Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 65123 |
| ensemblid | ENSG00000143624.14 |
| hgncid | 26153 |
| symbol | INTS3 |
| name | integrator complex subunit 3 |
| refseq_nuc | NM_023015.5 |
| refseq_prot | NP_075391.3 |
| ensembl_nuc | ENST00000318967.7 |
| ensembl_prot | ENSP00000318641.2 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 153728050 |
| end | 153774808 |
| strand | + |
| ver | v1.2 |
| region | chr1:153728050-153774808 |
| region5000 | chr1:153723050-153779808 |
| regionname0 | INTS3_chr1_153728050_153774808 |
| regionname5000 | INTS3_chr1_153723050_153779808 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 1042 | 347 | 88 | 60 | 144 | 12 | 42 | 102 | INTS3_chr1_153723050_153779808 | INTS3 | MELQK others(1037): Show |
chr1 | 153723050 | 153779808 |
| a0002 | 0/0 | 818 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | MELQK others(813): Show |
chr1 | 153723050 | 153779808 |
| a0003 | 0/0 | 1042 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | MELQK others(1037): Show |
chr1 | 153723050 | 153779808 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 3126 | 298 | 53 | 55 | 141 | 11 | 37 | INTS3_chr1_153723050_153779808 | INTS3 | ATGGA others(3121): Show |
chr1 | 153723050 | 153779808 | ||
| a0001c0002 | 0/0 | 3126 | 43 | 30 | 5 | 3 | 1 | 4 | INTS3_chr1_153723050_153779808 | INTS3 | ATGGA others(3121): Show |
chr1 | 153723050 | 153779808 | ||
| a0001c0003 | 0/0 | 3126 | 4 | 4 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | ATGGA others(3121): Show |
chr1 | 153723050 | 153779808 | ||
| a0001c0006 | 0/0 | 3126 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | ATGGA others(3121): Show |
chr1 | 153723050 | 153779808 | ||
| a0001c0007 | 0/0 | 3126 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | ATGGA others(3121): Show |
chr1 | 153723050 | 153779808 | ||
| a0002c0005 | 0/0 | 3110 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | ATGGA others(3105): Show |
chr1 | 153723050 | 153779808 | ||
| a0003c0004 | 0/0 | 3126 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | ATGGA others(3121): Show |
chr1 | 153723050 | 153779808 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5252 | 286 | 45 | 54 | 138 | 11 | 37 | INTS3_chr1_153723050_153779808 | INTS3 | GCCTT others(5247): Show |
chr1 | 153723050 | 153779808 |
| a0001c0001t0003 | 0/0 | 5252 | 8 | 7 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | GCCTT others(5247): Show |
chr1 | 153723050 | 153779808 |
| a0001c0001t0007 | 0/0 | 5230 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | GCCTT others(5225): Show |
chr1 | 153723050 | 153779808 |
| a0001c0001t0009 | 0/0 | 5252 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | GCCTT others(5247): Show |
chr1 | 153723050 | 153779808 |
| a0001c0001t0010 | 0/0 | 5252 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | GCCTT others(5247): Show |
chr1 | 153723050 | 153779808 |
| a0001c0001t0012 | 0/0 | 5252 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | GCCTT others(5247): Show |
chr1 | 153723050 | 153779808 |
| a0001c0002t0001 | 0/0 | 5252 | 6 | 5 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | GCCTT others(5247): Show |
chr1 | 153723050 | 153779808 |
| a0001c0002t0002 | 0/0 | 5252 | 29 | 17 | 4 | 3 | 1 | 4 | INTS3_chr1_153723050_153779808 | INTS3 | GCCTT others(5247): Show |
chr1 | 153723050 | 153779808 |
| a0001c0002t0004 | 0/0 | 5252 | 2 | 2 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | GCCTT others(5247): Show |
chr1 | 153723050 | 153779808 |
| a0001c0002t0005 | 0/0 | 5252 | 2 | 2 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | GCCTT others(5247): Show |
chr1 | 153723050 | 153779808 |
| a0001c0002t0006 | 0/0 | 5252 | 2 | 2 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | GCCTT others(5247): Show |
chr1 | 153723050 | 153779808 |
| a0001c0002t0008 | 0/0 | 5252 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | GCCTT others(5247): Show |
chr1 | 153723050 | 153779808 |
| a0001c0002t0011 | 0/0 | 5252 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | GCCTT others(5247): Show |
chr1 | 153723050 | 153779808 |
| a0001c0003t0001 | 0/0 | 5252 | 4 | 4 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | GCCTT others(5247): Show |
chr1 | 153723050 | 153779808 |
| a0001c0006t0001 | 0/0 | 5252 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | GCCTT others(5247): Show |
chr1 | 153723050 | 153779808 |
| a0001c0007t0003 | 0/0 | 5252 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | GCCTT others(5247): Show |
chr1 | 153723050 | 153779808 |
| a0002c0005t0001 | 0/0 | 5236 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | GCCTT others(5231): Show |
chr1 | 153723050 | 153779808 |
| a0003c0004t0001 | 0/0 | 5252 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | GCCTT others(5247): Show |
chr1 | 153723050 | 153779808 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0007 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0012 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0017 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0003g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0003g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0003g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0003g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0003g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0003g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0003g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0003g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0007g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0009g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0010g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0001t0012g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0002t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0002t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0002t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0002t0002g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0002t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0002t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0002t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0002t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0002t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0002t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0002t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0002t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0002t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0002t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0002t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0002t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0002t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0002t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0002t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0002t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0002t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0002t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0002t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0002t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0002t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0002t0004g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0002t0004g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0002t0005g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0002t0005g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0002t0006g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0002t0006g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0002t0008g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0002t0011g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0003t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0003t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0003t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0003t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0006t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0001c0007t0003g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0002c0005t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| a0003c0004t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0207 | EUR | GBR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0068 | EUR | GBR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0083 | EUR | GBR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0070 | EUR | GBR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG00408 | hp1 | a0001 | c0002 | t0002 | g0185 | EAS | CHS | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | CHS | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | CHS | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | CHS | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG00558 | hp2 | a0001 | c0001 | t0009 | g0215 | EAS | CHS | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | CHS | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | CHS | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG00673 | hp1 | a0001 | c0002 | t0002 | g0106 | EAS | CHS | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | CHS | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01074 | hp1 | a0001 | c0002 | t0002 | g0047 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01081 | hp1 | a0001 | c0002 | t0002 | g0006 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0148 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01167 | hp1 | a0001 | c0002 | t0002 | g0040 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01192 | hp2 | a0001 | c0002 | t0002 | g0006 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0317 | AMR | PUR | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | CLM | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | CLM | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | CLM | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0064 | EUR | IBS | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0324 | EUR | IBS | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | IBS | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0076 | EUR | IBS | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | ACB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01891 | hp1 | a0001 | c0002 | t0005 | g0306 | AFR | ACB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | ACB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PEL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PEL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0321 | AFR | ACB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | ACB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | KHV | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | KHV | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02145 | hp1 | a0001 | c0002 | t0008 | g0312 | AFR | ACB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02145 | hp2 | a0001 | c0003 | t0001 | g0279 | AFR | ACB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | CDX | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | CDX | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | CDX | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | CDX | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0320 | AFR | ACB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02258 | hp1 | a0001 | c0003 | t0001 | g0267 | AFR | ACB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0039 | AFR | ACB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0319 | AFR | ACB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | PEL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0299 | AFR | ACB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | KHV | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02602 | hp2 | a0001 | c0002 | t0002 | g0042 | SAS | PJL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0061 | AFR | GWD | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02622 | hp1 | a0001 | c0002 | t0006 | g0131 | AFR | GWD | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02630 | hp1 | a0001 | c0002 | t0006 | g0130 | AFR | GWD | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | GWD | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0318 | AFR | GWD | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02683 | hp1 | a0001 | c0002 | t0002 | g0048 | SAS | PJL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02723 | hp1 | a0001 | c0002 | t0002 | g0041 | AFR | GWD | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02723 | hp2 | a0001 | c0002 | t0002 | g0056 | AFR | GWD | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | GWD | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | GWD | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0307 | AFR | GWD | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02965 | hp1 | a0001 | c0002 | t0004 | g0313 | AFR | ESN | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02965 | hp2 | a0001 | c0002 | t0002 | g0046 | AFR | ESN | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ESN | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | ESN | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0310 | AFR | GWD | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0315 | AFR | GWD | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0010 | AFR | MSL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG03130 | hp1 | a0001 | c0002 | t0002 | g0037 | AFR | ESN | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG03130 | hp2 | a0001 | c0002 | t0002 | g0050 | AFR | ESN | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG03139 | hp1 | a0001 | c0003 | t0001 | g0223 | AFR | ESN | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG03139 | hp2 | a0002 | c0005 | t0001 | g0271 | AFR | ESN | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG03195 | hp1 | a0003 | c0004 | t0001 | g0149 | AFR | ESN | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG03195 | hp2 | a0001 | c0002 | t0002 | g0051 | AFR | ESN | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | MSL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG03209 | hp2 | a0001 | c0002 | t0005 | g0305 | AFR | MSL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0010 | AFR | MSL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | MSL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG03453 | hp1 | a0001 | c0002 | t0002 | g0055 | AFR | MSL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | MSL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG03486 | hp1 | a0001 | c0002 | t0002 | g0044 | AFR | MSL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | PJL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0322 | AFR | ESN | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG03540 | hp1 | a0001 | c0002 | t0004 | g0316 | AFR | GWD | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG03540 | hp2 | a0001 | c0001 | t0012 | g0138 | AFR | GWD | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG03579 | hp1 | a0001 | c0002 | t0011 | g0016 | AFR | MSL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0284 | SAS | BEB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | BEB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | BEB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | BEB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0288 | SAS | BEB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0291 | SAS | BEB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0293 | SAS | BEB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | BEB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0282 | SAS | STU | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0326 | SAS | STU | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG04184 | hp1 | a0001 | c0002 | t0002 | g0033 | SAS | BEB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | BEB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0265 | SAS | STU | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0280 | SAS | STU | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG04204 | hp1 | a0001 | c0006 | t0001 | g0074 | SAS | STU | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG04204 | hp2 | a0001 | c0002 | t0002 | g0036 | SAS | STU | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | STU | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | STU | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | YRI | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18522 | hp2 | a0001 | c0002 | t0002 | g0125 | AFR | YRI | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | CHB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | CHB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | CHB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | CHB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0300 | AFR | YRI | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18906 | hp2 | a0001 | c0007 | t0003 | g0314 | AFR | YRI | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18998 | hp1 | a0001 | c0001 | t0010 | g0221 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA19030 | hp1 | a0001 | c0003 | t0001 | g0262 | AFR | LWK | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0323 | AFR | LWK | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA19068 | hp2 | a0001 | c0001 | t0007 | g0197 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA19080 | hp1 | a0001 | c0002 | t0002 | g0073 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA19240 | hp1 | a0001 | c0002 | t0002 | g0049 | AFR | YRI | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | YRI | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ASW | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA20129 | hp2 | a0001 | c0002 | t0002 | g0034 | AFR | ASW | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0123 | EUR | TSI | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0188 | EUR | TSI | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0194 | EUR | TSI | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA20805 | hp2 | a0001 | c0002 | t0002 | g0038 | EUR | TSI | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0192 | SAS | GIH | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | GIH | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0243 | AMR | CLM | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02109 | hp1 | a0001 | c0002 | t0002 | g0052 | AFR | ACB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02109 | hp2 | a0001 | c0002 | t0002 | g0035 | AFR | ACB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | ACB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02486 | hp2 | a0001 | c0002 | t0002 | g0043 | AFR | ACB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | ACB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | ACB | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | MSL | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG06807 | hp1 | a0001 | c0002 | t0002 | g0053 | AFR | USA | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | USA | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | USA | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA20300 | hp2 | a0001 | c0002 | t0002 | g0054 | AFR | USA | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA21309 | hp1 | a0001 | c0002 | t0002 | g0045 | AFR | LWK | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | LWK | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0017 | REF | REF | INTS3_chr1_153723050_153779808 | INTS3 | chr1 | 153723050 | 153779808 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:153728720 | G | A | 1 | a0003 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.86G>A | p.Gly29Glu | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/30 | 671/5252 | 86/3129 | 29/1042 | chr1 | 153728720 | |||
| chr1:153770198 | TTCAGAGC others(9): Show |
T | 1 | a0002 | 1 | HG03139.hp2 | frameshift_variant&splice_region_variant | HIGH | c.2391_2406delTCAGAG others(10): Show |
p.Ile797fs | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 24/30 | 2976/5252 | 2391/3129 | 797/1042 | chr1 | 153770198 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:153767809 | G | A | 1 | a0001c0003 | 4 | HG02145.hp2 HG02258.hp1 HG03139.hp1 others(1): Show |
synonymous_variant | LOW | c.2226G>A | p.Thr742Thr | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 21/30 | 2811/5252 | 2226/3129 | 742/1042 | chr1 | 153767809 | |||
| chr1:153772397 | C | T | 1 | a0001c0007 | 1 | NA18906.hp2 | synonymous_variant | LOW | c.2778C>T | p.His926His | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 27/30 | 3363/5252 | 2778/3129 | 926/1042 | chr1 | 153772397 | |||
| chr1:153772652 | G | C | 1 | a0001c0002 | 43 | HG00408.hp1 HG00673.hp1 HG01074.hp1 others(40): Show |
synonymous_variant | LOW | c.2835G>C | p.Thr945Thr | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 28/30 | 3420/5252 | 2835/3129 | 945/1042 | chr1 | 153772652 | |||
| chr1:153773063 | G | A | 1 | a0001c0006 | 1 | HG04204.hp1 | synonymous_variant | LOW | c.3033G>A | p.Ser1011Ser | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 29/30 | 3618/5252 | 3033/3129 | 1011/1042 | chr1 | 153773063 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:153728115 | C | T | 1 | a0001c0001t0012 | 1 | HG03540.hp2 | 5_prime_UTR_variant | MODIFIER | c.-520C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/30 | 520 | chr1 | 153728115 | ||||||
| chr1:153728365 | A | G | 15 | a0001c0001t0001 a0001c0001t0007 a0001c0001t0009 others(12): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
5_prime_UTR_variant | MODIFIER | c.-270A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/30 | 270 | chr1 | 153728365 | ||||||
| chr1:153773750 | A | C | 1 | a0001c0002t0006 | 2 | HG02622.hp1 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*480A>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 30/30 | 480 | chr1 | 153773750 | ||||||
| chr1:153773783 | C | G | 2 | a0001c0002t0004 a0001c0002t0011 |
3 | HG02965.hp1 HG03540.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*513C>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 30/30 | 513 | chr1 | 153773783 | ||||||
| chr1:153773849 | G | T | 2 | a0001c0002t0004 a0001c0002t0011 |
3 | HG02965.hp1 HG03540.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*579G>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 30/30 | 579 | chr1 | 153773849 | ||||||
| chr1:153773984 | CTGTTTTT others(15): Show |
C | 1 | a0001c0001t0007 | 1 | NA19068.hp2 | 3_prime_UTR_variant | MODIFIER | c.*727_*748delTGTTTT others(16): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 30/30 | 727 | INFO_REALIGN_3_PRIME | chr1 | 153773984 | |||||
| chr1:153773998 | G | T | 1 | a0001c0001t0001 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*728G>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 30/30 | 728 | chr1 | 153773998 | ||||||
| chr1:153774134 | G | A | 1 | a0001c0002t0002 | 29 | HG00408.hp1 HG00673.hp1 HG01074.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*864G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 30/30 | 864 | chr1 | 153774134 | ||||||
| chr1:153774145 | C | T | 1 | a0001c0001t0010 | 1 | NA18998.hp1 | 3_prime_UTR_variant | MODIFIER | c.*875C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 30/30 | 875 | chr1 | 153774145 | ||||||
| chr1:153774148 | C | T | 1 | a0001c0002t0005 | 2 | HG01891.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*878C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 30/30 | 878 | chr1 | 153774148 | ||||||
| chr1:153774305 | G | A | 1 | a0001c0002t0002 | 29 | HG00408.hp1 HG00673.hp1 HG01074.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*1035G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 30/30 | 1035 | chr1 | 153774305 | ||||||
| chr1:153774537 | A | G | 1 | a0001c0001t0009 | 1 | HG00558.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1267A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 30/30 | 1267 | chr1 | 153774537 | ||||||
| chr1:153774619 | A | C | 1 | a0001c0002t0008 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1349A>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 30/30 | 1349 | chr1 | 153774619 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:153728867 | G | A | 1 | a0001c0002t0011g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.150+83G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153728867 | |||||||
| chr1:153729022 | T | C | 1 | a0001c0001t0001g0018 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.150+238T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153729022 | |||||||
| chr1:153729049 | T | A | 3 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 |
3 | HG01070.hp1 HG01071.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.150+265T>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153729049 | |||||||
| chr1:153729280 | T | C | 1 | a0001c0001t0001g0022 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.150+496T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153729280 | |||||||
| chr1:153729337 | G | T | 1 | a0001c0001t0001g0326 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.150+553G>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153729337 | |||||||
| chr1:153729429 | G | A | 1 | a0001c0001t0001g0023 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.150+645G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153729429 | |||||||
| chr1:153729819 | T | A | 1 | a0001c0001t0001g0024 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.150+1035T>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153729819 | |||||||
| chr1:153729865 | C | CA | 295 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(292): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.150+1098dupA | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 153729865 | ||||||
| chr1:153729865 | C | CAA | 8 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(5): Show |
8 | HG00423.hp2 HG01175.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.150+1097_150+1098d others(4): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 153729865 | ||||||
| chr1:153730184 | A | G | 1 | a0001c0001t0001g0304 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.150+1400A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153730184 | |||||||
| chr1:153730503 | C | T | 9 | a0001c0001t0001g0295 a0001c0001t0001g0296 a0001c0001t0001g0297 others(6): Show |
9 | HG02451.hp2 HG02559.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.150+1719C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153730503 | |||||||
| chr1:153730537 | C | T | 133 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(130): Show |
138 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.150+1753C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153730537 | |||||||
| chr1:153730541 | ATTGTGTC others(5): Show |
A | 1 | a0001c0001t0001g0186 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.150+1760_150+1771d others(14): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 153730541 | ||||||
| chr1:153730648 | G | A | 27 | a0001c0002t0001g0039 a0001c0002t0002g0006 a0001c0002t0002g0033 others(24): Show |
28 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.150+1864G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153730648 | |||||||
| chr1:153730654 | G | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0057 |
3 | HG01433.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.150+1870G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153730654 | |||||||
| chr1:153730989 | T | C | 2 | a0001c0001t0001g0187 a0001c0001t0001g0188 |
2 | HG04184.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.150+2205T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153730989 | |||||||
| chr1:153731066 | A | G | 1 | a0001c0002t0002g0185 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.150+2282A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153731066 | |||||||
| chr1:153731414 | C | G | 1 | a0001c0001t0001g0303 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.150+2630C>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153731414 | |||||||
| chr1:153731453 | A | G | 1 | a0001c0002t0011g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.150+2669A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153731453 | |||||||
| chr1:153731480 | C | T | 1 | a0001c0001t0001g0184 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.150+2696C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153731480 | |||||||
| chr1:153731558 | T | C | 305 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(302): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.150+2774T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153731558 | |||||||
| chr1:153731577 | C | CT | 140 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(137): Show |
150 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.150+2794dupT | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 153731577 | ||||||
| chr1:153731577 | C | CTT | 16 | a0001c0001t0001g0014 a0001c0001t0001g0174 a0001c0001t0001g0175 others(13): Show |
17 | HG00597.hp1 HG01891.hp2 HG02300.hp1 others(14): Show |
intron_variant | MODIFIER | c.150+2794_150+2795i others(4): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 153731577 | ||||||
| chr1:153731579 | C | CT | 16 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0155 others(13): Show |
16 | HG00621.hp2 HG01496.hp1 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.150+2816dupT | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 153731579 | ||||||
| chr1:153731579 | C | T | 156 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(153): Show |
167 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.150+2795C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153731579 | |||||||
| chr1:153731679 | G | A | 1 | a0001c0001t0001g0295 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.150+2895G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153731679 | |||||||
| chr1:153731680 | G | T | 1 | a0001c0001t0001g0152 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.150+2896G>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153731680 | |||||||
| chr1:153731747 | G | A | 1 | a0001c0002t0011g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.150+2963G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153731747 | |||||||
| chr1:153731901 | C | CT | 174 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(171): Show |
189 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.150+3141dupT | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 153731901 | ||||||
| chr1:153731901 | C | CTT | 23 | a0001c0001t0001g0022 a0001c0001t0001g0032 a0001c0001t0001g0150 others(20): Show |
23 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.150+3140_150+3141d others(4): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 153731901 | ||||||
| chr1:153731901 | CT | C | 25 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(22): Show |
26 | HG01081.hp1 HG01167.hp1 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.150+3141delT | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 153731901 | ||||||
| chr1:153731957 | G | C | 2 | a0001c0002t0001g0061 a0001c0002t0001g0307 |
2 | HG02615.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.150+3173G>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153731957 | |||||||
| chr1:153732193 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.150+3409G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153732193 | |||||||
| chr1:153732206 | G | A | 1 | a0001c0002t0002g0056 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.150+3422G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153732206 | |||||||
| chr1:153732242 | A | G | 1 | a0001c0001t0001g0272 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.150+3458A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153732242 | |||||||
| chr1:153732278 | A | G | 1 | a0001c0002t0011g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.150+3494A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153732278 | |||||||
| chr1:153732296 | A | G | 1 | a0002c0005t0001g0271 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.150+3512A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153732296 | |||||||
| chr1:153732299 | T | C | 1 | a0001c0002t0004g0313 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.150+3515T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153732299 | |||||||
| chr1:153732433 | G | A | 2 | a0001c0002t0001g0061 a0001c0002t0001g0307 |
2 | HG02615.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.150+3649G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153732433 | |||||||
| chr1:153732447 | A | AT | 7 | a0001c0001t0001g0026 a0001c0001t0001g0031 a0001c0001t0001g0123 others(4): Show |
7 | HG01175.hp2 HG01243.hp1 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.150+3679dupT | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 153732447 | ||||||
| chr1:153732447 | AT | A | 16 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0027 others(13): Show |
19 | HG01256.hp1 HG01433.hp1 HG01515.hp1 others(16): Show |
intron_variant | MODIFIER | c.150+3679delT | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 153732447 | ||||||
| chr1:153732501 | A | G | 2 | a0001c0002t0001g0148 a0001c0002t0008g0312 |
