Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 1520 |
| ensemblid | ENSG00000163131.12 |
| hgncid | 2545 |
| symbol | CTSS |
| name | cathepsin S |
| refseq_nuc | NM_004079.5 |
| refseq_prot | NP_004070.3 |
| ensembl_nuc | ENST00000368985.8 |
| ensembl_prot | ENSP00000357981.3 |
| mane_status | MANE Select |
| chr | chr1 |
| start | 150730188 |
| end | 150765778 |
| strand | - |
| ver | v1.2 |
| region | chr1:150730188-150765778 |
| region5000 | chr1:150725188-150770778 |
| regionname0 | CTSS_chr1_150730188_150765778 |
| regionname5000 | CTSS_chr1_150725188_150770778 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 331 | 228 | 61 | 29 | 105 | 10 | 22 | 81 | CTSS_chr1_150725188_150770778 | CTSS | MKRLV others(326): Show |
chr1 | 150725188 | 150770778 |
| a0002 | 0/1 | 331 | 110 | 21 | 18 | 51 | 5 | 14 | 41 | CTSS_chr1_150725188_150770778 | CTSS | MKRLV others(326): Show |
chr1 | 150725188 | 150770778 |
| a0003 | 0/0 | 331 | 6 | 0 | 3 | 0 | 1 | 2 | 0 | CTSS_chr1_150725188_150770778 | CTSS | MKRLV others(326): Show |
chr1 | 150725188 | 150770778 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 993 | 228 | 61 | 29 | 105 | 10 | 22 | CTSS_chr1_150725188_150770778 | CTSS | ATGAA others(988): Show |
chr1 | 150725188 | 150770778 | ||
| a0002c0002 | 0/1 | 993 | 110 | 21 | 18 | 51 | 5 | 14 | CTSS_chr1_150725188_150770778 | CTSS | ATGAA others(988): Show |
chr1 | 150725188 | 150770778 | ||
| a0003c0003 | 0/0 | 993 | 6 | 0 | 3 | 0 | 1 | 2 | CTSS_chr1_150725188_150770778 | CTSS | ATGAA others(988): Show |
chr1 | 150725188 | 150770778 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3935 | 131 | 8 | 26 | 73 | 7 | 17 | CTSS_chr1_150725188_150770778 | CTSS | CTCCT others(3930): Show |
chr1 | 150725188 | 150770778 |
| a0001c0001t0003 | 1/0 | 3935 | 89 | 50 | 3 | 29 | 3 | 3 | CTSS_chr1_150725188_150770778 | CTSS | CTCCT others(3930): Show |
chr1 | 150725188 | 150770778 |
| a0001c0001t0008 | 0/0 | 3935 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | CTCCT others(3930): Show |
chr1 | 150725188 | 150770778 |
| a0001c0001t0011 | 0/0 | 3935 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | CTCCT others(3930): Show |
chr1 | 150725188 | 150770778 |
| a0001c0001t0012 | 0/0 | 3935 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | CTCCT others(3930): Show |
chr1 | 150725188 | 150770778 |
| a0001c0001t0013 | 0/0 | 3935 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | CTCCT others(3930): Show |
chr1 | 150725188 | 150770778 |
| a0001c0001t0014 | 0/0 | 3935 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | CTCCT others(3930): Show |
chr1 | 150725188 | 150770778 |
| a0001c0001t0015 | 0/0 | 3926 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | CTCCT others(3921): Show |
chr1 | 150725188 | 150770778 |
| a0001c0001t0016 | 0/0 | 3935 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | CTCCT others(3930): Show |
chr1 | 150725188 | 150770778 |
| a0001c0001t0017 | 0/0 | 3935 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | CTCCT others(3930): Show |
chr1 | 150725188 | 150770778 |
| a0002c0002t0002 | 0/1 | 3928 | 94 | 7 | 17 | 50 | 5 | 14 | CTSS_chr1_150725188_150770778 | CTSS | CTCCT others(3923): Show |
chr1 | 150725188 | 150770778 |
| a0002c0002t0003 | 0/0 | 3935 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | CTCCT others(3930): Show |
chr1 | 150725188 | 150770778 |
| a0002c0002t0004 | 0/0 | 3932 | 6 | 6 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | CTCCT others(3927): Show |
chr1 | 150725188 | 150770778 |
| a0002c0002t0005 | 0/0 | 3926 | 6 | 6 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | CTCCT others(3921): Show |
chr1 | 150725188 | 150770778 |
| a0002c0002t0007 | 0/0 | 3928 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | CTCCT others(3923): Show |
chr1 | 150725188 | 150770778 |
| a0002c0002t0009 | 0/0 | 3928 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | CTCCT others(3923): Show |
chr1 | 150725188 | 150770778 |
| a0002c0002t0010 | 0/0 | 3928 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | CTCCT others(3923): Show |
chr1 | 150725188 | 150770778 |
| a0003c0003t0001 | 0/0 | 3935 | 4 | 0 | 3 | 0 | 1 | 0 | CTSS_chr1_150725188_150770778 | CTSS | CTCCT others(3930): Show |
chr1 | 150725188 | 150770778 |
| a0003c0003t0006 | 0/0 | 3935 | 2 | 0 | 0 | 0 | 0 | 2 | CTSS_chr1_150725188_150770778 | CTSS | CTCCT others(3930): Show |
chr1 | 150725188 | 150770778 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 7 | 0 | 1 | 3 | 3 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0004 | 0/0 | 7 | 0 | 0 | 5 | 0 | 2 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 3 | 2 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0002 | 0/0 | 13 | 0 | 0 | 13 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0005 | 1/0 | 7 | 6 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0012 | 0/0 | 4 | 0 | 0 | 2 | 1 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0008g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0011g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0012g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0013g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0014g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0015g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0016g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0001c0001t0017g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0001 | 0/0 | 15 | 1 | 5 | 8 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0013 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0014 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0015 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0024 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0025 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0058 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0004g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0004g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0005g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0005g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0005g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0005g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0007g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0009g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0002c0002t0010g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0003c0003t0001g0016 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0003c0003t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| a0003c0003t0006g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0160 | EUR | GBR | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | GBR | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0012 | EUR | GBR | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG00140 | hp2 | a0002 | c0002 | t0002 | g0015 | EUR | GBR | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG00280 | hp1 | a0003 | c0003 | t0001 | g0016 | EUR | FIN | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0029 | EUR | FIN | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG00323 | hp1 | a0002 | c0002 | t0002 | g0070 | EUR | FIN | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0159 | EUR | FIN | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG00408 | hp2 | a0002 | c0002 | t0002 | g0071 | EAS | CHS | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | CHS | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG00558 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | CHS | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | CHS | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG00597 | hp2 | a0002 | c0002 | t0002 | g0075 | EAS | CHS | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG00621 | hp1 | a0002 | c0002 | t0002 | g0064 | EAS | CHS | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0227 | EAS | CHS | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG00642 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG00735 | hp2 | a0002 | c0002 | t0002 | g0103 | AMR | PUR | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG00738 | hp2 | a0002 | c0002 | t0002 | g0060 | AMR | PUR | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG01069 | hp2 | a0002 | c0002 | t0002 | g0054 | AMR | PUR | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG01074 | hp2 | a0002 | c0002 | t0002 | g0069 | AMR | PUR | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG01109 | hp1 | a0002 | c0002 | t0002 | g0015 | AMR | PUR | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0211 | AMR | PUR | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG01243 | hp2 | a0003 | c0003 | t0001 | g0016 | AMR | PUR | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG01255 | hp1 | a0003 | c0003 | t0001 | g0016 | AMR | CLM | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG01255 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG01257 | hp1 | a0002 | c0002 | t0002 | g0014 | AMR | CLM | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG01257 | hp2 | a0003 | c0003 | t0001 | g0104 | AMR | CLM | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG01346 | hp2 | a0002 | c0002 | t0002 | g0024 | AMR | CLM | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG01358 | hp1 | a0002 | c0002 | t0002 | g0051 | AMR | CLM | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG01358 | hp2 | a0002 | c0002 | t0002 | g0101 | AMR | CLM | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0231 | AMR | CLM | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG01515 | hp2 | a0001 | c0001 | t0003 | g0224 | EUR | IBS | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG01517 | hp2 | a0002 | c0002 | t0002 | g0024 | EUR | IBS | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG01884 | hp1 | a0002 | c0002 | t0007 | g0076 | AFR | ACB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG01884 | hp2 | a0001 | c0001 | t0003 | g0213 | AFR | ACB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG01891 | hp1 | a0002 | c0002 | t0002 | g0072 | AFR | ACB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0212 | AFR | ACB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG01928 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG01934 | hp1 | a0002 | c0002 | t0002 | g0078 | AMR | PEL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG01943 | hp2 | a0002 | c0002 | t0009 | g0063 | AMR | PEL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG01978 | hp1 | a0002 | c0002 | t0002 | g0014 | AMR | PEL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG01981 | hp2 | a0002 | c0002 | t0002 | g0102 | AMR | PEL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0220 | AMR | PEL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PEL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0217 | EAS | KHV | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02015 | hp2 | a0002 | c0002 | t0002 | g0067 | EAS | KHV | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02027 | hp2 | a0002 | c0002 | t0002 | g0021 | EAS | KHV | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0207 | AFR | ACB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | KHV | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | KHV | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02083 | hp2 | a0001 | c0001 | t0008 | g0097 | EAS | KHV | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02129 | hp2 | a0001 | c0001 | t0003 | g0223 | EAS | KHV | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02132 | hp1 | a0002 | c0002 | t0002 | g0096 | EAS | KHV | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02132 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0240 | AFR | ACB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02145 | hp2 | a0001 | c0001 | t0003 | g0209 | AFR | ACB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | CDX | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02165 | hp2 | a0002 | c0002 | t0002 | g0055 | EAS | CDX | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02257 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | ACB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0198 | AFR | ACB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02258 | hp1 | a0002 | c0002 | t0005 | g0062 | AFR | ACB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02258 | hp2 | a0002 | c0002 | t0002 | g0001 | AFR | ACB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02273 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02280 | hp1 | a0001 | c0001 | t0003 | g0197 | AFR | ACB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02280 | hp2 | a0001 | c0001 | t0003 | g0204 | AFR | ACB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02293 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02602 | hp1 | a0002 | c0002 | t0002 | g0086 | SAS | PJL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0210 | AFR | GWD | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | GWD | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0233 | AFR | GWD | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02630 | hp1 | a0001 | c0001 | t0003 | g0202 | AFR | GWD | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0199 | AFR | GWD | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0195 | AFR | GWD | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02647 | hp2 | a0002 | c0002 | t0005 | g0065 | AFR | GWD | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0012 | SAS | PJL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02698 | hp2 | a0002 | c0002 | t0002 | g0050 | SAS | PJL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02735 | hp2 | a0002 | c0002 | t0002 | g0091 | SAS | PJL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02738 | hp1 | a0002 | c0002 | t0002 | g0047 | SAS | PJL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0201 | AFR | GWD | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02809 | hp2 | a0002 | c0002 | t0002 | g0073 | AFR | GWD | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0214 | AFR | GWD | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02886 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | GWD | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02886 | hp2 | a0002 | c0002 | t0005 | g0084 | AFR | GWD | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02895 | hp1 | a0002 | c0002 | t0005 | g0052 | AFR | GWD | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0193 | AFR | GWD | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02896 | hp1 | a0002 | c0002 | t0004 | g0041 | AFR | GWD | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0236 | AFR | GWD | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02897 | hp1 | a0002 | c0002 | t0005 | g0023 | AFR | GWD | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02897 | hp2 | a0002 | c0002 | t0004 | g0040 | AFR | GWD | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0206 | AFR | ESN | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02965 | hp2 | a0002 | c0002 | t0004 | g0039 | AFR | ESN | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02970 | hp1 | a0002 | c0002 | t0004 | g0042 | AFR | ESN | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | ESN | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02976 | hp1 | a0002 | c0002 | t0004 | g0048 | AFR | ESN | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02976 | hp2 | a0001 | c0001 | t0003 | g0216 | AFR | ESN | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG03041 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | GWD | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG03041 | hp2 | a0002 | c0002 | t0002 | g0056 | AFR | GWD | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0037 | AFR | MSL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0038 | AFR | MSL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG03130 | hp1 | a0002 | c0002 | t0003 | g0234 | AFR | ESN | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | ESN | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG03139 | hp1 | a0002 | c0002 | t0002 | g0074 | AFR | ESN | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | ESN | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG03209 | hp1 | a0001 | c0001 | t0014 | g0242 | AFR | MSL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG03209 | hp2 | a0002 | c0002 | t0004 | g0044 | AFR | MSL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0038 | AFR | MSL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0203 | AFR | MSL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG03239 | hp1 | a0001 | c0001 | t0016 | g0191 | SAS | PJL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG03239 | hp2 | a0002 | c0002 | t0002 | g0045 | SAS | PJL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0208 | AFR | MSL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0037 | AFR | MSL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0215 | AFR | MSL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0238 | AFR | MSL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG03490 | hp1 | a0002 | c0002 | t0002 | g0059 | SAS | PJL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG03490 | hp2 | a0003 | c0003 | t0006 | g0026 | SAS | PJL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0025 | SAS | PJL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG03492 | hp2 | a0003 | c0003 | t0006 | g0026 | SAS | PJL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ESN | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | ESN | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG03540 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | GWD | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG03540 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | GWD | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0194 | AFR | MSL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG03579 | hp2 | a0002 | c0002 | t0002 | g0013 | AFR | MSL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG03710 | hp1 | a0002 | c0002 | t0002 | g0092 | SAS | PJL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG03710 | hp2 | a0002 | c0002 | t0002 | g0095 | SAS | PJL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG03831 | hp1 | a0002 | c0002 | t0002 | g0014 | SAS | BEB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | BEB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG03834 | hp1 | a0001 | c0001 | t0011 | g0164 | SAS | BEB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | BEB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | BEB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG03942 | hp2 | a0002 | c0002 | t0002 | g0043 | SAS | BEB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | STU | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG04115 | hp2 | a0002 | c0002 | t0002 | g0001 | SAS | STU | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0221 | SAS | BEB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | BEB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | STU | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG04199 | hp2 | a0002 | c0002 | t0002 | g0046 | SAS | STU | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG04204 | hp1 | a0002 | c0002 | t0002 | g0087 | SAS | STU | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | STU | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | STU | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0226 | SAS | STU | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | YRI | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18522 | hp2 | a0002 | c0002 | t0005 | g0023 | AFR | YRI | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18612 | hp1 | a0002 | c0002 | t0002 | g0093 | EAS | CHB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18612 | hp2 | a0002 | c0002 | t0010 | g0082 | EAS | CHB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0229 | EAS | CHB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | YRI | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18906 | hp2 | a0002 | c0002 | t0002 | g0013 | AFR | YRI | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18939 | hp2 | a0002 | c0002 | t0002 | g0057 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18944 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18948 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18950 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18951 | hp1 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18952 | hp2 | a0002 | c0002 | t0002 | g0094 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18953 | hp2 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18954 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18960 | hp1 | a0002 | c0002 | t0002 | g0085 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18961 | hp1 | a0002 | c0002 | t0002 | g0013 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18962 | hp2 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18963 | hp2 | a0002 | c0002 | t0002 | g0081 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18965 | hp2 | a0002 | c0002 | t0002 | g0077 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18966 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18968 | hp1 | a0002 | c0002 | t0002 | g0066 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18970 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18972 | hp1 | a0002 | c0002 | t0002 | g0079 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18972 | hp2 | a0001 | c0001 | t0013 | g0218 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18973 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18974 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18978 | hp2 | a0002 | c0002 | t0002 | g0088 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18982 | hp1 | a0002 | c0002 | t0002 | g0022 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18982 | hp2 | a0002 | c0002 | t0002 | g0100 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18984 | hp1 | a0002 | c0002 | t0002 | g0098 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18986 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18988 | hp2 | a0001 | c0001 | t0003 | g0222 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18989 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18994 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18995 | hp1 | a0002 | c0002 | t0002 | g0021 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0228 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA19001 | hp1 | a0002 | c0002 | t0002 | g0025 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA19005 | hp1 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA19006 | hp1 | a0002 | c0002 | t0002 | g0061 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA19009 | hp2 | a0002 | c0002 | t0002 | g0080 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA19010 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA19010 | hp2 | a0002 | c0002 | t0002 | g0053 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0192 | AFR | LWK | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA19030 | hp2 | a0001 | c0001 | t0003 | g0200 | AFR | LWK | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA19043 | hp1 | a0001 | c0001 | t0017 | g0241 | AFR | LWK | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0237 | AFR | LWK | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA19054 | hp1 | a0001 | c0001 | t0012 | g0170 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA19054 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA19057 | hp2 | a0002 | c0002 | t0002 | g0083 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA19058 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA19062 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA19063 | hp1 | a0002 | c0002 | t0002 | g0099 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA19064 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA19065 | hp2 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA19066 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA19068 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA19070 | hp2 | a0002 | c0002 | t0002 | g0090 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA19078 | hp1 | a0002 | c0002 | t0002 | g0049 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA19079 | hp2 | a0002 | c0002 | t0002 | g0022 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0230 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA19085 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA19090 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | YRI | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | YRI | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA20752 | hp1 | a0002 | c0002 | t0002 | g0089 | EUR | TSI | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA20752 | hp2 | a0001 | c0001 | t0003 | g0219 | EUR | TSI | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0134 | EUR | TSI | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA20805 | hp2 | a0002 | c0002 | t0002 | g0068 | EUR | TSI | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | GIH | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | GIH | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0196 | AFR | ACB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0232 | AFR | ACB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | ACB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | MSL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0205 | AFR | MSL | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | USA | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| HG06807 | hp2 | a0001 | c0001 | t0015 | g0235 | AFR | USA | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0239 | AFR | LWK | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | LWK | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0002 | g0058 | REF | REF | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0005 | REF | REF | CTSS_chr1_150725188_150770778 | CTSS | chr1 | 150725188 | 150770778 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:150755063 | G | A | 1 | a0002 | 109 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(106): Show |
missense_variant | MODERATE | c.337C>T | p.Arg113Trp | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/8 | 419/3936 | 337/996 | 113/331 | chr1 | 150755063 | |||
| chr1:150764744 | A | G | 1 | a0003 | 6 | HG00280.hp1 HG01243.hp2 HG01255.hp1 others(3): Show |
missense_variant | MODERATE | c.20T>C | p.Val7Ala | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/8 | 102/3936 | 20/996 | 7/331 | chr1 | 150764744 |
| 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 |
|---|
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:150730241 | G | C | 8 | a0001c0001t0015 a0001c0001t0016 a0002c0002t0002 others(5): Show |
110 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*2805C>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 8/8 | 2805 | chr1 | 150730241 | ||||||
| chr1:150730293 | A | G | 1 | a0003c0003t0006 | 2 | HG03490.hp2 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2753T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 8/8 | 2753 | chr1 | 150730293 | ||||||
| chr1:150730558 | CAGA | C | 7 | a0001c0001t0015 a0002c0002t0002 a0002c0002t0004 others(4): Show |
109 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*2485_*2487delTCT | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 8/8 | 2485 | chr1 | 150730558 | ||||||
| chr1:150730815 | T | C | 1 | a0001c0001t0016 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2231A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 8/8 | 2231 | chr1 | 150730815 | ||||||
| chr1:150730880 | T | C | 1 | a0001c0001t0014 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2166A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 8/8 | 2166 | chr1 | 150730880 | ||||||
| chr1:150730890 | TAACA | T | 6 | a0001c0001t0015 a0002c0002t0002 a0002c0002t0005 others(3): Show |
103 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*2152_*2155delTGTT | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 8/8 | 2152 | chr1 | 150730890 | ||||||
| chr1:150730920 | CTG | C | 2 | a0001c0001t0015 a0002c0002t0005 |
7 | HG02258.hp1 HG02647.hp2 HG02886.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2124_*2125delCA | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 8/8 | 2124 | chr1 | 150730920 | ||||||
| chr1:150731008 | A | G | 1 | a0001c0001t0013 | 1 | NA18972.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2038T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 8/8 | 2038 | chr1 | 150731008 | ||||||
| chr1:150731722 | T | G | 1 | a0002c0002t0009 | 1 | HG01943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1324A>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 8/8 | 1324 | chr1 | 150731722 | ||||||
| chr1:150731739 | T | C | 1 | a0001c0001t0016 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1307A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 8/8 | 1307 | chr1 | 150731739 | ||||||
| chr1:150731882 | A | C | 1 | a0001c0001t0011 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1164T>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 8/8 | 1164 | chr1 | 150731882 | ||||||
| chr1:150732205 | G | A | 1 | a0001c0001t0012 | 1 | NA19054.hp1 | 3_prime_UTR_variant | MODIFIER | c.*841C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 8/8 | 841 | chr1 | 150732205 | ||||||
| chr1:150732378 | G | A | 1 | a0001c0001t0017 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*668C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 8/8 | 668 | chr1 | 150732378 | ||||||
| chr1:150732380 | T | C | 1 | a0002c0002t0010 | 1 | NA18612.hp2 | 3_prime_UTR_variant | MODIFIER | c.*666A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 8/8 | 666 | chr1 | 150732380 | ||||||
| chr1:150732604 | A | G | 1 | a0002c0002t0007 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*442T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 8/8 | 442 | chr1 | 150732604 | ||||||
| chr1:150765721 | C | T | 5 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0012 others(2): Show |
139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
5_prime_UTR_variant | MODIFIER | c.-25G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 1/8 | 958 | chr1 | 150765721 | ||||||
| chr1:150765724 | A | G | 7 | a0001c0001t0008 a0002c0002t0002 a0002c0002t0004 others(4): Show |
109 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(106): Show |
5_prime_UTR_variant | MODIFIER | c.-28T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 1/8 | 961 | chr1 | 150765724 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr1:150733180 | C | T | 1 | a0001c0001t0016g0191 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.897-35G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150733180 | |||||||
| chr1:150733279 | G | A | 77 | a0001c0001t0015g0235 a0001c0001t0016g0191 a0002c0002t0002g0001 others(74): Show |
110 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.897-134C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150733279 | |||||||
| chr1:150733306 | A | G | 1 | a0001c0001t0001g0137 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.897-161T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150733306 | |||||||
| chr1:150733403 | C | A | 1 | a0001c0001t0001g0167 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.897-258G>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150733403 | |||||||
| chr1:150733911 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.897-766C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150733911 | |||||||
| chr1:150734188 | C | T | 1 | a0002c0002t0002g0073 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.897-1043G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150734188 | |||||||
| chr1:150734265 | G | C | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG02615.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.897-1120C>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150734265 | |||||||
| chr1:150734318 | C | T | 20 | a0001c0001t0003g0002 a0001c0001t0003g0012 a0001c0001t0003g0019 others(17): Show |
38 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.897-1173G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150734318 | |||||||
| chr1:150734905 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.897-1760A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150734905 | |||||||
| chr1:150735096 | G | T | 1 | a0001c0001t0016g0191 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.897-1951C>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150735096 | |||||||
| chr1:150735120 | G | A | 76 | a0001c0001t0015g0235 a0002c0002t0002g0001 a0002c0002t0002g0006 others(73): Show |
109 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.897-1975C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150735120 | |||||||
| chr1:150735160 | A | T | 76 | a0001c0001t0015g0235 a0002c0002t0002g0001 a0002c0002t0002g0006 others(73): Show |
109 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.897-2015T>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150735160 | |||||||
| chr1:150735187 | T | C | 1 | a0001c0001t0001g0017 | 3 | HG00423.hp2 NA18988.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.897-2042A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150735187 | |||||||
| chr1:150735209 | G | A | 2 | a0001c0001t0001g0114 a0001c0001t0001g0118 |
2 | NA18979.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.897-2064C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150735209 | |||||||
