Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 25913 |
| ensemblid | ENSG00000128513.16 |
| hgncid | 17284 |
| symbol | POT1 |
| name | protection of telomeres 1 |
| refseq_nuc | NM_015450.3 |
| refseq_prot | NP_056265.2 |
| ensembl_nuc | ENST00000357628.8 |
| ensembl_prot | ENSP00000350249.3 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 124822386 |
| end | 124929825 |
| strand | - |
| ver | v1.2 |
| region | chr7:124822386-124929825 |
| region5000 | chr7:124817386-124934825 |
| regionname0 | POT1_chr7_124822386_124929825 |
| regionname5000 | POT1_chr7_124817386_124934825 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 634 | 337 | 80 | 57 | 145 | 18 | 35 | 113 | POT1_chr7_124817386_124934825 | POT1 | MSLVP others(629): Show |
chr7 | 124817386 | 124934825 |
| a0002 | 0/0 | 634 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | POT1_chr7_124817386_124934825 | POT1 | MSLVP others(629): Show |
chr7 | 124817386 | 124934825 |
| a0003 | 0/0 | 634 | 2 | 1 | 0 | 0 | 0 | 1 | 0 | POT1_chr7_124817386_124934825 | POT1 | MSLVP others(629): Show |
chr7 | 124817386 | 124934825 |
| a0004 | 0/0 | 634 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | POT1_chr7_124817386_124934825 | POT1 | MSLVP others(629): Show |
chr7 | 124817386 | 124934825 |
| a0005 | 0/0 | 634 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | MSLVP others(629): Show |
chr7 | 124817386 | 124934825 |
| a0006 | 0/0 | 634 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | MSLVP others(629): Show |
chr7 | 124817386 | 124934825 |
| a0007 | 0/0 | 634 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | MSLVP others(629): Show |
chr7 | 124817386 | 124934825 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1902 | 317 | 71 | 55 | 136 | 18 | 35 | POT1_chr7_124817386_124934825 | POT1 | ATGTC others(1897): Show |
chr7 | 124817386 | 124934825 | ||
| a0001c0002 | 0/0 | 1902 | 10 | 8 | 2 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | ATGTC others(1897): Show |
chr7 | 124817386 | 124934825 | ||
| a0001c0003 | 0/0 | 1902 | 7 | 0 | 0 | 7 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | ATGTC others(1897): Show |
chr7 | 124817386 | 124934825 | ||
| a0001c0007 | 0/0 | 1902 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | ATGTC others(1897): Show |
chr7 | 124817386 | 124934825 | ||
| a0001c0010 | 0/0 | 1902 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | ATGTC others(1897): Show |
chr7 | 124817386 | 124934825 | ||
| a0001c0011 | 0/0 | 1902 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | ATGTC others(1897): Show |
chr7 | 124817386 | 124934825 | ||
| a0002c0005 | 0/0 | 1902 | 2 | 0 | 0 | 2 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | ATGTC others(1897): Show |
chr7 | 124817386 | 124934825 | ||
| a0003c0006 | 0/0 | 1902 | 2 | 1 | 0 | 0 | 0 | 1 | POT1_chr7_124817386_124934825 | POT1 | ATGTC others(1897): Show |
chr7 | 124817386 | 124934825 | ||
| a0004c0004 | 0/0 | 1902 | 2 | 0 | 0 | 2 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | ATGTC others(1897): Show |
chr7 | 124817386 | 124934825 | ||
| a0005c0012 | 0/0 | 1902 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | ATGTC others(1897): Show |
chr7 | 124817386 | 124934825 | ||
| a0006c0008 | 0/0 | 1902 | 1 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | ATGTC others(1897): Show |
chr7 | 124817386 | 124934825 | ||
| a0007c0009 | 0/0 | 1902 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | ATGTC others(1897): Show |
chr7 | 124817386 | 124934825 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3924 | 182 | 65 | 32 | 54 | 11 | 18 | POT1_chr7_124817386_124934825 | POT1 | AAACT others(3919): Show |
chr7 | 124817386 | 124934825 |
| a0001c0001t0002 | 0/0 | 3924 | 67 | 0 | 7 | 48 | 6 | 6 | POT1_chr7_124817386_124934825 | POT1 | AAACT others(3919): Show |
chr7 | 124817386 | 124934825 |
| a0001c0001t0003 | 0/0 | 3924 | 62 | 4 | 14 | 34 | 0 | 10 | POT1_chr7_124817386_124934825 | POT1 | AAACT others(3919): Show |
chr7 | 124817386 | 124934825 |
| a0001c0001t0004 | 0/0 | 3924 | 2 | 0 | 2 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | AAACT others(3919): Show |
chr7 | 124817386 | 124934825 |
| a0001c0001t0006 | 0/0 | 3924 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | AAACT others(3919): Show |
chr7 | 124817386 | 124934825 |
| a0001c0001t0007 | 0/0 | 3924 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | AAACT others(3919): Show |
chr7 | 124817386 | 124934825 |
| a0001c0001t0008 | 0/0 | 3924 | 1 | 0 | 0 | 0 | 1 | 0 | POT1_chr7_124817386_124934825 | POT1 | AAACT others(3919): Show |
chr7 | 124817386 | 124934825 |
| a0001c0001t0010 | 0/0 | 3924 | 1 | 0 | 0 | 0 | 0 | 1 | POT1_chr7_124817386_124934825 | POT1 | AAACT others(3919): Show |
chr7 | 124817386 | 124934825 |
| a0001c0002t0001 | 0/0 | 3924 | 8 | 7 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | AAACT others(3919): Show |
chr7 | 124817386 | 124934825 |
| a0001c0002t0005 | 0/0 | 3924 | 2 | 1 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | AAACT others(3919): Show |
chr7 | 124817386 | 124934825 |
| a0001c0003t0001 | 0/0 | 3924 | 7 | 0 | 0 | 7 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | AAACT others(3919): Show |
chr7 | 124817386 | 124934825 |
| a0001c0007t0001 | 0/0 | 3924 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | AAACT others(3919): Show |
chr7 | 124817386 | 124934825 |
| a0001c0010t0002 | 0/0 | 3924 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | AAACT others(3919): Show |
chr7 | 124817386 | 124934825 |
| a0001c0011t0001 | 0/0 | 3924 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | AAACT others(3919): Show |
chr7 | 124817386 | 124934825 |
| a0002c0005t0001 | 0/0 | 3924 | 2 | 0 | 0 | 2 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | AAACT others(3919): Show |
chr7 | 124817386 | 124934825 |
| a0003c0006t0001 | 0/0 | 3924 | 1 | 0 | 0 | 0 | 0 | 1 | POT1_chr7_124817386_124934825 | POT1 | AAACT others(3919): Show |
chr7 | 124817386 | 124934825 |
| a0003c0006t0009 | 0/0 | 3924 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | AAACT others(3919): Show |
chr7 | 124817386 | 124934825 |
| a0004c0004t0002 | 0/0 | 3924 | 2 | 0 | 0 | 2 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | AAACT others(3919): Show |
chr7 | 124817386 | 124934825 |
| a0005c0012t0002 | 0/0 | 3924 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | AAACT others(3919): Show |
chr7 | 124817386 | 124934825 |
| a0006c0008t0003 | 0/0 | 3924 | 1 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | AAACT others(3919): Show |
chr7 | 124817386 | 124934825 |
| a0007c0009t0001 | 0/0 | 3924 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | AAACT others(3919): Show |
chr7 | 124817386 | 124934825 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0239 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0258 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0004g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0004g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0006g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0007g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0008g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0001t0010g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0002t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0002t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0002t0005g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0002t0005g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0003t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0003t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0003t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0003t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0003t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0003t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0003t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0007t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0010t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0001c0011t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0002c0005t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0002c0005t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0003c0006t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0003c0006t0009g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0004c0004t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0005c0012t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0006c0008t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| a0007c0009t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0132 | EUR | GBR | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG00099 | hp2 | a0001 | c0001 | t0008 | g0261 | EUR | GBR | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0085 | EUR | GBR | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0126 | EUR | GBR | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0287 | EUR | FIN | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0128 | EUR | FIN | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0104 | EUR | FIN | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0216 | EUR | FIN | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0161 | EAS | CHS | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | CHS | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | CHS | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | CHS | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | CHS | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG00544 | hp1 | a0001 | c0001 | t0003 | g0156 | EAS | CHS | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | CHS | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | CHS | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | CHS | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | CHS | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG00621 | hp1 | a0005 | c0012 | t0002 | g0039 | EAS | CHS | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG00621 | hp2 | a0002 | c0005 | t0001 | g0213 | EAS | CHS | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG00639 | hp2 | a0001 | c0002 | t0005 | g0197 | AMR | PUR | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0058 | AMR | PUR | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | CHS | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | CHS | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0081 | AMR | PUR | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PUR | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0022 | AMR | PUR | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0163 | AMR | PUR | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG01175 | hp1 | a0001 | c0001 | t0003 | g0164 | AMR | PUR | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | CLM | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG01255 | hp2 | a0001 | c0001 | t0003 | g0151 | AMR | CLM | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG01257 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | CLM | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0067 | AMR | CLM | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG01258 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | CLM | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0086 | AMR | CLM | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0317 | AMR | CLM | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG01261 | hp2 | a0001 | c0001 | t0004 | g0147 | AMR | CLM | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG01346 | hp2 | a0001 | c0001 | t0004 | g0149 | AMR | CLM | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0134 | AMR | CLM | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | CLM | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | CLM | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG01361 | hp2 | a0001 | c0001 | t0003 | g0162 | AMR | CLM | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | CLM | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0193 | AMR | CLM | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0034 | AMR | CLM | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0240 | AMR | CLM | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0262 | EUR | IBS | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0038 | EUR | IBS | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0018 | EUR | IBS | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0211 | EUR | IBS | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0265 | EUR | IBS | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0017 | EUR | IBS | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | ACB | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PEL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0166 | AMR | PEL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0057 | AMR | PEL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG01943 | hp2 | a0006 | c0008 | t0003 | g0148 | AMR | PEL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PEL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG01981 | hp2 | a0001 | c0001 | t0003 | g0146 | AMR | PEL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0076 | AMR | PEL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PEL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | PEL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02004 | hp2 | a0001 | c0001 | t0003 | g0165 | AMR | PEL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | KHV | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | KHV | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | KHV | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | KHV | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0172 | AFR | ACB | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | KHV | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | KHV | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0179 | EAS | KHV | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02135 | hp1 | a0001 | c0010 | t0002 | g0073 | EAS | KHV | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | KHV | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | CDX | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0181 | EAS | CDX | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0200 | AFR | ACB | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02258 | hp2 | a0003 | c0006 | t0009 | g0103 | AFR | ACB | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0143 | AMR | PEL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0178 | AMR | PEL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0303 | AMR | PEL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0145 | AMR | PEL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0299 | AMR | PEL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02523 | hp1 | a0001 | c0001 | t0003 | g0183 | EAS | KHV | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | GWD | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02602 | hp2 | a0001 | c0001 | t0010 | g0327 | SAS | PJL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02630 | hp1 | a0001 | c0002 | t0005 | g0198 | AFR | GWD | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0167 | SAS | PJL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0249 | SAS | PJL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02698 | hp1 | a0001 | c0001 | t0003 | g0150 | SAS | PJL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02723 | hp1 | a0001 | c0001 | t0006 | g0201 | AFR | GWD | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0030 | SAS | PJL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0074 | SAS | PJL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0322 | AFR | GWD | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02886 | hp2 | a0001 | c0001 | t0003 | g0159 | AFR | GWD | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0325 | AFR | GWD | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | GWD | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02897 | hp2 | a0007 | c0009 | t0001 | g0101 | AFR | GWD | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0196 | AFR | ESN | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | ESN | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0323 | AFR | ESN | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ESN | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0307 | SAS | PJL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0087 | SAS | PJL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0199 | AFR | ESN | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | ESN | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0194 | AFR | ESN | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG03209 | hp1 | a0001 | c0007 | t0001 | g0233 | AFR | MSL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | MSL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG03239 | hp1 | a0001 | c0001 | t0003 | g0184 | SAS | PJL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0321 | AFR | MSL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | MSL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | MSL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0010 | SAS | PJL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0010 | SAS | PJL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0324 | AFR | GWD | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0191 | AFR | MSL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG03579 | hp2 | a0001 | c0002 | t0001 | g0195 | AFR | MSL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0158 | SAS | PJL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0133 | SAS | PJL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG03688 | hp1 | a0001 | c0001 | t0003 | g0182 | SAS | STU | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | STU | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0316 | SAS | PJL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG03710 | hp2 | a0001 | c0001 | t0003 | g0180 | SAS | PJL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0173 | SAS | BEB | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | BEB | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0061 | SAS | BEB | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0315 | SAS | BEB | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0090 | SAS | STU | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | STU | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | BEB | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0070 | SAS | STU | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG04199 | hp2 | a0003 | c0006 | t0001 | g0235 | SAS | STU | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | YRI | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | YRI | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | CHB | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | CHB | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0241 | AFR | YRI | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18939 | hp2 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18952 | hp1 | a0001 | c0003 | t0001 | g0284 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18956 | hp2 | a0001 | c0003 | t0001 | g0313 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18965 | hp1 | a0004 | c0004 | t0002 | g0004 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18968 | hp1 | a0002 | c0005 | t0001 | g0250 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0135 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18972 | hp2 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18973 | hp2 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18974 | hp2 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18979 | hp1 | a0004 | c0004 | t0002 | g0004 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18979 | hp2 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18985 | hp2 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18987 | hp2 | a0001 | c0001 | t0003 | g0155 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18993 | hp1 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18993 | hp2 | a0001 | c0003 | t0001 | g0312 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18995 | hp1 | a0001 | c0003 | t0001 | g0309 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18995 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19004 | hp2 | a0001 | c0011 | t0001 | g0275 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19011 | hp2 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0157 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | LWK | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | LWK | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19054 | hp2 | a0001 | c0001 | t0003 | g0154 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19056 | hp2 | a0001 | c0003 | t0001 | g0300 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19057 | hp1 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19063 | hp2 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19074 | hp1 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0139 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19084 | hp2 | a0001 | c0003 | t0001 | g0314 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19087 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19088 | hp2 | a0001 | c0001 | t0003 | g0137 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19091 | hp1 | a0001 | c0003 | t0001 | g0311 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | YRI | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0160 | AFR | YRI | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ASW | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | ASW | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0123 | EUR | TSI | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0084 | EUR | TSI | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0130 | EUR | TSI | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0217 | EUR | TSI | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | CLM | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | ACB | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02486 | hp2 | a0001 | c0001 | t0007 | g0096 | AFR | ACB | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0185 | AFR | ACB | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | MSL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | MSL | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18955 | hp1 | a0001 | c0001 | t0003 | g0152 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | USA | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0144 | AFR | USA | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0244 | AFR | LWK | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | LWK | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0239 | REF | REF | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0258 | REF | REF | POT1_chr7_124817386_124934825 | POT1 | chr7 | 124817386 | 124934825 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:124841027 | C | A | 1 | a0006 | 1 | HG01943.hp2 | missense_variant | MODERATE | c.1315G>T | p.Val439Leu | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 14/19 | 1758/3924 | 1315/1905 | 439/634 | chr7 | 124841027 | |||
| chr7:124841114 | C | G | 1 | a0002 | 2 | HG00621.hp2 NA18968.hp1 |
missense_variant | MODERATE | c.1228G>C | p.Asp410His | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 14/19 | 1671/3924 | 1228/1905 | 410/634 | chr7 | 124841114 | |||
| chr7:124841144 | T | G | 1 | a0007 | 1 | HG02897.hp2 | missense_variant | MODERATE | c.1198A>C | p.Ile400Leu | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 14/19 | 1641/3924 | 1198/1905 | 400/634 | chr7 | 124841144 | |||
| chr7:124846971 | A | G | 1 | a0004 | 2 | NA18965.hp1 NA18979.hp1 |
missense_variant | MODERATE | c.977T>C | p.Val326Ala | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/19 | 1420/3924 | 977/1905 | 326/634 | chr7 | 124846971 | |||
| chr7:124853090 | T | C | 1 | a0003 | 2 | HG02258.hp2 HG04199.hp2 |
missense_variant | MODERATE | c.751A>G | p.Met251Val | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 10/19 | 1194/3924 | 751/1905 | 251/634 | chr7 | 124853090 | |||
| chr7:124892320 | T | C | 1 | a0005 | 1 | HG00621.hp1 | missense_variant | MODERATE | c.70A>G | p.Asn24Asp | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/19 | 513/3924 | 70/1905 | 24/634 | chr7 | 124892320 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:124823983 | T | G | 1 | a0001c0002 | 10 | HG00639.hp2 HG01433.hp2 HG02055.hp1 others(7): Show |
synonymous_variant | LOW | c.1884A>C | p.Thr628Thr | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 19/19 | 2327/3924 | 1884/1905 | 628/634 | chr7 | 124823983 | |||
| chr7:124842893 | T | C | 1 | a0001c0010 | 1 | HG02135.hp1 | synonymous_variant | LOW | c.1077A>G | p.Gln359Gln | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 13/19 | 1520/3924 | 1077/1905 | 359/634 | chr7 | 124842893 | |||
| chr7:124851897 | T | C | 1 | a0001c0003 | 7 | NA18952.hp1 NA18956.hp2 NA18993.hp2 others(4): Show |
synonymous_variant | LOW | c.924A>G | p.Gln308Gln | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 11/19 | 1367/3924 | 924/1905 | 308/634 | chr7 | 124851897 | |||
| chr7:124852995 | G | A | 1 | a0001c0011 | 1 | NA19004.hp2 | synonymous_variant | LOW | c.846C>T | p.Asn282Asn | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 10/19 | 1289/3924 | 846/1905 | 282/634 | chr7 | 124852995 | |||
| chr7:124853013 | C | T | 1 | a0001c0007 | 1 | HG03209.hp1 | synonymous_variant | LOW | c.828G>A | p.Arg276Arg | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 10/19 | 1271/3924 | 828/1905 | 276/634 | chr7 | 124853013 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:124822443 | C | T | 1 | a0001c0001t0006 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1519G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 19/19 | 1519 | chr7 | 124822443 | ||||||
| chr7:124822491 | C | G | 1 | a0001c0001t0006 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1471G>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 19/19 | 1471 | chr7 | 124822491 | ||||||
| chr7:124822590 | T | C | 1 | a0001c0002t0005 | 2 | HG00639.hp2 HG02630.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1372A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 19/19 | 1372 | chr7 | 124822590 | ||||||
| chr7:124822601 | T | C | 3 | a0001c0001t0003 a0001c0001t0004 a0006c0008t0003 |
65 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*1361A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 19/19 | 1361 | chr7 | 124822601 | ||||||
| chr7:124822607 | C | T | 5 | a0001c0001t0002 a0001c0001t0010 a0001c0010t0002 others(2): Show |
72 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*1355G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 19/19 | 1355 | chr7 | 124822607 | ||||||
| chr7:124822828 | A | C | 1 | a0001c0001t0007 | 1 | HG02486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1134T>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 19/19 | 1134 | chr7 | 124822828 | ||||||
| chr7:124823339 | A | C | 1 | a0001c0001t0006 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*623T>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 19/19 | 623 | chr7 | 124823339 | ||||||
| chr7:124823374 | T | G | 1 | a0001c0001t0008 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*588A>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 19/19 | 588 | chr7 | 124823374 | ||||||
