAS | BEB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0102 | SAS | BEB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG03834 | hp2 | a0001 | c0001 | t0003 | g0321 | SAS | BEB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0230 | SAS | STU | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0044 | SAS | STU | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0031 | SAS | BEB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0305 | SAS | BEB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0291 | SAS | STU | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | STU | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0138 | SAS | STU | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | STU | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0282 | SAS | STU | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0126 | SAS | STU | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0224 | AFR | YRI | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0311 | AFR | YRI | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | CHB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | CHB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18747 | hp1 | a0001 | c0001 | t0006 | g0178 | EAS | CHB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | CHB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | YRI | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | YRI | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18939 | hp2 | a0001 | c0001 | t0019 | g0350 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18941 | hp1 | a0001 | c0001 | t0006 | g0029 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18941 | hp2 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18952 | hp1 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18954 | hp1 | a0001 | c0001 | t0010 | g0344 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18966 | hp2 | a0001 | c0001 | t0009 | g0024 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18967 | hp1 | a0001 | c0001 | t0008 | g0347 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18969 | hp1 | a0001 | c0001 | t0009 | g0355 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18969 | hp2 | a0001 | c0001 | t0011 | g0352 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0276 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18977 | hp1 | a0001 | c0001 | t0007 | g0342 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18981 | hp1 | a0001 | c0001 | t0009 | g0353 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18981 | hp2 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18983 | hp2 | a0001 | c0001 | t0018 | g0343 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0333 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18988 | hp1 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18988 | hp2 | a0001 | c0001 | t0008 | g0340 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0278 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18997 | hp1 | a0001 | c0001 | t0006 | g0256 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18997 | hp2 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19002 | hp1 | a0001 | c0001 | t0007 | g0023 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19004 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0335 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0330 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0275 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0329 | AFR | LWK | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0042 | AFR | LWK | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | LWK | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0257 | AFR | LWK | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19056 | hp2 | a0001 | c0001 | t0011 | g0354 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19057 | hp2 | a0001 | c0001 | t0010 | g0348 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19058 | hp2 | a0001 | c0001 | t0008 | g0346 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19063 | hp1 | a0001 | c0001 | t0006 | g0177 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0055 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0249 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0152 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19077 | hp1 | a0001 | c0001 | t0008 | g0345 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19077 | hp2 | a0001 | c0001 | t0015 | g0280 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19079 | hp1 | a0001 | c0001 | t0011 | g0351 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19079 | hp2 | a0001 | c0001 | t0006 | g0099 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0270 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19084 | hp1 | a0001 | c0001 | t0007 | g0339 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19086 | hp1 | a0001 | c0001 | t0009 | g0024 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19089 | hp1 | a0001 | c0001 | t0010 | g0349 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0068 | AFR | YRI | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA19240 | hp2 | a0001 | c0001 | t0012 | g0358 | AFR | YRI | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0263 | EUR | TSI | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0238 | EUR | TSI | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0054 | EUR | TSI | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0252 | EUR | TSI | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | GIH | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0231 | SAS | GIH | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0185 | AMR | CLM | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG01123 | hp2 | a0001 | c0001 | t0007 | g0337 | AMR | CLM | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02109 | hp1 | a0001 | c0001 | t0005 | g0143 | AFR | ACB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02109 | hp2 | a0001 | c0007 | t0016 | g0221 | AFR | ACB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0310 | AFR | ACB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0140 | AFR | ACB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0083 | AFR | ACB | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | MSL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG03471 | hp2 | a0001 | c0001 | t0012 | g0356 | AFR | MSL | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0081 | AFR | USA | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| HG06807 | hp2 | a0002 | c0002 | t0002 | g0003 | AFR | USA | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18955 | hp1 | a0001 | c0001 | t0006 | g0176 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | USA | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA20300 | hp2 | a0001 | c0001 | t0002 | g0266 | AFR | USA | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | LWK | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0137 | AFR | LWK | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0328 | REF | REF | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0296 | REF | REF | GCK_chr7_44139275_44194439 | GCK | chr7 | 44139275 | 44194439 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:44188923 | C | T | 1 | a0002 | 3 | HG02257.hp1 HG03139.hp2 HG06807.hp2 |
missense_variant | MODERATE | c.31G>A | p.Ala11Thr | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/10 | 517/2745 | 31/1398 | 11/465 | chr7 | 44188923 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:44146528 | C | G | 1 | a0001c0004 | 1 | HG03041.hp2 | synonymous_variant | LOW | c.954G>C | p.Gly318Gly | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 8/10 | 1440/2745 | 954/1398 | 318/465 | chr7 | 44146528 | |||
| chr7:44149794 | G | A | 1 | a0001c0005 | 1 | HG02293.hp2 | synonymous_variant | LOW | c.645C>T | p.Tyr215Tyr | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 6/10 | 1131/2745 | 645/1398 | 215/465 | chr7 | 44149794 | |||
| chr7:44149821 | C | T | 1 | a0001c0003 | 1 | HG02717.hp1 | synonymous_variant | LOW | c.618G>A | p.Thr206Thr | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 6/10 | 1104/2745 | 618/1398 | 206/465 | chr7 | 44149821 | |||
| chr7:44152295 | G | A | 1 | a0001c0006 | 1 | HG00639.hp2 | synonymous_variant | LOW | c.339C>T | p.Asp113Asp | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 3/10 | 825/2745 | 339/1398 | 113/465 | chr7 | 44152295 | |||
| chr7:44152301 | G | A | 1 | a0001c0007 | 1 | HG02109.hp2 | synonymous_variant | LOW | c.333C>T | p.Pro111Pro | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 3/10 | 819/2745 | 333/1398 | 111/465 | chr7 | 44152301 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:44144289 | C | T | 1 | a0001c0001t0006 | 6 | NA18747.hp1 NA18941.hp1 NA18955.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*847G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 10/10 | 847 | chr7 | 44144289 | ||||||
| chr7:44144339 | G | A | 1 | a0001c0001t0005 | 11 | HG00741.hp2 HG01109.hp1 HG02109.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*797C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 10/10 | 797 | chr7 | 44144339 | ||||||
| chr7:44144376 | TG | T | 13 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(10): Show |
180 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(177): Show |
3_prime_UTR_variant | MODIFIER | c.*759delC | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 10/10 | 759 | chr7 | 44144376 | ||||||
| chr7:44144626 | G | A | 2 | a0001c0001t0015 a0001c0001t0018 |
2 | NA18983.hp2 NA19077.hp2 |
3_prime_UTR_variant | MODIFIER | c.*510C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 10/10 | 510 | chr7 | 44144626 | ||||||
| chr7:44144659 | G | A | 4 | a0001c0001t0004 a0001c0001t0005 a0001c0004t0004 others(1): Show |
29 | HG00741.hp2 HG01109.hp1 HG01433.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*477C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 10/10 | 477 | chr7 | 44144659 | ||||||
| chr7:44144761 | A | G | 1 | a0001c0001t0017 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*375T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 10/10 | 375 | chr7 | 44144761 | ||||||
| chr7:44144780 | C | T | 1 | a0001c0007t0016 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*356G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 10/10 | 356 | chr7 | 44144780 | ||||||
| chr7:44144804 | C | T | 4 | a0001c0001t0003 a0001c0001t0007 a0001c0001t0015 others(1): Show |
58 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*332G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 10/10 | 332 | chr7 | 44144804 | ||||||
| chr7:44189037 | G | C | 6 | a0001c0001t0007 a0001c0001t0008 a0001c0001t0010 others(3): Show |
21 | HG00423.hp1 HG00597.hp1 HG00733.hp1 others(18): Show |
5_prime_UTR_variant | MODIFIER | c.-84C>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/10 | 84 | chr7 | 44189037 | ||||||
| chr7:44189152 | G | A | 1 | a0001c0001t0019 | 1 | NA18939.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-199C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/10 | chr7 | 44189152 | |||||||
| chr7:44189168 | T | C | 2 | a0001c0001t0009 a0001c0001t0011 |
7 | NA18966.hp2 NA18969.hp1 NA18969.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-215A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/10 | 215 | chr7 | 44189168 | ||||||
| chr7:44189170 | G | C | 2 | a0001c0001t0012 a0001c0001t0013 |
5 | HG02922.hp1 HG03130.hp2 HG03471.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-217C>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/10 | 217 | chr7 | 44189170 | ||||||
| chr7:44189220 | C | A | 2 | a0001c0001t0012 a0001c0001t0013 |
5 | HG02922.hp1 HG03130.hp2 HG03471.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-267G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/10 | 267 | chr7 | 44189220 | ||||||
| chr7:44189406 | G | A | 1 | a0001c0001t0014 | 2 | HG01516.hp1 HG01517.hp1 |
5_prime_UTR_variant | MODIFIER | c.-453C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/10 | 453 | chr7 | 44189406 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:44145448 | C | T | 24 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0063 others(21): Show |
25 | HG01074.hp2 HG01256.hp1 HG02015.hp2 others(22): Show |
intron_variant | MODIFIER | c.1253+49G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 9/9 | chr7 | 44145448 | |||||||
| chr7:44145449 | G | A | 1 | a0001c0001t0002g0042 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1253+48C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 9/9 | chr7 | 44145449 | |||||||
| chr7:44145489 | G | A | 167 | a0001c0001t0001g0258 a0001c0001t0002g0001 a0001c0001t0002g0006 others(164): Show |
181 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(178): Show |
splice_region_variant&intron_variant | LOW | c.1253+8C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 9/9 | chr7 | 44145489 | |||||||
| chr7:44145784 | C | T | 1 | a0001c0001t0012g0356 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1020-54G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 8/9 | chr7 | 44145784 | |||||||
| chr7:44145825 | C | T | 1 | a0001c0003t0002g0286 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1020-95G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 8/9 | chr7 | 44145825 | |||||||
| chr7:44146057 | G | T | 51 | a0001c0001t0003g0004 a0001c0001t0003g0005 a0001c0001t0003g0009 others(48): Show |
58 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(55): Show |
intron_variant | MODIFIER | c.1020-327C>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 8/9 | chr7 | 44146057 | |||||||
| chr7:44146141 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1019+322G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 8/9 | chr7 | 44146141 | |||||||
| chr7:44146159 | C | G | 104 | a0001c0001t0001g0258 a0001c0001t0002g0001 a0001c0001t0002g0006 others(101): Show |
114 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.1019+304G>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 8/9 | chr7 | 44146159 | |||||||
| chr7:44146187 | GC | G | 78 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0060 others(75): Show |
86 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.1019+275delG | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 8/9 | chr7 | 44146187 | |||||||
| chr7:44146206 | C | G | 55 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0318 others(52): Show |
62 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(59): Show |
intron_variant | MODIFIER | c.1019+257G>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 8/9 | chr7 | 44146206 | |||||||
| chr7:44146218 | G | T | 1 | a0001c0001t0004g0218 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1019+245C>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 8/9 | chr7 | 44146218 | |||||||
| chr7:44146289 | C | A | 53 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0003g0004 others(50): Show |
60 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.1019+174G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 8/9 | chr7 | 44146289 | |||||||
| chr7:44146315 | C | T | 1 | a0001c0007t0016g0221 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1019+148G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 8/9 | chr7 | 44146315 | |||||||
| chr7:44146334 | C | A | 1 | a0001c0001t0008g0341 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1019+129G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 8/9 | chr7 | 44146334 | |||||||
| chr7:44146344 | C | T | 1 | a0001c0001t0003g0278 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1019+119G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 8/9 | chr7 | 44146344 | |||||||
| chr7:44146356 | A | G | 58 | a0001c0001t0002g0010 a0001c0001t0002g0013 a0001c0001t0002g0038 others(55): Show |
60 | HG00423.hp2 HG00544.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.1019+107T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 8/9 | chr7 | 44146356 | |||||||
| chr7:44146708 | A | G | 1 | a0001c0001t0003g0320 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.864-90T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 7/9 | chr7 | 44146708 | |||||||
| chr7:44146723 | C | T | 1 | a0001c0001t0014g0025 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.864-105G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 7/9 | chr7 | 44146723 | |||||||