| chr1:150735307 | T | C | 1 | a0001c0001t0016g0191 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.897-2162A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150735307 | |||||||
| chr1:150735516 | C | T | 70 | a0001c0001t0015g0235 a0002c0002t0002g0001 a0002c0002t0002g0006 others(67): Show |
103 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.897-2371G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150735516 | |||||||
| chr1:150735590 | T | C | 1 | a0001c0001t0001g0109 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.897-2445A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150735590 | |||||||
| chr1:150735623 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.897-2478C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150735623 | |||||||
| chr1:150735686 | T | C | 1 | a0002c0002t0002g0059 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.897-2541A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150735686 | |||||||
| chr1:150735755 | A | AT | 14 | a0001c0001t0001g0136 a0001c0001t0001g0148 a0001c0001t0001g0168 others(11): Show |
15 | HG01261.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.897-2611dupA | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150735755 | |||||||
| chr1:150735755 | AT | A | 76 | a0001c0001t0001g0106 a0001c0001t0001g0189 a0001c0001t0003g0229 others(73): Show |
109 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.897-2611delA | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150735755 | |||||||
| chr1:150736161 | G | A | 1 | a0002c0002t0002g0043 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.897-3016C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150736161 | |||||||
| chr1:150736320 | G | C | 1 | a0001c0001t0003g0223 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.897-3175C>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150736320 | |||||||
| chr1:150736585 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.897-3440A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150736585 | |||||||
| chr1:150736653 | T | A | 76 | a0001c0001t0015g0235 a0002c0002t0002g0001 a0002c0002t0002g0006 others(73): Show |
109 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.897-3508A>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150736653 | |||||||
| chr1:150736772 | T | TA | 18 | a0001c0001t0001g0140 a0001c0001t0001g0160 a0001c0001t0003g0009 others(15): Show |
25 | HG00099.hp1 HG01109.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.897-3628dupT | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150736772 | |||||||
| chr1:150736836 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.897-3691G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150736836 | |||||||
| chr1:150737175 | T | G | 2 | a0001c0001t0001g0159 a0001c0001t0001g0160 |
2 | HG00099.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.897-4030A>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150737175 | |||||||
| chr1:150737191 | C | T | 2 | a0001c0001t0001g0114 a0001c0001t0001g0118 |
2 | NA18979.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.897-4046G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150737191 | |||||||
| chr1:150737247 | C | T | 104 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(101): Show |
140 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.897-4102G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150737247 | |||||||
| chr1:150737309 | C | G | 76 | a0001c0001t0015g0235 a0002c0002t0002g0001 a0002c0002t0002g0006 others(73): Show |
109 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.897-4164G>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150737309 | |||||||
| chr1:150737354 | G | A | 1 | a0001c0001t0001g0125 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.897-4209C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150737354 | |||||||
| chr1:150737406 | C | T | 4 | a0001c0001t0003g0208 a0001c0001t0003g0209 a0001c0001t0003g0210 others(1): Show |
4 | HG01891.hp2 HG02145.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.897-4261G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150737406 | |||||||
| chr1:150737433 | G | A | 2 | a0001c0001t0001g0033 a0001c0001t0001g0178 |
3 | NA18999.hp1 NA19009.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.897-4288C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150737433 | |||||||
| chr1:150737791 | T | G | 1 | a0001c0001t0001g0139 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.897-4646A>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150737791 | |||||||
| chr1:150737810 | A | G | 1 | a0001c0001t0016g0191 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.897-4665T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150737810 | |||||||
| chr1:150737871 | G | A | 1 | a0001c0001t0003g0197 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.897-4726C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150737871 | |||||||
| chr1:150737984 | G | T | 5 | a0002c0002t0002g0006 a0002c0002t0002g0061 a0002c0002t0002g0088 others(2): Show |
9 | NA18950.hp2 NA18952.hp2 NA18954.hp1 others(6): Show |
intron_variant | MODIFIER | c.897-4839C>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150737984 | |||||||
| chr1:150738490 | A | AT | 15 | a0001c0001t0001g0033 a0001c0001t0001g0126 a0001c0001t0001g0140 others(12): Show |
17 | HG01109.hp2 HG01346.hp2 HG01517.hp2 others(14): Show |
intron_variant | MODIFIER | c.897-5346dupA | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150738490 | |||||||
| chr1:150738556 | G | A | 1 | a0001c0001t0001g0117 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.897-5411C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150738556 | |||||||
| chr1:150738598 | C | A | 1 | a0001c0001t0003g0240 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.897-5453G>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150738598 | |||||||
| chr1:150738624 | C | G | 1 | a0001c0001t0003g0240 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.897-5479G>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150738624 | |||||||
| chr1:150738681 | G | A | 11 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0231 others(8): Show |
13 | HG01433.hp2 HG02109.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.897-5536C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150738681 | |||||||
| chr1:150739081 | T | C | 1 | a0001c0001t0016g0191 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.897-5936A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150739081 | |||||||
| chr1:150739281 | C | G | 1 | a0002c0002t0002g0075 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.897-6136G>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150739281 | |||||||
| chr1:150739328 | A | T | 1 | a0001c0001t0001g0180 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.897-6183T>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150739328 | |||||||
| chr1:150739420 | A | T | 77 | a0001c0001t0015g0235 a0001c0001t0016g0191 a0002c0002t0002g0001 others(74): Show |
110 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.897-6275T>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150739420 | |||||||
| chr1:150739537 | T | G | 1 | a0001c0001t0001g0122 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.897-6392A>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150739537 | |||||||
| chr1:150739662 | TCAA | T | 226 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(223): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.897-6520_897-6518d others(5): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150739662 | |||||||
| chr1:150739722 | G | GA | 76 | a0001c0001t0015g0235 a0001c0001t0016g0191 a0002c0002t0002g0001 others(73): Show |
109 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.897-6578dupT | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150739722 | |||||||
| chr1:150739896 | GTTC | G | 76 | a0001c0001t0015g0235 a0002c0002t0002g0001 a0002c0002t0002g0006 others(73): Show |
109 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.897-6754_897-6752d others(5): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150739896 | |||||||
| chr1:150740450 | G | A | 76 | a0001c0001t0015g0235 a0002c0002t0002g0001 a0002c0002t0002g0006 others(73): Show |
109 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.897-7305C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150740450 | |||||||
| chr1:150740515 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.896+7262G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150740515 | |||||||
| chr1:150740592 | C | T | 1 | a0001c0001t0003g0195 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.896+7185G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150740592 | |||||||
| chr1:150740594 | G | A | 2 | a0001c0001t0001g0114 a0001c0001t0001g0118 |
2 | NA18979.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.896+7183C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150740594 | |||||||
| chr1:150740618 | T | G | 3 | a0002c0002t0002g0068 a0002c0002t0002g0069 a0002c0002t0002g0070 |
3 | HG00323.hp1 HG01074.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.896+7159A>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150740618 | |||||||
| chr1:150741009 | A | C | 1 | a0001c0001t0003g0198 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.896+6768T>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150741009 | |||||||
| chr1:150741536 | A | G | 2 | a0001c0001t0001g0185 a0001c0001t0001g0186 |
2 | NA19006.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.896+6241T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150741536 | |||||||
| chr1:150741884 | AG | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(100): Show |
139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.896+5892delC | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150741884 | |||||||
| chr1:150741886 | G | C | 1 | a0002c0002t0002g0070 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.896+5891C>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150741886 | |||||||
| chr1:150741887 | G | C | 8 | a0001c0001t0003g0009 a0001c0001t0003g0192 a0001c0001t0003g0194 others(5): Show |
12 | HG02055.hp1 HG02109.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.896+5890C>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150741887 | |||||||
| chr1:150741891 | G | C | 1 | a0001c0001t0016g0191 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.896+5886C>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150741891 | |||||||
| chr1:150742102 | C | G | 1 | a0001c0001t0001g0129 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.896+5675G>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150742102 | |||||||
| chr1:150742175 | TGAACCTT others(7): Show |
T | 104 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(101): Show |
140 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.896+5588_896+5601d others(16): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150742175 | |||||||
| chr1:150742189 | A | G | 123 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0011 others(120): Show |
182 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.896+5588T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150742189 | |||||||
| chr1:150742682 | T | C | 11 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0231 others(8): Show |
13 | HG01433.hp2 HG02109.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.896+5095A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150742682 | |||||||
| chr1:150742756 | A | G | 11 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0231 others(8): Show |
13 | HG01433.hp2 HG02109.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.896+5021T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150742756 | |||||||
| chr1:150742918 | T | C | 4 | a0001c0001t0003g0208 a0001c0001t0003g0209 a0001c0001t0003g0210 others(1): Show |
4 | HG01891.hp2 HG02145.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.896+4859A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150742918 | |||||||
| chr1:150742937 | G | T | 1 | a0002c0002t0002g0088 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.896+4840C>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150742937 | |||||||
| chr1:150742976 | G | A | 3 | a0002c0002t0002g0022 a0002c0002t0002g0077 a0002c0002t0002g0081 |
4 | NA18963.hp2 NA18965.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.896+4801C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150742976 | |||||||
| chr1:150743109 | T | A | 1 | a0002c0002t0002g0095 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.896+4668A>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743109 | |||||||
| chr1:150743192 | G | T | 1 | a0001c0001t0016g0191 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.896+4585C>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743192 | |||||||
| chr1:150743306 | G | A | 90 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0231 others(87): Show |
125 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.896+4471C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743306 | |||||||
| chr1:150743366 | C | CAACAGTC others(28): Show |
1 | a0002c0002t0002g0079 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.896+4376_896+4410d others(37): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743366 | |||||||
| chr1:150743496 | GAT | G | 136 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(133): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.896+4279_896+4280d others(4): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743496 | |||||||
| chr1:150743496 | GATAT | G | 82 | a0001c0001t0003g0208 a0001c0001t0003g0209 a0001c0001t0003g0210 others(79): Show |
115 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.896+4277_896+4280d others(6): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743496 | |||||||
| chr1:150743546 | T | G | 7 | a0001c0001t0001g0135 a0001c0001t0001g0150 a0001c0001t0001g0151 others(4): Show |
7 | HG00741.hp2 HG01981.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.896+4231A>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743546 | |||||||
| chr1:150743561 | G | GTATGTAT others(24): Show |
5 | a0002c0002t0002g0013 a0002c0002t0002g0021 a0002c0002t0002g0068 others(2): Show |
6 | HG00323.hp1 HG02027.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.896+4185_896+4215d others(33): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743561 | |||||||
| chr1:150743561 | G | GTATGTAT others(55): Show |
2 | a0001c0001t0003g0240 a0002c0002t0002g0087 |
2 | HG02145.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.896+4154_896+4215d others(64): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743561 | |||||||
| chr1:150743561 | GTATGTAT others(24): Show |
G | 2 | a0001c0001t0001g0150 a0001c0001t0001g0177 |
2 | HG03017.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.896+4185_896+4215d others(33): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743561 | |||||||
| chr1:150743561 | GTATGTAT others(55): Show |
G | 2 | a0001c0001t0001g0127 a0001c0001t0001g0131 |
2 | NA18954.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.896+4154_896+4215d others(64): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743561 | |||||||
| chr1:150743569 | A | G | 1 | a0001c0001t0003g0226 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.896+4208T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743569 | |||||||
| chr1:150743606 | T | TATACATA others(102): Show |
1 | a0001c0001t0016g0191 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.896+4170_896+4171i others(111): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743606 | |||||||
| chr1:150743610 | T | A | 2 | a0002c0002t0004g0040 a0002c0002t0004g0041 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.896+4167A>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743610 | |||||||
| chr1:150743611 | T | A | 2 | a0001c0001t0003g0213 a0001c0001t0016g0191 |
2 | HG01884.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.896+4166A>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743611 | |||||||
| chr1:150743612 | A | ATATAT | 54 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(51): Show |
81 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(78): Show |
intron_variant | MODIFIER | c.896+4160_896+4164d others(7): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743612 | |||||||
| chr1:150743612 | A | ATATATTA others(134): Show |
1 | a0002c0002t0002g0079 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.896+4164_896+4165i others(143): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743612 | |||||||
| chr1:150743612 | A | T | 2 | a0001c0001t0003g0213 a0001c0001t0016g0191 |