| chr7:124823469 | C | T | 1 | a0001c0001t0004 | 2 | HG01261.hp2 HG01346.hp2 |
3_prime_UTR_variant | MODIFIER | c.*493G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 19/19 | 493 | chr7 | 124823469 | ||||||
| chr7:124823873 | T | C | 1 | a0003c0006t0009 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*89A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 19/19 | 89 | chr7 | 124823873 | ||||||
| chr7:124929817 | G | A | 1 | a0001c0001t0010 | 1 | HG02602.hp2 | 5_prime_UTR_variant | MODIFIER | c.-435C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 1/19 | 32644 | chr7 | 124929817 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:124824289 | T | C | 1 | a0001c0001t0003g0179 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1793-215A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 18/18 | chr7 | 124824289 | |||||||
| chr7:124824377 | T | C | 5 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0034 others(2): Show |
5 | HG01496.hp1 HG01515.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1793-303A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 18/18 | chr7 | 124824377 | |||||||
| chr7:124824475 | A | G | 5 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
5 | HG02055.hp2 HG02280.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1793-401T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 18/18 | chr7 | 124824475 | |||||||
| chr7:124824480 | G | A | 1 | a0001c0001t0003g0182 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1793-406C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 18/18 | chr7 | 124824480 | |||||||
| chr7:124824583 | A | G | 20 | a0001c0001t0001g0007 a0001c0001t0001g0097 a0001c0001t0001g0098 others(17): Show |
21 | HG01361.hp1 HG01884.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.1793-509T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 18/18 | chr7 | 124824583 | |||||||
| chr7:124824855 | CTAGT | C | 119 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(116): Show |
124 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.1792+393_1792+396d others(6): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 18/18 | chr7 | 124824855 | |||||||
| chr7:124824863 | C | T | 131 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(128): Show |
137 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.1792+389G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 18/18 | chr7 | 124824863 | |||||||
| chr7:124824864 | A | G | 237 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(234): Show |
248 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.1792+388T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 18/18 | chr7 | 124824864 | |||||||
| chr7:124824909 | T | C | 1 | a0001c0001t0001g0088 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1792+343A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 18/18 | chr7 | 124824909 | |||||||
| chr7:124824975 | G | A | 1 | a0003c0006t0001g0235 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1792+277C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 18/18 | chr7 | 124824975 | |||||||
| chr7:124825043 | A | T | 131 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(128): Show |
137 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.1792+209T>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 18/18 | chr7 | 124825043 | |||||||
| chr7:124825202 | T | C | 2 | a0001c0001t0002g0076 a0001c0001t0002g0104 |
2 | HG00323.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.1792+50A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 18/18 | chr7 | 124825202 | |||||||
| chr7:124825455 | A | C | 131 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(128): Show |
137 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.1687-98T>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 17/18 | chr7 | 124825455 | |||||||
| chr7:124825810 | C | T | 1 | a0001c0001t0002g0034 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1687-453G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 17/18 | chr7 | 124825810 | |||||||
| chr7:124825822 | C | G | 131 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(128): Show |
137 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.1687-465G>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 17/18 | chr7 | 124825822 | |||||||
| chr7:124825854 | A | C | 4 | a0001c0001t0001g0007 a0001c0001t0001g0097 a0001c0001t0001g0098 others(1): Show |
5 | HG01361.hp1 HG02572.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1687-497T>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 17/18 | chr7 | 124825854 | |||||||
| chr7:124825894 | A | G | 3 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 |
3 | HG02622.hp2 HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1687-537T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 17/18 | chr7 | 124825894 | |||||||
| chr7:124825897 | A | C | 131 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(128): Show |
137 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.1687-540T>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 17/18 | chr7 | 124825897 | |||||||
| chr7:124826186 | T | C | 2 | a0001c0001t0001g0263 a0001c0001t0001g0266 |
2 | HG01070.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.1687-829A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 17/18 | chr7 | 124826186 | |||||||
| chr7:124826203 | T | C | 1 | a0001c0001t0003g0160 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1687-846A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 17/18 | chr7 | 124826203 | |||||||
| chr7:124826267 | T | C | 20 | a0001c0001t0001g0007 a0001c0001t0001g0097 a0001c0001t0001g0098 others(17): Show |
21 | HG01361.hp1 HG01884.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.1687-910A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 17/18 | chr7 | 124826267 | |||||||
| chr7:124826458 | T | G | 131 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(128): Show |
137 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.1686+756A>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 17/18 | chr7 | 124826458 | |||||||
| chr7:124826599 | C | T | 1 | a0001c0001t0002g0082 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1686+615G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 17/18 | chr7 | 124826599 | |||||||
| chr7:124826614 | G | A | 80 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0036 others(77): Show |
83 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.1686+600C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 17/18 | chr7 | 124826614 | |||||||
| chr7:124826760 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1686+454G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 17/18 | chr7 | 124826760 | |||||||
| chr7:124826812 | T | C | 1 | a0001c0002t0005g0197 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1686+402A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 17/18 | chr7 | 124826812 | |||||||
| chr7:124826871 | A | AAAAC | 139 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0013 others(136): Show |
146 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.1686+339_1686+342d others(6): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 17/18 | chr7 | 124826871 | |||||||
| chr7:124826871 | A | AAAACAAA others(1): Show |
10 | a0001c0001t0001g0108 a0001c0001t0001g0110 a0001c0001t0001g0112 others(7): Show |
10 | HG02055.hp2 HG02451.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1686+335_1686+342d others(10): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 17/18 | chr7 | 124826871 | |||||||
| chr7:124826871 | AAAAC | A | 80 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0036 others(77): Show |
83 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.1686+339_1686+342d others(6): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 17/18 | chr7 | 124826871 | |||||||
| chr7:124826999 | T | C | 4 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 others(1): Show |
4 | HG02647.hp2 HG02965.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1686+215A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 17/18 | chr7 | 124826999 | |||||||
| chr7:124827007 | T | C | 1 | a0001c0001t0003g0151 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1686+207A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 17/18 | chr7 | 124827007 | |||||||
| chr7:124827416 | T | C | 80 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0036 others(77): Show |
83 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.1595-111A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 16/18 | chr7 | 124827416 | |||||||
| chr7:124827472 | T | C | 1 | a0001c0002t0001g0185 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1595-167A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 16/18 | chr7 | 124827472 | |||||||
| chr7:124827559 | T | C | 8 | a0001c0001t0001g0016 a0001c0001t0001g0319 a0001c0001t0001g0320 others(5): Show |
9 | HG02486.hp1 HG02818.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.1595-254A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 16/18 | chr7 | 124827559 | |||||||
| chr7:124827964 | C | A | 1 | a0001c0001t0001g0088 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1595-659G>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 16/18 | chr7 | 124827964 | |||||||
| chr7:124828272 | T | C | 1 | a0001c0001t0001g0273 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1595-967A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 16/18 | chr7 | 124828272 | |||||||
| chr7:124828412 | A | G | 1 | a0001c0001t0002g0087 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1594+842T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 16/18 | chr7 | 124828412 | |||||||
| chr7:124828465 | T | G | 131 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(128): Show |
137 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.1594+789A>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 16/18 | chr7 | 124828465 | |||||||
| chr7:124828545 | G | A | 122 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(119): Show |
127 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.1594+709C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 16/18 | chr7 | 124828545 | |||||||
| chr7:124829213 | A | T | 131 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(128): Show |
137 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.1594+41T>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 16/18 | chr7 | 124829213 | |||||||
| chr7:124829420 | CAT | C | 5 | a0001c0001t0001g0008 a0001c0001t0001g0100 a0001c0001t0001g0102 others(2): Show |
6 | HG02717.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1506-80_1506-79del others(2): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124829420 | |||||||
| chr7:124829533 | G | A | 131 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(128): Show |
137 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.1506-191C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124829533 | |||||||
| chr7:124829699 | G | GATCTAT | 101 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0099 others(98): Show |
104 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.1506-363_1506-358d others(8): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124829699 | |||||||
| chr7:124829699 | G | GATCTATA others(5): Show |
24 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0036 others(21): Show |
26 | HG00609.hp1 HG00621.hp1 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.1506-369_1506-358d others(14): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124829699 | |||||||
| chr7:124829699 | G | GATCTATA others(11): Show |
1 | a0001c0001t0001g0095 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1506-375_1506-358d others(20): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124829699 | |||||||
| chr7:124829699 | GATCTAT | G | 5 | a0001c0001t0001g0008 a0001c0001t0001g0100 a0001c0001t0001g0102 others(2): Show |
6 | HG02717.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1506-363_1506-358d others(8): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124829699 | |||||||
| chr7:124829732 | A | C | 1 | a0001c0001t0006g0201 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1506-390T>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124829732 | |||||||
| chr7:124829752 | G | A | 1 | a0001c0001t0001g0297 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1506-410C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124829752 | |||||||
| chr7:124829803 | G | A | 1 | a0001c0001t0001g0280 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1506-461C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124829803 | |||||||
| chr7:124829820 | C | T | 2 | a0001c0001t0001g0225 a0001c0001t0001g0227 |
2 | HG01255.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.1506-478G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124829820 | |||||||
| chr7:124830071 | C | G | 128 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(125): Show |
134 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.1506-729G>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124830071 | |||||||
| chr7:124830172 | T | C | 1 | a0001c0001t0001g0286 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1506-830A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124830172 | |||||||
| chr7:124830193 | C | T | 1 | a0001c0001t0003g0136 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1506-851G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124830193 | |||||||
| chr7:124830337 | T | C | 2 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
2 | HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1506-995A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124830337 | |||||||
| chr7:124830340 | A | G | 2 | a0001c0001t0002g0052 a0001c0001t0002g0080 |
2 | NA19011.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1506-998T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124830340 | |||||||
| chr7:124830813 | A | T | 22 | a0001c0001t0001g0003 a0001c0001t0001g0205 a0001c0001t0001g0207 others(19): Show |
24 | HG00323.hp2 HG01169.hp1 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.1506-1471T>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124830813 | |||||||
| chr7:124830907 | C | A | 131 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(128): Show |
137 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.1506-1565G>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124830907 | |||||||
| chr7:124831362 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0091 |
3 | HG02257.hp2 HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1506-2020C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124831362 | |||||||
| chr7:124831535 | A | G | 1 | a0001c0001t0001g0285 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1506-2193T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124831535 | |||||||
| chr7:124831603 | G | A | 6 | a0001c0002t0001g0193 a0001c0002t0001g0194 a0001c0002t0001g0199 others(3): Show |
6 | HG00639.hp2 HG01433.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1506-2261C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124831603 | |||||||
| chr7:124831609 | T | A | 4 | a0001c0001t0001g0289 a0001c0001t0001g0291 a0001c0001t0001g0292 others(1): Show |
4 | HG02040.hp1 NA18953.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.1506-2267A>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124831609 | |||||||
| chr7:124831700 | A | T | 232 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(229): Show |
242 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.1506-2358T>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124831700 | |||||||
| chr7:124831799 | C | T | 8 | a0001c0001t0001g0016 a0001c0001t0001g0319 a0001c0001t0001g0320 others(5): Show |
9 | HG02486.hp1 HG02818.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.1506-2457G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124831799 | |||||||
| chr7:124831835 | T | C | 131 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(128): Show |
137 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.1506-2493A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124831835 | |||||||
| chr7:124831961 | A | G | 131 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(128): Show |
137 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.1506-2619T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124831961 | |||||||
| chr7:124831999 | T | TAA | 8 | a0001c0001t0001g0014 a0001c0001t0001g0230 a0001c0001t0001g0231 others(5): Show |
9 | HG02280.hp2 HG02622.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.1506-2659_1506-265 others(6): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124831999 | |||||||
| chr7:124831999 | TA | T | 27 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0008 others(24): Show |
29 | HG01070.hp2 HG01074.hp2 HG01257.hp2 others(26): Show |
intron_variant | MODIFIER | c.1506-2658delT | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124831999 | |||||||
| chr7:124832007 | A | AAT | 118 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0015 others(115): Show |
123 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(120): Show |
intron_variant | MODIFIER | c.1506-2666_1506-266 others(6): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124832007 | |||||||
| chr7:124832007 | A | T | 3 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0317 |
3 | HG01261.hp1 HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1506-2665T>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124832007 | |||||||
| chr7:124832008 | A | AT | 3 | a0001c0001t0001g0222 a0001c0001t0001g0263 a0001c0001t0001g0294 |
3 | HG01070.hp1 NA18962.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1506-2667_1506-266 others(5): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124832008 | |||||||
| chr7:124832010 | A | T | 2 | a0001c0002t0001g0172 a0001c0002t0001g0185 |
2 | HG02055.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1506-2668T>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124832010 | |||||||
| chr7:124832013 | A | T | 1 | a0001c0001t0006g0201 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1506-2671T>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124832013 | |||||||
| chr7:124832196 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1506-2854G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124832196 | |||||||
| chr7:124832252 | C | CA | 178 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(175): Show |
187 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.1506-2911dupT | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124832252 | |||||||
| chr7:124832252 | C | CAA | 17 | a0001c0001t0001g0099 a0001c0001t0001g0207 a0001c0001t0001g0234 others(14): Show |
17 | HG01934.hp2 HG02015.hp1 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.1506-2912_1506-291 others(6): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124832252 | |||||||
| chr7:124832272 | A | T | 1 | a0001c0001t0001g0224 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1506-2930T>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124832272 | |||||||
| chr7:124832275 | G | T | 131 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(128): Show |
137 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.1506-2933C>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124832275 | |||||||
| chr7:124832351 | T | A | 16 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(13): Show |
16 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1505+2928A>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124832351 | |||||||
| chr7:124832719 | G | C | 1 | a0001c0001t0001g0289 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1505+2560C>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124832719 | |||||||
| chr7:124832721 | T | C | 1 | a0001c0001t0001g0316 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1505+2558A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124832721 | |||||||
| chr7:124832800 | C | T | 2 | a0001c0001t0002g0047 a0001c0001t0002g0050 |
2 | HG00597.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.1505+2479G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124832800 | |||||||
| chr7:124832803 | T | C | 1 | a0001c0001t0001g0229 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1505+2476A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124832803 | |||||||
| chr7:124832805 | G | C | 1 | a0001c0001t0003g0158 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1505+2474C>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124832805 | |||||||
| chr7:124832821 | CA | C | 128 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0013 others(125): Show |
134 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.1505+2457delT | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124832821 | |||||||
| chr7:124832980 | G | A | 131 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(128): Show |
137 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.1505+2299C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124832980 | |||||||
| chr7:124833016 | T | C | 1 | a0001c0001t0001g0008 | 2 | HG02717.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1505+2263A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124833016 | |||||||
| chr7:124833097 | ATTAAAAA others(5): Show |
A | 1 | a0001c0001t0001g0112 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1505+2170_1505+218 others(16): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124833097 | |||||||
| chr7:124833228 | C | T | 2 | a0001c0002t0001g0195 a0001c0002t0001g0196 |
2 | HG02922.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1505+2051G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124833228 | |||||||
| chr7:124833249 | T | C | 8 | a0001c0001t0001g0013 a0001c0001t0001g0203 a0001c0001t0001g0204 others(5): Show |
9 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(6): Show |
intron_variant | MODIFIER | c.1505+2030A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124833249 | |||||||
| chr7:124833452 | C | G | 8 | a0001c0001t0001g0014 a0001c0001t0001g0229 a0001c0001t0001g0230 others(5): Show |
9 | HG02280.hp2 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.1505+1827G>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124833452 | |||||||
| chr7:124833771 | C | T | 131 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(128): Show |
137 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.1505+1508G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124833771 | |||||||
| chr7:124833792 | A | G | 1 | a0001c0001t0001g0035 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1505+1487T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124833792 | |||||||
| chr7:124833803 | A | G | 1 | a0001c0001t0001g0035 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1505+1476T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124833803 | |||||||
| chr7:124833884 | T | C | 5 | a0001c0001t0001g0008 a0001c0001t0001g0100 a0001c0001t0001g0102 others(2): Show |
6 | HG02717.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1505+1395A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124833884 | |||||||
| chr7:124834192 | T | C | 3 | a0001c0001t0001g0100 a0001c0001t0001g0102 a0007c0009t0001g0101 |
3 | HG02895.hp2 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1505+1087A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124834192 | |||||||
| chr7:124834233 | A | G | 80 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0036 others(77): Show |
83 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.1505+1046T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124834233 | |||||||
| chr7:124834556 | G | A | 1 | a0001c0001t0001g0008 | 2 | HG02717.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1505+723C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124834556 | |||||||
| chr7:124834659 | G | C | 1 | a0001c0001t0001g0255 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1505+620C>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124834659 | |||||||
| chr7:124834798 | C | T | 122 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(119): Show |
127 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.1505+481G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124834798 | |||||||
| chr7:124834807 | C | T | 2 | a0001c0001t0001g0035 a0003c0006t0009g0103 |
2 | HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1505+472G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124834807 | |||||||
| chr7:124834857 | G | C | 131 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(128): Show |
137 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.1505+422C>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124834857 | |||||||
| chr7:124835095 | G | A | 3 | a0001c0001t0002g0052 a0001c0001t0002g0079 a0001c0001t0002g0080 |
3 | NA18978.hp1 NA19011.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1505+184C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124835095 | |||||||
| chr7:124835175 | T | C | 1 | a0001c0001t0001g0298 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1505+104A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124835175 | |||||||
| chr7:124835226 | G | T | 1 | a0001c0001t0001g0226 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1505+53C>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124835226 | |||||||
| chr7:124835242 | T | TAAACA | 70 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0036 others(67): Show |
72 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.1505+32_1505+36dup others(5): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124835242 | |||||||
| chr7:124835242 | T | TAAACAAA others(3): Show |
1 | a0001c0001t0002g0030 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1505+27_1505+36dup others(10): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124835242 | |||||||
| chr7:124835242 | TAAACA | T | 136 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0013 others(133): Show |
143 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.1505+32_1505+36del others(5): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124835242 | |||||||
| chr7:124835242 | TAAACAAA others(3): Show |
T | 1 | a0001c0001t0002g0070 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1505+27_1505+36del others(10): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 15/18 | chr7 | 124835242 | |||||||
| chr7:124835695 | T | C | 1 | a0001c0001t0006g0201 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1370-281A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 14/18 | chr7 | 124835695 | |||||||
| chr7:124835857 | A | G | 5 | a0001c0001t0001g0007 a0001c0001t0001g0097 a0001c0001t0001g0098 others(2): Show |
6 | HG01361.hp1 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1370-443T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 14/18 | chr7 | 124835857 | |||||||
| chr7:124836110 | T | C | 2 | a0001c0001t0001g0113 a0001c0001t0001g0114 |
2 | HG02976.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1370-696A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 14/18 | chr7 | 124836110 | |||||||
| chr7:124836369 | C | A | 1 | a0001c0001t0002g0027 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1370-955G>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 14/18 | chr7 | 124836369 | |||||||