| chr7:44146729 | C | T | 5 | a0001c0001t0001g0093 a0001c0001t0001g0158 a0001c0001t0008g0341 others(2): Show |
6 | HG00597.hp1 HG02040.hp2 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.864-111G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 7/9 | chr7 | 44146729 | |||||||
| chr7:44146752 | C | A | 1 | a0001c0001t0003g0175 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.864-134G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 7/9 | chr7 | 44146752 | |||||||
| chr7:44147058 | G | C | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG00140.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.864-440C>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 7/9 | chr7 | 44147058 | |||||||
| chr7:44147408 | G | A | 2 | a0001c0001t0001g0318 a0001c0001t0001g0319 |
2 | HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.863+242C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 7/9 | chr7 | 44147408 | |||||||
| chr7:44147569 | A | T | 1 | a0001c0001t0002g0137 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.863+81T>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 7/9 | chr7 | 44147569 | |||||||
| chr7:44147853 | G | C | 1 | a0001c0001t0001g0082 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.680-20C>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 6/9 | chr7 | 44147853 | |||||||
| chr7:44147879 | C | T | 1 | a0001c0001t0003g0217 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.680-46G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 6/9 | chr7 | 44147879 | |||||||
| chr7:44148005 | C | G | 1 | a0001c0001t0002g0105 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.680-172G>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 6/9 | chr7 | 44148005 | |||||||
| chr7:44148510 | GT | G | 163 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0054 others(160): Show |
179 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.680-678delA | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 6/9 | chr7 | 44148510 | |||||||
| chr7:44148621 | T | C | 239 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0054 others(236): Show |
259 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.680-788A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 6/9 | chr7 | 44148621 | |||||||
| chr7:44148802 | G | A | 1 | a0001c0001t0003g0201 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.679+958C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 6/9 | chr7 | 44148802 | |||||||
| chr7:44148810 | C | T | 1 | a0001c0001t0001g0332 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.679+950G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 6/9 | chr7 | 44148810 | |||||||
| chr7:44149168 | A | G | 1 | a0001c0001t0002g0259 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.679+592T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 6/9 | chr7 | 44149168 | |||||||
| chr7:44149275 | C | T | 1 | a0001c0001t0005g0144 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.679+485G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 6/9 | chr7 | 44149275 | |||||||
| chr7:44149411 | C | T | 74 | a0001c0001t0001g0082 a0001c0001t0001g0165 a0001c0001t0001g0232 others(71): Show |
78 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.679+349G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 6/9 | chr7 | 44149411 | |||||||
| chr7:44149424 | T | C | 239 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0054 others(236): Show |
259 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.679+336A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 6/9 | chr7 | 44149424 | |||||||
| chr7:44149484 | A | G | 1 | a0001c0001t0001g0233 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.679+276T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 6/9 | chr7 | 44149484 | |||||||
| chr7:44149591 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.679+169C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 6/9 | chr7 | 44149591 | |||||||
| chr7:44149675 | T | C | 76 | a0001c0001t0001g0082 a0001c0001t0001g0165 a0001c0001t0001g0232 others(73): Show |
80 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.679+85A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 6/9 | chr7 | 44149675 | |||||||
| chr7:44149722 | A | G | 239 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0054 others(236): Show |
259 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(256): Show |
intron_variant | MODIFIER | c.679+38T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 6/9 | chr7 | 44149722 | |||||||
| chr7:44149940 | C | A | 5 | a0001c0001t0001g0155 a0001c0001t0001g0239 a0001c0001t0001g0240 others(2): Show |
5 | NA18949.hp2 NA18962.hp1 NA18987.hp1 others(2): Show |
intron_variant | MODIFIER | c.579+29G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 5/9 | chr7 | 44149940 | |||||||
| chr7:44150093 | C | G | 6 | a0001c0001t0001g0015 a0001c0001t0001g0168 a0001c0001t0001g0226 others(3): Show |
7 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.484-29G>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 4/9 | chr7 | 44150093 | |||||||
| chr7:44150298 | T | C | 1 | a0001c0001t0010g0348 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.484-234A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 4/9 | chr7 | 44150298 | |||||||
| chr7:44150538 | T | C | 1 | a0001c0001t0003g0271 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.483+418A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 4/9 | chr7 | 44150538 | |||||||
| chr7:44150869 | T | G | 241 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0054 others(238): Show |
261 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.483+87A>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 4/9 | chr7 | 44150869 | |||||||
| chr7:44150898 | T | A | 15 | a0001c0001t0002g0022 a0001c0001t0002g0114 a0001c0001t0002g0166 others(12): Show |
16 | HG02055.hp1 HG02280.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.483+58A>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 4/9 | chr7 | 44150898 | |||||||
| chr7:44151113 | G | C | 1 | a0001c0001t0001g0291 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.364-38C>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 3/9 | chr7 | 44151113 | |||||||
| chr7:44151453 | A | C | 3 | a0001c0001t0001g0037 a0001c0001t0001g0075 a0001c0001t0001g0077 |
3 | NA18983.hp1 NA19062.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.364-378T>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 3/9 | chr7 | 44151453 | |||||||
| chr7:44151525 | G | A | 1 | a0001c0001t0002g0248 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.364-450C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 3/9 | chr7 | 44151525 | |||||||
| chr7:44151581 | C | T | 1 | a0001c0001t0001g0260 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.364-506G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 3/9 | chr7 | 44151581 | |||||||
| chr7:44151591 | T | A | 69 | a0001c0001t0001g0165 a0001c0001t0001g0258 a0001c0001t0001g0303 others(66): Show |
73 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.364-516A>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 3/9 | chr7 | 44151591 | |||||||
| chr7:44151591 | T | G | 45 | a0001c0001t0001g0186 a0001c0001t0001g0187 a0001c0001t0001g0229 others(42): Show |
51 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.364-516A>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 3/9 | chr7 | 44151591 | |||||||
| chr7:44151710 | C | T | 106 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0054 others(103): Show |
116 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.363+561G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 3/9 | chr7 | 44151710 | |||||||
| chr7:44151747 | T | C | 118 | a0001c0001t0001g0041 a0001c0001t0001g0165 a0001c0001t0001g0172 others(115): Show |
128 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.363+524A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 3/9 | chr7 | 44151747 | |||||||
| chr7:44151763 | T | C | 119 | a0001c0001t0001g0093 a0001c0001t0001g0165 a0001c0001t0001g0172 others(116): Show |
129 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.363+508A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 3/9 | chr7 | 44151763 | |||||||
| chr7:44151953 | C | T | 11 | a0001c0001t0002g0114 a0001c0001t0002g0139 a0001c0001t0005g0112 others(8): Show |
11 | HG00741.hp2 HG01109.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.363+318G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 3/9 | chr7 | 44151953 | |||||||
| chr7:44151954 | G | A | 1 | a0001c0001t0003g0201 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.363+317C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 3/9 | chr7 | 44151954 | |||||||
| chr7:44152106 | G | A | 7 | a0001c0001t0002g0038 a0001c0001t0002g0039 a0001c0001t0002g0080 others(4): Show |
7 | HG02015.hp1 NA18956.hp2 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.363+165C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 3/9 | chr7 | 44152106 | |||||||
| chr7:44152201 | C | T | 1 | a0001c0001t0002g0142 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.363+70G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 3/9 | chr7 | 44152201 | |||||||
| chr7:44152604 | A | G | 127 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0018 others(124): Show |
143 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.209-179T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 2/9 | chr7 | 44152604 | |||||||
| chr7:44152661 | C | A | 118 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0054 others(115): Show |
128 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.209-236G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 2/9 | chr7 | 44152661 | |||||||
| chr7:44152758 | C | CT | 269 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(266): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.209-334dupA | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 2/9 | chr7 | 44152758 | |||||||
| chr7:44152758 | C | CTT | 76 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0040 others(73): Show |
87 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.209-335_209-334dup others(2): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 2/9 | chr7 | 44152758 | |||||||
| chr7:44152794 | C | T | 1 | a0001c0001t0003g0217 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.209-369G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 2/9 | chr7 | 44152794 | |||||||
| chr7:44152950 | G | A | 6 | a0001c0001t0002g0022 a0001c0001t0002g0166 a0001c0001t0002g0167 others(3): Show |
7 | HG02055.hp1 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.208+351C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 2/9 | chr7 | 44152950 | |||||||
| chr7:44152953 | G | A | 126 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0054 others(123): Show |
137 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.208+348C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 2/9 | chr7 | 44152953 | |||||||
| chr7:44153079 | G | A | 1 | a0001c0001t0001g0281 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.208+222C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 2/9 | chr7 | 44153079 | |||||||
| chr7:44153525 | G | T | 1 | a0001c0004t0004g0261 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.46-62C>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44153525 | |||||||
| chr7:44153805 | C | T | 126 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0054 others(123): Show |
137 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.46-342G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44153805 | |||||||
| chr7:44153863 | G | T | 107 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0054 others(104): Show |
117 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.46-400C>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44153863 | |||||||
| chr7:44153952 | T | G | 13 | a0001c0001t0001g0318 a0001c0001t0001g0319 a0001c0001t0002g0047 others(10): Show |
15 | HG00639.hp2 HG02145.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.46-489A>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44153952 | |||||||
| chr7:44153986 | C | T | 1 | a0001c0001t0006g0176 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.46-523G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44153986 | |||||||
| chr7:44154142 | G | A | 1 | a0001c0001t0002g0207 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.46-679C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44154142 | |||||||
| chr7:44154248 | T | G | 1 | a0001c0001t0002g0128 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.46-785A>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44154248 | |||||||
| chr7:44154323 | G | T | 1 | a0001c0001t0002g0017 | 2 | HG02074.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.46-860C>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44154323 | |||||||
| chr7:44154638 | GA | G | 3 | a0001c0001t0002g0014 a0001c0001t0002g0027 a0001c0001t0002g0222 |
4 | HG00099.hp2 HG00323.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-1176delT | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44154638 | |||||||
| chr7:44154883 | G | A | 47 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0060 others(44): Show |
53 | HG00140.hp1 HG00741.hp2 HG01074.hp2 others(50): Show |
intron_variant | MODIFIER | c.46-1420C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44154883 | |||||||
| chr7:44154924 | T | G | 356 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(353): Show |
388 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(385): Show |
intron_variant | MODIFIER | c.46-1461A>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44154924 | |||||||
| chr7:44154952 | G | A | 125 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0054 others(122): Show |
136 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.46-1489C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44154952 | |||||||
| chr7:44154952 | G | C | 1 | a0001c0001t0001g0063 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.46-1489C>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44154952 | |||||||
| chr7:44154987 | A | G | 13 | a0001c0001t0001g0318 a0001c0001t0001g0319 a0001c0001t0002g0047 others(10): Show |
15 | HG00639.hp2 HG02145.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.46-1524T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44154987 | |||||||
| chr7:44155112 | T | C | 3 | a0001c0001t0001g0037 a0001c0001t0001g0075 a0001c0001t0001g0077 |
3 | NA18983.hp1 NA19062.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.46-1649A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44155112 | |||||||
| chr7:44155152 | C | A | 1 | a0001c0001t0005g0236 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.46-1689G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44155152 | |||||||
| chr7:44155222 | C | T | 1 | a0001c0001t0002g0131 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.46-1759G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44155222 | |||||||
| chr7:44155239 | C | A | 30 | a0001c0001t0001g0194 a0001c0001t0002g0001 a0001c0001t0002g0026 others(27): Show |
35 | HG00741.hp2 HG01109.hp1 HG01433.hp2 others(32): Show |
intron_variant | MODIFIER | c.46-1776G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44155239 | |||||||
| chr7:44155351 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.46-1888C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44155351 | |||||||
| chr7:44155397 | G | A | 8 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0036 others(5): Show |
11 | HG01884.hp1 HG01891.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.46-1934C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44155397 | |||||||
| chr7:44155410 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.46-1947G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44155410 | |||||||
| chr7:44155477 | G | A | 1 | a0001c0001t0007g0342 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.46-2014C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44155477 | |||||||
| chr7:44155516 | A | G | 1 | a0001c0001t0001g0190 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.46-2053T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44155516 | |||||||
