Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 5188 |
| ensemblid | ENSG00000059691.12 |
| hgncid | 8849 |
| symbol | GATB |
| name | glutamyl-tRNA amidotransferase subunit B |
| refseq_nuc | NM_004564.3 |
| refseq_prot | NP_004555.1 |
| ensembl_nuc | ENST00000263985.11 |
| ensembl_prot | ENSP00000263985.6 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 151670504 |
| end | 151761007 |
| strand | - |
| ver | v1.2 |
| region | chr4:151670504-151761007 |
| region5000 | chr4:151665504-151766007 |
| regionname0 | GATB_chr4_151670504_151761007 |
| regionname5000 | GATB_chr4_151665504_151766007 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 557 | 260 | 60 | 48 | 114 | 8 | 28 | 92 | GATB_chr4_151665504_151766007 | GATB | MAAPM others(552): Show |
chr4 | 151665504 | 151766007 |
| a0002 | 0/0 | 557 | 47 | 22 | 3 | 20 | 2 | 0 | 11 | GATB_chr4_151665504_151766007 | GATB | MAAPM others(552): Show |
chr4 | 151665504 | 151766007 |
| a0003 | 0/0 | 557 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | MAAPM others(552): Show |
chr4 | 151665504 | 151766007 |
| a0004 | 0/0 | 557 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | MAAPM others(552): Show |
chr4 | 151665504 | 151766007 |
| a0005 | 0/0 | 557 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | MAAPM others(552): Show |
chr4 | 151665504 | 151766007 |
| a0006 | 0/0 | 557 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | MAAPM others(552): Show |
chr4 | 151665504 | 151766007 |
| a0007 | 0/0 | 557 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | MAAPM others(552): Show |
chr4 | 151665504 | 151766007 |
| a0008 | 0/0 | 557 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | MAAPM others(552): Show |
chr4 | 151665504 | 151766007 |
| a0009 | 0/0 | 557 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | MAAPM others(552): Show |
chr4 | 151665504 | 151766007 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1671 | 244 | 58 | 45 | 106 | 7 | 27 | GATB_chr4_151665504_151766007 | GATB | ATGGC others(1666): Show |
chr4 | 151665504 | 151766007 | ||
| a0001c0003 | 0/0 | 1671 | 9 | 0 | 2 | 6 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | ATGGC others(1666): Show |
chr4 | 151665504 | 151766007 | ||
| a0001c0005 | 0/1 | 1671 | 3 | 0 | 1 | 0 | 1 | 0 | GATB_chr4_151665504_151766007 | GATB | ATGGC others(1666): Show |
chr4 | 151665504 | 151766007 | ||
| a0001c0009 | 0/0 | 1671 | 2 | 1 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | ATGGC others(1666): Show |
chr4 | 151665504 | 151766007 | ||
| a0001c0011 | 0/0 | 1671 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | ATGGC others(1666): Show |
chr4 | 151665504 | 151766007 | ||
| a0001c0012 | 0/0 | 1671 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | ATGGC others(1666): Show |
chr4 | 151665504 | 151766007 | ||
| a0002c0002 | 0/0 | 1671 | 47 | 22 | 3 | 20 | 2 | 0 | GATB_chr4_151665504_151766007 | GATB | ATGGC others(1666): Show |
chr4 | 151665504 | 151766007 | ||
| a0003c0004 | 0/0 | 1671 | 4 | 4 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | ATGGC others(1666): Show |
chr4 | 151665504 | 151766007 | ||
| a0004c0006 | 0/0 | 1671 | 2 | 2 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | ATGGC others(1666): Show |
chr4 | 151665504 | 151766007 | ||
| a0005c0007 | 0/0 | 1671 | 2 | 2 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | ATGGC others(1666): Show |
chr4 | 151665504 | 151766007 | ||
| a0006c0008 | 0/0 | 1671 | 2 | 2 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | ATGGC others(1666): Show |
chr4 | 151665504 | 151766007 | ||
| a0007c0013 | 0/0 | 1671 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | ATGGC others(1666): Show |
chr4 | 151665504 | 151766007 | ||
| a0008c0010 | 0/0 | 1671 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | ATGGC others(1666): Show |
chr4 | 151665504 | 151766007 | ||
| a0009c0014 | 0/0 | 1671 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | ATGGC others(1666): Show |
chr4 | 151665504 | 151766007 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2369 | 153 | 52 | 22 | 57 | 6 | 16 | GATB_chr4_151665504_151766007 | GATB | ACCTG others(2364): Show |
chr4 | 151665504 | 151766007 |
| a0001c0001t0002 | 1/0 | 2369 | 91 | 6 | 23 | 49 | 1 | 11 | GATB_chr4_151665504_151766007 | GATB | ACCTG others(2364): Show |
chr4 | 151665504 | 151766007 |
| a0001c0003t0001 | 0/0 | 2369 | 3 | 0 | 0 | 3 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | ACCTG others(2364): Show |
chr4 | 151665504 | 151766007 |
| a0001c0003t0002 | 0/0 | 2369 | 6 | 0 | 2 | 3 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | ACCTG others(2364): Show |
chr4 | 151665504 | 151766007 |
| a0001c0005t0002 | 0/1 | 2369 | 3 | 0 | 1 | 0 | 1 | 0 | GATB_chr4_151665504_151766007 | GATB | ACCTG others(2364): Show |
chr4 | 151665504 | 151766007 |
| a0001c0009t0001 | 0/0 | 2369 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | ACCTG others(2364): Show |
chr4 | 151665504 | 151766007 |
| a0001c0009t0002 | 0/0 | 2369 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | ACCTG others(2364): Show |
chr4 | 151665504 | 151766007 |
| a0001c0011t0002 | 0/0 | 2369 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | ACCTG others(2364): Show |
chr4 | 151665504 | 151766007 |
| a0001c0012t0001 | 0/0 | 2369 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | ACCTG others(2364): Show |
chr4 | 151665504 | 151766007 |
| a0002c0002t0001 | 0/0 | 2369 | 47 | 22 | 3 | 20 | 2 | 0 | GATB_chr4_151665504_151766007 | GATB | ACCTG others(2364): Show |
chr4 | 151665504 | 151766007 |
| a0003c0004t0001 | 0/0 | 2369 | 4 | 4 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | ACCTG others(2364): Show |
chr4 | 151665504 | 151766007 |
| a0004c0006t0001 | 0/0 | 2369 | 2 | 2 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | ACCTG others(2364): Show |
chr4 | 151665504 | 151766007 |
| a0005c0007t0002 | 0/0 | 2369 | 2 | 2 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | ACCTG others(2364): Show |
chr4 | 151665504 | 151766007 |
| a0006c0008t0001 | 0/0 | 2369 | 2 | 2 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | ACCTG others(2364): Show |
chr4 | 151665504 | 151766007 |
| a0007c0013t0001 | 0/0 | 2369 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | ACCTG others(2364): Show |
chr4 | 151665504 | 151766007 |
| a0008c0010t0001 | 0/0 | 2369 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | ACCTG others(2364): Show |
chr4 | 151665504 | 151766007 |
| a0009c0014t0002 | 0/0 | 2369 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | ACCTG others(2364): Show |
chr4 | 151665504 | 151766007 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0003 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0004 | 1/0 | 3 | 0 | 2 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0005 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0003t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0003t0002g0013 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0003t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0003t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0003t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0003t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0005t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0005t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0005t0002g0269 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0009t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0009t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0011t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0001c0012t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0002c0002t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0002c0002t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0002c0002t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0002c0002t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0002c0002t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0002c0002t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0002c0002t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0002c0002t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0002c0002t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0002c0002t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0002c0002t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0002c0002t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0002c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0002c0002t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0002c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0002c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0002c0002t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0002c0002t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0002c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0002c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0002c0002t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0002c0002t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0002c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0002c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0002c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0002c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0002c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0002c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0002c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0003c0004t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0003c0004t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0003c0004t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0003c0004t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0004c0006t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0004c0006t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0005c0007t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0005c0007t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0006c0008t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0006c0008t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0007c0013t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0008c0010t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| a0009c0014t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0089 | EUR | GBR | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0215 | EUR | GBR | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0179 | EUR | FIN | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0147 | EUR | FIN | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG00323 | hp1 | a0001 | c0005 | t0002 | g0263 | EUR | FIN | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0044 | EUR | FIN | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0235 | EAS | CHS | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | CHS | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG00597 | hp2 | a0002 | c0002 | t0001 | g0049 | EAS | CHS | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0036 | AMR | PUR | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG00642 | hp2 | a0001 | c0001 | t0002 | g0273 | AMR | PUR | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0281 | AMR | PUR | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0217 | AMR | PUR | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0283 | AMR | PUR | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0224 | AMR | PUR | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0208 | AMR | PUR | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG01109 | hp1 | a0002 | c0002 | t0001 | g0026 | AMR | PUR | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0240 | AMR | PUR | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0223 | AMR | PUR | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PUR | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0257 | AMR | PUR | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0265 | AMR | CLM | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG01255 | hp2 | a0001 | c0005 | t0002 | g0207 | AMR | CLM | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0264 | AMR | CLM | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG01258 | hp2 | a0007 | c0013 | t0001 | g0098 | AMR | CLM | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0201 | AMR | CLM | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0272 | AMR | CLM | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0243 | AMR | CLM | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG01361 | hp1 | a0001 | c0003 | t0002 | g0212 | AMR | CLM | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | CLM | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0200 | AMR | CLM | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0038 | EUR | IBS | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0119 | EUR | IBS | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG01884 | hp1 | a0003 | c0004 | t0001 | g0294 | AFR | ACB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0018 | AFR | ACB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG01891 | hp1 | a0002 | c0002 | t0001 | g0020 | AFR | ACB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0285 | AMR | PEL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0209 | AMR | PEL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0244 | AMR | PEL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0196 | AMR | PEL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG01978 | hp1 | a0001 | c0003 | t0002 | g0231 | AMR | PEL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PEL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG01993 | hp2 | a0002 | c0002 | t0001 | g0037 | AMR | PEL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | KHV | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ACB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | ACB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02056 | hp2 | a0002 | c0002 | t0001 | g0045 | EAS | KHV | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0225 | EAS | KHV | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | KHV | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02074 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | KHV | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | KHV | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0048 | EAS | KHV | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | KHV | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | KHV | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02145 | hp1 | a0002 | c0002 | t0001 | g0051 | AFR | ACB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ACB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02155 | hp1 | a0002 | c0002 | t0001 | g0046 | EAS | CDX | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | CDX | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | CDX | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02165 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CDX | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0035 | AFR | ACB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | ACB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02451 | hp2 | a0001 | c0012 | t0001 | g0275 | AFR | ACB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | KHV | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02523 | hp2 | a0008 | c0010 | t0001 | g0058 | EAS | KHV | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02572 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | GWD | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02622 | hp2 | a0004 | c0006 | t0001 | g0050 | AFR | GWD | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0032 | AFR | GWD | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02630 | hp2 | a0002 | c0002 | t0001 | g0021 | AFR | GWD | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02717 | hp2 | a0002 | c0002 | t0001 | g0054 | AFR | GWD | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02723 | hp2 | a0002 | c0002 | t0001 | g0019 | AFR | GWD | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02735 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02809 | hp1 | a0004 | c0006 | t0001 | g0041 | AFR | GWD | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02809 | hp2 | a0002 | c0002 | t0001 | g0052 | AFR | GWD | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | GWD | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | GWD | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0022 | AFR | GWD | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | GWD | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02897 | hp1 | a0005 | c0007 | t0002 | g0025 | AFR | GWD | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | GWD | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | ESN | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | ESN | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ESN | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ESN | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | ESN | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02970 | hp2 | a0003 | c0004 | t0001 | g0296 | AFR | ESN | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ESN | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02976 | hp2 | a0003 | c0004 | t0001 | g0293 | AFR | ESN | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0008 | AFR | GWD | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | MSL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | MSL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ESN | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0053 | AFR | ESN | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG03139 | hp1 | a0002 | c0002 | t0001 | g0028 | AFR | ESN | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG03195 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ESN | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | ESN | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG03209 | hp2 | a0006 | c0008 | t0001 | g0194 | AFR | MSL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | MSL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | MSL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG03453 | hp1 | a0003 | c0004 | t0001 | g0295 | AFR | MSL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG03453 | hp2 | a0001 | c0009 | t0001 | g0186 | AFR | MSL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | MSL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | ESN | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG03540 | hp1 | a0005 | c0007 | t0002 | g0024 | AFR | GWD | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | MSL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | MSL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0233 | SAS | PJL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0267 | SAS | PJL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0012 | SAS | PJL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0245 | SAS | STU | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | STU | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0211 | SAS | BEB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0274 | SAS | BEB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | BEB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | BEB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0109 | SAS | STU | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | STU | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0012 | SAS | BEB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | BEB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | STU | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0232 | SAS | STU | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | CHB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CHB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18747 | hp1 | a0002 | c0002 | t0001 | g0047 | EAS | CHB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18747 | hp2 | a0001 | c0003 | t0002 | g0228 | EAS | CHB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | YRI | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18906 | hp2 | a0002 | c0002 | t0001 | g0031 | AFR | YRI | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18939 | hp2 | a0001 | c0009 | t0002 | g0239 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18940 | hp1 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18945 | hp2 | a0001 | c0003 | t0001 | g0149 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18948 | hp1 | a0001 | c0003 | t0001 | g0165 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18949 | hp2 | a0009 | c0014 | t0002 | g0284 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18954 | hp2 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18959 | hp2 | a0002 | c0002 | t0001 | g0056 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18962 | hp1 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0254 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18979 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18980 | hp1 | a0002 | c0002 | t0001 | g0040 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0034 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18987 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA19000 | hp2 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA19030 | hp1 | a0002 | c0002 | t0001 | g0023 | AFR | LWK | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | LWK | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA19043 | hp1 | a0006 | c0008 | t0001 | g0195 | AFR | LWK | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA19043 | hp2 | a0002 | c0002 | t0001 | g0029 | AFR | LWK | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA19054 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA19057 | hp1 | a0001 | c0003 | t0001 | g0166 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA19060 | hp2 | a0001 | c0003 | t0002 | g0013 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0261 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA19068 | hp2 | a0001 | c0011 | t0002 | g0226 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA19074 | hp2 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA19082 | hp1 | a0001 | c0003 | t0002 | g0218 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA19085 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA19240 | hp1 | a0002 | c0002 | t0001 | g0008 | AFR | YRI | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0055 | AFR | YRI | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ASW | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ASW | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0088 | EUR | TSI | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0227 | EUR | TSI | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA20905 | hp1 | a0001 | c0003 | t0002 | g0013 | SAS | GIH | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | GIH | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ACB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | ACB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | ACB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0256 | AFR | ACB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0198 | AFR | ACB | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG03471 | hp1 | a0002 | c0002 | t0001 | g0033 | AFR | MSL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | MSL | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | USA | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| HG06807 | hp2 | a0002 | c0002 | t0001 | g0027 | AFR | USA | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0262 | AFR | USA | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | USA | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | LWK | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | LWK | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| homoSapiens | chm13v2 | a0001 | c0005 | t0002 | g0269 | REF | REF | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0004 | REF | REF | GATB_chr4_151665504_151766007 | GATB | chr4 | 151665504 | 151766007 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:151688651 | T | C | 1 | a0007 | 1 | HG01258.hp2 | missense_variant | MODERATE | c.1310A>G | p.Gln437Arg | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/13 | 1335/2369 | 1310/1674 | 437/557 | chr4 | 151688651 | |||
| chr4:151701381 | T | C | 1 | a0006 | 2 | HG03209.hp2 NA19043.hp1 |
missense_variant | MODERATE | c.1145A>G | p.Glu382Gly | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/13 | 1170/2369 | 1145/1674 | 382/557 | chr4 | 151701381 | |||
| chr4:151705266 | T | C | 1 | a0004 | 2 | HG02622.hp2 HG02809.hp1 |
missense_variant | MODERATE | c.881A>G | p.Tyr294Cys | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 7/13 | 906/2369 | 881/1674 | 294/557 | chr4 | 151705266 | |||
| chr4:151717074 | C | A | 1 | a0005 | 2 | HG02897.hp1 HG03540.hp1 |
missense_variant&splice_region_variant | MODERATE | c.442G>T | p.Ala148Ser | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 4/13 | 467/2369 | 442/1674 | 148/557 | chr4 | 151717074 | |||
| chr4:151758837 | G | A | 1 | a0009 | 1 | NA18949.hp2 | missense_variant | MODERATE | c.262C>T | p.Arg88Cys | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/13 | 287/2369 | 262/1674 | 88/557 | chr4 | 151758837 | |||
| chr4:151760834 | A | G | 1 | a0008 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.149T>C | p.Leu50Pro | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 1/13 | 174/2369 | 149/1674 | 50/557 | chr4 | 151760834 | |||
| chr4:151760846 | G | A | 1 | a0003 | 4 | HG01884.hp1 HG02970.hp2 HG02976.hp2 others(1): Show |
missense_variant | MODERATE | c.137C>T | p.Ala46Val | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 1/13 | 162/2369 | 137/1674 | 46/557 | chr4 | 151760846 | |||
| chr4:151760894 | G | T | 3 | a0002 a0004 a0005 |
51 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(48): Show |
missense_variant | MODERATE | c.89C>A | p.Ala30Asp | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 1/13 | 114/2369 | 89/1674 | 30/557 | chr4 | 151760894 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:151671237 | C | T | 1 | a0001c0012 | 1 | HG02451.hp2 | synonymous_variant | LOW | c.1611G>A | p.Ala537Ala | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 13/13 | 1636/2369 | 1611/1674 | 537/557 | chr4 | 151671237 | |||
| chr4:151688632 | C | T | 1 | a0001c0003 | 9 | HG01361.hp1 HG01978.hp1 NA18747.hp2 others(6): Show |
splice_region_variant&synonymous_variant | LOW | c.1329G>A | p.Glu443Glu | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/13 | 1354/2369 | 1329/1674 | 443/557 | chr4 | 151688632 | |||
| chr4:151688674 | A | C | 1 | a0001c0005 | 2 | HG00323.hp1 HG01255.hp2 |
synonymous_variant | LOW | c.1287T>G | p.Thr429Thr | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/13 | 1312/2369 | 1287/1674 | 429/557 | chr4 | 151688674 | |||
| chr4:151701476 | G | A | 1 | a0001c0009 | 2 | HG03453.hp2 NA18939.hp2 |
synonymous_variant | LOW | c.1050C>T | p.Asp350Asp | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/13 | 1075/2369 | 1050/1674 | 350/557 | chr4 | 151701476 | |||
| chr4:151708048 | A | G | 1 | a0001c0011 | 1 | NA19068.hp2 | synonymous_variant | LOW | c.817T>C | p.Leu273Leu | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 6/13 | 842/2369 | 817/1674 | 273/557 | chr4 | 151708048 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:151671039 | T | C | 10 | a0001c0001t0001 a0001c0003t0001 a0001c0009t0001 others(7): Show |
215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*135A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 13/13 | 135 | chr4 | 151671039 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:151671317 | A | ATTAC | 206 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(203): Show |
214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.1546-19_1546-16dup others(4): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 12/12 | chr4 | 151671317 | |||||||
| chr4:151671563 | G | T | 4 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(1): Show |
4 | HG02965.hp1 HG03195.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1546-261C>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 12/12 | chr4 | 151671563 | |||||||
| chr4:151671781 | A | G | 206 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(203): Show |
214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.1546-479T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 12/12 | chr4 | 151671781 | |||||||
| chr4:151671794 | G | A | 1 | a0002c0002t0001g0039 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1546-492C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 12/12 | chr4 | 151671794 | |||||||
| chr4:151671801 | C | T | 208 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(205): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1546-499G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 12/12 | chr4 | 151671801 | |||||||
| chr4:151671803 | G | C | 5 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(2): Show |
5 | HG01891.hp2 HG02258.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1546-501C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 12/12 | chr4 | 151671803 | |||||||
| chr4:151671979 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1546-677G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 12/12 | chr4 | 151671979 | |||||||
| chr4:151672054 | G | C | 2 | a0005c0007t0002g0024 a0005c0007t0002g0025 |
2 | HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1545+708C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 12/12 | chr4 | 151672054 | |||||||