| chr7:124836780 | A | G | 20 | a0001c0001t0001g0007 a0001c0001t0001g0097 a0001c0001t0001g0098 others(17): Show |
21 | HG01361.hp1 HG01884.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.1370-1366T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 14/18 | chr7 | 124836780 | |||||||
| chr7:124836946 | TA | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0105 |
3 | HG02717.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1370-1533delT | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 14/18 | chr7 | 124836946 | |||||||
| chr7:124837103 | T | C | 6 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0242 others(3): Show |
6 | HG01496.hp2 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1370-1689A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 14/18 | chr7 | 124837103 | |||||||
| chr7:124837128 | A | G | 236 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(233): Show |
247 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.1370-1714T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 14/18 | chr7 | 124837128 | |||||||
| chr7:124837216 | A | G | 2 | a0001c0001t0001g0129 a0001c0001t0001g0131 |
2 | HG01346.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1370-1802T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 14/18 | chr7 | 124837216 | |||||||
| chr7:124837236 | T | C | 1 | a0001c0001t0002g0063 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1370-1822A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 14/18 | chr7 | 124837236 | |||||||
| chr7:124837332 | A | G | 1 | a0001c0001t0001g0229 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1370-1918T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 14/18 | chr7 | 124837332 | |||||||
| chr7:124837347 | T | C | 2 | a0001c0001t0001g0268 a0001c0001t0001g0269 |
2 | NA18957.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.1370-1933A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 14/18 | chr7 | 124837347 | |||||||
| chr7:124837426 | TAATA | T | 8 | a0001c0002t0001g0193 a0001c0002t0001g0194 a0001c0002t0001g0195 others(5): Show |
8 | HG00639.hp2 HG01433.hp2 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1370-2016_1370-201 others(8): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 14/18 | chr7 | 124837426 | |||||||
| chr7:124837451 | C | T | 1 | a0001c0001t0006g0201 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1370-2037G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 14/18 | chr7 | 124837451 | |||||||
| chr7:124837604 | G | C | 1 | a0001c0001t0001g0273 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1370-2190C>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 14/18 | chr7 | 124837604 | |||||||
| chr7:124837779 | C | T | 1 | a0001c0001t0010g0327 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1370-2365G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 14/18 | chr7 | 124837779 | |||||||
| chr7:124837966 | T | C | 1 | a0001c0001t0001g0008 | 2 | HG02717.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1370-2552A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 14/18 | chr7 | 124837966 | |||||||
| chr7:124838044 | G | A | 5 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 others(2): Show |
5 | HG00140.hp2 HG00280.hp2 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.1370-2630C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 14/18 | chr7 | 124838044 | |||||||
| chr7:124838154 | C | T | 1 | a0001c0001t0006g0201 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1370-2740G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 14/18 | chr7 | 124838154 | |||||||
| chr7:124838178 | T | C | 132 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(129): Show |
138 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.1370-2764A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 14/18 | chr7 | 124838178 | |||||||
| chr7:124838245 | G | A | 131 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(128): Show |
137 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.1369+2728C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 14/18 | chr7 | 124838245 | |||||||
| chr7:124838396 | A | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0323 |
3 | HG02976.hp1 HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1369+2577T>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 14/18 | chr7 | 124838396 | |||||||
| chr7:124838444 | T | C | 1 | a0001c0001t0001g0315 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1369+2529A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 14/18 | chr7 | 124838444 | |||||||
| chr7:124838550 | C | T | 1 | a0001c0001t0001g0290 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1369+2423G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 14/18 | chr7 | 124838550 | |||||||
| chr7:124838693 | C | T | 1 | a0001c0001t0003g0165 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1369+2280G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 14/18 | chr7 | 124838693 | |||||||
| chr7:124838759 | T | C | 131 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(128): Show |
137 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.1369+2214A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 14/18 | chr7 | 124838759 | |||||||
| chr7:124838910 | T | A | 9 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0036 others(6): Show |
10 | HG02257.hp2 HG02258.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1369+2063A>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 14/18 | chr7 | 124838910 | |||||||
| chr7:124838993 | T | G | 3 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 |
3 | HG01099.hp2 HG01943.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1369+1980A>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 14/18 | chr7 | 124838993 | |||||||
| chr7:124839126 | G | A | 70 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0018 others(67): Show |
72 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.1369+1847C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 14/18 | chr7 | 124839126 | |||||||
| chr7:124839298 | A | G | 131 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(128): Show |
137 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.1369+1675T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 14/18 | chr7 | 124839298 | |||||||
| chr7:124839589 | A | G | 1 | a0001c0001t0001g0310 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1369+1384T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 14/18 | chr7 | 124839589 | |||||||
| chr7:124839624 | C | T | 122 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(119): Show |
127 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.1369+1349G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 14/18 | chr7 | 124839624 | |||||||
| chr7:124839755 | C | T | 1 | a0002c0005t0001g0213 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1369+1218G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 14/18 | chr7 | 124839755 | |||||||
| chr7:124839850 | C | G | 1 | a0001c0001t0001g0093 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1369+1123G>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 14/18 | chr7 | 124839850 | |||||||
| chr7:124839997 | A | AT | 128 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(125): Show |
133 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.1369+975dupA | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 14/18 | chr7 | 124839997 | |||||||
| chr7:124839998 | T | C | 4 | a0001c0001t0001g0108 a0001c0001t0001g0110 a0001c0001t0001g0111 others(1): Show |
4 | HG02055.hp2 HG02280.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.1369+975A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 14/18 | chr7 | 124839998 | |||||||
| chr7:124840021 | T | C | 101 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0035 others(98): Show |
105 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.1369+952A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 14/18 | chr7 | 124840021 | |||||||
| chr7:124840176 | T | C | 1 | a0001c0001t0002g0083 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1369+797A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 14/18 | chr7 | 124840176 | |||||||
| chr7:124840236 | T | C | 1 | a0001c0001t0003g0186 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1369+737A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 14/18 | chr7 | 124840236 | |||||||
| chr7:124840268 | G | A | 6 | a0001c0001t0001g0006 a0001c0001t0001g0091 a0001c0001t0001g0092 others(3): Show |
7 | HG02257.hp2 HG02622.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1369+705C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 14/18 | chr7 | 124840268 | |||||||
| chr7:124840412 | G | C | 6 | a0001c0001t0001g0006 a0001c0001t0001g0091 a0001c0001t0001g0092 others(3): Show |
7 | HG02257.hp2 HG02622.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.1369+561C>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 14/18 | chr7 | 124840412 | |||||||
| chr7:124840452 | A | G | 122 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(119): Show |
127 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.1369+521T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 14/18 | chr7 | 124840452 | |||||||
| chr7:124840523 | C | T | 131 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(128): Show |
137 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.1369+450G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 14/18 | chr7 | 124840523 | |||||||
| chr7:124840569 | CTTT | C | 3 | a0001c0001t0001g0220 a0001c0001t0001g0236 a0001c0001t0001g0260 |
3 | HG01074.hp1 HG02895.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1369+401_1369+403d others(5): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 14/18 | chr7 | 124840569 | |||||||
| chr7:124840584 | A | G | 5 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
5 | HG02055.hp2 HG02280.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1369+389T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 14/18 | chr7 | 124840584 | |||||||
| chr7:124840815 | T | C | 131 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(128): Show |
137 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.1369+158A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 14/18 | chr7 | 124840815 | |||||||
| chr7:124841191 | G | A | 131 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(128): Show |
137 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.1164-13C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 13/18 | chr7 | 124841191 | |||||||
| chr7:124841349 | T | A | 122 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(119): Show |
127 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.1164-171A>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 13/18 | chr7 | 124841349 | |||||||
| chr7:124841366 | T | A | 131 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(128): Show |
137 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.1164-188A>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 13/18 | chr7 | 124841366 | |||||||
| chr7:124841394 | C | G | 16 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(13): Show |
16 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1164-216G>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 13/18 | chr7 | 124841394 | |||||||
| chr7:124841573 | C | T | 9 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0036 others(6): Show |
10 | HG02257.hp2 HG02258.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1164-395G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 13/18 | chr7 | 124841573 | |||||||
| chr7:124841581 | G | A | 131 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(128): Show |
137 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.1164-403C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 13/18 | chr7 | 124841581 | |||||||
| chr7:124841658 | C | T | 131 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(128): Show |
137 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.1164-480G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 13/18 | chr7 | 124841658 | |||||||
| chr7:124841744 | C | T | 131 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(128): Show |
137 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.1164-566G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 13/18 | chr7 | 124841744 | |||||||
| chr7:124841751 | C | T | 1 | a0001c0001t0001g0019 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1164-573G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 13/18 | chr7 | 124841751 | |||||||
| chr7:124841766 | T | C | 1 | a0001c0001t0001g0035 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1164-588A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 13/18 | chr7 | 124841766 | |||||||
| chr7:124841914 | A | C | 1 | a0001c0001t0003g0158 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1164-736T>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 13/18 | chr7 | 124841914 | |||||||
| chr7:124842260 | G | A | 1 | a0001c0001t0003g0186 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1163+547C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 13/18 | chr7 | 124842260 | |||||||
| chr7:124842270 | T | C | 8 | a0001c0001t0001g0016 a0001c0001t0001g0319 a0001c0001t0001g0320 others(5): Show |
9 | HG02486.hp1 HG02818.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.1163+537A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 13/18 | chr7 | 124842270 | |||||||
| chr7:124843122 | C | T | 1 | a0001c0001t0001g0227 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1007-159G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124843122 | |||||||
| chr7:124843168 | T | C | 80 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0036 others(77): Show |
83 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.1007-205A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124843168 | |||||||
| chr7:124843218 | A | T | 122 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(119): Show |
127 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.1007-255T>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124843218 | |||||||
| chr7:124843282 | C | T | 1 | a0001c0002t0001g0172 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1007-319G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124843282 | |||||||
| chr7:124843403 | C | A | 1 | a0001c0001t0007g0096 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1007-440G>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124843403 | |||||||
| chr7:124843467 | T | A | 9 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0036 others(6): Show |
10 | HG02257.hp2 HG02258.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1007-504A>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124843467 | |||||||
| chr7:124843470 | T | C | 1 | a0001c0001t0001g0326 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1007-507A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124843470 | |||||||
| chr7:124843554 | C | A | 8 | a0001c0001t0001g0016 a0001c0001t0001g0319 a0001c0001t0001g0320 others(5): Show |
9 | HG02486.hp1 HG02818.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.1007-591G>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124843554 | |||||||
| chr7:124843653 | T | A | 131 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(128): Show |
137 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.1007-690A>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124843653 | |||||||
| chr7:124843677 | A | C | 1 | a0001c0001t0001g0222 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1007-714T>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124843677 | |||||||
| chr7:124843742 | C | A | 80 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0036 others(77): Show |
83 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.1007-779G>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124843742 | |||||||
| chr7:124843837 | G | T | 1 | a0001c0001t0001g0222 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1007-874C>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124843837 | |||||||
| chr7:124843916 | T | A | 4 | a0001c0001t0002g0059 a0001c0001t0002g0060 a0001c0001t0002g0077 others(1): Show |
4 | NA18955.hp2 NA18956.hp1 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.1007-953A>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124843916 | |||||||
| chr7:124843988 | T | C | 1 | a0001c0001t0002g0078 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.1007-1025A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124843988 | |||||||
| chr7:124844050 | TATCAGAG others(15): Show |
T | 1 | a0001c0001t0003g0183 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1007-1109_1007-108 others(26): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124844050 | |||||||
| chr7:124844112 | T | C | 131 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(128): Show |
137 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.1007-1149A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124844112 | |||||||
| chr7:124844126 | G | GT | 86 | a0001c0001t0001g0006 a0001c0001t0001g0036 a0001c0001t0001g0088 others(83): Show |
89 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.1007-1164dupA | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124844126 | |||||||
| chr7:124844126 | GT | G | 126 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(123): Show |
132 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.1007-1164delA | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124844126 | |||||||
| chr7:124844143 | T | C | 6 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 others(3): Show |
6 | HG02486.hp1 HG02818.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1007-1180A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124844143 | |||||||
| chr7:124844232 | G | A | 131 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(128): Show |
137 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.1007-1269C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124844232 | |||||||
| chr7:124844286 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1007-1323C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124844286 | |||||||
| chr7:124844380 | C | T | 1 | a0001c0001t0003g0191 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1007-1417G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124844380 | |||||||
| chr7:124844462 | C | T | 1 | a0001c0002t0001g0195 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1007-1499G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124844462 | |||||||
| chr7:124844505 | G | A | 1 | a0001c0001t0001g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1007-1542C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124844505 | |||||||
| chr7:124844514 | A | C | 122 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(119): Show |
127 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.1007-1551T>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124844514 | |||||||
| chr7:124844568 | C | G | 8 | a0001c0001t0003g0022 a0001c0001t0003g0142 a0001c0001t0003g0144 others(5): Show |
8 | HG01070.hp2 HG01261.hp2 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.1007-1605G>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124844568 | |||||||
| chr7:124844603 | C | T | 1 | a0001c0001t0006g0201 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1007-1640G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124844603 | |||||||
| chr7:124844616 | T | C | 1 | a0001c0001t0001g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1007-1653A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124844616 | |||||||
| chr7:124844652 | G | A | 6 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 others(3): Show |
6 | HG02486.hp1 HG02818.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1007-1689C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124844652 | |||||||
| chr7:124844662 | A | G | 131 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(128): Show |
137 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.1007-1699T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124844662 | |||||||
| chr7:124844732 | CA | C | 199 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(196): Show |
211 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(208): Show |
intron_variant | MODIFIER | c.1007-1770delT | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124844732 | |||||||
| chr7:124844732 | CAA | C | 101 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0020 others(98): Show |
104 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.1007-1771_1007-177 others(6): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124844732 | |||||||
| chr7:124844732 | CAAA | C | 6 | a0001c0001t0001g0008 a0001c0001t0001g0105 a0001c0001t0002g0017 others(3): Show |
7 | HG01496.hp1 HG01515.hp2 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.1007-1772_1007-177 others(7): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124844732 | |||||||
| chr7:124844864 | G | A | 1 | a0001c0001t0003g0150 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1007-1901C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124844864 | |||||||
| chr7:124844978 | C | G | 1 | a0001c0001t0003g0187 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1006+1964G>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124844978 | |||||||
| chr7:124845045 | C | T | 1 | a0001c0001t0001g0270 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1006+1897G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124845045 | |||||||
| chr7:124845218 | T | C | 1 | a0001c0001t0002g0033 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1006+1724A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124845218 | |||||||
| chr7:124845257 | C | T | 131 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(128): Show |
137 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.1006+1685G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124845257 | |||||||
| chr7:124845308 | C | T | 8 | a0001c0001t0001g0016 a0001c0001t0001g0319 a0001c0001t0001g0320 others(5): Show |
9 | HG02486.hp1 HG02818.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.1006+1634G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124845308 | |||||||
| chr7:124845475 | C | T | 7 | a0001c0003t0001g0284 a0001c0003t0001g0300 a0001c0003t0001g0309 others(4): Show |
7 | NA18952.hp1 NA18956.hp2 NA18993.hp2 others(4): Show |
intron_variant | MODIFIER | c.1006+1467G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124845475 | |||||||
| chr7:124845699 | T | C | 5 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
5 | HG02055.hp2 HG02280.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1006+1243A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124845699 | |||||||
| chr7:124846063 | ATCTGAGC others(6): Show |
A | 1 | a0001c0001t0001g0292 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1006+866_1006+878d others(15): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124846063 | |||||||
| chr7:124846111 | T | C | 59 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0010 others(56): Show |
65 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.1006+831A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124846111 | |||||||
| chr7:124846114 | T | C | 131 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(128): Show |
137 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.1006+828A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124846114 | |||||||
| chr7:124846162 | G | GACACAC | 11 | a0001c0001t0001g0016 a0001c0001t0001g0210 a0001c0001t0001g0319 others(8): Show |
12 | HG00621.hp2 HG02486.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.1006+774_1006+779d others(8): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124846162 | |||||||
| chr7:124846162 | G | GACACACA others(3): Show |
117 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(114): Show |
122 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(119): Show |
intron_variant | MODIFIER | c.1006+770_1006+779d others(12): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124846162 | |||||||
| chr7:124846162 | G | GACACACA others(5): Show |
67 | a0001c0001t0001g0088 a0001c0001t0001g0117 a0001c0001t0002g0005 others(64): Show |
69 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.1006+768_1006+779d others(14): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124846162 | |||||||
| chr7:124846162 | G | GACACACA others(7): Show |
14 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0020 others(11): Show |
15 | HG01099.hp2 HG01943.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.1006+766_1006+779d others(16): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124846162 | |||||||
| chr7:124846162 | G | GACACACA others(9): Show |
16 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0105 others(13): Show |
17 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.1006+764_1006+779d others(18): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124846162 | |||||||
| chr7:124846162 | G | GACACACA others(11): Show |
2 | a0001c0001t0001g0035 a0001c0001t0001g0114 |
2 | NA19240.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1006+762_1006+779d others(20): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124846162 | |||||||
| chr7:124846162 | G | GACACACA others(15): Show |
3 | a0001c0001t0001g0100 a0001c0001t0001g0102 a0007c0009t0001g0101 |
3 | HG02895.hp2 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1006+758_1006+779d others(24): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124846162 | |||||||
| chr7:124846183 | A | ACACACAC others(9): Show |
1 | a0003c0006t0009g0103 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1006+758_1006+759i others(18): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124846183 | |||||||
| chr7:124846184 | C | CACACACA others(4): Show |
1 | a0001c0001t0001g0230 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1006+757_1006+758i others(13): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124846184 | |||||||
| chr7:124846225 | C | G | 2 | a0001c0001t0001g0206 a0001c0001t0001g0234 |
2 | NA18950.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.1006+717G>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124846225 | |||||||
| chr7:124846315 | A | C | 7 | a0001c0003t0001g0284 a0001c0003t0001g0300 a0001c0003t0001g0309 others(4): Show |
7 | NA18952.hp1 NA18956.hp2 NA18993.hp2 others(4): Show |
intron_variant | MODIFIER | c.1006+627T>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124846315 | |||||||
| chr7:124846337 | T | C | 131 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(128): Show |
137 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.1006+605A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124846337 | |||||||
| chr7:124846359 | C | A | 85 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0035 others(82): Show |
89 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.1006+583G>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124846359 | |||||||
| chr7:124846447 | T | A | 8 | a0001c0001t0001g0016 a0001c0001t0001g0319 a0001c0001t0001g0320 others(5): Show |
9 | HG02486.hp1 HG02818.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.1006+495A>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124846447 | |||||||