2 | HG01884.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.896+4165T>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743612 | |||||||
| chr1:150743612 | ATATATGT others(60): Show |
A | 1 | a0001c0001t0001g0135 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.896+4098_896+4164d others(69): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743612 | |||||||
| chr1:150743636 | ATATAT | A | 20 | a0001c0001t0003g0002 a0001c0001t0003g0012 a0001c0001t0003g0019 others(17): Show |
38 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.896+4136_896+4140d others(7): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743636 | |||||||
| chr1:150743642 | T | A | 1 | a0001c0001t0016g0191 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.896+4135A>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743642 | |||||||
| chr1:150743643 | A | ATATAT | 111 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(108): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.896+4129_896+4133d others(7): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743643 | |||||||
| chr1:150743643 | A | ATATATGT others(60): Show |
2 | a0002c0002t0002g0086 a0002c0002t0004g0039 |
2 | HG02602.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.896+4133_896+4134i others(69): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743643 | |||||||
| chr1:150743643 | A | ATATATGT others(235): Show |
1 | a0001c0001t0003g0199 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.896+4133_896+4134i others(244): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743643 | |||||||
| chr1:150743643 | A | ATATATGT others(132): Show |
2 | a0001c0001t0003g0195 a0001c0001t0003g0196 |
2 | HG02109.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.896+4133_896+4134i others(141): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743643 | |||||||
| chr1:150743643 | A | ATATATGT others(168): Show |
1 | a0002c0002t0004g0042 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.896+4133_896+4134i others(177): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743643 | |||||||
| chr1:150743643 | A | ATATATGT others(132): Show |
1 | a0001c0001t0003g0215 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.896+4133_896+4134i others(141): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743643 | |||||||
| chr1:150743649 | G | A | 1 | a0001c0001t0016g0191 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.896+4128C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743649 | |||||||
| chr1:150743674 | ATATAT | A | 7 | a0001c0001t0003g0237 a0001c0001t0017g0241 a0002c0002t0002g0069 others(4): Show |
7 | HG00408.hp2 HG01074.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.896+4098_896+4102d others(7): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743674 | |||||||
| chr1:150743675 | T | C | 2 | a0002c0002t0004g0040 a0002c0002t0004g0041 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.896+4102A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743675 | |||||||
| chr1:150743679 | T | TGTATATT others(19): Show |
1 | a0002c0002t0002g0059 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.896+4097_896+4098i others(28): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743679 | |||||||
| chr1:150743710 | ATATAT | A | 5 | a0001c0001t0001g0030 a0001c0001t0017g0241 a0002c0002t0002g0049 others(2): Show |
6 | HG00621.hp1 HG01074.hp2 NA18978.hp1 others(3): Show |
intron_variant | MODIFIER | c.896+4062_896+4066d others(7): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743710 | |||||||
| chr1:150743744 | T | TTATATAT others(132): Show |
2 | a0001c0001t0003g0209 a0001c0001t0003g0210 |
2 | HG02145.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.896+3894_896+4032d others(141): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743744 | |||||||
| chr1:150743796 | T | C | 1 | a0002c0002t0002g0060 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.896+3981A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743796 | |||||||
| chr1:150743852 | T | TTATATAT others(24): Show |
1 | a0002c0002t0002g0078 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.896+3894_896+3924d others(33): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743852 | |||||||
| chr1:150743887 | A | ACATATAA others(423): Show |
1 | a0001c0001t0003g0214 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.896+3889_896+3890i others(432): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743887 | |||||||
| chr1:150743888 | T | TATTATAT others(167): Show |
1 | a0001c0001t0003g0208 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.896+3888_896+3889i others(176): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743888 | |||||||
| chr1:150743948 | A | T | 1 | a0001c0001t0001g0186 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.896+3829T>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743948 | |||||||
| chr1:150743959 | A | ATTATATA others(28): Show |
4 | a0002c0002t0002g0015 a0002c0002t0002g0047 a0002c0002t0002g0101 others(1): Show |
6 | HG00140.hp2 HG00735.hp2 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.896+3783_896+3817d others(37): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743959 | |||||||
| chr1:150743959 | A | ATTATATA others(63): Show |
1 | a0002c0002t0002g0089 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.896+3817_896+3818i others(72): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743959 | |||||||
| chr1:150743994 | T | G | 3 | a0001c0001t0001g0151 a0001c0001t0001g0155 a0001c0001t0001g0178 |
3 | HG01981.hp1 HG04204.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.896+3783A>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743994 | |||||||
| chr1:150743994 | TA | T | 3 | a0001c0001t0003g0037 a0001c0001t0003g0213 a0001c0001t0003g0231 |
4 | HG01433.hp2 HG01884.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.896+3782delT | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150743994 | |||||||
| chr1:150744030 | T | G | 8 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0150 others(5): Show |
10 | HG00741.hp2 HG03017.hp2 HG03654.hp2 others(7): Show |
intron_variant | MODIFIER | c.896+3747A>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744030 | |||||||
| chr1:150744030 | TA | T | 12 | a0001c0001t0003g0038 a0001c0001t0003g0232 a0001c0001t0003g0233 others(9): Show |
14 | HG01346.hp2 HG01517.hp2 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.896+3746delT | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744030 | |||||||
| chr1:150744031 | ATTATATA others(28): Show |
A | 3 | a0001c0001t0001g0128 a0001c0001t0001g0155 a0001c0001t0001g0168 |
3 | HG01346.hp1 HG01981.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.896+3711_896+3745d others(37): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744031 | |||||||
| chr1:150744031 | ATTATATA others(252): Show |
A | 1 | a0001c0001t0003g0207 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.896+3487_896+3745d others(2): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744031 | |||||||
| chr1:150744057 | TACATAAT others(77): Show |
T | 1 | a0001c0001t0001g0126 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.896+3636_896+3719d others(86): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744057 | |||||||
| chr1:150744063 | ATATT | A | 3 | a0002c0002t0002g0014 a0002c0002t0002g0059 a0002c0002t0002g0060 |
4 | HG00738.hp2 HG01978.hp1 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.896+3710_896+3713d others(6): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744063 | |||||||
| chr1:150744065 | A | AG | 16 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0033 others(13): Show |
17 | HG00558.hp2 HG00738.hp1 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.896+3711_896+3712i others(3): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744065 | |||||||
| chr1:150744066 | T | A | 16 | a0001c0001t0001g0003 a0001c0001t0001g0032 a0001c0001t0001g0033 others(13): Show |
17 | HG00558.hp2 HG00738.hp1 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.896+3711A>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744066 | |||||||
| chr1:150744066 | T | TA | 187 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(184): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.896+3710_896+3711i others(3): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744066 | |||||||
| chr1:150744066 | T | TATTATAT others(138): Show |
1 | a0001c0001t0001g0114 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.896+3710_896+3711i others(147): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744066 | |||||||
| chr1:150744066 | TTTATATA others(76): Show |
T | 5 | a0001c0001t0001g0008 a0001c0001t0001g0123 a0001c0001t0001g0151 others(2): Show |
10 | HG01243.hp2 HG01255.hp1 HG01257.hp2 others(7): Show |
intron_variant | MODIFIER | c.896+3628_896+3710d others(85): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744066 | |||||||
| chr1:150744082 | A | G | 1 | a0002c0002t0002g0078 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.896+3695T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744082 | |||||||
| chr1:150744092 | TACATAAT others(42): Show |
T | 1 | a0001c0001t0003g0038 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.896+3636_896+3684d others(51): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744092 | |||||||
| chr1:150744101 | T | G | 23 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0032 others(20): Show |
29 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(26): Show |
intron_variant | MODIFIER | c.896+3676A>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744101 | |||||||
| chr1:150744101 | TA | T | 9 | a0001c0001t0001g0129 a0001c0001t0003g0213 a0001c0001t0003g0232 others(6): Show |
9 | HG01884.hp2 HG01928.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.896+3675delT | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744101 | |||||||
| chr1:150744102 | ATTATATA others(41): Show |
A | 9 | a0001c0001t0001g0007 a0001c0001t0001g0018 a0001c0001t0001g0028 others(6): Show |
15 | HG01069.hp1 HG01071.hp1 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.896+3627_896+3674d others(50): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744102 | |||||||
| chr1:150744102 | ATTATATA others(76): Show |
A | 2 | a0001c0001t0003g0037 a0001c0001t0003g0231 |
3 | HG01433.hp2 HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.896+3592_896+3674d others(85): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744102 | |||||||
| chr1:150744113 | T | C | 1 | a0001c0001t0003g0206 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.896+3664A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744113 | |||||||
| chr1:150744118 | A | G | 3 | a0002c0002t0002g0001 a0002c0002t0002g0102 a0002c0002t0009g0063 |
6 | HG01255.hp2 HG01928.hp2 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.896+3659T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744118 | |||||||
| chr1:150744128 | TACATAAT others(6): Show |
T | 16 | a0001c0001t0001g0007 a0001c0001t0001g0121 a0001c0001t0001g0128 others(13): Show |
17 | HG00642.hp1 HG01167.hp1 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.896+3636_896+3648d others(15): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744128 | |||||||
| chr1:150744134 | A | ATAGATTA others(16): Show |
2 | a0001c0001t0001g0032 a0001c0001t0001g0114 |
2 | NA18947.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.896+3642_896+3643i others(25): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATAGATTA others(52): Show |
2 | a0001c0001t0001g0141 a0001c0001t0001g0143 |
2 | HG02602.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.896+3642_896+3643i others(61): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATAGATTA others(88): Show |
3 | a0001c0001t0001g0119 a0001c0001t0001g0146 a0001c0001t0001g0183 |
3 | HG00408.hp1 HG02027.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.896+3642_896+3643i others(97): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATAGATTA others(124): Show |
3 | a0001c0001t0001g0029 a0001c0001t0001g0147 a0001c0001t0001g0149 |
3 | HG01192.hp1 HG03834.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.896+3642_896+3643i others(133): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATAGATTA others(88): Show |
6 | a0001c0001t0001g0003 a0001c0001t0001g0115 a0001c0001t0001g0117 others(3): Show |
9 | HG00099.hp2 HG00597.hp1 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.896+3642_896+3643i others(97): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATAGATTA others(52): Show |
2 | a0001c0001t0001g0148 a0001c0001t0001g0189 |
2 | HG00558.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.896+3642_896+3643i others(61): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATAGATTA others(124): Show |
3 | a0001c0001t0001g0003 a0001c0001t0001g0140 a0001c0001t0001g0184 |
3 | HG01109.hp2 HG01433.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.896+3642_896+3643i others(133): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATAGATTA others(88): Show |
1 | a0001c0001t0001g0174 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.896+3642_896+3643i others(97): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATATTA others(16): Show |
32 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(29): Show |
38 | HG00408.hp2 HG00735.hp2 HG01358.hp1 others(35): Show |
intron_variant | MODIFIER | c.896+3642_896+3643i others(25): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATATTA others(88): Show |
1 | a0001c0001t0001g0116 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.896+3642_896+3643i others(97): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATATTA others(196): Show |
1 | a0001c0001t0001g0003 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.896+3642_896+3643i others(205): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATATTA others(158): Show |
1 | a0001c0001t0001g0138 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.896+3642_896+3643i others(167): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATATTA others(88): Show |
8 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0144 others(5): Show |
8 | HG00280.hp2 HG00438.hp1 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.896+3642_896+3643i others(97): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATATTA others(159): Show |
2 | a0001c0001t0001g0106 a0001c0001t0001g0139 |
2 | NA18953.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.896+3642_896+3643i others(168): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATATTA others(124): Show |
4 | a0001c0001t0001g0105 a0001c0001t0001g0120 a0001c0001t0001g0142 others(1): Show |
4 | HG00735.hp1 HG02165.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.896+3642_896+3643i others(133): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATATTA others(225): Show |
1 | a0001c0001t0003g0002 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.896+3642_896+3643i others(234): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATATTA others(52): Show |
21 | a0001c0001t0001g0113 a0001c0001t0001g0175 a0002c0002t0002g0001 others(18): Show |
33 | HG00558.hp1 HG00597.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.896+3642_896+3643i others(61): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATATTA others(124): Show |
1 | a0001c0001t0001g0118 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.896+3642_896+3643i others(133): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATATTA others(160): Show |
1 | a0001c0001t0001g0182 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.896+3642_896+3643i others(169): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATATTA others(88): Show |
4 | a0001c0001t0001g0004 a0001c0001t0001g0161 a0002c0002t0002g0001 others(1): Show |
6 | HG01074.hp1 HG02258.hp2 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.896+3642_896+3643i others(97): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATATTA others(155): Show |
1 | a0001c0001t0001g0111 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.896+3642_896+3643i others(164): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATATTA others(124): Show |
3 | a0001c0001t0001g0162 a0002c0002t0002g0068 a0002c0002t0005g0065 |
3 | HG00423.hp1 HG02647.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.896+3642_896+3643i others(133): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATATTA others(160): Show |
10 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(7): Show |
12 | HG00099.hp1 HG00323.hp2 HG00423.hp2 others(9): Show |
intron_variant | MODIFIER | c.896+3642_896+3643i others(169): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATATTA others(196): Show |
8 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0133 others(5): Show |
10 | HG03017.hp1 HG03942.hp1 NA18951.hp2 others(7): Show |