| chr4:151672127 | C | T | 2 | a0001c0001t0001g0108 a0001c0001t0001g0215 |
2 | HG00140.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.1545+635G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 12/12 | chr4 | 151672127 | |||||||
| chr4:151672198 | C | T | 4 | a0001c0001t0001g0117 a0001c0001t0001g0123 a0001c0001t0001g0124 others(1): Show |
4 | HG02083.hp1 HG02132.hp1 NA18953.hp1 others(1): Show |
intron_variant | MODIFIER | c.1545+564G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 12/12 | chr4 | 151672198 | |||||||
| chr4:151672230 | A | G | 29 | a0001c0001t0001g0145 a0002c0002t0001g0002 a0002c0002t0001g0009 others(26): Show |
33 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.1545+532T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 12/12 | chr4 | 151672230 | |||||||
| chr4:151672257 | T | C | 206 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(203): Show |
214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.1545+505A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 12/12 | chr4 | 151672257 | |||||||
| chr4:151672258 | C | T | 3 | a0003c0004t0001g0293 a0003c0004t0001g0294 a0003c0004t0001g0296 |
3 | HG01884.hp1 HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1545+504G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 12/12 | chr4 | 151672258 | |||||||
| chr4:151672318 | C | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0189 |
2 | HG00639.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.1545+444G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 12/12 | chr4 | 151672318 | |||||||
| chr4:151672383 | G | GTTC | 3 | a0001c0001t0002g0259 a0001c0001t0002g0260 a0001c0001t0002g0261 |
3 | NA19057.hp2 NA19064.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.1545+376_1545+378d others(5): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 12/12 | chr4 | 151672383 | |||||||
| chr4:151672397 | G | A | 1 | a0001c0001t0002g0285 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1545+365C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 12/12 | chr4 | 151672397 | |||||||
| chr4:151672424 | A | G | 1 | a0001c0001t0001g0169 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1545+338T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 12/12 | chr4 | 151672424 | |||||||
| chr4:151673046 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1411-150G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151673046 | |||||||
| chr4:151673068 | G | T | 1 | a0002c0002t0001g0049 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1411-172C>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151673068 | |||||||
| chr4:151673252 | T | TG | 57 | a0001c0001t0001g0016 a0001c0001t0001g0060 a0001c0001t0001g0061 others(54): Show |
59 | HG00280.hp1 HG00558.hp1 HG01109.hp2 others(56): Show |
intron_variant | MODIFIER | c.1411-357dupC | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151673252 | |||||||
| chr4:151673252 | T | TGG | 83 | a0001c0001t0001g0059 a0001c0001t0001g0063 a0001c0001t0001g0065 others(80): Show |
83 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(80): Show |
intron_variant | MODIFIER | c.1411-358_1411-357d others(4): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151673252 | |||||||
| chr4:151673252 | T | TGGG | 6 | a0001c0001t0001g0011 a0001c0001t0001g0147 a0001c0001t0001g0182 others(3): Show |
7 | HG00140.hp2 HG00280.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.1411-357_1411-356i others(5): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151673252 | |||||||
| chr4:151673253 | G | T | 2 | a0004c0006t0001g0041 a0004c0006t0001g0050 |
2 | HG02622.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.1411-357C>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151673253 | |||||||
| chr4:151673254 | G | GT | 5 | a0001c0001t0001g0110 a0001c0001t0001g0112 a0001c0001t0001g0204 others(2): Show |
5 | HG02040.hp2 NA18948.hp2 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.1411-359_1411-358i others(3): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151673254 | |||||||
| chr4:151673254 | GC | G | 24 | a0001c0001t0001g0145 a0001c0009t0001g0186 a0002c0002t0001g0002 others(21): Show |
27 | HG00323.hp2 HG01515.hp1 HG02132.hp2 others(24): Show |
intron_variant | MODIFIER | c.1411-359delG | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151673254 | |||||||
| chr4:151673255 | C | CG | 27 | a0001c0001t0001g0242 a0001c0001t0002g0004 a0001c0001t0002g0012 others(24): Show |
29 | HG00642.hp2 HG00735.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.1411-360dupC | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151673255 | |||||||
| chr4:151673255 | C | G | 182 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(179): Show |
187 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1411-359G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151673255 | |||||||
| chr4:151673572 | G | A | 28 | a0001c0001t0001g0145 a0002c0002t0001g0002 a0002c0002t0001g0009 others(25): Show |
32 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1411-676C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151673572 | |||||||
| chr4:151673573 | A | G | 28 | a0001c0001t0001g0145 a0002c0002t0001g0002 a0002c0002t0001g0009 others(25): Show |
32 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1411-677T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151673573 | |||||||
| chr4:151673662 | T | C | 207 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(204): Show |
215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1411-766A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151673662 | |||||||
| chr4:151674145 | C | T | 6 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(3): Show |
6 | HG02486.hp2 HG03139.hp2 NA18906.hp1 others(3): Show |
intron_variant | MODIFIER | c.1411-1249G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151674145 | |||||||
| chr4:151674147 | C | T | 2 | a0001c0001t0002g0205 a0001c0001t0002g0206 |
2 | NA19005.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1411-1251G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151674147 | |||||||
| chr4:151674221 | A | G | 207 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(204): Show |
215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1411-1325T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151674221 | |||||||
| chr4:151674386 | A | T | 68 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(65): Show |
68 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.1411-1490T>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151674386 | |||||||
| chr4:151674645 | C | T | 8 | a0001c0009t0001g0186 a0002c0002t0001g0008 a0002c0002t0001g0023 others(5): Show |
9 | HG02630.hp1 HG03041.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.1411-1749G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151674645 | |||||||
| chr4:151674676 | A | G | 1 | a0001c0001t0002g0236 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1411-1780T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151674676 | |||||||
| chr4:151674684 | C | G | 206 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(203): Show |
214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.1411-1788G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151674684 | |||||||
| chr4:151674994 | G | A | 3 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 |
3 | HG01243.hp1 HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1411-2098C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151674994 | |||||||
| chr4:151674996 | A | G | 1 | a0002c0002t0001g0051 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1411-2100T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151674996 | |||||||
| chr4:151675150 | G | A | 2 | a0005c0007t0002g0024 a0005c0007t0002g0025 |
2 | HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1411-2254C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151675150 | |||||||
| chr4:151675218 | C | T | 2 | a0005c0007t0002g0024 a0005c0007t0002g0025 |
2 | HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1411-2322G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151675218 | |||||||
| chr4:151675356 | T | C | 207 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(204): Show |
215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1411-2460A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151675356 | |||||||
| chr4:151675374 | C | T | 28 | a0001c0001t0001g0145 a0002c0002t0001g0002 a0002c0002t0001g0009 others(25): Show |
32 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1411-2478G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151675374 | |||||||
| chr4:151675388 | T | C | 209 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(206): Show |
217 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(214): Show |
intron_variant | MODIFIER | c.1411-2492A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151675388 | |||||||
| chr4:151675516 | G | A | 206 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(203): Show |
214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.1411-2620C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151675516 | |||||||
| chr4:151675673 | G | A | 1 | a0002c0002t0001g0019 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1411-2777C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151675673 | |||||||
| chr4:151675676 | C | T | 1 | a0001c0001t0002g0205 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1411-2780G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151675676 | |||||||
| chr4:151675918 | A | G | 1 | a0002c0002t0001g0029 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1411-3022T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151675918 | |||||||
| chr4:151675995 | A | G | 29 | a0001c0001t0001g0145 a0002c0002t0001g0002 a0002c0002t0001g0009 others(26): Show |
33 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.1411-3099T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151675995 | |||||||
| chr4:151676050 | C | G | 207 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(204): Show |
215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1411-3154G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151676050 | |||||||
| chr4:151676153 | G | A | 2 | a0001c0001t0001g0085 a0001c0001t0001g0086 |
2 | HG02602.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1411-3257C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151676153 | |||||||
| chr4:151676225 | C | T | 1 | a0001c0001t0002g0234 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1411-3329G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151676225 | |||||||
| chr4:151676388 | A | G | 207 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(204): Show |
215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1410+3425T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151676388 | |||||||
| chr4:151676389 | A | G | 2 | a0005c0007t0002g0024 a0005c0007t0002g0025 |
2 | HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1410+3424T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151676389 | |||||||
| chr4:151676530 | AGGCTTGG others(7): Show |
A | 31 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(28): Show |
31 | HG00558.hp1 HG00597.hp1 HG01433.hp1 others(28): Show |
intron_variant | MODIFIER | c.1410+3269_1410+328 others(18): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151676530 | |||||||
| chr4:151676873 | G | C | 1 | a0001c0001t0001g0076 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1410+2940C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151676873 | |||||||
| chr4:151677353 | C | T | 2 | a0001c0001t0001g0241 a0002c0002t0001g0051 |
2 | HG02145.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.1410+2460G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151677353 | |||||||
| chr4:151677451 | C | T | 206 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(203): Show |
214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.1410+2362G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151677451 | |||||||
| chr4:151677465 | TAC | T | 28 | a0001c0001t0001g0145 a0002c0002t0001g0002 a0002c0002t0001g0009 others(25): Show |
32 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1410+2346_1410+234 others(6): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151677465 | |||||||
| chr4:151677515 | G | A | 4 | a0001c0001t0001g0073 a0001c0001t0001g0080 a0001c0001t0001g0081 others(1): Show |
4 | NA18969.hp1 NA19009.hp1 NA19082.hp2 others(1): Show |
intron_variant | MODIFIER | c.1410+2298C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151677515 | |||||||
| chr4:151677546 | T | C | 206 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(203): Show |
214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.1410+2267A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151677546 | |||||||
| chr4:151677670 | G | A | 2 | a0001c0001t0002g0003 a0001c0001t0002g0217 |
4 | HG00639.hp2 HG00741.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.1410+2143C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151677670 | |||||||
| chr4:151677724 | C | G | 208 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(205): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1410+2089G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151677724 | |||||||
| chr4:151677840 | C | T | 206 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(203): Show |
214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.1410+1973G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151677840 | |||||||
| chr4:151677874 | T | TA | 8 | a0001c0009t0001g0186 a0002c0002t0001g0008 a0002c0002t0001g0023 others(5): Show |
9 | HG02630.hp1 HG03041.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.1410+1938dupT | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151677874 | |||||||
| chr4:151678094 | G | C | 1 | a0001c0001t0001g0088 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1410+1719C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151678094 | |||||||
| chr4:151678153 | C | G | 1 | a0001c0001t0001g0127 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1410+1660G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151678153 | |||||||
| chr4:151678222 | C | A | 208 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(205): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1410+1591G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151678222 | |||||||
| chr4:151678316 | C | G | 1 | a0001c0001t0001g0156 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1410+1497G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151678316 | |||||||
| chr4:151678356 | T | C | 1 | a0001c0001t0001g0292 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1410+1457A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151678356 | |||||||
| chr4:151678437 | TTC | T | 198 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(195): Show |
206 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.1410+1374_1410+137 others(6): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151678437 | |||||||
| chr4:151678437 | TTCTC | T | 3 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 |
3 | NA18612.hp2 NA18977.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.1410+1372_1410+137 others(8): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151678437 | |||||||
| chr4:151678500 | A | T | 208 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(205): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1410+1313T>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151678500 | |||||||
| chr4:151678620 | A | AAACAGAG others(304): Show |
1 | a0001c0001t0001g0160 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1410+1192_1410+119 others(315): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151678620 | |||||||
| chr4:151678620 | A | AAACAGAG others(308): Show |
2 | a0001c0003t0001g0165 a0001c0003t0001g0166 |
2 | NA18948.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.1410+1192_1410+119 others(319): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151678620 | |||||||
| chr4:151678620 | A | AAACAGAG others(316): Show |
1 | a0001c0001t0001g0159 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1410+1192_1410+119 others(327): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151678620 | |||||||
| chr4:151678620 | A | AAACAGAG others(317): Show |
1 | a0001c0001t0001g0157 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1410+1192_1410+119 others(328): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151678620 | |||||||
| chr4:151678620 | A | AAACAGAG others(318): Show |
1 | a0001c0001t0001g0158 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1410+1192_1410+119 others(329): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151678620 | |||||||
| chr4:151678620 | A | AAACAGAG others(328): Show |
1 | a0001c0001t0001g0155 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1410+1192_1410+119 others(339): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151678620 | |||||||
| chr4:151678620 | A | AAACAGAG others(329): Show |
1 | a0001c0001t0001g0162 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1410+1192_1410+119 others(340): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151678620 | |||||||
| chr4:151678620 | A | AAACAGAG others(348): Show |
2 | a0001c0001t0001g0142 a0001c0003t0001g0149 |
2 | NA18945.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.1410+1192_1410+119 others(359): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151678620 | |||||||
| chr4:151678620 | A | AAACAGAG others(351): Show |
1 | a0001c0001t0001g0143 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1410+1192_1410+119 others(362): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151678620 | |||||||
| chr4:151678750 | G | A | 208 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(205): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1410+1063C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151678750 | |||||||
| chr4:151678841 | A | C | 2 | a0001c0001t0001g0138 a0001c0001t0001g0168 |
2 | HG03942.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1410+972T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151678841 | |||||||
| chr4:151678883 | G | GT | 197 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(194): Show |
205 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(202): Show |
intron_variant | MODIFIER | c.1410+929dupA | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151678883 | |||||||
| chr4:151678883 | G | GTTT | 11 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0155 others(8): Show |
11 | HG00597.hp1 NA18941.hp2 NA18945.hp2 others(8): Show |
intron_variant | MODIFIER | c.1410+927_1410+929d others(5): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151678883 | |||||||
| chr4:151678935 | C | T | 2 | a0005c0007t0002g0024 a0005c0007t0002g0025 |
2 | HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1410+878G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151678935 | |||||||
| chr4:151679063 | T | C | 1 | a0001c0001t0001g0133 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1410+750A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151679063 | |||||||
| chr4:151679218 | C | T | 208 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(205): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1410+595G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151679218 | |||||||
| chr4:151679299 | A | G | 208 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(205): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1410+514T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151679299 | |||||||
| chr4:151679445 | C | A | 1 | a0004c0006t0001g0041 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1410+368G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151679445 | |||||||
| chr4:151679456 | C | T | 1 | a0001c0001t0002g0202 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1410+357G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151679456 | |||||||
| chr4:151679547 | T | C | 200 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(197): Show |
207 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1410+266A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 11/12 | chr4 | 151679547 | |||||||
| chr4:151679994 | T | G | 200 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(197): Show |
207 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1332-103A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151679994 | |||||||
| chr4:151680171 | A | G | 7 | a0002c0002t0001g0008 a0002c0002t0001g0023 a0002c0002t0001g0027 others(4): Show |
8 | HG02630.hp1 HG03041.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.1332-280T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151680171 | |||||||
| chr4:151680201 | A | G | 208 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(205): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1332-310T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151680201 | |||||||
| chr4:151680202 | T | C | 1 | a0001c0001t0002g0267 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1332-311A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151680202 | |||||||
| chr4:151680253 | C | T | 2 | a0005c0007t0002g0024 a0005c0007t0002g0025 |
2 | HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1332-362G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151680253 | |||||||
| chr4:151680278 | T | TA | 202 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(199): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1332-388dupT | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151680278 | |||||||
| chr4:151680278 | T | TAA | 8 | a0001c0001t0001g0063 a0001c0001t0001g0094 a0001c0001t0001g0124 others(5): Show |
8 | HG00280.hp2 HG00735.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1332-389_1332-388d others(4): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151680278 | |||||||
| chr4:151680314 | C | T | 4 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(1): Show |
4 | HG02965.hp1 HG03195.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1332-423G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151680314 | |||||||
| chr4:151680423 | T | TA | 7 | a0002c0002t0001g0008 a0002c0002t0001g0023 a0002c0002t0001g0027 others(4): Show |
8 | HG02630.hp1 HG03041.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.1332-533dupT | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151680423 | |||||||
| chr4:151680515 | A | G | 1 | a0001c0001t0002g0268 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1332-624T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151680515 | |||||||
| chr4:151680612 | C | T | 1 | a0002c0002t0001g0019 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1332-721G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151680612 | |||||||
| chr4:151680689 | G | A | 170 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(167): Show |
173 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.1332-798C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151680689 | |||||||
| chr4:151680750 | G | A | 208 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(205): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1332-859C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151680750 | |||||||
| chr4:151680799 | G | A | 5 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0152 others(2): Show |
5 | HG02055.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1332-908C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151680799 | |||||||
| chr4:151680814 | G | A | 5 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(2): Show |
5 | HG02280.hp1 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1332-923C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151680814 | |||||||
| chr4:151680890 | T | C | 2 | a0001c0001t0002g0244 a0001c0001t0002g0265 |
2 | HG01255.hp1 HG01934.hp2 |
intron_variant | MODIFIER | c.1332-999A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151680890 | |||||||
| chr4:151681095 | A | C | 208 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(205): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1332-1204T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151681095 | |||||||
| chr4:151681178 | A | G | 2 | a0001c0001t0001g0085 a0001c0001t0001g0086 |
2 | HG02602.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1332-1287T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151681178 | |||||||
| chr4:151681197 | A | G | 1 | a0001c0009t0002g0239 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1332-1306T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151681197 | |||||||
| chr4:151681433 | G | A | 208 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(205): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1332-1542C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151681433 | |||||||
| chr4:151681447 | TA | T | 208 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(205): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1332-1557delT | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151681447 | |||||||
| chr4:151681511 | C | G | 1 | a0001c0001t0001g0155 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1332-1620G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151681511 | |||||||
| chr4:151681646 | A | G | 208 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(205): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1332-1755T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151681646 | |||||||
| chr4:151681834 | A | G | 8 | a0001c0009t0001g0186 a0002c0002t0001g0008 a0002c0002t0001g0023 others(5): Show |
9 | HG02630.hp1 HG03041.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.1332-1943T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151681834 | |||||||
| chr4:151681953 | A | G | 29 | a0001c0001t0001g0145 a0002c0002t0001g0002 a0002c0002t0001g0009 others(26): Show |
33 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.1332-2062T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151681953 | |||||||
| chr4:151681979 | A | T | 8 | a0001c0009t0001g0186 a0002c0002t0001g0008 a0002c0002t0001g0023 others(5): Show |
9 | HG02630.hp1 HG03041.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.1332-2088T>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151681979 | |||||||
| chr4:151682012 | T | C | 208 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(205): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1332-2121A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151682012 | |||||||
| chr4:151682025 | A | G | 208 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(205): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1332-2134T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151682025 | |||||||
| chr4:151682126 | G | A | 208 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(205): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1332-2235C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151682126 | |||||||
| chr4:151682205 | G | A | 208 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(205): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1332-2314C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151682205 | |||||||
| chr4:151682263 | G | A | 28 | a0001c0001t0001g0145 a0002c0002t0001g0002 a0002c0002t0001g0009 others(25): Show |
32 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.1332-2372C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151682263 | |||||||
| chr4:151682323 | C | T | 208 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(205): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1332-2432G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151682323 | |||||||
| chr4:151682376 | C | G | 208 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(205): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1332-2485G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151682376 | |||||||
| chr4:151682463 | T | C | 208 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(205): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1332-2572A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151682463 | |||||||
| chr4:151682503 | C | T | 208 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(205): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1332-2612G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151682503 | |||||||
| chr4:151682553 | C | T | 1 | a0002c0002t0001g0044 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1332-2662G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151682553 | |||||||
| chr4:151682597 | A | G | 1 | a0003c0004t0001g0293 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1332-2706T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151682597 | |||||||
| chr4:151682691 | C | T | 36 | a0001c0001t0001g0145 a0001c0001t0001g0288 a0001c0001t0001g0289 others(33): Show |
41 | HG00323.hp2 HG00597.hp2 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.1332-2800G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151682691 | |||||||
| chr4:151682713 | T | C | 208 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(205): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1332-2822A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151682713 | |||||||
| chr4:151682784 | G | A | 2 | a0001c0001t0001g0146 a0001c0001t0001g0188 |
2 | HG02129.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.1332-2893C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151682784 | |||||||