| chr7:124846604 | T | C | 234 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(231): Show |
244 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.1006+338A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124846604 | |||||||
| chr7:124846764 | T | C | 3 | a0001c0001t0001g0221 a0001c0001t0001g0237 a0001c0001t0001g0246 |
3 | NA18942.hp2 NA18989.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.1006+178A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124846764 | |||||||
| chr7:124846926 | T | C | 239 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(236): Show |
250 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.1006+16A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 12/18 | chr7 | 124846926 | |||||||
| chr7:124847232 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.950-234G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 11/18 | chr7 | 124847232 | |||||||
| chr7:124847255 | A | G | 240 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(237): Show |
255 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.950-257T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 11/18 | chr7 | 124847255 | |||||||
| chr7:124847256 | G | A | 240 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(237): Show |
255 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.950-258C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 11/18 | chr7 | 124847256 | |||||||
| chr7:124847389 | C | G | 232 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0008 others(229): Show |
242 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.950-391G>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 11/18 | chr7 | 124847389 | |||||||
| chr7:124847411 | T | C | 130 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0014 others(127): Show |
136 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.950-413A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 11/18 | chr7 | 124847411 | |||||||
| chr7:124847427 | G | A | 2 | a0001c0001t0001g0129 a0001c0001t0001g0131 |
2 | HG01346.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.950-429C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 11/18 | chr7 | 124847427 | |||||||
| chr7:124847981 | T | C | 70 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0018 others(67): Show |
72 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.950-983A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 11/18 | chr7 | 124847981 | |||||||
| chr7:124848055 | G | A | 1 | a0001c0001t0006g0201 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.950-1057C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 11/18 | chr7 | 124848055 | |||||||
| chr7:124848099 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.950-1101A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 11/18 | chr7 | 124848099 | |||||||
| chr7:124848138 | T | G | 1 | a0001c0001t0003g0186 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.950-1140A>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 11/18 | chr7 | 124848138 | |||||||
| chr7:124848262 | T | G | 4 | a0001c0001t0001g0007 a0001c0001t0001g0097 a0001c0001t0001g0098 others(1): Show |
5 | HG01361.hp1 HG02572.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.950-1264A>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 11/18 | chr7 | 124848262 | |||||||
| chr7:124848667 | G | GA | 16 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0020 others(13): Show |
17 | HG01099.hp2 HG01943.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.950-1670dupT | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 11/18 | chr7 | 124848667 | |||||||
| chr7:124848667 | G | GAA | 16 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(13): Show |
16 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.950-1671_950-1670d others(4): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 11/18 | chr7 | 124848667 | |||||||
| chr7:124848667 | GA | G | 92 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0036 others(89): Show |
101 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.950-1670delT | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 11/18 | chr7 | 124848667 | |||||||
| chr7:124848798 | T | C | 3 | a0001c0001t0003g0022 a0001c0001t0003g0142 a0001c0001t0003g0145 |
3 | HG01070.hp2 HG02300.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.950-1800A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 11/18 | chr7 | 124848798 | |||||||
| chr7:124848851 | G | A | 8 | a0001c0001t0001g0016 a0001c0001t0001g0319 a0001c0001t0001g0320 others(5): Show |
9 | HG02486.hp1 HG02818.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.950-1853C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 11/18 | chr7 | 124848851 | |||||||
| chr7:124848923 | TCTAACAA others(5): Show |
T | 1 | a0001c0001t0001g0282 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.950-1937_950-1926d others(14): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 11/18 | chr7 | 124848923 | |||||||
| chr7:124848943 | A | G | 5 | a0001c0001t0001g0007 a0001c0001t0001g0097 a0001c0001t0001g0098 others(2): Show |
6 | HG01361.hp1 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.950-1945T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 11/18 | chr7 | 124848943 | |||||||
| chr7:124848956 | T | C | 19 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0123 others(16): Show |
21 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(18): Show |
intron_variant | MODIFIER | c.950-1958A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 11/18 | chr7 | 124848956 | |||||||
| chr7:124848991 | T | G | 1 | a0001c0001t0006g0201 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.950-1993A>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 11/18 | chr7 | 124848991 | |||||||
| chr7:124849054 | C | T | 1 | a0001c0001t0001g0035 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.950-2056G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 11/18 | chr7 | 124849054 | |||||||
| chr7:124849091 | C | A | 1 | a0001c0001t0003g0189 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.950-2093G>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 11/18 | chr7 | 124849091 | |||||||
| chr7:124849097 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.950-2099G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 11/18 | chr7 | 124849097 | |||||||
| chr7:124849147 | C | A | 3 | a0001c0001t0001g0100 a0001c0001t0001g0102 a0007c0009t0001g0101 |
3 | HG02895.hp2 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.950-2149G>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 11/18 | chr7 | 124849147 | |||||||
| chr7:124849427 | T | G | 1 | a0001c0001t0003g0191 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.950-2429A>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 11/18 | chr7 | 124849427 | |||||||
| chr7:124849568 | C | A | 1 | a0001c0001t0002g0090 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.949+2304G>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 11/18 | chr7 | 124849568 | |||||||
| chr7:124849639 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.949+2233C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 11/18 | chr7 | 124849639 | |||||||
| chr7:124849724 | T | C | 1 | a0001c0001t0001g0278 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.949+2148A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 11/18 | chr7 | 124849724 | |||||||
| chr7:124849850 | G | A | 1 | a0001c0001t0001g0244 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.949+2022C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 11/18 | chr7 | 124849850 | |||||||
| chr7:124850075 | AAG | A | 101 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0035 others(98): Show |
105 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.949+1795_949+1796d others(4): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 11/18 | chr7 | 124850075 | |||||||
| chr7:124850247 | T | C | 8 | a0001c0001t0001g0016 a0001c0001t0001g0319 a0001c0001t0001g0320 others(5): Show |
9 | HG02486.hp1 HG02818.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.949+1625A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 11/18 | chr7 | 124850247 | |||||||
| chr7:124850384 | T | C | 8 | a0001c0001t0001g0016 a0001c0001t0001g0319 a0001c0001t0001g0320 others(5): Show |
9 | HG02486.hp1 HG02818.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.949+1488A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 11/18 | chr7 | 124850384 | |||||||
| chr7:124850592 | T | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.949+1280A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 11/18 | chr7 | 124850592 | |||||||
| chr7:124850630 | C | T | 2 | a0001c0001t0003g0136 a0001c0001t0003g0139 |
2 | NA19074.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.949+1242G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 11/18 | chr7 | 124850630 | |||||||
| chr7:124850655 | C | T | 1 | a0001c0001t0003g0133 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.949+1217G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 11/18 | chr7 | 124850655 | |||||||
| chr7:124850687 | C | T | 1 | a0001c0001t0002g0075 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.949+1185G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 11/18 | chr7 | 124850687 | |||||||
| chr7:124850688 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.949+1184C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 11/18 | chr7 | 124850688 | |||||||
| chr7:124850736 | A | C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0105 |
3 | HG02717.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.949+1136T>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 11/18 | chr7 | 124850736 | |||||||
| chr7:124850806 | C | T | 8 | a0001c0001t0001g0016 a0001c0001t0001g0319 a0001c0001t0001g0320 others(5): Show |
9 | HG02486.hp1 HG02818.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.949+1066G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 11/18 | chr7 | 124850806 | |||||||
| chr7:124850884 | T | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.949+988A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 11/18 | chr7 | 124850884 | |||||||
| chr7:124850905 | GA | G | 92 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0097 others(89): Show |
101 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.949+966delT | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 11/18 | chr7 | 124850905 | |||||||
| chr7:124850913 | A | C | 8 | a0001c0001t0001g0016 a0001c0001t0001g0319 a0001c0001t0001g0320 others(5): Show |
9 | HG02486.hp1 HG02818.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.949+959T>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 11/18 | chr7 | 124850913 | |||||||
| chr7:124850916 | A | C | 24 | a0001c0001t0001g0016 a0001c0001t0001g0106 a0001c0001t0001g0107 others(21): Show |
25 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(22): Show |
intron_variant | MODIFIER | c.949+956T>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 11/18 | chr7 | 124850916 | |||||||
| chr7:124851085 | G | T | 1 | a0001c0001t0001g0035 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.949+787C>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 11/18 | chr7 | 124851085 | |||||||
| chr7:124851253 | T | C | 70 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0018 others(67): Show |
72 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.949+619A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 11/18 | chr7 | 124851253 | |||||||
| chr7:124851483 | T | A | 93 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0097 others(90): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.949+389A>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 11/18 | chr7 | 124851483 | |||||||
| chr7:124851507 | CTA | C | 6 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 others(3): Show |
6 | HG02486.hp1 HG02818.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.949+363_949+364del others(2): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 11/18 | chr7 | 124851507 | |||||||
| chr7:124851542 | G | A | 1 | a0001c0001t0003g0150 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.949+330C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 11/18 | chr7 | 124851542 | |||||||
| chr7:124851623 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.949+249G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 11/18 | chr7 | 124851623 | |||||||
| chr7:124851686 | T | C | 1 | a0001c0001t0001g0094 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.949+186A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 11/18 | chr7 | 124851686 | |||||||
| chr7:124851984 | T | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0097 others(90): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.870-33A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 10/18 | chr7 | 124851984 | |||||||
| chr7:124852089 | C | A | 1 | a0001c0001t0002g0044 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.870-138G>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 10/18 | chr7 | 124852089 | |||||||
| chr7:124852245 | A | G | 3 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 |
3 | HG01099.hp2 HG01943.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.870-294T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 10/18 | chr7 | 124852245 | |||||||
| chr7:124852313 | T | C | 1 | a0001c0001t0003g0184 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.870-362A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 10/18 | chr7 | 124852313 | |||||||
| chr7:124852398 | G | C | 1 | a0001c0001t0002g0066 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.870-447C>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 10/18 | chr7 | 124852398 | |||||||
| chr7:124852709 | A | G | 70 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0018 others(67): Show |
72 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.869+263T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 10/18 | chr7 | 124852709 | |||||||
| chr7:124852777 | T | G | 1 | a0001c0001t0001g0228 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.869+195A>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 10/18 | chr7 | 124852777 | |||||||
| chr7:124852829 | T | G | 2 | a0001c0001t0002g0056 a0001c0001t0002g0082 |
2 | NA18954.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.869+143A>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 10/18 | chr7 | 124852829 | |||||||
| chr7:124852959 | A | T | 1 | a0001c0001t0001g0282 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.869+13T>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 10/18 | chr7 | 124852959 | |||||||
| chr7:124853181 | T | G | 1 | a0001c0001t0001g0267 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.703-43A>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124853181 | |||||||
| chr7:124853400 | T | C | 4 | a0001c0001t0001g0108 a0001c0001t0001g0110 a0001c0001t0001g0111 others(1): Show |
4 | HG02055.hp2 HG02280.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.703-262A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124853400 | |||||||
| chr7:124853589 | G | C | 1 | a0001c0003t0001g0309 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.703-451C>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124853589 | |||||||
| chr7:124853677 | C | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.703-539G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124853677 | |||||||
| chr7:124853689 | T | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.703-551A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124853689 | |||||||
| chr7:124853725 | G | GT | 178 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(175): Show |
191 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(188): Show |
intron_variant | MODIFIER | c.703-588dupA | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124853725 | |||||||
| chr7:124853726 | TA | T | 16 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(13): Show |
16 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.703-589delT | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124853726 | |||||||
| chr7:124853728 | A | T | 16 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(13): Show |
16 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.703-590T>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124853728 | |||||||
| chr7:124853810 | T | C | 1 | a0001c0001t0003g0023 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.703-672A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124853810 | |||||||
| chr7:124853998 | T | C | 1 | a0001c0001t0001g0218 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.703-860A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124853998 | |||||||
| chr7:124854037 | T | A | 1 | a0001c0001t0003g0191 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.703-899A>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124854037 | |||||||
| chr7:124854077 | T | C | 5 | a0001c0001t0001g0007 a0001c0001t0001g0097 a0001c0001t0001g0098 others(2): Show |
6 | HG01361.hp1 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.703-939A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124854077 | |||||||
| chr7:124854168 | G | A | 8 | a0001c0001t0001g0016 a0001c0001t0001g0319 a0001c0001t0001g0320 others(5): Show |
9 | HG02486.hp1 HG02818.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.703-1030C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124854168 | |||||||
| chr7:124854356 | G | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.703-1218C>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124854356 | |||||||
| chr7:124854411 | T | C | 114 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(111): Show |
124 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.703-1273A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124854411 | |||||||
| chr7:124854415 | G | A | 1 | a0001c0001t0006g0201 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.703-1277C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124854415 | |||||||
| chr7:124854441 | TA | T | 5 | a0001c0001t0001g0007 a0001c0001t0001g0097 a0001c0001t0001g0098 others(2): Show |
6 | HG01361.hp1 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.703-1304delT | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124854441 | |||||||
| chr7:124854807 | A | G | 70 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0018 others(67): Show |
72 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.703-1669T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124854807 | |||||||
| chr7:124854812 | T | C | 16 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(13): Show |
16 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.703-1674A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124854812 | |||||||
| chr7:124854880 | A | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.703-1742T>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124854880 | |||||||
| chr7:124854922 | T | C | 1 | a0001c0001t0003g0023 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.703-1784A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124854922 | |||||||
| chr7:124855085 | C | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0123 others(85): Show |
96 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.703-1947G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124855085 | |||||||
| chr7:124855190 | C | A | 1 | a0003c0006t0001g0235 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.703-2052G>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124855190 | |||||||
| chr7:124855218 | C | CA | 21 | a0001c0001t0001g0016 a0001c0001t0001g0093 a0001c0001t0001g0094 others(18): Show |
22 | HG01175.hp2 HG01261.hp1 HG01496.hp2 others(19): Show |
intron_variant | MODIFIER | c.703-2081dupT | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124855218 | |||||||
| chr7:124855218 | C | CAA | 6 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0100 others(3): Show |
6 | HG01943.hp1 HG02723.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.703-2082_703-2081d others(4): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124855218 | |||||||
| chr7:124855218 | CA | C | 115 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0035 others(112): Show |
123 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.703-2081delT | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124855218 | |||||||
| chr7:124855218 | CAA | C | 50 | a0001c0001t0001g0008 a0001c0001t0001g0105 a0001c0001t0002g0005 others(47): Show |
53 | HG00323.hp1 HG00423.hp2 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.703-2082_703-2081d others(4): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124855218 | |||||||
| chr7:124855501 | G | A | 5 | a0001c0001t0001g0008 a0001c0001t0001g0100 a0001c0001t0001g0102 others(2): Show |
6 | HG02717.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.703-2363C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124855501 | |||||||
| chr7:124855534 | T | C | 1 | a0003c0006t0009g0103 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.703-2396A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124855534 | |||||||
| chr7:124855680 | T | TA | 7 | a0001c0001t0001g0036 a0001c0001t0001g0319 a0001c0001t0001g0320 others(4): Show |
7 | HG02486.hp1 HG02818.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.703-2543dupT | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124855680 | |||||||
| chr7:124855692 | C | CA | 6 | a0001c0001t0001g0006 a0001c0001t0001g0091 a0001c0001t0001g0092 others(3): Show |
7 | HG02257.hp2 HG02622.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.703-2555dupT | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124855692 | |||||||
| chr7:124855918 | G | C | 2 | a0001c0001t0001g0035 a0003c0006t0009g0103 |
2 | HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.703-2780C>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124855918 | |||||||
| chr7:124855950 | T | C | 8 | a0001c0001t0001g0016 a0001c0001t0001g0319 a0001c0001t0001g0320 others(5): Show |
9 | HG02486.hp1 HG02818.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.703-2812A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124855950 | |||||||
| chr7:124856116 | C | T | 203 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(200): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.702+2841G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124856116 | |||||||
| chr7:124856173 | T | C | 1 | a0001c0001t0004g0149 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.702+2784A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124856173 | |||||||
| chr7:124856431 | AAC | A | 16 | a0001c0001t0001g0016 a0001c0001t0001g0319 a0001c0001t0001g0320 others(13): Show |
17 | HG00639.hp2 HG01433.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.702+2524_702+2525d others(4): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124856431 | |||||||
| chr7:124856445 | CATTTTCT others(2): Show |
C | 16 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(13): Show |
16 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.702+2503_702+2511d others(11): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124856445 | |||||||
| chr7:124856559 | T | C | 7 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0001g0278 others(4): Show |
7 | HG00597.hp2 HG00609.hp2 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.702+2398A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124856559 | |||||||
| chr7:124856624 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.702+2333C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124856624 | |||||||
| chr7:124856816 | G | C | 8 | a0001c0001t0001g0016 a0001c0001t0001g0319 a0001c0001t0001g0320 others(5): Show |
9 | HG02486.hp1 HG02818.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.702+2141C>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124856816 | |||||||
| chr7:124856818 | A | T | 1 | a0001c0001t0003g0151 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.702+2139T>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124856818 | |||||||
| chr7:124856935 | G | A | 1 | a0001c0001t0001g0287 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.702+2022C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124856935 | |||||||
| chr7:124857183 | T | A | 1 | a0001c0001t0003g0023 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.702+1774A>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124857183 | |||||||
| chr7:124857372 | C | T | 8 | a0001c0001t0001g0016 a0001c0001t0001g0319 a0001c0001t0001g0320 others(5): Show |
9 | HG02486.hp1 HG02818.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.702+1585G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124857372 | |||||||
| chr7:124857434 | C | T | 5 | a0001c0001t0003g0144 a0001c0001t0003g0146 a0001c0001t0004g0147 others(2): Show |
5 | HG01261.hp2 HG01346.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.702+1523G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124857434 | |||||||
| chr7:124857439 | C | T | 2 | a0001c0001t0001g0315 a0003c0006t0001g0235 |
2 | HG03942.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.702+1518G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124857439 | |||||||
| chr7:124857757 | T | A | 193 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(190): Show |
206 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.702+1200A>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124857757 | |||||||
| chr7:124857802 | C | T | 2 | a0001c0001t0002g0059 a0001c0001t0002g0060 |
2 | NA18955.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.702+1155G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124857802 | |||||||
| chr7:124857981 | G | A | 100 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0035 others(97): Show |
104 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.702+976C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124857981 | |||||||
| chr7:124857990 | A | G | 2 | a0001c0001t0001g0008 a0001c0001t0001g0105 |
3 | HG02717.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.702+967T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124857990 | |||||||
| chr7:124858101 | T | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(190): Show |
206 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.702+856A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124858101 | |||||||
| chr7:124858251 | G | T | 4 | a0001c0001t0001g0108 a0001c0001t0001g0110 a0001c0001t0001g0111 others(1): Show |
4 | HG02055.hp2 HG02280.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.702+706C>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124858251 | |||||||
| chr7:124858324 | C | A | 1 | a0001c0001t0001g0006 | 2 | HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.702+633G>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124858324 | |||||||
| chr7:124858363 | G | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(190): Show |
206 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.702+594C>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124858363 | |||||||
| chr7:124858427 | T | C | 1 | a0001c0001t0001g0088 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.702+530A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124858427 | |||||||
| chr7:124858653 | C | G | 80 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0036 others(77): Show |