2 | HG01109.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.150+3717A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153732501 | |||||||
| chr1:153732622 | A | G | 1 | a0001c0001t0001g0270 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.150+3838A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153732622 | |||||||
| chr1:153732706 | C | T | 2 | a0001c0001t0001g0005 a0001c0001t0001g0181 |
4 | HG00735.hp1 HG01123.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.150+3922C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153732706 | |||||||
| chr1:153732808 | C | CT | 154 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(151): Show |
165 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.150+4037dupT | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 153732808 | ||||||
| chr1:153732808 | CT | C | 12 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0057 others(9): Show |
15 | HG01433.hp1 HG02257.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.150+4037delT | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 153732808 | ||||||
| chr1:153732810 | T | G | 1 | a0001c0002t0002g0033 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.150+4026T>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153732810 | |||||||
| chr1:153733002 | C | T | 2 | a0001c0002t0005g0305 a0001c0002t0005g0306 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.150+4218C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153733002 | |||||||
| chr1:153733130 | C | T | 1 | a0001c0002t0001g0148 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.150+4346C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153733130 | |||||||
| chr1:153733134 | C | G | 1 | a0001c0001t0001g0121 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.150+4350C>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153733134 | |||||||
| chr1:153733174 | T | C | 3 | a0001c0002t0001g0010 a0001c0002t0006g0130 a0001c0002t0006g0131 |
4 | HG02622.hp1 HG02630.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.150+4390T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153733174 | |||||||
| chr1:153733197 | CTT | C | 40 | a0001c0001t0001g0026 a0001c0001t0001g0062 a0001c0001t0001g0103 others(37): Show |
40 | HG00408.hp1 HG00621.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.150+4444_150+4445d others(4): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 153733197 | ||||||
| chr1:153733197 | CTTT | C | 134 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(131): Show |
142 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(139): Show |
intron_variant | MODIFIER | c.150+4443_150+4445d others(5): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 153733197 | ||||||
| chr1:153733197 | CTTTT | C | 115 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(112): Show |
126 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.150+4442_150+4445d others(6): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 153733197 | ||||||
| chr1:153733197 | CTTTTT | C | 25 | a0001c0001t0001g0007 a0001c0001t0001g0057 a0001c0001t0001g0198 others(22): Show |
27 | HG01081.hp1 HG01109.hp2 HG01192.hp2 others(24): Show |
intron_variant | MODIFIER | c.150+4441_150+4445d others(7): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 153733197 | ||||||
| chr1:153733197 | CTTTTTTT others(8): Show |
C | 8 | a0001c0001t0001g0003 a0001c0001t0001g0124 a0001c0001t0001g0126 others(5): Show |
10 | HG02257.hp1 HG02486.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.150+4431_150+4445d others(17): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 153733197 | ||||||
| chr1:153733299 | G | A | 2 | a0001c0002t0001g0061 a0001c0002t0001g0307 |
2 | HG02615.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.150+4515G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153733299 | |||||||
| chr1:153733369 | C | T | 2 | a0001c0002t0001g0061 a0001c0002t0001g0307 |
2 | HG02615.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.150+4585C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153733369 | |||||||
| chr1:153733622 | T | G | 1 | a0001c0002t0011g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.150+4838T>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153733622 | |||||||
| chr1:153733666 | G | A | 12 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 others(9): Show |
12 | HG02258.hp2 HG02451.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.150+4882G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153733666 | |||||||
| chr1:153733753 | C | T | 2 | a0001c0002t0001g0061 a0001c0002t0001g0307 |
2 | HG02615.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.150+4969C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153733753 | |||||||
| chr1:153733766 | G | A | 1 | a0001c0001t0001g0248 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.150+4982G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153733766 | |||||||
| chr1:153733820 | C | G | 1 | a0001c0001t0001g0146 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.150+5036C>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153733820 | |||||||
| chr1:153733841 | G | T | 1 | a0001c0001t0001g0060 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.150+5057G>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153733841 | |||||||
| chr1:153733869 | T | C | 1 | a0001c0001t0007g0197 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.150+5085T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153733869 | |||||||
| chr1:153734209 | T | C | 1 | a0001c0002t0002g0045 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.150+5425T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153734209 | |||||||
| chr1:153734223 | T | G | 217 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(214): Show |
233 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(230): Show |
intron_variant | MODIFIER | c.150+5439T>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153734223 | |||||||
| chr1:153734375 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.150+5591T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153734375 | |||||||
| chr1:153734413 | ACTT | A | 3 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 |
3 | HG03490.hp1 HG03492.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.150+5633_150+5635d others(5): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 153734413 | ||||||
| chr1:153734563 | T | C | 1 | a0001c0002t0002g0045 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.150+5779T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153734563 | |||||||
| chr1:153734616 | G | T | 1 | a0001c0001t0001g0186 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.150+5832G>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153734616 | |||||||
| chr1:153734749 | A | C | 1 | a0001c0001t0001g0286 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.151-5902A>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153734749 | |||||||
| chr1:153734784 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.151-5867A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153734784 | |||||||
| chr1:153734831 | A | G | 2 | a0001c0001t0001g0019 a0001c0001t0001g0020 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.151-5820A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153734831 | |||||||
| chr1:153734884 | A | G | 3 | a0001c0002t0001g0010 a0001c0002t0006g0130 a0001c0002t0006g0131 |
4 | HG02622.hp1 HG02630.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.151-5767A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153734884 | |||||||
| chr1:153734953 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.151-5698C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153734953 | |||||||
| chr1:153736002 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.151-4649G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153736002 | |||||||
| chr1:153736063 | C | T | 1 | a0001c0001t0001g0300 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.151-4588C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153736063 | |||||||
| chr1:153736157 | A | G | 30 | a0001c0002t0001g0039 a0001c0002t0001g0061 a0001c0002t0001g0307 others(27): Show |
31 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.151-4494A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153736157 | |||||||
| chr1:153736276 | T | G | 1 | a0001c0001t0001g0066 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.151-4375T>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153736276 | |||||||
| chr1:153736355 | A | T | 1 | a0001c0001t0012g0138 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.151-4296A>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153736355 | |||||||
| chr1:153736381 | T | A | 1 | a0001c0001t0001g0200 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.151-4270T>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153736381 | |||||||
| chr1:153736430 | G | A | 29 | a0001c0002t0001g0039 a0001c0002t0001g0061 a0001c0002t0001g0307 others(26): Show |
30 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.151-4221G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153736430 | |||||||
| chr1:153736451 | C | CT | 156 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(153): Show |
167 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.151-4187dupT | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 153736451 | ||||||
| chr1:153736508 | G | A | 9 | a0001c0001t0001g0005 a0001c0001t0001g0176 a0001c0001t0001g0177 others(6): Show |
11 | HG00621.hp2 HG00735.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.151-4143G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153736508 | |||||||
| chr1:153736571 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.151-4080C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153736571 | |||||||
| chr1:153736761 | C | CT | 173 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(170): Show |
186 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(183): Show |
intron_variant | MODIFIER | c.151-3870dupT | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 153736761 | ||||||
| chr1:153736761 | C | CTT | 19 | a0001c0001t0001g0164 a0001c0001t0001g0244 a0001c0001t0001g0269 others(16): Show |
19 | HG02055.hp2 HG02056.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.151-3871_151-3870d others(4): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 153736761 | ||||||
| chr1:153736856 | C | T | 2 | a0001c0002t0006g0130 a0001c0002t0006g0131 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.151-3795C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153736856 | |||||||
| chr1:153736905 | A | G | 1 | a0001c0001t0001g0066 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.151-3746A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153736905 | |||||||
| chr1:153737213 | C | T | 1 | a0001c0002t0002g0045 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.151-3438C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153737213 | |||||||
| chr1:153737495 | G | A | 30 | a0001c0002t0001g0039 a0001c0002t0001g0061 a0001c0002t0001g0307 others(27): Show |
31 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.151-3156G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153737495 | |||||||
| chr1:153737500 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.151-3151C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153737500 | |||||||
| chr1:153737820 | T | C | 1 | a0001c0002t0011g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.151-2831T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153737820 | |||||||
| chr1:153737841 | T | A | 1 | a0001c0002t0001g0039 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.151-2810T>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153737841 | |||||||
| chr1:153738072 | G | A | 1 | a0001c0001t0001g0068 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.151-2579G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153738072 | |||||||
| chr1:153738140 | C | T | 1 | a0001c0001t0001g0015 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.151-2511C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153738140 | |||||||
| chr1:153738220 | T | C | 68 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(65): Show |
73 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.151-2431T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153738220 | |||||||
| chr1:153738326 | C | T | 1 | a0001c0002t0011g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.151-2325C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153738326 | |||||||
| chr1:153738335 | A | G | 1 | a0001c0001t0001g0194 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.151-2316A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153738335 | |||||||
| chr1:153738390 | A | C | 1 | a0001c0001t0001g0183 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.151-2261A>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153738390 | |||||||
| chr1:153738442 | T | C | 4 | a0001c0001t0001g0186 a0001c0002t0001g0010 a0001c0002t0006g0130 others(1): Show |
5 | HG02622.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.151-2209T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153738442 | |||||||
| chr1:153738627 | G | A | 1 | a0001c0002t0002g0045 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.151-2024G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153738627 | |||||||
| chr1:153738634 | T | C | 1 | a0001c0001t0001g0195 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.151-2017T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153738634 | |||||||
| chr1:153738788 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.151-1863A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153738788 | |||||||
| chr1:153738792 | T | C | 156 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(153): Show |
167 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(164): Show |
intron_variant | MODIFIER | c.151-1859T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153738792 | |||||||
| chr1:153738893 | CT | C | 36 | a0001c0001t0001g0069 a0001c0001t0001g0201 a0001c0001t0001g0202 others(33): Show |
38 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.151-1741delT | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | INFO_REALIGN_3_PRIME | chr1 | 153738893 | ||||||
| chr1:153738927 | C | T | 1 | a0001c0002t0011g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.151-1724C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153738927 | |||||||
| chr1:153738940 | C | G | 4 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0115 others(1): Show |
4 | HG01433.hp2 HG01952.hp2 HG02027.hp2 others(1): Show |
intron_variant | MODIFIER | c.151-1711C>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153738940 | |||||||
| chr1:153739189 | G | A | 1 | a0001c0001t0001g0301 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.151-1462G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153739189 | |||||||
| chr1:153739211 | G | A | 1 | a0001c0002t0011g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.151-1440G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153739211 | |||||||
| chr1:153739435 | T | C | 30 | a0001c0002t0001g0039 a0001c0002t0001g0061 a0001c0002t0001g0307 others(27): Show |
31 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.151-1216T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153739435 | |||||||
| chr1:153739467 | C | T | 2 | a0001c0002t0001g0148 a0001c0002t0008g0312 |
2 | HG01109.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.151-1184C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153739467 | |||||||
| chr1:153739486 | A | G | 304 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(301): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.151-1165A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153739486 | |||||||
| chr1:153739585 | C | T | 1 | a0001c0002t0011g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.151-1066C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153739585 | |||||||
| chr1:153739888 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.151-763G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153739888 | |||||||
| chr1:153739899 | A | G | 1 | a0001c0001t0001g0280 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.151-752A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153739899 | |||||||
| chr1:153739907 | G | T | 16 | a0001c0002t0001g0039 a0001c0002t0002g0006 a0001c0002t0002g0033 others(13): Show |
17 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.151-744G>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153739907 | |||||||