intron_variant | MODIFIER | c.896+3642_896+3643i others(205): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATATTA others(232): Show |
4 | a0001c0001t0001g0004 a0001c0001t0001g0107 a0001c0001t0001g0163 others(1): Show |
4 | HG02004.hp2 HG02735.hp1 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.896+3642_896+3643i others(241): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATATTA others(268): Show |
1 | a0001c0001t0001g0004 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.896+3642_896+3643i others(277): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATATTA others(267): Show |
1 | a0001c0001t0001g0035 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.896+3642_896+3643i others(276): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATATTA others(302): Show |
1 | a0001c0001t0013g0218 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.896+3642_896+3643i others(311): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATATTA others(302): Show |
2 | a0001c0001t0003g0002 a0001c0001t0003g0230 |
2 | NA18947.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.896+3642_896+3643i others(311): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATATTA others(195): Show |
4 | a0001c0001t0001g0034 a0001c0001t0001g0108 a0002c0002t0005g0052 others(1): Show |
4 | HG02818.hp1 HG02886.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.896+3642_896+3643i others(204): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATATTA others(267): Show |
1 | a0002c0002t0002g0073 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.896+3642_896+3643i others(276): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATATTA others(266): Show |
1 | a0001c0001t0003g0190 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.896+3642_896+3643i others(275): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATATTA others(301): Show |
2 | a0001c0001t0003g0002 a0001c0001t0003g0012 |
4 | HG00438.hp2 NA18970.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.896+3642_896+3643i others(310): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATATTA others(230): Show |
1 | a0001c0001t0001g0188 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.896+3642_896+3643i others(239): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATATTA others(159): Show |
3 | a0001c0001t0001g0110 a0002c0002t0002g0070 a0002c0002t0005g0023 |
3 | HG00323.hp1 HG02055.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.896+3642_896+3643i others(168): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATATTA others(265): Show |
13 | a0001c0001t0003g0002 a0001c0001t0003g0012 a0001c0001t0003g0019 others(10): Show |
21 | HG00621.hp2 HG01515.hp2 HG02004.hp1 others(18): Show |
intron_variant | MODIFIER | c.896+3642_896+3643i others(274): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATATTA others(442): Show |
1 | a0001c0001t0003g0201 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.896+3642_896+3643i others(451): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATATTA others(336): Show |
3 | a0001c0001t0003g0011 a0001c0001t0003g0193 a0001c0001t0003g0200 |
6 | HG02622.hp1 HG02895.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.896+3642_896+3643i others(345): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATATTA others(300): Show |
2 | a0001c0001t0003g0002 a0001c0001t0003g0012 |
2 | HG02132.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.896+3642_896+3643i others(309): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATATTA others(1262): Show |
1 | a0001c0001t0003g0217 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.896+3642_896+3643i others(1271): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATATTA others(159): Show |
4 | a0001c0001t0003g0212 a0002c0002t0002g0072 a0002c0002t0002g0074 others(1): Show |
4 | HG01891.hp1 HG01891.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.896+3642_896+3643i others(168): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATATTA others(194): Show |
1 | a0001c0001t0003g0206 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.896+3642_896+3643i others(203): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATATTA others(229): Show |
2 | a0001c0001t0003g0012 a0001c0001t0003g0211 |
2 | HG00140.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.896+3642_896+3643i others(238): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATATTA others(585): Show |
1 | a0001c0001t0003g0216 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.896+3642_896+3643i others(594): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATATTA others(264): Show |
1 | a0001c0001t0003g0019 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.896+3642_896+3643i others(273): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATATTA others(87): Show |
2 | a0001c0001t0003g0009 a0002c0002t0002g0014 |
3 | HG01257.hp1 HG03516.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.896+3642_896+3643i others(96): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATATTA others(123): Show |
1 | a0002c0002t0002g0098 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.896+3642_896+3643i others(132): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATATTA others(158): Show |
4 | a0001c0001t0003g0009 a0001c0001t0003g0192 a0001c0001t0003g0197 others(1): Show |
4 | HG02280.hp1 HG02630.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.896+3642_896+3643i others(167): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATATTA others(479): Show |
1 | a0001c0001t0003g0005 | 2 | HG02257.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.896+3642_896+3643i others(488): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATATTA others(193): Show |
1 | a0001c0001t0003g0219 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.896+3642_896+3643i others(202): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATATTA others(122): Show |
1 | a0001c0001t0003g0198 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.896+3642_896+3643i others(131): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATATTA others(478): Show |
1 | a0001c0001t0003g0203 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.896+3642_896+3643i others(487): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATATTA others(51): Show |
5 | a0002c0002t0002g0014 a0002c0002t0002g0059 a0002c0002t0002g0060 others(2): Show |
6 | HG00738.hp2 HG01074.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.896+3642_896+3643i others(60): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATATTA others(87): Show |
3 | a0002c0002t0002g0006 a0002c0002t0002g0010 a0002c0002t0002g0061 |
7 | NA18950.hp2 NA18954.hp1 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.896+3642_896+3643i others(96): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATATTA others(123): Show |
1 | a0002c0002t0002g0088 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.896+3642_896+3643i others(132): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATATTA others(122): Show |
2 | a0001c0001t0003g0009 a0001c0001t0003g0194 |
2 | HG03579.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.896+3642_896+3643i others(131): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATATTA others(443): Show |
1 | a0001c0001t0003g0005 | 2 | HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.896+3642_896+3643i others(452): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATATTA others(372): Show |
1 | a0001c0001t0003g0205 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.896+3642_896+3643i others(381): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATATTA others(157): Show |
1 | a0001c0001t0003g0009 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.896+3642_896+3643i others(166): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATATTA others(369): Show |
1 | a0001c0001t0003g0226 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.896+3642_896+3643i others(378): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATTTAT others(15): Show |
2 | a0001c0001t0003g0195 a0001c0001t0003g0196 |
2 | HG02109.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.896+3642_896+3643i others(24): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATTTAT others(51): Show |
4 | a0002c0002t0002g0045 a0002c0002t0002g0046 a0002c0002t0002g0049 others(1): Show |
4 | HG00621.hp1 HG03239.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.896+3642_896+3643i others(60): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATTTAT others(336): Show |
2 | a0001c0001t0003g0005 a0001c0001t0003g0204 |
3 | HG02280.hp2 HG02970.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.896+3642_896+3643i others(345): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATTTAT others(230): Show |
1 | a0002c0002t0002g0092 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.896+3642_896+3643i others(239): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATTTAT others(120): Show |
1 | a0001c0001t0003g0214 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.896+3642_896+3643i others(129): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATTTAT others(406): Show |
1 | a0001c0001t0003g0215 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.896+3642_896+3643i others(415): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744134 | A | ATATTTAT others(121): Show |
1 | a0001c0001t0003g0199 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.896+3642_896+3643i others(130): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744134 | |||||||
| chr1:150744136 | ATGTACAC others(5): Show |
A | 2 | a0001c0001t0001g0153 a0001c0001t0001g0155 |
2 | HG00741.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.896+3629_896+3640d others(14): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744136 | |||||||
| chr1:150744136 | ATGTACAC others(40): Show |
A | 1 | a0001c0001t0001g0173 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.896+3594_896+3640d others(49): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744136 | |||||||
| chr1:150744137 | TGTACACA others(5): Show |
T | 28 | a0001c0001t0001g0033 a0001c0001t0001g0124 a0001c0001t0001g0127 others(25): Show |
32 | HG00140.hp2 HG00280.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.896+3628_896+3639d others(14): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744137 | |||||||
| chr1:150744141 | C | T | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0017 others(174): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.896+3636G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744141 | |||||||
| chr1:150744149 | A | G | 2 | a0001c0001t0001g0153 a0001c0001t0001g0155 |
2 | HG00741.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.896+3628T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744149 | |||||||
| chr1:150744150 | T | A | 35 | a0001c0001t0001g0008 a0001c0001t0001g0033 a0001c0001t0001g0123 others(32): Show |
45 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(42): Show |
intron_variant | MODIFIER | c.896+3627A>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744150 | |||||||
| chr1:150744150 | T | TA | 67 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0031 others(64): Show |
85 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.896+3626_896+3627i others(3): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744150 | |||||||
| chr1:150744184 | A | AG | 7 | a0001c0001t0001g0033 a0001c0001t0001g0152 a0001c0001t0001g0153 others(4): Show |
8 | HG00558.hp2 HG00741.hp2 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.896+3592_896+3593i others(3): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744184 | |||||||
| chr1:150744184 | A | G | 1 | a0001c0001t0001g0173 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.896+3593T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744184 | |||||||
| chr1:150744185 | T | A | 8 | a0001c0001t0001g0033 a0001c0001t0001g0152 a0001c0001t0001g0153 others(5): Show |
9 | HG00558.hp2 HG00741.hp2 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.896+3592A>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744185 | |||||||
| chr1:150744185 | T | TA | 63 | a0001c0001t0001g0119 a0001c0001t0001g0141 a0001c0001t0001g0143 others(60): Show |
96 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.896+3591_896+3592i others(3): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744185 | |||||||
| chr1:150744185 | T | TATTATAT others(101): Show |
2 | a0002c0002t0002g0053 a0002c0002t0002g0095 |
2 | HG03710.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.896+3591_896+3592i others(110): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744185 | |||||||
| chr1:150744199 | G | GTATATTA others(29): Show |
1 | a0001c0001t0003g0212 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.896+3577_896+3578i others(38): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744199 | |||||||
| chr1:150744220 | T | A | 2 | a0001c0001t0001g0155 a0001c0001t0001g0173 |
2 | HG01981.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.896+3557A>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744220 | |||||||
| chr1:150744220 | T | TA | 57 | a0001c0001t0001g0033 a0001c0001t0001g0152 a0001c0001t0001g0153 others(54): Show |
82 | HG00408.hp2 HG00558.hp1 HG00558.hp2 others(79): Show |
intron_variant | MODIFIER | c.896+3556_896+3557i others(3): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744220 | |||||||
| chr1:150744220 | T | TATTATAT others(56): Show |
1 | a0001c0001t0016g0191 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.896+3556_896+3557i others(65): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744220 | |||||||
| chr1:150744220 | T | TTTATATA others(65): Show |
2 | a0002c0002t0002g0013 a0002c0002t0002g0081 |
4 | HG03579.hp2 NA18906.hp2 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.896+3556_896+3557i others(74): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744220 | |||||||
| chr1:150744220 | T | TTTATATA others(101): Show |
1 | a0002c0002t0005g0062 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.896+3556_896+3557i others(110): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744220 | |||||||
| chr1:150744223 | ATATAT | A | 3 | a0001c0001t0001g0135 a0001c0001t0001g0150 a0001c0001t0001g0151 |
3 | HG03017.hp2 HG04184.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.896+3549_896+3553d others(7): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744223 | |||||||
| chr1:150744255 | T | TA | 24 | a0001c0001t0001g0033 a0001c0001t0001g0152 a0001c0001t0001g0173 others(21): Show |
26 | HG00558.hp2 HG01074.hp2 HG01346.hp2 others(23): Show |
intron_variant | MODIFIER | c.896+3521_896+3522i others(3): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744255 | |||||||
| chr1:150744290 | T | TA | 18 | a0001c0001t0001g0129 a0001c0001t0003g0037 a0001c0001t0003g0038 others(15): Show |
20 | HG00735.hp2 HG01433.hp2 HG01928.hp1 others(17): Show |
intron_variant | MODIFIER | c.896+3486_896+3487i others(3): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744290 | |||||||
| chr1:150744290 | TTTATATA others(29): Show |
T | 3 | a0001c0001t0001g0153 a0001c0001t0001g0155 a0001c0001t0001g0177 |
3 | HG00741.hp2 HG01981.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.896+3451_896+3486d others(38): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744290 | |||||||
| chr1:150744325 | T | TTTATATA others(27): Show |
1 | a0001c0001t0001g0162 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.896+3451_896+3452i others(36): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744325 | |||||||
| chr1:150744325 | TA | T | 125 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(122): Show |
180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.896+3451delT | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744325 | |||||||
| chr1:150744326 | A | T | 1 | a0001c0001t0001g0162 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.896+3451T>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744326 | |||||||
| chr1:150744361 | T | TTTATATA others(27): Show |
1 | a0001c0001t0001g0112 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.896+3415_896+3416i others(36): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744361 | |||||||
| chr1:150744361 | TA | T | 18 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0167 others(15): Show |
19 | HG00735.hp2 HG01074.hp2 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.896+3415delT | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744361 | |||||||
| chr1:150744361 | TATTATAT others(30): Show |
T | 3 | a0001c0001t0001g0121 a0001c0001t0001g0126 a0001c0001t0001g0168 |
3 | HG01167.hp1 HG02293.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.896+3379_896+3415d others(39): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744361 | |||||||