83 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.702+304G>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124858653 | |||||||
| chr7:124858810 | C | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0105 |
3 | HG02717.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.702+147G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124858810 | |||||||
| chr7:124858850 | T | C | 6 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 others(3): Show |
6 | HG02015.hp1 HG02056.hp2 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.702+107A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124858850 | |||||||
| chr7:124858927 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.702+30T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124858927 | |||||||
| chr7:124858948 | A | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.702+9T>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124858948 | |||||||
| chr7:124858949 | T | A | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
splice_region_variant&intron_variant | LOW | c.702+8A>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 9/18 | chr7 | 124858949 | |||||||
| chr7:124859303 | G | T | 1 | a0001c0001t0001g0266 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.547-191C>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 8/18 | chr7 | 124859303 | |||||||
| chr7:124859334 | G | T | 80 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0036 others(77): Show |
83 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.547-222C>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 8/18 | chr7 | 124859334 | |||||||
| chr7:124859348 | C | G | 193 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(190): Show |
206 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.547-236G>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 8/18 | chr7 | 124859348 | |||||||
| chr7:124859426 | A | C | 80 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0036 others(77): Show |
83 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.547-314T>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 8/18 | chr7 | 124859426 | |||||||
| chr7:124859460 | T | C | 205 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(202): Show |
219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.547-348A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 8/18 | chr7 | 124859460 | |||||||
| chr7:124859656 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.547-544C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 8/18 | chr7 | 124859656 | |||||||
| chr7:124859722 | T | TA | 7 | a0001c0001t0001g0013 a0001c0001t0001g0203 a0001c0001t0001g0204 others(4): Show |
8 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(5): Show |
intron_variant | MODIFIER | c.547-611dupT | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 8/18 | chr7 | 124859722 | |||||||
| chr7:124859722 | TA | T | 80 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0036 others(77): Show |
83 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.547-611delT | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 8/18 | chr7 | 124859722 | |||||||
| chr7:124859723 | A | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0097 others(90): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.547-611T>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 8/18 | chr7 | 124859723 | |||||||
| chr7:124859765 | C | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0105 |
3 | HG02717.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.547-653G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 8/18 | chr7 | 124859765 | |||||||
| chr7:124860004 | T | C | 1 | a0001c0001t0001g0102 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.547-892A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 8/18 | chr7 | 124860004 | |||||||
| chr7:124860006 | G | A | 15 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(12): Show |
15 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.547-894C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 8/18 | chr7 | 124860006 | |||||||
| chr7:124860051 | C | T | 1 | a0001c0001t0006g0201 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.547-939G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 8/18 | chr7 | 124860051 | |||||||
| chr7:124860081 | C | T | 6 | a0001c0001t0001g0006 a0001c0001t0001g0091 a0001c0001t0001g0092 others(3): Show |
7 | HG02257.hp2 HG02622.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.547-969G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 8/18 | chr7 | 124860081 | |||||||
| chr7:124860140 | C | T | 1 | a0001c0002t0001g0185 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.547-1028G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 8/18 | chr7 | 124860140 | |||||||
| chr7:124860141 | G | A | 5 | a0001c0001t0001g0008 a0001c0001t0001g0100 a0001c0001t0001g0102 others(2): Show |
6 | HG02717.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.547-1029C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 8/18 | chr7 | 124860141 | |||||||
| chr7:124860156 | C | T | 193 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(190): Show |
206 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.547-1044G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 8/18 | chr7 | 124860156 | |||||||
| chr7:124860290 | A | G | 2 | a0001c0001t0003g0159 a0001c0001t0003g0160 |
2 | HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.547-1178T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 8/18 | chr7 | 124860290 | |||||||
| chr7:124860682 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.547-1570G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 8/18 | chr7 | 124860682 | |||||||
| chr7:124860756 | C | T | 193 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(190): Show |
206 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.547-1644G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 8/18 | chr7 | 124860756 | |||||||
| chr7:124860763 | C | T | 1 | a0001c0001t0010g0327 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.547-1651G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 8/18 | chr7 | 124860763 | |||||||
| chr7:124860868 | C | T | 8 | a0001c0001t0001g0016 a0001c0001t0001g0319 a0001c0001t0001g0320 others(5): Show |
9 | HG02486.hp1 HG02818.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.547-1756G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 8/18 | chr7 | 124860868 | |||||||
| chr7:124860989 | C | CT | 70 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0018 others(67): Show |
72 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.547-1878dupA | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 8/18 | chr7 | 124860989 | |||||||
| chr7:124861069 | G | A | 93 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0097 others(90): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.547-1957C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 8/18 | chr7 | 124861069 | |||||||
| chr7:124861263 | C | A | 193 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(190): Show |
206 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.546+2087G>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 8/18 | chr7 | 124861263 | |||||||
| chr7:124861400 | CTTCTT | C | 26 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 others(23): Show |
27 | HG00609.hp1 HG00621.hp1 HG01934.hp2 others(24): Show |
intron_variant | MODIFIER | c.546+1945_546+1949d others(7): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 8/18 | chr7 | 124861400 | |||||||
| chr7:124861449 | G | T | 1 | a0001c0001t0002g0024 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.546+1901C>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 8/18 | chr7 | 124861449 | |||||||
| chr7:124861457 | T | C | 5 | a0001c0001t0001g0008 a0001c0001t0001g0100 a0001c0001t0001g0102 others(2): Show |
6 | HG02717.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.546+1893A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 8/18 | chr7 | 124861457 | |||||||
| chr7:124861479 | T | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(190): Show |
206 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.546+1871A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 8/18 | chr7 | 124861479 | |||||||
| chr7:124861550 | TG | T | 193 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(190): Show |
206 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.546+1799delC | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 8/18 | chr7 | 124861550 | |||||||
| chr7:124861569 | A | G | 1 | a0001c0001t0001g0190 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.546+1781T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 8/18 | chr7 | 124861569 | |||||||
| chr7:124861760 | T | C | 205 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(202): Show |
219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.546+1590A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 8/18 | chr7 | 124861760 | |||||||
| chr7:124861947 | C | T | 3 | a0001c0001t0001g0100 a0001c0001t0001g0102 a0007c0009t0001g0101 |
3 | HG02895.hp2 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.546+1403G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 8/18 | chr7 | 124861947 | |||||||
| chr7:124861963 | A | G | 3 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 |
3 | HG02647.hp1 HG02896.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.546+1387T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 8/18 | chr7 | 124861963 | |||||||
| chr7:124862082 | T | C | 193 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(190): Show |
206 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.546+1268A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 8/18 | chr7 | 124862082 | |||||||
| chr7:124862137 | A | C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0105 |
3 | HG02717.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.546+1213T>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 8/18 | chr7 | 124862137 | |||||||
| chr7:124862473 | T | G | 8 | a0001c0001t0001g0014 a0001c0001t0001g0229 a0001c0001t0001g0230 others(5): Show |
9 | HG02280.hp2 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.546+877A>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 8/18 | chr7 | 124862473 | |||||||
| chr7:124862896 | AATGCTTC others(21): Show |
A | 1 | a0001c0001t0001g0212 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.546+426_546+453del others(28): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 8/18 | chr7 | 124862896 | |||||||
| chr7:124862950 | G | A | 4 | a0001c0001t0001g0007 a0001c0001t0001g0097 a0001c0001t0001g0098 others(1): Show |
5 | HG01361.hp1 HG02572.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.546+400C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 8/18 | chr7 | 124862950 | |||||||
| chr7:124862993 | G | A | 5 | a0001c0001t0001g0008 a0001c0001t0001g0100 a0001c0001t0001g0102 others(2): Show |
6 | HG02717.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.546+357C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 8/18 | chr7 | 124862993 | |||||||
| chr7:124863058 | T | C | 8 | a0001c0001t0001g0016 a0001c0001t0001g0319 a0001c0001t0001g0320 others(5): Show |
9 | HG02486.hp1 HG02818.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.546+292A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 8/18 | chr7 | 124863058 | |||||||
| chr7:124863084 | T | C | 1 | a0001c0001t0003g0158 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.546+266A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 8/18 | chr7 | 124863084 | |||||||
| chr7:124863135 | A | G | 193 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(190): Show |
206 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.546+215T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 8/18 | chr7 | 124863135 | |||||||
| chr7:124863136 | A | G | 2 | a0001c0001t0001g0008 a0001c0001t0001g0105 |
3 | HG02717.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.546+214T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 8/18 | chr7 | 124863136 | |||||||
| chr7:124863142 | C | T | 49 | a0001c0001t0001g0003 a0001c0001t0001g0109 a0001c0001t0001g0205 others(46): Show |
51 | HG00099.hp2 HG00323.hp2 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.546+208G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 8/18 | chr7 | 124863142 | |||||||
| chr7:124863704 | C | T | 1 | a0001c0001t0001g0007 | 2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.256-64G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124863704 | |||||||
| chr7:124863766 | A | T | 8 | a0001c0001t0001g0014 a0001c0001t0001g0229 a0001c0001t0001g0230 others(5): Show |
9 | HG02280.hp2 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.256-126T>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124863766 | |||||||
| chr7:124863939 | T | C | 15 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(12): Show |
15 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.256-299A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124863939 | |||||||
| chr7:124864020 | C | A | 80 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0036 others(77): Show |
83 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.256-380G>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124864020 | |||||||
| chr7:124864022 | G | A | 1 | a0001c0001t0001g0294 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.256-382C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124864022 | |||||||
| chr7:124864046 | A | G | 1 | a0001c0001t0001g0322 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.256-406T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124864046 | |||||||
| chr7:124864208 | T | C | 2 | a0001c0001t0001g0295 a0001c0011t0001g0275 |
2 | NA18982.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.256-568A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124864208 | |||||||
| chr7:124864346 | A | G | 1 | a0001c0001t0001g0008 | 2 | HG02717.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.256-706T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124864346 | |||||||
| chr7:124864395 | G | A | 1 | a0001c0001t0003g0180 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.256-755C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124864395 | |||||||
| chr7:124865248 | T | C | 3 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 |
3 | HG01099.hp2 HG01943.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.256-1608A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124865248 | |||||||
| chr7:124865417 | G | A | 1 | a0001c0001t0001g0303 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.256-1777C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124865417 | |||||||
| chr7:124865656 | T | G | 6 | a0001c0001t0001g0006 a0001c0001t0001g0091 a0001c0001t0001g0092 others(3): Show |
7 | HG02257.hp2 HG02622.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.256-2016A>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124865656 | |||||||
| chr7:124865661 | C | G | 1 | a0001c0001t0001g0204 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.256-2021G>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124865661 | |||||||
| chr7:124865707 | T | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.256-2067A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124865707 | |||||||
| chr7:124865730 | C | A | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.256-2090G>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124865730 | |||||||
| chr7:124865797 | C | G | 1 | a0001c0001t0001g0324 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.256-2157G>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124865797 | |||||||
| chr7:124865897 | C | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.256-2257G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124865897 | |||||||
| chr7:124865952 | C | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0097 others(90): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.256-2312G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124865952 | |||||||
| chr7:124865971 | A | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.256-2331T>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124865971 | |||||||
| chr7:124865972 | G | C | 1 | a0001c0001t0002g0075 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.256-2332C>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124865972 | |||||||
| chr7:124866209 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.256-2569C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124866209 | |||||||
| chr7:124866249 | CAT | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.256-2611_256-2610d others(4): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124866249 | |||||||
| chr7:124866287 | C | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.256-2647G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124866287 | |||||||
| chr7:124866305 | TG | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.256-2666delC | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124866305 | |||||||
| chr7:124866432 | C | CATGTTCA others(6): Show |
194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.256-2805_256-2793d others(15): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124866432 | |||||||
| chr7:124866525 | G | A | 1 | a0001c0001t0002g0034 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.256-2885C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124866525 | |||||||
| chr7:124866569 | A | G | 1 | a0001c0001t0002g0038 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.256-2929T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124866569 | |||||||
| chr7:124866696 | T | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.256-3056A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124866696 | |||||||
| chr7:124866714 | C | A | 1 | a0001c0001t0003g0177 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.256-3074G>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124866714 | |||||||
| chr7:124866848 | T | C | 1 | a0001c0001t0006g0201 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.256-3208A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124866848 | |||||||
| chr7:124866870 | C | T | 1 | a0001c0001t0001g0298 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.256-3230G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124866870 | |||||||
| chr7:124866949 | G | A | 80 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0036 others(77): Show |
83 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.256-3309C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124866949 | |||||||
| chr7:124867025 | C | T | 3 | a0001c0001t0001g0106 a0001c0001t0001g0116 a0001c0001t0001g0118 |
3 | HG03491.hp2 HG03688.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.256-3385G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124867025 | |||||||
| chr7:124867081 | C | A | 3 | a0001c0001t0001g0100 a0001c0001t0001g0102 a0007c0009t0001g0101 |
3 | HG02895.hp2 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.256-3441G>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124867081 | |||||||
| chr7:124867205 | G | A | 1 | a0001c0001t0001g0317 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.256-3565C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124867205 | |||||||
| chr7:124867236 | T | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0097 others(90): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.256-3596A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124867236 | |||||||
| chr7:124867250 | A | T | 6 | a0001c0001t0001g0006 a0001c0001t0001g0091 a0001c0001t0001g0092 others(3): Show |
7 | HG02257.hp2 HG02622.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.256-3610T>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124867250 | |||||||
| chr7:124867271 | T | A | 3 | a0001c0001t0002g0005 a0001c0001t0002g0043 a0001c0001t0002g0072 |
4 | NA18986.hp2 NA19056.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.256-3631A>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124867271 | |||||||
| chr7:124867297 | C | CAT | 323 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(320): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.255+3613_255+3614i others(4): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124867297 | |||||||
| chr7:124867512 | T | C | 1 | a0001c0001t0001g0220 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.255+3399A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124867512 | |||||||
| chr7:124867532 | C | T | 1 | a0001c0001t0001g0130 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.255+3379G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124867532 | |||||||
| chr7:124867634 | T | TTTTA | 5 | a0001c0001t0001g0008 a0001c0001t0001g0100 a0001c0001t0001g0102 others(2): Show |
6 | HG02717.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.255+3273_255+3276d others(6): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124867634 | |||||||
| chr7:124867657 | A | T | 4 | a0001c0001t0001g0106 a0001c0001t0001g0116 a0001c0001t0001g0118 others(1): Show |
4 | HG02723.hp1 HG03491.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.255+3254T>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124867657 | |||||||
| chr7:124867676 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.255+3235C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124867676 | |||||||
| chr7:124867795 | C | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0097 others(90): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.255+3116G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124867795 | |||||||
| chr7:124867809 | A | G | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.255+3102T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124867809 | |||||||
| chr7:124867976 | C | T | 3 | a0001c0001t0002g0062 a0001c0001t0002g0068 a0001c0001t0002g0069 |
3 | NA18948.hp1 NA18952.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.255+2935G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124867976 | |||||||
| chr7:124868092 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.255+2819C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124868092 | |||||||
| chr7:124868260 | T | C | 5 | a0001c0001t0003g0144 a0001c0001t0003g0146 a0001c0001t0004g0147 others(2): Show |
5 | HG01261.hp2 HG01346.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.255+2651A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124868260 | |||||||
| chr7:124868303 | T | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.255+2608A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124868303 | |||||||
| chr7:124868355 | C | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0323 |
3 | HG02976.hp1 HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.255+2556G>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124868355 | |||||||
| chr7:124868651 | A | G | 1 | a0001c0001t0002g0076 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.255+2260T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124868651 | |||||||
| chr7:124868843 | T | C | 5 | a0001c0001t0001g0008 a0001c0001t0001g0100 a0001c0001t0001g0102 others(2): Show |
6 | HG02717.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.255+2068A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124868843 | |||||||
| chr7:124868850 | CCTCT | C | 2 | a0001c0001t0001g0006 a0001c0001t0001g0091 |
3 | HG02257.hp2 HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.255+2057_255+2060d others(6): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124868850 | |||||||
| chr7:124868875 | G | A | 80 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0036 others(77): Show |
83 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.255+2036C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124868875 | |||||||
| chr7:124868904 | T | C | 3 | a0001c0001t0001g0100 a0001c0001t0001g0102 a0007c0009t0001g0101 |
3 | HG02895.hp2 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.255+2007A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124868904 | |||||||
| chr7:124868936 | T | C | 16 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(13): Show |
16 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.255+1975A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124868936 | |||||||
| chr7:124869234 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.255+1677G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124869234 | |||||||
| chr7:124869255 | T | C | 1 | a0001c0001t0001g0114 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.255+1656A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124869255 | |||||||
| chr7:124869366 | G | A | 1 | a0001c0001t0001g0318 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.255+1545C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124869366 | |||||||
| chr7:124869397 | T | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.255+1514A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124869397 | |||||||
| chr7:124869511 | GT | G | 6 | a0001c0001t0001g0006 a0001c0001t0001g0091 a0001c0001t0001g0092 others(3): Show |
7 | HG02257.hp2 HG02622.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.255+1399delA | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124869511 | |||||||
| chr7:124869525 | AT | A | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.255+1385delA | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124869525 | |||||||
| chr7:124869615 | T | G | 16 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(13): Show |
16 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.255+1296A>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124869615 | |||||||
| chr7:124869723 | C | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0097 others(90): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.255+1188G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124869723 | |||||||
| chr7:124869772 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.255+1139C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124869772 | |||||||
| chr7:124869845 | T | A | 1 | a0001c0001t0006g0201 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.255+1066A>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124869845 | |||||||
| chr7:124870222 | G | A | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.255+689C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124870222 | |||||||
| chr7:124870416 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.255+495A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124870416 | |||||||
| chr7:124870423 | C | G | 3 | a0001c0001t0001g0100 a0001c0001t0001g0102 a0007c0009t0001g0101 |
3 | HG02895.hp2 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.255+488G>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124870423 | |||||||
| chr7:124870522 | ATATAATC others(3): Show |
A | 1 | a0001c0001t0001g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.255+379_255+388del others(10): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 7/18 | chr7 | 124870522 | |||||||
| chr7:124871332 | A | C | 1 | a0001c0001t0001g0310 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.125-291T>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124871332 | |||||||