| chr1:153739914 | T | C | 1 | a0001c0001t0001g0070 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.151-737T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153739914 | |||||||
| chr1:153739949 | C | A | 27 | a0001c0002t0001g0039 a0001c0002t0002g0006 a0001c0002t0002g0033 others(24): Show |
28 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.151-702C>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153739949 | |||||||
| chr1:153740163 | G | A | 3 | a0001c0001t0001g0295 a0001c0001t0001g0297 a0001c0001t0001g0302 |
3 | HG02647.hp1 HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.151-488G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153740163 | |||||||
| chr1:153740204 | A | C | 1 | a0001c0001t0001g0186 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.151-447A>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153740204 | |||||||
| chr1:153740257 | G | A | 1 | a0001c0001t0001g0281 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.151-394G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153740257 | |||||||
| chr1:153740300 | G | A | 1 | a0001c0001t0001g0066 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.151-351G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153740300 | |||||||
| chr1:153740315 | G | A | 29 | a0001c0002t0001g0039 a0001c0002t0001g0061 a0001c0002t0001g0307 others(26): Show |
30 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.151-336G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 1/29 | chr1 | 153740315 | |||||||
| chr1:153740890 | G | A | 1 | a0001c0002t0006g0131 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.234+156G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 2/29 | chr1 | 153740890 | |||||||
| chr1:153741143 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.235-142G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 2/29 | chr1 | 153741143 | |||||||
| chr1:153741407 | A | G | 1 | a0001c0002t0002g0049 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.318+39A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153741407 | |||||||
| chr1:153741454 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.318+86G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153741454 | |||||||
| chr1:153741703 | T | C | 1 | a0001c0001t0003g0320 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.318+335T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153741703 | |||||||
| chr1:153741748 | G | A | 1 | a0001c0002t0011g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.318+380G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153741748 | |||||||
| chr1:153741776 | G | A | 124 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(121): Show |
129 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.318+408G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153741776 | |||||||
| chr1:153741942 | C | T | 169 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(166): Show |
176 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(173): Show |
intron_variant | MODIFIER | c.318+574C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153741942 | |||||||
| chr1:153741958 | C | T | 1 | a0001c0001t0001g0172 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.318+590C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153741958 | |||||||
| chr1:153742282 | G | A | 1 | a0001c0001t0001g0280 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.318+914G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153742282 | |||||||
| chr1:153742343 | T | C | 6 | a0001c0001t0001g0011 a0001c0001t0001g0244 a0001c0001t0001g0249 others(3): Show |
7 | NA18950.hp2 NA18953.hp2 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.318+975T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153742343 | |||||||
| chr1:153742425 | G | T | 1 | a0001c0001t0010g0221 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.318+1057G>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153742425 | |||||||
| chr1:153742478 | C | CTCTGTGT others(3): Show |
1 | a0001c0002t0011g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.318+1111_318+1112i others(12): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153742478 | ||||||
| chr1:153742478 | C | CTCTGTGT others(15): Show |
1 | a0001c0002t0002g0045 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.318+1111_318+1112i others(24): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153742478 | ||||||
| chr1:153742478 | C | CTG | 73 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(70): Show |
80 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.318+1139_318+1140d others(4): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153742478 | ||||||
| chr1:153742478 | C | CTGTG | 5 | a0001c0001t0001g0129 a0001c0001t0001g0220 a0001c0001t0001g0261 others(2): Show |
5 | HG01496.hp2 HG02080.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.318+1137_318+1140d others(6): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153742478 | ||||||
| chr1:153742478 | C | CTGTGTGT others(1): Show |
3 | a0001c0002t0002g0050 a0001c0002t0002g0053 a0001c0002t0002g0054 |
3 | HG03130.hp2 HG06807.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.318+1133_318+1140d others(10): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153742478 | ||||||
| chr1:153742478 | C | CTGTGTGT others(3): Show |
2 | a0001c0002t0002g0051 a0001c0002t0006g0130 |
2 | HG02630.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.318+1131_318+1140d others(12): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153742478 | ||||||
| chr1:153742478 | C | CTGTGTGT others(5): Show |
2 | a0001c0002t0002g0047 a0001c0002t0002g0055 |
2 | HG01074.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.318+1129_318+1140d others(14): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153742478 | ||||||
| chr1:153742478 | C | CTGTGTGT others(7): Show |
6 | a0001c0001t0001g0186 a0001c0002t0001g0010 a0001c0002t0002g0033 others(3): Show |
7 | HG02109.hp1 HG02622.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.318+1127_318+1140d others(16): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153742478 | ||||||
| chr1:153742478 | C | CTGTGTGT others(9): Show |
2 | a0001c0002t0001g0307 a0001c0002t0002g0040 |
2 | HG01167.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.318+1125_318+1140d others(18): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153742478 | ||||||
| chr1:153742478 | C | CTGTGTGT others(11): Show |
7 | a0001c0002t0001g0061 a0001c0002t0002g0034 a0001c0002t0002g0035 others(4): Show |
7 | HG01891.hp1 HG02109.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.318+1123_318+1140d others(20): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153742478 | ||||||
| chr1:153742478 | C | CTGTGTGT others(13): Show |
5 | a0001c0002t0001g0039 a0001c0002t0002g0006 a0001c0002t0002g0037 others(2): Show |
6 | HG01081.hp1 HG01192.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.318+1121_318+1140d others(22): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153742478 | ||||||
| chr1:153742478 | C | CTGTGTGT others(15): Show |
1 | a0001c0002t0002g0046 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.318+1119_318+1140d others(24): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153742478 | ||||||
| chr1:153742478 | C | G | 2 | a0001c0002t0001g0148 a0001c0002t0008g0312 |
2 | HG01109.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.318+1110C>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153742478 | |||||||
| chr1:153742478 | CTG | C | 192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(189): Show |
203 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.318+1139_318+1140d others(4): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153742478 | ||||||
| chr1:153742505 | T | TGTGTGTG others(9): Show |
1 | a0001c0002t0002g0049 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.318+1140_318+1141i others(18): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153742505 | ||||||
| chr1:153742507 | T | C | 2 | a0001c0001t0001g0103 a0001c0001t0001g0183 |
2 | HG00621.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.318+1139T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153742507 | |||||||
| chr1:153742507 | T | TGTGTGTG others(9): Show |
1 | a0001c0002t0008g0312 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.318+1140_318+1141i others(18): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153742507 | ||||||
| chr1:153742547 | C | G | 2 | a0001c0002t0001g0061 a0001c0002t0001g0307 |
2 | HG02615.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.318+1179C>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153742547 | |||||||
| chr1:153742559 | C | CATCTCAG others(5): Show |
1 | a0001c0001t0001g0283 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.318+1193_318+1194i others(14): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153742559 | ||||||
| chr1:153742666 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.318+1298G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153742666 | |||||||
| chr1:153742925 | C | A | 1 | a0001c0001t0001g0140 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.318+1557C>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153742925 | |||||||
| chr1:153743028 | G | A | 13 | a0001c0001t0001g0001 a0001c0001t0001g0156 a0001c0001t0001g0157 others(10): Show |
17 | HG01069.hp1 HG01255.hp2 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.318+1660G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153743028 | |||||||
| chr1:153743605 | CCTT | C | 133 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(130): Show |
138 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(135): Show |
intron_variant | MODIFIER | c.318+2241_318+2243d others(5): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153743605 | ||||||
| chr1:153743646 | T | A | 2 | a0001c0002t0006g0130 a0001c0002t0006g0131 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.318+2278T>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153743646 | |||||||
| chr1:153743710 | C | G | 2 | a0001c0002t0006g0130 a0001c0002t0006g0131 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.318+2342C>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153743710 | |||||||
| chr1:153743759 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.318+2391C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153743759 | |||||||
| chr1:153743973 | C | T | 2 | a0001c0001t0001g0195 a0001c0001t0001g0247 |
2 | HG03704.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.318+2605C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153743973 | |||||||
| chr1:153744007 | T | G | 3 | a0001c0001t0001g0193 a0001c0001t0001g0196 a0001c0001t0001g0273 |
3 | HG01081.hp2 HG01975.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.318+2639T>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153744007 | |||||||
| chr1:153744038 | C | CGT | 7 | a0001c0001t0001g0062 a0001c0001t0001g0140 a0001c0001t0001g0151 others(4): Show |
7 | HG02055.hp1 HG02622.hp2 HG03492.hp2 others(4): Show |
intron_variant | MODIFIER | c.318+2713_318+2714d others(4): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153744038 | ||||||
| chr1:153744038 | C | CGTGTGTG others(5): Show |
1 | a0001c0002t0001g0148 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.318+2703_318+2714d others(14): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153744038 | ||||||
| chr1:153744038 | CGT | C | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(92): Show |
107 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.318+2713_318+2714d others(4): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153744038 | ||||||
| chr1:153744038 | CGTGT | C | 45 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0057 others(42): Show |
50 | HG00099.hp1 HG00621.hp2 HG01081.hp1 others(47): Show |
intron_variant | MODIFIER | c.318+2711_318+2714d others(6): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153744038 | ||||||
| chr1:153744038 | CGTGTGT | C | 120 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(117): Show |
125 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(122): Show |
intron_variant | MODIFIER | c.318+2709_318+2714d others(8): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153744038 | ||||||
| chr1:153744038 | CGTGTGTG others(3): Show |
C | 3 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0243 |
3 | HG01123.hp2 HG02717.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.318+2705_318+2714d others(12): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153744038 | ||||||
| chr1:153744038 | CGTGTGTG others(9): Show |
C | 1 | a0001c0001t0001g0177 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.318+2699_318+2714d others(18): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153744038 | ||||||
| chr1:153744038 | CGTGTGTG others(11): Show |
C | 1 | a0001c0001t0001g0246 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.318+2697_318+2714d others(20): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153744038 | ||||||
| chr1:153744038 | CGTGTGTG others(13): Show |
C | 8 | a0001c0001t0001g0023 a0001c0001t0001g0065 a0001c0001t0001g0098 others(5): Show |
8 | HG02080.hp1 NA18982.hp1 NA18982.hp2 others(5): Show |
intron_variant | MODIFIER | c.318+2695_318+2714d others(22): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153744038 | ||||||
| chr1:153744046 | T | C | 1 | a0001c0001t0001g0285 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.318+2678T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153744046 | |||||||
| chr1:153744065 | GTGTGTGT others(10): Show |
G | 1 | a0001c0001t0001g0245 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.318+2699_318+2715d others(19): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153744065 | ||||||
| chr1:153744088 | C | A | 1 | a0001c0003t0001g0223 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.318+2720C>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153744088 | |||||||
| chr1:153744396 | T | C | 1 | a0001c0001t0001g0302 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.319-2561T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153744396 | |||||||
| chr1:153744649 | G | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0104 |
3 | HG00639.hp1 HG01074.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.319-2308G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153744649 | |||||||
| chr1:153744682 | C | G | 1 | a0001c0001t0001g0190 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.319-2275C>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153744682 | |||||||
| chr1:153744706 | G | A | 29 | a0001c0002t0001g0039 a0001c0002t0001g0061 a0001c0002t0001g0307 others(26): Show |
30 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.319-2251G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153744706 | |||||||
| chr1:153744848 | C | T | 3 | a0001c0001t0001g0095 a0001c0001t0001g0163 a0001c0001t0001g0171 |
3 | HG00408.hp2 NA18983.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.319-2109C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153744848 | |||||||
| chr1:153745083 | C | CAT | 4 | a0001c0001t0001g0186 a0001c0002t0001g0010 a0001c0002t0006g0130 others(1): Show |
5 | HG02622.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.319-1863_319-1862d others(4): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153745083 | ||||||
| chr1:153745083 | CAT | C | 13 | a0001c0001t0001g0099 a0001c0001t0001g0132 a0001c0001t0001g0133 others(10): Show |
13 | HG02258.hp2 HG02451.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.319-1863_319-1862d others(4): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153745083 | ||||||
| chr1:153745161 | C | CT | 190 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(187): Show |
200 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(197): Show |
intron_variant | MODIFIER | c.319-1781dupT | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | INFO_REALIGN_3_PRIME | chr1 | 153745161 | ||||||
| chr1:153745220 | G | C | 2 | a0001c0002t0006g0130 a0001c0002t0006g0131 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.319-1737G>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153745220 | |||||||
| chr1:153745303 | C | T | 13 | a0001c0001t0001g0099 a0001c0001t0001g0132 a0001c0001t0001g0133 others(10): Show |
13 | HG02258.hp2 HG02451.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.319-1654C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153745303 | |||||||
| chr1:153745304 | G | A | 2 | a0001c0001t0001g0165 a0001c0001t0001g0283 |
2 | HG02300.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.319-1653G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153745304 | |||||||