| chr1:150744362 | A | ATTATATA others(28): Show |
1 | a0001c0001t0003g0240 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.896+3380_896+3414d others(37): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744362 | |||||||
| chr1:150744362 | A | ATTATATA others(64): Show |
1 | a0001c0001t0003g0011 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.896+3344_896+3414d others(73): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744362 | |||||||
| chr1:150744362 | A | ATTATATA others(775): Show |
1 | a0001c0001t0003g0224 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.896+3414_896+3415i others(784): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744362 | |||||||
| chr1:150744362 | A | T | 1 | a0001c0001t0001g0112 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.896+3415T>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744362 | |||||||
| chr1:150744397 | T | TTTATATA others(27): Show |
11 | a0002c0002t0002g0001 a0002c0002t0002g0010 a0002c0002t0002g0020 others(8): Show |
14 | HG01069.hp2 HG02015.hp2 HG02273.hp1 others(11): Show |
intron_variant | MODIFIER | c.896+3379_896+3380i others(36): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744397 | |||||||
| chr1:150744397 | TA | T | 103 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(100): Show |
155 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.896+3379delT | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744397 | |||||||
| chr1:150744398 | A | ATTATATA others(23): Show |
1 | a0002c0002t0002g0072 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.896+3378_896+3379i others(32): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744398 | |||||||
| chr1:150744398 | A | T | 11 | a0002c0002t0002g0001 a0002c0002t0002g0010 a0002c0002t0002g0020 others(8): Show |
14 | HG01069.hp2 HG02015.hp2 HG02273.hp1 others(11): Show |
intron_variant | MODIFIER | c.896+3379T>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744398 | |||||||
| chr1:150744406 | T | TTATATGT others(130): Show |
1 | a0002c0002t0002g0103 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.896+3370_896+3371i others(139): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744406 | |||||||
| chr1:150744430 | A | T | 1 | a0001c0001t0016g0191 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.896+3347T>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744430 | |||||||
| chr1:150744430 | ATATT | A | 5 | a0001c0001t0015g0235 a0002c0002t0002g0024 a0002c0002t0002g0069 others(2): Show |
6 | HG01074.hp2 HG01346.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.896+3343_896+3346d others(6): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744430 | |||||||
| chr1:150744433 | T | TA | 15 | a0001c0001t0001g0112 a0001c0001t0001g0128 a0001c0001t0001g0129 others(12): Show |
16 | HG01346.hp1 HG01515.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.896+3343_896+3344i others(3): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744433 | |||||||
| chr1:150744433 | T | TATATTAT others(201): Show |
1 | a0001c0001t0016g0191 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.896+3343_896+3344i others(210): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744433 | |||||||
| chr1:150744433 | T | TTTATATA others(29): Show |
1 | a0001c0001t0001g0027 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.896+3308_896+3343d others(38): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744433 | |||||||
| chr1:150744433 | TTTATATA others(29): Show |
T | 7 | a0001c0001t0003g0037 a0001c0001t0003g0231 a0001c0001t0003g0233 others(4): Show |
8 | HG01433.hp2 HG02622.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.896+3308_896+3343d others(38): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744433 | |||||||
| chr1:150744440 | A | T | 5 | a0001c0001t0015g0235 a0002c0002t0002g0024 a0002c0002t0002g0069 others(2): Show |
6 | HG01074.hp2 HG01346.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.896+3337T>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744440 | |||||||
| chr1:150744441 | T | A | 5 | a0001c0001t0015g0235 a0002c0002t0002g0024 a0002c0002t0002g0069 others(2): Show |
6 | HG01074.hp2 HG01346.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.896+3336A>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744441 | |||||||
| chr1:150744441 | T | TTATATGT others(15): Show |
1 | a0002c0002t0002g0103 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.896+3335_896+3336i others(24): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744441 | |||||||
| chr1:150744447 | G | T | 1 | a0001c0001t0003g0192 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.896+3330C>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744447 | |||||||
| chr1:150744468 | T | TTTATATA others(94): Show |
30 | a0002c0002t0002g0001 a0002c0002t0002g0010 a0002c0002t0002g0013 others(27): Show |
47 | HG00558.hp1 HG00597.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.896+3308_896+3309i others(103): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744468 | |||||||
| chr1:150744468 | T | TTTATATA others(99): Show |
3 | a0002c0002t0004g0040 a0002c0002t0004g0044 a0002c0002t0004g0048 |
3 | HG02897.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.896+3308_896+3309i others(108): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744468 | |||||||
| chr1:150744468 | T | TTTATATA others(93): Show |
1 | a0002c0002t0002g0066 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.896+3308_896+3309i others(102): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744468 | |||||||
| chr1:150744468 | T | TTTATATA others(129): Show |
15 | a0002c0002t0002g0006 a0002c0002t0002g0015 a0002c0002t0002g0045 others(12): Show |
21 | HG00140.hp2 HG01109.hp1 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.896+3308_896+3309i others(138): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744468 | |||||||
| chr1:150744468 | TA | T | 19 | a0001c0001t0003g0038 a0001c0001t0003g0203 a0001c0001t0003g0224 others(16): Show |
22 | HG00323.hp1 HG00408.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.896+3308delT | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744468 | |||||||
| chr1:150744469 | A | ATTATATA others(28): Show |
3 | a0001c0001t0001g0154 a0002c0002t0002g0073 a0002c0002t0002g0074 |
3 | HG00438.hp1 HG02809.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.896+3273_896+3307d others(37): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744469 | |||||||
| chr1:150744469 | A | ATTATATA others(59): Show |
14 | a0002c0002t0002g0001 a0002c0002t0002g0010 a0002c0002t0002g0020 others(11): Show |
18 | HG01069.hp2 HG02015.hp2 HG02273.hp1 others(15): Show |
intron_variant | MODIFIER | c.896+3307_896+3308i others(68): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744469 | |||||||
| chr1:150744469 | A | ATTATATA others(64): Show |
1 | a0002c0002t0004g0041 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.896+3237_896+3307d others(73): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744469 | |||||||
| chr1:150744469 | A | ATTATATA others(95): Show |
1 | a0002c0002t0005g0084 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.896+3307_896+3308i others(104): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744469 | |||||||
| chr1:150744469 | A | T | 49 | a0002c0002t0002g0001 a0002c0002t0002g0006 a0002c0002t0002g0010 others(46): Show |
72 | HG00140.hp2 HG00558.hp1 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.896+3308T>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744469 | |||||||
| chr1:150744477 | T | TTA | 4 | a0001c0001t0001g0029 a0001c0001t0001g0112 a0001c0001t0001g0129 others(1): Show |
5 | HG00280.hp2 HG01192.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.896+3298_896+3299d others(4): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744477 | |||||||
| chr1:150744477 | T | TTATATGT others(55): Show |
1 | a0002c0002t0002g0070 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.896+3299_896+3300i others(64): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744477 | |||||||
| chr1:150744504 | T | TATTATAT others(58): Show |
1 | a0001c0001t0003g0240 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.896+3272_896+3273i others(67): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744504 | |||||||
| chr1:150744504 | TA | T | 48 | a0001c0001t0001g0003 a0001c0001t0001g0029 a0001c0001t0001g0032 others(45): Show |
57 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.896+3272delT | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744504 | |||||||
| chr1:150744505 | A | ATTATATA others(23): Show |
1 | a0002c0002t0002g0081 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.896+3271_896+3272i others(32): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744505 | |||||||
| chr1:150744505 | A | ATTATATA others(94): Show |
2 | a0002c0002t0002g0021 a0002c0002t0002g0071 |
3 | HG00408.hp2 HG02027.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.896+3271_896+3272i others(103): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744505 | |||||||
| chr1:150744513 | T | TTA | 4 | a0001c0001t0001g0112 a0001c0001t0001g0128 a0001c0001t0001g0129 others(1): Show |
4 | HG00438.hp1 HG01346.hp1 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.896+3262_896+3263d others(4): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744513 | |||||||
| chr1:150744513 | TTATATGT others(31): Show |
T | 1 | a0001c0001t0001g0172 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.896+3226_896+3263d others(40): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744513 | |||||||
| chr1:150744528 | G | A | 1 | a0001c0001t0003g0038 | 2 | HG03098.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.896+3249C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744528 | |||||||
| chr1:150744537 | A | G | 1 | a0001c0001t0016g0191 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.896+3240T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744537 | |||||||
| chr1:150744542 | T | A | 1 | a0001c0001t0003g0198 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.896+3235A>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744542 | |||||||
| chr1:150744550 | T | C | 1 | a0001c0001t0017g0241 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.896+3227A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744550 | |||||||
| chr1:150744575 | ATATAT | A | 18 | a0001c0001t0003g0002 a0001c0001t0003g0012 a0001c0001t0003g0019 others(15): Show |
36 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.896+3197_896+3201d others(7): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744575 | |||||||
| chr1:150744580 | T | TATTATAT others(21): Show |
1 | a0001c0001t0003g0220 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.896+3196_896+3197i others(30): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744580 | |||||||
| chr1:150744580 | T | TTATATAT others(26): Show |
1 | a0001c0001t0003g0224 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.896+3196_896+3197i others(35): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744580 | |||||||
| chr1:150744604 | G | A | 20 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(17): Show |
31 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(28): Show |
intron_variant | MODIFIER | c.896+3173C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744604 | |||||||
| chr1:150744604 | G | GTATACAT others(31): Show |
1 | a0001c0001t0001g0111 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.896+3172_896+3173i others(40): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744604 | |||||||
| chr1:150744624 | T | TATA | 77 | a0001c0001t0015g0235 a0001c0001t0016g0191 a0002c0002t0002g0001 others(74): Show |
110 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.896+3150_896+3152d others(5): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744624 | |||||||
| chr1:150744633 | G | GATTATGT others(24): Show |
3 | a0001c0001t0001g0147 a0001c0001t0001g0183 a0001c0001t0016g0191 |
3 | HG02738.hp2 HG03239.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.896+3113_896+3143d others(33): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744633 | |||||||
| chr1:150744670 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.896+3107C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744670 | |||||||
| chr1:150744676 | A | T | 1 | a0001c0001t0001g0143 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.896+3101T>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744676 | |||||||
| chr1:150744848 | T | G | 5 | a0001c0001t0003g0011 a0001c0001t0003g0193 a0001c0001t0003g0199 others(2): Show |
8 | HG02622.hp1 HG02630.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.896+2929A>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744848 | |||||||
| chr1:150744938 | A | T | 1 | a0001c0001t0001g0030 | 2 | NA18978.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.896+2839T>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744938 | |||||||
| chr1:150744999 | A | T | 4 | a0001c0001t0003g0011 a0001c0001t0003g0193 a0001c0001t0003g0199 others(1): Show |
7 | HG02622.hp1 HG02630.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.896+2778T>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150744999 | |||||||
| chr1:150745075 | C | T | 1 | a0001c0001t0016g0191 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.896+2702G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150745075 | |||||||
| chr1:150745367 | A | G | 3 | a0002c0002t0002g0068 a0002c0002t0002g0069 a0002c0002t0002g0070 |
3 | HG00323.hp1 HG01074.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.896+2410T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150745367 | |||||||
| chr1:150745703 | G | A | 8 | a0001c0001t0003g0009 a0001c0001t0003g0192 a0001c0001t0003g0194 others(5): Show |
12 | HG02055.hp1 HG02109.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.896+2074C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150745703 | |||||||
| chr1:150745710 | G | A | 1 | a0001c0001t0017g0241 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.896+2067C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150745710 | |||||||
| chr1:150745887 | T | G | 1 | a0001c0001t0001g0156 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.896+1890A>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150745887 | |||||||
| chr1:150745913 | A | G | 1 | a0001c0001t0016g0191 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.896+1864T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150745913 | |||||||
| chr1:150745994 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.896+1783A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150745994 | |||||||
| chr1:150746126 | T | G | 23 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0018 others(20): Show |
36 | HG00280.hp1 HG00642.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.896+1651A>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150746126 | |||||||
| chr1:150746146 | G | A | 3 | a0001c0001t0003g0208 a0001c0001t0003g0209 a0001c0001t0003g0210 |
3 | HG02145.hp2 HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.896+1631C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150746146 | |||||||
| chr1:150746477 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.896+1300G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150746477 | |||||||
| chr1:150747063 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.896+714T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150747063 | |||||||
| chr1:150747423 | T | C | 1 | a0001c0001t0014g0242 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.896+354A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150747423 | |||||||
| chr1:150747458 | G | T | 1 | a0001c0001t0001g0181 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.896+319C>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150747458 | |||||||
| chr1:150747723 | T | C | 1 | a0001c0001t0003g0240 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.896+54A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 7/7 | chr1 | 150747723 | |||||||
| chr1:150747902 | A | G | 1 | a0001c0001t0003g0233 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.794-23T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 6/7 | chr1 | 150747902 | |||||||
| chr1:150748036 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.794-157T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 6/7 | chr1 | 150748036 | |||||||
| chr1:150748087 | C | T | 1 | a0001c0001t0003g0212 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.794-208G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 6/7 | chr1 | 150748087 | |||||||
| chr1:150748147 | G | A | 24 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0027 others(21): Show |
