Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 203522 |
| ensemblid | ENSG00000165359.16 |
| hgncid | 27334 |
| symbol | INTS6L |
| name | integrator complex subunit 6 like |
| refseq_nuc | NM_001351601.3 |
| refseq_prot | NP_001338530.1 |
| ensembl_nuc | ENST00000639893.2 |
| ensembl_prot | ENSP00000491427.1 |
| mane_status | MANE Select |
| chr | chrX |
| start | 135520660 |
| end | 135582510 |
| strand | + |
| ver | v1.2 |
| region | chrX:135520660-135582510 |
| region5000 | chrX:135515660-135587510 |
| regionname0 | INTS6L_chrX_135520660_135582510 |
| regionname5000 | INTS6L_chrX_135515660_135587510 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 898 | 240 | 60 | 36 | 111 | 9 | 22 | 90 | INTS6L_chrX_135515660_135587510 | INTS6L | MPILL others(893): Show |
chrX | 135515660 | 135587510 |
| a0002 | 0/0 | 898 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | MPILL others(893): Show |
chrX | 135515660 | 135587510 |
| a0003 | 0/0 | 898 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | MPILL others(893): Show |
chrX | 135515660 | 135587510 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2694 | 185 | 41 | 33 | 85 | 7 | 17 | INTS6L_chrX_135515660_135587510 | INTS6L | ATGCC others(2689): Show |
chrX | 135515660 | 135587510 | ||
| a0001c0002 | 0/0 | 2694 | 33 | 15 | 0 | 16 | 0 | 2 | INTS6L_chrX_135515660_135587510 | INTS6L | ATGCC others(2689): Show |
chrX | 135515660 | 135587510 | ||
| a0001c0003 | 0/0 | 2694 | 21 | 4 | 3 | 10 | 2 | 2 | INTS6L_chrX_135515660_135587510 | INTS6L | ATGCC others(2689): Show |
chrX | 135515660 | 135587510 | ||
| a0001c0005 | 0/0 | 2694 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | ATGCC others(2689): Show |
chrX | 135515660 | 135587510 | ||
| a0002c0004 | 0/0 | 2694 | 3 | 0 | 3 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | ATGCC others(2689): Show |
chrX | 135515660 | 135587510 | ||
| a0003c0006 | 0/0 | 2694 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | ATGCC others(2689): Show |
chrX | 135515660 | 135587510 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3904 | 165 | 37 | 30 | 73 | 7 | 17 | INTS6L_chrX_135515660_135587510 | INTS6L | AGTCT others(3899): Show |
chrX | 135515660 | 135587510 |
| a0001c0001t0002 | 1/0 | 3904 | 18 | 4 | 2 | 11 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | AGTCT others(3899): Show |
chrX | 135515660 | 135587510 |
| a0001c0001t0003 | 0/0 | 3904 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | AGTCT others(3899): Show |
chrX | 135515660 | 135587510 |
| a0001c0001t0004 | 0/0 | 3904 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | AGTCT others(3899): Show |
chrX | 135515660 | 135587510 |
| a0001c0002t0001 | 0/0 | 3904 | 33 | 15 | 0 | 16 | 0 | 2 | INTS6L_chrX_135515660_135587510 | INTS6L | AGTCT others(3899): Show |
chrX | 135515660 | 135587510 |
| a0001c0003t0001 | 0/0 | 3904 | 21 | 4 | 3 | 10 | 2 | 2 | INTS6L_chrX_135515660_135587510 | INTS6L | AGTCT others(3899): Show |
chrX | 135515660 | 135587510 |
| a0001c0005t0001 | 0/0 | 3904 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | AGTCT others(3899): Show |
chrX | 135515660 | 135587510 |
| a0002c0004t0001 | 0/0 | 3904 | 3 | 0 | 3 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | AGTCT others(3899): Show |
chrX | 135515660 | 135587510 |
| a0003c0006t0001 | 0/0 | 3904 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | AGTCT others(3899): Show |
chrX | 135515660 | 135587510 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 5 | 1 | 0 | 4 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0042 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0002g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0002g0040 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0003t0001g0009 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0003t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0003t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0003t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0003t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0003t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0003t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0003t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0003t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0003t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0003t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0003t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0001c0005t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0002c0004t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0002c0004t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0002c0004t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| a0003c0006t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0075 | EUR | GBR | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0155 | EUR | GBR | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0125 | EUR | GBR | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0156 | EUR | FIN | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0166 | EAS | CHS | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG00621 | hp1 | a0001 | c0002 | t0001 | g0031 | EAS | CHS | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | CHS | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0049 | AMR | PUR | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01099 | hp1 | a0001 | c0003 | t0001 | g0062 | AMR | PUR | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0045 | AMR | PUR | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | CLM | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0074 | AMR | CLM | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01346 | hp1 | a0002 | c0004 | t0001 | g0181 | AMR | CLM | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01433 | hp1 | a0002 | c0004 | t0001 | g0153 | AMR | CLM | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01496 | hp1 | a0001 | c0003 | t0001 | g0146 | AMR | CLM | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0145 | EUR | IBS | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01516 | hp2 | a0001 | c0003 | t0001 | g0071 | EUR | IBS | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0084 | AFR | ACB | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01978 | hp1 | a0002 | c0004 | t0001 | g0111 | AMR | PEL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01978 | hp2 | a0001 | c0003 | t0001 | g0061 | AMR | PEL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02015 | hp1 | a0001 | c0003 | t0001 | g0056 | EAS | KHV | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02040 | hp1 | a0001 | c0003 | t0001 | g0070 | EAS | KHV | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02056 | hp1 | a0001 | c0002 | t0001 | g0030 | EAS | KHV | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | KHV | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0034 | EAS | KHV | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | CDX | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02257 | hp1 | a0001 | c0003 | t0001 | g0199 | AFR | ACB | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0079 | AFR | ACB | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0011 | AFR | ACB | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ACB | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0027 | SAS | PJL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02615 | hp1 | a0001 | c0003 | t0001 | g0076 | AFR | GWD | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0078 | AFR | GWD | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0209 | AFR | GWD | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ESN | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | ESN | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0004 | AFR | ESN | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0086 | AFR | ESN | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03098 | hp1 | a0001 | c0003 | t0001 | g0198 | AFR | MSL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0004 | AFR | ESN | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03139 | hp1 | a0001 | c0002 | t0001 | g0087 | AFR | ESN | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | MSL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | MSL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0072 | AFR | MSL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0043 | AFR | MSL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0004 | AFR | MSL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03492 | hp1 | a0001 | c0005 | t0001 | g0126 | SAS | PJL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ESN | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0085 | AFR | GWD | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | MSL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03654 | hp1 | a0001 | c0003 | t0001 | g0009 | SAS | PJL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | STU | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03831 | hp1 | a0001 | c0002 | t0001 | g0024 | SAS | BEB | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | BEB | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | BEB | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | STU | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG04199 | hp1 | a0001 | c0003 | t0001 | g0036 | SAS | STU | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | STU | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | STU | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | YRI | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CHB | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | CHB | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | YRI | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0083 | AFR | YRI | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18952 | hp1 | a0001 | c0003 | t0001 | g0063 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18956 | hp2 | a0001 | c0003 | t0001 | g0064 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18963 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18969 | hp1 | a0001 | c0003 | t0001 | g0057 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18978 | hp1 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0058 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18991 | hp1 | a0001 | c0003 | t0001 | g0009 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18994 | hp1 | a0001 | c0003 | t0001 | g0069 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19006 | hp1 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | LWK | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0052 | AFR | LWK | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | LWK | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19056 | hp1 | a0001 | c0003 | t0001 | g0041 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19058 | hp1 | a0001 | c0003 | t0001 | g0065 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19068 | hp1 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19070 | hp1 | a0001 | c0003 | t0001 | g0068 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19078 | hp1 | a0003 | c0006 | t0001 | g0025 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0054 | AFR | YRI | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | YRI | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0088 | AFR | ASW | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0053 | AFR | ASW | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0122 | EUR | TSI | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA20805 | hp1 | a0001 | c0003 | t0001 | g0066 | EUR | TSI | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | GIH | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02559 | hp1 | a0001 | c0003 | t0001 | g0067 | AFR | ACB | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0011 | AFR | USA | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | USA | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0042 | REF | REF | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0040 | REF | REF | INTS6L_chrX_135515660_135587510 | INTS6L | chrX | 135515660 | 135587510 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:135556253 | A | C | 1 | a0003 | 1 | NA19078.hp1 | missense_variant | MODERATE | c.1145A>C | p.Asn382Thr | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/18 | 1478/3904 | 1145/2697 | 382/898 | chrX | 135556253 | |||
| chrX:135577340 | A | T | 1 | a0002 | 3 | HG01346.hp1 HG01433.hp1 HG01978.hp1 |