| chr1:153745350 | T | G | 1 | a0001c0002t0002g0055 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.319-1607T>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153745350 | |||||||
| chr1:153745402 | A | G | 44 | a0001c0001t0001g0099 a0001c0001t0001g0132 a0001c0001t0001g0133 others(41): Show |
45 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.319-1555A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153745402 | |||||||
| chr1:153745408 | C | T | 10 | a0001c0001t0001g0003 a0001c0001t0001g0124 a0001c0001t0001g0126 others(7): Show |
12 | HG02257.hp1 HG02486.hp1 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.319-1549C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153745408 | |||||||
| chr1:153745409 | G | A | 2 | a0001c0001t0001g0007 a0001c0001t0001g0057 |
3 | HG01433.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.319-1548G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153745409 | |||||||
| chr1:153745484 | T | G | 18 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(15): Show |
18 | HG01433.hp2 HG01952.hp2 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.319-1473T>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153745484 | |||||||
| chr1:153745547 | C | T | 3 | a0001c0001t0001g0137 a0001c0001t0001g0151 a0001c0001t0001g0155 |
3 | HG02622.hp2 HG02630.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.319-1410C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153745547 | |||||||
| chr1:153745593 | G | A | 2 | a0001c0002t0001g0061 a0001c0002t0001g0307 |
2 | HG02615.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.319-1364G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153745593 | |||||||
| chr1:153745740 | T | C | 2 | a0001c0002t0002g0037 a0001c0002t0011g0016 |
2 | HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.319-1217T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153745740 | |||||||
| chr1:153745832 | A | G | 14 | a0001c0001t0001g0099 a0001c0001t0001g0132 a0001c0001t0001g0133 others(11): Show |
14 | HG02258.hp2 HG02451.hp1 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.319-1125A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153745832 | |||||||
| chr1:153745862 | T | C | 32 | a0001c0001t0001g0186 a0001c0002t0001g0039 a0001c0002t0001g0061 others(29): Show |
33 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(30): Show |
intron_variant | MODIFIER | c.319-1095T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153745862 | |||||||
| chr1:153745864 | A | G | 29 | a0001c0002t0001g0039 a0001c0002t0002g0006 a0001c0002t0002g0033 others(26): Show |
30 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(27): Show |
intron_variant | MODIFIER | c.319-1093A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153745864 | |||||||
| chr1:153745965 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.319-992C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153745965 | |||||||
| chr1:153745966 | G | A | 3 | a0001c0001t0003g0315 a0001c0002t0005g0305 a0001c0002t0005g0306 |
3 | HG01891.hp1 HG03041.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.319-991G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153745966 | |||||||
| chr1:153745996 | G | T | 183 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(180): Show |
190 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(187): Show |
intron_variant | MODIFIER | c.319-961G>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153745996 | |||||||
| chr1:153746034 | C | G | 2 | a0001c0002t0001g0061 a0001c0002t0001g0307 |
2 | HG02615.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.319-923C>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153746034 | |||||||
| chr1:153746270 | G | A | 171 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(168): Show |
178 | HG00099.hp1 HG00423.hp2 HG00544.hp1 others(175): Show |
intron_variant | MODIFIER | c.319-687G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153746270 | |||||||
| chr1:153746421 | G | A | 3 | a0001c0001t0001g0178 a0001c0001t0001g0180 a0001c0001t0001g0182 |
3 | HG01106.hp1 HG01175.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.319-536G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153746421 | |||||||
| chr1:153746425 | C | T | 145 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0018 others(142): Show |
149 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.319-532C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153746425 | |||||||
| chr1:153746463 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.319-494C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153746463 | |||||||
| chr1:153746464 | G | A | 1 | a0001c0002t0008g0312 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.319-493G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153746464 | |||||||
| chr1:153746511 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.319-446C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153746511 | |||||||
| chr1:153746556 | G | A | 1 | a0001c0001t0001g0166 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.319-401G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153746556 | |||||||
| chr1:153746557 | T | C | 1 | a0001c0001t0001g0166 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.319-400T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153746557 | |||||||
| chr1:153746562 | G | A | 5 | a0001c0001t0001g0003 a0001c0001t0001g0124 a0001c0001t0001g0126 others(2): Show |
7 | HG02257.hp1 HG02486.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.319-395G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153746562 | |||||||
| chr1:153746602 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.319-355C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153746602 | |||||||
| chr1:153746652 | T | C | 3 | a0001c0001t0001g0005 a0001c0001t0001g0173 a0001c0001t0001g0181 |
5 | HG00735.hp1 HG01123.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.319-305T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153746652 | |||||||
| chr1:153746653 | G | A | 1 | a0001c0001t0001g0173 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.319-304G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153746653 | |||||||
| chr1:153746692 | C | T | 11 | a0001c0001t0001g0099 a0001c0001t0001g0132 a0001c0001t0001g0133 others(8): Show |
11 | HG02258.hp2 HG02451.hp1 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.319-265C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153746692 | |||||||
| chr1:153746837 | A | C | 1 | a0001c0001t0001g0120 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.319-120A>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153746837 | |||||||
| chr1:153746920 | C | T | 1 | a0001c0001t0001g0026 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.319-37C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 3/29 | chr1 | 153746920 | |||||||
| chr1:153747169 | T | C | 9 | a0001c0001t0001g0005 a0001c0001t0001g0176 a0001c0001t0001g0177 others(6): Show |
11 | HG00621.hp2 HG00735.hp1 HG01106.hp1 others(8): Show |
intron_variant | MODIFIER | c.432+99T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 4/29 | chr1 | 153747169 | |||||||
| chr1:153747582 | T | C | 1 | a0001c0002t0011g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.517+219T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 5/29 | chr1 | 153747582 | |||||||
| chr1:153747943 | C | G | 1 | a0001c0002t0011g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.517+580C>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 5/29 | chr1 | 153747943 | |||||||
| chr1:153748069 | A | C | 4 | a0001c0001t0001g0186 a0001c0002t0001g0010 a0001c0002t0006g0130 others(1): Show |
5 | HG02622.hp1 HG02630.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.518-620A>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 5/29 | chr1 | 153748069 | |||||||
| chr1:153748214 | G | A | 190 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(187): Show |
198 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(195): Show |
intron_variant | MODIFIER | c.518-475G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 5/29 | chr1 | 153748214 | |||||||
| chr1:153748255 | G | A | 1 | a0001c0002t0011g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.518-434G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 5/29 | chr1 | 153748255 | |||||||
| chr1:153748454 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.518-235G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 5/29 | chr1 | 153748454 | |||||||
| chr1:153748574 | G | A | 1 | a0001c0002t0011g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.518-115G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 5/29 | chr1 | 153748574 | |||||||
| chr1:153748827 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.584+72G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 6/29 | chr1 | 153748827 | |||||||
| chr1:153748863 | T | C | 2 | a0001c0002t0005g0305 a0001c0002t0005g0306 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.584+108T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 6/29 | chr1 | 153748863 | |||||||
| chr1:153748919 | A | T | 2 | a0001c0002t0005g0305 a0001c0002t0005g0306 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.584+164A>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 6/29 | chr1 | 153748919 | |||||||
| chr1:153749129 | G | A | 15 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0032 others(12): Show |
17 | HG00423.hp2 HG00673.hp2 HG01516.hp1 others(14): Show |
intron_variant | MODIFIER | c.584+374G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 6/29 | chr1 | 153749129 | |||||||
| chr1:153749131 | T | C | 1 | a0001c0001t0001g0225 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.584+376T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 6/29 | chr1 | 153749131 | |||||||
| chr1:153749158 | A | G | 1 | a0001c0001t0001g0161 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.584+403A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 6/29 | chr1 | 153749158 | |||||||
| chr1:153749232 | T | A | 2 | a0001c0002t0001g0061 a0001c0002t0001g0307 |
2 | HG02615.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.584+477T>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 6/29 | chr1 | 153749232 | |||||||
| chr1:153749543 | G | A | 7 | a0001c0002t0002g0050 a0001c0002t0002g0051 a0001c0002t0002g0052 others(4): Show |
7 | HG02109.hp1 HG02723.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.584+788G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 6/29 | chr1 | 153749543 | |||||||
| chr1:153749608 | C | T | 2 | a0001c0002t0001g0061 a0001c0002t0001g0307 |
2 | HG02615.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.584+853C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 6/29 | chr1 | 153749608 | |||||||
| chr1:153749706 | T | C | 6 | a0001c0001t0001g0008 a0001c0001t0001g0068 a0001c0001t0001g0070 others(3): Show |
7 | HG00099.hp2 HG00140.hp2 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.584+951T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 6/29 | chr1 | 153749706 | |||||||
| chr1:153749791 | C | T | 4 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0136 others(1): Show |
4 | HG02717.hp1 HG03540.hp2 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.584+1036C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 6/29 | chr1 | 153749791 | |||||||
| chr1:153750059 | G | A | 1 | a0001c0002t0002g0049 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.585-1036G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 6/29 | chr1 | 153750059 | |||||||
| chr1:153750229 | A | G | 1 | a0001c0002t0002g0045 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.585-866A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 6/29 | chr1 | 153750229 | |||||||
| chr1:153750276 | G | A | 1 | a0001c0001t0001g0248 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.585-819G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 6/29 | chr1 | 153750276 | |||||||
| chr1:153750561 | T | C | 16 | a0001c0002t0001g0039 a0001c0002t0002g0006 a0001c0002t0002g0033 others(13): Show |
17 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.585-534T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 6/29 | chr1 | 153750561 | |||||||
| chr1:153750568 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.585-527C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 6/29 | chr1 | 153750568 | |||||||
| chr1:153750574 | G | T | 1 | a0001c0001t0001g0208 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.585-521G>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 6/29 | chr1 | 153750574 | |||||||
| chr1:153750994 | C | T | 8 | a0001c0002t0002g0045 a0001c0002t0002g0050 a0001c0002t0002g0051 others(5): Show |
8 | HG02109.hp1 HG02723.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.585-101C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 6/29 | chr1 | 153750994 | |||||||
| chr1:153751017 | C | T | 1 | a0001c0001t0001g0301 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.585-78C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 6/29 | chr1 | 153751017 | |||||||
| chr1:153751354 | C | G | 1 | a0001c0002t0002g0045 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.729+115C>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 7/29 | chr1 | 153751354 | |||||||
| chr1:153751414 | A | G | 1 | a0001c0001t0001g0113 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.729+175A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 7/29 | chr1 | 153751414 | |||||||
| chr1:153751856 | T | C | 1 | a0001c0001t0001g0261 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.730-423T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 7/29 | chr1 | 153751856 | |||||||
| chr1:153752252 | G | A | 4 | a0001c0002t0002g0050 a0001c0002t0002g0051 a0001c0002t0002g0053 others(1): Show |
4 | HG03130.hp2 HG03195.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.730-27G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 7/29 | chr1 | 153752252 | |||||||
| chr1:153752506 | C | T | 5 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0057 others(2): Show |
7 | HG01433.hp1 HG02895.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.859+98C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153752506 | |||||||
| chr1:153752769 | C | T | 2 | a0001c0002t0001g0061 a0001c0002t0001g0307 |
2 | HG02615.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.859+361C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153752769 | |||||||
| chr1:153752770 | G | A | 3 | a0001c0001t0001g0015 a0001c0001t0001g0310 a0003c0004t0001g0149 |
4 | HG02896.hp1 HG02897.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.859+362G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153752770 | |||||||
| chr1:153752828 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.859+420G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153752828 | |||||||
| chr1:153752834 | T | A | 5 | a0001c0001t0001g0132 a0001c0001t0001g0135 a0001c0001t0001g0143 others(2): Show |
5 | HG02258.hp2 HG02451.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.859+426T>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153752834 | |||||||
| chr1:153752873 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.859+465C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153752873 | |||||||
| chr1:153753007 | C | T | 1 | a0001c0001t0001g0242 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.859+599C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153753007 | |||||||
| chr1:153753016 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.859+608G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153753016 | |||||||
| chr1:153753042 | T | TAC | 34 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0023 others(31): Show |
36 | HG00099.hp2 HG00140.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.859+661_859+662dup others(2): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr1 | 153753042 | ||||||
| chr1:153753042 | T | TACAC | 16 | a0001c0001t0001g0147 a0001c0002t0001g0010 a0001c0002t0002g0006 others(13): Show |
18 | HG01081.hp1 HG01192.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.859+659_859+662dup others(4): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr1 | 153753042 | ||||||
| chr1:153753042 | T | TACACAC | 4 | a0001c0002t0002g0040 a0001c0002t0002g0042 a0001c0002t0006g0130 others(1): Show |
4 | HG01167.hp1 HG02602.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.859+657_859+662dup others(6): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr1 | 153753042 | ||||||
| chr1:153753042 | TAC | T | 3 | a0001c0001t0001g0057 a0001c0001t0001g0177 a0001c0001t0001g0191 |