| chr7:44155635 | A | C | 1 | a0001c0001t0001g0291 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.46-2172T>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44155635 | |||||||
| chr7:44155820 | G | A | 10 | a0001c0001t0001g0082 a0001c0001t0001g0232 a0001c0001t0001g0233 others(7): Show |
10 | HG02258.hp2 HG02280.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.46-2357C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44155820 | |||||||
| chr7:44155855 | G | A | 1 | a0001c0001t0003g0183 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.46-2392C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44155855 | |||||||
| chr7:44155927 | T | C | 1 | a0001c0001t0012g0358 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.46-2464A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44155927 | |||||||
| chr7:44156167 | G | A | 1 | a0001c0001t0018g0343 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.46-2704C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44156167 | |||||||
| chr7:44156312 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.46-2849C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44156312 | |||||||
| chr7:44156342 | C | T | 1 | a0001c0001t0001g0203 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.46-2879G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44156342 | |||||||
| chr7:44156381 | GT | G | 3 | a0001c0001t0001g0195 a0001c0001t0001g0202 a0001c0001t0001g0334 |
3 | HG01255.hp1 HG01952.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.46-2919delA | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44156381 | |||||||
| chr7:44156435 | A | G | 1 | a0001c0001t0002g0035 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.46-2972T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44156435 | |||||||
| chr7:44156470 | C | T | 173 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0018 others(170): Show |
194 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.46-3007G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44156470 | |||||||
| chr7:44156949 | G | C | 3 | a0001c0001t0002g0139 a0001c0001t0005g0145 a0001c0001t0005g0146 |
3 | HG01109.hp1 HG02976.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.46-3486C>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44156949 | |||||||
| chr7:44156983 | A | G | 1 | a0001c0001t0017g0072 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.46-3520T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44156983 | |||||||
| chr7:44157214 | A | G | 2 | a0001c0001t0002g0056 a0001c0001t0003g0055 |
2 | NA18979.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.46-3751T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44157214 | |||||||
| chr7:44157241 | C | T | 1 | a0001c0001t0002g0225 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.46-3778G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44157241 | |||||||
| chr7:44157276 | T | C | 1 | a0001c0001t0002g0231 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.46-3813A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44157276 | |||||||
| chr7:44157377 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.46-3914C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44157377 | |||||||
| chr7:44157464 | C | G | 5 | a0001c0001t0002g0006 a0001c0001t0002g0030 a0001c0001t0002g0032 others(2): Show |
6 | NA18940.hp2 NA18944.hp1 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.46-4001G>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44157464 | |||||||
| chr7:44157560 | G | A | 1 | a0001c0001t0002g0132 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.46-4097C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44157560 | |||||||
| chr7:44157631 | G | A | 1 | a0001c0001t0004g0046 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.46-4168C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44157631 | |||||||
| chr7:44157678 | A | G | 1 | a0002c0002t0002g0003 | 3 | HG02257.hp1 HG03139.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.46-4215T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44157678 | |||||||
| chr7:44157824 | C | T | 1 | a0001c0001t0002g0088 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.46-4361G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44157824 | |||||||
| chr7:44157854 | A | G | 3 | a0001c0001t0013g0359 a0001c0001t0013g0360 a0002c0002t0002g0003 |
5 | HG02257.hp1 HG02922.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.46-4391T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44157854 | |||||||
| chr7:44157901 | G | A | 4 | a0001c0001t0001g0228 a0001c0001t0001g0230 a0001c0001t0003g0149 others(1): Show |
4 | HG01496.hp1 HG02293.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-4438C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44157901 | |||||||
| chr7:44157929 | G | A | 3 | a0001c0001t0002g0132 a0001c0001t0002g0287 a0001c0001t0003g0179 |
3 | HG00544.hp1 HG02293.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.46-4466C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44157929 | |||||||
| chr7:44157968 | C | T | 2 | a0001c0001t0001g0155 a0001c0001t0001g0240 |
2 | NA18949.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.46-4505G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44157968 | |||||||
| chr7:44157984 | G | T | 100 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0054 others(97): Show |
110 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.46-4521C>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44157984 | |||||||
| chr7:44158080 | T | C | 1 | a0001c0001t0005g0144 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.46-4617A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44158080 | |||||||
| chr7:44158167 | T | C | 1 | a0001c0001t0001g0260 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.46-4704A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44158167 | |||||||
| chr7:44158176 | C | T | 11 | a0001c0001t0001g0082 a0001c0001t0001g0232 a0001c0001t0001g0233 others(8): Show |
11 | HG02258.hp2 HG02280.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.46-4713G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44158176 | |||||||
| chr7:44158360 | G | C | 1 | a0001c0001t0001g0054 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.46-4897C>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44158360 | |||||||
| chr7:44158451 | C | G | 2 | a0001c0001t0012g0357 a0001c0001t0012g0358 |
2 | HG03130.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.46-4988G>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44158451 | |||||||
| chr7:44158495 | G | A | 2 | a0001c0001t0002g0091 a0001c0001t0002g0138 |
2 | HG02602.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.46-5032C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44158495 | |||||||
| chr7:44158558 | A | G | 1 | a0001c0001t0017g0072 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.46-5095T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44158558 | |||||||
| chr7:44158679 | C | T | 4 | a0001c0001t0004g0050 a0001c0001t0004g0084 a0001c0001t0004g0214 others(1): Show |
4 | HG02451.hp2 HG02630.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.46-5216G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44158679 | |||||||
| chr7:44158733 | C | T | 1 | a0001c0001t0001g0093 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.46-5270G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44158733 | |||||||
| chr7:44159021 | C | T | 1 | a0001c0001t0001g0297 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.46-5558G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44159021 | |||||||
| chr7:44159057 | T | C | 1 | a0002c0002t0002g0003 | 3 | HG02257.hp1 HG03139.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.46-5594A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44159057 | |||||||
| chr7:44159061 | T | A | 1 | a0001c0001t0001g0104 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.46-5598A>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44159061 | |||||||
| chr7:44159144 | A | G | 2 | a0001c0001t0002g0056 a0001c0001t0003g0055 |
2 | NA18979.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.46-5681T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44159144 | |||||||
| chr7:44159164 | G | A | 10 | a0001c0001t0001g0082 a0001c0001t0001g0232 a0001c0001t0001g0233 others(7): Show |
10 | HG02258.hp2 HG02280.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.46-5701C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44159164 | |||||||
| chr7:44159402 | C | A | 1 | a0001c0001t0001g0240 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.46-5939G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44159402 | |||||||
| chr7:44159413 | C | T | 1 | a0001c0001t0003g0278 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.46-5950G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44159413 | |||||||
| chr7:44159543 | C | T | 95 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0054 others(92): Show |
104 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.46-6080G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44159543 | |||||||
| chr7:44159693 | G | A | 2 | a0001c0001t0013g0359 a0001c0001t0013g0360 |
2 | HG02922.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.46-6230C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44159693 | |||||||
| chr7:44159852 | C | T | 1 | a0001c0001t0002g0108 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.46-6389G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44159852 | |||||||
| chr7:44159930 | C | A | 1 | a0001c0001t0002g0185 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.46-6467G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44159930 | |||||||
| chr7:44160350 | C | T | 1 | a0001c0001t0005g0274 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.46-6887G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44160350 | |||||||
| chr7:44160487 | C | T | 1 | a0001c0003t0002g0286 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.46-7024G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44160487 | |||||||
| chr7:44160500 | G | T | 50 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0040 others(47): Show |
60 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.46-7037C>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44160500 | |||||||
| chr7:44160637 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.46-7174C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44160637 | |||||||
| chr7:44160666 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.46-7203G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44160666 | |||||||
| chr7:44160727 | T | C | 1 | a0001c0001t0002g0032 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.46-7264A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44160727 | |||||||
| chr7:44160798 | T | G | 1 | a0001c0001t0002g0083 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.46-7335A>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44160798 | |||||||
| chr7:44160884 | A | G | 1 | a0001c0001t0001g0325 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.46-7421T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44160884 | |||||||
| chr7:44160929 | G | A | 5 | a0001c0001t0001g0219 a0001c0001t0002g0014 a0001c0001t0002g0222 others(2): Show |
6 | HG00323.hp1 HG01256.hp2 HG01257.hp2 others(3): Show |
intron_variant | MODIFIER | c.46-7466C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44160929 | |||||||
| chr7:44161079 | C | T | 1 | a0001c0001t0001g0301 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.46-7616G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44161079 | |||||||
| chr7:44161080 | G | A | 1 | a0001c0001t0002g0027 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.46-7617C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44161080 | |||||||
| chr7:44161116 | T | TTAATTA | 123 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0054 others(120): Show |
133 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.46-7654_46-7653ins others(6): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44161116 | |||||||
| chr7:44161157 | G | A | 6 | a0001c0001t0001g0082 a0001c0001t0001g0233 a0001c0001t0001g0323 others(3): Show |
6 | HG02258.hp2 HG02280.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.46-7694C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44161157 | |||||||
| chr7:44161285 | T | C | 242 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0015 others(239): Show |
267 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.46-7822A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44161285 | |||||||
| chr7:44161323 | T | C | 3 | a0001c0001t0003g0169 a0001c0001t0003g0170 a0001c0001t0003g0171 |
3 | HG00280.hp1 HG01074.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.46-7860A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44161323 | |||||||
| chr7:44161403 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.46-7940C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44161403 | |||||||
| chr7:44161550 | C | T | 47 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0040 others(44): Show |
56 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.46-8087G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44161550 | |||||||
| chr7:44161716 | T | A | 2 | a0001c0001t0002g0276 a0001c0001t0002g0308 |
2 | NA18950.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.46-8253A>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44161716 | |||||||
| chr7:44161943 | G | C | 7 | a0001c0001t0002g0064 a0001c0001t0002g0065 a0001c0001t0002g0066 others(4): Show |
7 | HG02258.hp1 HG02630.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.46-8480C>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44161943 | |||||||
| chr7:44162283 | C | T | 1 | a0001c0007t0016g0221 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.46-8820G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44162283 | |||||||
| chr7:44162634 | A | C | 1 | a0001c0001t0002g0132 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.46-9171T>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44162634 | |||||||
| chr7:44162790 | T | C | 15 | a0001c0001t0002g0022 a0001c0001t0002g0064 a0001c0001t0002g0065 others(12): Show |
16 | HG02055.hp1 HG02258.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.46-9327A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44162790 | |||||||
| chr7:44163117 | C | T | 7 | a0001c0001t0002g0022 a0001c0001t0002g0166 a0001c0001t0002g0167 others(4): Show |
8 | HG00639.hp2 HG02055.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.46-9654G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44163117 | |||||||
| chr7:44163223 | A | T | 1 | a0001c0001t0001g0258 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.46-9760T>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44163223 | |||||||
| chr7:44163295 | G | A | 1 | a0001c0001t0002g0225 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.46-9832C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44163295 | |||||||
| chr7:44163334 | T | C | 1 | a0001c0001t0002g0059 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.46-9871A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44163334 | |||||||
| chr7:44163407 | C | T | 243 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(240): Show |
272 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(269): Show |
intron_variant | MODIFIER | c.46-9944G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44163407 | |||||||
| chr7:44163619 | G | A | 1 | a0001c0001t0002g0125 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.46-10156C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44163619 | |||||||
| chr7:44164135 | T | C | 6 | a0001c0001t0002g0022 a0001c0001t0002g0166 a0001c0001t0002g0167 others(3): Show |
7 | HG02055.hp1 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.46-10672A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44164135 | |||||||
| chr7:44164150 | G | A | 1 | a0001c0001t0002g0139 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.46-10687C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44164150 | |||||||
| chr7:44164163 | A | G | 1 | a0001c0001t0001g0210 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.46-10700T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44164163 | |||||||