| chr7:124871670 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.125-629G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124871670 | |||||||
| chr7:124871680 | A | G | 1 | a0001c0001t0001g0270 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.125-639T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124871680 | |||||||
| chr7:124871731 | A | AT | 74 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(71): Show |
80 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(77): Show |
intron_variant | MODIFIER | c.125-691dupA | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124871731 | |||||||
| chr7:124871731 | A | ATT | 18 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(15): Show |
18 | HG01496.hp2 HG02055.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.125-692_125-691dup others(2): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124871731 | |||||||
| chr7:124871731 | A | ATTT | 6 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 others(3): Show |
6 | HG01884.hp1 HG02976.hp2 NA19002.hp2 others(3): Show |
intron_variant | MODIFIER | c.125-693_125-691dup others(3): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124871731 | |||||||
| chr7:124871731 | A | T | 1 | a0001c0001t0001g0141 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.125-690T>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124871731 | |||||||
| chr7:124871731 | AT | A | 122 | a0001c0001t0001g0008 a0001c0001t0001g0035 a0001c0001t0001g0088 others(119): Show |
130 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.125-691delA | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124871731 | |||||||
| chr7:124871731 | ATT | A | 23 | a0001c0001t0001g0036 a0001c0001t0001g0100 a0001c0001t0001g0102 others(20): Show |
24 | HG00323.hp1 HG01070.hp2 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.125-692_125-691del others(2): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124871731 | |||||||
| chr7:124871879 | AG | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0323 |
3 | HG02976.hp1 HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.125-839delC | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124871879 | |||||||
| chr7:124871890 | C | T | 1 | a0001c0001t0002g0057 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.125-849G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124871890 | |||||||
| chr7:124872195 | G | A | 80 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0036 others(77): Show |
83 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.125-1154C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124872195 | |||||||
| chr7:124872208 | A | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0097 others(90): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.125-1167T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124872208 | |||||||
| chr7:124872264 | T | C | 1 | a0001c0001t0003g0180 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.125-1223A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124872264 | |||||||
| chr7:124872333 | A | T | 3 | a0001c0001t0002g0005 a0001c0001t0002g0043 a0001c0001t0002g0072 |
4 | NA18986.hp2 NA19056.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.125-1292T>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124872333 | |||||||
| chr7:124872362 | T | C | 1 | a0001c0001t0006g0201 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.125-1321A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124872362 | |||||||
| chr7:124872376 | T | C | 9 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0036 others(6): Show |
10 | HG02257.hp2 HG02258.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.125-1335A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124872376 | |||||||
| chr7:124872446 | T | C | 1 | a0001c0001t0001g0322 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.125-1405A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124872446 | |||||||
| chr7:124872463 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.125-1422G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124872463 | |||||||
| chr7:124872476 | C | G | 16 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(13): Show |
16 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.125-1435G>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124872476 | |||||||
| chr7:124872488 | G | A | 1 | a0001c0002t0001g0185 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.125-1447C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124872488 | |||||||
| chr7:124872501 | T | A | 70 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0018 others(67): Show |
72 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.125-1460A>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124872501 | |||||||
| chr7:124872593 | C | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0097 others(90): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.125-1552G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124872593 | |||||||
| chr7:124872653 | A | G | 1 | a0001c0001t0002g0070 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.125-1612T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124872653 | |||||||
| chr7:124872669 | T | C | 1 | a0001c0001t0003g0191 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.125-1628A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124872669 | |||||||
| chr7:124872711 | C | T | 1 | a0001c0001t0001g0317 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.125-1670G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124872711 | |||||||
| chr7:124872852 | C | T | 2 | a0001c0002t0005g0197 a0001c0002t0005g0198 |
2 | HG00639.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.125-1811G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124872852 | |||||||
| chr7:124872858 | G | A | 1 | a0001c0001t0003g0145 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.125-1817C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124872858 | |||||||
| chr7:124872966 | C | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0097 others(90): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.125-1925G>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124872966 | |||||||
| chr7:124872969 | T | C | 3 | a0001c0001t0001g0100 a0001c0001t0001g0102 a0007c0009t0001g0101 |
3 | HG02895.hp2 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.125-1928A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124872969 | |||||||
| chr7:124872996 | A | G | 80 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0036 others(77): Show |
83 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.125-1955T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124872996 | |||||||
| chr7:124873038 | C | A | 1 | a0001c0001t0001g0122 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.125-1997G>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124873038 | |||||||
| chr7:124873229 | G | A | 70 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0018 others(67): Show |
72 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.125-2188C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124873229 | |||||||
| chr7:124873301 | G | C | 85 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0035 others(82): Show |
89 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.125-2260C>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124873301 | |||||||
| chr7:124873309 | T | C | 4 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 others(1): Show |
4 | NA19002.hp2 NA19012.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.125-2268A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124873309 | |||||||
| chr7:124873396 | C | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.125-2355G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124873396 | |||||||
| chr7:124873564 | T | C | 1 | a0001c0001t0001g0008 | 2 | HG02717.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.125-2523A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124873564 | |||||||
| chr7:124873571 | T | C | 1 | a0001c0001t0001g0253 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.125-2530A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124873571 | |||||||
| chr7:124873643 | A | C | 8 | a0001c0001t0001g0014 a0001c0001t0001g0229 a0001c0001t0001g0230 others(5): Show |
9 | HG02280.hp2 HG02451.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.125-2602T>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124873643 | |||||||
| chr7:124873693 | T | G | 1 | a0001c0001t0001g0255 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.125-2652A>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124873693 | |||||||
| chr7:124873716 | A | G | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.125-2675T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124873716 | |||||||
| chr7:124873854 | T | G | 5 | a0001c0001t0001g0008 a0001c0001t0001g0100 a0001c0001t0001g0102 others(2): Show |
6 | HG02717.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.125-2813A>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124873854 | |||||||
| chr7:124873885 | CAG | C | 16 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(13): Show |
16 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.125-2846_125-2845d others(4): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124873885 | |||||||
| chr7:124874045 | C | T | 2 | a0001c0001t0001g0263 a0001c0001t0001g0266 |
2 | HG01070.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.125-3004G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124874045 | |||||||
| chr7:124874048 | T | G | 2 | a0001c0001t0002g0017 a0001c0001t0002g0018 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.125-3007A>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124874048 | |||||||
| chr7:124874338 | C | A | 1 | a0001c0001t0001g0088 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.125-3297G>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124874338 | |||||||
| chr7:124874366 | C | T | 1 | a0001c0001t0003g0134 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.125-3325G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124874366 | |||||||
| chr7:124874399 | A | G | 2 | a0001c0001t0001g0008 a0001c0001t0001g0105 |
3 | HG02717.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.125-3358T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124874399 | |||||||
| chr7:124874465 | T | C | 2 | a0001c0001t0002g0031 a0001c0001t0002g0032 |
2 | NA18940.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.125-3424A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124874465 | |||||||
| chr7:124874490 | T | A | 80 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0036 others(77): Show |
83 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.125-3449A>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124874490 | |||||||
| chr7:124874530 | A | C | 9 | a0001c0001t0001g0016 a0001c0001t0001g0319 a0001c0001t0001g0320 others(6): Show |
10 | HG02486.hp1 HG02723.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.125-3489T>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124874530 | |||||||
| chr7:124874647 | A | T | 1 | a0001c0001t0001g0088 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.125-3606T>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124874647 | |||||||
| chr7:124874714 | G | A | 3 | a0001c0001t0002g0081 a0001c0001t0002g0084 a0001c0001t0002g0085 |
3 | HG00140.hp1 HG00735.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.125-3673C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124874714 | |||||||
| chr7:124874733 | C | CA | 9 | a0001c0001t0001g0016 a0001c0001t0001g0093 a0001c0001t0001g0319 others(6): Show |
10 | HG02486.hp1 HG02818.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.125-3693dupT | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124874733 | |||||||
| chr7:124874831 | G | C | 2 | a0001c0001t0002g0056 a0001c0001t0002g0082 |
2 | NA18954.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.125-3790C>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124874831 | |||||||
| chr7:124874945 | C | CA | 9 | a0001c0001t0001g0093 a0001c0001t0001g0210 a0001c0001t0001g0304 others(6): Show |
9 | HG00438.hp2 HG01934.hp2 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.125-3905dupT | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124874945 | |||||||
| chr7:124875292 | T | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.125-4251A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124875292 | |||||||
| chr7:124875319 | G | A | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.125-4278C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124875319 | |||||||
| chr7:124875377 | G | C | 1 | a0001c0001t0001g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.125-4336C>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124875377 | |||||||
| chr7:124875439 | T | G | 8 | a0001c0001t0001g0016 a0001c0001t0001g0319 a0001c0001t0001g0320 others(5): Show |
9 | HG02486.hp1 HG02818.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.125-4398A>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124875439 | |||||||
| chr7:124875751 | T | G | 1 | a0001c0001t0001g0116 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.125-4710A>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124875751 | |||||||
| chr7:124875845 | A | G | 2 | a0001c0001t0002g0068 a0001c0001t0002g0069 |
2 | NA18952.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.125-4804T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124875845 | |||||||
| chr7:124875973 | G | A | 8 | a0001c0001t0001g0016 a0001c0001t0001g0319 a0001c0001t0001g0320 others(5): Show |
9 | HG02486.hp1 HG02818.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.125-4932C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124875973 | |||||||
| chr7:124876068 | G | A | 1 | a0001c0001t0003g0188 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.125-5027C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124876068 | |||||||
| chr7:124876335 | C | CTTTTTT | 16 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(13): Show |
16 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.125-5295_125-5294i others(8): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124876335 | |||||||
| chr7:124876340 | A | C | 1 | a0001c0001t0001g0088 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.125-5299T>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124876340 | |||||||
| chr7:124876346 | C | T | 324 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(321): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.125-5305G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124876346 | |||||||
| chr7:124876413 | C | G | 1 | a0001c0001t0006g0201 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.125-5372G>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124876413 | |||||||
| chr7:124876631 | AACAT | A | 3 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0061 |
3 | HG01516.hp1 HG01517.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.125-5594_125-5591d others(6): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124876631 | |||||||
| chr7:124876636 | A | G | 3 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0061 |
3 | HG01516.hp1 HG01517.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.125-5595T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124876636 | |||||||
| chr7:124876638 | G | A | 3 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0061 |
3 | HG01516.hp1 HG01517.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.125-5597C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124876638 | |||||||
| chr7:124876759 | G | GA | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.125-5719dupT | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124876759 | |||||||
| chr7:124876817 | C | T | 5 | a0001c0001t0001g0007 a0001c0001t0001g0097 a0001c0001t0001g0098 others(2): Show |
6 | HG01361.hp1 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.125-5776G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124876817 | |||||||
| chr7:124877018 | C | T | 1 | a0001c0001t0007g0096 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.125-5977G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124877018 | |||||||
| chr7:124877076 | C | A | 3 | a0001c0001t0001g0100 a0001c0001t0001g0102 a0007c0009t0001g0101 |
3 | HG02895.hp2 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.125-6035G>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124877076 | |||||||
| chr7:124877108 | T | C | 3 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 |
3 | HG01099.hp2 HG01943.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.125-6067A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124877108 | |||||||
| chr7:124877226 | A | G | 80 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0036 others(77): Show |
83 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.125-6185T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124877226 | |||||||
| chr7:124877441 | T | C | 1 | a0001c0001t0002g0074 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.125-6400A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124877441 | |||||||
| chr7:124877558 | C | T | 3 | a0001c0001t0002g0017 a0001c0001t0002g0018 a0001c0001t0002g0061 |
3 | HG01516.hp1 HG01517.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.125-6517G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124877558 | |||||||
| chr7:124877576 | C | A | 16 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(13): Show |
16 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.125-6535G>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124877576 | |||||||
| chr7:124877599 | G | A | 1 | a0001c0001t0002g0030 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.125-6558C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124877599 | |||||||
| chr7:124877632 | A | T | 1 | a0001c0001t0001g0219 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.125-6591T>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124877632 | |||||||
| chr7:124877664 | C | G | 1 | a0001c0001t0006g0201 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.125-6623G>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124877664 | |||||||
| chr7:124877676 | A | G | 6 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(3): Show |
6 | HG00099.hp2 HG01070.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.125-6635T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124877676 | |||||||
| chr7:124877750 | G | A | 1 | a0001c0001t0001g0035 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.125-6709C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124877750 | |||||||
| chr7:124877758 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.125-6717C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124877758 | |||||||
| chr7:124877792 | C | T | 8 | a0001c0001t0001g0013 a0001c0001t0001g0203 a0001c0001t0001g0204 others(5): Show |
9 | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(6): Show |
intron_variant | MODIFIER | c.125-6751G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124877792 | |||||||
| chr7:124877803 | A | G | 80 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0036 others(77): Show |
83 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.125-6762T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124877803 | |||||||
| chr7:124877840 | C | CA | 26 | a0001c0001t0001g0020 a0001c0001t0001g0100 a0001c0001t0001g0102 others(23): Show |
26 | HG00099.hp2 HG00609.hp2 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.125-6800dupT | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124877840 | |||||||
| chr7:124877840 | C | CAA | 7 | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0105 others(4): Show |
7 | HG01943.hp1 HG02074.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.125-6801_125-6800d others(4): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124877840 | |||||||
| chr7:124877840 | C | CAAA | 7 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0092 others(4): Show |
8 | HG02976.hp2 HG03041.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.125-6802_125-6800d others(5): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124877840 | |||||||
| chr7:124877840 | C | CAAAA | 8 | a0001c0001t0001g0091 a0001c0001t0001g0094 a0001c0001t0001g0109 others(5): Show |
8 | HG02257.hp2 HG02280.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.125-6803_125-6800d others(6): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124877840 | |||||||
| chr7:124877840 | C | CAAAAAAA others(4): Show |
2 | a0001c0001t0001g0088 a0001c0001t0002g0030 |
2 | HG01243.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.125-6810_125-6800d others(13): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124877840 | |||||||
| chr7:124877840 | C | CAAAAAAA others(5): Show |
16 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0002g0051 others(13): Show |
17 | HG00323.hp1 HG00673.hp1 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.125-6811_125-6800d others(14): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124877840 | |||||||
| chr7:124877840 | C | CAAAAAAA others(6): Show |
21 | a0001c0001t0002g0005 a0001c0001t0002g0033 a0001c0001t0002g0037 others(18): Show |
22 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.125-6812_125-6800d others(15): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124877840 | |||||||
| chr7:124877840 | C | CAAAAAAA others(7): Show |
10 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0041 others(7): Show |
10 | HG00423.hp2 HG00735.hp2 HG02015.hp1 others(7): Show |
intron_variant | MODIFIER | c.125-6813_125-6800d others(16): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124877840 | |||||||
| chr7:124877840 | C | CAAAAAAA others(8): Show |
4 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0052 others(1): Show |
4 | HG00621.hp1 HG02056.hp2 HG02074.hp2 others(1): Show |
intron_variant | MODIFIER | c.125-6814_125-6800d others(17): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124877840 | |||||||
| chr7:124877840 | C | CAAAAAAA others(9): Show |
3 | a0001c0001t0002g0026 a0001c0001t0002g0027 a0001c0001t0002g0086 |
3 | HG01258.hp2 NA18967.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.125-6815_125-6800d others(18): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124877840 | |||||||
| chr7:124877840 | C | CAAAAAAA others(11): Show |
3 | a0001c0001t0002g0034 a0001c0001t0002g0080 a0001c0001t0002g0082 |
3 | HG01496.hp1 NA18954.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.125-6817_125-6800d others(20): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124877840 | |||||||
| chr7:124877840 | C | CAAAAAAA others(13): Show |
2 | a0001c0001t0002g0056 a0001c0001t0002g0057 |
2 | HG01934.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.125-6819_125-6800d others(22): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124877840 | |||||||
| chr7:124877840 | C | CAAAAAAA others(21): Show |
1 | a0001c0001t0002g0075 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.125-6827_125-6800d others(30): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124877840 | |||||||
| chr7:124877840 | CA | C | 7 | a0001c0001t0001g0211 a0001c0001t0001g0216 a0001c0001t0001g0229 others(4): Show |
7 | HG00323.hp2 HG01515.hp1 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.125-6800delT | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124877840 | |||||||
| chr7:124877840 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0002g0038 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.125-6810_125-6800d others(13): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124877840 | |||||||
| chr7:124877840 | CAAAAAAA others(5): Show |
C | 8 | a0001c0001t0001g0016 a0001c0001t0001g0319 a0001c0001t0001g0320 others(5): Show |
9 | HG02486.hp1 HG02818.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.125-6811_125-6800d others(14): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124877840 | |||||||
| chr7:124877840 | CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0001g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.125-6813_125-6800d others(16): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124877840 | |||||||
| chr7:124877840 | CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0003g0157 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.125-6814_125-6800d others(17): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124877840 | |||||||
| chr7:124877840 | CAAAAAAA others(9): Show |
C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0097 others(83): Show |
95 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.125-6815_125-6800d others(18): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124877840 | |||||||
| chr7:124877840 | CAAAAAAA others(13): Show |
C | 6 | a0001c0002t0001g0193 a0001c0002t0001g0194 a0001c0002t0001g0199 others(3): Show |
6 | HG00639.hp2 HG01433.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.125-6819_125-6800d others(22): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124877840 | |||||||
| chr7:124877918 | A | C | 16 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(13): Show |
16 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.125-6877T>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124877918 | |||||||
| chr7:124878004 | T | C | 1 | a0001c0001t0001g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.125-6963A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124878004 | |||||||
| chr7:124878017 | C | T | 1 | a0001c0001t0003g0023 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.125-6976G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124878017 | |||||||
| chr7:124878116 | T | A | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.125-7075A>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124878116 | |||||||
| chr7:124878118 | G | C | 80 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0036 others(77): Show |
83 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.125-7077C>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124878118 | |||||||
| chr7:124878193 | G | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0105 |
3 | HG02717.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.125-7152C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124878193 | |||||||
| chr7:124878221 | A | C | 16 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(13): Show |
16 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.125-7180T>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124878221 | |||||||
| chr7:124878415 | GCA | G | 5 | a0001c0001t0001g0008 a0001c0001t0001g0100 a0001c0001t0001g0102 others(2): Show |
6 | HG02717.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.125-7376_125-7375d others(4): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124878415 | |||||||
| chr7:124878588 | C | A | 1 | a0001c0001t0001g0091 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.125-7547G>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124878588 | |||||||
| chr7:124878706 | T | C | 1 | a0001c0001t0002g0086 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.125-7665A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124878706 | |||||||
| chr7:124878712 | T | C | 206 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(203): Show |
220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.125-7671A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124878712 | |||||||