3 | HG02897.hp2 HG03834.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.859+661_859+662del others(2): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr1 | 153753042 | ||||||
| chr1:153753042 | TACAC | T | 7 | a0001c0001t0001g0189 a0001c0001t0001g0218 a0001c0001t0001g0219 others(4): Show |
7 | HG02056.hp1 NA18951.hp2 NA18971.hp1 others(4): Show |
intron_variant | MODIFIER | c.859+659_859+662del others(4): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr1 | 153753042 | ||||||
| chr1:153753077 | T | G | 1 | a0001c0002t0002g0037 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.859+669T>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153753077 | |||||||
| chr1:153753138 | C | G | 1 | a0001c0002t0002g0035 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.859+730C>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153753138 | |||||||
| chr1:153753179 | A | G | 7 | a0001c0001t0001g0190 a0001c0001t0001g0217 a0001c0001t0001g0255 others(4): Show |
7 | NA18948.hp2 NA18962.hp2 NA18988.hp2 others(4): Show |
intron_variant | MODIFIER | c.859+771A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153753179 | |||||||
| chr1:153753287 | G | A | 1 | a0001c0001t0001g0301 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.859+879G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153753287 | |||||||
| chr1:153753314 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.859+906T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153753314 | |||||||
| chr1:153753325 | G | T | 1 | a0001c0002t0002g0047 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.859+917G>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153753325 | |||||||
| chr1:153753329 | C | A | 1 | a0001c0001t0001g0230 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.859+921C>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153753329 | |||||||
| chr1:153753341 | G | A | 1 | a0001c0002t0002g0033 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.859+933G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153753341 | |||||||
| chr1:153753382 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.859+974C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153753382 | |||||||
| chr1:153753402 | C | T | 3 | a0001c0001t0001g0241 a0001c0001t0001g0301 a0001c0001t0001g0303 |
3 | HG02559.hp1 HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.859+994C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153753402 | |||||||
| chr1:153753476 | G | A | 1 | a0001c0001t0001g0231 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.859+1068G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153753476 | |||||||
| chr1:153753478 | A | G | 2 | a0001c0002t0001g0061 a0001c0002t0001g0307 |
2 | HG02615.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.859+1070A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153753478 | |||||||
| chr1:153753512 | G | T | 1 | a0001c0001t0001g0092 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.859+1104G>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153753512 | |||||||
| chr1:153753555 | C | CA | 5 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0057 others(2): Show |
7 | HG01433.hp1 HG02895.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.860-1079dupA | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr1 | 153753555 | ||||||
| chr1:153753655 | C | CT | 13 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0112 others(10): Show |
16 | HG00735.hp1 HG01106.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.860-969dupT | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr1 | 153753655 | ||||||
| chr1:153753655 | CT | C | 13 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0067 others(10): Show |
13 | HG01070.hp2 HG01256.hp2 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.860-969delT | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr1 | 153753655 | ||||||
| chr1:153753655 | CTT | C | 12 | a0001c0001t0001g0099 a0001c0001t0001g0132 a0001c0001t0001g0133 others(9): Show |
12 | HG02258.hp2 HG02451.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.860-970_860-969del others(2): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr1 | 153753655 | ||||||
| chr1:153753758 | C | T | 1 | a0001c0002t0008g0312 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.860-884C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153753758 | |||||||
| chr1:153753929 | A | G | 4 | a0001c0001t0001g0008 a0001c0001t0001g0068 a0001c0001t0001g0105 others(1): Show |
5 | HG00099.hp2 HG00741.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.860-713A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153753929 | |||||||
| chr1:153753939 | G | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0068 a0001c0001t0001g0105 others(1): Show |
5 | HG00099.hp2 HG00741.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.860-703G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153753939 | |||||||
| chr1:153753940 | C | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0068 a0001c0001t0001g0105 others(1): Show |
5 | HG00099.hp2 HG00741.hp1 HG01069.hp2 others(2): Show |
intron_variant | MODIFIER | c.860-702C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153753940 | |||||||
| chr1:153753956 | CT | C | 175 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(172): Show |
181 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.860-667delT | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr1 | 153753956 | ||||||
| chr1:153753956 | CTT | C | 8 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0057 others(5): Show |
10 | HG01433.hp1 HG02145.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.860-668_860-667del others(2): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | INFO_REALIGN_3_PRIME | chr1 | 153753956 | ||||||
| chr1:153754144 | G | T | 1 | a0001c0001t0001g0216 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.860-498G>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153754144 | |||||||
| chr1:153754280 | T | C | 1 | a0001c0001t0001g0188 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.860-362T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 8/29 | chr1 | 153754280 | |||||||
| chr1:153754797 | C | T | 2 | a0001c0002t0005g0305 a0001c0002t0005g0306 |
2 | HG01891.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.957+58C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 9/29 | chr1 | 153754797 | |||||||
| chr1:153754946 | C | G | 2 | a0001c0002t0001g0061 a0001c0002t0001g0307 |
2 | HG02615.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.957+207C>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 9/29 | chr1 | 153754946 | |||||||
| chr1:153755060 | A | G | 1 | a0001c0001t0001g0288 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.957+321A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 9/29 | chr1 | 153755060 | |||||||
| chr1:153755086 | G | A | 5 | a0001c0001t0001g0203 a0001c0001t0001g0207 a0001c0001t0001g0214 others(2): Show |
5 | HG00099.hp1 HG01258.hp2 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.957+347G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 9/29 | chr1 | 153755086 | |||||||
| chr1:153755156 | T | C | 30 | a0001c0002t0001g0039 a0001c0002t0001g0061 a0001c0002t0001g0307 others(27): Show |
31 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.957+417T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 9/29 | chr1 | 153755156 | |||||||
| chr1:153755249 | G | GT | 12 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0063 others(9): Show |
12 | HG00423.hp1 HG00621.hp1 HG00621.hp2 others(9): Show |
intron_variant | MODIFIER | c.957+520dupT | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 9/29 | INFO_REALIGN_3_PRIME | chr1 | 153755249 | ||||||
| chr1:153755327 | G | C | 2 | a0001c0001t0001g0229 a0001c0001t0001g0240 |
2 | HG01884.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.957+588G>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 9/29 | chr1 | 153755327 | |||||||
| chr1:153755332 | C | T | 2 | a0001c0002t0001g0148 a0001c0002t0008g0312 |
2 | HG01109.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.957+593C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 9/29 | chr1 | 153755332 | |||||||
| chr1:153755441 | A | G | 1 | a0001c0002t0002g0047 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.957+702A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 9/29 | chr1 | 153755441 | |||||||
| chr1:153755616 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.957+877G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 9/29 | chr1 | 153755616 | |||||||
| chr1:153755763 | A | G | 194 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(191): Show |
206 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(203): Show |
intron_variant | MODIFIER | c.957+1024A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 9/29 | chr1 | 153755763 | |||||||
| chr1:153755854 | C | T | 30 | a0001c0002t0001g0039 a0001c0002t0001g0061 a0001c0002t0001g0307 others(27): Show |
31 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.957+1115C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 9/29 | chr1 | 153755854 | |||||||
| chr1:153755982 | A | G | 192 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(189): Show |
204 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(201): Show |
intron_variant | MODIFIER | c.957+1243A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 9/29 | chr1 | 153755982 | |||||||
| chr1:153755982 | A | T | 2 | a0001c0001t0001g0219 a0001c0001t0001g0260 |
2 | NA18971.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.957+1243A>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 9/29 | chr1 | 153755982 | |||||||
| chr1:153756100 | C | T | 1 | a0001c0001t0001g0095 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.957+1361C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 9/29 | chr1 | 153756100 | |||||||
| chr1:153756166 | A | G | 1 | a0001c0001t0001g0238 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.958-1406A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 9/29 | chr1 | 153756166 | |||||||
| chr1:153756229 | G | C | 1 | a0001c0001t0001g0030 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.958-1343G>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 9/29 | chr1 | 153756229 | |||||||
| chr1:153756274 | A | G | 2 | a0001c0001t0001g0005 a0001c0001t0001g0181 |
4 | HG00735.hp1 HG01123.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.958-1298A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 9/29 | chr1 | 153756274 | |||||||
| chr1:153756317 | A | T | 1 | a0001c0002t0011g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.958-1255A>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 9/29 | chr1 | 153756317 | |||||||
| chr1:153756476 | C | T | 1 | a0001c0002t0002g0049 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.958-1096C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 9/29 | chr1 | 153756476 | |||||||
| chr1:153756544 | G | A | 1 | a0001c0002t0011g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.958-1028G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 9/29 | chr1 | 153756544 | |||||||
| chr1:153756644 | C | T | 30 | a0001c0002t0001g0039 a0001c0002t0001g0061 a0001c0002t0001g0307 others(27): Show |
31 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.958-928C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 9/29 | chr1 | 153756644 | |||||||
| chr1:153756994 | G | A | 1 | a0001c0002t0011g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.958-578G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 9/29 | chr1 | 153756994 | |||||||
| chr1:153757113 | T | A | 1 | a0001c0001t0001g0066 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.958-459T>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 9/29 | chr1 | 153757113 | |||||||
| chr1:153757186 | T | G | 1 | a0001c0001t0001g0123 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.958-386T>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 9/29 | chr1 | 153757186 | |||||||
| chr1:153757245 | C | T | 8 | a0001c0002t0002g0045 a0001c0002t0002g0050 a0001c0002t0002g0051 others(5): Show |
8 | HG02109.hp1 HG02723.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.958-327C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 9/29 | chr1 | 153757245 | |||||||
| chr1:153757847 | C | G | 1 | a0001c0002t0008g0312 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1149+84C>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 10/29 | chr1 | 153757847 | |||||||
| chr1:153757855 | C | T | 3 | a0001c0002t0002g0049 a0001c0002t0005g0305 a0001c0002t0005g0306 |
3 | HG01891.hp1 HG03209.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1149+92C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 10/29 | chr1 | 153757855 | |||||||
| chr1:153758257 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1149+494T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 10/29 | chr1 | 153758257 | |||||||
| chr1:153758412 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1149+649T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 10/29 | chr1 | 153758412 | |||||||
| chr1:153758526 | T | C | 3 | a0001c0001t0001g0224 a0001c0001t0001g0229 a0001c0001t0001g0240 |
3 | HG01884.hp1 HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1149+763T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 10/29 | chr1 | 153758526 | |||||||
| chr1:153758531 | A | G | 1 | a0001c0001t0001g0222 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1149+768A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 10/29 | chr1 | 153758531 | |||||||
| chr1:153758535 | C | T | 316 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(313): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.1149+772C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 10/29 | chr1 | 153758535 | |||||||
| chr1:153758583 | A | G | 2 | a0001c0001t0001g0009 a0001c0001t0001g0104 |
3 | HG00639.hp1 HG01074.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1149+820A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 10/29 | chr1 | 153758583 | |||||||
| chr1:153759059 | G | A | 2 | a0001c0002t0006g0130 a0001c0002t0006g0131 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1150-467G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 10/29 | chr1 | 153759059 | |||||||
| chr1:153759082 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1150-444G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 10/29 | chr1 | 153759082 | |||||||
| chr1:153759085 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1150-441C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 10/29 | chr1 | 153759085 | |||||||
| chr1:153759274 | G | GA | 34 | a0001c0001t0001g0081 a0001c0001t0001g0099 a0001c0002t0001g0039 others(31): Show |
35 | HG00544.hp2 HG01074.hp1 HG01081.hp1 others(32): Show |
intron_variant | MODIFIER | c.1150-237dupA | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr1 | 153759274 | ||||||
| chr1:153759274 | GA | G | 135 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(132): Show |
139 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.1150-237delA | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 10/29 | INFO_REALIGN_3_PRIME | chr1 | 153759274 | ||||||
| chr1:153759295 | G | A | 2 | a0001c0002t0006g0130 a0001c0002t0006g0131 |
2 | HG02622.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1150-231G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 10/29 | chr1 | 153759295 | |||||||
| chr1:153759432 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1150-94C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 10/29 | chr1 | 153759432 | |||||||
| chr1:153759830 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1237+217G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 11/29 | chr1 | 153759830 | |||||||
| chr1:153760095 | G | A | 1 | a0001c0001t0001g0190 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1238-216G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 11/29 | chr1 | 153760095 | |||||||
| chr1:153760164 | A | G | 177 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(174): Show |
183 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(180): Show |
intron_variant | MODIFIER | c.1238-147A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 11/29 | chr1 | 153760164 | |||||||
| chr1:153760232 | C | A | 5 | a0001c0001t0001g0200 a0001c0001t0001g0226 a0001c0001t0001g0232 others(2): Show |
5 | HG01099.hp1 HG01123.hp2 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.1238-79C>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 11/29 | chr1 | 153760232 | |||||||