| chr7:44164313 | A | G | 242 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(239): Show |
271 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.46-10850T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44164313 | |||||||
| chr7:44164349 | A | G | 1 | a0001c0001t0012g0356 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.46-10886T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44164349 | |||||||
| chr7:44164419 | A | G | 4 | a0001c0001t0001g0318 a0001c0001t0001g0319 a0001c0001t0002g0103 others(1): Show |
6 | HG02257.hp1 HG02818.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.46-10956T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44164419 | |||||||
| chr7:44164723 | G | A | 242 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(239): Show |
271 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(268): Show |
intron_variant | MODIFIER | c.46-11260C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44164723 | |||||||
| chr7:44164827 | C | T | 62 | a0001c0001t0001g0015 a0001c0001t0001g0063 a0001c0001t0001g0141 others(59): Show |
67 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.46-11364G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44164827 | |||||||
| chr7:44164927 | G | T | 1 | a0001c0001t0001g0302 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.46-11464C>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44164927 | |||||||
| chr7:44165078 | C | T | 2 | a0001c0001t0001g0155 a0001c0001t0001g0240 |
2 | NA18949.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.46-11615G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44165078 | |||||||
| chr7:44165133 | A | G | 1 | a0001c0001t0002g0042 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.46-11670T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44165133 | |||||||
| chr7:44165135 | G | A | 1 | a0001c0001t0002g0042 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.46-11672C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44165135 | |||||||
| chr7:44165236 | C | T | 2 | a0001c0001t0003g0009 a0001c0001t0004g0220 |
3 | HG01070.hp1 HG01071.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.46-11773G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44165236 | |||||||
| chr7:44165253 | A | G | 5 | a0001c0001t0001g0164 a0001c0001t0001g0172 a0001c0001t0001g0180 others(2): Show |
5 | HG01934.hp1 NA18967.hp2 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.46-11790T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44165253 | |||||||
| chr7:44165345 | A | AAAT | 59 | a0001c0001t0001g0015 a0001c0001t0001g0063 a0001c0001t0001g0141 others(56): Show |
63 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.46-11885_46-11883d others(5): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44165345 | |||||||
| chr7:44165345 | A | AAATAAT | 4 | a0001c0001t0002g0010 a0001c0001t0002g0085 a0001c0001t0002g0154 others(1): Show |
5 | HG00423.hp2 NA18943.hp2 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.46-11888_46-11883d others(8): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44165345 | |||||||
| chr7:44165345 | A | AAATAATA others(2): Show |
50 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0018 others(47): Show |
60 | HG00423.hp1 HG00597.hp2 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.46-11891_46-11883d others(11): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44165345 | |||||||
| chr7:44165345 | A | AAATAATA others(5): Show |
1 | a0001c0001t0003g0255 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.46-11894_46-11883d others(14): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44165345 | |||||||
| chr7:44165345 | A | AAATAATA others(8): Show |
1 | a0001c0001t0003g0171 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.46-11897_46-11883d others(17): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44165345 | |||||||
| chr7:44165395 | G | A | 240 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(237): Show |
268 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.46-11932C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44165395 | |||||||
| chr7:44165550 | T | C | 62 | a0001c0001t0001g0007 a0001c0001t0001g0049 a0001c0001t0001g0053 others(59): Show |
66 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.46-12087A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44165550 | |||||||
| chr7:44165915 | A | T | 50 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0018 others(47): Show |
60 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.46-12452T>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44165915 | |||||||
| chr7:44166006 | G | A | 50 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0018 others(47): Show |
60 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.46-12543C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44166006 | |||||||
| chr7:44166147 | T | C | 1 | a0001c0001t0003g0115 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.46-12684A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44166147 | |||||||
| chr7:44166211 | C | T | 2 | a0001c0001t0001g0226 a0001c0001t0001g0229 |
2 | HG02698.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.46-12748G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44166211 | |||||||
| chr7:44166296 | C | T | 5 | a0001c0001t0002g0086 a0001c0001t0002g0087 a0001c0001t0002g0088 others(2): Show |
5 | HG00558.hp2 HG00673.hp1 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.46-12833G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44166296 | |||||||
| chr7:44166307 | A | C | 184 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0015 others(181): Show |
199 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.46-12844T>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44166307 | |||||||
| chr7:44166387 | G | A | 2 | a0001c0001t0003g0169 a0001c0001t0003g0170 |
2 | HG01074.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.46-12924C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44166387 | |||||||
| chr7:44166535 | TA | T | 226 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(223): Show |
251 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.46-13073delT | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44166535 | |||||||
| chr7:44166592 | C | T | 1 | a0001c0003t0002g0286 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.46-13129G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44166592 | |||||||
| chr7:44166749 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.46-13286T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44166749 | |||||||
| chr7:44166756 | GAT | G | 50 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0018 others(47): Show |
60 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.46-13295_46-13294d others(4): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44166756 | |||||||
| chr7:44166795 | T | A | 50 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0018 others(47): Show |
60 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.46-13332A>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44166795 | |||||||
| chr7:44166862 | T | TA | 324 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(321): Show |
350 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(347): Show |
intron_variant | MODIFIER | c.46-13400dupT | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44166862 | |||||||
| chr7:44167004 | C | A | 3 | a0001c0001t0001g0318 a0001c0001t0001g0319 a0001c0001t0002g0103 |
3 | HG02818.hp1 HG02965.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.46-13541G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44167004 | |||||||
| chr7:44167083 | C | T | 50 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0018 others(47): Show |
60 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.46-13620G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44167083 | |||||||
| chr7:44167225 | T | C | 3 | a0001c0001t0001g0163 a0001c0001t0001g0208 a0001c0001t0001g0331 |
3 | HG00280.hp2 HG01109.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.46-13762A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44167225 | |||||||
| chr7:44167344 | C | G | 7 | a0001c0001t0002g0022 a0001c0001t0002g0166 a0001c0001t0002g0167 others(4): Show |
10 | HG02055.hp1 HG02257.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.46-13881G>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44167344 | |||||||
| chr7:44167346 | G | A | 3 | a0001c0001t0002g0128 a0001c0001t0002g0131 a0001c0001t0019g0350 |
3 | NA18939.hp2 NA18978.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.46-13883C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44167346 | |||||||
| chr7:44167497 | G | A | 11 | a0001c0001t0001g0082 a0001c0001t0001g0232 a0001c0001t0001g0233 others(8): Show |
11 | HG02258.hp1 HG02258.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.46-14034C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44167497 | |||||||
| chr7:44167510 | C | T | 1 | a0001c0001t0002g0160 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.46-14047G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44167510 | |||||||
| chr7:44167567 | T | C | 1 | a0001c0001t0002g0035 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.46-14104A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44167567 | |||||||
| chr7:44167642 | T | C | 3 | a0001c0001t0003g0169 a0001c0001t0003g0170 a0001c0001t0003g0171 |
3 | HG00280.hp1 HG01074.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.46-14179A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44167642 | |||||||
| chr7:44167889 | C | T | 1 | a0001c0001t0002g0253 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.46-14426G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44167889 | |||||||
| chr7:44167895 | T | C | 105 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0037 others(102): Show |
115 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.46-14432A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44167895 | |||||||
| chr7:44167956 | G | A | 4 | a0001c0001t0012g0357 a0001c0001t0012g0358 a0001c0001t0013g0359 others(1): Show |
4 | HG02922.hp1 HG03130.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-14493C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44167956 | |||||||
| chr7:44168012 | C | G | 2 | a0001c0001t0001g0049 a0001c0001t0001g0194 |
2 | HG02647.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.46-14549G>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44168012 | |||||||
| chr7:44168408 | G | A | 50 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0018 others(47): Show |
60 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.46-14945C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44168408 | |||||||
| chr7:44168431 | C | A | 1 | a0001c0001t0001g0293 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.46-14968G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44168431 | |||||||
| chr7:44168448 | C | CT | 8 | a0001c0001t0001g0007 a0001c0001t0001g0168 a0001c0001t0001g0246 others(5): Show |
9 | HG01433.hp1 HG02145.hp2 HG03579.hp2 others(6): Show |
intron_variant | MODIFIER | c.46-14986dupA | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44168448 | |||||||
| chr7:44168448 | CT | C | 7 | a0001c0001t0001g0263 a0001c0001t0001g0293 a0001c0001t0001g0294 others(4): Show |
7 | HG01099.hp2 HG01257.hp2 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.46-14986delA | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44168448 | |||||||
| chr7:44168487 | C | T | 4 | a0001c0001t0002g0022 a0001c0001t0002g0309 a0001c0001t0002g0315 others(1): Show |
5 | HG02055.hp1 HG02280.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.46-15024G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44168487 | |||||||
| chr7:44168637 | G | A | 1 | a0001c0001t0001g0288 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.46-15174C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44168637 | |||||||
| chr7:44169023 | T | C | 1 | a0001c0001t0005g0145 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.46-15560A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44169023 | |||||||
| chr7:44169028 | T | C | 1 | a0001c0001t0012g0356 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.46-15565A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44169028 | |||||||
| chr7:44169464 | C | A | 4 | a0001c0001t0012g0357 a0001c0001t0012g0358 a0001c0001t0013g0359 others(1): Show |
4 | HG02922.hp1 HG03130.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.46-16001G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44169464 | |||||||
| chr7:44169723 | G | A | 64 | a0001c0001t0001g0015 a0001c0001t0001g0063 a0001c0001t0001g0141 others(61): Show |
69 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.46-16260C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44169723 | |||||||
| chr7:44169912 | A | T | 1 | a0001c0001t0001g0011 | 2 | NA18948.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.46-16449T>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44169912 | |||||||
| chr7:44170275 | G | A | 3 | a0001c0001t0001g0318 a0001c0001t0001g0319 a0001c0001t0002g0103 |
3 | HG02818.hp1 HG02965.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.46-16812C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44170275 | |||||||
| chr7:44170306 | C | A | 2 | a0001c0001t0002g0128 a0001c0001t0019g0350 |
2 | NA18939.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.46-16843G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44170306 | |||||||
| chr7:44170482 | C | T | 1 | a0001c0001t0002g0051 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.46-17019G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44170482 | |||||||
| chr7:44170681 | T | C | 1 | a0001c0001t0003g0171 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.46-17218A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44170681 | |||||||
| chr7:44170881 | G | A | 1 | a0001c0001t0002g0108 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.46-17418C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44170881 | |||||||
| chr7:44171111 | C | T | 74 | a0001c0001t0001g0015 a0001c0001t0001g0063 a0001c0001t0001g0082 others(71): Show |
79 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.46-17648G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44171111 | |||||||
| chr7:44171422 | A | AAAAT | 64 | a0001c0001t0001g0015 a0001c0001t0001g0063 a0001c0001t0001g0141 others(61): Show |
69 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.45+17483_45+17486d others(6): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44171422 | |||||||
| chr7:44171422 | A | AAAATAAA others(1): Show |
104 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0037 others(101): Show |
114 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.45+17479_45+17486d others(10): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44171422 | |||||||
| chr7:44171422 | A | AAAATAAA others(5): Show |
1 | a0001c0001t0001g0049 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.45+17475_45+17486d others(14): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44171422 | |||||||
| chr7:44171470 | C | T | 1 | a0001c0001t0003g0157 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.45+17439G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44171470 | |||||||
| chr7:44171498 | A | T | 3 | a0001c0001t0003g0043 a0001c0001t0003g0290 a0001c0001t0003g0292 |
3 | HG00140.hp2 HG01361.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.45+17411T>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44171498 | |||||||
| chr7:44171568 | C | T | 1 | a0001c0001t0001g0213 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.45+17341G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44171568 | |||||||
| chr7:44171694 | A | G | 1 | a0001c0001t0001g0260 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.45+17215T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44171694 | |||||||
| chr7:44171738 | T | C | 74 | a0001c0001t0001g0015 a0001c0001t0001g0063 a0001c0001t0001g0082 others(71): Show |
79 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.45+17171A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44171738 | |||||||