missense_variant | MODERATE | c.2032A>T | p.Thr678Ser | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 15/18 | 2365/3904 | 2032/2697 | 678/898 | chrX | 135577340 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:135575208 | G | A | 1 | a0001c0005 | 1 | HG03492.hp1 | synonymous_variant | LOW | c.1866G>A | p.Pro622Pro | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 14/18 | 2199/3904 | 1866/2697 | 622/898 | chrX | 135575208 | |||
| chrX:135579930 | G | A | 1 | a0001c0003 | 21 | HG01099.hp1 HG01496.hp1 HG01516.hp2 others(18): Show |
synonymous_variant | LOW | c.2262G>A | p.Leu754Leu | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 16/18 | 2595/3904 | 2262/2697 | 754/898 | chrX | 135579930 | |||
| chrX:135579936 | C | T | 2 | a0001c0002 a0003c0006 |
34 | HG00621.hp1 HG00673.hp1 HG01884.hp1 others(31): Show |
synonymous_variant | LOW | c.2268C>T | p.Asp756Asp | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 16/18 | 2601/3904 | 2268/2697 | 756/898 | chrX | 135579936 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:135520697 | C | T | 1 | a0001c0001t0004 | 1 | HG01261.hp1 | 5_prime_UTR_variant | MODIFIER | c.-296C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 1/18 | 296 | chrX | 135520697 | ||||||
| chrX:135520798 | G | A | 1 | a0001c0001t0004 | 1 | HG01261.hp1 | 5_prime_UTR_variant | MODIFIER | c.-195G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 1/18 | 195 | chrX | 135520798 | ||||||
| chrX:135520893 | T | C | 8 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(5): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
5_prime_UTR_variant | MODIFIER | c.-100T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 1/18 | 100 | chrX | 135520893 | ||||||
| chrX:135582196 | G | A | 1 | a0001c0001t0003 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*560G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 18/18 | 560 | chrX | 135582196 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:135521415 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.189+97C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135521415 | |||||||
| chrX:135521453 | G | A | 17 | a0001c0001t0001g0039 a0001c0002t0001g0003 a0001c0002t0001g0024 others(14): Show |
19 | HG00621.hp1 HG00673.hp1 HG02056.hp1 others(16): Show |
intron_variant | MODIFIER | c.189+135G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135521453 | |||||||
| chrX:135521752 | C | G | 207 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(204): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.189+434C>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135521752 | |||||||
| chrX:135521755 | C | G | 1 | a0001c0003t0001g0041 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.189+437C>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135521755 | |||||||
| chrX:135521758 | G | C | 1 | a0001c0003t0001g0041 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.189+440G>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135521758 | |||||||
| chrX:135521759 | C | G | 1 | a0001c0003t0001g0041 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.189+441C>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135521759 | |||||||
| chrX:135521770 | A | C | 1 | a0001c0003t0001g0056 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.189+452A>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135521770 | |||||||
| chrX:135521770 | A | G | 193 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(190): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.189+452A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135521770 | |||||||
| chrX:135522043 | G | A | 18 | a0001c0001t0001g0060 a0001c0002t0001g0058 a0001c0002t0001g0059 others(15): Show |
19 | HG01099.hp1 HG01516.hp2 HG01928.hp1 others(16): Show |
intron_variant | MODIFIER | c.189+725G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135522043 | |||||||
| chrX:135522422 | T | C | 1 | a0001c0002t0001g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.189+1104T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135522422 | |||||||
| chrX:135522447 | G | A | 1 | a0001c0001t0001g0073 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.189+1129G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135522447 | |||||||
| chrX:135522673 | G | C | 1 | a0001c0001t0004g0074 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.189+1355G>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135522673 | |||||||
| chrX:135522969 | C | T | 1 | a0001c0002t0001g0209 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.189+1651C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135522969 | |||||||
| chrX:135522973 | G | A | 1 | a0001c0003t0001g0057 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.189+1655G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135522973 | |||||||
| chrX:135523107 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.189+1789G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135523107 | |||||||
| chrX:135523173 | T | C | 1 | a0001c0003t0001g0076 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.189+1855T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135523173 | |||||||
| chrX:135523247 | A | C | 147 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(144): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.189+1929A>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135523247 | |||||||
| chrX:135523258 | C | T | 1 | a0001c0003t0001g0056 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.189+1940C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135523258 | |||||||
| chrX:135523269 | G | C | 2 | a0001c0001t0001g0010 a0001c0001t0001g0077 |
3 | HG01884.hp2 HG02818.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.189+1951G>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135523269 | |||||||
| chrX:135523402 | C | CA | 13 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(10): Show |
13 | HG01069.hp1 HG01167.hp1 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.189+2109dupA | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135523402 | ||||||
| chrX:135523402 | C | CAA | 114 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(111): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(133): Show |
intron_variant | MODIFIER | c.189+2108_189+2109d others(4): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135523402 | ||||||
| chrX:135523402 | C | CAAA | 18 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0106 others(15): Show |
18 | HG00642.hp1 HG00735.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.189+2107_189+2109d others(5): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135523402 | ||||||
| chrX:135523402 | C | CAAAA | 6 | a0001c0001t0001g0060 a0001c0001t0001g0099 a0001c0001t0001g0100 others(3): Show |
6 | HG01928.hp1 HG02071.hp1 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.189+2106_189+2109d others(6): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135523402 | ||||||
| chrX:135523402 | CA | C | 14 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0077 others(11): Show |
16 | HG00639.hp2 HG01884.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.189+2109delA | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135523402 | ||||||
| chrX:135523402 | CAAAAAAA | C | 3 | a0001c0001t0001g0005 a0001c0001t0001g0097 a0001c0001t0001g0098 |
5 | HG02080.hp1 HG02155.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.189+2103_189+2109d others(9): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135523402 | ||||||
| chrX:135524039 | T | G | 1 | a0001c0001t0001g0099 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.189+2721T>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135524039 | |||||||
| chrX:135524450 | G | GT | 36 | a0001c0001t0001g0005 a0001c0001t0001g0081 a0001c0001t0001g0082 others(33): Show |
43 | HG00621.hp1 HG00673.hp1 HG01884.hp1 others(40): Show |
intron_variant | MODIFIER | c.189+3144dupT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135524450 | ||||||
| chrX:135524802 | C | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(191): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.189+3484C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135524802 | |||||||
| chrX:135525834 | G | T | 3 | a0001c0001t0001g0023 a0001c0001t0001g0200 a0001c0001t0001g0207 |
4 | HG01167.hp1 HG02895.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.189+4516G>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135525834 | |||||||
| chrX:135525979 | A | G | 44 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0012 others(41): Show |
53 | HG00621.hp1 HG00639.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.189+4661A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135525979 | |||||||
| chrX:135526242 | G | A | 194 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(191): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.189+4924G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135526242 | |||||||
| chrX:135526524 | A | T | 47 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0012 others(44): Show |
56 | HG00621.hp1 HG00639.hp2 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.189+5206A>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135526524 | |||||||
| chrX:135526791 | A | G | 3 | a0001c0002t0001g0079 a0001c0002t0001g0088 a0001c0002t0001g0209 |
3 | HG02257.hp2 HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.189+5473A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135526791 | |||||||
| chrX:135527211 | T | A | 3 | a0001c0001t0001g0013 a0001c0001t0001g0104 a0001c0001t0001g0121 |
4 | HG02129.hp1 NA18942.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.189+5893T>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135527211 | |||||||
| chrX:135527258 | A | G | 2 | a0001c0001t0002g0052 a0001c0001t0002g0053 |
2 | NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.189+5940A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135527258 | |||||||
| chrX:135527299 | T | C | 1 | a0001c0001t0001g0104 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.189+5981T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135527299 | |||||||
| chrX:135527347 | G | A | 1 | a0001c0001t0002g0044 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.189+6029G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135527347 | |||||||
| chrX:135527475 | T | C | 1 | a0001c0001t0001g0122 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.189+6157T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135527475 | |||||||
| chrX:135527843 | G | C | 12 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0077 others(9): Show |
14 | HG00639.hp2 HG01123.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.189+6525G>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135527843 | |||||||
| chrX:135527982 | T | C | 44 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0012 others(41): Show |
53 | HG00621.hp1 HG00639.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.189+6664T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135527982 | |||||||
| chrX:135528180 | G | A | 3 | a0001c0001t0001g0014 a0001c0001t0001g0123 a0001c0001t0001g0202 |
4 | NA18945.hp1 NA18990.hp1 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.189+6862G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135528180 | |||||||
| chrX:135528496 | G | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(191): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.189+7178G>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135528496 | |||||||
| chrX:135528549 | G | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0081 a0001c0001t0001g0082 others(2): Show |
7 | HG02080.hp1 HG02155.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.189+7231G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135528549 | |||||||
| chrX:135528561 | C | T | 3 | a0001c0003t0001g0076 a0001c0003t0001g0198 a0001c0003t0001g0199 |
3 | HG02257.hp1 HG02615.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.189+7243C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135528561 | |||||||
| chrX:135528809 | C | A | 1 | a0001c0001t0001g0124 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.189+7491C>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135528809 | |||||||
| chrX:135528866 | A | AC | 89 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(86): Show |
104 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.189+7559dupC | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135528866 | ||||||
| chrX:135528866 | A | ACC | 51 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(48): Show |