| chr1:153760232 | C | CA | 16 | a0001c0001t0001g0032 a0001c0001t0001g0102 a0001c0001t0001g0112 others(13): Show |
16 | HG00423.hp2 HG02080.hp2 HG02165.hp1 others(13): Show |
intron_variant | MODIFIER | c.1238-53dupA | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 11/29 | INFO_REALIGN_3_PRIME | chr1 | 153760232 | ||||||
| chr1:153760232 | CA | C | 48 | a0001c0001t0001g0020 a0001c0001t0001g0027 a0001c0001t0001g0063 others(45): Show |
49 | HG00099.hp1 HG00544.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.1238-53delA | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 11/29 | INFO_REALIGN_3_PRIME | chr1 | 153760232 | ||||||
| chr1:153760232 | CAAA | C | 6 | a0001c0002t0002g0050 a0001c0002t0002g0052 a0001c0002t0002g0053 others(3): Show |
6 | HG02109.hp1 HG02723.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1238-55_1238-53del others(3): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 11/29 | INFO_REALIGN_3_PRIME | chr1 | 153760232 | ||||||
| chr1:153760257 | A | G | 2 | a0001c0001t0001g0280 a0001c0002t0001g0010 |
3 | HG03098.hp2 HG03225.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1238-54A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 11/29 | chr1 | 153760257 | |||||||
| chr1:153760497 | G | A | 28 | a0001c0002t0001g0039 a0001c0002t0002g0006 a0001c0002t0002g0033 others(25): Show |
29 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.1317+107G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 12/29 | chr1 | 153760497 | |||||||
| chr1:153760538 | C | A | 8 | a0001c0001t0001g0099 a0001c0001t0001g0133 a0001c0001t0001g0134 others(5): Show |
8 | HG02622.hp2 HG02630.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1317+148C>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 12/29 | chr1 | 153760538 | |||||||
| chr1:153760540 | T | C | 1 | a0001c0001t0003g0320 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1317+150T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 12/29 | chr1 | 153760540 | |||||||
| chr1:153761561 | C | G | 1 | a0001c0001t0001g0237 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1410-9C>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 13/29 | chr1 | 153761561 | |||||||
| chr1:153762064 | T | C | 3 | a0001c0002t0004g0313 a0001c0002t0004g0316 a0001c0002t0011g0016 |
3 | HG02965.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1516+388T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 14/29 | chr1 | 153762064 | |||||||
| chr1:153762249 | G | A | 1 | a0001c0002t0008g0312 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1517-479G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 14/29 | chr1 | 153762249 | |||||||
| chr1:153762278 | G | A | 7 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0057 others(4): Show |
9 | HG01433.hp1 HG02615.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1517-450G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 14/29 | chr1 | 153762278 | |||||||
| chr1:153762373 | C | G | 3 | a0001c0002t0004g0313 a0001c0002t0004g0316 a0001c0002t0011g0016 |
3 | HG02965.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1517-355C>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 14/29 | chr1 | 153762373 | |||||||
| chr1:153762961 | T | C | 1 | a0001c0001t0001g0201 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1636+114T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 15/29 | chr1 | 153762961 | |||||||
| chr1:153763181 | C | T | 1 | a0001c0001t0001g0099 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1637-52C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 15/29 | chr1 | 153763181 | |||||||
| chr1:153763529 | G | A | 1 | a0001c0002t0008g0312 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1766+167G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 16/29 | chr1 | 153763529 | |||||||
| chr1:153763590 | C | G | 2 | a0001c0001t0001g0178 a0001c0001t0001g0182 |
2 | HG01175.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1766+228C>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 16/29 | chr1 | 153763590 | |||||||
| chr1:153763595 | G | C | 3 | a0001c0002t0004g0313 a0001c0002t0004g0316 a0001c0002t0011g0016 |
3 | HG02965.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1766+233G>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 16/29 | chr1 | 153763595 | |||||||
| chr1:153763672 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1767-160A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 16/29 | chr1 | 153763672 | |||||||
| chr1:153763804 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1767-28G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 16/29 | chr1 | 153763804 | |||||||
| chr1:153763904 | C | T | 1 | a0001c0001t0001g0191 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1821+18C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 17/29 | chr1 | 153763904 | |||||||
| chr1:153764235 | T | TCC | 13 | a0001c0001t0001g0099 a0001c0001t0001g0132 a0001c0001t0001g0133 others(10): Show |
13 | HG02258.hp2 HG02451.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.1925+16_1925+17dup others(2): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 18/29 | INFO_REALIGN_3_PRIME | chr1 | 153764235 | ||||||
| chr1:153764285 | C | T | 2 | a0001c0001t0001g0245 a0001c0001t0001g0246 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1925+64C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 18/29 | chr1 | 153764285 | |||||||
| chr1:153764520 | G | A | 1 | a0001c0002t0011g0016 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1926-170G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 18/29 | chr1 | 153764520 | |||||||
| chr1:153764538 | C | A | 1 | a0001c0001t0001g0280 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1926-152C>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 18/29 | chr1 | 153764538 | |||||||
| chr1:153764634 | G | A | 2 | a0001c0002t0002g0043 a0001c0002t0002g0044 |
2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1926-56G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 18/29 | chr1 | 153764634 | |||||||
| chr1:153764660 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1926-30G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 18/29 | chr1 | 153764660 | |||||||
| chr1:153765144 | T | C | 1 | a0001c0002t0002g0049 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2090+81T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 20/29 | chr1 | 153765144 | |||||||
| chr1:153765182 | T | C | 1 | a0001c0001t0001g0068 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2090+119T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 20/29 | chr1 | 153765182 | |||||||
| chr1:153765252 | T | C | 1 | a0001c0001t0001g0134 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2090+189T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 20/29 | chr1 | 153765252 | |||||||
| chr1:153765257 | C | T | 13 | a0001c0001t0001g0099 a0001c0001t0001g0132 a0001c0001t0001g0133 others(10): Show |
13 | HG02258.hp2 HG02451.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.2090+194C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 20/29 | chr1 | 153765257 | |||||||
| chr1:153765293 | C | T | 5 | a0001c0001t0001g0002 a0001c0001t0001g0081 a0001c0001t0001g0086 others(2): Show |
8 | HG00544.hp2 NA18957.hp2 NA18962.hp1 others(5): Show |
intron_variant | MODIFIER | c.2090+230C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 20/29 | chr1 | 153765293 | |||||||
| chr1:153765515 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2090+452T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 20/29 | chr1 | 153765515 | |||||||
| chr1:153765789 | C | T | 1 | a0001c0002t0002g0038 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.2090+726C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 20/29 | chr1 | 153765789 | |||||||
| chr1:153765986 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2090+923A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 20/29 | chr1 | 153765986 | |||||||
| chr1:153766021 | G | C | 2 | a0001c0002t0001g0061 a0001c0002t0001g0307 |
2 | HG02615.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.2090+958G>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 20/29 | chr1 | 153766021 | |||||||
| chr1:153766115 | C | CT | 42 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0026 others(39): Show |
43 | HG00438.hp2 HG01081.hp1 HG01109.hp1 others(40): Show |
intron_variant | MODIFIER | c.2090+1076dupT | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr1 | 153766115 | ||||||
| chr1:153766115 | CT | C | 16 | a0001c0001t0001g0020 a0001c0001t0001g0060 a0001c0001t0001g0077 others(13): Show |
16 | HG00558.hp2 HG01069.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.2090+1076delT | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr1 | 153766115 | ||||||
| chr1:153766339 | C | T | 3 | a0001c0002t0001g0010 a0001c0002t0006g0130 a0001c0002t0006g0131 |
4 | HG02622.hp1 HG02630.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2090+1276C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 20/29 | chr1 | 153766339 | |||||||
| chr1:153766347 | G | A | 2 | a0001c0001t0001g0019 a0001c0001t0001g0020 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2090+1284G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 20/29 | chr1 | 153766347 | |||||||
| chr1:153766423 | G | A | 16 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0032 others(13): Show |
18 | HG00423.hp2 HG00673.hp2 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.2091-1251G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 20/29 | chr1 | 153766423 | |||||||
| chr1:153766551 | G | A | 2 | a0001c0001t0001g0222 a0001c0001t0001g0234 |
2 | HG00609.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.2091-1123G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 20/29 | chr1 | 153766551 | |||||||
| chr1:153766591 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2091-1083G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 20/29 | chr1 | 153766591 | |||||||
| chr1:153766687 | A | AT | 10 | a0001c0001t0001g0007 a0001c0001t0001g0057 a0001c0001t0001g0075 others(7): Show |
11 | HG01109.hp2 HG01433.hp1 HG02083.hp2 others(8): Show |
intron_variant | MODIFIER | c.2091-967dupT | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr1 | 153766687 | ||||||
| chr1:153766687 | AT | A | 36 | a0001c0001t0001g0179 a0001c0001t0001g0198 a0001c0001t0001g0325 others(33): Show |
38 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.2091-967delT | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 20/29 | INFO_REALIGN_3_PRIME | chr1 | 153766687 | ||||||
| chr1:153766793 | A | G | 198 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(195): Show |
210 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(207): Show |
intron_variant | MODIFIER | c.2091-881A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 20/29 | chr1 | 153766793 | |||||||
| chr1:153766883 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2091-791G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 20/29 | chr1 | 153766883 | |||||||
| chr1:153766999 | C | G | 1 | a0001c0001t0001g0116 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2091-675C>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 20/29 | chr1 | 153766999 | |||||||
| chr1:153767005 | C | T | 1 | a0001c0001t0001g0282 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2091-669C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 20/29 | chr1 | 153767005 | |||||||
| chr1:153767343 | T | A | 1 | a0001c0001t0001g0204 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2091-331T>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 20/29 | chr1 | 153767343 | |||||||
| chr1:153767479 | G | A | 30 | a0001c0002t0001g0039 a0001c0002t0001g0061 a0001c0002t0001g0307 others(27): Show |
31 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.2091-195G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 20/29 | chr1 | 153767479 | |||||||
| chr1:153767552 | G | A | 3 | a0001c0002t0004g0313 a0001c0002t0004g0316 a0001c0002t0011g0016 |
3 | HG02965.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2091-122G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 20/29 | chr1 | 153767552 | |||||||
| chr1:153767611 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.2091-63C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 20/29 | chr1 | 153767611 | |||||||
| chr1:153767831 | A | G | 1 | a0001c0001t0001g0255 | 1 | NA19064.hp2 | splice_region_variant&intron_variant | LOW | c.2244+4A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 21/29 | chr1 | 153767831 | |||||||
| chr1:153768018 | C | T | 36 | a0001c0002t0001g0010 a0001c0002t0001g0039 a0001c0002t0001g0061 others(33): Show |
38 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.2244+191C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 21/29 | chr1 | 153768018 | |||||||
| chr1:153768021 | T | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0057 |
3 | HG01433.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2244+194T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 21/29 | chr1 | 153768021 | |||||||
| chr1:153768177 | C | A | 1 | a0001c0001t0001g0031 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2244+350C>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 21/29 | chr1 | 153768177 | |||||||
| chr1:153768215 | G | T | 1 | a0001c0001t0001g0166 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2244+388G>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 21/29 | chr1 | 153768215 | |||||||
| chr1:153768566 | C | T | 3 | a0001c0001t0003g0317 a0001c0001t0003g0318 a0001c0001t0003g0322 |
3 | HG01243.hp2 HG02647.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2245-327C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 21/29 | chr1 | 153768566 | |||||||
| chr1:153768580 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2245-313A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 21/29 | chr1 | 153768580 | |||||||
| chr1:153768661 | A | G | 5 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0057 others(2): Show |
7 | HG01433.hp1 HG02895.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.2245-232A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 21/29 | chr1 | 153768661 | |||||||
| chr1:153768817 | TAAGG | T | 3 | a0001c0002t0004g0313 a0001c0002t0004g0316 a0001c0002t0011g0016 |
3 | HG02965.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2245-70_2245-67del others(4): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 21/29 | INFO_REALIGN_3_PRIME | chr1 | 153768817 | ||||||
| chr1:153768836 | A | G | 3 | a0001c0002t0004g0313 a0001c0002t0004g0316 a0001c0002t0011g0016 |
3 | HG02965.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2245-57A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 21/29 | chr1 | 153768836 | |||||||
| chr1:153769036 | C | A | 33 | a0001c0002t0001g0010 a0001c0002t0001g0039 a0001c0002t0001g0061 others(30): Show |
35 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(32): Show |
intron_variant | MODIFIER | c.2313+75C>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 22/29 | chr1 | 153769036 | |||||||
| chr1:153769350 | G | A | 5 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0111 others(2): Show |
5 | NA18947.hp2 NA18963.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.2313+389G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 22/29 | chr1 | 153769350 | |||||||
| chr1:153769419 | G | C | 1 | a0001c0001t0001g0093 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2314-350G>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 22/29 | chr1 | 153769419 | |||||||
| chr1:153769597 | C | A | 1 | a0001c0002t0002g0006 | 2 | HG01081.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.2314-172C>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 22/29 | chr1 | 153769597 | |||||||
| chr1:153769613 | C | T | 1 | a0001c0001t0001g0276 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2314-156C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 22/29 | chr1 | 153769613 | |||||||
| chr1:153769666 | AT | A | 42 | a0001c0001t0001g0003 a0001c0001t0001g0124 a0001c0001t0001g0126 others(39): Show |
46 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.2314-92delT | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 22/29 | INFO_REALIGN_3_PRIME | chr1 | 153769666 | ||||||
| chr1:153769894 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2389+50G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | chr1 | 153769894 | |||||||
| chr1:153769961 | T | C | 37 | a0001c0001t0001g0201 a0001c0002t0001g0010 a0001c0002t0001g0039 others(34): Show |