| chr7:44171808 | T | C | 50 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0018 others(47): Show |
60 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.45+17101A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44171808 | |||||||
| chr7:44171844 | G | GT | 49 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0018 others(46): Show |
59 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.45+17064dupA | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44171844 | |||||||
| chr7:44171851 | G | GT | 10 | a0001c0001t0001g0155 a0001c0001t0001g0205 a0001c0001t0001g0240 others(7): Show |
11 | HG00140.hp2 HG01361.hp1 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.45+17057dupA | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44171851 | |||||||
| chr7:44171851 | G | T | 50 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0018 others(47): Show |
60 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.45+17058C>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44171851 | |||||||
| chr7:44171862 | T | G | 1 | a0001c0001t0002g0039 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.45+17047A>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44171862 | |||||||
| chr7:44172019 | C | T | 50 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0018 others(47): Show |
60 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.45+16890G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44172019 | |||||||
| chr7:44172135 | G | A | 1 | a0001c0001t0003g0324 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.45+16774C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44172135 | |||||||
| chr7:44172196 | G | A | 6 | a0001c0001t0002g0022 a0001c0001t0002g0166 a0001c0001t0002g0167 others(3): Show |
7 | HG02055.hp1 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.45+16713C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44172196 | |||||||
| chr7:44172302 | C | G | 1 | a0001c0001t0002g0108 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.45+16607G>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44172302 | |||||||
| chr7:44172332 | C | G | 1 | a0001c0001t0001g0335 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.45+16577G>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44172332 | |||||||
| chr7:44172332 | C | T | 1 | a0001c0001t0002g0108 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.45+16577G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44172332 | |||||||
| chr7:44172526 | G | C | 1 | a0001c0001t0005g0145 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.45+16383C>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44172526 | |||||||
| chr7:44172677 | A | C | 1 | a0001c0001t0008g0346 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.45+16232T>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44172677 | |||||||
| chr7:44172686 | G | T | 50 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0018 others(47): Show |
60 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.45+16223C>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44172686 | |||||||
| chr7:44172826 | C | A | 1 | a0001c0001t0002g0035 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.45+16083G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44172826 | |||||||
| chr7:44172894 | T | A | 1 | a0001c0001t0002g0127 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.45+16015A>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44172894 | |||||||
| chr7:44172967 | C | T | 6 | a0001c0001t0002g0022 a0001c0001t0002g0166 a0001c0001t0002g0167 others(3): Show |
7 | HG02055.hp1 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.45+15942G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44172967 | |||||||
| chr7:44172985 | C | T | 10 | a0001c0001t0001g0082 a0001c0001t0001g0232 a0001c0001t0001g0233 others(7): Show |
10 | HG02258.hp1 HG02258.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.45+15924G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44172985 | |||||||
| chr7:44173346 | C | T | 2 | a0001c0001t0010g0349 a0001c0001t0018g0343 |
2 | NA18983.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.45+15563G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44173346 | |||||||
| chr7:44173494 | T | C | 1 | a0001c0004t0004g0261 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.45+15415A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44173494 | |||||||
| chr7:44173623 | A | T | 229 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(226): Show |
257 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(254): Show |
intron_variant | MODIFIER | c.45+15286T>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44173623 | |||||||
| chr7:44173699 | G | A | 4 | a0001c0001t0001g0263 a0001c0001t0001g0293 a0001c0001t0001g0294 others(1): Show |
4 | HG01099.hp2 HG01261.hp1 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+15210C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44173699 | |||||||
| chr7:44173760 | T | C | 3 | a0001c0001t0001g0318 a0001c0001t0001g0319 a0001c0001t0002g0103 |
3 | HG02818.hp1 HG02965.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.45+15149A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44173760 | |||||||
| chr7:44173777 | T | C | 1 | a0001c0001t0012g0356 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.45+15132A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44173777 | |||||||
| chr7:44173833 | G | A | 10 | a0001c0001t0001g0082 a0001c0001t0001g0232 a0001c0001t0001g0233 others(7): Show |
10 | HG02258.hp1 HG02258.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.45+15076C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44173833 | |||||||
| chr7:44173943 | G | A | 1 | a0001c0001t0001g0282 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.45+14966C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44173943 | |||||||
| chr7:44174029 | G | A | 10 | a0001c0001t0001g0082 a0001c0001t0001g0232 a0001c0001t0001g0233 others(7): Show |
10 | HG02258.hp1 HG02258.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.45+14880C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174029 | |||||||
| chr7:44174275 | C | T | 53 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0018 others(50): Show |
63 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.45+14634G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174275 | |||||||
| chr7:44174531 | G | C | 1 | a0001c0001t0001g0074 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.45+14378C>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174531 | |||||||
| chr7:44174557 | C | CCTT | 245 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(242): Show |
273 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.45+14349_45+14351d others(5): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174557 | |||||||
| chr7:44174641 | T | C | 7 | a0001c0001t0002g0022 a0001c0001t0002g0166 a0001c0001t0002g0167 others(4): Show |
10 | HG02055.hp1 HG02257.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.45+14268A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174641 | |||||||
| chr7:44174643 | C | A | 4 | a0001c0001t0004g0021 a0001c0001t0004g0257 a0001c0001t0004g0310 others(1): Show |
5 | HG01433.hp2 HG02257.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+14266G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174643 | |||||||
| chr7:44174676 | CT | C | 11 | a0001c0001t0001g0164 a0001c0001t0002g0094 a0001c0001t0003g0115 others(8): Show |
12 | HG00423.hp1 HG00597.hp2 NA18954.hp1 others(9): Show |
intron_variant | MODIFIER | c.45+14232delA | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174676 | |||||||
| chr7:44174695 | TTCC | T | 102 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0037 others(99): Show |
112 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.45+14211_45+14213d others(5): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174695 | |||||||
| chr7:44174725 | T | C | 1 | a0001c0001t0004g0020 | 2 | HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.45+14184A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174725 | |||||||
| chr7:44174774 | T | A | 1 | a0001c0001t0004g0214 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.45+14135A>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174774 | |||||||
| chr7:44174842 | T | C | 1 | a0001c0001t0002g0235 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.45+14067A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174842 | |||||||
| chr7:44174844 | G | C | 1 | a0001c0001t0002g0235 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.45+14065C>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174844 | |||||||
| chr7:44174844 | G | GTTCCTC | 10 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0018 others(7): Show |
15 | NA18942.hp2 NA18948.hp1 NA18950.hp1 others(12): Show |
intron_variant | MODIFIER | c.45+14059_45+14064d others(8): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174844 | |||||||
| chr7:44174848 | C | CTCTTCTT others(2): Show |
3 | a0001c0001t0001g0263 a0001c0001t0002g0167 a0001c0001t0002g0316 |
3 | HG02280.hp1 HG02622.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.45+14060_45+14061i others(11): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174848 | |||||||
| chr7:44174848 | C | CTCTTCTT others(5): Show |
1 | a0001c0001t0002g0022 | 2 | HG03098.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.45+14060_45+14061i others(14): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174848 | |||||||
| chr7:44174848 | C | CTCTTCTT others(8): Show |
1 | a0001c0001t0002g0315 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.45+14060_45+14061i others(17): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174848 | |||||||
| chr7:44174848 | C | CTCTTCTT others(11): Show |
2 | a0001c0001t0002g0166 a0001c0001t0002g0309 |
2 | HG02055.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.45+14060_45+14061i others(20): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174848 | |||||||
| chr7:44174848 | C | CTCTTCTT others(17): Show |
1 | a0001c0001t0003g0278 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.45+14060_45+14061i others(26): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174848 | |||||||
| chr7:44174848 | CTCTTCCT others(14): Show |
C | 1 | a0001c0001t0002g0253 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.45+14040_45+14060d others(23): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174848 | |||||||
| chr7:44174854 | C | CTCCTCTT others(11): Show |
1 | a0001c0001t0004g0050 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.45+14054_45+14055i others(20): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | |||||||
| chr7:44174854 | C | CTCCTCTT others(20): Show |
2 | a0001c0001t0001g0284 a0001c0001t0008g0347 |
2 | NA18967.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.45+14054_45+14055i others(29): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | |||||||
| chr7:44174854 | C | CTCT | 13 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0001g0205 others(10): Show |
13 | HG01109.hp2 HG01255.hp1 HG02698.hp2 others(10): Show |
intron_variant | MODIFIER | c.45+14052_45+14054d others(5): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | |||||||
| chr7:44174854 | C | CTCTTCCT others(11): Show |
1 | a0001c0001t0002g0103 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.45+14054_45+14055i others(20): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | |||||||
| chr7:44174854 | C | CTCTTCCT others(14): Show |
1 | a0001c0001t0001g0318 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.45+14054_45+14055i others(23): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | |||||||
| chr7:44174854 | C | CTCTTCCT others(17): Show |
1 | a0001c0001t0001g0319 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.45+14054_45+14055i others(26): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | |||||||
| chr7:44174854 | C | CTCTTCCT others(2): Show |
10 | a0001c0001t0001g0264 a0001c0001t0002g0150 a0001c0001t0002g0188 others(7): Show |
12 | HG00733.hp1 HG00738.hp1 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.45+14054_45+14055i others(11): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | |||||||
| chr7:44174854 | C | CTCTTCCT others(8): Show |
1 | a0001c0001t0003g0115 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.45+14054_45+14055i others(17): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | |||||||
| chr7:44174854 | C | CTCTTCCT others(5): Show |
7 | a0001c0001t0001g0164 a0001c0001t0001g0180 a0001c0001t0001g0187 others(4): Show |
7 | HG00280.hp1 HG00609.hp2 HG01123.hp2 others(4): Show |
intron_variant | MODIFIER | c.45+14054_45+14055i others(14): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | |||||||
| chr7:44174854 | C | CTCTTCCT others(8): Show |
3 | a0001c0001t0001g0189 a0001c0001t0007g0339 a0001c0001t0008g0345 |
3 | NA19074.hp2 NA19077.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.45+14054_45+14055i others(17): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | |||||||
| chr7:44174854 | C | CTCTTCCT others(11): Show |
6 | a0001c0001t0002g0083 a0001c0001t0003g0116 a0001c0001t0003g0275 others(3): Show |
7 | HG00423.hp1 HG02559.hp2 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.45+14054_45+14055i others(20): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | |||||||
| chr7:44174854 | C | CTCTTCCT others(14): Show |
1 | a0001c0001t0007g0342 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.45+14054_45+14055i others(23): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | |||||||
| chr7:44174854 | C | CTCTTCCT others(20): Show |
1 | a0001c0001t0003g0101 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.45+14054_45+14055i others(29): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | |||||||
| chr7:44174854 | C | CTCTTCT | 24 | a0001c0001t0001g0028 a0001c0001t0001g0092 a0001c0001t0001g0120 others(21): Show |
25 | HG01099.hp1 HG01106.hp1 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.45+14049_45+14054d others(8): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | |||||||
| chr7:44174854 | C | CTCTTCTT others(2): Show |
15 | a0001c0001t0001g0100 a0001c0001t0001g0119 a0001c0001t0001g0163 others(12): Show |
15 | HG00597.hp1 HG01074.hp2 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.45+14046_45+14054d others(11): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | |||||||
| chr7:44174854 | C | CTCTTCTT others(5): Show |
11 | a0001c0001t0001g0155 a0001c0001t0001g0158 a0001c0001t0001g0200 others(8): Show |
11 | HG00140.hp2 HG00733.hp2 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.45+14043_45+14054d others(14): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | |||||||
| chr7:44174854 | C | CTCTTCTT others(8): Show |
14 | a0001c0001t0001g0097 a0001c0001t0001g0118 a0001c0001t0001g0197 others(11): Show |
14 | HG00544.hp2 HG00673.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.45+14040_45+14054d others(17): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | |||||||
| chr7:44174854 | C | CTCTTCTT others(11): Show |
7 | a0001c0001t0001g0148 a0001c0001t0001g0196 a0001c0001t0001g0291 others(4): Show |
8 | HG00621.hp2 HG01358.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.45+14037_45+14054d others(20): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | |||||||
| chr7:44174854 | C | CTCTTCTT others(14): Show |
2 | a0001c0001t0002g0058 a0001c0001t0002g0059 |
2 | NA18946.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.45+14054_45+14055i others(23): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | |||||||
| chr7:44174854 | C | CTCTTCTT others(23): Show |
1 | a0001c0001t0002g0215 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.45+14054_45+14055i others(32): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | |||||||
| chr7:44174854 | C | CTCTTCTT others(14): Show |
3 | a0001c0001t0001g0111 a0001c0001t0001g0199 a0001c0001t0001g0335 |
3 | HG02080.hp1 NA18956.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.45+14034_45+14054d others(23): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | |||||||
| chr7:44174854 | C | CTCTTCTT others(17): Show |
1 | a0001c0001t0003g0290 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.45+14031_45+14054d others(26): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | |||||||