| chr4:151682831 | G | A | 8 | a0001c0009t0001g0186 a0002c0002t0001g0008 a0002c0002t0001g0023 others(5): Show |
9 | HG02630.hp1 HG03041.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.1332-2940C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151682831 | |||||||
| chr4:151682879 | G | A | 208 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(205): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1332-2988C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151682879 | |||||||
| chr4:151683065 | C | T | 4 | a0002c0002t0001g0049 a0003c0004t0001g0293 a0003c0004t0001g0294 others(1): Show |
4 | HG00597.hp2 HG01884.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1332-3174G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151683065 | |||||||
| chr4:151683150 | C | T | 1 | a0002c0002t0001g0051 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1332-3259G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151683150 | |||||||
| chr4:151683169 | T | C | 1 | a0001c0001t0002g0233 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1332-3278A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151683169 | |||||||
| chr4:151683179 | C | G | 208 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(205): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1332-3288G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151683179 | |||||||
| chr4:151683194 | C | CTTTAT | 208 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(205): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1332-3304_1332-330 others(9): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151683194 | |||||||
| chr4:151683315 | T | G | 208 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(205): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1332-3424A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151683315 | |||||||
| chr4:151683368 | C | T | 208 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(205): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1332-3477G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151683368 | |||||||
| chr4:151683391 | T | C | 208 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(205): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1332-3500A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151683391 | |||||||
| chr4:151683406 | C | T | 208 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(205): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1332-3515G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151683406 | |||||||
| chr4:151683472 | G | A | 2 | a0001c0001t0002g0209 a0001c0001t0002g0243 |
2 | HG01346.hp1 HG01928.hp2 |
intron_variant | MODIFIER | c.1332-3581C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151683472 | |||||||
| chr4:151683567 | T | C | 208 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(205): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1332-3676A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151683567 | |||||||
| chr4:151683571 | T | C | 208 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(205): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1332-3680A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151683571 | |||||||
| chr4:151683711 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1332-3820G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151683711 | |||||||
| chr4:151683774 | A | C | 1 | a0001c0001t0001g0093 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1332-3883T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151683774 | |||||||
| chr4:151683842 | A | C | 1 | a0001c0001t0001g0101 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1332-3951T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151683842 | |||||||
| chr4:151683860 | A | G | 30 | a0001c0001t0001g0145 a0002c0002t0001g0002 a0002c0002t0001g0009 others(27): Show |
34 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.1332-3969T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151683860 | |||||||
| chr4:151683875 | C | T | 200 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(197): Show |
207 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1332-3984G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151683875 | |||||||
| chr4:151684018 | A | G | 200 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(197): Show |
207 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.1332-4127T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151684018 | |||||||
| chr4:151684128 | T | C | 8 | a0001c0009t0001g0186 a0002c0002t0001g0008 a0002c0002t0001g0023 others(5): Show |
9 | HG02630.hp1 HG03041.hp2 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.1332-4237A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151684128 | |||||||
| chr4:151684147 | C | A | 2 | a0005c0007t0002g0024 a0005c0007t0002g0025 |
2 | HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1332-4256G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151684147 | |||||||
| chr4:151684160 | C | A | 208 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(205): Show |
216 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.1332-4269G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151684160 | |||||||
| chr4:151684297 | A | G | 203 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(200): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.1331+4333T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151684297 | |||||||
| chr4:151684442 | G | C | 1 | a0001c0001t0002g0202 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1331+4188C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151684442 | |||||||
| chr4:151684469 | G | A | 207 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(204): Show |
215 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.1331+4161C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151684469 | |||||||
| chr4:151684568 | G | C | 32 | a0001c0001t0001g0145 a0001c0001t0001g0280 a0001c0001t0001g0292 others(29): Show |
36 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.1331+4062C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151684568 | |||||||
| chr4:151684684 | G | A | 1 | a0001c0001t0002g0233 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1331+3946C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151684684 | |||||||
| chr4:151684991 | T | C | 1 | a0001c0001t0001g0150 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1331+3639A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151684991 | |||||||
| chr4:151685046 | G | A | 2 | a0002c0002t0001g0037 a0002c0002t0001g0044 |
2 | HG00323.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.1331+3584C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151685046 | |||||||
| chr4:151685109 | C | T | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1331+3521G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151685109 | |||||||
| chr4:151685395 | G | A | 140 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(137): Show |
142 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.1331+3235C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151685395 | |||||||
| chr4:151685421 | T | C | 204 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(201): Show |
212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.1331+3209A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151685421 | |||||||
| chr4:151685430 | C | T | 1 | a0001c0001t0002g0257 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1331+3200G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151685430 | |||||||
| chr4:151685529 | G | T | 2 | a0002c0002t0001g0029 a0002c0002t0001g0052 |
2 | HG02809.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1331+3101C>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151685529 | |||||||
| chr4:151685550 | T | G | 204 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(201): Show |
212 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(209): Show |
intron_variant | MODIFIER | c.1331+3080A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151685550 | |||||||
| chr4:151685571 | C | T | 148 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(145): Show |
150 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.1331+3059G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151685571 | |||||||
| chr4:151685587 | A | T | 1 | a0001c0001t0002g0281 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1331+3043T>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151685587 | |||||||
| chr4:151685666 | A | G | 146 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(143): Show |
148 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.1331+2964T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151685666 | |||||||
| chr4:151685671 | G | A | 146 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(143): Show |
148 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.1331+2959C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151685671 | |||||||
| chr4:151685823 | T | G | 146 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(143): Show |
148 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.1331+2807A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151685823 | |||||||
| chr4:151685890 | AG | A | 145 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(142): Show |
147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1331+2739delC | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151685890 | |||||||
| chr4:151685891 | G | A | 1 | a0001c0001t0001g0144 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1331+2739C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151685891 | |||||||
| chr4:151685896 | T | C | 1 | a0001c0001t0002g0267 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1331+2734A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151685896 | |||||||
| chr4:151686039 | C | T | 145 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(142): Show |
147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1331+2591G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686039 | |||||||
| chr4:151686064 | A | C | 1 | a0001c0001t0002g0224 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1331+2566T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686064 | |||||||
| chr4:151686068 | C | CA | 145 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(142): Show |
147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1331+2561dupT | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686068 | |||||||
| chr4:151686126 | C | T | 145 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(142): Show |
147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1331+2504G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686126 | |||||||
| chr4:151686166 | C | A | 141 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(138): Show |
143 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.1331+2464G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686166 | |||||||
| chr4:151686192 | C | T | 2 | a0001c0001t0001g0090 a0001c0001t0001g0112 |
2 | NA19010.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.1331+2438G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686192 | |||||||
| chr4:151686200 | C | A | 1 | a0001c0001t0001g0292 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1331+2430G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686200 | |||||||
| chr4:151686290 | T | C | 145 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(142): Show |
147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1331+2340A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686290 | |||||||
| chr4:151686304 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1331+2326C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686304 | |||||||
| chr4:151686396 | A | C | 142 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(139): Show |
144 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.1331+2234T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686396 | |||||||
| chr4:151686416 | G | C | 145 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(142): Show |
147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1331+2214C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686416 | |||||||
| chr4:151686434 | A | G | 145 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(142): Show |
147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1331+2196T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686434 | |||||||
| chr4:151686471 | A | G | 145 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(142): Show |
147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1331+2159T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686471 | |||||||
| chr4:151686510 | G | A | 145 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(142): Show |
147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1331+2120C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686510 | |||||||
| chr4:151686535 | T | G | 1 | a0001c0001t0002g0214 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1331+2095A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686535 | |||||||
| chr4:151686652 | G | GC | 69 | a0001c0001t0001g0097 a0001c0001t0001g0145 a0001c0001t0001g0230 others(66): Show |
75 | HG00438.hp2 HG00597.hp2 HG00642.hp1 others(72): Show |
intron_variant | MODIFIER | c.1331+1977dupG | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686652 | |||||||
| chr4:151686652 | G | GCC | 27 | a0001c0001t0001g0108 a0001c0001t0001g0190 a0001c0001t0001g0215 others(24): Show |
29 | HG00140.hp2 HG00323.hp2 HG01109.hp1 others(26): Show |
intron_variant | MODIFIER | c.1331+1976_1331+197 others(6): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686652 | |||||||
| chr4:151686652 | G | GCCC | 15 | a0001c0001t0001g0011 a0001c0012t0001g0275 a0002c0002t0001g0002 others(12): Show |
16 | HG01515.hp1 HG02074.hp2 HG02135.hp2 others(13): Show |
intron_variant | MODIFIER | c.1331+1975_1331+197 others(7): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686652 | |||||||
| chr4:151686652 | G | GCCCCGCC | 33 | a0001c0001t0001g0061 a0001c0001t0001g0065 a0001c0001t0001g0070 others(30): Show |
33 | HG00140.hp1 HG01070.hp1 HG01346.hp2 others(30): Show |
intron_variant | MODIFIER | c.1331+1977_1331+197 others(11): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686652 | |||||||
| chr4:151686652 | G | GCCCCGCC others(1): Show |
51 | a0001c0001t0001g0059 a0001c0001t0001g0063 a0001c0001t0001g0064 others(48): Show |
51 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(48): Show |
intron_variant | MODIFIER | c.1331+1977_1331+197 others(12): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686652 | |||||||
| chr4:151686652 | G | GCCCCGCC others(2): Show |
23 | a0001c0001t0001g0060 a0001c0001t0001g0062 a0001c0001t0001g0067 others(20): Show |
23 | HG00597.hp1 HG00639.hp1 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.1331+1977_1331+197 others(13): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686652 | |||||||
| chr4:151686652 | G | GCCCCGCC others(3): Show |
8 | a0001c0001t0001g0077 a0001c0001t0001g0090 a0001c0001t0001g0095 others(5): Show |
8 | HG01109.hp2 HG02257.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1331+1977_1331+197 others(14): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686652 | |||||||
| chr4:151686652 | G | GCCCCGCC others(4): Show |
3 | a0001c0001t0001g0133 a0001c0001t0001g0176 a0001c0003t0001g0166 |
3 | HG02572.hp1 NA18939.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.1331+1977_1331+197 others(15): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686652 | |||||||
| chr4:151686652 | G | GCCCCGCC others(5): Show |
3 | a0001c0001t0001g0106 a0001c0001t0001g0162 a0001c0003t0001g0165 |
3 | NA18948.hp1 NA18961.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1331+1977_1331+197 others(16): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686652 | |||||||
| chr4:151686652 | G | GCCCCGCC others(6): Show |
2 | a0001c0001t0001g0099 a0001c0001t0001g0183 |
2 | HG01978.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1331+1977_1331+197 others(17): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686652 | |||||||
| chr4:151686652 | GCCCCCC | G | 13 | a0001c0001t0001g0016 a0001c0001t0001g0073 a0001c0001t0001g0076 others(10): Show |
14 | HG01934.hp1 HG01981.hp2 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.1331+1972_1331+197 others(10): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686652 | |||||||
| chr4:151686654 | C | A | 1 | a0001c0001t0002g0267 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1331+1976G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686654 | |||||||
| chr4:151686657 | C | G | 1 | a0001c0001t0001g0122 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1331+1973G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686657 | |||||||
| chr4:151686662 | C | G | 1 | a0001c0001t0001g0068 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1331+1968G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686662 | |||||||
| chr4:151686663 | A | C | 2 | a0001c0001t0001g0068 a0001c0001t0001g0142 |
2 | NA18963.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.1331+1967T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686663 | |||||||
| chr4:151686663 | A | G | 143 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(140): Show |
145 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.1331+1967T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686663 | |||||||
| chr4:151686700 | C | A | 1 | a0001c0001t0001g0190 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1331+1930G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686700 | |||||||
| chr4:151686705 | C | T | 3 | a0001c0001t0002g0248 a0001c0001t0002g0249 a0001c0001t0002g0250 |
3 | HG02155.hp2 NA18612.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.1331+1925G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686705 | |||||||
| chr4:151686721 | T | C | 1 | a0001c0001t0001g0180 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1331+1909A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686721 | |||||||
| chr4:151686729 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1331+1901G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686729 | |||||||
| chr4:151686779 | T | C | 147 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(144): Show |
149 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.1331+1851A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686779 | |||||||
| chr4:151686828 | G | A | 1 | a0001c0001t0002g0109 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1331+1802C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151686828 | |||||||
| chr4:151687069 | C | T | 38 | a0001c0001t0001g0145 a0002c0002t0001g0002 a0002c0002t0001g0008 others(35): Show |
43 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.1331+1561G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151687069 | |||||||
| chr4:151687183 | G | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0255 |
3 | HG01934.hp1 HG01981.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.1331+1447C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151687183 | |||||||
| chr4:151687187 | T | G | 145 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(142): Show |
147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1331+1443A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151687187 | |||||||
| chr4:151687319 | G | A | 1 | a0001c0001t0001g0072 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1331+1311C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151687319 | |||||||
| chr4:151687436 | C | T | 1 | a0005c0007t0002g0025 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1331+1194G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151687436 | |||||||
| chr4:151687721 | T | A | 1 | a0001c0001t0001g0152 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1331+909A>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151687721 | |||||||
| chr4:151687738 | C | T | 9 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(6): Show |
9 | HG01891.hp1 HG02280.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1331+892G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151687738 | |||||||
| chr4:151688003 | G | C | 1 | a0002c0002t0001g0030 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1331+627C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151688003 | |||||||
| chr4:151688137 | C | T | 145 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(142): Show |
147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1331+493G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151688137 | |||||||
| chr4:151688152 | G | A | 145 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(142): Show |
147 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1331+478C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151688152 | |||||||
| chr4:151688178 | G | A | 2 | a0001c0001t0001g0092 a0008c0010t0001g0058 |
2 | HG02523.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.1331+452C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151688178 | |||||||
| chr4:151688404 | C | A | 5 | a0001c0009t0001g0186 a0003c0004t0001g0293 a0003c0004t0001g0294 others(2): Show |
5 | HG01884.hp1 HG02970.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1331+226G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151688404 | |||||||
| chr4:151688542 | A | G | 185 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(182): Show |
191 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.1331+88T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151688542 | |||||||
| chr4:151688548 | A | C | 185 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(182): Show |
191 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(188): Show |
intron_variant | MODIFIER | c.1331+82T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 10/12 | chr4 | 151688548 | |||||||
| chr4:151688768 | TA | T | 197 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(194): Show |
204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
splice_region_variant&intron_variant | LOW | c.1198-6delT | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151688768 | |||||||
| chr4:151688777 | A | G | 1 | a0001c0001t0001g0063 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1198-14T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151688777 | |||||||
| chr4:151688846 | C | CA | 137 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(134): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.1198-84_1198-83ins others(1): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151688846 | |||||||
| chr4:151688876 | T | G | 1 | a0002c0002t0001g0008 | 2 | HG03041.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1198-113A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151688876 | |||||||
| chr4:151688965 | T | C | 188 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(185): Show |
194 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.1198-202A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151688965 | |||||||
| chr4:151689028 | G | C | 1 | a0001c0001t0001g0162 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1198-265C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151689028 | |||||||
| chr4:151689150 | T | C | 5 | a0001c0001t0001g0090 a0001c0001t0001g0110 a0001c0001t0001g0111 others(2): Show |
5 | HG02040.hp2 HG02071.hp2 NA19010.hp1 others(2): Show |
intron_variant | MODIFIER | c.1198-387A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151689150 | |||||||
| chr4:151689166 | C | T | 40 | a0001c0001t0001g0145 a0002c0002t0001g0002 a0002c0002t0001g0008 others(37): Show |
45 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.1198-403G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151689166 | |||||||
| chr4:151689391 | A | G | 143 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(140): Show |
144 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.1198-628T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151689391 | |||||||
| chr4:151689435 | T | G | 149 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(146): Show |
150 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.1198-672A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151689435 | |||||||
| chr4:151689496 | G | A | 1 | a0001c0001t0002g0256 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1198-733C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151689496 | |||||||
| chr4:151689517 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1198-754T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151689517 | |||||||
| chr4:151689698 | A | G | 5 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(2): Show |
5 | HG02280.hp1 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1198-935T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151689698 | |||||||
| chr4:151689742 | T | C | 62 | a0001c0001t0001g0145 a0001c0001t0001g0276 a0001c0001t0001g0277 others(59): Show |
68 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.1198-979A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151689742 | |||||||
| chr4:151689797 | A | G | 42 | a0001c0001t0001g0145 a0001c0001t0001g0288 a0001c0001t0001g0289 others(39): Show |
47 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.1198-1034T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151689797 | |||||||
| chr4:151689807 | C | T | 5 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(2): Show |
5 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1198-1044G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151689807 | |||||||
| chr4:151689980 | G | A | 2 | a0001c0001t0002g0012 a0001c0001t0002g0227 |
3 | HG03669.hp2 HG04184.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.1198-1217C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151689980 | |||||||
| chr4:151690162 | C | T | 13 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0001g0278 others(10): Show |
14 | HG01884.hp2 HG01891.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1198-1399G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151690162 | |||||||
| chr4:151690314 | T | G | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1198-1551A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151690314 | |||||||
| chr4:151690375 | C | T | 2 | a0001c0001t0002g0198 a0001c0001t0002g0281 |
2 | HG00741.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1198-1612G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151690375 | |||||||
| chr4:151690388 | T | G | 40 | a0001c0001t0001g0145 a0002c0002t0001g0002 a0002c0002t0001g0008 others(37): Show |
45 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.1198-1625A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151690388 | |||||||
| chr4:151690465 | T | C | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1198-1702A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151690465 | |||||||
| chr4:151690522 | C | T | 28 | a0001c0001t0001g0011 a0001c0001t0001g0087 a0001c0001t0001g0088 others(25): Show |
29 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.1198-1759G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151690522 | |||||||
| chr4:151690924 | A | G | 9 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(6): Show |
9 | HG01891.hp1 HG02280.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1198-2161T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151690924 | |||||||
| chr4:151690986 | G | C | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1198-2223C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151690986 | |||||||
| chr4:151691297 | T | C | 62 | a0001c0001t0001g0145 a0001c0001t0001g0276 a0001c0001t0001g0277 others(59): Show |
68 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.1198-2534A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151691297 | |||||||
| chr4:151691536 | C | T | 5 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(2): Show |
5 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1198-2773G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151691536 | |||||||
| chr4:151691635 | C | T | 1 | a0001c0001t0002g0283 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1198-2872G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151691635 | |||||||
| chr4:151691842 | G | A | 42 | a0001c0001t0001g0145 a0001c0001t0001g0288 a0001c0001t0001g0289 others(39): Show |
47 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.1198-3079C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151691842 | |||||||
| chr4:151691997 | CAG | C | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1198-3236_1198-323 others(6): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151691997 | |||||||
| chr4:151692083 | G | A | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1198-3320C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151692083 | |||||||
| chr4:151692102 | T | C | 42 | a0001c0001t0001g0145 a0001c0001t0001g0288 a0001c0001t0001g0289 others(39): Show |
47 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.1198-3339A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151692102 | |||||||
| chr4:151692145 | C | G | 4 | a0001c0001t0001g0276 a0001c0012t0001g0275 a0002c0002t0001g0007 others(1): Show |
5 | HG01884.hp2 HG02451.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1198-3382G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151692145 | |||||||
| chr4:151692328 | C | T | 42 | a0001c0001t0001g0145 a0001c0001t0001g0288 a0001c0001t0001g0289 others(39): Show |