56 | HG00642.hp1 HG00741.hp1 HG01099.hp1 others(53): Show |
intron_variant | MODIFIER | c.189+7558_189+7559d others(4): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135528866 | ||||||
| chrX:135528866 | A | ACCC | 13 | a0001c0001t0001g0005 a0001c0001t0001g0097 a0001c0001t0001g0100 others(10): Show |
15 | HG00140.hp1 HG01109.hp1 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.189+7557_189+7559d others(5): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135528866 | ||||||
| chrX:135528873 | C | CT | 3 | a0001c0001t0001g0120 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | HG00735.hp1 HG01074.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.189+7555_189+7556i others(3): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135528873 | |||||||
| chrX:135528877 | C | G | 6 | a0001c0002t0001g0003 a0001c0002t0001g0026 a0001c0002t0001g0038 others(3): Show |
8 | NA18943.hp1 NA18957.hp1 NA18963.hp2 others(5): Show |
intron_variant | MODIFIER | c.189+7559C>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135528877 | |||||||
| chrX:135529141 | G | A | 1 | a0001c0002t0001g0079 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.189+7823G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135529141 | |||||||
| chrX:135529204 | G | A | 5 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0001t0001g0125 others(2): Show |
7 | HG00099.hp2 HG00140.hp1 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.189+7886G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135529204 | |||||||
| chrX:135529406 | G | A | 2 | a0001c0002t0001g0004 a0001c0002t0001g0084 |
4 | HG01884.hp1 HG02970.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.189+8088G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135529406 | |||||||
| chrX:135529518 | A | G | 1 | a0001c0001t0001g0192 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.189+8200A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135529518 | |||||||
| chrX:135529526 | T | C | 4 | a0001c0001t0001g0075 a0001c0001t0001g0120 a0001c0001t0001g0196 others(1): Show |
4 | HG00099.hp1 HG00735.hp1 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.189+8208T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135529526 | |||||||
| chrX:135529694 | T | C | 3 | a0001c0002t0001g0079 a0001c0002t0001g0088 a0001c0002t0001g0209 |
3 | HG02257.hp2 HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.189+8376T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135529694 | |||||||
| chrX:135529742 | T | A | 1 | a0001c0001t0001g0112 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.189+8424T>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135529742 | |||||||
| chrX:135530182 | A | G | 1 | a0001c0001t0002g0053 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.189+8864A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135530182 | |||||||
| chrX:135530228 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.189+8910C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135530228 | |||||||
| chrX:135530490 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.189+9172G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135530490 | |||||||
| chrX:135530562 | G | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0081 a0001c0001t0001g0082 others(2): Show |
7 | HG02080.hp1 HG02155.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.189+9244G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135530562 | |||||||
| chrX:135530753 | T | G | 39 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0077 others(36): Show |
46 | HG00621.hp1 HG00639.hp2 HG00673.hp1 others(43): Show |
intron_variant | MODIFIER | c.189+9435T>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135530753 | |||||||
| chrX:135530902 | A | C | 4 | a0001c0001t0001g0022 a0001c0001t0001g0103 a0001c0001t0001g0119 others(1): Show |
5 | HG02451.hp1 HG02572.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.189+9584A>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135530902 | |||||||
| chrX:135531152 | A | T | 1 | a0001c0002t0001g0084 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.189+9834A>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135531152 | |||||||
| chrX:135531292 | C | A | 64 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(61): Show |
73 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.189+9974C>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135531292 | |||||||
| chrX:135531320 | G | A | 5 | a0001c0001t0001g0005 a0001c0001t0001g0081 a0001c0001t0001g0082 others(2): Show |
7 | HG02080.hp1 HG02155.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.189+10002G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135531320 | |||||||
| chrX:135531489 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.189+10171G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135531489 | |||||||
| chrX:135531667 | C | G | 5 | a0001c0001t0001g0005 a0001c0001t0001g0081 a0001c0001t0001g0082 others(2): Show |
7 | HG02080.hp1 HG02155.hp2 NA18747.hp1 others(4): Show |
intron_variant | MODIFIER | c.189+10349C>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135531667 | |||||||
| chrX:135531749 | T | C | 1 | a0001c0001t0001g0208 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.189+10431T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135531749 | |||||||
| chrX:135531761 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.189+10443C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135531761 | |||||||
| chrX:135531911 | G | C | 3 | a0001c0002t0001g0079 a0001c0002t0001g0088 a0001c0002t0001g0209 |
3 | HG02257.hp2 HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.189+10593G>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135531911 | |||||||
| chrX:135532220 | G | T | 1 | a0001c0001t0001g0173 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.189+10902G>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135532220 | |||||||
| chrX:135532469 | A | G | 1 | a0001c0002t0001g0037 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.189+11151A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135532469 | |||||||
| chrX:135532514 | G | A | 3 | a0001c0002t0001g0079 a0001c0002t0001g0088 a0001c0002t0001g0209 |
3 | HG02257.hp2 HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.189+11196G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135532514 | |||||||
| chrX:135532636 | A | G | 1 | a0002c0004t0001g0111 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.189+11318A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135532636 | |||||||
| chrX:135532701 | G | A | 3 | a0001c0002t0001g0079 a0001c0002t0001g0088 a0001c0002t0001g0209 |
3 | HG02257.hp2 HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.189+11383G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135532701 | |||||||
| chrX:135533100 | CA | C | 4 | a0001c0001t0001g0099 a0001c0001t0001g0128 a0001c0001t0001g0137 others(1): Show |
4 | NA18953.hp1 NA18957.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.189+11789delA | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135533100 | ||||||
| chrX:135533107 | AC | A | 26 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0011 others(23): Show |
31 | HG00621.hp1 HG00673.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.189+11790delC | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135533107 | |||||||
| chrX:135533178 | T | C | 1 | a0001c0002t0001g0032 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.189+11860T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135533178 | |||||||
| chrX:135533647 | G | A | 3 | a0001c0002t0001g0079 a0001c0002t0001g0088 a0001c0002t0001g0209 |
3 | HG02257.hp2 HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.190-11776G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135533647 | |||||||
| chrX:135533672 | G | C | 3 | a0001c0002t0001g0079 a0001c0002t0001g0088 a0001c0002t0001g0209 |
3 | HG02257.hp2 HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.190-11751G>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135533672 | |||||||
| chrX:135533755 | T | C | 27 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0011 others(24): Show |
32 | HG00621.hp1 HG00673.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.190-11668T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135533755 | |||||||
| chrX:135533826 | T | C | 47 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0012 others(44): Show |
56 | HG00621.hp1 HG00639.hp2 HG00673.hp1 others(53): Show |
intron_variant | MODIFIER | c.190-11597T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135533826 | |||||||
| chrX:135533933 | T | G | 3 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0174 |
3 | HG02145.hp1 HG02647.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.190-11490T>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135533933 | |||||||
| chrX:135534039 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.190-11384G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135534039 | |||||||
| chrX:135534450 | G | A | 1 | a0001c0001t0001g0203 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.190-10973G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135534450 | |||||||
| chrX:135534568 | G | A | 1 | a0001c0002t0001g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.190-10855G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135534568 | |||||||
| chrX:135534682 | C | CT | 24 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0011 others(21): Show |
29 | HG00673.hp1 HG01884.hp1 HG02056.hp1 others(26): Show |
intron_variant | MODIFIER | c.190-10722dupT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135534682 | ||||||
| chrX:135534682 | C | CTT | 5 | a0001c0002t0001g0026 a0001c0002t0001g0031 a0001c0002t0001g0079 others(2): Show |
5 | HG00621.hp1 HG02257.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.190-10723_190-1072 others(6): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135534682 | ||||||
| chrX:135534682 | CT | C | 8 | a0001c0001t0001g0039 a0001c0001t0001g0119 a0001c0001t0001g0140 others(5): Show |
8 | HG01070.hp2 HG01256.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.190-10722delT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135534682 | ||||||
| chrX:135534687 | T | C | 10 | a0001c0001t0002g0002 a0001c0001t0002g0044 a0001c0001t0002g0045 others(7): Show |
13 | HG00741.hp2 HG01192.hp1 NA18946.hp1 others(10): Show |
intron_variant | MODIFIER | c.190-10736T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135534687 | |||||||
| chrX:135534701 | T | A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(153): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.190-10722T>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135534701 | |||||||
| chrX:135534701 | T | TA | 3 | a0001c0001t0001g0118 a0001c0002t0001g0072 a0002c0004t0001g0153 |
3 | HG01433.hp1 HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.190-10719dupA | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135534701 | ||||||
| chrX:135534708 | A | T | 1 | a0001c0003t0001g0199 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.190-10715A>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135534708 | |||||||
| chrX:135534750 | G | A | 13 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0077 others(10): Show |
15 | HG00639.hp2 HG01123.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.190-10673G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135534750 | |||||||
| chrX:135534895 | G | C | 42 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0077 others(39): Show |
49 | HG00621.hp1 HG00639.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.190-10528G>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135534895 | |||||||
| chrX:135535149 | A | C | 1 | a0001c0002t0001g0030 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.190-10274A>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135535149 | |||||||
| chrX:135535284 | A | G | 3 | a0001c0002t0001g0079 a0001c0002t0001g0088 a0001c0002t0001g0209 |
3 | HG02257.hp2 HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.190-10139A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135535284 | |||||||
| chrX:135536672 | T | A | 1 | a0001c0001t0001g0192 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.190-8751T>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135536672 | |||||||