| chr7:44174854 | C | T | 13 | a0001c0001t0001g0263 a0001c0001t0002g0022 a0001c0001t0002g0064 others(10): Show |
16 | HG02055.hp1 HG02257.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.45+14055G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | |||||||
| chr7:44174854 | CTCT | C | 16 | a0001c0001t0001g0016 a0001c0001t0001g0237 a0001c0001t0001g0254 others(13): Show |
18 | HG00438.hp2 HG01099.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.45+14052_45+14054d others(5): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | |||||||
| chr7:44174854 | CTCTTCT | C | 19 | a0001c0001t0001g0208 a0001c0001t0001g0277 a0001c0001t0002g0010 others(16): Show |
22 | HG00280.hp2 HG00323.hp2 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.45+14049_45+14054d others(8): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | |||||||
| chr7:44174854 | CTCTTCTT others(2): Show |
C | 23 | a0001c0001t0001g0268 a0001c0001t0001g0288 a0001c0001t0001g0303 others(20): Show |
23 | HG00423.hp2 HG00558.hp1 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.45+14046_45+14054d others(11): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | |||||||
| chr7:44174854 | CTCTTCTT others(5): Show |
C | 4 | a0001c0001t0001g0093 a0001c0001t0001g0165 a0001c0001t0002g0225 others(1): Show |
4 | HG01071.hp2 HG02738.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+14043_45+14054d others(14): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | |||||||
| chr7:44174854 | CTCTTCTT others(8): Show |
C | 4 | a0001c0001t0001g0063 a0001c0001t0001g0141 a0001c0001t0005g0112 others(1): Show |
4 | HG01256.hp1 HG02486.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+14040_45+14054d others(17): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | |||||||
| chr7:44174854 | CTCTTCTT others(11): Show |
C | 8 | a0001c0001t0002g0114 a0001c0001t0002g0142 a0001c0001t0005g0113 others(5): Show |
8 | HG00741.hp2 HG02109.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.45+14037_45+14054d others(20): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | |||||||
| chr7:44174854 | CTCTTCTT others(14): Show |
C | 2 | a0001c0001t0001g0209 a0001c0001t0005g0146 |
2 | HG01109.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.45+14034_45+14054d others(23): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174854 | |||||||
| chr7:44174857 | T | TTCC | 5 | a0001c0001t0001g0191 a0001c0001t0002g0185 a0001c0001t0003g0184 others(2): Show |
5 | HG01123.hp1 HG01981.hp2 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+14051_45+14052i others(5): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174857 | |||||||
| chr7:44174860 | T | C | 4 | a0001c0001t0001g0186 a0001c0001t0001g0192 a0001c0001t0003g0009 others(1): Show |
6 | HG01070.hp1 HG01071.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.45+14049A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174860 | |||||||
| chr7:44174863 | T | C | 1 | a0001c0001t0003g0151 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.45+14046A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174863 | |||||||
| chr7:44174914 | T | C | 49 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0018 others(46): Show |
59 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.45+13995A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174914 | |||||||
| chr7:44174915 | T | C | 73 | a0001c0001t0001g0015 a0001c0001t0001g0063 a0001c0001t0001g0141 others(70): Show |
78 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.45+13994A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174915 | |||||||
| chr7:44174915 | T | TCTC | 5 | a0001c0001t0002g0034 a0001c0001t0002g0057 a0001c0001t0002g0062 others(2): Show |
5 | HG01255.hp2 HG01891.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.45+13993_45+13994i others(5): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174915 | |||||||
| chr7:44174915 | T | TCTTCTC | 5 | a0001c0001t0002g0033 a0001c0001t0002g0042 a0001c0001t0002g0056 others(2): Show |
5 | HG02071.hp2 HG02895.hp2 NA18979.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+13993_45+13994i others(8): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174915 | |||||||
| chr7:44174915 | T | TCTTCTTC others(2): Show |
7 | a0001c0001t0002g0006 a0001c0001t0002g0032 a0001c0001t0002g0088 others(4): Show |
8 | HG00558.hp2 HG02135.hp1 NA18940.hp2 others(5): Show |
intron_variant | MODIFIER | c.45+13993_45+13994i others(11): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174915 | |||||||
| chr7:44174915 | T | TCTTCTTC others(5): Show |
13 | a0001c0001t0001g0233 a0001c0001t0002g0019 a0001c0001t0002g0027 others(10): Show |
14 | HG00099.hp2 HG00438.hp1 HG00609.hp1 others(11): Show |
intron_variant | MODIFIER | c.45+13993_45+13994i others(14): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174915 | |||||||
| chr7:44174915 | T | TCTTCTTC others(8): Show |
13 | a0001c0001t0001g0007 a0001c0001t0001g0053 a0001c0001t0001g0054 others(10): Show |
17 | HG00323.hp1 HG01891.hp2 HG02015.hp2 others(14): Show |
intron_variant | MODIFIER | c.45+13993_45+13994i others(17): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174915 | |||||||
| chr7:44174915 | T | TCTTCTTC others(11): Show |
15 | a0001c0001t0001g0061 a0001c0001t0001g0078 a0001c0001t0001g0104 others(12): Show |
17 | HG00140.hp1 HG00673.hp1 HG01256.hp2 others(14): Show |
intron_variant | MODIFIER | c.45+13993_45+13994i others(20): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174915 | |||||||
| chr7:44174915 | T | TCTTCTTC others(14): Show |
14 | a0001c0001t0001g0049 a0001c0001t0001g0076 a0001c0001t0001g0077 others(11): Show |
14 | HG02015.hp1 HG02647.hp1 HG02896.hp1 others(11): Show |
intron_variant | MODIFIER | c.45+13993_45+13994i others(23): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174915 | |||||||
| chr7:44174915 | T | TCTTCTTC others(17): Show |
12 | a0001c0001t0001g0060 a0001c0001t0001g0246 a0001c0001t0001g0260 others(9): Show |
12 | HG01884.hp1 HG02615.hp2 HG02683.hp1 others(9): Show |
intron_variant | MODIFIER | c.45+13993_45+13994i others(26): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174915 | |||||||
| chr7:44174915 | T | TCTTCTTC others(20): Show |
9 | a0001c0001t0001g0008 a0001c0001t0001g0037 a0001c0001t0001g0075 others(6): Show |
11 | HG01433.hp2 HG01934.hp2 HG02148.hp2 others(8): Show |
intron_variant | MODIFIER | c.45+13993_45+13994i others(29): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174915 | |||||||
| chr7:44174915 | T | TCTTCTTC others(23): Show |
6 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0002g0069 others(3): Show |
6 | HG01257.hp2 NA18522.hp2 NA18999.hp2 others(3): Show |
intron_variant | MODIFIER | c.45+13993_45+13994i others(32): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174915 | |||||||
| chr7:44174915 | T | TCTTCTTC others(26): Show |
4 | a0001c0001t0002g0036 a0001c0001t0002g0287 a0001c0001t0004g0310 others(1): Show |
4 | HG00544.hp1 HG02486.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+13993_45+13994i others(35): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174915 | |||||||
| chr7:44174915 | T | TCTTCTTC others(29): Show |
1 | a0001c0001t0001g0305 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.45+13993_45+13994i others(38): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174915 | |||||||
| chr7:44174937 | C | T | 1 | a0001c0001t0001g0277 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.45+13972G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44174937 | |||||||
| chr7:44175056 | T | G | 2 | a0001c0001t0002g0315 a0001c0001t0002g0316 |
2 | HG02280.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.45+13853A>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44175056 | |||||||
| chr7:44175168 | G | A | 4 | a0001c0001t0012g0357 a0001c0001t0012g0358 a0001c0001t0013g0359 others(1): Show |
4 | HG02922.hp1 HG03130.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+13741C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44175168 | |||||||
| chr7:44175310 | A | T | 1 | a0001c0001t0001g0237 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.45+13599T>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44175310 | |||||||
| chr7:44175349 | T | G | 1 | a0001c0001t0001g0210 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.45+13560A>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44175349 | |||||||
| chr7:44175415 | T | C | 53 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0018 others(50): Show |
63 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.45+13494A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44175415 | |||||||
| chr7:44175467 | T | C | 1 | a0001c0001t0001g0187 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.45+13442A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44175467 | |||||||
| chr7:44175551 | G | A | 1 | a0001c0001t0005g0146 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.45+13358C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44175551 | |||||||
| chr7:44175789 | C | T | 1 | a0001c0001t0002g0127 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.45+13120G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44175789 | |||||||
| chr7:44176062 | C | A | 1 | a0001c0001t0002g0147 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.45+12847G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44176062 | |||||||
| chr7:44176272 | G | A | 50 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0018 others(47): Show |
60 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.45+12637C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44176272 | |||||||
| chr7:44176398 | C | T | 3 | a0001c0001t0004g0272 a0001c0001t0004g0273 a0001c0001t0005g0274 |
3 | HG02895.hp1 HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.45+12511G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44176398 | |||||||
| chr7:44176417 | G | A | 1 | a0001c0001t0002g0091 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.45+12492C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44176417 | |||||||
| chr7:44176513 | G | A | 50 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0018 others(47): Show |
60 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.45+12396C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44176513 | |||||||
| chr7:44176538 | G | A | 180 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0015 others(177): Show |
195 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(192): Show |
intron_variant | MODIFIER | c.45+12371C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44176538 | |||||||
| chr7:44176575 | C | T | 6 | a0001c0001t0002g0022 a0001c0001t0002g0166 a0001c0001t0002g0167 others(3): Show |
7 | HG02055.hp1 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.45+12334G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44176575 | |||||||
| chr7:44176625 | C | A | 2 | a0001c0001t0009g0353 a0001c0001t0011g0352 |
2 | NA18969.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.45+12284G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44176625 | |||||||
| chr7:44176681 | G | A | 63 | a0001c0001t0001g0007 a0001c0001t0001g0037 a0001c0001t0001g0053 others(60): Show |
67 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.45+12228C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44176681 | |||||||
| chr7:44176698 | C | T | 50 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0018 others(47): Show |
60 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.45+12211G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44176698 | |||||||
| chr7:44176800 | C | T | 11 | a0001c0001t0001g0104 a0001c0001t0002g0006 a0001c0001t0002g0017 others(8): Show |
13 | HG00609.hp1 HG02074.hp1 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.45+12109G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44176800 | |||||||
| chr7:44176808 | C | T | 3 | a0001c0001t0004g0272 a0001c0001t0004g0273 a0001c0001t0005g0274 |
3 | HG02895.hp1 HG02970.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.45+12101G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44176808 | |||||||
| chr7:44176941 | C | T | 1 | a0001c0001t0003g0171 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.45+11968G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44176941 | |||||||
| chr7:44176947 | G | T | 68 | a0001c0001t0001g0007 a0001c0001t0001g0037 a0001c0001t0001g0049 others(65): Show |
72 | HG00099.hp2 HG00438.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.45+11962C>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44176947 | |||||||
| chr7:44176999 | T | C | 54 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0018 others(51): Show |
66 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.45+11910A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44176999 | |||||||
| chr7:44177010 | C | T | 7 | a0001c0001t0001g0318 a0001c0001t0001g0319 a0001c0001t0002g0103 others(4): Show |
7 | HG02818.hp1 HG02922.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.45+11899G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44177010 | |||||||
| chr7:44177057 | C | A | 4 | a0001c0001t0002g0047 a0001c0001t0002g0068 a0001c0001t0004g0046 others(1): Show |
4 | HG00639.hp2 HG02145.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+11852G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44177057 | |||||||
| chr7:44177155 | C | T | 235 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(232): Show |
262 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.45+11754G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44177155 | |||||||
| chr7:44177229 | C | G | 2 | a0001c0001t0002g0013 a0001c0001t0003g0198 |
3 | HG01070.hp2 HG01081.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.45+11680G>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44177229 | |||||||
| chr7:44177342 | G | A | 3 | a0001c0001t0001g0318 a0001c0001t0001g0319 a0001c0001t0002g0103 |
3 | HG02818.hp1 HG02965.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.45+11567C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44177342 | |||||||
| chr7:44177412 | T | C | 1 | a0001c0001t0002g0329 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.45+11497A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44177412 | |||||||
| chr7:44177527 | C | T | 241 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(238): Show |
269 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.45+11382G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44177527 | |||||||
| chr7:44177595 | A | C | 2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | HG00544.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.45+11314T>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44177595 | |||||||
| chr7:44177617 | C | CA | 235 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(232): Show |
262 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.45+11291dupT | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44177617 | |||||||
| chr7:44177680 | G | A | 1 | a0001c0001t0002g0222 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.45+11229C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44177680 | |||||||
| chr7:44177762 | A | G | 54 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0018 others(51): Show |
66 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.45+11147T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44177762 | |||||||
| chr7:44177765 | T | C | 1 | a0001c0001t0003g0211 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.45+11144A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44177765 | |||||||
| chr7:44177842 | T | C | 1 | a0001c0001t0001g0332 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.45+11067A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44177842 | |||||||
| chr7:44177847 | A | C | 1 | a0001c0001t0001g0288 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.45+11062T>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44177847 | |||||||
| chr7:44177976 | C | T | 1 | a0001c0001t0001g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.45+10933G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44177976 | |||||||
| chr7:44177977 | T | C | 5 | a0001c0001t0002g0001 a0001c0001t0002g0026 a0001c0001t0002g0071 others(2): Show |