47 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.1198-3565G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151692328 | |||||||
| chr4:151692390 | A | G | 42 | a0001c0001t0001g0145 a0001c0001t0001g0288 a0001c0001t0001g0289 others(39): Show |
47 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.1198-3627T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151692390 | |||||||
| chr4:151692434 | T | A | 5 | a0001c0009t0001g0186 a0003c0004t0001g0293 a0003c0004t0001g0294 others(2): Show |
5 | HG01884.hp1 HG02970.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1198-3671A>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151692434 | |||||||
| chr4:151692687 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1198-3924G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151692687 | |||||||
| chr4:151692800 | G | A | 201 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(198): Show |
208 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.1198-4037C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151692800 | |||||||
| chr4:151692951 | G | C | 1 | a0001c0001t0001g0276 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1198-4188C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151692951 | |||||||
| chr4:151693084 | C | T | 2 | a0006c0008t0001g0194 a0006c0008t0001g0195 |
2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1198-4321G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151693084 | |||||||
| chr4:151693092 | C | T | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1198-4329G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151693092 | |||||||
| chr4:151693100 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1198-4337G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151693100 | |||||||
| chr4:151693112 | T | C | 138 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(135): Show |
139 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.1198-4349A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151693112 | |||||||
| chr4:151693176 | TAA | T | 42 | a0001c0001t0001g0145 a0001c0001t0001g0288 a0001c0001t0001g0289 others(39): Show |
47 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.1198-4415_1198-441 others(6): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151693176 | |||||||
| chr4:151693187 | A | T | 1 | a0001c0001t0001g0292 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1198-4424T>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151693187 | |||||||
| chr4:151693281 | T | C | 42 | a0001c0001t0001g0145 a0001c0001t0001g0288 a0001c0001t0001g0289 others(39): Show |
47 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.1198-4518A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151693281 | |||||||
| chr4:151693337 | C | G | 42 | a0001c0001t0001g0145 a0001c0001t0001g0288 a0001c0001t0001g0289 others(39): Show |
47 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.1198-4574G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151693337 | |||||||
| chr4:151693337 | C | T | 5 | a0001c0009t0001g0186 a0003c0004t0001g0293 a0003c0004t0001g0294 others(2): Show |
5 | HG01884.hp1 HG02970.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1198-4574G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151693337 | |||||||
| chr4:151693387 | T | A | 42 | a0001c0001t0001g0145 a0001c0001t0001g0288 a0001c0001t0001g0289 others(39): Show |
47 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.1198-4624A>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151693387 | |||||||
| chr4:151693502 | AC | A | 57 | a0001c0001t0001g0145 a0001c0001t0001g0276 a0001c0001t0001g0277 others(54): Show |
63 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.1198-4740delG | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151693502 | |||||||
| chr4:151693576 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1198-4813T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151693576 | |||||||
| chr4:151693668 | C | G | 6 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(3): Show |
6 | HG02486.hp2 HG03139.hp2 NA18906.hp1 others(3): Show |
intron_variant | MODIFIER | c.1198-4905G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151693668 | |||||||
| chr4:151693712 | G | A | 3 | a0001c0001t0001g0011 a0001c0001t0001g0108 a0001c0001t0001g0215 |
4 | HG00140.hp2 HG01361.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.1198-4949C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151693712 | |||||||
| chr4:151693805 | T | G | 1 | a0001c0001t0001g0180 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1198-5042A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151693805 | |||||||
| chr4:151693828 | G | C | 38 | a0001c0001t0001g0145 a0002c0002t0001g0002 a0002c0002t0001g0008 others(35): Show |
43 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.1198-5065C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151693828 | |||||||
| chr4:151694044 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1198-5281A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151694044 | |||||||
| chr4:151694641 | A | C | 13 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0001g0278 others(10): Show |
14 | HG01884.hp2 HG01891.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1198-5878T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151694641 | |||||||
| chr4:151694865 | A | C | 2 | a0006c0008t0001g0194 a0006c0008t0001g0195 |
2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1198-6102T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151694865 | |||||||
| chr4:151695084 | G | A | 42 | a0001c0001t0001g0145 a0001c0001t0001g0288 a0001c0001t0001g0289 others(39): Show |
47 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.1197+6245C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151695084 | |||||||
| chr4:151695092 | G | A | 1 | a0001c0009t0002g0239 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1197+6237C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151695092 | |||||||
| chr4:151695403 | C | G | 1 | a0001c0001t0001g0241 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1197+5926G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151695403 | |||||||
| chr4:151695543 | G | A | 3 | a0001c0001t0001g0134 a0001c0001t0001g0181 a0002c0002t0001g0051 |
3 | HG02145.hp1 HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1197+5786C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151695543 | |||||||
| chr4:151695608 | G | T | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1197+5721C>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151695608 | |||||||
| chr4:151695732 | C | T | 1 | a0001c0001t0002g0211 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1197+5597G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151695732 | |||||||
| chr4:151695930 | A | AT | 15 | a0001c0001t0001g0061 a0001c0001t0001g0097 a0001c0001t0001g0122 others(12): Show |
16 | HG01106.hp2 HG01361.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.1197+5398dupA | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151695930 | |||||||
| chr4:151695930 | A | ATTTTTTT | 32 | a0001c0001t0001g0145 a0001c0009t0001g0186 a0002c0002t0001g0002 others(29): Show |
37 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1197+5392_1197+539 others(11): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151695930 | |||||||
| chr4:151695930 | A | ATTTTTTT others(3): Show |
1 | a0002c0002t0001g0026 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1197+5389_1197+539 others(14): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151695930 | |||||||
| chr4:151695930 | AT | A | 12 | a0001c0001t0001g0118 a0001c0001t0001g0277 a0001c0001t0001g0278 others(9): Show |
12 | HG00639.hp1 HG01891.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1197+5398delA | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151695930 | |||||||
| chr4:151696164 | A | G | 1 | a0001c0001t0001g0179 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1197+5165T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151696164 | |||||||
| chr4:151696167 | T | G | 40 | a0001c0001t0001g0145 a0002c0002t0001g0002 a0002c0002t0001g0008 others(37): Show |
45 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.1197+5162A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151696167 | |||||||
| chr4:151696293 | C | A | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1197+5036G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151696293 | |||||||
| chr4:151696350 | T | A | 7 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0150 others(4): Show |
7 | HG02055.hp1 HG02451.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1197+4979A>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151696350 | |||||||
| chr4:151696357 | T | C | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1197+4972A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151696357 | |||||||
| chr4:151696427 | G | A | 1 | a0001c0001t0002g0268 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1197+4902C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151696427 | |||||||
| chr4:151696430 | T | C | 62 | a0001c0001t0001g0145 a0001c0001t0001g0276 a0001c0001t0001g0277 others(59): Show |
68 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.1197+4899A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151696430 | |||||||
| chr4:151697016 | T | C | 3 | a0002c0002t0001g0023 a0002c0002t0001g0031 a0002c0002t0001g0033 |
3 | HG03471.hp1 NA18906.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1197+4313A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697016 | |||||||
| chr4:151697229 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1197+4100C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697229 | |||||||
| chr4:151697512 | G | A | 2 | a0006c0008t0001g0194 a0006c0008t0001g0195 |
2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1197+3817C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697512 | |||||||
| chr4:151697536 | C | T | 13 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0001g0278 others(10): Show |
14 | HG01884.hp2 HG01891.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1197+3793G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697536 | |||||||
| chr4:151697671 | A | G | 1 | a0001c0001t0001g0076 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1197+3658T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697671 | |||||||
| chr4:151697832 | G | A | 1 | a0001c0001t0001g0148 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1197+3497C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697832 | |||||||
| chr4:151697917 | C | A | 201 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(198): Show |
208 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(205): Show |
intron_variant | MODIFIER | c.1197+3412G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697917 | |||||||
| chr4:151697937 | A | ATG | 5 | a0001c0001t0002g0196 a0001c0001t0002g0254 a0001c0001t0002g0270 others(2): Show |
5 | HG00741.hp1 HG01975.hp2 NA18945.hp1 others(2): Show |
intron_variant | MODIFIER | c.1197+3390_1197+339 others(6): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697937 | |||||||
| chr4:151697937 | A | ATGTG | 4 | a0003c0004t0001g0293 a0003c0004t0001g0294 a0003c0004t0001g0295 others(1): Show |
4 | HG01884.hp1 HG02970.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1197+3388_1197+339 others(8): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697937 | |||||||
| chr4:151697937 | A | G | 42 | a0001c0001t0001g0145 a0001c0001t0001g0288 a0001c0001t0001g0289 others(39): Show |
47 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.1197+3392T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697937 | |||||||
| chr4:151697943 | G | GTGTGTGT others(97): Show |
1 | a0001c0001t0001g0148 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1197+3385_1197+338 others(108): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697943 | |||||||
| chr4:151697943 | GTGTGTGT others(7): Show |
G | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1197+3372_1197+338 others(18): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697943 | |||||||
| chr4:151697947 | G | GTGTATAT others(11): Show |
1 | a0001c0001t0001g0128 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1197+3381_1197+338 others(22): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697947 | |||||||
| chr4:151697949 | G | GTATATAT others(7): Show |
2 | a0001c0001t0001g0127 a0001c0001t0001g0192 |
2 | NA20129.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1197+3379_1197+338 others(18): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697949 | |||||||
| chr4:151697949 | G | GTATATAT others(9): Show |
3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0002c0002t0001g0055 |
3 | HG03139.hp2 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1197+3379_1197+338 others(20): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697949 | |||||||
| chr4:151697949 | G | GTATATAT others(35): Show |
1 | a0001c0001t0001g0151 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1197+3379_1197+338 others(46): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697949 | |||||||
| chr4:151697949 | G | GTATATAT others(39): Show |
4 | a0001c0001t0001g0097 a0001c0001t0001g0134 a0001c0001t0001g0181 others(1): Show |
4 | HG02055.hp1 HG02145.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1197+3379_1197+338 others(50): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697949 | |||||||
| chr4:151697949 | G | GTATATAT others(41): Show |
1 | a0001c0001t0001g0191 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1197+3379_1197+338 others(52): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697949 | |||||||
| chr4:151697949 | G | GTATATAT others(43): Show |
1 | a0001c0001t0001g0096 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1197+3379_1197+338 others(54): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697949 | |||||||
| chr4:151697949 | G | GTATATAT others(45): Show |
1 | a0001c0001t0001g0150 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1197+3379_1197+338 others(56): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697949 | |||||||
| chr4:151697949 | G | GTATATAT others(71): Show |
1 | a0001c0001t0001g0180 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1197+3379_1197+338 others(82): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697949 | |||||||
| chr4:151697949 | GTGTGTAT others(3): Show |
G | 1 | a0001c0001t0001g0011 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1197+3370_1197+337 others(14): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697949 | |||||||
| chr4:151697949 | GTGTGTAT others(5): Show |
G | 48 | a0001c0001t0001g0063 a0001c0001t0001g0073 a0001c0001t0001g0074 others(45): Show |
48 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(45): Show |
intron_variant | MODIFIER | c.1197+3368_1197+337 others(16): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697949 | |||||||
| chr4:151697949 | GTGTGTAT others(7): Show |
G | 1 | a0001c0001t0001g0087 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1197+3366_1197+337 others(18): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697949 | |||||||
| chr4:151697951 | G | A | 76 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(73): Show |
76 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(73): Show |
intron_variant | MODIFIER | c.1197+3378C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697951 | |||||||
| chr4:151697951 | G | GTATATAT others(3): Show |
2 | a0002c0002t0001g0035 a0002c0002t0001g0038 |
2 | HG01515.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.1197+3377_1197+337 others(14): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697951 | |||||||
| chr4:151697951 | G | GTATATAT others(45): Show |
1 | a0001c0001t0001g0156 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1197+3377_1197+337 others(56): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697951 | |||||||
| chr4:151697951 | GTGTA | G | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0287 |
3 | HG02970.hp1 HG03486.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1197+3374_1197+337 others(8): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697951 | |||||||
| chr4:151697953 | G | A | 82 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(79): Show |
82 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(79): Show |
intron_variant | MODIFIER | c.1197+3376C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697953 | |||||||
| chr4:151697953 | G | GTA | 31 | a0001c0001t0001g0204 a0001c0001t0001g0230 a0001c0001t0001g0255 others(28): Show |
33 | HG00438.hp2 HG00639.hp2 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.1197+3374_1197+337 others(6): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697953 | |||||||
| chr4:151697953 | G | GTATA | 21 | a0001c0001t0001g0016 a0001c0001t0001g0282 a0001c0001t0002g0001 others(18): Show |
23 | HG01361.hp1 HG01934.hp1 HG02056.hp1 others(20): Show |
intron_variant | MODIFIER | c.1197+3372_1197+337 others(8): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697953 | |||||||
| chr4:151697953 | G | GTATATA | 17 | a0001c0001t0001g0016 a0001c0001t0002g0004 a0001c0001t0002g0198 others(14): Show |
17 | HG01109.hp1 HG01192.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.1197+3370_1197+337 others(10): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697953 | |||||||
| chr4:151697953 | G | GTATATAT others(1): Show |
9 | a0001c0001t0001g0145 a0001c0001t0001g0253 a0001c0001t0002g0203 others(6): Show |
11 | HG00597.hp2 HG02074.hp2 HG02129.hp1 others(8): Show |
intron_variant | MODIFIER | c.1197+3368_1197+337 others(12): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697953 | |||||||
| chr4:151697953 | G | GTATATAT others(3): Show |
8 | a0001c0001t0002g0012 a0001c0001t0002g0197 a0001c0001t0002g0247 others(5): Show |
9 | HG00642.hp2 HG02451.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1197+3366_1197+337 others(14): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697953 | |||||||
| chr4:151697953 | G | GTATATAT others(5): Show |
1 | a0002c0002t0001g0023 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1197+3364_1197+337 others(16): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697953 | |||||||
| chr4:151697953 | G | GTATATAT others(7): Show |
3 | a0001c0001t0002g0202 a0001c0001t0002g0286 a0002c0002t0001g0047 |
3 | NA18747.hp1 NA19011.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1197+3362_1197+337 others(18): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697953 | |||||||
| chr4:151697953 | G | GTATATAT others(9): Show |
2 | a0001c0001t0002g0220 a0001c0001t0002g0245 |
2 | HG03688.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.1197+3360_1197+337 others(20): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697953 | |||||||
| chr4:151697953 | G | GTATATAT others(13): Show |
1 | a0001c0001t0002g0005 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1197+3356_1197+337 others(24): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697953 | |||||||
| chr4:151697953 | G | GTGTA | 5 | a0001c0001t0002g0014 a0001c0001t0002g0250 a0001c0009t0002g0239 others(2): Show |
5 | HG02135.hp1 HG02717.hp2 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.1197+3375_1197+337 others(8): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697953 | |||||||
| chr4:151697953 | G | GTGTATA | 12 | a0001c0001t0002g0200 a0001c0001t0002g0208 a0001c0001t0002g0248 others(9): Show |
12 | HG01106.hp1 HG01496.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1197+3375_1197+337 others(10): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697953 | |||||||
| chr4:151697953 | G | GTGTATAT others(1): Show |
8 | a0001c0001t0001g0276 a0001c0001t0002g0246 a0001c0001t0002g0259 others(5): Show |
10 | HG02486.hp1 HG02572.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1197+3375_1197+337 others(12): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697953 | |||||||
| chr4:151697953 | G | GTGTATAT others(7): Show |
1 | a0002c0002t0001g0033 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1197+3375_1197+337 others(18): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697953 | |||||||
| chr4:151697953 | GTATATAT others(9): Show |
G | 1 | a0001c0001t0002g0201 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1197+3360_1197+337 others(20): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697953 | |||||||
| chr4:151697953 | GTATATAT others(17): Show |
G | 1 | a0001c0001t0002g0006 | 3 | HG02055.hp2 HG02922.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1197+3352_1197+337 others(28): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697953 | |||||||
| chr4:151697955 | A | G | 9 | a0001c0001t0001g0096 a0001c0001t0001g0127 a0001c0001t0001g0150 others(6): Show |
9 | HG00323.hp1 HG01255.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1197+3374T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697955 | |||||||
| chr4:151697957 | A | ATATATAT others(37): Show |
1 | a0001c0001t0001g0152 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1197+3371_1197+337 others(48): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697957 | |||||||
| chr4:151697957 | A | ATATATAT others(33): Show |
1 | a0001c0001t0001g0154 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1197+3371_1197+337 others(44): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697957 | |||||||
| chr4:151697965 | A | ATGTGTGT others(37): Show |
1 | a0001c0001t0001g0065 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1197+3363_1197+336 others(48): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697965 | |||||||
| chr4:151697965 | A | ATGTGTGT others(35): Show |
3 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0164 |
3 | HG01981.hp1 NA18957.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.1197+3363_1197+336 others(46): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697965 | |||||||
| chr4:151697965 | A | ATGTGTGT others(33): Show |
25 | a0001c0001t0001g0059 a0001c0001t0001g0061 a0001c0001t0001g0062 others(22): Show |
25 | HG00558.hp1 HG00597.hp1 HG01433.hp1 others(22): Show |
intron_variant | MODIFIER | c.1197+3363_1197+336 others(44): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697965 | |||||||
| chr4:151697965 | A | ATGTGTGT others(31): Show |
6 | a0001c0001t0001g0068 a0001c0001t0001g0131 a0001c0001t0001g0138 others(3): Show |
6 | HG00438.hp1 HG01975.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1197+3363_1197+336 others(42): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697965 | |||||||
| chr4:151697965 | A | ATGTGTGT others(33): Show |
1 | a0001c0001t0001g0071 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1197+3363_1197+336 others(44): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697965 | |||||||
| chr4:151697965 | A | ATGTGTGT others(29): Show |
14 | a0001c0001t0001g0060 a0001c0001t0001g0085 a0001c0001t0001g0086 others(11): Show |
14 | HG01243.hp1 HG01891.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1197+3363_1197+336 others(40): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697965 | |||||||
| chr4:151697965 | A | ATGTGTGT others(31): Show |
3 | a0001c0001t0001g0105 a0001c0001t0001g0146 a0001c0001t0001g0188 |
3 | HG02129.hp2 HG02165.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.1197+3363_1197+336 others(42): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697965 | |||||||
| chr4:151697965 | A | ATGTGTGT others(27): Show |
4 | a0001c0001t0001g0093 a0001c0001t0001g0133 a0001c0001t0001g0175 others(1): Show |
4 | HG02572.hp1 HG03492.hp2 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.1197+3363_1197+336 others(38): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697965 | |||||||
| chr4:151697965 | A | ATGTGTGT others(29): Show |
1 | a0001c0001t0001g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1197+3363_1197+336 others(40): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697965 | |||||||
| chr4:151697965 | A | ATGTGTGT others(25): Show |
4 | a0001c0001t0001g0104 a0001c0001t0001g0132 a0001c0001t0001g0174 others(1): Show |
4 | HG02922.hp1 NA18939.hp1 NA18946.hp1 others(1): Show |
intron_variant | MODIFIER | c.1197+3363_1197+336 others(36): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697965 | |||||||
| chr4:151697965 | A | ATGTGTGT others(57): Show |
1 | a0001c0001t0001g0169 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1197+3363_1197+336 others(68): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697965 | |||||||
| chr4:151697965 | A | ATGTGTGT others(55): Show |
1 | a0001c0001t0001g0170 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1197+3363_1197+336 others(66): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697965 | |||||||
| chr4:151697965 | A | ATGTGTGT others(33): Show |
2 | a0001c0001t0001g0101 a0001c0001t0001g0172 |
2 | HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1197+3363_1197+336 others(44): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697965 | |||||||
| chr4:151697965 | A | ATGTGTGT others(31): Show |
1 | a0001c0001t0001g0171 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1197+3363_1197+336 others(42): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697965 | |||||||
| chr4:151697965 | A | ATGTGTGT others(27): Show |
2 | a0001c0001t0001g0126 a0001c0001t0001g0179 |
2 | HG00280.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1197+3363_1197+336 others(38): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697965 | |||||||
| chr4:151697967 | A | G | 64 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(61): Show |
64 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.1197+3362T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697967 | |||||||
| chr4:151697977 | A | ATATGTG | 3 | a0001c0001t0001g0134 a0001c0001t0001g0181 a0002c0002t0001g0051 |
3 | HG02145.hp1 HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1197+3351_1197+335 others(10): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697977 | |||||||
| chr4:151697979 | A | G | 50 | a0001c0001t0001g0011 a0001c0001t0001g0063 a0001c0001t0001g0073 others(47): Show |
51 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.1197+3350T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697979 | |||||||
| chr4:151697981 | A | G | 50 | a0001c0001t0001g0011 a0001c0001t0001g0063 a0001c0001t0001g0073 others(47): Show |
51 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.1197+3348T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697981 | |||||||
| chr4:151697983 | A | G | 5 | a0001c0001t0001g0096 a0001c0001t0001g0150 a0001c0001t0001g0152 others(2): Show |
5 | HG03130.hp1 HG03209.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1197+3346T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697983 | |||||||
| chr4:151697985 | A | G | 7 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0150 others(4): Show |
7 | HG02055.hp1 HG02451.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.1197+3344T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151697985 | |||||||
| chr4:151698256 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1197+3073G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151698256 | |||||||
| chr4:151698265 | A | G | 9 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(6): Show |
9 | HG01891.hp1 HG02280.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.1197+3064T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151698265 | |||||||
| chr4:151698298 | T | A | 1 | a0001c0001t0002g0244 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1197+3031A>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151698298 | |||||||
| chr4:151698408 | A | C | 3 | a0001c0001t0001g0152 a0001c0001t0001g0154 a0001c0001t0001g0191 |
3 | HG03209.hp1 HG03225.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1197+2921T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151698408 | |||||||
| chr4:151698810 | C | T | 1 | a0001c0001t0002g0240 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1197+2519G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151698810 | |||||||
| chr4:151698811 | C | T | 1 | a0001c0001t0002g0262 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1197+2518G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151698811 | |||||||
| chr4:151698849 | C | T | 1 | a0001c0001t0002g0109 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1197+2480G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151698849 | |||||||
| chr4:151698878 | T | G | 1 | a0001c0001t0001g0060 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1197+2451A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151698878 | |||||||
| chr4:151698966 | G | T | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1197+2363C>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151698966 | |||||||
| chr4:151698987 | T | G | 1 | a0002c0002t0001g0056 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1197+2342A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151698987 | |||||||
| chr4:151699071 | G | A | 1 | a0001c0001t0002g0201 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1197+2258C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151699071 | |||||||
| chr4:151699344 | G | A | 9 | a0001c0001t0001g0073 a0001c0001t0001g0076 a0001c0001t0001g0078 others(6): Show |
9 | NA18612.hp2 NA18977.hp2 NA18998.hp2 others(6): Show |
intron_variant | MODIFIER | c.1197+1985C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151699344 | |||||||