35 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(32): Show |
intron_variant | MODIFIER | c.794-268C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 6/7 | chr1 | 150748147 | |||||||
| chr1:150748677 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.794-798C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 6/7 | chr1 | 150748677 | |||||||
| chr1:150748699 | G | T | 76 | a0001c0001t0015g0235 a0002c0002t0002g0001 a0002c0002t0002g0006 others(73): Show |
109 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.794-820C>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 6/7 | chr1 | 150748699 | |||||||
| chr1:150748711 | C | T | 3 | a0001c0001t0001g0105 a0001c0001t0001g0120 a0001c0001t0012g0170 |
3 | HG02165.hp1 NA18998.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.794-832G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 6/7 | chr1 | 150748711 | |||||||
| chr1:150748977 | A | G | 1 | a0001c0001t0003g0240 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.793+1029T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 6/7 | chr1 | 150748977 | |||||||
| chr1:150749085 | A | G | 1 | a0001c0001t0014g0242 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.793+921T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 6/7 | chr1 | 150749085 | |||||||
| chr1:150749257 | C | A | 1 | a0001c0001t0003g0207 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.793+749G>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 6/7 | chr1 | 150749257 | |||||||
| chr1:150749424 | C | T | 2 | a0001c0001t0001g0033 a0001c0001t0001g0178 |
3 | NA18999.hp1 NA19009.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.793+582G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 6/7 | chr1 | 150749424 | |||||||
| chr1:150749524 | G | A | 3 | a0002c0002t0002g0010 a0002c0002t0002g0066 a0002c0002t0002g0100 |
6 | NA18944.hp1 NA18962.hp2 NA18968.hp1 others(3): Show |
intron_variant | MODIFIER | c.793+482C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 6/7 | chr1 | 150749524 | |||||||
| chr1:150749550 | TCGCCTCA others(8): Show |
T | 1 | a0001c0001t0017g0241 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.793+441_793+455del others(15): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 6/7 | chr1 | 150749550 | |||||||
| chr1:150749592 | G | T | 1 | a0001c0001t0016g0191 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.793+414C>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 6/7 | chr1 | 150749592 | |||||||
| chr1:150749597 | A | G | 2 | a0001c0001t0003g0217 a0001c0001t0003g0224 |
2 | HG01515.hp2 HG02015.hp1 |
intron_variant | MODIFIER | c.793+409T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 6/7 | chr1 | 150749597 | |||||||
| chr1:150749606 | T | C | 1 | a0001c0001t0003g0212 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.793+400A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 6/7 | chr1 | 150749606 | |||||||
| chr1:150750368 | A | G | 78 | a0001c0001t0003g0222 a0001c0001t0003g0223 a0001c0001t0015g0235 others(75): Show |
111 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.628-197T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 5/7 | chr1 | 150750368 | |||||||
| chr1:150750587 | G | A | 1 | a0001c0001t0003g0240 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.628-416C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 5/7 | chr1 | 150750587 | |||||||
| chr1:150750723 | A | G | 1 | a0002c0002t0002g0020 | 2 | NA18966.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.628-552T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 5/7 | chr1 | 150750723 | |||||||
| chr1:150750894 | G | A | 1 | a0001c0001t0003g0240 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.628-723C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 5/7 | chr1 | 150750894 | |||||||
| chr1:150750901 | C | G | 3 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 |
3 | HG00735.hp1 HG01109.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.628-730G>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 5/7 | chr1 | 150750901 | |||||||
| chr1:150751175 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.627+606C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 5/7 | chr1 | 150751175 | |||||||
| chr1:150751271 | T | C | 78 | a0001c0001t0001g0035 a0001c0001t0003g0240 a0001c0001t0016g0191 others(75): Show |
112 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.627+510A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 5/7 | chr1 | 150751271 | |||||||
| chr1:150751291 | G | A | 1 | a0002c0002t0005g0084 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.627+490C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 5/7 | chr1 | 150751291 | |||||||
| chr1:150751382 | G | A | 2 | a0001c0001t0001g0107 a0001c0001t0001g0163 |
2 | HG02004.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.627+399C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 5/7 | chr1 | 150751382 | |||||||
| chr1:150751390 | G | A | 1 | a0002c0002t0002g0092 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.627+391C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 5/7 | chr1 | 150751390 | |||||||
| chr1:150751406 | C | T | 1 | a0001c0001t0003g0198 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.627+375G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 5/7 | chr1 | 150751406 | |||||||
| chr1:150751772 | A | T | 1 | a0002c0002t0004g0048 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.627+9T>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 5/7 | chr1 | 150751772 | |||||||
| chr1:150752055 | G | A | 1 | a0001c0001t0001g0134 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.400-47C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150752055 | |||||||
| chr1:150752163 | G | A | 1 | a0001c0001t0017g0241 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.400-155C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150752163 | |||||||
| chr1:150752382 | C | T | 1 | a0002c0002t0002g0101 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.400-374G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150752382 | |||||||
| chr1:150752567 | C | T | 1 | a0002c0002t0002g0094 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.400-559G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150752567 | |||||||
| chr1:150752712 | C | T | 1 | a0001c0001t0003g0240 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.400-704G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150752712 | |||||||
| chr1:150752859 | G | T | 76 | a0001c0001t0016g0191 a0002c0002t0002g0001 a0002c0002t0002g0006 others(73): Show |
109 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.400-851C>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150752859 | |||||||
| chr1:150752860 | T | G | 1 | a0002c0002t0002g0024 | 2 | HG01346.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.400-852A>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150752860 | |||||||
| chr1:150752925 | C | A | 32 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0018 others(29): Show |
48 | HG00280.hp1 HG00642.hp1 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.400-917G>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150752925 | |||||||
| chr1:150753191 | T | G | 1 | a0002c0002t0002g0099 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.400-1183A>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150753191 | |||||||
| chr1:150753262 | A | G | 1 | a0001c0001t0016g0191 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.400-1254T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150753262 | |||||||
| chr1:150753480 | A | G | 1 | a0001c0001t0003g0231 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.400-1472T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150753480 | |||||||
| chr1:150753573 | C | T | 6 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(3): Show |
6 | HG00735.hp1 HG00741.hp1 HG01109.hp2 others(3): Show |
intron_variant | MODIFIER | c.399+1428G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150753573 | |||||||
| chr1:150753683 | C | A | 1 | a0001c0001t0001g0169 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.399+1318G>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150753683 | |||||||
| chr1:150753762 | C | T | 75 | a0002c0002t0002g0001 a0002c0002t0002g0006 a0002c0002t0002g0010 others(72): Show |
108 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.399+1239G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150753762 | |||||||
| chr1:150753940 | C | CAAACA | 73 | a0002c0002t0002g0001 a0002c0002t0002g0006 a0002c0002t0002g0010 others(70): Show |
105 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.399+1056_399+1060d others(7): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150753940 | |||||||
| chr1:150753940 | C | CAAACAAA others(3): Show |
2 | a0002c0002t0002g0025 a0002c0002t0010g0082 |
3 | HG03492.hp1 NA18612.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.399+1051_399+1060d others(12): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150753940 | |||||||
| chr1:150754111 | C | CT | 22 | a0001c0001t0001g0106 a0001c0001t0001g0108 a0001c0001t0001g0110 others(19): Show |
26 | HG01891.hp2 HG01978.hp2 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.399+889dupA | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150754111 | |||||||
| chr1:150754111 | CT | C | 90 | a0001c0001t0001g0033 a0001c0001t0001g0169 a0001c0001t0001g0178 others(87): Show |
142 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.399+889delA | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150754111 | |||||||
| chr1:150754128 | T | C | 2 | a0002c0002t0002g0083 a0002c0002t0002g0085 |
2 | NA18960.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.399+873A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150754128 | |||||||
| chr1:150754136 | C | T | 1 | a0001c0001t0003g0194 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.399+865G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150754136 | |||||||
| chr1:150754261 | C | G | 1 | a0002c0002t0005g0062 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.399+740G>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150754261 | |||||||
| chr1:150754395 | T | C | 1 | a0001c0001t0012g0170 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.399+606A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150754395 | |||||||
| chr1:150754430 | C | CT | 75 | a0001c0001t0001g0185 a0001c0001t0001g0186 a0001c0001t0003g0227 others(72): Show |
108 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.399+570dupA | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150754430 | |||||||
| chr1:150754435 | T | A | 9 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0231 others(6): Show |
11 | HG01433.hp2 HG02109.hp2 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.399+566A>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150754435 | |||||||
| chr1:150754561 | G | A | 1 | a0001c0001t0016g0191 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.399+440C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150754561 | |||||||
| chr1:150754853 | C | T | 75 | a0002c0002t0002g0001 a0002c0002t0002g0006 a0002c0002t0002g0010 others(72): Show |
108 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.399+148G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150754853 | |||||||
| chr1:150754918 | G | A | 20 | a0001c0001t0003g0002 a0001c0001t0003g0012 a0001c0001t0003g0019 others(17): Show |
38 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.399+83C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 4/7 | chr1 | 150754918 | |||||||
| chr1:150755511 | G | A | 15 | a0001c0001t0003g0009 a0001c0001t0003g0011 a0001c0001t0003g0192 others(12): Show |
22 | HG02055.hp1 HG02109.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.250-361C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 3/7 | chr1 | 150755511 | |||||||
| chr1:150755556 | A | G | 75 | a0002c0002t0002g0001 a0002c0002t0002g0006 a0002c0002t0002g0010 others(72): Show |
108 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.250-406T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 3/7 | chr1 | 150755556 | |||||||
| chr1:150755672 | G | T | 2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | NA18977.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.250-522C>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 3/7 | chr1 | 150755672 | |||||||
| chr1:150756152 | C | T | 6 | a0002c0002t0004g0039 a0002c0002t0004g0040 a0002c0002t0004g0041 others(3): Show |
6 | HG02896.hp1 HG02897.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.250-1002G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 3/7 | chr1 | 150756152 | |||||||
| chr1:150756200 | T | C | 76 | a0001c0001t0016g0191 a0002c0002t0002g0001 a0002c0002t0002g0006 others(73): Show |
109 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.250-1050A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 3/7 | chr1 | 150756200 | |||||||
| chr1:150756290 | G | A | 3 | a0002c0002t0002g0050 a0002c0002t0002g0086 a0002c0002t0002g0087 |
3 | HG02602.hp1 HG02698.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.250-1140C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 3/7 | chr1 | 150756290 | |||||||
| chr1:150756543 | T | C | 2 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
2 | HG04199.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.249+1315A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 3/7 | chr1 | 150756543 | |||||||
| chr1:150756558 | C | T | 1 | a0001c0001t0001g0028 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.249+1300G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 3/7 | chr1 | 150756558 | |||||||
| chr1:150756708 | C | CT | 60 | a0001c0001t0001g0110 a0001c0001t0001g0135 a0001c0001t0003g0220 others(57): Show |
87 | HG00323.hp1 HG00408.hp2 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.249+1149dupA | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 3/7 | chr1 | 150756708 | |||||||
| chr1:150756708 | CT | C | 9 | a0001c0001t0001g0112 a0001c0001t0001g0130 a0001c0001t0001g0131 others(6): Show |
11 | HG00558.hp2 HG02273.hp2 HG02976.hp2 others(8): Show |
intron_variant | MODIFIER | c.249+1149delA | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 3/7 | chr1 | 150756708 | |||||||
| chr1:150756712 | T | C | 1 | a0001c0001t0001g0132 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.249+1146A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 3/7 | chr1 | 150756712 | |||||||
| chr1:150756738 | C | T | 1 | a0001c0001t0001g0134 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.249+1120G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 3/7 | chr1 | 150756738 | |||||||
| chr1:150756871 | C | T | 2 | a0001c0001t0003g0240 a0001c0001t0017g0241 |
2 | HG02145.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.249+987G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 3/7 | chr1 | 150756871 | |||||||
| chr1:150757317 | G | A | 104 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(101): Show |
140 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.249+541C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 3/7 | chr1 | 150757317 | |||||||
| chr1:150757507 | G | A | 76 | a0001c0001t0016g0191 a0002c0002t0002g0001 a0002c0002t0002g0006 others(73): Show |
109 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.249+351C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 3/7 | chr1 | 150757507 | |||||||
| chr1:150757621 | T | C | 1 | a0002c0002t0002g0093 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.249+237A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 3/7 | chr1 | 150757621 | |||||||
| chr1:150757657 | G | A | 1 | a0002c0002t0004g0039 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.249+201C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 3/7 | chr1 | 150757657 | |||||||
| chr1:150757708 | C | A | 76 | a0001c0001t0016g0191 a0002c0002t0002g0001 a0002c0002t0002g0006 others(73): Show |
109 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.249+150G>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 3/7 | chr1 | 150757708 | |||||||
| chr1:150757785 | T | C | 1 | a0001c0001t0003g0226 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.249+73A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 3/7 | chr1 | 150757785 | |||||||
| chr1:150757803 | A | G | 76 | a0001c0001t0008g0097 a0002c0002t0002g0001 a0002c0002t0002g0006 others(73): Show |
109 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.249+55T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 3/7 | chr1 | 150757803 | |||||||
| chr1:150758053 | A | AT | 10 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0133 others(7): Show |