| chrX:135536756 | A | G | 189 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(186): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.190-8667A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135536756 | |||||||
| chrX:135536821 | A | G | 147 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(144): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.190-8602A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135536821 | |||||||
| chrX:135537144 | C | T | 1 | a0001c0003t0001g0036 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.190-8279C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135537144 | |||||||
| chrX:135537247 | TCACTGAT others(8): Show |
T | 1 | a0001c0001t0002g0051 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.190-8174_190-8160d others(17): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135537247 | ||||||
| chrX:135537437 | G | C | 1 | a0001c0001t0001g0109 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.190-7986G>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135537437 | |||||||
| chrX:135537574 | C | T | 4 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(1): Show |
4 | HG00621.hp1 HG02056.hp1 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.190-7849C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135537574 | |||||||
| chrX:135537953 | A | G | 147 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(144): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.190-7470A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135537953 | |||||||
| chrX:135538546 | G | A | 206 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(203): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.190-6877G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135538546 | |||||||
| chrX:135538563 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.190-6860C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135538563 | |||||||
| chrX:135538725 | A | G | 189 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(186): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.190-6698A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135538725 | |||||||
| chrX:135539228 | A | T | 1 | a0001c0001t0001g0171 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.190-6195A>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135539228 | |||||||
| chrX:135539525 | GTTTTTCT others(3): Show |
G | 3 | a0001c0002t0001g0079 a0001c0002t0001g0088 a0001c0002t0001g0209 |
3 | HG02257.hp2 HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.190-5896_190-5887d others(12): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135539525 | ||||||
| chrX:135539709 | C | A | 1 | a0001c0001t0001g0097 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.190-5714C>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135539709 | |||||||
| chrX:135539939 | C | G | 17 | a0001c0001t0001g0005 a0001c0001t0001g0081 a0001c0001t0001g0082 others(14): Show |
22 | HG00741.hp2 HG01192.hp1 HG02080.hp1 others(19): Show |
intron_variant | MODIFIER | c.190-5484C>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135539939 | |||||||
| chrX:135540615 | A | G | 1 | a0001c0001t0002g0050 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.190-4808A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135540615 | |||||||
| chrX:135540704 | A | C | 3 | a0001c0002t0001g0079 a0001c0002t0001g0088 a0001c0002t0001g0209 |
3 | HG02257.hp2 HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.190-4719A>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135540704 | |||||||
| chrX:135540716 | G | GCTC | 184 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(181): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.190-4685_190-4683d others(5): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135540716 | ||||||
| chrX:135541115 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.190-4308A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135541115 | |||||||
| chrX:135541149 | G | C | 2 | a0001c0001t0001g0142 a0001c0001t0001g0205 |
2 | HG01256.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.190-4274G>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135541149 | |||||||
| chrX:135541178 | G | T | 1 | a0001c0001t0001g0170 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.190-4245G>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135541178 | |||||||
| chrX:135541900 | C | A | 3 | a0001c0002t0001g0079 a0001c0002t0001g0088 a0001c0002t0001g0209 |
3 | HG02257.hp2 HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.190-3523C>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135541900 | |||||||
| chrX:135542303 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.190-3120C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135542303 | |||||||
| chrX:135542308 | G | A | 3 | a0001c0002t0001g0079 a0001c0002t0001g0088 a0001c0002t0001g0209 |
3 | HG02257.hp2 HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.190-3115G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135542308 | |||||||
| chrX:135542373 | T | C | 186 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(183): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.190-3050T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135542373 | |||||||
| chrX:135542395 | G | A | 27 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0011 others(24): Show |
32 | HG00621.hp1 HG00673.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.190-3028G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135542395 | |||||||
| chrX:135542553 | GGGAA | G | 13 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0077 others(10): Show |
15 | HG00639.hp2 HG01123.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.190-2849_190-2846d others(6): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chrX | 135542553 | ||||||
| chrX:135543066 | C | G | 1 | a0001c0001t0001g0095 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.190-2357C>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135543066 | |||||||
| chrX:135543098 | A | G | 1 | a0001c0001t0001g0169 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.190-2325A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135543098 | |||||||
| chrX:135543150 | T | C | 1 | a0001c0001t0002g0052 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.190-2273T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135543150 | |||||||
| chrX:135543533 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.190-1890A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135543533 | |||||||
| chrX:135543602 | C | T | 3 | a0001c0001t0001g0102 a0001c0001t0001g0141 a0001c0001t0001g0150 |
3 | NA18951.hp1 NA19001.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.190-1821C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135543602 | |||||||
| chrX:135543766 | T | A | 1 | a0001c0001t0001g0175 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.190-1657T>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135543766 | |||||||
| chrX:135543940 | C | T | 1 | a0001c0002t0001g0078 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.190-1483C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135543940 | |||||||
| chrX:135544292 | C | T | 2 | a0001c0001t0001g0092 a0001c0001t0001g0093 |
2 | HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.190-1131C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135544292 | |||||||
| chrX:135544322 | C | A | 1 | a0001c0002t0001g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.190-1101C>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135544322 | |||||||
| chrX:135544338 | G | A | 26 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0011 others(23): Show |
31 | HG00621.hp1 HG00673.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.190-1085G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135544338 | |||||||
| chrX:135544353 | A | C | 2 | a0001c0001t0001g0103 a0001c0001t0001g0119 |
2 | HG02922.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.190-1070A>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135544353 | |||||||
| chrX:135544363 | T | A | 5 | a0001c0001t0001g0020 a0001c0001t0001g0039 a0001c0001t0001g0159 others(2): Show |
6 | HG03017.hp1 NA18948.hp1 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.190-1060T>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135544363 | |||||||
| chrX:135544742 | A | G | 1 | a0001c0002t0001g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.190-681A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135544742 | |||||||
| chrX:135544925 | C | G | 159 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(156): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.190-498C>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 2/17 | chrX | 135544925 | |||||||
| chrX:135545583 | T | A | 5 | a0001c0001t0001g0140 a0001c0001t0001g0143 a0001c0001t0001g0176 others(2): Show |
5 | HG02280.hp1 HG02451.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.339+11T>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 3/17 | chrX | 135545583 | |||||||
| chrX:135545844 | A | T | 1 | a0001c0001t0001g0149 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.339+272A>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 3/17 | chrX | 135545844 | |||||||
| chrX:135545932 | T | A | 27 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0011 others(24): Show |
32 | HG00621.hp1 HG00673.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.339+360T>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 3/17 | chrX | 135545932 | |||||||
| chrX:135546136 | G | A | 1 | a0001c0001t0001g0169 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.340-244G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 3/17 | chrX | 135546136 | |||||||
| chrX:135546607 | T | C | 1 | a0001c0001t0001g0132 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.430-95T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 4/17 | chrX | 135546607 | |||||||
| chrX:135546616 | A | G | 1 | a0001c0001t0001g0168 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.430-86A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 4/17 | chrX | 135546616 | |||||||
| chrX:135546893 | C | T | 3 | a0001c0002t0001g0079 a0001c0002t0001g0088 a0001c0002t0001g0209 |
3 | HG02257.hp2 HG02818.hp2 NA20129.hp1 |
splice_region_variant&intron_variant | LOW | c.613+8C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 5/17 | chrX | 135546893 | |||||||
| chrX:135547314 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.742+49G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 6/17 | chrX | 135547314 | |||||||
| chrX:135547587 | C | T | 3 | a0001c0002t0001g0079 a0001c0002t0001g0088 a0001c0002t0001g0209 |
3 | HG02257.hp2 HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.742+322C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 6/17 | chrX | 135547587 | |||||||
| chrX:135548039 | G | T | 147 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(144): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.742+774G>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 6/17 | chrX | 135548039 | |||||||
| chrX:135548047 | G | GTATA | 2 | a0001c0002t0001g0004 a0001c0002t0001g0084 |
4 | HG01884.hp1 HG02970.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.742+799_742+802dup others(4): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chrX | 135548047 | ||||||
| chrX:135548047 | G | GTATATA | 3 | a0001c0002t0001g0083 a0001c0002t0001g0086 a0001c0002t0001g0087 |
3 | HG02976.hp1 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.742+797_742+802dup others(6): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chrX | 135548047 | ||||||
| chrX:135548047 | GTA | G | 126 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(123): Show |
146 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(143): Show |
intron_variant | MODIFIER | c.742+801_742+802del others(2): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chrX | 135548047 | ||||||
| chrX:135548161 | T | C | 1 | a0001c0001t0001g0102 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.742+896T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 6/17 | chrX | 135548161 | |||||||
| chrX:135548367 | G | A | 3 | a0001c0002t0001g0079 a0001c0002t0001g0088 a0001c0002t0001g0209 |
3 | HG02257.hp2 HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.742+1102G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 6/17 | chrX | 135548367 | |||||||
| chrX:135548505 | C | A | 1 | a0001c0002t0001g0085 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.743-1137C>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 6/17 | chrX | 135548505 | |||||||