| chr7:124878956 | T | C | 16 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(13): Show |
16 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.125-7915A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124878956 | |||||||
| chr7:124879054 | A | G | 3 | a0001c0001t0001g0100 a0001c0001t0001g0102 a0007c0009t0001g0101 |
3 | HG02895.hp2 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.125-8013T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124879054 | |||||||
| chr7:124879302 | G | T | 1 | a0001c0001t0003g0181 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.125-8261C>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124879302 | |||||||
| chr7:124879322 | T | G | 2 | a0001c0001t0001g0006 a0001c0001t0001g0091 |
3 | HG02257.hp2 HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.125-8281A>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124879322 | |||||||
| chr7:124879345 | T | C | 7 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(4): Show |
7 | HG00323.hp2 HG01358.hp2 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.125-8304A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124879345 | |||||||
| chr7:124879418 | C | G | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.125-8377G>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124879418 | |||||||
| chr7:124879573 | C | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.125-8532G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124879573 | |||||||
| chr7:124879622 | T | C | 2 | a0001c0001t0003g0011 a0001c0001t0003g0174 |
3 | NA18965.hp2 NA18985.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.125-8581A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124879622 | |||||||
| chr7:124879653 | T | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.125-8612A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124879653 | |||||||
| chr7:124879966 | G | A | 1 | a0003c0006t0009g0103 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.125-8925C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124879966 | |||||||
| chr7:124880060 | T | A | 1 | a0001c0001t0003g0175 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.125-9019A>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124880060 | |||||||
| chr7:124880138 | G | C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0105 |
3 | HG02717.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.125-9097C>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124880138 | |||||||
| chr7:124880254 | G | A | 80 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0036 others(77): Show |
83 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.125-9213C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124880254 | |||||||
| chr7:124880312 | T | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.125-9271A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124880312 | |||||||
| chr7:124880397 | T | C | 1 | a0001c0001t0007g0096 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.125-9356A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124880397 | |||||||
| chr7:124880713 | C | T | 16 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(13): Show |
16 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.125-9672G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124880713 | |||||||
| chr7:124880727 | G | C | 1 | a0001c0001t0001g0274 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.125-9686C>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124880727 | |||||||
| chr7:124880775 | C | G | 1 | a0001c0001t0003g0159 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.125-9734G>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124880775 | |||||||
| chr7:124880821 | GA | G | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.125-9781delT | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124880821 | |||||||
| chr7:124880870 | C | T | 1 | a0001c0001t0006g0201 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.125-9829G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124880870 | |||||||
| chr7:124880912 | C | A | 101 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0035 others(98): Show |
105 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.125-9871G>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124880912 | |||||||
| chr7:124881050 | C | G | 1 | a0001c0001t0001g0088 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.125-10009G>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124881050 | |||||||
| chr7:124881092 | C | T | 203 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(200): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.125-10051G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124881092 | |||||||
| chr7:124881093 | G | A | 1 | a0001c0001t0001g0223 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.125-10052C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124881093 | |||||||
| chr7:124881161 | G | C | 1 | a0001c0001t0001g0269 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.125-10120C>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124881161 | |||||||
| chr7:124881163 | C | T | 203 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(200): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.125-10122G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124881163 | |||||||
| chr7:124881193 | T | A | 1 | a0001c0001t0001g0310 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.125-10152A>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124881193 | |||||||
| chr7:124881311 | T | A | 1 | a0003c0006t0009g0103 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.125-10270A>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124881311 | |||||||
| chr7:124881337 | C | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.125-10296G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124881337 | |||||||
| chr7:124881373 | T | C | 1 | a0001c0001t0001g0303 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.125-10332A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124881373 | |||||||
| chr7:124881376 | C | A | 71 | a0001c0001t0001g0088 a0001c0001t0002g0005 a0001c0001t0002g0017 others(68): Show |
73 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.125-10335G>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124881376 | |||||||
| chr7:124881668 | C | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.124+10598G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124881668 | |||||||
| chr7:124881857 | T | C | 1 | a0001c0001t0001g0308 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.124+10409A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124881857 | |||||||
| chr7:124881876 | A | G | 1 | a0001c0001t0003g0145 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.124+10390T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124881876 | |||||||
| chr7:124881897 | T | C | 8 | a0001c0001t0001g0016 a0001c0001t0001g0319 a0001c0001t0001g0320 others(5): Show |
9 | HG02486.hp1 HG02818.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.124+10369A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124881897 | |||||||
| chr7:124881905 | G | C | 1 | a0001c0001t0001g0020 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.124+10361C>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124881905 | |||||||
| chr7:124882114 | T | C | 2 | a0001c0001t0002g0047 a0001c0001t0002g0050 |
2 | HG00597.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.124+10152A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124882114 | |||||||
| chr7:124882302 | T | C | 1 | a0003c0006t0009g0103 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.124+9964A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124882302 | |||||||
| chr7:124882479 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.124+9787G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124882479 | |||||||
| chr7:124882524 | A | C | 1 | a0001c0001t0003g0144 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.124+9742T>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124882524 | |||||||
| chr7:124882645 | AG | A | 4 | a0001c0001t0001g0007 a0001c0001t0001g0097 a0001c0001t0001g0098 others(1): Show |
5 | HG01361.hp1 HG02572.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.124+9620delC | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124882645 | |||||||
| chr7:124882699 | T | TA | 203 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(200): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.124+9566dupT | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124882699 | |||||||
| chr7:124882865 | C | T | 8 | a0001c0001t0001g0016 a0001c0001t0001g0319 a0001c0001t0001g0320 others(5): Show |
9 | HG02486.hp1 HG02818.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.124+9401G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124882865 | |||||||
| chr7:124882992 | G | C | 1 | a0001c0002t0001g0195 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.124+9274C>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124882992 | |||||||
| chr7:124883103 | T | C | 324 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(321): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.124+9163A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124883103 | |||||||
| chr7:124883118 | C | T | 1 | a0001c0001t0003g0167 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.124+9148G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124883118 | |||||||
| chr7:124883219 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.124+9047G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124883219 | |||||||
| chr7:124883243 | A | C | 1 | a0001c0001t0006g0201 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.124+9023T>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124883243 | |||||||
| chr7:124883257 | C | A | 1 | a0001c0001t0003g0191 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.124+9009G>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124883257 | |||||||
| chr7:124883367 | G | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0097 others(90): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.124+8899C>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124883367 | |||||||
| chr7:124883516 | C | T | 1 | a0001c0001t0003g0009 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.124+8750G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124883516 | |||||||
| chr7:124883533 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.124+8733T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124883533 | |||||||
| chr7:124883572 | G | GTTCTAAT others(6): Show |
1 | a0001c0001t0002g0084 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.124+8693_124+8694i others(15): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124883572 | |||||||
| chr7:124883573 | A | T | 1 | a0001c0001t0002g0084 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.124+8693T>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124883573 | |||||||
| chr7:124883574 | C | A | 1 | a0001c0001t0002g0084 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.124+8692G>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124883574 | |||||||
| chr7:124883577 | C | T | 1 | a0001c0001t0002g0084 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.124+8689G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124883577 | |||||||
| chr7:124883578 | C | A | 1 | a0001c0001t0002g0084 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.124+8688G>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124883578 | |||||||
| chr7:124883705 | C | T | 1 | a0001c0001t0002g0058 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.124+8561G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124883705 | |||||||
| chr7:124883719 | A | G | 1 | a0001c0001t0001g0008 | 2 | HG02717.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.124+8547T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124883719 | |||||||
| chr7:124883730 | G | A | 1 | a0006c0008t0003g0148 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.124+8536C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124883730 | |||||||
| chr7:124883733 | T | C | 1 | a0001c0001t0003g0023 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.124+8533A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124883733 | |||||||
| chr7:124883979 | A | T | 1 | a0001c0001t0002g0024 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.124+8287T>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124883979 | |||||||
| chr7:124884077 | G | A | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.124+8189C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124884077 | |||||||
| chr7:124884459 | A | G | 1 | a0001c0003t0001g0284 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.124+7807T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124884459 | |||||||
| chr7:124884508 | A | C | 16 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(13): Show |
16 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.124+7758T>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124884508 | |||||||
| chr7:124884622 | A | AG | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.124+7643dupC | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124884622 | |||||||
| chr7:124884646 | C | A | 1 | a0003c0006t0009g0103 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.124+7620G>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124884646 | |||||||
| chr7:124884963 | C | CTAGGAAA others(2): Show |
16 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(13): Show |
16 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.124+7294_124+7302d others(11): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124884963 | |||||||
| chr7:124885128 | A | C | 88 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0123 others(85): Show |
96 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.124+7138T>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124885128 | |||||||
| chr7:124885293 | C | CA | 31 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0088 others(28): Show |
33 | HG00597.hp2 HG01243.hp1 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.124+6972dupT | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124885293 | |||||||
| chr7:124885293 | C | CAA | 87 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0035 others(84): Show |
96 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.124+6971_124+6972d others(4): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124885293 | |||||||
| chr7:124885293 | C | CAAA | 69 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0129 others(66): Show |
71 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.124+6970_124+6972d others(5): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124885293 | |||||||
| chr7:124885293 | C | CAAAA | 11 | a0001c0001t0002g0032 a0001c0001t0002g0048 a0001c0001t0002g0049 others(8): Show |
11 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(8): Show |
intron_variant | MODIFIER | c.124+6969_124+6972d others(6): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124885293 | |||||||
| chr7:124885293 | CA | C | 6 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0242 others(3): Show |
6 | HG01496.hp2 HG02630.hp2 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.124+6972delT | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124885293 | |||||||
| chr7:124885362 | A | T | 1 | a0001c0001t0001g0282 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.124+6904T>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124885362 | |||||||
| chr7:124885463 | C | T | 101 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0035 others(98): Show |
105 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.124+6803G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124885463 | |||||||
| chr7:124885488 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.124+6778G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124885488 | |||||||
| chr7:124885722 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.124+6544A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124885722 | |||||||
| chr7:124885736 | A | G | 1 | a0001c0001t0002g0053 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.124+6530T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124885736 | |||||||
| chr7:124885791 | A | AAAAT | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.124+6471_124+6474d others(6): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124885791 | |||||||
| chr7:124885918 | A | C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0105 |
3 | HG02717.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.124+6348T>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124885918 | |||||||
| chr7:124885936 | T | C | 2 | a0001c0001t0001g0255 a0001c0001t0001g0317 |
2 | HG01099.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.124+6330A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124885936 | |||||||
| chr7:124886094 | G | A | 93 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0097 others(90): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.124+6172C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124886094 | |||||||
| chr7:124886159 | C | T | 80 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0036 others(77): Show |
83 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.124+6107G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124886159 | |||||||
| chr7:124886239 | T | C | 5 | a0001c0001t0001g0007 a0001c0001t0001g0097 a0001c0001t0001g0098 others(2): Show |
6 | HG01361.hp1 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.124+6027A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124886239 | |||||||
| chr7:124886277 | C | T | 70 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0018 others(67): Show |
72 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.124+5989G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124886277 | |||||||
| chr7:124886488 | C | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.124+5778G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124886488 | |||||||
| chr7:124886571 | G | A | 1 | a0001c0001t0001g0249 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.124+5695C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124886571 | |||||||
| chr7:124886685 | C | T | 79 | a0001c0001t0001g0007 a0001c0001t0001g0097 a0001c0001t0001g0098 others(76): Show |
86 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.124+5581G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124886685 | |||||||
| chr7:124886697 | G | C | 5 | a0001c0001t0001g0008 a0001c0001t0001g0100 a0001c0001t0001g0102 others(2): Show |
6 | HG02717.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.124+5569C>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124886697 | |||||||
| chr7:124886743 | T | C | 1 | a0001c0001t0006g0201 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.124+5523A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124886743 | |||||||
| chr7:124887042 | C | A | 1 | a0001c0001t0002g0050 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.124+5224G>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124887042 | |||||||
| chr7:124887070 | A | G | 5 | a0001c0001t0001g0007 a0001c0001t0001g0097 a0001c0001t0001g0098 others(2): Show |
6 | HG01361.hp1 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.124+5196T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124887070 | |||||||
| chr7:124887144 | A | G | 1 | a0001c0001t0006g0201 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.124+5122T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124887144 | |||||||
| chr7:124887178 | T | C | 1 | a0001c0001t0006g0201 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.124+5088A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124887178 | |||||||
| chr7:124887214 | T | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0323 |
3 | HG02976.hp1 HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.124+5052A>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124887214 | |||||||
| chr7:124887376 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.124+4890C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124887376 | |||||||
| chr7:124887396 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.124+4870A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124887396 | |||||||
| chr7:124887427 | C | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.124+4839G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124887427 | |||||||
| chr7:124887467 | T | C | 1 | a0001c0001t0001g0255 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.124+4799A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124887467 | |||||||
| chr7:124887470 | T | C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0323 |
3 | HG02976.hp1 HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.124+4796A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124887470 | |||||||
| chr7:124887505 | T | G | 1 | a0001c0001t0002g0089 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.124+4761A>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124887505 | |||||||
| chr7:124887679 | C | T | 206 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(203): Show |
220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.124+4587G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124887679 | |||||||
| chr7:124887711 | G | A | 1 | a0001c0001t0001g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.124+4555C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124887711 | |||||||
| chr7:124887913 | A | G | 3 | a0001c0001t0001g0106 a0001c0001t0001g0116 a0001c0001t0001g0118 |
3 | HG03491.hp2 HG03688.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.124+4353T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124887913 | |||||||
| chr7:124887926 | C | G | 1 | a0001c0001t0001g0281 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.124+4340G>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124887926 | |||||||
| chr7:124888001 | C | T | 203 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(200): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.124+4265G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124888001 | |||||||
| chr7:124888032 | G | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.124+4234C>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124888032 | |||||||
| chr7:124888233 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.124+4033A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124888233 | |||||||
| chr7:124888366 | T | C | 1 | a0001c0001t0002g0034 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.124+3900A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124888366 | |||||||
| chr7:124888413 | T | C | 1 | a0001c0001t0002g0028 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.124+3853A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124888413 | |||||||
| chr7:124888741 | A | T | 1 | a0001c0001t0001g0249 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.124+3525T>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124888741 | |||||||
| chr7:124888780 | T | A | 1 | a0001c0001t0002g0038 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.124+3486A>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124888780 | |||||||
| chr7:124888894 | C | CCT | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.124+3370_124+3371d others(4): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124888894 | |||||||
| chr7:124889260 | C | T | 1 | a0001c0001t0002g0058 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.124+3006G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124889260 | |||||||
| chr7:124889290 | T | G | 1 | a0001c0001t0001g0223 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.124+2976A>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124889290 | |||||||
| chr7:124889511 | A | T | 2 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
2 | HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.124+2755T>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124889511 | |||||||
| chr7:124889543 | G | A | 1 | a0001c0001t0006g0201 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.124+2723C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124889543 | |||||||
| chr7:124889568 | T | C | 70 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0018 others(67): Show |
72 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.124+2698A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124889568 | |||||||
| chr7:124889700 | A | AG | 203 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(200): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.124+2565dupC | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124889700 | |||||||
| chr7:124889778 | T | C | 1 | a0001c0001t0001g0122 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.124+2488A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124889778 | |||||||
| chr7:124889800 | C | T | 1 | a0001c0002t0001g0195 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.124+2466G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124889800 | |||||||
| chr7:124890012 | C | A | 1 | a0001c0001t0001g0307 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.124+2254G>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124890012 | |||||||
| chr7:124890041 | C | G | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.124+2225G>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124890041 | |||||||
| chr7:124890061 | C | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.124+2205G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124890061 | |||||||
| chr7:124890247 | A | T | 2 | a0001c0001t0001g0100 a0007c0009t0001g0101 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.124+2019T>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124890247 | |||||||
| chr7:124890260 | A | G | 214 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(211): Show |
229 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(226): Show |
intron_variant | MODIFIER | c.124+2006T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124890260 | |||||||
| chr7:124890314 | C | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.124+1952G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124890314 | |||||||
| chr7:124890536 | G | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0105 |
3 | HG02717.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.124+1730C>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124890536 | |||||||
| chr7:124890596 | T | C | 203 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(200): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.124+1670A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124890596 | |||||||
| chr7:124890769 | C | T | 16 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(13): Show |
16 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.124+1497G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124890769 | |||||||
| chr7:124890881 | A | G | 1 | a0001c0001t0003g0184 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.124+1385T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124890881 | |||||||
| chr7:124891018 | C | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0097 others(90): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.124+1248G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124891018 | |||||||