10 | HG01891.hp2 HG02145.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.127-74dupA | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150758053 | |||||||
| chr1:150758350 | A | C | 1 | a0001c0001t0001g0122 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.127-370T>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150758350 | |||||||
| chr1:150758484 | ATAT | A | 12 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0231 others(9): Show |
14 | HG01433.hp2 HG02109.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.127-507_127-505del others(3): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150758484 | |||||||
| chr1:150758634 | G | C | 1 | a0002c0002t0002g0094 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.127-654C>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150758634 | |||||||
| chr1:150758849 | A | AT | 7 | a0001c0001t0001g0027 a0001c0001t0001g0113 a0001c0001t0003g0219 others(4): Show |
8 | HG00738.hp2 HG02071.hp1 HG03490.hp1 others(5): Show |
intron_variant | MODIFIER | c.127-870dupA | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150758849 | |||||||
| chr1:150758894 | G | A | 1 | a0001c0001t0017g0241 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.127-914C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150758894 | |||||||
| chr1:150758942 | G | T | 1 | a0001c0001t0001g0187 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.127-962C>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150758942 | |||||||
| chr1:150758983 | G | A | 1 | a0002c0002t0002g0095 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.127-1003C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150758983 | |||||||
| chr1:150759035 | A | AT | 3 | a0001c0001t0003g0233 a0001c0001t0015g0235 a0002c0002t0003g0234 |
3 | HG02622.hp2 HG03130.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.127-1056dupA | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150759035 | |||||||
| chr1:150759037 | TA | T | 76 | a0001c0001t0008g0097 a0001c0001t0017g0241 a0002c0002t0002g0001 others(73): Show |
108 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.127-1058delT | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150759037 | |||||||
| chr1:150759038 | A | T | 33 | a0001c0001t0003g0009 a0001c0001t0003g0011 a0001c0001t0003g0012 others(30): Show |
40 | HG00140.hp1 HG00735.hp2 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.127-1058T>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150759038 | |||||||
| chr1:150759041 | T | A | 1 | a0001c0001t0001g0105 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.127-1061A>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150759041 | |||||||
| chr1:150759129 | C | G | 13 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0123 others(10): Show |
21 | HG00642.hp1 HG01071.hp1 HG01346.hp1 others(18): Show |
intron_variant | MODIFIER | c.127-1149G>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150759129 | |||||||
| chr1:150759142 | T | C | 76 | a0001c0001t0008g0097 a0002c0002t0002g0001 a0002c0002t0002g0006 others(73): Show |
109 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.127-1162A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150759142 | |||||||
| chr1:150759538 | G | A | 1 | a0001c0001t0003g0230 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.127-1558C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150759538 | |||||||
| chr1:150759597 | A | G | 1 | a0001c0001t0003g0193 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.127-1617T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150759597 | |||||||
| chr1:150759686 | C | A | 1 | a0001c0001t0001g0122 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.127-1706G>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150759686 | |||||||
| chr1:150759695 | T | C | 8 | a0001c0001t0003g0002 a0001c0001t0003g0019 a0001c0001t0003g0036 others(5): Show |
23 | HG00438.hp2 HG00621.hp2 HG02071.hp2 others(20): Show |
intron_variant | MODIFIER | c.127-1715A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150759695 | |||||||
| chr1:150759811 | C | A | 9 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0231 others(6): Show |
11 | HG01433.hp2 HG02109.hp2 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.127-1831G>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150759811 | |||||||
| chr1:150759822 | G | C | 1 | a0001c0001t0016g0191 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.127-1842C>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150759822 | |||||||
| chr1:150760226 | A | T | 1 | a0002c0002t0002g0057 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.127-2246T>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150760226 | |||||||
| chr1:150760241 | A | C | 2 | a0001c0001t0001g0185 a0001c0001t0001g0186 |
2 | NA19006.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.127-2261T>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150760241 | |||||||
| chr1:150760249 | C | T | 1 | a0002c0002t0002g0056 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.127-2269G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150760249 | |||||||
| chr1:150760455 | G | A | 1 | a0002c0002t0004g0048 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.127-2475C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150760455 | |||||||
| chr1:150760507 | G | A | 1 | a0001c0001t0017g0241 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.127-2527C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150760507 | |||||||
| chr1:150760569 | G | A | 1 | a0001c0001t0001g0173 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.127-2589C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150760569 | |||||||
| chr1:150760880 | C | CA | 16 | a0001c0001t0001g0032 a0001c0001t0001g0174 a0001c0001t0001g0175 others(13): Show |
19 | HG01433.hp2 HG02109.hp2 HG02132.hp1 others(16): Show |
intron_variant | MODIFIER | c.127-2901dupT | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150760880 | |||||||
| chr1:150760880 | CA | C | 8 | a0001c0001t0001g0121 a0001c0001t0001g0122 a0001c0001t0003g0193 others(5): Show |
8 | HG01069.hp2 HG01167.hp1 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.127-2901delT | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150760880 | |||||||
| chr1:150760911 | C | T | 1 | a0001c0001t0001g0120 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.127-2931G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150760911 | |||||||
| chr1:150760912 | G | A | 1 | a0001c0001t0008g0097 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.127-2932C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150760912 | |||||||
| chr1:150760940 | G | A | 15 | a0001c0001t0003g0009 a0001c0001t0003g0011 a0001c0001t0003g0192 others(12): Show |
22 | HG02055.hp1 HG02109.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.127-2960C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150760940 | |||||||
| chr1:150761048 | G | A | 12 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0231 others(9): Show |
14 | HG01433.hp2 HG02109.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.127-3068C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150761048 | |||||||
| chr1:150761101 | C | T | 6 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(3): Show |
6 | HG00597.hp1 HG02027.hp1 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-3121G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150761101 | |||||||
| chr1:150761136 | G | A | 1 | a0001c0001t0016g0191 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.127-3156C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150761136 | |||||||
| chr1:150761173 | C | G | 1 | a0001c0001t0001g0113 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.127-3193G>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150761173 | |||||||
| chr1:150761178 | CA | C | 132 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(129): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.127-3199delT | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150761178 | |||||||
| chr1:150761178 | CAA | C | 82 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0003g0208 others(79): Show |
115 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.127-3200_127-3199d others(4): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150761178 | |||||||
| chr1:150761266 | A | G | 1 | a0001c0001t0003g0192 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.127-3286T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150761266 | |||||||
| chr1:150761329 | GGAAAACA others(31): Show |
G | 1 | a0001c0001t0001g0179 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.126+3271_126+3308d others(40): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150761329 | |||||||
| chr1:150761561 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.126+3077C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150761561 | |||||||
| chr1:150761603 | T | C | 20 | a0001c0001t0003g0002 a0001c0001t0003g0012 a0001c0001t0003g0019 others(17): Show |
38 | HG00140.hp1 HG00438.hp2 HG00621.hp2 others(35): Show |
intron_variant | MODIFIER | c.126+3035A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150761603 | |||||||
| chr1:150761735 | A | G | 1 | a0001c0001t0003g0212 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.126+2903T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150761735 | |||||||
| chr1:150761739 | CAAGAAAA others(8): Show |
C | 103 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0007 others(100): Show |
139 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.126+2884_126+2898d others(17): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150761739 | |||||||
| chr1:150761850 | C | T | 1 | a0001c0001t0003g0232 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.126+2788G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150761850 | |||||||
| chr1:150761855 | G | A | 1 | a0001c0001t0016g0191 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.126+2783C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150761855 | |||||||
| chr1:150761960 | A | G | 76 | a0001c0001t0008g0097 a0002c0002t0002g0001 a0002c0002t0002g0006 others(73): Show |
109 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.126+2678T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150761960 | |||||||
| chr1:150762118 | A | C | 1 | a0002c0002t0002g0053 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.126+2520T>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150762118 | |||||||
| chr1:150762179 | G | A | 76 | a0001c0001t0008g0097 a0002c0002t0002g0001 a0002c0002t0002g0006 others(73): Show |
109 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.126+2459C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150762179 | |||||||
| chr1:150762316 | A | G | 1 | a0001c0001t0003g0240 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.126+2322T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150762316 | |||||||
| chr1:150762373 | G | GT | 5 | a0001c0001t0001g0183 a0001c0001t0003g0211 a0002c0002t0002g0051 others(2): Show |
5 | HG01243.hp1 HG01358.hp1 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.126+2264dupA | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150762373 | |||||||
| chr1:150762901 | C | G | 3 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 |
3 | HG02055.hp2 HG02818.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.126+1737G>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150762901 | |||||||
| chr1:150762938 | C | T | 3 | a0001c0001t0001g0107 a0001c0001t0003g0037 a0001c0001t0003g0231 |
4 | HG01433.hp2 HG02004.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+1700G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150762938 | |||||||
| chr1:150763029 | G | C | 1 | a0001c0001t0016g0191 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.126+1609C>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150763029 | |||||||
| chr1:150763104 | TA | T | 80 | a0001c0001t0001g0106 a0001c0001t0003g0208 a0001c0001t0003g0209 others(77): Show |
113 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.126+1533delT | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150763104 | |||||||
| chr1:150763350 | A | T | 1 | a0002c0002t0002g0050 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.126+1288T>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150763350 | |||||||
| chr1:150763852 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.126+786G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150763852 | |||||||
| chr1:150763886 | G | A | 1 | a0001c0001t0001g0181 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.126+752C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150763886 | |||||||
| chr1:150764324 | G | A | 15 | a0001c0001t0003g0009 a0001c0001t0003g0011 a0001c0001t0003g0192 others(12): Show |
22 | HG02055.hp1 HG02109.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.126+314C>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150764324 | |||||||
| chr1:150764331 | C | T | 15 | a0001c0001t0003g0009 a0001c0001t0003g0011 a0001c0001t0003g0192 others(12): Show |
22 | HG02055.hp1 HG02109.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.126+307G>A | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150764331 | |||||||
| chr1:150764411 | T | C | 1 | a0002c0002t0002g0100 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.126+227A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 2/7 | chr1 | 150764411 | |||||||
| chr1:150764768 | T | A | 1 | a0001c0001t0001g0182 | 1 | NA18971.hp2 | splice_region_variant&intron_variant | LOW | c.-1-4A>T | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 1/7 | chr1 | 150764768 | |||||||
| chr1:150764889 | A | C | 1 | a0001c0001t0003g0240 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-1-125T>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 1/7 | chr1 | 150764889 | |||||||
| chr1:150765089 | T | TTCTC | 72 | a0001c0001t0008g0097 a0001c0001t0016g0191 a0002c0002t0002g0001 others(69): Show |
105 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.-1-329_-1-326dupGA others(2): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 1/7 | chr1 | 150765089 | |||||||
| chr1:150765101 | C | CA | 6 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0003g0206 others(3): Show |
6 | HG01433.hp1 HG02055.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.-1-338dupT | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 1/7 | chr1 | 150765101 | |||||||
| chr1:150765101 | C | CTCTCA | 3 | a0002c0002t0002g0101 a0002c0002t0002g0102 a0002c0002t0002g0103 |
3 | HG00735.hp2 HG01358.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.-1-338_-1-337insTG others(3): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 1/7 | chr1 | 150765101 | |||||||
| chr1:150765102 | A | C | 2 | a0002c0002t0002g0049 a0002c0002t0004g0039 |
2 | HG02965.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.-1-338T>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 1/7 | chr1 | 150765102 | |||||||
| chr1:150765210 | A | G | 2 | a0002c0002t0004g0040 a0002c0002t0004g0041 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-1-446T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 1/7 | chr1 | 150765210 | |||||||
| chr1:150765269 | G | C | 1 | a0001c0001t0014g0242 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-2+429C>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 1/7 | chr1 | 150765269 | |||||||
| chr1:150765287 | GT | G | 35 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0185 others(32): Show |
55 | HG00140.hp1 HG00438.hp2 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.-2+410delA | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 1/7 | chr1 | 150765287 | |||||||
| chr1:150765300 | T | C | 66 | a0001c0001t0008g0097 a0002c0002t0002g0001 a0002c0002t0002g0006 others(63): Show |
99 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(96): Show |
intron_variant | MODIFIER | c.-2+398A>G | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 1/7 | chr1 | 150765300 | |||||||
| chr1:150765300 | T | TC | 24 | a0001c0001t0003g0037 a0001c0001t0003g0038 a0001c0001t0003g0231 others(21): Show |
26 | HG01433.hp2 HG02109.hp2 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.-2+397_-2+398insG | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 1/7 | chr1 | 150765300 | |||||||
| chr1:150765619 | A | G | 1 | a0001c0001t0016g0191 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-2+79T>C | CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 1/7 | chr1 | 150765619 | |||||||
| chr1:150765696 | A | ACGTGATA others(29): Show |
1 | a0001c0001t0003g0190 | 1 | NA18953.hp2 | splice_donor_variant&intron_variant | HIGH | c.-36_-2+1dupACTCTTA others(29): Show |
CTSS | ENSG00000163131.12 | transcript | ENST00000368985.8 | protein_coding | 1/7 | chr1 | 150765696 |