| chrX:135548639 | A | G | 150 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(147): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.743-1003A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 6/17 | chrX | 135548639 | |||||||
| chrX:135548721 | C | T | 3 | a0001c0002t0001g0079 a0001c0002t0001g0088 a0001c0002t0001g0209 |
3 | HG02257.hp2 HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.743-921C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 6/17 | chrX | 135548721 | |||||||
| chrX:135548783 | A | G | 1 | a0001c0001t0001g0132 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.743-859A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 6/17 | chrX | 135548783 | |||||||
| chrX:135549218 | A | G | 27 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0011 others(24): Show |
32 | HG00621.hp1 HG00673.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.743-424A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 6/17 | chrX | 135549218 | |||||||
| chrX:135549224 | A | G | 206 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(203): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.743-418A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 6/17 | chrX | 135549224 | |||||||
| chrX:135549939 | A | G | 159 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(156): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.906+134A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 7/17 | chrX | 135549939 | |||||||
| chrX:135550026 | G | A | 1 | a0001c0002t0001g0031 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.906+221G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 7/17 | chrX | 135550026 | |||||||
| chrX:135550127 | G | T | 25 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0011 others(22): Show |
30 | HG00621.hp1 HG00673.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.906+322G>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 7/17 | chrX | 135550127 | |||||||
| chrX:135550370 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.906+565C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 7/17 | chrX | 135550370 | |||||||
| chrX:135550430 | C | CT | 155 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(152): Show |
179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.906+641dupT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chrX | 135550430 | ||||||
| chrX:135550430 | CT | C | 26 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0011 others(23): Show |
31 | HG00621.hp1 HG00673.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.906+641delT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chrX | 135550430 | ||||||
| chrX:135550584 | C | G | 3 | a0001c0002t0001g0079 a0001c0002t0001g0088 a0001c0002t0001g0209 |
3 | HG02257.hp2 HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.906+779C>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 7/17 | chrX | 135550584 | |||||||
| chrX:135550844 | G | A | 1 | a0001c0003t0001g0063 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.906+1039G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 7/17 | chrX | 135550844 | |||||||
| chrX:135550950 | T | A | 1 | a0001c0001t0002g0051 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.907-1044T>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 7/17 | chrX | 135550950 | |||||||
| chrX:135550951 | C | T | 1 | a0001c0001t0002g0051 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.907-1043C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 7/17 | chrX | 135550951 | |||||||
| chrX:135551899 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.907-95A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 7/17 | chrX | 135551899 | |||||||
| chrX:135551983 | A | T | 12 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0077 others(9): Show |
14 | HG00639.hp2 HG01123.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.907-11A>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 7/17 | chrX | 135551983 | |||||||
| chrX:135552298 | G | A | 26 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0011 others(23): Show |
31 | HG00621.hp1 HG00673.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.1059+152G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | chrX | 135552298 | |||||||
| chrX:135552527 | A | G | 1 | a0001c0001t0001g0188 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1059+381A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | chrX | 135552527 | |||||||
| chrX:135552599 | T | C | 11 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0077 others(8): Show |
13 | HG00639.hp2 HG01123.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1059+453T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | chrX | 135552599 | |||||||
| chrX:135552601 | G | A | 1 | a0001c0001t0001g0094 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1059+455G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | chrX | 135552601 | |||||||
| chrX:135552613 | A | C | 5 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0001t0001g0125 others(2): Show |
7 | HG00099.hp2 HG00140.hp1 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.1059+467A>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | chrX | 135552613 | |||||||
| chrX:135552682 | A | G | 1 | a0001c0001t0002g0053 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1059+536A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | chrX | 135552682 | |||||||
| chrX:135553168 | C | CAG | 27 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0011 others(24): Show |
32 | HG00621.hp1 HG00673.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.1059+1030_1059+103 others(6): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chrX | 135553168 | ||||||
| chrX:135553427 | C | G | 2 | a0001c0001t0001g0113 a0001c0001t0001g0131 |
2 | HG03669.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1059+1281C>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | chrX | 135553427 | |||||||
| chrX:135553481 | AT | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0186 a0001c0001t0001g0187 others(1): Show |
6 | NA18954.hp2 NA18974.hp1 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.1059+1358delT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chrX | 135553481 | ||||||
| chrX:135553482 | T | TC | 9 | a0001c0001t0001g0105 a0001c0001t0001g0121 a0001c0001t0001g0131 others(6): Show |
9 | HG01099.hp1 HG02040.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1059+1336_1059+133 others(5): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | chrX | 135553482 | |||||||
| chrX:135553483 | T | C | 136 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(133): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.1059+1337T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | chrX | 135553483 | |||||||
| chrX:135553485 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1059+1339T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | chrX | 135553485 | |||||||
| chrX:135553512 | C | T | 1 | a0001c0002t0001g0024 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1059+1366C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | chrX | 135553512 | |||||||
| chrX:135553619 | G | A | 1 | a0001c0001t0001g0141 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1059+1473G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | chrX | 135553619 | |||||||
| chrX:135553647 | C | A | 1 | a0001c0001t0001g0160 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1059+1501C>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | chrX | 135553647 | |||||||
| chrX:135553919 | T | C | 162 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(159): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.1059+1773T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | chrX | 135553919 | |||||||
| chrX:135554118 | C | T | 14 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0001t0001g0110 others(11): Show |
16 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(13): Show |
intron_variant | MODIFIER | c.1059+1972C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | chrX | 135554118 | |||||||
| chrX:135554310 | A | T | 1 | a0001c0001t0001g0060 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1060-1858A>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | chrX | 135554310 | |||||||
| chrX:135554409 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1060-1759A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | chrX | 135554409 | |||||||
| chrX:135554575 | G | C | 1 | a0002c0004t0001g0181 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1060-1593G>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | chrX | 135554575 | |||||||
| chrX:135554640 | G | A | 162 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(159): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.1060-1528G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | chrX | 135554640 | |||||||
| chrX:135554883 | C | CT | 43 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0012 others(40): Show |
53 | HG00621.hp1 HG00639.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.1060-1260dupT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chrX | 135554883 | ||||||
| chrX:135554883 | C | CTT | 16 | a0001c0001t0001g0022 a0001c0001t0001g0113 a0001c0001t0001g0151 others(13): Show |
19 | HG00741.hp2 HG01070.hp1 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.1060-1261_1060-126 others(6): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chrX | 135554883 | ||||||
| chrX:135554883 | C | CTTT | 123 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(120): Show |
142 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(139): Show |
intron_variant | MODIFIER | c.1060-1262_1060-126 others(7): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chrX | 135554883 | ||||||
| chrX:135554883 | C | CTTTT | 20 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0060 others(17): Show |
22 | HG00609.hp1 HG01358.hp1 HG01928.hp1 others(19): Show |
intron_variant | MODIFIER | c.1060-1263_1060-126 others(8): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chrX | 135554883 | ||||||
| chrX:135554977 | A | T | 14 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0001t0001g0110 others(11): Show |
16 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(13): Show |
intron_variant | MODIFIER | c.1060-1191A>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | chrX | 135554977 | |||||||
| chrX:135555720 | G | A | 1 | a0001c0005t0001g0126 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.1060-448G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | chrX | 135555720 | |||||||
| chrX:135555764 | C | T | 1 | a0001c0001t0001g0134 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1060-404C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | chrX | 135555764 | |||||||
| chrX:135556031 | T | C | 4 | a0001c0001t0002g0002 a0001c0001t0002g0044 a0001c0001t0002g0051 others(1): Show |
7 | NA18946.hp1 NA18947.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.1060-137T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 8/17 | chrX | 135556031 | |||||||
| chrX:135556390 | G | A | 3 | a0001c0002t0001g0079 a0001c0002t0001g0088 a0001c0002t0001g0209 |
3 | HG02257.hp2 HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1192+90G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135556390 | |||||||
| chrX:135556549 | C | T | 1 | a0001c0001t0001g0165 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1192+249C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135556549 | |||||||
| chrX:135556655 | C | G | 1 | a0001c0003t0001g0069 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1192+355C>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135556655 | |||||||
| chrX:135556902 | A | G | 27 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0011 others(24): Show |
32 | HG00621.hp1 HG00673.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.1192+602A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135556902 | |||||||
| chrX:135556903 | G | T | 1 | a0001c0002t0001g0085 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1192+603G>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135556903 | |||||||
| chrX:135557266 | T | G | 1 | a0001c0001t0001g0174 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1192+966T>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135557266 | |||||||
| chrX:135557349 | A | C | 150 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(147): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.1192+1049A>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135557349 | |||||||