| chr4:151699387 | C | CA | 50 | a0001c0001t0001g0090 a0001c0001t0001g0097 a0001c0001t0001g0110 others(47): Show |
55 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.1197+1941dupT | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151699387 | |||||||
| chr4:151699387 | CA | C | 12 | a0001c0001t0001g0078 a0001c0001t0001g0082 a0001c0001t0001g0084 others(9): Show |
12 | HG01891.hp1 HG02486.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1197+1941delT | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151699387 | |||||||
| chr4:151699452 | A | G | 13 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0001g0278 others(10): Show |
14 | HG01884.hp2 HG01891.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.1197+1877T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151699452 | |||||||
| chr4:151699636 | C | T | 2 | a0006c0008t0001g0194 a0006c0008t0001g0195 |
2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1197+1693G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151699636 | |||||||
| chr4:151699737 | A | G | 40 | a0001c0001t0001g0145 a0002c0002t0001g0002 a0002c0002t0001g0008 others(37): Show |
45 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.1197+1592T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151699737 | |||||||
| chr4:151699777 | T | TAC | 55 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0117 others(52): Show |
60 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.1197+1550_1197+155 others(6): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151699777 | |||||||
| chr4:151699777 | T | TACAC | 5 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(2): Show |
5 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1197+1548_1197+155 others(8): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151699777 | |||||||
| chr4:151699998 | A | C | 50 | a0001c0001t0001g0011 a0001c0001t0001g0063 a0001c0001t0001g0073 others(47): Show |
51 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.1197+1331T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151699998 | |||||||
| chr4:151700085 | C | T | 50 | a0001c0001t0001g0011 a0001c0001t0001g0063 a0001c0001t0001g0073 others(47): Show |
51 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.1197+1244G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151700085 | |||||||
| chr4:151700546 | A | T | 1 | a0001c0001t0001g0105 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1197+783T>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151700546 | |||||||
| chr4:151700617 | A | G | 1 | a0001c0009t0001g0186 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1197+712T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151700617 | |||||||
| chr4:151700710 | C | T | 1 | a0001c0001t0002g0232 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1197+619G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151700710 | |||||||
| chr4:151700983 | T | C | 2 | a0001c0001t0001g0182 a0001c0001t0001g0185 |
2 | HG03579.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1197+346A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151700983 | |||||||
| chr4:151701070 | T | C | 4 | a0003c0004t0001g0293 a0003c0004t0001g0294 a0003c0004t0001g0295 others(1): Show |
4 | HG01884.hp1 HG02970.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1197+259A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151701070 | |||||||
| chr4:151701288 | C | T | 5 | a0001c0001t0001g0204 a0001c0001t0002g0017 a0001c0001t0002g0285 others(2): Show |
6 | HG01928.hp1 NA18949.hp1 NA18949.hp2 others(3): Show |
intron_variant | MODIFIER | c.1197+41G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 9/12 | chr4 | 151701288 | |||||||
| chr4:151701647 | C | G | 1 | a0001c0001t0001g0292 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1008-129G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 8/12 | chr4 | 151701647 | |||||||
| chr4:151701651 | T | G | 2 | a0001c0001t0002g0232 a0001c0001t0002g0245 |
2 | HG03688.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.1008-133A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 8/12 | chr4 | 151701651 | |||||||
| chr4:151702133 | T | C | 293 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0059 others(290): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.1008-615A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 8/12 | chr4 | 151702133 | |||||||
| chr4:151702151 | C | T | 1 | a0001c0001t0001g0083 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1008-633G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 8/12 | chr4 | 151702151 | |||||||
| chr4:151702185 | T | C | 4 | a0001c0001t0002g0233 a0001c0009t0001g0186 a0006c0008t0001g0194 others(1): Show |
4 | HG03209.hp2 HG03453.hp2 HG03654.hp2 others(1): Show |
intron_variant | MODIFIER | c.1008-667A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 8/12 | chr4 | 151702185 | |||||||
| chr4:151702245 | AT | A | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1008-728delA | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 8/12 | chr4 | 151702245 | |||||||
| chr4:151702333 | A | C | 1 | a0001c0001t0001g0118 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1008-815T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 8/12 | chr4 | 151702333 | |||||||
| chr4:151702343 | A | G | 38 | a0001c0001t0001g0145 a0002c0002t0001g0002 a0002c0002t0001g0008 others(35): Show |
43 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.1008-825T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 8/12 | chr4 | 151702343 | |||||||
| chr4:151702702 | C | T | 1 | a0002c0002t0001g0051 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1007+1149G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 8/12 | chr4 | 151702702 | |||||||
| chr4:151703269 | C | G | 1 | a0003c0004t0001g0296 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1007+582G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 8/12 | chr4 | 151703269 | |||||||
| chr4:151703399 | T | C | 1 | a0001c0001t0001g0290 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1007+452A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 8/12 | chr4 | 151703399 | |||||||
| chr4:151703815 | G | A | 10 | a0001c0001t0001g0142 a0001c0001t0001g0157 a0001c0001t0001g0158 others(7): Show |
11 | HG01884.hp2 HG01891.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1007+36C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 8/12 | chr4 | 151703815 | |||||||
| chr4:151703820 | A | G | 43 | a0001c0001t0001g0145 a0001c0001t0001g0277 a0001c0001t0001g0278 others(40): Show |
48 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(45): Show |
intron_variant | MODIFIER | c.1007+31T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 8/12 | chr4 | 151703820 | |||||||
| chr4:151704063 | G | A | 1 | a0001c0001t0002g0109 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.963-168C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 7/12 | chr4 | 151704063 | |||||||
| chr4:151704080 | C | CT | 6 | a0001c0001t0001g0152 a0001c0001t0001g0154 a0001c0001t0001g0277 others(3): Show |
6 | HG01243.hp2 HG02145.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.963-186dupA | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 7/12 | chr4 | 151704080 | |||||||
| chr4:151704080 | CT | C | 17 | a0001c0001t0001g0176 a0001c0001t0001g0288 a0001c0001t0001g0289 others(14): Show |
21 | HG00597.hp2 HG01515.hp1 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.963-186delA | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 7/12 | chr4 | 151704080 | |||||||
| chr4:151704193 | T | C | 6 | a0002c0002t0001g0007 a0002c0002t0001g0018 a0002c0002t0001g0019 others(3): Show |
7 | HG01884.hp2 HG01891.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.963-298A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 7/12 | chr4 | 151704193 | |||||||
| chr4:151704208 | T | C | 1 | a0001c0001t0002g0210 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.963-313A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 7/12 | chr4 | 151704208 | |||||||
| chr4:151704225 | T | C | 38 | a0001c0001t0001g0145 a0002c0002t0001g0002 a0002c0002t0001g0008 others(35): Show |
43 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.963-330A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 7/12 | chr4 | 151704225 | |||||||
| chr4:151704265 | T | C | 4 | a0001c0001t0002g0193 a0001c0001t0002g0213 a0001c0001t0002g0234 others(1): Show |
4 | HG00438.hp2 NA19010.hp2 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.963-370A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 7/12 | chr4 | 151704265 | |||||||
| chr4:151704294 | A | G | 50 | a0001c0001t0001g0145 a0001c0001t0001g0288 a0001c0001t0001g0289 others(47): Show |
56 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.963-399T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 7/12 | chr4 | 151704294 | |||||||
| chr4:151704297 | T | C | 2 | a0001c0001t0002g0012 a0001c0001t0002g0227 |
3 | HG03669.hp2 HG04184.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.963-402A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 7/12 | chr4 | 151704297 | |||||||
| chr4:151704310 | A | C | 1 | a0001c0001t0001g0163 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.963-415T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 7/12 | chr4 | 151704310 | |||||||
| chr4:151704493 | G | A | 1 | a0002c0002t0001g0022 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.963-598C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 7/12 | chr4 | 151704493 | |||||||
| chr4:151704539 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.963-644G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 7/12 | chr4 | 151704539 | |||||||
| chr4:151704542 | C | T | 3 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0114 |
3 | HG01070.hp1 HG01192.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.962+643G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 7/12 | chr4 | 151704542 | |||||||
| chr4:151704552 | T | C | 12 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(9): Show |
13 | HG01884.hp2 HG01891.hp1 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.962+633A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 7/12 | chr4 | 151704552 | |||||||
| chr4:151704643 | C | T | 6 | a0002c0002t0001g0007 a0002c0002t0001g0018 a0002c0002t0001g0019 others(3): Show |
7 | HG01884.hp2 HG01891.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.962+542G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 7/12 | chr4 | 151704643 | |||||||
| chr4:151704738 | C | A | 1 | a0001c0001t0001g0276 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.962+447G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 7/12 | chr4 | 151704738 | |||||||
| chr4:151704742 | G | C | 46 | a0001c0001t0001g0145 a0002c0002t0001g0002 a0002c0002t0001g0007 others(43): Show |
52 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.962+443C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 7/12 | chr4 | 151704742 | |||||||
| chr4:151704868 | C | T | 5 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(2): Show |
5 | HG02280.hp1 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.962+317G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 7/12 | chr4 | 151704868 | |||||||
| chr4:151705142 | C | T | 5 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(2): Show |
5 | HG02280.hp1 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.962+43G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 7/12 | chr4 | 151705142 | |||||||
| chr4:151705164 | C | T | 1 | a0001c0001t0001g0292 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.962+21G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 7/12 | chr4 | 151705164 | |||||||
| chr4:151705325 | A | G | 7 | a0002c0002t0001g0008 a0002c0002t0001g0023 a0002c0002t0001g0027 others(4): Show |
8 | HG02630.hp1 HG03041.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.878-56T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 6/12 | chr4 | 151705325 | |||||||
| chr4:151705363 | TA | T | 26 | a0001c0001t0001g0063 a0001c0001t0001g0094 a0001c0001t0001g0117 others(23): Show |
27 | HG00280.hp2 HG00323.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.878-95delT | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 6/12 | chr4 | 151705363 | |||||||
| chr4:151705486 | G | A | 1 | a0001c0012t0001g0275 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.878-217C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 6/12 | chr4 | 151705486 | |||||||
| chr4:151705732 | C | A | 1 | a0001c0001t0001g0160 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.878-463G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 6/12 | chr4 | 151705732 | |||||||
| chr4:151705766 | A | G | 2 | a0001c0001t0002g0012 a0001c0001t0002g0227 |
3 | HG03669.hp2 HG04184.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.878-497T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 6/12 | chr4 | 151705766 | |||||||
| chr4:151706078 | G | C | 50 | a0001c0001t0001g0011 a0001c0001t0001g0063 a0001c0001t0001g0073 others(47): Show |
51 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.878-809C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 6/12 | chr4 | 151706078 | |||||||
| chr4:151706116 | A | G | 1 | a0001c0001t0001g0160 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.878-847T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 6/12 | chr4 | 151706116 | |||||||
| chr4:151706132 | A | G | 3 | a0001c0001t0001g0093 a0001c0001t0001g0178 a0001c0001t0001g0187 |
3 | NA18953.hp2 NA19006.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.878-863T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 6/12 | chr4 | 151706132 | |||||||
| chr4:151706194 | G | A | 38 | a0001c0001t0001g0145 a0002c0002t0001g0002 a0002c0002t0001g0008 others(35): Show |
43 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.878-925C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 6/12 | chr4 | 151706194 | |||||||
| chr4:151706216 | A | T | 1 | a0001c0001t0001g0156 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.878-947T>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 6/12 | chr4 | 151706216 | |||||||
| chr4:151706287 | G | A | 1 | a0001c0001t0001g0016 | 2 | HG01934.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.878-1018C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 6/12 | chr4 | 151706287 | |||||||
| chr4:151706368 | GGCT | G | 50 | a0001c0001t0001g0011 a0001c0001t0001g0063 a0001c0001t0001g0073 others(47): Show |
51 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.878-1102_878-1100d others(5): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 6/12 | chr4 | 151706368 | |||||||
| chr4:151706409 | C | T | 5 | a0001c0001t0002g0246 a0001c0001t0002g0247 a0001c0001t0002g0248 others(2): Show |
5 | HG02155.hp2 NA18612.hp1 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.878-1140G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 6/12 | chr4 | 151706409 | |||||||
| chr4:151706421 | C | CACT | 50 | a0001c0001t0001g0145 a0001c0001t0001g0288 a0001c0001t0001g0289 others(47): Show |
56 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.878-1155_878-1153d others(5): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 6/12 | chr4 | 151706421 | |||||||
| chr4:151706647 | C | G | 2 | a0001c0001t0001g0288 a0001c0001t0001g0291 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.877+1341G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 6/12 | chr4 | 151706647 | |||||||
| chr4:151706675 | G | GGC | 195 | a0001c0001t0001g0011 a0001c0001t0001g0060 a0001c0001t0001g0061 others(192): Show |
202 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.877+1312_877+1313i others(4): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 6/12 | chr4 | 151706675 | |||||||
| chr4:151706751 | T | C | 2 | a0001c0001t0001g0276 a0001c0012t0001g0275 |
2 | HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.877+1237A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 6/12 | chr4 | 151706751 | |||||||
| chr4:151706793 | T | C | 46 | a0001c0001t0001g0145 a0002c0002t0001g0002 a0002c0002t0001g0007 others(43): Show |
52 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.877+1195A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 6/12 | chr4 | 151706793 | |||||||
| chr4:151706807 | G | A | 46 | a0001c0001t0001g0145 a0002c0002t0001g0002 a0002c0002t0001g0007 others(43): Show |
52 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.877+1181C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 6/12 | chr4 | 151706807 | |||||||
| chr4:151706964 | G | T | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.877+1024C>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 6/12 | chr4 | 151706964 | |||||||
| chr4:151707307 | T | C | 1 | a0002c0002t0001g0037 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.877+681A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 6/12 | chr4 | 151707307 | |||||||
| chr4:151707519 | G | C | 38 | a0001c0001t0001g0145 a0002c0002t0001g0002 a0002c0002t0001g0008 others(35): Show |
43 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.877+469C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 6/12 | chr4 | 151707519 | |||||||
| chr4:151707676 | G | A | 4 | a0001c0001t0002g0014 a0001c0001t0002g0197 a0001c0001t0002g0236 others(1): Show |
5 | HG02135.hp1 HG02523.hp1 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.877+312C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 6/12 | chr4 | 151707676 | |||||||
| chr4:151707680 | T | A | 1 | a0001c0001t0002g0109 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.877+308A>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 6/12 | chr4 | 151707680 | |||||||
| chr4:151708234 | G | T | 1 | a0001c0001t0002g0283 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.764-133C>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151708234 | |||||||
| chr4:151708468 | G | T | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.764-367C>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151708468 | |||||||
| chr4:151708471 | GT | G | 5 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(2): Show |
5 | HG02280.hp1 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.764-371delA | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151708471 | |||||||
| chr4:151709234 | C | T | 1 | a0001c0001t0002g0272 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.764-1133G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151709234 | |||||||
| chr4:151709266 | C | T | 2 | a0006c0008t0001g0194 a0006c0008t0001g0195 |
2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.764-1165G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151709266 | |||||||
| chr4:151709775 | CTATA | C | 193 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(190): Show |
200 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(197): Show |
intron_variant | MODIFIER | c.764-1678_764-1675d others(6): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151709775 | |||||||
| chr4:151709798 | T | C | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.764-1697A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151709798 | |||||||
| chr4:151709835 | C | T | 2 | a0001c0001t0001g0092 a0008c0010t0001g0058 |
2 | HG02523.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.764-1734G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151709835 | |||||||
| chr4:151710032 | A | C | 38 | a0001c0001t0001g0145 a0002c0002t0001g0002 a0002c0002t0001g0008 others(35): Show |
43 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.764-1931T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151710032 | |||||||
| chr4:151710049 | C | T | 5 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(2): Show |
5 | HG02280.hp1 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.764-1948G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151710049 | |||||||
| chr4:151710159 | T | A | 38 | a0001c0001t0001g0145 a0002c0002t0001g0002 a0002c0002t0001g0008 others(35): Show |
43 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.764-2058A>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151710159 | |||||||
| chr4:151710248 | A | G | 2 | a0001c0001t0001g0083 a0001c0009t0002g0239 |
2 | NA18939.hp2 NA18977.hp2 |
intron_variant | MODIFIER | c.764-2147T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151710248 | |||||||
| chr4:151710320 | A | G | 140 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(137): Show |
141 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.764-2219T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151710320 | |||||||
| chr4:151710439 | C | A | 3 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 |
3 | HG02145.hp2 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.764-2338G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151710439 | |||||||
| chr4:151710485 | G | A | 197 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(194): Show |
204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.764-2384C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151710485 | |||||||
| chr4:151710668 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.764-2567C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151710668 | |||||||
| chr4:151710745 | A | T | 4 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0175 others(1): Show |
4 | HG03492.hp2 HG03654.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.764-2644T>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151710745 | |||||||
| chr4:151710775 | C | T | 3 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 |
3 | HG01243.hp1 HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.764-2674G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151710775 | |||||||
| chr4:151710992 | C | T | 4 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(1): Show |
4 | HG02257.hp1 HG02572.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.764-2891G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151710992 | |||||||
| chr4:151711077 | C | T | 6 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(3): Show |
6 | HG02486.hp2 HG03139.hp2 NA18906.hp1 others(3): Show |
intron_variant | MODIFIER | c.764-2976G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151711077 | |||||||
| chr4:151711225 | T | A | 1 | a0001c0001t0001g0116 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.764-3124A>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151711225 | |||||||
| chr4:151711249 | T | C | 5 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(2): Show |
5 | HG02280.hp1 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.764-3148A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151711249 | |||||||
| chr4:151711305 | C | A | 2 | a0001c0001t0002g0272 a0001c0001t0002g0273 |
2 | HG00642.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.764-3204G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151711305 | |||||||
| chr4:151711817 | C | T | 37 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0009 others(34): Show |
42 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.764-3716G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151711817 | |||||||
| chr4:151711821 | G | A | 1 | a0001c0001t0002g0285 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.764-3720C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151711821 | |||||||
| chr4:151711853 | T | C | 1 | a0004c0006t0001g0050 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.764-3752A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151711853 | |||||||
| chr4:151711949 | G | T | 1 | a0001c0001t0001g0274 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.764-3848C>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151711949 | |||||||
| chr4:151712515 | C | T | 197 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(194): Show |
204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.763+3494G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151712515 | |||||||
| chr4:151712693 | C | G | 1 | a0001c0001t0001g0148 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.763+3316G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151712693 | |||||||
| chr4:151712780 | A | C | 2 | a0001c0001t0002g0259 a0001c0001t0002g0260 |
2 | NA19057.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.763+3229T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151712780 | |||||||
| chr4:151712902 | G | A | 5 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(2): Show |
5 | HG02280.hp1 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.763+3107C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151712902 | |||||||
| chr4:151712969 | C | T | 37 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0009 others(34): Show |
42 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.763+3040G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151712969 | |||||||
| chr4:151713085 | A | T | 10 | a0001c0001t0001g0276 a0001c0012t0001g0275 a0002c0002t0001g0007 others(7): Show |
11 | HG01884.hp2 HG01891.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.763+2924T>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151713085 | |||||||
| chr4:151713278 | C | T | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.763+2731G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151713278 | |||||||
| chr4:151713370 | C | T | 2 | a0002c0002t0001g0007 a0002c0002t0001g0018 |
3 | HG01884.hp2 HG02572.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.763+2639G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151713370 | |||||||
| chr4:151713417 | G | A | 4 | a0002c0002t0001g0019 a0002c0002t0001g0020 a0002c0002t0001g0021 others(1): Show |
4 | HG01891.hp1 HG02630.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.763+2592C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151713417 | |||||||
| chr4:151713447 | C | T | 1 | a0001c0009t0001g0186 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.763+2562G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151713447 | |||||||
| chr4:151713656 | A | G | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.763+2353T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151713656 | |||||||
| chr4:151714126 | G | A | 2 | a0001c0001t0002g0003 a0001c0001t0002g0217 |
4 | HG00639.hp2 HG00741.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.763+1883C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151714126 | |||||||
| chr4:151714435 | C | A | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.763+1574G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151714435 | |||||||
| chr4:151714599 | C | T | 4 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(1): Show |
4 | HG02965.hp1 HG03195.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.763+1410G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151714599 | |||||||
| chr4:151714600 | G | A | 5 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(2): Show |
5 | HG02280.hp1 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.763+1409C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151714600 | |||||||
| chr4:151714651 | A | G | 197 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(194): Show |
204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.763+1358T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151714651 | |||||||
| chr4:151715012 | G | A | 2 | a0001c0001t0002g0270 a0001c0001t0002g0271 |
2 | NA18945.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.763+997C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151715012 | |||||||
| chr4:151715159 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.763+850A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151715159 | |||||||
| chr4:151715499 | A | G | 1 | a0001c0001t0002g0285 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.763+510T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 5/12 | chr4 | 151715499 | |||||||
| chr4:151716236 | A | G | 1 | a0001c0001t0001g0078 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.641-105T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 4/12 | chr4 | 151716236 | |||||||
| chr4:151716277 | C | CT | 10 | a0001c0001t0001g0070 a0001c0001t0001g0073 a0001c0001t0001g0097 others(7): Show |
10 | HG01169.hp1 HG01175.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.641-147dupA | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 4/12 | chr4 | 151716277 | |||||||
| chr4:151716277 | CT | C | 13 | a0001c0001t0001g0091 a0001c0001t0001g0117 a0001c0001t0001g0123 others(10): Show |
13 | HG01070.hp1 HG01515.hp1 HG02523.hp2 others(10): Show |
intron_variant | MODIFIER | c.641-147delA | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 4/12 | chr4 | 151716277 | |||||||
| chr4:151716370 | A | G | 1 | a0001c0001t0001g0292 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.641-239T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 4/12 | chr4 | 151716370 | |||||||
| chr4:151716473 | G | A | 1 | a0001c0001t0002g0238 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.641-342C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 4/12 | chr4 | 151716473 | |||||||
| chr4:151716505 | G | A | 17 | a0002c0002t0001g0002 a0002c0002t0001g0009 a0002c0002t0001g0010 others(14): Show |
21 | HG00597.hp2 HG01109.hp1 HG02056.hp2 others(18): Show |
intron_variant | MODIFIER | c.640+371C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 4/12 | chr4 | 151716505 | |||||||
| chr4:151716548 | C | T | 24 | a0002c0002t0001g0002 a0002c0002t0001g0009 a0002c0002t0001g0010 others(21): Show |