39 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.2389+117T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | chr1 | 153769961 | |||||||
| chr1:153769979 | C | T | 6 | a0001c0001t0003g0315 a0001c0001t0003g0319 a0001c0001t0003g0320 others(3): Show |
6 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.2389+135C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | chr1 | 153769979 | |||||||
| chr1:153769980 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2389+136G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | chr1 | 153769980 | |||||||
| chr1:153769993 | A | G | 36 | a0001c0002t0001g0010 a0001c0002t0001g0039 a0001c0002t0001g0061 others(33): Show |
38 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.2389+149A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | chr1 | 153769993 | |||||||
| chr1:153770058 | G | GGT | 4 | a0001c0001t0001g0060 a0001c0001t0001g0094 a0001c0001t0001g0122 others(1): Show |
4 | HG01167.hp2 HG02055.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.2390-96_2390-95dup others(2): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr1 | 153770058 | ||||||
| chr1:153770058 | GGT | G | 46 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0001c0001t0001g0026 others(43): Show |
46 | HG00140.hp1 HG00423.hp1 HG00558.hp1 others(43): Show |
intron_variant | MODIFIER | c.2390-96_2390-95del others(2): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr1 | 153770058 | ||||||
| chr1:153770058 | GGTGT | G | 35 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(32): Show |
37 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(34): Show |
intron_variant | MODIFIER | c.2390-98_2390-95del others(4): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr1 | 153770058 | ||||||
| chr1:153770058 | GGTGTGT | G | 26 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(23): Show |
28 | HG00408.hp1 HG01106.hp1 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.2390-100_2390-95de others(7): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr1 | 153770058 | ||||||
| chr1:153770058 | GGTGTGTG others(1): Show |
G | 3 | a0001c0001t0001g0007 a0001c0001t0001g0057 a0001c0001t0001g0087 |
4 | HG00639.hp2 HG01433.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.2390-102_2390-95de others(9): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr1 | 153770058 | ||||||
| chr1:153770058 | GGTGTGTG others(9): Show |
G | 2 | a0001c0002t0001g0148 a0001c0002t0008g0312 |
2 | HG01109.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.2390-110_2390-95de others(17): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr1 | 153770058 | ||||||
| chr1:153770058 | GGTGTGTG others(25): Show |
G | 36 | a0001c0002t0001g0010 a0001c0002t0001g0039 a0001c0002t0001g0061 others(33): Show |
38 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.2390-126_2390-95de others(33): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr1 | 153770058 | ||||||
| chr1:153770059 | GT | G | 13 | a0001c0001t0001g0011 a0001c0001t0001g0193 a0001c0001t0001g0194 others(10): Show |
13 | HG00673.hp2 HG01081.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.2390-138delT | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | chr1 | 153770059 | |||||||
| chr1:153770059 | GTGT | G | 66 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(63): Show |
68 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.2390-138_2390-136d others(5): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | chr1 | 153770059 | |||||||
| chr1:153770059 | GTGTGT | G | 41 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0019 others(38): Show |
42 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.2390-138_2390-134d others(7): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | chr1 | 153770059 | |||||||
| chr1:153770059 | GTGTGTGT | G | 30 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0031 others(27): Show |
33 | HG00558.hp2 HG01069.hp1 HG01099.hp1 others(30): Show |
intron_variant | MODIFIER | c.2390-138_2390-132d others(9): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | chr1 | 153770059 | |||||||
| chr1:153770059 | GTGTGTGT others(4): Show |
G | 2 | a0001c0001t0001g0256 a0001c0001t0001g0280 |
2 | HG04199.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.2390-138_2390-128d others(13): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | chr1 | 153770059 | |||||||
| chr1:153770059 | GTGTGTGT others(12): Show |
G | 1 | a0001c0001t0001g0261 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2390-138_2390-120d others(21): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | chr1 | 153770059 | |||||||
| chr1:153770062 | T | G | 2 | a0001c0001t0001g0063 a0001c0002t0002g0073 |
2 | NA19056.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.2390-136T>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | chr1 | 153770062 | |||||||
| chr1:153770064 | T | G | 2 | a0001c0001t0001g0274 a0001c0002t0002g0106 |
2 | HG00673.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.2390-134T>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | chr1 | 153770064 | |||||||
| chr1:153770066 | T | G | 3 | a0001c0001t0001g0235 a0001c0001t0001g0239 a0001c0002t0002g0185 |
3 | HG00408.hp1 HG03017.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.2390-132T>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | chr1 | 153770066 | |||||||
| chr1:153770100 | T | C | 1 | a0001c0001t0001g0082 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2390-98T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | chr1 | 153770100 | |||||||
| chr1:153770102 | T | C | 44 | a0001c0001t0001g0008 a0001c0001t0001g0030 a0001c0001t0001g0068 others(41): Show |
47 | HG00099.hp2 HG00140.hp2 HG00735.hp2 others(44): Show |
intron_variant | MODIFIER | c.2390-96T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | chr1 | 153770102 | |||||||
| chr1:153770121 | G | A | 1 | a0001c0002t0001g0010 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2390-77G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | chr1 | 153770121 | |||||||
| chr1:153770127 | T | G | 1 | a0001c0001t0001g0190 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.2390-71T>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | chr1 | 153770127 | |||||||
| chr1:153770127 | T | TG | 23 | a0001c0001t0001g0026 a0001c0001t0001g0032 a0001c0001t0001g0060 others(20): Show |
23 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.2390-63dupG | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr1 | 153770127 | ||||||
| chr1:153770132 | G | T | 1 | a0001c0001t0001g0099 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.2390-66G>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | chr1 | 153770132 | |||||||
| chr1:153770134 | G | GGT | 15 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 others(12): Show |
15 | HG01978.hp2 HG02258.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.2390-47_2390-46dup others(2): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr1 | 153770134 | ||||||
| chr1:153770134 | G | T | 9 | a0001c0001t0001g0099 a0001c0001t0001g0203 a0001c0001t0001g0207 others(6): Show |
9 | HG00099.hp1 HG01258.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.2390-64G>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | chr1 | 153770134 | |||||||
| chr1:153770134 | GGT | G | 25 | a0001c0002t0001g0039 a0001c0002t0002g0006 a0001c0002t0002g0033 others(22): Show |
26 | HG01074.hp1 HG01081.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.2390-47_2390-46del others(2): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | INFO_REALIGN_3_PRIME | chr1 | 153770134 | ||||||
| chr1:153770136 | T | G | 4 | a0001c0001t0001g0002 a0001c0001t0001g0086 a0001c0001t0001g0142 others(1): Show |
4 | HG04199.hp1 NA18957.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.2390-62T>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 23/29 | chr1 | 153770136 | |||||||
| chr1:153770555 | G | A | 1 | a0001c0001t0001g0281 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.2504-130G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 24/29 | chr1 | 153770555 | |||||||
| chr1:153770758 | T | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(161): Show |
174 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(171): Show |
intron_variant | MODIFIER | c.2552+25T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 25/29 | chr1 | 153770758 | |||||||
| chr1:153770779 | C | T | 1 | a0001c0002t0008g0312 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2552+46C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 25/29 | chr1 | 153770779 | |||||||
| chr1:153770813 | C | G | 113 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0012 others(110): Show |
121 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(118): Show |
intron_variant | MODIFIER | c.2552+80C>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 25/29 | chr1 | 153770813 | |||||||
| chr1:153770841 | G | A | 96 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(93): Show |
106 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.2552+108G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 25/29 | chr1 | 153770841 | |||||||
| chr1:153770924 | T | G | 1 | a0001c0007t0003g0314 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2552+191T>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 25/29 | chr1 | 153770924 | |||||||
| chr1:153770926 | C | G | 5 | a0001c0002t0001g0061 a0001c0002t0001g0307 a0001c0002t0004g0313 others(2): Show |
5 | HG02615.hp1 HG02896.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2552+193C>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 25/29 | chr1 | 153770926 | |||||||
| chr1:153770964 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2552+231G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 25/29 | chr1 | 153770964 | |||||||
| chr1:153771043 | C | G | 1 | a0001c0001t0001g0164 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2552+310C>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 25/29 | chr1 | 153771043 | |||||||
| chr1:153771068 | C | T | 1 | a0001c0001t0001g0072 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2552+335C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 25/29 | chr1 | 153771068 | |||||||
| chr1:153771117 | G | A | 1 | a0001c0001t0001g0266 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2552+384G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 25/29 | chr1 | 153771117 | |||||||
| chr1:153771147 | C | T | 3 | a0001c0001t0001g0203 a0001c0001t0001g0207 a0001c0001t0001g0261 |
3 | HG00099.hp1 HG01496.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.2552+414C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 25/29 | chr1 | 153771147 | |||||||
| chr1:153771185 | G | A | 5 | a0001c0001t0001g0132 a0001c0001t0001g0135 a0001c0001t0001g0143 others(2): Show |
5 | HG02258.hp2 HG02451.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2552+452G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 25/29 | chr1 | 153771185 | |||||||
| chr1:153771219 | G | A | 1 | a0001c0001t0001g0259 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2552+486G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 25/29 | chr1 | 153771219 | |||||||
| chr1:153771304 | T | C | 1 | a0001c0001t0001g0259 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2553-492T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 25/29 | chr1 | 153771304 | |||||||
| chr1:153771376 | T | C | 1 | a0001c0001t0001g0192 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2553-420T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 25/29 | chr1 | 153771376 | |||||||
| chr1:153771451 | A | G | 44 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0057 others(41): Show |
48 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.2553-345A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 25/29 | chr1 | 153771451 | |||||||
| chr1:153771473 | T | C | 41 | a0001c0001t0001g0015 a0001c0001t0001g0201 a0001c0001t0001g0310 others(38): Show |
44 | HG01074.hp1 HG01081.hp1 HG01109.hp2 others(41): Show |
intron_variant | MODIFIER | c.2553-323T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 25/29 | chr1 | 153771473 | |||||||
| chr1:153771541 | G | T | 1 | a0001c0001t0001g0192 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2553-255G>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 25/29 | chr1 | 153771541 | |||||||
| chr1:153771582 | T | C | 3 | a0001c0001t0001g0015 a0001c0001t0001g0310 a0003c0004t0001g0149 |
4 | HG02896.hp1 HG02897.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.2553-214T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 25/29 | chr1 | 153771582 | |||||||
| chr1:153771662 | T | C | 2 | a0001c0002t0001g0061 a0001c0002t0001g0307 |
2 | HG02615.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.2553-134T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 25/29 | chr1 | 153771662 | |||||||
| chr1:153771768 | A | G | 1 | a0001c0001t0001g0261 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2553-28A>G | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 25/29 | chr1 | 153771768 | |||||||
| chr1:153772020 | C | CGGT | 6 | a0001c0001t0001g0126 a0001c0001t0001g0137 a0001c0001t0001g0151 others(3): Show |
6 | HG02486.hp1 HG02622.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.2720+86_2720+88dup others(3): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr1 | 153772020 | ||||||
| chr1:153772020 | CGG | C | 3 | a0001c0002t0004g0313 a0001c0002t0004g0316 a0001c0002t0011g0016 |
3 | HG02965.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2720+58_2720+59del others(2): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 26/29 | chr1 | 153772020 | |||||||
| chr1:153772020 | CGGT | C | 34 | a0001c0002t0001g0010 a0001c0002t0001g0039 a0001c0002t0001g0061 others(31): Show |
36 | HG00408.hp1 HG01074.hp1 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.2720+86_2720+88del others(3): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr1 | 153772020 | ||||||
| chr1:153772020 | CGGTGGTG others(8): Show |
C | 1 | a0001c0002t0008g0312 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2720+74_2720+88del others(15): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr1 | 153772020 | ||||||
| chr1:153772020 | CGGTGGTG others(11): Show |
C | 9 | a0001c0001t0001g0189 a0001c0001t0001g0191 a0001c0001t0001g0218 others(6): Show |
9 | HG02056.hp1 NA18941.hp1 NA18951.hp2 others(6): Show |
intron_variant | MODIFIER | c.2720+71_2720+88del others(18): Show |
INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 26/29 | INFO_REALIGN_3_PRIME | chr1 | 153772020 | ||||||
| chr1:153772023 | T | C | 3 | a0001c0002t0004g0313 a0001c0002t0004g0316 a0001c0002t0011g0016 |
3 | HG02965.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2720+60T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 26/29 | chr1 | 153772023 | |||||||
| chr1:153772032 | T | C | 7 | a0001c0002t0002g0050 a0001c0002t0002g0051 a0001c0002t0002g0052 others(4): Show |
7 | HG02109.hp1 HG02723.hp2 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.2720+69T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 26/29 | chr1 | 153772032 | |||||||
| chr1:153772119 | C | T | 1 | a0001c0002t0004g0316 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2720+156C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 26/29 | chr1 | 153772119 | |||||||
| chr1:153772139 | C | T | 1 | a0001c0001t0001g0086 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.2720+176C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 26/29 | chr1 | 153772139 | |||||||
| chr1:153772140 | T | C | 1 | a0001c0001t0001g0086 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.2720+177T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 26/29 | chr1 | 153772140 | |||||||
| chr1:153772238 | T | C | 5 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0111 others(2): Show |
5 | NA18947.hp2 NA18963.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.2721-102T>C | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 26/29 | chr1 | 153772238 | |||||||
| chr1:153772306 | C | T | 1 | a0001c0001t0001g0308 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2721-34C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 26/29 | chr1 | 153772306 | |||||||
| chr1:153772839 | C | T | 1 | a0001c0002t0002g0049 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2895-86C>T | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 28/29 | chr1 | 153772839 | |||||||
| chr1:153772904 | G | A | 2 | a0001c0001t0001g0201 a0001c0001t0001g0275 |
2 | HG01109.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.2895-21G>A | INTS3 | ENSG00000143624.14 | transcript | ENST00000318967.7 | protein_coding | 28/29 | chr1 | 153772904 |