| chrX:135557426 | A | C | 1 | a0003c0006t0001g0025 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1192+1126A>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135557426 | |||||||
| chrX:135557526 | A | G | 11 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0077 others(8): Show |
13 | HG00639.hp2 HG01123.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1192+1226A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135557526 | |||||||
| chrX:135558180 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1192+1880C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135558180 | |||||||
| chrX:135558226 | T | A | 1 | a0001c0001t0001g0210 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1192+1926T>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135558226 | |||||||
| chrX:135558281 | C | A | 27 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0011 others(24): Show |
32 | HG00621.hp1 HG00673.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.1192+1981C>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135558281 | |||||||
| chrX:135558390 | A | G | 2 | a0001c0001t0001g0022 a0001c0001t0001g0195 |
3 | HG02451.hp1 HG02572.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1192+2090A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135558390 | |||||||
| chrX:135558552 | A | G | 1 | a0001c0001t0001g0082 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1192+2252A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135558552 | |||||||
| chrX:135558584 | A | G | 1 | a0001c0001t0004g0074 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1192+2284A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135558584 | |||||||
| chrX:135558787 | C | CT | 7 | a0001c0001t0001g0023 a0001c0001t0001g0116 a0001c0001t0001g0122 others(4): Show |
8 | HG01167.hp1 HG02055.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.1192+2503dupT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135558787 | ||||||
| chrX:135558788 | T | C | 1 | a0003c0006t0001g0025 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1192+2488T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135558788 | |||||||
| chrX:135558933 | G | A | 14 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0001t0001g0110 others(11): Show |
16 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(13): Show |
intron_variant | MODIFIER | c.1192+2633G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135558933 | |||||||
| chrX:135559003 | G | A | 27 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0011 others(24): Show |
32 | HG00621.hp1 HG00673.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.1192+2703G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135559003 | |||||||
| chrX:135559181 | A | G | 27 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0011 others(24): Show |
32 | HG00621.hp1 HG00673.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.1192+2881A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135559181 | |||||||
| chrX:135559252 | G | A | 27 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0011 others(24): Show |
32 | HG00621.hp1 HG00673.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.1192+2952G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135559252 | |||||||
| chrX:135559308 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1192+3008T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135559308 | |||||||
| chrX:135559749 | T | G | 1 | a0001c0001t0002g0045 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1192+3449T>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135559749 | |||||||
| chrX:135560057 | G | A | 27 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0011 others(24): Show |
32 | HG00621.hp1 HG00673.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.1192+3757G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135560057 | |||||||
| chrX:135560065 | C | A | 2 | a0001c0001t0002g0052 a0001c0001t0002g0053 |
2 | NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1192+3765C>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135560065 | |||||||
| chrX:135560214 | G | T | 12 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0077 others(9): Show |
14 | HG00639.hp2 HG01123.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1192+3914G>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135560214 | |||||||
| chrX:135560375 | T | C | 149 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(146): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.1192+4075T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135560375 | |||||||
| chrX:135560395 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1192+4095T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135560395 | |||||||
| chrX:135560458 | T | C | 3 | a0001c0001t0001g0120 a0001c0001t0001g0196 a0001c0001t0001g0197 |
3 | HG00735.hp1 HG01074.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.1192+4158T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135560458 | |||||||
| chrX:135560558 | T | C | 1 | a0001c0003t0001g0071 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1192+4258T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135560558 | |||||||
| chrX:135560759 | A | G | 188 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(185): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.1192+4459A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135560759 | |||||||
| chrX:135560769 | G | A | 3 | a0001c0001t0001g0021 a0001c0001t0001g0144 a0001c0001t0001g0149 |
4 | HG01496.hp2 HG01943.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.1192+4469G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135560769 | |||||||
| chrX:135560958 | T | C | 1 | a0003c0006t0001g0025 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1192+4658T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135560958 | |||||||
| chrX:135560959 | C | CT | 162 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(159): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.1192+4670dupT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135560959 | ||||||
| chrX:135560959 | C | T | 1 | a0003c0006t0001g0025 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1192+4659C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135560959 | |||||||
| chrX:135561392 | C | T | 11 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0077 others(8): Show |
13 | HG00639.hp2 HG01123.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1192+5092C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135561392 | |||||||
| chrX:135561821 | A | G | 188 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(185): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.1192+5521A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135561821 | |||||||
| chrX:135561891 | C | G | 1 | a0001c0001t0001g0207 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1192+5591C>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135561891 | |||||||
| chrX:135562013 | A | T | 148 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(145): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.1192+5713A>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135562013 | |||||||
| chrX:135562066 | CTTTTT | C | 27 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0011 others(24): Show |
32 | HG00621.hp1 HG00673.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.1192+5768_1192+577 others(9): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135562066 | ||||||
| chrX:135562140 | T | C | 149 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(146): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(168): Show |
intron_variant | MODIFIER | c.1192+5840T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135562140 | |||||||
| chrX:135562196 | T | C | 27 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0011 others(24): Show |
32 | HG00621.hp1 HG00673.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.1192+5896T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135562196 | |||||||
| chrX:135562328 | A | G | 12 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0077 others(9): Show |
14 | HG00639.hp2 HG01123.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1192+6028A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135562328 | |||||||
| chrX:135562486 | G | A | 12 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0077 others(9): Show |
14 | HG00639.hp2 HG01123.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1192+6186G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135562486 | |||||||
| chrX:135562777 | T | A | 161 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(158): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.1192+6477T>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135562777 | |||||||
| chrX:135562955 | T | G | 1 | a0001c0003t0001g0064 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1193-6382T>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135562955 | |||||||
| chrX:135563341 | C | T | 1 | a0001c0001t0002g0050 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1193-5996C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135563341 | |||||||
| chrX:135563584 | C | CAT | 148 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(145): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.1193-5744_1193-574 others(6): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135563584 | ||||||
| chrX:135563619 | A | ATGTG | 3 | a0001c0001t0001g0080 a0001c0001t0001g0094 a0001c0001t0001g0096 |
3 | HG01123.hp1 HG02615.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1193-5706_1193-570 others(8): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135563619 | ||||||
| chrX:135563619 | A | ATGTGTG | 5 | a0001c0001t0001g0012 a0001c0001t0001g0077 a0001c0001t0001g0090 others(2): Show |
6 | HG02280.hp2 HG02717.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1193-5708_1193-570 others(10): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135563619 | ||||||
| chrX:135563619 | A | ATGTGTGT others(1): Show |
2 | a0001c0001t0001g0010 a0001c0001t0001g0089 |
3 | HG01884.hp2 HG02922.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1193-5710_1193-570 others(12): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135563619 | ||||||
| chrX:135563619 | A | G | 3 | a0001c0002t0001g0079 a0001c0002t0001g0088 a0001c0002t0001g0209 |
3 | HG02257.hp2 HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1193-5718A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135563619 | |||||||
| chrX:135563619 | ATGTG | A | 7 | a0001c0002t0001g0027 a0001c0002t0001g0032 a0001c0002t0001g0033 others(4): Show |
7 | HG00673.hp1 HG02602.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1193-5706_1193-570 others(8): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135563619 | ||||||
| chrX:135563631 | G | A | 18 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0024 others(15): Show |
22 | HG00621.hp1 HG01884.hp1 HG02056.hp1 others(19): Show |
intron_variant | MODIFIER | c.1193-5706G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135563631 | |||||||
| chrX:135563631 | G | GTATA | 10 | a0001c0001t0001g0005 a0001c0001t0001g0060 a0001c0001t0001g0081 others(7): Show |
12 | HG00741.hp2 HG01928.hp1 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.1193-5705_1193-570 others(8): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135563631 | ||||||
| chrX:135563631 | G | GTATATAT others(1): Show |
4 | a0001c0001t0002g0002 a0001c0001t0002g0044 a0001c0001t0002g0051 others(1): Show |
7 | NA18946.hp1 NA18947.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.1193-5705_1193-570 others(12): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135563631 | ||||||
| chrX:135563633 | G | A | 36 | a0001c0001t0001g0005 a0001c0001t0001g0060 a0001c0001t0001g0081 others(33): Show |
45 | HG00621.hp1 HG00741.hp2 HG01192.hp1 others(42): Show |
intron_variant | MODIFIER | c.1193-5704G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135563633 | |||||||
| chrX:135563633 | G | GTGTGTGT others(3): Show |
2 | a0001c0001t0001g0091 a0001c0001t0001g0093 |
2 | HG00639.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1193-5703_1193-570 others(14): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135563633 | ||||||
| chrX:135563635 | A | G | 157 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(154): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.1193-5702A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135563635 | |||||||