28 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.640+328G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 4/12 | chr4 | 151716548 | |||||||
| chr4:151716870 | G | A | 1 | a0001c0001t0002g0250 | 1 | NA18612.hp1 | splice_region_variant&intron_variant | LOW | c.640+6C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 4/12 | chr4 | 151716870 | |||||||
| chr4:151717163 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.442-89G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 3/12 | chr4 | 151717163 | |||||||
| chr4:151717482 | T | C | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-408A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 3/12 | chr4 | 151717482 | |||||||
| chr4:151717653 | C | T | 1 | a0001c0001t0001g0292 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.442-579G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 3/12 | chr4 | 151717653 | |||||||
| chr4:151717708 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.442-634G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 3/12 | chr4 | 151717708 | |||||||
| chr4:151717879 | C | G | 2 | a0001c0001t0001g0276 a0001c0012t0001g0275 |
2 | HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.442-805G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 3/12 | chr4 | 151717879 | |||||||
| chr4:151717919 | G | A | 1 | a0001c0001t0002g0208 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.442-845C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 3/12 | chr4 | 151717919 | |||||||
| chr4:151717956 | A | C | 1 | a0001c0001t0001g0151 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.442-882T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 3/12 | chr4 | 151717956 | |||||||
| chr4:151717957 | G | C | 1 | a0001c0001t0001g0151 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.442-883C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 3/12 | chr4 | 151717957 | |||||||
| chr4:151717959 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.442-885A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 3/12 | chr4 | 151717959 | |||||||
| chr4:151717962 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.442-888A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 3/12 | chr4 | 151717962 | |||||||
| chr4:151717963 | G | C | 1 | a0001c0001t0001g0151 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.442-889C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 3/12 | chr4 | 151717963 | |||||||
| chr4:151718095 | C | T | 1 | a0001c0001t0001g0292 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.442-1021G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 3/12 | chr4 | 151718095 | |||||||
| chr4:151718124 | A | T | 1 | a0001c0001t0002g0198 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.442-1050T>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 3/12 | chr4 | 151718124 | |||||||
| chr4:151718132 | G | A | 28 | a0001c0001t0001g0011 a0001c0001t0001g0087 a0001c0001t0001g0088 others(25): Show |
29 | HG00140.hp1 HG00140.hp2 HG00558.hp2 others(26): Show |
intron_variant | MODIFIER | c.442-1058C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 3/12 | chr4 | 151718132 | |||||||
| chr4:151718137 | T | G | 1 | a0001c0001t0001g0073 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.442-1063A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 3/12 | chr4 | 151718137 | |||||||
| chr4:151718762 | A | ATTTCAGT others(3): Show |
1 | a0001c0001t0001g0073 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.441+653_441+662dup others(10): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 3/12 | chr4 | 151718762 | |||||||
| chr4:151718887 | AGTAACTG others(10): Show |
A | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+521_441+537del others(17): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 3/12 | chr4 | 151718887 | |||||||
| chr4:151719147 | GC | G | 3 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0077 |
3 | HG01109.hp2 HG01175.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.441+277delG | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 3/12 | chr4 | 151719147 | |||||||
| chr4:151719153 | A | G | 260 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(257): Show |
278 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.441+272T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 3/12 | chr4 | 151719153 | |||||||
| chr4:151719235 | C | T | 191 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(188): Show |
198 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.441+190G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 3/12 | chr4 | 151719235 | |||||||
| chr4:151719242 | C | T | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.441+183G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 3/12 | chr4 | 151719242 | |||||||
| chr4:151719262 | G | A | 2 | a0001c0001t0001g0097 a0001c0001t0001g0180 |
2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.441+163C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 3/12 | chr4 | 151719262 | |||||||
| chr4:151719287 | C | T | 3 | a0001c0001t0001g0134 a0001c0001t0001g0181 a0002c0002t0001g0051 |
3 | HG02145.hp1 HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.441+138G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 3/12 | chr4 | 151719287 | |||||||
| chr4:151719364 | C | G | 2 | a0001c0001t0001g0276 a0001c0012t0001g0275 |
2 | HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.441+61G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 3/12 | chr4 | 151719364 | |||||||
| chr4:151719573 | C | T | 1 | a0001c0001t0002g0225 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.328-35G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151719573 | |||||||
| chr4:151719574 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.328-36C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151719574 | |||||||
| chr4:151719614 | G | A | 3 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0175 |
3 | HG03492.hp2 HG03688.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.328-76C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151719614 | |||||||
| chr4:151719658 | C | T | 1 | a0001c0001t0002g0262 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.328-120G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151719658 | |||||||
| chr4:151719743 | G | A | 5 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(2): Show |
5 | HG02280.hp1 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.328-205C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151719743 | |||||||
| chr4:151719764 | A | T | 2 | a0002c0002t0001g0053 a0002c0002t0001g0054 |
2 | HG02717.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.328-226T>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151719764 | |||||||
| chr4:151719827 | G | A | 1 | a0001c0001t0001g0101 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.328-289C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151719827 | |||||||
| chr4:151719857 | T | C | 1 | a0001c0001t0001g0292 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.328-319A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151719857 | |||||||
| chr4:151719963 | T | C | 2 | a0005c0007t0002g0024 a0005c0007t0002g0025 |
2 | HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.328-425A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151719963 | |||||||
| chr4:151720050 | G | A | 50 | a0001c0001t0001g0011 a0001c0001t0001g0063 a0001c0001t0001g0073 others(47): Show |
51 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.328-512C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151720050 | |||||||
| chr4:151720070 | C | T | 1 | a0001c0009t0001g0186 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.328-532G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151720070 | |||||||
| chr4:151720434 | C | A | 2 | a0006c0008t0001g0194 a0006c0008t0001g0195 |
2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.328-896G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151720434 | |||||||
| chr4:151720489 | G | C | 2 | a0006c0008t0001g0194 a0006c0008t0001g0195 |
2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.328-951C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151720489 | |||||||
| chr4:151720504 | T | C | 8 | a0002c0002t0001g0007 a0002c0002t0001g0018 a0002c0002t0001g0019 others(5): Show |
9 | HG01884.hp2 HG01891.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.328-966A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151720504 | |||||||
| chr4:151720515 | C | T | 6 | a0002c0002t0001g0007 a0002c0002t0001g0018 a0002c0002t0001g0019 others(3): Show |
7 | HG01884.hp2 HG01891.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.328-977G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151720515 | |||||||
| chr4:151720789 | G | C | 197 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(194): Show |
204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.328-1251C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151720789 | |||||||
| chr4:151720809 | A | G | 10 | a0001c0001t0001g0276 a0001c0012t0001g0275 a0002c0002t0001g0007 others(7): Show |
11 | HG01884.hp2 HG01891.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.328-1271T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151720809 | |||||||
| chr4:151720844 | TGGGATGA others(3): Show |
T | 6 | a0002c0002t0001g0007 a0002c0002t0001g0018 a0002c0002t0001g0019 others(3): Show |
7 | HG01884.hp2 HG01891.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.328-1316_328-1307d others(12): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151720844 | |||||||
| chr4:151721023 | G | T | 1 | a0001c0001t0001g0152 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.328-1485C>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151721023 | |||||||
| chr4:151721025 | T | G | 1 | a0001c0001t0001g0079 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.328-1487A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151721025 | |||||||
| chr4:151721221 | G | A | 5 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(2): Show |
5 | HG02280.hp1 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.328-1683C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151721221 | |||||||
| chr4:151721422 | G | C | 1 | a0001c0001t0002g0217 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.328-1884C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151721422 | |||||||
| chr4:151721446 | A | C | 1 | a0001c0001t0001g0153 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.328-1908T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151721446 | |||||||
| chr4:151721491 | C | T | 1 | a0002c0002t0001g0046 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.328-1953G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151721491 | |||||||
| chr4:151721644 | G | A | 1 | a0001c0001t0002g0210 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.328-2106C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151721644 | |||||||
| chr4:151721872 | C | T | 2 | a0006c0008t0001g0194 a0006c0008t0001g0195 |
2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.328-2334G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151721872 | |||||||
| chr4:151722032 | G | A | 197 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(194): Show |
204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.328-2494C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151722032 | |||||||
| chr4:151722237 | T | A | 5 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(2): Show |
5 | HG02280.hp1 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.328-2699A>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151722237 | |||||||
| chr4:151722408 | C | T | 1 | a0001c0001t0001g0287 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.328-2870G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151722408 | |||||||
| chr4:151722601 | C | T | 1 | a0001c0001t0002g0198 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.328-3063G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151722601 | |||||||
| chr4:151722820 | C | T | 186 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(183): Show |
192 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.328-3282G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151722820 | |||||||
| chr4:151723099 | A | G | 1 | a0001c0001t0001g0127 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.328-3561T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151723099 | |||||||
| chr4:151723125 | G | A | 3 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 |
3 | HG01243.hp1 HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.328-3587C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151723125 | |||||||
| chr4:151723519 | G | A | 1 | a0002c0002t0001g0010 | 2 | HG02074.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.328-3981C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151723519 | |||||||
| chr4:151723723 | T | C | 1 | a0001c0001t0002g0109 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.328-4185A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151723723 | |||||||
| chr4:151723939 | G | A | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-4401C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151723939 | |||||||
| chr4:151724006 | C | T | 8 | a0001c0001t0001g0101 a0001c0001t0001g0135 a0001c0001t0001g0136 others(5): Show |
8 | HG02145.hp2 HG02280.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.328-4468G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151724006 | |||||||
| chr4:151724177 | C | T | 1 | a0001c0001t0002g0219 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.328-4639G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151724177 | |||||||
| chr4:151724318 | C | G | 2 | a0001c0001t0001g0156 a0001c0009t0001g0186 |
2 | HG01169.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.328-4780G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151724318 | |||||||
| chr4:151724336 | C | T | 1 | a0001c0001t0001g0011 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.328-4798G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151724336 | |||||||
| chr4:151724356 | T | C | 2 | a0001c0001t0001g0134 a0001c0001t0001g0181 |
2 | HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.328-4818A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151724356 | |||||||
| chr4:151724518 | A | G | 1 | a0001c0001t0002g0193 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.328-4980T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151724518 | |||||||
| chr4:151724570 | C | T | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-5032G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151724570 | |||||||
| chr4:151724876 | G | C | 1 | a0001c0001t0002g0245 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.328-5338C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151724876 | |||||||
| chr4:151725024 | G | C | 1 | a0001c0001t0001g0276 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.328-5486C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151725024 | |||||||
| chr4:151725174 | T | A | 2 | a0001c0001t0001g0126 a0001c0001t0001g0179 |
2 | HG00280.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.328-5636A>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151725174 | |||||||
| chr4:151725396 | T | A | 186 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(183): Show |
192 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(189): Show |
intron_variant | MODIFIER | c.328-5858A>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151725396 | |||||||
| chr4:151725433 | T | C | 2 | a0001c0001t0001g0092 a0008c0010t0001g0058 |
2 | HG02523.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.328-5895A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151725433 | |||||||
| chr4:151725538 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.328-6000C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151725538 | |||||||
| chr4:151725745 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.328-6207G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151725745 | |||||||
| chr4:151725839 | A | G | 2 | a0001c0001t0002g0223 a0001c0001t0002g0224 |
2 | HG01074.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.328-6301T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151725839 | |||||||
| chr4:151726425 | T | A | 136 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(133): Show |
137 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.328-6887A>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151726425 | |||||||
| chr4:151726496 | C | A | 3 | a0001c0001t0002g0248 a0001c0001t0002g0249 a0001c0001t0002g0250 |
3 | HG02155.hp2 NA18612.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.328-6958G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151726496 | |||||||
| chr4:151726573 | T | C | 1 | a0002c0002t0001g0048 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.328-7035A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151726573 | |||||||
| chr4:151726679 | A | G | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-7141T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151726679 | |||||||
| chr4:151726690 | T | C | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-7152A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151726690 | |||||||
| chr4:151727109 | C | T | 7 | a0002c0002t0001g0008 a0002c0002t0001g0023 a0002c0002t0001g0027 others(4): Show |
8 | HG02630.hp1 HG03041.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.328-7571G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151727109 | |||||||
| chr4:151727238 | G | A | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-7700C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151727238 | |||||||
| chr4:151727884 | T | A | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-8346A>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151727884 | |||||||
| chr4:151727909 | T | C | 1 | a0001c0001t0001g0187 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.328-8371A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151727909 | |||||||
| chr4:151727987 | G | A | 2 | a0001c0001t0002g0202 a0001c0001t0002g0203 |
2 | NA18960.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.328-8449C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151727987 | |||||||
| chr4:151728213 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.328-8675G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151728213 | |||||||
| chr4:151728274 | A | G | 1 | a0007c0013t0001g0098 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.328-8736T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151728274 | |||||||
| chr4:151728456 | T | G | 2 | a0001c0001t0001g0103 a0001c0001t0001g0105 |
2 | HG02258.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.328-8918A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151728456 | |||||||
| chr4:151728583 | C | T | 1 | a0001c0001t0002g0219 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.328-9045G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151728583 | |||||||
| chr4:151728629 | A | G | 1 | a0002c0002t0001g0026 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.328-9091T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151728629 | |||||||
| chr4:151728775 | T | C | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-9237A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151728775 | |||||||
| chr4:151728784 | T | C | 1 | a0002c0002t0001g0029 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.328-9246A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151728784 | |||||||
| chr4:151728811 | T | C | 1 | a0001c0001t0001g0067 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.328-9273A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151728811 | |||||||
| chr4:151728859 | T | C | 2 | a0001c0001t0001g0276 a0001c0012t0001g0275 |
2 | HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.328-9321A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151728859 | |||||||
| chr4:151728880 | T | C | 43 | a0001c0001t0001g0011 a0001c0001t0001g0073 a0001c0001t0001g0074 others(40): Show |
44 | HG00140.hp1 HG00280.hp2 HG00558.hp2 others(41): Show |
intron_variant | MODIFIER | c.328-9342A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151728880 | |||||||
| chr4:151729280 | A | T | 1 | a0001c0001t0001g0097 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.328-9742T>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151729280 | |||||||
| chr4:151729374 | C | T | 5 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(2): Show |
5 | HG02486.hp2 HG03139.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.328-9836G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151729374 | |||||||
| chr4:151729405 | G | A | 7 | a0002c0002t0001g0008 a0002c0002t0001g0023 a0002c0002t0001g0027 others(4): Show |
8 | HG02630.hp1 HG03041.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.328-9867C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151729405 | |||||||
| chr4:151729573 | G | T | 2 | a0001c0001t0002g0259 a0001c0001t0002g0260 |
2 | NA19057.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.328-10035C>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151729573 | |||||||
| chr4:151729730 | T | G | 196 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(193): Show |
203 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.328-10192A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151729730 | |||||||
| chr4:151729927 | T | C | 2 | a0006c0008t0001g0194 a0006c0008t0001g0195 |
2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.328-10389A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151729927 | |||||||
| chr4:151729959 | G | A | 3 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0077 |
3 | HG01109.hp2 HG01175.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.328-10421C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151729959 | |||||||
| chr4:151730137 | C | T | 2 | a0006c0008t0001g0194 a0006c0008t0001g0195 |
2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.328-10599G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151730137 | |||||||
| chr4:151730175 | C | T | 5 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(2): Show |
5 | HG02486.hp2 HG03139.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.328-10637G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151730175 | |||||||
| chr4:151730282 | G | A | 1 | a0001c0003t0001g0149 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.328-10744C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151730282 | |||||||
| chr4:151730351 | A | G | 192 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(189): Show |
199 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.328-10813T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151730351 | |||||||
| chr4:151730683 | C | T | 6 | a0002c0002t0001g0007 a0002c0002t0001g0018 a0002c0002t0001g0019 others(3): Show |
7 | HG01884.hp2 HG01891.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.328-11145G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151730683 | |||||||
| chr4:151730929 | C | A | 3 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 |
3 | HG01243.hp1 HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.328-11391G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151730929 | |||||||
| chr4:151730990 | G | A | 5 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(2): Show |
5 | HG02280.hp1 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.328-11452C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151730990 | |||||||
| chr4:151731067 | T | C | 1 | a0001c0001t0002g0273 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.328-11529A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731067 | |||||||
| chr4:151731088 | TCCCTCCC others(11): Show |
T | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-11568_328-1155 others(22): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731088 | |||||||
| chr4:151731255 | C | T | 9 | a0001c0001t0001g0073 a0001c0001t0001g0076 a0001c0001t0001g0078 others(6): Show |
9 | NA18612.hp2 NA18977.hp2 NA18998.hp2 others(6): Show |
intron_variant | MODIFIER | c.328-11717G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731255 | |||||||
| chr4:151731267 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.328-11729C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731267 | |||||||
| chr4:151731325 | C | T | 1 | a0001c0001t0002g0109 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.328-11787G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731325 | |||||||
| chr4:151731349 | A | G | 196 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(193): Show |
203 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.328-11811T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731349 | |||||||
| chr4:151731405 | G | A | 1 | a0001c0001t0002g0267 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.328-11867C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731405 | |||||||
| chr4:151731447 | C | T | 1 | a0001c0001t0002g0222 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.328-11909G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731447 | |||||||
| chr4:151731494 | G | C | 1 | a0001c0001t0001g0146 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.328-11956C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731494 | |||||||
| chr4:151731508 | C | T | 6 | a0002c0002t0001g0007 a0002c0002t0001g0018 a0002c0002t0001g0019 others(3): Show |
7 | HG01884.hp2 HG01891.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.328-11970G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731508 | |||||||
| chr4:151731531 | T | C | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-11993A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731531 | |||||||
| chr4:151731665 | G | A | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-12127C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731665 | |||||||
| chr4:151731674 | G | A | 1 | a0001c0001t0002g0285 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.328-12136C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731674 | |||||||
| chr4:151731694 | C | T | 6 | a0002c0002t0001g0007 a0002c0002t0001g0018 a0002c0002t0001g0019 others(3): Show |
7 | HG01884.hp2 HG01891.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.328-12156G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731694 | |||||||
| chr4:151731713 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.328-12175C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731713 | |||||||
| chr4:151731715 | C | A | 3 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 |
3 | HG02257.hp1 HG02572.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.328-12177G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731715 | |||||||
| chr4:151731726 | T | C | 196 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(193): Show |
203 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.328-12188A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731726 | |||||||
| chr4:151731760 | G | A | 1 | a0001c0001t0001g0151 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.328-12222C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731760 | |||||||
| chr4:151731809 | GTCTGAGA others(33): Show |
G | 1 | a0001c0001t0001g0168 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.328-12311_328-1227 others(44): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731809 | |||||||
| chr4:151731832 | T | C | 195 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(192): Show |
202 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(199): Show |
intron_variant | MODIFIER | c.328-12294A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731832 | |||||||
| chr4:151731843 | C | T | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-12305G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731843 | |||||||
| chr4:151731849 | A | G | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-12311T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731849 | |||||||
| chr4:151731878 | GCAGCCAC others(50): Show |
G | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-12397_328-1234 others(61): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731878 | |||||||
| chr4:151731900 | A | C | 69 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(66): Show |
69 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.328-12362T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731900 | |||||||
| chr4:151731932 | GGGCCAGC others(40): Show |
G | 46 | a0001c0001t0001g0092 a0001c0001t0001g0145 a0001c0001t0001g0147 others(43): Show |
51 | HG00280.hp2 HG00323.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.328-12441_328-1239 others(51): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731932 | |||||||
| chr4:151731940 | C | T | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-12402G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731940 | |||||||
| chr4:151731948 | CCGGG | C | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-12414_328-1241 others(8): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731948 | |||||||
| chr4:151731953 | A | T | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-12415T>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731953 | |||||||
| chr4:151731955 | G | A | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-12417C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731955 | |||||||