8 | HG01884.hp1 HG01891.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.45+10932A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44177977 | |||||||
| chr7:44178062 | GT | G | 4 | a0001c0001t0001g0318 a0001c0001t0001g0319 a0001c0001t0002g0103 others(1): Show |
6 | HG02257.hp1 HG02818.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.45+10846delA | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44178062 | |||||||
| chr7:44178224 | G | A | 1 | a0001c0001t0001g0299 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.45+10685C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44178224 | |||||||
| chr7:44178250 | A | C | 1 | a0001c0001t0001g0195 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.45+10659T>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44178250 | |||||||
| chr7:44178261 | G | A | 1 | a0001c0001t0002g0231 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.45+10648C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44178261 | |||||||
| chr7:44178409 | A | T | 1 | a0001c0001t0012g0356 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.45+10500T>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44178409 | |||||||
| chr7:44178453 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.45+10456C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44178453 | |||||||
| chr7:44178742 | G | A | 53 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0018 others(50): Show |
63 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.45+10167C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44178742 | |||||||
| chr7:44178746 | C | A | 1 | a0001c0001t0003g0171 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.45+10163G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44178746 | |||||||
| chr7:44179195 | T | C | 50 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0018 others(47): Show |
60 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.45+9714A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44179195 | |||||||
| chr7:44179257 | G | A | 98 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0037 others(95): Show |
108 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.45+9652C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44179257 | |||||||
| chr7:44179330 | C | T | 1 | a0001c0001t0008g0340 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.45+9579G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44179330 | |||||||
| chr7:44179436 | T | C | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG04204.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.45+9473A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44179436 | |||||||
| chr7:44179475 | T | C | 242 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(239): Show |
270 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(267): Show |
intron_variant | MODIFIER | c.45+9434A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44179475 | |||||||
| chr7:44179498 | T | C | 1 | a0001c0001t0008g0347 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.45+9411A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44179498 | |||||||
| chr7:44179502 | C | G | 1 | a0001c0001t0008g0347 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.45+9407G>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44179502 | |||||||
| chr7:44179505 | A | C | 1 | a0001c0001t0008g0347 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.45+9404T>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44179505 | |||||||
| chr7:44179506 | T | G | 1 | a0001c0001t0008g0347 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.45+9403A>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44179506 | |||||||
| chr7:44179507 | T | C | 1 | a0001c0001t0008g0347 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.45+9402A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44179507 | |||||||
| chr7:44179509 | G | T | 1 | a0001c0001t0008g0347 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.45+9400C>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44179509 | |||||||
| chr7:44179511 | C | T | 1 | a0001c0001t0008g0347 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.45+9398G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44179511 | |||||||
| chr7:44179512 | A | T | 1 | a0001c0001t0008g0347 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.45+9397T>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44179512 | |||||||
| chr7:44179602 | G | T | 1 | a0001c0001t0004g0314 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.45+9307C>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44179602 | |||||||
| chr7:44179683 | G | A | 11 | a0001c0001t0001g0082 a0001c0001t0001g0232 a0001c0001t0001g0233 others(8): Show |
11 | HG02258.hp1 HG02258.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.45+9226C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44179683 | |||||||
| chr7:44179739 | A | G | 65 | a0001c0001t0001g0015 a0001c0001t0001g0063 a0001c0001t0001g0141 others(62): Show |
70 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.45+9170T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44179739 | |||||||
| chr7:44179835 | T | C | 1 | a0001c0001t0002g0287 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.45+9074A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44179835 | |||||||
| chr7:44179970 | T | A | 4 | a0001c0001t0012g0357 a0001c0001t0012g0358 a0001c0001t0013g0359 others(1): Show |
4 | HG02922.hp1 HG03130.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+8939A>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44179970 | |||||||
| chr7:44179973 | C | T | 1 | a0001c0001t0005g0224 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.45+8936G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44179973 | |||||||
| chr7:44180004 | A | T | 1 | a0001c0001t0001g0194 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.45+8905T>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44180004 | |||||||
| chr7:44180005 | C | T | 1 | a0001c0001t0001g0193 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.45+8904G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44180005 | |||||||
| chr7:44180006 | G | A | 1 | a0001c0001t0001g0223 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.45+8903C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44180006 | |||||||
| chr7:44180106 | T | C | 64 | a0001c0001t0001g0015 a0001c0001t0001g0063 a0001c0001t0001g0141 others(61): Show |
69 | HG00323.hp2 HG00423.hp2 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.45+8803A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44180106 | |||||||
| chr7:44180143 | C | A | 49 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0018 others(46): Show |
59 | HG00280.hp1 HG00423.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.45+8766G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44180143 | |||||||
| chr7:44180220 | G | C | 1 | a0001c0001t0003g0171 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.45+8689C>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44180220 | |||||||
| chr7:44180226 | G | T | 1 | a0001c0001t0002g0096 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.45+8683C>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44180226 | |||||||
| chr7:44180251 | G | A | 1 | a0001c0001t0012g0356 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.45+8658C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44180251 | |||||||
| chr7:44180314 | G | A | 3 | a0001c0001t0002g0269 a0001c0001t0002g0289 a0001c0001t0002g0333 |
3 | HG02148.hp1 NA18939.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.45+8595C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44180314 | |||||||
| chr7:44180320 | A | G | 1 | a0001c0001t0005g0236 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.45+8589T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44180320 | |||||||
| chr7:44180352 | G | A | 2 | a0001c0001t0001g0233 a0001c0001t0002g0042 |
2 | HG02280.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.45+8557C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44180352 | |||||||
| chr7:44180396 | G | T | 2 | a0001c0001t0002g0188 a0001c0001t0002g0235 |
2 | NA18948.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.45+8513C>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44180396 | |||||||
| chr7:44180590 | T | C | 1 | a0001c0001t0001g0148 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.45+8319A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44180590 | |||||||
| chr7:44180628 | G | A | 1 | a0001c0001t0004g0314 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.45+8281C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44180628 | |||||||
| chr7:44180812 | A | G | 2 | a0001c0001t0003g0162 a0001c0001t0003g0173 |
2 | NA18941.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.45+8097T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44180812 | |||||||
| chr7:44180822 | A | G | 11 | a0001c0001t0001g0082 a0001c0001t0001g0232 a0001c0001t0001g0233 others(8): Show |
11 | HG02258.hp1 HG02258.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.45+8087T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44180822 | |||||||
| chr7:44181001 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.45+7908A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44181001 | |||||||
| chr7:44181006 | A | T | 1 | a0001c0001t0002g0248 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.45+7903T>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44181006 | |||||||
| chr7:44181074 | C | G | 3 | a0001c0001t0002g0086 a0001c0001t0002g0276 a0001c0001t0002g0308 |
3 | NA18950.hp2 NA18970.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.45+7835G>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44181074 | |||||||
| chr7:44181320 | C | A | 7 | a0001c0001t0001g0226 a0001c0001t0001g0228 a0001c0001t0001g0229 others(4): Show |
7 | HG01496.hp1 HG02293.hp2 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.45+7589G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44181320 | |||||||
| chr7:44181394 | G | C | 1 | a0001c0001t0012g0356 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.45+7515C>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44181394 | |||||||
| chr7:44181483 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.45+7426C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44181483 | |||||||
| chr7:44181696 | G | A | 49 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0018 others(46): Show |
59 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.45+7213C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44181696 | |||||||
| chr7:44181703 | A | G | 49 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0018 others(46): Show |
59 | HG00280.hp1 HG00423.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.45+7206T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44181703 | |||||||
| chr7:44181806 | G | A | 23 | a0001c0001t0001g0011 a0001c0001t0001g0028 a0001c0001t0001g0164 others(20): Show |
28 | HG00423.hp2 HG00609.hp2 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.45+7103C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44181806 | |||||||
| chr7:44181944 | C | G | 2 | a0001c0001t0009g0353 a0001c0001t0011g0352 |
2 | NA18969.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.45+6965G>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44181944 | |||||||
| chr7:44181982 | A | C | 314 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(311): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.45+6927T>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44181982 | |||||||
| chr7:44182176 | G | C | 2 | a0001c0001t0002g0069 a0001c0001t0002g0070 |
2 | NA18978.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.45+6733C>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44182176 | |||||||
| chr7:44182294 | A | G | 4 | a0001c0001t0002g0114 a0001c0001t0004g0272 a0001c0001t0004g0273 others(1): Show |
4 | HG02717.hp2 HG02895.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+6615T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44182294 | |||||||
| chr7:44182326 | A | G | 8 | a0001c0001t0001g0318 a0001c0001t0002g0022 a0001c0001t0002g0315 others(5): Show |
9 | HG02280.hp1 HG02622.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.45+6583T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44182326 | |||||||
| chr7:44182343 | C | A | 1 | a0001c0001t0001g0234 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.45+6566G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44182343 | |||||||
| chr7:44182389 | C | T | 2 | a0001c0001t0007g0337 a0001c0001t0008g0338 |
2 | HG01123.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.45+6520G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44182389 | |||||||
| chr7:44182404 | G | T | 160 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(157): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.45+6505C>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44182404 | |||||||
| chr7:44182405 | A | T | 160 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(157): Show |
173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.45+6504T>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44182405 | |||||||
| chr7:44182470 | A | G | 4 | a0001c0001t0001g0037 a0001c0001t0002g0038 a0001c0001t0002g0039 others(1): Show |
4 | NA18965.hp1 NA18985.hp1 NA19055.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+6439T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44182470 | |||||||
| chr7:44182621 | C | G | 40 | a0001c0001t0001g0011 a0001c0001t0001g0028 a0001c0001t0001g0100 others(37): Show |
45 | HG00280.hp1 HG00609.hp2 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.45+6288G>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44182621 | |||||||
| chr7:44182626 | G | C | 289 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(286): Show |
316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.45+6283C>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44182626 | |||||||
| chr7:44182854 | G | A | 3 | a0001c0001t0002g0083 a0001c0001t0002g0309 a0001c0001t0004g0084 |
3 | HG02055.hp1 HG02451.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.45+6055C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44182854 | |||||||
| chr7:44182872 | A | G | 298 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(295): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.45+6037T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44182872 | |||||||
| chr7:44183155 | C | T | 1 | a0001c0001t0002g0081 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.45+5754G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44183155 | |||||||
| chr7:44183189 | G | A | 1 | a0001c0001t0001g0306 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.45+5720C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44183189 | |||||||
| chr7:44183197 | C | T | 1 | a0001c0004t0004g0261 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.45+5712G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44183197 | |||||||
| chr7:44183203 | C | T | 113 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0015 others(110): Show |
126 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.45+5706G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44183203 | |||||||
| chr7:44183246 | C | A | 1 | a0001c0001t0002g0090 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.45+5663G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44183246 | |||||||
| chr7:44183399 | C | A | 3 | a0001c0001t0001g0163 a0001c0001t0001g0331 a0001c0001t0001g0332 |
3 | HG01109.hp2 HG01358.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.45+5510G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44183399 | |||||||
| chr7:44183433 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.45+5476G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44183433 | |||||||
| chr7:44183693 | T | TA | 19 | a0001c0001t0007g0023 a0001c0001t0007g0336 a0001c0001t0007g0337 others(16): Show |
20 | HG00423.hp1 HG00597.hp1 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.45+5215_45+5216ins others(1): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44183693 | |||||||
| chr7:44183696 | G | A | 14 | a0001c0001t0007g0023 a0001c0001t0007g0336 a0001c0001t0007g0337 others(11): Show |