| chrX:135563637 | A | G | 147 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(144): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.1193-5700A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135563637 | |||||||
| chrX:135563639 | A | G | 5 | a0001c0001t0001g0094 a0001c0001t0001g0155 a0001c0001t0001g0168 others(2): Show |
5 | HG00099.hp2 HG01261.hp1 HG01516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1193-5698A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135563639 | |||||||
| chrX:135563645 | ATATATAT others(19): Show |
A | 143 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(140): Show |
165 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.1193-5681_1193-565 others(30): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135563645 | ||||||
| chrX:135563647 | ATATATAT others(17): Show |
A | 3 | a0001c0001t0001g0155 a0001c0001t0001g0168 a0001c0001t0001g0208 |
3 | HG00099.hp2 HG02523.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1193-5675_1193-565 others(28): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135563647 | ||||||
| chrX:135563655 | ATAGCTAT others(9): Show |
A | 2 | a0001c0002t0001g0028 a0001c0002t0001g0034 |
2 | HG02074.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.1193-5679_1193-566 others(20): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135563655 | ||||||
| chrX:135563657 | AGC | A | 24 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0011 others(21): Show |
29 | HG00621.hp1 HG00673.hp1 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.1193-5679_1193-567 others(6): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135563657 | |||||||
| chrX:135563658 | G | T | 16 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0077 others(13): Show |
18 | HG00639.hp2 HG01123.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.1193-5679G>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135563658 | |||||||
| chrX:135563659 | C | A | 16 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0077 others(13): Show |
18 | HG00639.hp2 HG01123.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.1193-5678C>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135563659 | |||||||
| chrX:135563669 | AGC | A | 12 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0024 others(9): Show |
15 | HG00621.hp1 HG02602.hp1 HG02809.hp2 others(12): Show |
intron_variant | MODIFIER | c.1193-5667_1193-566 others(6): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135563669 | |||||||
| chrX:135563670 | G | T | 29 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0077 others(26): Show |
32 | HG00639.hp2 HG00673.hp1 HG01123.hp1 others(29): Show |
intron_variant | MODIFIER | c.1193-5667G>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135563670 | |||||||
| chrX:135563671 | C | A | 29 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0077 others(26): Show |
32 | HG00639.hp2 HG00673.hp1 HG01123.hp1 others(29): Show |
intron_variant | MODIFIER | c.1193-5666C>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135563671 | |||||||
| chrX:135564145 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1193-5192T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135564145 | |||||||
| chrX:135564244 | A | G | 2 | a0001c0001t0001g0112 a0001c0001t0001g0167 |
2 | HG02083.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.1193-5093A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135564244 | |||||||
| chrX:135564367 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1193-4970C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135564367 | |||||||
| chrX:135564376 | T | C | 12 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0077 others(9): Show |
14 | HG00639.hp2 HG01123.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1193-4961T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135564376 | |||||||
| chrX:135564584 | T | C | 12 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0077 others(9): Show |
14 | HG00639.hp2 HG01123.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1193-4753T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135564584 | |||||||
| chrX:135564721 | T | A | 1 | a0001c0001t0001g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-4616T>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135564721 | |||||||
| chrX:135564722 | A | C | 1 | a0001c0001t0001g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-4615A>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135564722 | |||||||
| chrX:135564731 | C | CA | 7 | a0001c0001t0001g0039 a0001c0001t0001g0117 a0001c0001t0001g0178 others(4): Show |
7 | HG02257.hp2 HG02723.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1193-4592dupA | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135564731 | ||||||
| chrX:135564731 | C | CAA | 133 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(130): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): Show |
intron_variant | MODIFIER | c.1193-4593_1193-459 others(6): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135564731 | ||||||
| chrX:135564731 | C | CAAA | 10 | a0001c0001t0001g0023 a0001c0001t0001g0106 a0001c0001t0001g0113 others(7): Show |
11 | HG01167.hp1 HG02055.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.1193-4594_1193-459 others(7): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135564731 | ||||||
| chrX:135564731 | CA | C | 13 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0077 others(10): Show |
15 | HG00639.hp2 HG01123.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.1193-4592delA | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chrX | 135564731 | ||||||
| chrX:135564806 | A | G | 1 | a0001c0003t0001g0146 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1193-4531A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135564806 | |||||||
| chrX:135565303 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1193-4034G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135565303 | |||||||
| chrX:135565396 | A | G | 3 | a0001c0002t0001g0079 a0001c0002t0001g0088 a0001c0002t0001g0209 |
3 | HG02257.hp2 HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1193-3941A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135565396 | |||||||
| chrX:135565696 | A | G | 12 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0077 others(9): Show |
14 | HG00639.hp2 HG01123.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1193-3641A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135565696 | |||||||
| chrX:135565710 | C | G | 12 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0077 others(9): Show |
14 | HG00639.hp2 HG01123.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1193-3627C>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135565710 | |||||||
| chrX:135565774 | A | C | 1 | a0001c0001t0001g0094 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1193-3563A>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135565774 | |||||||
| chrX:135565877 | G | C | 1 | a0001c0001t0001g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-3460G>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135565877 | |||||||
| chrX:135566041 | A | G | 27 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0011 others(24): Show |
32 | HG00621.hp1 HG00673.hp1 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.1193-3296A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135566041 | |||||||
| chrX:135566078 | G | A | 1 | a0001c0001t0001g0134 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1193-3259G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135566078 | |||||||
| chrX:135566805 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1193-2532G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135566805 | |||||||
| chrX:135566842 | T | C | 1 | a0001c0002t0001g0027 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1193-2495T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135566842 | |||||||
| chrX:135566926 | G | A | 1 | a0001c0001t0001g0132 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1193-2411G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135566926 | |||||||
| chrX:135566950 | G | A | 1 | a0001c0001t0001g0186 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1193-2387G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135566950 | |||||||
| chrX:135566951 | C | A | 1 | a0001c0001t0001g0186 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1193-2386C>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135566951 | |||||||
| chrX:135567122 | C | G | 3 | a0001c0001t0001g0102 a0001c0001t0001g0141 a0001c0001t0001g0150 |
3 | NA18951.hp1 NA19001.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1193-2215C>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135567122 | |||||||
| chrX:135567272 | C | T | 3 | a0001c0001t0001g0102 a0001c0001t0001g0141 a0001c0001t0001g0150 |
3 | NA18951.hp1 NA19001.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1193-2065C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135567272 | |||||||
| chrX:135567301 | T | C | 161 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(158): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.1193-2036T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135567301 | |||||||
| chrX:135567687 | A | T | 161 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(158): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.1193-1650A>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135567687 | |||||||
| chrX:135567689 | A | C | 161 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(158): Show |
185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.1193-1648A>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135567689 | |||||||
| chrX:135568018 | T | A | 3 | a0001c0001t0001g0135 a0001c0001t0001g0183 a0001c0003t0001g0057 |
3 | HG02148.hp2 HG02523.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.1193-1319T>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135568018 | |||||||
| chrX:135568019 | A | T | 4 | a0001c0001t0001g0144 a0001c0002t0001g0079 a0001c0002t0001g0088 others(1): Show |
4 | HG02257.hp2 HG02300.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1193-1318A>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135568019 | |||||||
| chrX:135568175 | T | C | 1 | a0001c0001t0001g0160 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1193-1162T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135568175 | |||||||
| chrX:135568582 | C | T | 1 | a0001c0001t0001g0172 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1193-755C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135568582 | |||||||
| chrX:135568790 | T | G | 158 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(155): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.1193-547T>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135568790 | |||||||
| chrX:135568885 | A | T | 1 | a0001c0001t0001g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-452A>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135568885 | |||||||
| chrX:135568886 | T | A | 1 | a0001c0001t0001g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-451T>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135568886 | |||||||
| chrX:135568891 | G | T | 1 | a0001c0001t0001g0129 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1193-446G>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135568891 | |||||||
| chrX:135569183 | T | G | 158 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(155): Show |
182 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(179): Show |
intron_variant | MODIFIER | c.1193-154T>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135569183 | |||||||
| chrX:135569265 | A | C | 4 | a0001c0001t0002g0046 a0001c0001t0002g0047 a0001c0001t0002g0048 others(1): Show |
4 | HG00741.hp2 NA18964.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1193-72A>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 9/17 | chrX | 135569265 | |||||||
| chrX:135570032 | C | T | 3 | a0001c0002t0001g0079 a0001c0002t0001g0088 a0001c0002t0001g0209 |
3 | HG02257.hp2 HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1288-404C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 10/17 | chrX | 135570032 | |||||||
| chrX:135571110 | C | A | 1 | a0001c0001t0001g0145 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1398+564C>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 11/17 | chrX | 135571110 | |||||||