| chr4:151731958 | A | G | 146 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(143): Show |
148 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(145): Show |
intron_variant | MODIFIER | c.328-12420T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731958 | |||||||
| chr4:151731962 | G | A | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-12424C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731962 | |||||||
| chr4:151731975 | T | C | 144 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(141): Show |
146 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(143): Show |
intron_variant | MODIFIER | c.328-12437A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731975 | |||||||
| chr4:151731975 | T | TCC | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-12438_328-1243 others(6): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731975 | |||||||
| chr4:151731979 | C | T | 16 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0106 others(13): Show |
16 | HG00438.hp1 HG02129.hp2 HG02165.hp1 others(13): Show |
intron_variant | MODIFIER | c.328-12441G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731979 | |||||||
| chr4:151731982 | C | CAGCCACC others(3): Show |
4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-12445_328-1244 others(14): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731982 | |||||||
| chr4:151731992 | C | T | 69 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(66): Show |
69 | HG00280.hp1 HG00438.hp1 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.328-12454G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731992 | |||||||
| chr4:151731993 | G | A | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-12455C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151731993 | |||||||
| chr4:151732007 | TGGGGGGT others(41): Show |
T | 2 | a0006c0008t0001g0194 a0006c0008t0001g0195 |
2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.328-12517_328-1247 others(52): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151732007 | |||||||
| chr4:151732023 | G | A | 2 | a0001c0001t0002g0216 a0001c0001t0002g0251 |
2 | NA18940.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.328-12485C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151732023 | |||||||
| chr4:151732026 | C | G | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-12488G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151732026 | |||||||
| chr4:151732054 | TG | T | 193 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(190): Show |
200 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.328-12517delC | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151732054 | |||||||
| chr4:151732055 | G | A | 2 | a0001c0003t0002g0013 a0001c0003t0002g0218 |
3 | NA19060.hp2 NA19082.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.328-12517C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151732055 | |||||||
| chr4:151732071 | G | A | 20 | a0001c0001t0001g0011 a0001c0001t0001g0088 a0001c0001t0001g0089 others(17): Show |
21 | HG00140.hp1 HG01106.hp2 HG01346.hp2 others(18): Show |
intron_variant | MODIFIER | c.328-12533C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151732071 | |||||||
| chr4:151732092 | G | C | 39 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0009 others(36): Show |
44 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.328-12554C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151732092 | |||||||
| chr4:151732115 | CGCCCGGC others(33): Show |
C | 8 | a0001c0001t0002g0005 a0001c0001t0002g0205 a0001c0001t0002g0206 others(5): Show |
10 | HG02056.hp1 HG02155.hp2 HG02602.hp2 others(7): Show |
intron_variant | MODIFIER | c.328-12617_328-1257 others(44): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151732115 | |||||||
| chr4:151732132 | G | A | 4 | a0002c0002t0001g0019 a0002c0002t0001g0020 a0002c0002t0001g0021 others(1): Show |
4 | HG01891.hp1 HG02630.hp2 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-12594C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151732132 | |||||||
| chr4:151732138 | G | A | 23 | a0001c0001t0001g0230 a0001c0001t0001g0258 a0001c0001t0002g0001 others(20): Show |
27 | HG00438.hp2 HG01361.hp1 HG01978.hp1 others(24): Show |
intron_variant | MODIFIER | c.328-12600C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151732138 | |||||||
| chr4:151732159 | CGGCCACC others(30): Show |
C | 2 | a0001c0001t0001g0276 a0001c0012t0001g0275 |
2 | HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.328-12658_328-1262 others(41): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151732159 | |||||||
| chr4:151732527 | A | G | 5 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(2): Show |
5 | HG01928.hp1 HG02818.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.328-12989T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151732527 | |||||||
| chr4:151732694 | A | G | 1 | a0001c0001t0002g0219 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.328-13156T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151732694 | |||||||
| chr4:151732714 | TA | T | 20 | a0001c0001t0001g0087 a0001c0001t0001g0091 a0001c0001t0001g0096 others(17): Show |
20 | HG00639.hp1 HG01070.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.328-13177delT | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151732714 | |||||||
| chr4:151732728 | A | G | 2 | a0001c0001t0001g0178 a0001c0001t0001g0187 |
2 | NA18953.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.328-13190T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151732728 | |||||||
| chr4:151732783 | C | T | 1 | a0001c0003t0002g0218 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.328-13245G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151732783 | |||||||
| chr4:151732849 | T | C | 2 | a0006c0008t0001g0194 a0006c0008t0001g0195 |
2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.328-13311A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151732849 | |||||||
| chr4:151732923 | G | A | 3 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0077 |
3 | HG01109.hp2 HG01175.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.328-13385C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151732923 | |||||||
| chr4:151732977 | G | A | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-13439C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151732977 | |||||||
| chr4:151733421 | A | G | 6 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
6 | HG02109.hp2 HG02280.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.328-13883T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151733421 | |||||||
| chr4:151733610 | A | G | 2 | a0006c0008t0001g0194 a0006c0008t0001g0195 |
2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.328-14072T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151733610 | |||||||
| chr4:151733899 | T | A | 1 | a0001c0001t0001g0066 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.328-14361A>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151733899 | |||||||
| chr4:151734214 | G | T | 1 | a0001c0001t0001g0147 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.328-14676C>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151734214 | |||||||
| chr4:151734293 | C | T | 1 | a0001c0001t0002g0198 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.328-14755G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151734293 | |||||||
| chr4:151734350 | CA | C | 141 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(138): Show |
142 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.328-14813delT | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151734350 | |||||||
| chr4:151734363 | A | T | 2 | a0001c0001t0002g0003 a0001c0001t0002g0217 |
4 | HG00639.hp2 HG00741.hp2 HG02735.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-14825T>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151734363 | |||||||
| chr4:151734572 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.328-15034G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151734572 | |||||||
| chr4:151734577 | CAG | C | 8 | a0001c0001t0001g0101 a0001c0001t0001g0135 a0001c0001t0001g0136 others(5): Show |
8 | HG02145.hp2 HG02280.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.328-15041_328-1504 others(6): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151734577 | |||||||
| chr4:151734654 | G | C | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-15116C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151734654 | |||||||
| chr4:151734682 | T | G | 1 | a0001c0003t0001g0149 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.328-15144A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151734682 | |||||||
| chr4:151734731 | T | C | 3 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 |
3 | NA18941.hp2 NA18957.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.328-15193A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151734731 | |||||||
| chr4:151734830 | GA | G | 5 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(2): Show |
5 | HG02486.hp2 HG03139.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.328-15293delT | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151734830 | |||||||
| chr4:151735053 | A | G | 1 | a0001c0001t0001g0290 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.328-15515T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735053 | |||||||
| chr4:151735235 | G | GA | 15 | a0001c0001t0002g0251 a0002c0002t0001g0007 a0002c0002t0001g0008 others(12): Show |
17 | HG01884.hp2 HG01891.hp1 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.328-15698dupT | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735235 | |||||||
| chr4:151735235 | G | GAA | 30 | a0002c0002t0001g0002 a0002c0002t0001g0009 a0002c0002t0001g0010 others(27): Show |
34 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.328-15699_328-1569 others(6): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735235 | |||||||
| chr4:151735247 | A | C | 6 | a0001c0001t0001g0134 a0001c0001t0001g0181 a0001c0001t0001g0182 others(3): Show |
6 | HG02965.hp1 HG03195.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.328-15709T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735247 | |||||||
| chr4:151735405 | T | C | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-15867A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735405 | |||||||
| chr4:151735503 | C | A | 1 | a0001c0001t0001g0125 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.328-15965G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735503 | |||||||
| chr4:151735588 | T | C | 182 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(179): Show |
189 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.328-16050A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735588 | |||||||
| chr4:151735734 | G | GTATATAT others(3): Show |
2 | a0001c0001t0001g0113 a0001c0001t0001g0134 |
2 | HG03516.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.328-16197_328-1619 others(14): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735734 | |||||||
| chr4:151735734 | G | GTATATAT others(5): Show |
1 | a0001c0001t0001g0168 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.328-16197_328-1619 others(16): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735734 | |||||||
| chr4:151735734 | G | GTATATAT others(9): Show |
4 | a0001c0001t0001g0096 a0001c0001t0001g0136 a0001c0001t0001g0150 others(1): Show |
4 | HG02717.hp1 HG02965.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-16197_328-1619 others(20): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735734 | |||||||
| chr4:151735734 | G | GTATATAT others(11): Show |
8 | a0001c0001t0001g0073 a0001c0001t0001g0076 a0001c0001t0001g0078 others(5): Show |
8 | HG00280.hp1 HG02735.hp1 HG03225.hp1 others(5): Show |
intron_variant | MODIFIER | c.328-16197_328-1619 others(22): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735734 | |||||||
| chr4:151735734 | G | GTATATAT others(13): Show |
16 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0077 others(13): Show |
16 | HG01070.hp1 HG01109.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.328-16197_328-1619 others(24): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735734 | |||||||
| chr4:151735734 | G | GTATATAT others(15): Show |
16 | a0001c0001t0001g0080 a0001c0001t0001g0083 a0001c0001t0001g0084 others(13): Show |
16 | HG01074.hp1 HG01258.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.328-16197_328-1619 others(26): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735734 | |||||||
| chr4:151735734 | G | GTATATAT others(17): Show |
13 | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0001t0001g0090 others(10): Show |
13 | HG00639.hp1 HG01169.hp1 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.328-16197_328-1619 others(28): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735734 | |||||||
| chr4:151735734 | G | GTATATAT others(19): Show |
19 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0061 others(16): Show |
20 | HG00140.hp1 HG00558.hp2 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.328-16197_328-1619 others(30): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735734 | |||||||
| chr4:151735734 | G | GTATATAT others(21): Show |
7 | a0001c0001t0001g0062 a0001c0001t0001g0106 a0001c0001t0001g0139 others(4): Show |
7 | HG01243.hp1 HG01433.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.328-16197_328-1619 others(32): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735734 | |||||||
| chr4:151735734 | G | GTATATAT others(23): Show |
9 | a0001c0001t0001g0063 a0001c0001t0001g0067 a0001c0001t0001g0095 others(6): Show |
9 | HG00280.hp2 HG00597.hp1 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.328-16197_328-1619 others(34): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735734 | |||||||
| chr4:151735734 | G | GTATATAT others(25): Show |
14 | a0001c0001t0001g0060 a0001c0001t0001g0068 a0001c0001t0001g0093 others(11): Show |
14 | HG00438.hp1 HG01106.hp2 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.328-16197_328-1619 others(36): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735734 | |||||||
| chr4:151735734 | G | GTATATAT others(27): Show |
14 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0069 others(11): Show |
14 | HG00558.hp1 HG02129.hp2 HG02148.hp1 others(11): Show |
intron_variant | MODIFIER | c.328-16197_328-1619 others(38): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735734 | |||||||
| chr4:151735734 | G | GTATATAT others(29): Show |
3 | a0001c0001t0001g0070 a0001c0001t0001g0176 a0001c0003t0001g0165 |
3 | NA18939.hp1 NA18948.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.328-16197_328-1619 others(40): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735734 | |||||||
| chr4:151735734 | G | GTATATAT others(31): Show |
2 | a0001c0001t0001g0190 a0001c0003t0001g0166 |
2 | HG02258.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.328-16197_328-1619 others(42): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735734 | |||||||
| chr4:151735734 | G | GTATATAT others(33): Show |
7 | a0001c0001t0001g0105 a0001c0001t0001g0107 a0001c0001t0001g0123 others(4): Show |
7 | HG02258.hp2 HG03225.hp2 HG03654.hp1 others(4): Show |
intron_variant | MODIFIER | c.328-16197_328-1619 others(44): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735734 | |||||||
| chr4:151735734 | G | GTATATAT others(35): Show |
3 | a0001c0001t0001g0066 a0001c0001t0001g0071 a0001c0001t0001g0274 |
3 | HG03927.hp2 NA18973.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.328-16197_328-1619 others(46): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735734 | |||||||
| chr4:151735734 | G | GTATATAT others(37): Show |
1 | a0001c0001t0001g0072 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.328-16197_328-1619 others(48): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735734 | |||||||
| chr4:151735736 | G | A | 140 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(137): Show |
141 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.328-16198C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735736 | |||||||
| chr4:151735736 | G | GTA | 5 | a0001c0001t0002g0201 a0001c0001t0002g0210 a0001c0001t0002g0252 others(2): Show |
5 | HG01261.hp1 HG02523.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.328-16200_328-1619 others(6): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735736 | |||||||
| chr4:151735736 | G | GTATATAT others(21): Show |
1 | a0001c0001t0001g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.328-16199_328-1619 others(32): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735736 | |||||||
| chr4:151735736 | GTA | G | 44 | a0002c0002t0001g0002 a0002c0002t0001g0007 a0002c0002t0001g0008 others(41): Show |
50 | HG00323.hp2 HG00642.hp1 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.328-16200_328-1619 others(6): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735736 | |||||||
| chr4:151735788 | T | G | 1 | a0001c0001t0001g0167 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.328-16250A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735788 | |||||||
| chr4:151735866 | C | T | 2 | a0006c0008t0001g0194 a0006c0008t0001g0195 |
2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.328-16328G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735866 | |||||||
| chr4:151735908 | A | C | 4 | a0001c0001t0001g0276 a0001c0012t0001g0275 a0006c0008t0001g0194 others(1): Show |
4 | HG02451.hp2 HG02486.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-16370T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151735908 | |||||||
| chr4:151736198 | T | A | 6 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
6 | HG02109.hp2 HG02280.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.328-16660A>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151736198 | |||||||
| chr4:151736289 | A | G | 1 | a0001c0001t0002g0257 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.328-16751T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151736289 | |||||||
| chr4:151736672 | T | C | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-17134A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151736672 | |||||||
| chr4:151736781 | C | T | 4 | a0001c0001t0001g0276 a0001c0012t0001g0275 a0006c0008t0001g0194 others(1): Show |
4 | HG02451.hp2 HG02486.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-17243G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151736781 | |||||||
| chr4:151736794 | G | A | 1 | a0002c0002t0001g0026 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.328-17256C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151736794 | |||||||
| chr4:151736839 | G | C | 1 | a0001c0001t0002g0211 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.328-17301C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151736839 | |||||||
| chr4:151737037 | G | A | 5 | a0001c0001t0001g0145 a0001c0001t0001g0182 a0001c0001t0001g0183 others(2): Show |
5 | HG02896.hp2 HG02965.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.328-17499C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151737037 | |||||||
| chr4:151737076 | G | A | 1 | a0001c0001t0002g0203 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.328-17538C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151737076 | |||||||
| chr4:151737121 | G | T | 1 | a0001c0001t0001g0148 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.328-17583C>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151737121 | |||||||
| chr4:151737206 | G | A | 39 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0009 others(36): Show |
44 | HG00323.hp2 HG00597.hp2 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.328-17668C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151737206 | |||||||
| chr4:151737286 | G | A | 34 | a0001c0001t0001g0085 a0001c0001t0001g0086 a0001c0001t0001g0101 others(31): Show |
34 | HG00438.hp1 HG01243.hp1 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.328-17748C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151737286 | |||||||
| chr4:151737555 | CG | C | 4 | a0001c0001t0001g0276 a0001c0012t0001g0275 a0006c0008t0001g0194 others(1): Show |
4 | HG02451.hp2 HG02486.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-18018delC | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151737555 | |||||||
| chr4:151737637 | C | T | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-18099G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151737637 | |||||||
| chr4:151737751 | C | T | 4 | a0001c0001t0001g0090 a0001c0001t0001g0110 a0001c0001t0001g0111 others(1): Show |
4 | HG02040.hp2 HG02071.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-18213G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151737751 | |||||||
| chr4:151737829 | G | A | 3 | a0001c0001t0002g0006 a0005c0007t0002g0024 a0005c0007t0002g0025 |
5 | HG02055.hp2 HG02897.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.328-18291C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151737829 | |||||||
| chr4:151737909 | A | G | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-18371T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151737909 | |||||||
| chr4:151737916 | G | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0253 a0001c0001t0001g0255 others(1): Show |
5 | HG01934.hp1 HG01981.hp2 HG01993.hp1 others(2): Show |
intron_variant | MODIFIER | c.328-18378C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151737916 | |||||||
| chr4:151737995 | G | A | 6 | a0002c0002t0001g0007 a0002c0002t0001g0018 a0002c0002t0001g0019 others(3): Show |
7 | HG01884.hp2 HG01891.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.328-18457C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151737995 | |||||||
| chr4:151738239 | C | A | 1 | a0001c0001t0001g0081 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.328-18701G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151738239 | |||||||
| chr4:151738446 | C | T | 1 | a0001c0001t0001g0095 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.328-18908G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151738446 | |||||||
| chr4:151738767 | C | T | 2 | a0001c0001t0001g0094 a0001c0001t0001g0147 |
2 | HG00280.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.328-19229G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151738767 | |||||||
| chr4:151738804 | G | A | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-19266C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151738804 | |||||||
| chr4:151739109 | T | C | 4 | a0001c0001t0001g0276 a0001c0012t0001g0275 a0006c0008t0001g0194 others(1): Show |
4 | HG02451.hp2 HG02486.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.328-19571A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151739109 | |||||||
| chr4:151739281 | A | T | 1 | a0001c0001t0001g0146 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.327+19491T>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151739281 | |||||||
| chr4:151739385 | T | G | 2 | a0005c0007t0002g0024 a0005c0007t0002g0025 |
2 | HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.327+19387A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151739385 | |||||||
| chr4:151739429 | G | A | 6 | a0002c0002t0001g0007 a0002c0002t0001g0018 a0002c0002t0001g0019 others(3): Show |
7 | HG01884.hp2 HG01891.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.327+19343C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151739429 | |||||||
| chr4:151739442 | A | G | 1 | a0001c0001t0002g0216 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.327+19330T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151739442 | |||||||
| chr4:151739480 | G | A | 6 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0079 others(3): Show |
6 | NA18612.hp2 NA18977.hp2 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.327+19292C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151739480 | |||||||
| chr4:151739534 | T | C | 1 | a0001c0001t0001g0192 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.327+19238A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151739534 | |||||||
| chr4:151739663 | C | G | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+19109G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151739663 | |||||||
| chr4:151739695 | G | C | 1 | a0001c0001t0002g0256 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.327+19077C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151739695 | |||||||
| chr4:151739909 | G | A | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.327+18863C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151739909 | |||||||
| chr4:151739975 | G | A | 4 | a0001c0001t0001g0276 a0001c0012t0001g0275 a0006c0008t0001g0194 others(1): Show |
4 | HG02451.hp2 HG02486.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+18797C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151739975 | |||||||
| chr4:151740049 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.327+18723C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151740049 | |||||||
| chr4:151740073 | C | G | 1 | a0001c0001t0001g0145 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.327+18699G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151740073 | |||||||
| chr4:151740238 | C | T | 1 | a0002c0002t0001g0029 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.327+18534G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151740238 | |||||||
| chr4:151740244 | T | C | 2 | a0001c0001t0001g0178 a0001c0001t0001g0187 |
2 | NA18953.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.327+18528A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151740244 | |||||||
| chr4:151740272 | A | G | 2 | a0001c0001t0001g0215 a0001c0001t0002g0283 |
2 | HG00140.hp2 HG01070.hp2 |
intron_variant | MODIFIER | c.327+18500T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151740272 | |||||||
| chr4:151740751 | TG | T | 6 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(3): Show |
6 | HG02109.hp2 HG02280.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.327+18020delC | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151740751 | |||||||
| chr4:151740874 | G | A | 1 | a0001c0001t0002g0257 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.327+17898C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151740874 | |||||||
| chr4:151741042 | A | G | 1 | a0001c0001t0002g0214 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.327+17730T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151741042 | |||||||
| chr4:151741072 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.327+17700G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151741072 | |||||||
| chr4:151741304 | G | C | 1 | a0001c0001t0001g0179 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.327+17468C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151741304 | |||||||
| chr4:151741388 | C | G | 2 | a0001c0001t0001g0060 a0001c0001t0001g0093 |
2 | NA19060.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.327+17384G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151741388 | |||||||
| chr4:151741795 | G | T | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+16977C>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151741795 | |||||||
| chr4:151742090 | G | GT | 174 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(171): Show |
181 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.327+16681dupA | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151742090 | |||||||
| chr4:151742090 | G | GTT | 13 | a0001c0001t0001g0076 a0001c0001t0001g0085 a0001c0001t0001g0087 others(10): Show |
13 | HG00597.hp1 HG01243.hp1 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.327+16680_327+1668 others(6): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151742090 | |||||||
| chr4:151742174 | T | C | 198 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(195): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.327+16598A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151742174 | |||||||
| chr4:151742242 | T | C | 196 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(193): Show |
203 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.327+16530A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151742242 | |||||||
| chr4:151742289 | C | T | 2 | a0001c0001t0001g0088 a0001c0001t0001g0089 |
2 | HG00140.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.327+16483G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151742289 | |||||||
| chr4:151742310 | G | A | 5 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(2): Show |
5 | HG02280.hp1 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.327+16462C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151742310 | |||||||
| chr4:151742553 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.327+16219C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151742553 | |||||||
| chr4:151742638 | C | A | 1 | a0006c0008t0001g0195 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.327+16134G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151742638 | |||||||
| chr4:151742722 | C | A | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+16050G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151742722 | |||||||
| chr4:151742819 | G | A | 196 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(193): Show |
203 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.327+15953C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151742819 | |||||||