15 | HG00423.hp1 HG00597.hp1 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.45+5213C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44183696 | |||||||
| chr7:44183837 | T | G | 1 | a0001c0001t0002g0156 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.45+5072A>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44183837 | |||||||
| chr7:44183880 | G | A | 267 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(264): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.45+5029C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44183880 | |||||||
| chr7:44183909 | C | A | 4 | a0001c0001t0004g0021 a0001c0001t0004g0310 a0001c0001t0004g0311 others(1): Show |
7 | HG01433.hp2 HG02257.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.45+5000G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44183909 | |||||||
| chr7:44183959 | C | T | 18 | a0001c0001t0007g0023 a0001c0001t0007g0336 a0001c0001t0007g0337 others(15): Show |
19 | HG00423.hp1 HG00597.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.45+4950G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44183959 | |||||||
| chr7:44184122 | G | A | 77 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0097 others(74): Show |
81 | HG00323.hp2 HG00597.hp2 HG00621.hp1 others(78): Show |
intron_variant | MODIFIER | c.45+4787C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44184122 | |||||||
| chr7:44184259 | G | A | 2 | a0001c0001t0001g0305 a0001c0001t0001g0306 |
2 | HG03688.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.45+4650C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44184259 | |||||||
| chr7:44184343 | G | A | 82 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0097 others(79): Show |
87 | HG00323.hp2 HG00597.hp2 HG00621.hp1 others(84): Show |
intron_variant | MODIFIER | c.45+4566C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44184343 | |||||||
| chr7:44184356 | G | A | 1 | a0001c0001t0002g0253 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.45+4553C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44184356 | |||||||
| chr7:44184377 | T | C | 2 | a0001c0001t0001g0313 a0001c0001t0002g0312 |
2 | HG02970.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.45+4532A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44184377 | |||||||
| chr7:44184499 | C | T | 12 | a0001c0001t0001g0168 a0001c0001t0002g0006 a0001c0001t0002g0030 others(9): Show |
13 | HG00280.hp1 HG01074.hp1 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.45+4410G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44184499 | |||||||
| chr7:44184551 | C | T | 5 | a0001c0001t0002g0091 a0001c0001t0012g0357 a0001c0001t0012g0358 others(2): Show |
5 | HG02602.hp1 HG02922.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.45+4358G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44184551 | |||||||
| chr7:44184569 | C | G | 1 | a0002c0002t0002g0003 | 3 | HG02257.hp1 HG03139.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.45+4340G>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44184569 | |||||||
| chr7:44184840 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.45+4069C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44184840 | |||||||
| chr7:44184845 | T | C | 1 | a0001c0001t0001g0254 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.45+4064A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44184845 | |||||||
| chr7:44184933 | GAT | G | 18 | a0001c0001t0007g0023 a0001c0001t0007g0336 a0001c0001t0007g0337 others(15): Show |
19 | HG00423.hp1 HG00597.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.45+3974_45+3975del others(2): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44184933 | |||||||
| chr7:44184937 | T | TAC | 4 | a0001c0001t0001g0307 a0001c0001t0001g0313 a0001c0001t0002g0017 others(1): Show |
5 | HG01099.hp1 HG02074.hp1 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.45+3970_45+3971dup others(2): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44184937 | |||||||
| chr7:44184939 | C | T | 2 | a0001c0001t0002g0166 a0001c0001t0002g0167 |
2 | HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.45+3970G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44184939 | |||||||
| chr7:44185003 | G | A | 4 | a0001c0001t0012g0357 a0001c0001t0012g0358 a0001c0001t0013g0359 others(1): Show |
4 | HG02922.hp1 HG03130.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+3906C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44185003 | |||||||
| chr7:44185015 | T | TAC | 267 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(264): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.45+3892_45+3893dup others(2): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44185015 | |||||||
| chr7:44185015 | T | TACAC | 5 | a0001c0001t0001g0158 a0001c0001t0001g0165 a0001c0001t0003g0157 others(2): Show |
5 | HG01106.hp2 HG01981.hp2 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.45+3890_45+3893dup others(4): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44185015 | |||||||
| chr7:44185031 | C | CACAG | 5 | a0001c0001t0001g0258 a0001c0001t0001g0260 a0001c0001t0002g0259 others(2): Show |
5 | HG01257.hp1 HG02615.hp2 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.45+3877_45+3878ins others(4): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44185031 | |||||||
| chr7:44185031 | CAG | C | 18 | a0001c0001t0007g0023 a0001c0001t0007g0336 a0001c0001t0007g0337 others(15): Show |
19 | HG00423.hp1 HG00597.hp1 HG00733.hp1 others(16): Show |
intron_variant | MODIFIER | c.45+3876_45+3877del others(2): Show |
GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44185031 | |||||||
| chr7:44185087 | C | G | 2 | a0001c0001t0001g0318 a0001c0001t0001g0319 |
2 | HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.45+3822G>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44185087 | |||||||
| chr7:44185252 | G | A | 114 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0015 others(111): Show |
127 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.45+3657C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44185252 | |||||||
| chr7:44185322 | G | T | 1 | a0001c0001t0006g0256 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.45+3587C>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44185322 | |||||||
| chr7:44185657 | A | G | 4 | a0001c0001t0012g0357 a0001c0001t0012g0358 a0001c0001t0013g0359 others(1): Show |
4 | HG02922.hp1 HG03130.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+3252T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44185657 | |||||||
| chr7:44185741 | T | A | 1 | a0001c0001t0006g0256 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.45+3168A>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44185741 | |||||||
| chr7:44185887 | G | C | 15 | a0001c0001t0007g0023 a0001c0001t0007g0336 a0001c0001t0007g0337 others(12): Show |
16 | HG00423.hp1 HG00597.hp1 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.45+3022C>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44185887 | |||||||
| chr7:44185938 | G | A | 1 | a0001c0001t0002g0080 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.45+2971C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44185938 | |||||||
| chr7:44185948 | C | T | 2 | a0001c0001t0012g0357 a0001c0001t0012g0358 |
2 | HG03130.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.45+2961G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44185948 | |||||||
| chr7:44185957 | C | T | 4 | a0001c0001t0012g0357 a0001c0001t0012g0358 a0001c0001t0013g0359 others(1): Show |
4 | HG02922.hp1 HG03130.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+2952G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44185957 | |||||||
| chr7:44186106 | G | T | 1 | a0001c0001t0002g0161 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.45+2803C>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44186106 | |||||||
| chr7:44186161 | G | A | 1 | a0001c0001t0002g0317 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.45+2748C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44186161 | |||||||
| chr7:44186209 | G | A | 4 | a0001c0001t0012g0357 a0001c0001t0012g0358 a0001c0001t0013g0359 others(1): Show |
4 | HG02922.hp1 HG03130.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+2700C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44186209 | |||||||
| chr7:44186217 | C | A | 1 | a0001c0001t0002g0081 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.45+2692G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44186217 | |||||||
| chr7:44186230 | A | G | 19 | a0001c0001t0007g0023 a0001c0001t0007g0336 a0001c0001t0007g0337 others(16): Show |
20 | HG00423.hp1 HG00597.hp1 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.45+2679T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44186230 | |||||||
| chr7:44186320 | G | A | 1 | a0001c0001t0001g0082 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.45+2589C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44186320 | |||||||
| chr7:44186384 | C | T | 1 | a0001c0001t0002g0160 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.45+2525G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44186384 | |||||||
| chr7:44186388 | G | C | 1 | a0001c0001t0001g0159 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.45+2521C>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44186388 | |||||||
| chr7:44186412 | C | T | 4 | a0001c0001t0012g0357 a0001c0001t0012g0358 a0001c0001t0013g0359 others(1): Show |
4 | HG02922.hp1 HG03130.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.45+2497G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44186412 | |||||||
| chr7:44186491 | C | G | 119 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0015 others(116): Show |
132 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.45+2418G>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44186491 | |||||||
| chr7:44186502 | C | T | 74 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0097 others(71): Show |
78 | HG00323.hp2 HG00597.hp2 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.45+2407G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44186502 | |||||||
| chr7:44186757 | A | G | 6 | a0001c0001t0002g0085 a0001c0001t0002g0086 a0001c0001t0002g0087 others(3): Show |
6 | HG00423.hp2 HG00558.hp2 HG00673.hp1 others(3): Show |
intron_variant | MODIFIER | c.45+2152T>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44186757 | |||||||
| chr7:44187089 | C | G | 15 | a0001c0001t0007g0023 a0001c0001t0007g0336 a0001c0001t0007g0337 others(12): Show |
16 | HG00423.hp1 HG00597.hp1 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.45+1820G>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44187089 | |||||||
| chr7:44187114 | G | A | 5 | a0001c0001t0002g0022 a0001c0001t0002g0315 a0001c0001t0002g0316 others(2): Show |
6 | HG02280.hp1 HG02809.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.45+1795C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44187114 | |||||||
| chr7:44187266 | C | T | 1 | a0001c0001t0002g0026 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.45+1643G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44187266 | |||||||
| chr7:44187345 | G | A | 19 | a0001c0001t0007g0023 a0001c0001t0007g0336 a0001c0001t0007g0337 others(16): Show |
20 | HG00423.hp1 HG00597.hp1 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.45+1564C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44187345 | |||||||
| chr7:44187357 | T | G | 15 | a0001c0001t0007g0023 a0001c0001t0007g0336 a0001c0001t0007g0337 others(12): Show |
16 | HG00423.hp1 HG00597.hp1 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.45+1552A>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44187357 | |||||||
| chr7:44187358 | G | T | 2 | a0001c0001t0002g0083 a0001c0001t0004g0084 |
2 | HG02451.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.45+1551C>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44187358 | |||||||
| chr7:44187421 | G | T | 60 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0037 others(57): Show |
66 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.45+1488C>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44187421 | |||||||
| chr7:44187495 | T | C | 2 | a0001c0001t0001g0318 a0001c0001t0001g0319 |
2 | HG02818.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.45+1414A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44187495 | |||||||
| chr7:44187523 | T | C | 2 | a0001c0001t0003g0320 a0001c0001t0003g0321 |
2 | HG02145.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.45+1386A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44187523 | |||||||
| chr7:44187686 | A | C | 20 | a0001c0001t0007g0023 a0001c0001t0007g0336 a0001c0001t0007g0337 others(17): Show |
21 | HG00423.hp1 HG00597.hp1 HG00733.hp1 others(18): Show |
intron_variant | MODIFIER | c.45+1223T>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44187686 | |||||||
| chr7:44187697 | G | A | 1 | a0001c0001t0002g0322 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.45+1212C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44187697 | |||||||
| chr7:44187774 | C | T | 1 | a0001c0001t0011g0351 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.45+1135G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44187774 | |||||||
| chr7:44187790 | T | A | 5 | a0001c0001t0012g0356 a0001c0001t0012g0357 a0001c0001t0012g0358 others(2): Show |
5 | HG02922.hp1 HG03130.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.45+1119A>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44187790 | |||||||
| chr7:44187874 | G | A | 1 | a0001c0001t0001g0323 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.45+1035C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44187874 | |||||||
| chr7:44187941 | C | T | 1 | a0001c0001t0001g0028 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.45+968G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44187941 | |||||||
| chr7:44188037 | C | T | 1 | a0001c0001t0002g0027 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.45+872G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44188037 | |||||||
| chr7:44188039 | T | G | 4 | a0001c0001t0001g0325 a0001c0001t0001g0326 a0001c0001t0001g0327 others(1): Show |
4 | HG00738.hp1 HG01358.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.45+870A>C | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44188039 | |||||||
| chr7:44188293 | T | C | 1 | a0001c0001t0002g0329 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.45+616A>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44188293 | |||||||
| chr7:44188298 | C | T | 15 | a0001c0001t0007g0023 a0001c0001t0007g0336 a0001c0001t0007g0337 others(12): Show |
16 | HG00423.hp1 HG00597.hp1 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.45+611G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44188298 | |||||||
| chr7:44188321 | C | A | 1 | a0001c0001t0002g0330 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.45+588G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44188321 | |||||||
| chr7:44188380 | C | A | 2 | a0001c0001t0001g0331 a0001c0001t0001g0332 |
2 | HG01109.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.45+529G>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44188380 | |||||||
| chr7:44188480 | C | T | 1 | a0001c0001t0002g0026 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.45+429G>A | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44188480 | |||||||
| chr7:44188512 | G | A | 1 | a0001c0001t0002g0333 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.45+397C>T | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44188512 | |||||||
| chr7:44188548 | GC | G | 15 | a0001c0001t0007g0023 a0001c0001t0007g0336 a0001c0001t0007g0337 others(12): Show |
16 | HG00423.hp1 HG00597.hp1 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.45+360delG | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44188548 | |||||||
| chr7:44188608 | G | C | 1 | a0001c0001t0001g0334 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.45+301C>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44188608 | |||||||
| chr7:44188737 | G | C | 1 | a0001c0001t0001g0335 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.45+172C>G | GCK | ENSG00000106633.18 | transcript | ENST00000403799.8 | protein_coding | 1/9 | chr7 | 44188737 |