| chrX:135571731 | T | A | 1 | a0001c0002t0001g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1399-1084T>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 11/17 | chrX | 135571731 | |||||||
| chrX:135571934 | T | A | 1 | a0001c0001t0001g0091 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1399-881T>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 11/17 | chrX | 135571934 | |||||||
| chrX:135571963 | A | G | 1 | a0001c0001t0002g0046 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1399-852A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 11/17 | chrX | 135571963 | |||||||
| chrX:135572344 | G | T | 25 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0011 others(22): Show |
30 | HG00621.hp1 HG00673.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.1399-471G>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 11/17 | chrX | 135572344 | |||||||
| chrX:135572586 | T | C | 150 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(147): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.1399-229T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 11/17 | chrX | 135572586 | |||||||
| chrX:135572671 | G | A | 1 | a0001c0001t0001g0162 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1399-144G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 11/17 | chrX | 135572671 | |||||||
| chrX:135572678 | G | A | 26 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0011 others(23): Show |
31 | HG00621.hp1 HG00673.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.1399-137G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 11/17 | chrX | 135572678 | |||||||
| chrX:135573523 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1618-416G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 12/17 | chrX | 135573523 | |||||||
| chrX:135573526 | T | G | 1 | a0001c0001t0001g0184 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1618-413T>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 12/17 | chrX | 135573526 | |||||||
| chrX:135573839 | G | A | 1 | a0001c0001t0001g0102 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1618-100G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 12/17 | chrX | 135573839 | |||||||
| chrX:135573843 | T | C | 2 | a0001c0001t0001g0163 a0001c0001t0001g0208 |
2 | HG02735.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1618-96T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 12/17 | chrX | 135573843 | |||||||
| chrX:135574082 | C | CT | 15 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0077 others(12): Show |
17 | HG00639.hp2 HG01123.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.1741+35dupT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chrX | 135574082 | ||||||
| chrX:135574082 | CT | C | 6 | a0001c0001t0001g0121 a0001c0001t0001g0164 a0001c0001t0001g0165 others(3): Show |
6 | HG01167.hp1 NA18956.hp1 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.1741+35delT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chrX | 135574082 | ||||||
| chrX:135574166 | T | C | 12 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0077 others(9): Show |
14 | HG00639.hp2 HG01123.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1741+104T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 13/17 | chrX | 135574166 | |||||||
| chrX:135574704 | T | C | 188 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(185): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.1742-380T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 13/17 | chrX | 135574704 | |||||||
| chrX:135574792 | G | C | 1 | a0001c0002t0001g0029 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1742-292G>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 13/17 | chrX | 135574792 | |||||||
| chrX:135574915 | T | G | 1 | a0001c0001t0001g0192 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1742-169T>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 13/17 | chrX | 135574915 | |||||||
| chrX:135575390 | G | T | 1 | a0001c0002t0001g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1884+164G>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 14/17 | chrX | 135575390 | |||||||
| chrX:135575644 | G | A | 159 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(156): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.1884+418G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 14/17 | chrX | 135575644 | |||||||
| chrX:135575785 | A | AGT | 152 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(149): Show |
176 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.1884+582_1884+583d others(4): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chrX | 135575785 | ||||||
| chrX:135575785 | A | AGTGT | 4 | a0001c0001t0001g0075 a0001c0001t0001g0089 a0001c0001t0001g0091 others(1): Show |
4 | HG00099.hp1 HG00639.hp2 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.1884+580_1884+583d others(6): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chrX | 135575785 | ||||||
| chrX:135575785 | AGT | A | 46 | a0001c0001t0001g0005 a0001c0001t0001g0060 a0001c0001t0001g0081 others(43): Show |
56 | HG00621.hp1 HG00673.hp1 HG00741.hp2 others(53): Show |
intron_variant | MODIFIER | c.1884+582_1884+583d others(4): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chrX | 135575785 | ||||||
| chrX:135575810 | A | G | 1 | a0001c0003t0001g0036 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1884+584A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 14/17 | chrX | 135575810 | |||||||
| chrX:135575992 | A | G | 6 | a0001c0001t0001g0007 a0001c0001t0001g0157 a0001c0001t0001g0162 others(3): Show |
8 | HG00609.hp1 NA18947.hp2 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.1884+766A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 14/17 | chrX | 135575992 | |||||||
| chrX:135576024 | G | A | 159 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(156): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.1884+798G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 14/17 | chrX | 135576024 | |||||||
| chrX:135576083 | C | T | 206 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(203): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.1884+857C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 14/17 | chrX | 135576083 | |||||||
| chrX:135576327 | C | CA | 20 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0077 others(17): Show |
22 | HG00639.hp2 HG01123.hp1 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.1885-848dupA | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chrX | 135576327 | ||||||
| chrX:135576327 | C | CAA | 133 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(130): Show |
155 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.1885-849_1885-848d others(4): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chrX | 135576327 | ||||||
| chrX:135576327 | C | CAAA | 7 | a0001c0001t0001g0121 a0001c0001t0001g0125 a0001c0001t0001g0135 others(4): Show |
7 | HG00140.hp1 HG02148.hp1 HG02148.hp2 others(4): Show |
intron_variant | MODIFIER | c.1885-850_1885-848d others(5): Show |
INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chrX | 135576327 | ||||||
| chrX:135576391 | A | C | 1 | a0001c0001t0001g0131 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1885-802A>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 14/17 | chrX | 135576391 | |||||||
| chrX:135576396 | C | T | 188 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(185): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.1885-797C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 14/17 | chrX | 135576396 | |||||||
| chrX:135576685 | G | GA | 206 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(203): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.1885-507dupA | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chrX | 135576685 | ||||||
| chrX:135576688 | G | T | 206 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(203): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.1885-505G>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 14/17 | chrX | 135576688 | |||||||
| chrX:135576690 | G | A | 206 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(203): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.1885-503G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 14/17 | chrX | 135576690 | |||||||
| chrX:135577053 | AT | A | 12 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0077 others(9): Show |
14 | HG00639.hp2 HG01123.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.1885-137delT | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chrX | 135577053 | ||||||
| chrX:135577862 | C | T | 2 | a0001c0001t0002g0052 a0001c0001t0002g0053 |
2 | NA19030.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2119+435C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 15/17 | chrX | 135577862 | |||||||
| chrX:135578011 | G | A | 3 | a0001c0002t0001g0079 a0001c0002t0001g0088 a0001c0002t0001g0209 |
3 | HG02257.hp2 HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2119+584G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 15/17 | chrX | 135578011 | |||||||
| chrX:135578041 | C | T | 1 | a0001c0001t0001g0094 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2119+614C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 15/17 | chrX | 135578041 | |||||||
| chrX:135578074 | T | A | 188 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(185): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.2119+647T>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 15/17 | chrX | 135578074 | |||||||
| chrX:135578165 | G | A | 4 | a0001c0001t0001g0105 a0001c0001t0001g0127 a0001c0001t0001g0154 others(1): Show |
4 | HG03490.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.2119+738G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 15/17 | chrX | 135578165 | |||||||
| chrX:135578169 | T | A | 1 | a0001c0001t0001g0130 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2119+742T>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 15/17 | chrX | 135578169 | |||||||
| chrX:135578616 | T | C | 150 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(147): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.2120-1172T>C | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 15/17 | chrX | 135578616 | |||||||
| chrX:135579271 | A | G | 1 | a0001c0001t0001g0174 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2120-517A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 15/17 | chrX | 135579271 | |||||||
| chrX:135579480 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2120-308C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 15/17 | chrX | 135579480 | |||||||
| chrX:135579498 | T | A | 188 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(185): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.2120-290T>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 15/17 | chrX | 135579498 | |||||||
| chrX:135580243 | C | G | 4 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 others(1): Show |
4 | HG00621.hp1 HG02056.hp1 NA18956.hp1 others(1): Show |
intron_variant | MODIFIER | c.2494+81C>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 16/17 | chrX | 135580243 | |||||||
| chrX:135580358 | A | T | 1 | a0001c0001t0002g0052 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2494+196A>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 16/17 | chrX | 135580358 | |||||||
| chrX:135580671 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2495-379C>T | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 16/17 | chrX | 135580671 | |||||||
| chrX:135580973 | C | G | 1 | a0001c0002t0001g0072 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2495-77C>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 16/17 | chrX | 135580973 | |||||||
| chrX:135581037 | T | A | 26 | a0001c0002t0001g0003 a0001c0002t0001g0004 a0001c0002t0001g0011 others(23): Show |
31 | HG00621.hp1 HG00673.hp1 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.2495-13T>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 16/17 | chrX | 135581037 | |||||||
| chrX:135581349 | G | A | 71 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(68): Show |
80 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.2589-179G>A | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 17/17 | chrX | 135581349 | |||||||
| chrX:135581367 | A | G | 3 | a0001c0002t0001g0079 a0001c0002t0001g0088 a0001c0002t0001g0209 |
3 | HG02257.hp2 HG02818.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2589-161A>G | INTS6L | ENSG00000165359.16 | transcript | ENST00000639893.2 | protein_coding | 17/17 | chrX | 135581367 |