| chr4:151743011 | A | T | 191 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(188): Show |
198 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.327+15761T>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151743011 | |||||||
| chr4:151743191 | TCA | T | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+15579_327+1558 others(6): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151743191 | |||||||
| chr4:151743381 | T | C | 3 | a0001c0001t0002g0259 a0001c0001t0002g0260 a0001c0001t0002g0261 |
3 | NA19057.hp2 NA19064.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.327+15391A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151743381 | |||||||
| chr4:151743673 | T | C | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+15099A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151743673 | |||||||
| chr4:151743972 | T | C | 1 | a0001c0001t0001g0292 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.327+14800A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151743972 | |||||||
| chr4:151744200 | A | G | 3 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 |
3 | HG01243.hp1 HG02109.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.327+14572T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151744200 | |||||||
| chr4:151744252 | A | C | 1 | a0001c0001t0001g0138 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.327+14520T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151744252 | |||||||
| chr4:151744372 | G | A | 5 | a0001c0001t0002g0201 a0001c0001t0002g0262 a0001c0001t0002g0264 others(2): Show |
5 | HG00323.hp1 HG01255.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.327+14400C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151744372 | |||||||
| chr4:151744410 | T | C | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+14362A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151744410 | |||||||
| chr4:151744510 | G | C | 4 | a0001c0001t0001g0276 a0001c0012t0001g0275 a0006c0008t0001g0194 others(1): Show |
4 | HG02451.hp2 HG02486.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+14262C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151744510 | |||||||
| chr4:151744853 | C | T | 3 | a0002c0002t0001g0008 a0002c0002t0001g0027 a0002c0002t0001g0028 |
4 | HG03041.hp2 HG03139.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+13919G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151744853 | |||||||
| chr4:151744870 | A | T | 3 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 |
3 | HG02145.hp2 HG02717.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.327+13902T>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151744870 | |||||||
| chr4:151744991 | C | A | 1 | a0001c0001t0002g0208 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.327+13781G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151744991 | |||||||
| chr4:151745026 | A | C | 6 | a0002c0002t0001g0007 a0002c0002t0001g0018 a0002c0002t0001g0019 others(3): Show |
7 | HG01884.hp2 HG01891.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.327+13746T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151745026 | |||||||
| chr4:151745446 | G | A | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+13326C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151745446 | |||||||
| chr4:151745531 | C | T | 1 | a0001c0001t0002g0209 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.327+13241G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151745531 | |||||||
| chr4:151745616 | A | C | 188 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(185): Show |
195 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.327+13156T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151745616 | |||||||
| chr4:151745918 | C | T | 1 | a0001c0001t0001g0088 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.327+12854G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151745918 | |||||||
| chr4:151746019 | T | C | 196 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(193): Show |
203 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.327+12753A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151746019 | |||||||
| chr4:151746036 | T | C | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+12736A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151746036 | |||||||
| chr4:151746151 | C | G | 2 | a0001c0001t0001g0134 a0001c0001t0001g0181 |
2 | HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.327+12621G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151746151 | |||||||
| chr4:151746419 | T | A | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+12353A>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151746419 | |||||||
| chr4:151746622 | C | A | 1 | a0002c0002t0001g0044 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.327+12150G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151746622 | |||||||
| chr4:151746654 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.327+12118G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151746654 | |||||||
| chr4:151746795 | T | C | 1 | a0001c0001t0002g0266 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.327+11977A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151746795 | |||||||
| chr4:151746894 | T | G | 2 | a0001c0001t0002g0272 a0001c0001t0002g0273 |
2 | HG00642.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.327+11878A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151746894 | |||||||
| chr4:151747072 | A | G | 192 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(189): Show |
199 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.327+11700T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151747072 | |||||||
| chr4:151747291 | A | G | 1 | a0006c0008t0001g0195 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.327+11481T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151747291 | |||||||
| chr4:151747632 | T | A | 1 | a0001c0001t0001g0180 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.327+11140A>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151747632 | |||||||
| chr4:151747633 | A | C | 196 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(193): Show |
203 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.327+11139T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151747633 | |||||||
| chr4:151748154 | A | G | 1 | a0001c0001t0001g0126 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.327+10618T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151748154 | |||||||
| chr4:151748198 | A | G | 1 | a0001c0001t0002g0208 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.327+10574T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151748198 | |||||||
| chr4:151748356 | A | G | 5 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(2): Show |
5 | HG02280.hp1 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.327+10416T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151748356 | |||||||
| chr4:151748357 | C | CCG | 5 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(2): Show |
5 | HG02280.hp1 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.327+10414_327+1041 others(6): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151748357 | |||||||
| chr4:151748360 | C | T | 5 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(2): Show |
5 | HG02280.hp1 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.327+10412G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151748360 | |||||||
| chr4:151748453 | A | G | 1 | a0005c0007t0002g0024 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.327+10319T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151748453 | |||||||
| chr4:151749116 | T | C | 8 | a0002c0002t0001g0002 a0002c0002t0001g0009 a0002c0002t0001g0010 others(5): Show |
12 | HG00597.hp2 HG02056.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.327+9656A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151749116 | |||||||
| chr4:151749135 | T | G | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+9637A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151749135 | |||||||
| chr4:151749146 | A | C | 1 | a0001c0005t0002g0207 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.327+9626T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151749146 | |||||||
| chr4:151749171 | A | G | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+9601T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151749171 | |||||||
| chr4:151749461 | A | G | 196 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(193): Show |
203 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.327+9311T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151749461 | |||||||
| chr4:151749613 | C | T | 137 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(134): Show |
138 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.327+9159G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151749613 | |||||||
| chr4:151749628 | C | A | 196 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(193): Show |
203 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.327+9144G>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151749628 | |||||||
| chr4:151749632 | T | TATA | 196 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(193): Show |
203 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.327+9137_327+9139d others(5): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151749632 | |||||||
| chr4:151749760 | G | A | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+9012C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151749760 | |||||||
| chr4:151749850 | C | T | 5 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(2): Show |
5 | HG02280.hp1 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.327+8922G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151749850 | |||||||
| chr4:151749951 | G | A | 1 | a0001c0001t0002g0267 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.327+8821C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151749951 | |||||||
| chr4:151750035 | C | T | 2 | a0001c0001t0002g0205 a0001c0001t0002g0206 |
2 | NA19005.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.327+8737G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151750035 | |||||||
| chr4:151750072 | A | G | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+8700T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151750072 | |||||||
| chr4:151750120 | A | G | 5 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(2): Show |
5 | HG02486.hp2 HG03139.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.327+8652T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151750120 | |||||||
| chr4:151750125 | C | T | 3 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 |
3 | HG02257.hp1 HG02572.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.327+8647G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151750125 | |||||||
| chr4:151750148 | T | A | 1 | a0001c0001t0002g0017 | 2 | NA18994.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.327+8624A>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151750148 | |||||||
| chr4:151750173 | G | A | 143 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(140): Show |
145 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(142): Show |
intron_variant | MODIFIER | c.327+8599C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151750173 | |||||||
| chr4:151750208 | T | C | 4 | a0001c0001t0001g0276 a0001c0012t0001g0275 a0006c0008t0001g0194 others(1): Show |
4 | HG02451.hp2 HG02486.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+8564A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151750208 | |||||||
| chr4:151750253 | T | C | 192 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(189): Show |
199 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.327+8519A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151750253 | |||||||
| chr4:151750280 | G | A | 2 | a0005c0007t0002g0024 a0005c0007t0002g0025 |
2 | HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.327+8492C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151750280 | |||||||
| chr4:151750318 | C | T | 1 | a0001c0001t0001g0287 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.327+8454G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151750318 | |||||||
| chr4:151750418 | GCTATGTG others(10): Show |
G | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+8337_327+8353d others(19): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151750418 | |||||||
| chr4:151750488 | C | G | 182 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(179): Show |
189 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.327+8284G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151750488 | |||||||
| chr4:151750866 | T | C | 1 | a0001c0001t0002g0268 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.327+7906A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151750866 | |||||||
| chr4:151750901 | T | C | 1 | a0003c0004t0001g0296 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.327+7871A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151750901 | |||||||
| chr4:151750969 | C | G | 182 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(179): Show |
189 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.327+7803G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151750969 | |||||||
| chr4:151751084 | T | C | 1 | a0001c0001t0001g0180 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.327+7688A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151751084 | |||||||
| chr4:151751569 | A | G | 1 | a0001c0001t0001g0204 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.327+7203T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151751569 | |||||||
| chr4:151751688 | C | T | 1 | a0001c0001t0002g0109 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.327+7084G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151751688 | |||||||
| chr4:151751730 | T | G | 182 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(179): Show |
189 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.327+7042A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151751730 | |||||||
| chr4:151751969 | A | T | 1 | a0001c0001t0001g0108 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.327+6803T>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151751969 | |||||||
| chr4:151752034 | T | C | 8 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0001g0278 others(5): Show |
8 | HG02109.hp2 HG02280.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.327+6738A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151752034 | |||||||
| chr4:151752386 | T | C | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+6386A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151752386 | |||||||
| chr4:151752593 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.327+6179C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151752593 | |||||||
| chr4:151752753 | T | G | 1 | a0001c0001t0001g0066 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.327+6019A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151752753 | |||||||
| chr4:151752781 | T | C | 2 | a0006c0008t0001g0194 a0006c0008t0001g0195 |
2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.327+5991A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151752781 | |||||||
| chr4:151753166 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.327+5606A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151753166 | |||||||
| chr4:151753181 | T | C | 2 | a0006c0008t0001g0194 a0006c0008t0001g0195 |
2 | HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.327+5591A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151753181 | |||||||
| chr4:151753240 | A | C | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+5532T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151753240 | |||||||
| chr4:151753251 | T | C | 2 | a0001c0001t0002g0270 a0001c0001t0002g0271 |
2 | NA18945.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.327+5521A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151753251 | |||||||
| chr4:151753767 | C | G | 5 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(2): Show |
5 | HG02486.hp2 HG03139.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.327+5005G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151753767 | |||||||
| chr4:151754286 | C | T | 1 | a0002c0002t0001g0052 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.327+4486G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151754286 | |||||||
| chr4:151754295 | T | C | 27 | a0001c0001t0001g0011 a0001c0001t0001g0087 a0001c0001t0001g0088 others(24): Show |
28 | HG00140.hp1 HG00558.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.327+4477A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151754295 | |||||||
| chr4:151754369 | C | T | 1 | a0002c0002t0001g0051 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.327+4403G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151754369 | |||||||
| chr4:151754406 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.327+4366G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151754406 | |||||||
| chr4:151754621 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.327+4151G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151754621 | |||||||
| chr4:151754810 | G | C | 3 | a0001c0001t0001g0073 a0001c0001t0001g0080 a0001c0001t0001g0081 |
3 | NA19009.hp1 NA19082.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.327+3962C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151754810 | |||||||
| chr4:151754873 | T | C | 2 | a0001c0001t0002g0272 a0001c0001t0002g0273 |
2 | HG00642.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.327+3899A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151754873 | |||||||
| chr4:151755198 | T | C | 194 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(191): Show |
201 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(198): Show |
intron_variant | MODIFIER | c.327+3574A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151755198 | |||||||
| chr4:151755257 | A | G | 1 | a0002c0002t0001g0026 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.327+3515T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151755257 | |||||||
| chr4:151755269 | T | C | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+3503A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151755269 | |||||||
| chr4:151755310 | A | G | 2 | a0005c0007t0002g0024 a0005c0007t0002g0025 |
2 | HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.327+3462T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151755310 | |||||||
| chr4:151755339 | G | GTATTATG others(5): Show |
1 | a0001c0001t0001g0292 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.327+3432_327+3433i others(14): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151755339 | |||||||
| chr4:151755340 | T | C | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+3432A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151755340 | |||||||
| chr4:151755344 | G | T | 1 | a0001c0001t0001g0292 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.327+3428C>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151755344 | |||||||
| chr4:151755676 | T | G | 6 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(3): Show |
6 | NA18944.hp1 NA18964.hp1 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.327+3096A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151755676 | |||||||
| chr4:151755705 | G | A | 1 | a0001c0001t0001g0181 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.327+3067C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151755705 | |||||||
| chr4:151755775 | T | C | 4 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 others(1): Show |
4 | HG02965.hp1 HG03195.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+2997A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151755775 | |||||||
| chr4:151756257 | A | C | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+2515T>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151756257 | |||||||
| chr4:151756375 | T | C | 182 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(179): Show |
189 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.327+2397A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151756375 | |||||||
| chr4:151756409 | T | C | 4 | a0003c0004t0001g0293 a0003c0004t0001g0294 a0003c0004t0001g0295 others(1): Show |
4 | HG01884.hp1 HG02970.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+2363A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151756409 | |||||||
| chr4:151756428 | C | T | 27 | a0001c0001t0001g0011 a0001c0001t0001g0087 a0001c0001t0001g0088 others(24): Show |
28 | HG00140.hp1 HG00558.hp2 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.327+2344G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151756428 | |||||||
| chr4:151756465 | C | T | 2 | a0001c0001t0001g0106 a0001c0001t0001g0107 |
2 | HG03688.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.327+2307G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151756465 | |||||||
| chr4:151756677 | A | G | 2 | a0001c0001t0002g0202 a0001c0001t0002g0203 |
2 | NA18960.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.327+2095T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151756677 | |||||||
| chr4:151756758 | A | G | 4 | a0001c0001t0001g0102 a0001c0001t0001g0103 a0001c0001t0001g0104 others(1): Show |
4 | HG01891.hp2 HG02258.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.327+2014T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151756758 | |||||||
| chr4:151756917 | T | C | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+1855A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151756917 | |||||||
| chr4:151757195 | G | A | 8 | a0002c0002t0001g0002 a0002c0002t0001g0009 a0002c0002t0001g0010 others(5): Show |
12 | HG00597.hp2 HG02056.hp2 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.327+1577C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151757195 | |||||||
| chr4:151757467 | A | AT | 175 | a0001c0001t0001g0011 a0001c0001t0001g0060 a0001c0001t0001g0061 others(172): Show |
182 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.327+1304dupA | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151757467 | |||||||
| chr4:151757467 | A | ATT | 24 | a0001c0001t0001g0059 a0001c0001t0001g0073 a0001c0001t0001g0074 others(21): Show |
24 | HG00140.hp1 HG01070.hp1 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.327+1303_327+1304d others(4): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151757467 | |||||||
| chr4:151757512 | G | A | 1 | a0001c0001t0001g0187 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.327+1260C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151757512 | |||||||
| chr4:151757677 | C | T | 2 | a0001c0001t0001g0276 a0001c0012t0001g0275 |
2 | HG02451.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.327+1095G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151757677 | |||||||
| chr4:151757756 | C | T | 1 | a0001c0001t0001g0073 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.327+1016G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151757756 | |||||||
| chr4:151757772 | C | T | 2 | a0001c0001t0001g0085 a0001c0001t0001g0086 |
2 | HG02602.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.327+1000G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151757772 | |||||||
| chr4:151757773 | G | A | 3 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0084 |
3 | NA18612.hp2 NA18977.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.327+999C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151757773 | |||||||
| chr4:151757822 | T | C | 198 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(195): Show |
205 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(202): Show |
intron_variant | MODIFIER | c.327+950A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151757822 | |||||||
| chr4:151757836 | T | C | 1 | a0001c0001t0001g0282 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.327+936A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151757836 | |||||||
| chr4:151758060 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.327+712A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151758060 | |||||||
| chr4:151758258 | T | G | 1 | a0001c0001t0001g0292 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.327+514A>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151758258 | |||||||
| chr4:151758260 | T | C | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+512A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151758260 | |||||||
| chr4:151758295 | C | G | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.327+477G>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151758295 | |||||||
| chr4:151758373 | C | T | 12 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(9): Show |
12 | HG01109.hp2 HG01175.hp1 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.327+399G>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151758373 | |||||||
| chr4:151758390 | A | G | 14 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(11): Show |
14 | HG00558.hp1 HG00735.hp2 NA18944.hp1 others(11): Show |
intron_variant | MODIFIER | c.327+382T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151758390 | |||||||
| chr4:151758498 | T | C | 1 | a0001c0001t0002g0283 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.327+274A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151758498 | |||||||
| chr4:151758537 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.327+235C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151758537 | |||||||
| chr4:151758570 | A | G | 142 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(139): Show |
143 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.327+202T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151758570 | |||||||
| chr4:151758664 | A | G | 136 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(133): Show |
137 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.327+108T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 2/12 | chr4 | 151758664 | |||||||
| chr4:151758948 | G | GATGTATT others(12): Show |
2 | a0001c0001t0002g0285 a0001c0001t0002g0286 |
2 | HG01928.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.177-45_177-27dupGG others(17): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 1/12 | chr4 | 151758948 | |||||||
| chr4:151759246 | T | A | 1 | a0001c0001t0002g0193 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.177-324A>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 1/12 | chr4 | 151759246 | |||||||
| chr4:151759281 | T | A | 6 | a0002c0002t0001g0051 a0002c0002t0001g0052 a0002c0002t0001g0053 others(3): Show |
6 | HG02145.hp1 HG02622.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.177-359A>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 1/12 | chr4 | 151759281 | |||||||
| chr4:151759385 | A | G | 6 | a0002c0002t0001g0007 a0002c0002t0001g0018 a0002c0002t0001g0019 others(3): Show |
7 | HG01884.hp2 HG01891.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.177-463T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 1/12 | chr4 | 151759385 | |||||||
| chr4:151759454 | T | C | 1 | a0001c0001t0001g0190 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.177-532A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 1/12 | chr4 | 151759454 | |||||||
| chr4:151759469 | A | T | 1 | a0001c0001t0002g0193 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.177-547T>A | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 1/12 | chr4 | 151759469 | |||||||
| chr4:151759549 | T | C | 138 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(135): Show |
139 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.177-627A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 1/12 | chr4 | 151759549 | |||||||
| chr4:151759741 | T | C | 1 | a0001c0001t0001g0287 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.177-819A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 1/12 | chr4 | 151759741 | |||||||
| chr4:151759791 | C | CAT | 8 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(5): Show |
8 | HG01884.hp1 HG02818.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.177-871_177-870dup others(2): Show |
GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 1/12 | chr4 | 151759791 | |||||||
| chr4:151760174 | CT | C | 4 | a0001c0001t0001g0288 a0001c0001t0001g0289 a0001c0001t0001g0290 others(1): Show |
4 | HG02818.hp2 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.176+632delA | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 1/12 | chr4 | 151760174 | |||||||
| chr4:151760305 | T | C | 1 | a0001c0001t0001g0292 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.176+502A>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 1/12 | chr4 | 151760305 | |||||||
| chr4:151760354 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.176+453C>T | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 1/12 | chr4 | 151760354 | |||||||
| chr4:151760683 | G | C | 1 | a0001c0001t0001g0192 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.176+124C>G | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 1/12 | chr4 | 151760683 | |||||||
| chr4:151760800 | A | G | 136 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0060 others(133): Show |
137 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(134): Show |
splice_region_variant&intron_variant | LOW | c.176+7T>C | GATB | ENSG00000059691.12 | transcript | ENST00000263985.11 | protein_coding | 1/12 | chr4 | 151760800 |