| chr7:124891222 | A | G | 1 | a0001c0001t0006g0201 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.124+1044T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124891222 | |||||||
| chr7:124891284 | C | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.124+982G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124891284 | |||||||
| chr7:124891316 | G | A | 47 | a0001c0001t0001g0003 a0001c0001t0001g0205 a0001c0001t0001g0207 others(44): Show |
49 | HG00099.hp2 HG00323.hp2 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.124+950C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124891316 | |||||||
| chr7:124891394 | T | G | 1 | a0001c0001t0001g0228 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.124+872A>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124891394 | |||||||
| chr7:124891413 | A | C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0105 |
3 | HG02717.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.124+853T>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124891413 | |||||||
| chr7:124891415 | G | A | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.124+851C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124891415 | |||||||
| chr7:124891450 | G | A | 1 | a0001c0001t0001g0228 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.124+816C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124891450 | |||||||
| chr7:124891477 | A | C | 1 | a0001c0001t0001g0228 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.124+789T>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124891477 | |||||||
| chr7:124891515 | T | C | 1 | a0001c0001t0006g0201 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.124+751A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124891515 | |||||||
| chr7:124891515 | T | G | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.124+751A>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124891515 | |||||||
| chr7:124891543 | G | A | 1 | a0001c0001t0006g0201 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.124+723C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124891543 | |||||||
| chr7:124891591 | C | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0097 others(90): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.124+675G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124891591 | |||||||
| chr7:124891804 | A | AC | 92 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0097 others(89): Show |
101 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.124+461dupG | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124891804 | |||||||
| chr7:124892026 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.124+240C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124892026 | |||||||
| chr7:124892091 | A | G | 1 | a0001c0001t0001g0016 | 2 | HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.124+175T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124892091 | |||||||
| chr7:124892133 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.124+133A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 6/18 | chr7 | 124892133 | |||||||
| chr7:124892407 | A | G | 1 | a0001c0002t0001g0196 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.10-27T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 5/18 | chr7 | 124892407 | |||||||
| chr7:124892497 | A | G | 1 | a0001c0001t0001g0008 | 2 | HG02717.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.10-117T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 5/18 | chr7 | 124892497 | |||||||
| chr7:124892561 | A | T | 1 | a0001c0001t0001g0215 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.10-181T>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 5/18 | chr7 | 124892561 | |||||||
| chr7:124892662 | C | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.10-282G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 5/18 | chr7 | 124892662 | |||||||
| chr7:124892696 | A | T | 1 | a0001c0001t0002g0038 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.10-316T>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 5/18 | chr7 | 124892696 | |||||||
| chr7:124892703 | A | G | 3 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 |
3 | HG01099.hp2 HG01943.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.10-323T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 5/18 | chr7 | 124892703 | |||||||
| chr7:124892789 | G | GT | 8 | a0001c0001t0001g0016 a0001c0001t0001g0319 a0001c0001t0001g0320 others(5): Show |
9 | HG02486.hp1 HG02818.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.10-410dupA | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 5/18 | chr7 | 124892789 | |||||||
| chr7:124892876 | C | CT | 5 | a0001c0001t0001g0007 a0001c0001t0001g0097 a0001c0001t0001g0098 others(2): Show |
6 | HG01361.hp1 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.10-497dupA | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 5/18 | chr7 | 124892876 | |||||||
| chr7:124892884 | T | A | 85 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0035 others(82): Show |
89 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.10-504A>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 5/18 | chr7 | 124892884 | |||||||
| chr7:124893203 | T | C | 1 | a0001c0001t0001g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.10-823A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 5/18 | chr7 | 124893203 | |||||||
| chr7:124893214 | T | G | 1 | a0001c0002t0001g0172 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.10-834A>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 5/18 | chr7 | 124893214 | |||||||
| chr7:124893238 | A | C | 6 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(3): Show |
6 | HG00099.hp2 HG01070.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.10-858T>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 5/18 | chr7 | 124893238 | |||||||
| chr7:124893626 | C | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.10-1246G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 5/18 | chr7 | 124893626 | |||||||
| chr7:124893673 | C | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0105 |
3 | HG02717.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.10-1293G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 5/18 | chr7 | 124893673 | |||||||
| chr7:124893686 | C | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.10-1306G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 5/18 | chr7 | 124893686 | |||||||
| chr7:124893876 | T | G | 1 | a0001c0001t0002g0028 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.10-1496A>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 5/18 | chr7 | 124893876 | |||||||
| chr7:124894332 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.10-1952C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 5/18 | chr7 | 124894332 | |||||||
| chr7:124894371 | C | T | 5 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
5 | HG02055.hp2 HG02280.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.10-1991G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 5/18 | chr7 | 124894371 | |||||||
| chr7:124894392 | G | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0097 others(90): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.10-2012C>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 5/18 | chr7 | 124894392 | |||||||
| chr7:124894907 | C | T | 1 | a0001c0001t0001g0169 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.9+2258G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 5/18 | chr7 | 124894907 | |||||||
| chr7:124895199 | A | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.9+1966T>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 5/18 | chr7 | 124895199 | |||||||
| chr7:124895320 | C | T | 2 | a0001c0001t0001g0016 a0001c0001t0001g0323 |
3 | HG02976.hp1 HG03486.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.9+1845G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 5/18 | chr7 | 124895320 | |||||||
| chr7:124895396 | G | A | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.9+1769C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 5/18 | chr7 | 124895396 | |||||||
| chr7:124895523 | C | T | 2 | a0001c0001t0003g0180 a0001c0001t0003g0183 |
2 | HG02523.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.9+1642G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 5/18 | chr7 | 124895523 | |||||||
| chr7:124895560 | T | TA | 93 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0097 others(90): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.9+1604_9+1605insT | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 5/18 | chr7 | 124895560 | |||||||
| chr7:124895562 | A | C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0105 |
3 | HG02717.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.9+1603T>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 5/18 | chr7 | 124895562 | |||||||
| chr7:124895663 | G | A | 1 | a0001c0001t0002g0078 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.9+1502C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 5/18 | chr7 | 124895663 | |||||||
| chr7:124895842 | G | A | 2 | a0001c0001t0001g0129 a0001c0001t0001g0131 |
2 | HG01346.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.9+1323C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 5/18 | chr7 | 124895842 | |||||||
| chr7:124896052 | A | ACACTTTT others(13): Show |
1 | a0001c0001t0003g0133 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.9+1093_9+1112dupAG others(18): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 5/18 | chr7 | 124896052 | |||||||
| chr7:124896184 | A | G | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.9+981T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 5/18 | chr7 | 124896184 | |||||||
| chr7:124896280 | G | A | 1 | a0001c0001t0001g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.9+885C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 5/18 | chr7 | 124896280 | |||||||
| chr7:124896348 | A | C | 16 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(13): Show |
16 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.9+817T>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 5/18 | chr7 | 124896348 | |||||||
| chr7:124896490 | C | T | 2 | a0001c0001t0001g0279 a0001c0001t0001g0280 |
2 | HG00673.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.9+675G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 5/18 | chr7 | 124896490 | |||||||
| chr7:124896504 | C | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.9+661G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 5/18 | chr7 | 124896504 | |||||||
| chr7:124896622 | C | T | 1 | a0001c0001t0003g0158 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.9+543G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 5/18 | chr7 | 124896622 | |||||||
| chr7:124896859 | C | A | 80 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0036 others(77): Show |
83 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.9+306G>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 5/18 | chr7 | 124896859 | |||||||
| chr7:124896986 | T | C | 8 | a0001c0001t0001g0016 a0001c0001t0001g0319 a0001c0001t0001g0320 others(5): Show |
9 | HG02486.hp1 HG02818.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.9+179A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 5/18 | chr7 | 124896986 | |||||||
| chr7:124897049 | A | G | 1 | a0001c0001t0003g0158 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.9+116T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 5/18 | chr7 | 124897049 | |||||||
| chr7:124897380 | A | G | 3 | a0001c0001t0001g0100 a0001c0001t0001g0102 a0007c0009t0001g0101 |
3 | HG02895.hp2 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-39-168T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 4/18 | chr7 | 124897380 | |||||||
| chr7:124897393 | TA | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.-39-182delT | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 4/18 | chr7 | 124897393 | |||||||
| chr7:124897422 | A | C | 71 | a0001c0001t0001g0088 a0001c0001t0002g0005 a0001c0001t0002g0017 others(68): Show |
73 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.-39-210T>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 4/18 | chr7 | 124897422 | |||||||
| chr7:124897438 | A | G | 1 | a0001c0001t0003g0023 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-39-226T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 4/18 | chr7 | 124897438 | |||||||
| chr7:124897560 | T | C | 1 | a0001c0001t0003g0139 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.-39-348A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 4/18 | chr7 | 124897560 | |||||||
| chr7:124897615 | A | C | 3 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 |
3 | HG01099.hp2 HG01943.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-39-403T>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 4/18 | chr7 | 124897615 | |||||||
| chr7:124897859 | A | G | 6 | a0001c0001t0002g0053 a0001c0001t0002g0054 a0001c0001t0002g0055 others(3): Show |
6 | HG01934.hp2 NA18954.hp2 NA18995.hp2 others(3): Show |
intron_variant | MODIFIER | c.-40+402T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 4/18 | chr7 | 124897859 | |||||||
| chr7:124897980 | G | A | 1 | a0001c0001t0003g0167 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-40+281C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 4/18 | chr7 | 124897980 | |||||||
| chr7:124897982 | C | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.-40+279G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 4/18 | chr7 | 124897982 | |||||||
| chr7:124897994 | G | C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0105 |
3 | HG02717.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-40+267C>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 4/18 | chr7 | 124897994 | |||||||
| chr7:124898099 | C | A | 5 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 others(2): Show |
5 | HG00140.hp2 HG00280.hp2 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.-40+162G>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 4/18 | chr7 | 124898099 | |||||||
| chr7:124898211 | T | C | 3 | a0001c0001t0001g0100 a0001c0001t0001g0102 a0007c0009t0001g0101 |
3 | HG02895.hp2 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-40+50A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 4/18 | chr7 | 124898211 | |||||||
| chr7:124898231 | G | A | 206 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(203): Show |
220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.-40+30C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 4/18 | chr7 | 124898231 | |||||||
| chr7:124898382 | GA | G | 5 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
5 | HG02055.hp2 HG02280.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-153-9delT | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124898382 | |||||||
| chr7:124898536 | A | G | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.-153-162T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124898536 | |||||||
| chr7:124898561 | C | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0097 others(90): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.-153-187G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124898561 | |||||||
| chr7:124898764 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-153-390G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124898764 | |||||||
| chr7:124898831 | T | C | 3 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 |
3 | HG01099.hp2 HG01943.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-153-457A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124898831 | |||||||
| chr7:124899297 | A | C | 7 | a0001c0001t0001g0003 a0001c0001t0001g0205 a0001c0001t0001g0224 others(4): Show |
9 | HG01255.hp1 HG01433.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.-153-923T>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124899297 | |||||||
| chr7:124899483 | T | C | 206 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(203): Show |
220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.-153-1109A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124899483 | |||||||
| chr7:124899488 | C | T | 195 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(192): Show |
208 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.-153-1114G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124899488 | |||||||
| chr7:124899505 | T | C | 17 | a0001c0001t0003g0002 a0001c0001t0003g0135 a0001c0001t0003g0136 others(14): Show |
19 | HG00423.hp1 HG00544.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.-153-1131A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124899505 | |||||||
| chr7:124899683 | C | T | 1 | a0001c0001t0001g0223 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-153-1309G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124899683 | |||||||
| chr7:124899684 | G | A | 1 | a0001c0001t0001g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-153-1310C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124899684 | |||||||
| chr7:124899699 | G | A | 3 | a0001c0001t0001g0100 a0001c0001t0001g0102 a0007c0009t0001g0101 |
3 | HG02895.hp2 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-153-1325C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124899699 | |||||||
| chr7:124899741 | GA | G | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.-153-1368delT | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124899741 | |||||||
| chr7:124899804 | T | A | 3 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 |
3 | HG02647.hp1 HG02896.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-153-1430A>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124899804 | |||||||
| chr7:124899888 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-153-1514C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124899888 | |||||||
| chr7:124900114 | A | G | 1 | a0001c0001t0002g0089 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-153-1740T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124900114 | |||||||
| chr7:124900400 | T | C | 3 | a0001c0001t0002g0052 a0001c0001t0002g0079 a0001c0001t0002g0080 |
3 | NA18978.hp1 NA19011.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.-153-2026A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124900400 | |||||||
| chr7:124900481 | T | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.-153-2107A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124900481 | |||||||
| chr7:124900525 | T | C | 1 | a0001c0001t0001g0202 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-153-2151A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124900525 | |||||||
| chr7:124900597 | C | T | 1 | a0001c0001t0001g0036 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-153-2223G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124900597 | |||||||
| chr7:124900718 | T | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.-153-2344A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124900718 | |||||||
| chr7:124900728 | C | T | 13 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(10): Show |
13 | HG00544.hp1 NA18954.hp1 NA18955.hp1 others(10): Show |
intron_variant | MODIFIER | c.-153-2354G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124900728 | |||||||
| chr7:124900787 | A | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.-153-2413T>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124900787 | |||||||
| chr7:124900818 | C | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.-153-2444G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124900818 | |||||||
| chr7:124900859 | C | A | 5 | a0001c0001t0001g0008 a0001c0001t0001g0100 a0001c0001t0001g0102 others(2): Show |
6 | HG02717.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-153-2485G>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124900859 | |||||||
| chr7:124900877 | T | G | 1 | a0001c0001t0002g0081 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-153-2503A>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124900877 | |||||||
| chr7:124900915 | C | G | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.-153-2541G>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124900915 | |||||||
| chr7:124900939 | G | A | 1 | a0001c0001t0006g0201 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-153-2565C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124900939 | |||||||
| chr7:124900968 | T | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0097 others(90): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.-153-2594A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124900968 | |||||||
| chr7:124900993 | G | A | 5 | a0001c0001t0001g0008 a0001c0001t0001g0100 a0001c0001t0001g0102 others(2): Show |
6 | HG02717.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-153-2619C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124900993 | |||||||
| chr7:124901338 | G | A | 2 | a0001c0001t0002g0087 a0001c0001t0010g0327 |
2 | HG02602.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.-153-2964C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124901338 | |||||||
| chr7:124901587 | A | G | 1 | a0001c0001t0003g0153 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-153-3213T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124901587 | |||||||
| chr7:124901614 | C | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.-153-3240G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124901614 | |||||||
| chr7:124901760 | C | T | 9 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0319 others(6): Show |
11 | HG02486.hp1 HG02717.hp2 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.-153-3386G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124901760 | |||||||
| chr7:124901823 | G | T | 1 | a0001c0001t0003g0133 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-153-3449C>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124901823 | |||||||
| chr7:124901952 | A | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(192): Show |
208 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.-153-3578T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124901952 | |||||||
| chr7:124902048 | G | C | 3 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 |
3 | HG01099.hp2 HG01943.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-153-3674C>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124902048 | |||||||
| chr7:124902072 | G | A | 93 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0097 others(90): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.-153-3698C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124902072 | |||||||
| chr7:124902134 | C | T | 206 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(203): Show |
220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.-153-3760G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124902134 | |||||||
| chr7:124902176 | C | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.-153-3802G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124902176 | |||||||
| chr7:124902221 | C | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.-153-3847G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124902221 | |||||||
| chr7:124902395 | T | G | 5 | a0001c0001t0001g0007 a0001c0001t0001g0097 a0001c0001t0001g0098 others(2): Show |
6 | HG01361.hp1 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-153-4021A>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124902395 | |||||||
| chr7:124902626 | A | G | 1 | a0001c0001t0002g0083 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-153-4252T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124902626 | |||||||
| chr7:124902721 | A | C | 1 | a0001c0001t0002g0052 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-153-4347T>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124902721 | |||||||
| chr7:124902726 | A | C | 206 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(203): Show |
220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.-153-4352T>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124902726 | |||||||
| chr7:124902780 | C | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.-153-4406G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124902780 | |||||||
| chr7:124902803 | T | C | 1 | a0001c0001t0006g0201 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-153-4429A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124902803 | |||||||
| chr7:124902943 | G | A | 1 | a0001c0001t0001g0308 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-153-4569C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124902943 | |||||||
| chr7:124902957 | G | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.-153-4583C>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124902957 | |||||||
| chr7:124902968 | A | G | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.-153-4594T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124902968 | |||||||
| chr7:124903155 | C | T | 102 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0035 others(99): Show |
106 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.-153-4781G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124903155 | |||||||
| chr7:124903170 | C | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0105 |
3 | HG02717.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-153-4796G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124903170 | |||||||
| chr7:124903171 | G | A | 1 | a0001c0001t0003g0186 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-153-4797C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124903171 | |||||||
| chr7:124903249 | C | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.-153-4875G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124903249 | |||||||
| chr7:124903257 | C | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.-153-4883G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124903257 | |||||||
| chr7:124903734 | G | C | 1 | a0001c0001t0002g0051 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-153-5360C>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124903734 | |||||||
| chr7:124903739 | A | T | 1 | a0001c0001t0002g0033 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-153-5365T>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124903739 | |||||||
| chr7:124903786 | A | G | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.-153-5412T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124903786 | |||||||
| chr7:124903791 | GAAGAA | G | 59 | a0001c0001t0003g0002 a0001c0001t0003g0009 a0001c0001t0003g0010 others(56): Show |
65 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.-153-5422_-153-541 others(9): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124903791 | |||||||
| chr7:124903794 | G | A | 3 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 |
3 | HG00140.hp2 HG00280.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.-153-5420C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124903794 | |||||||
| chr7:124903848 | T | A | 101 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0035 others(98): Show |
105 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.-153-5474A>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124903848 | |||||||
| chr7:124903926 | G | T | 9 | a0001c0001t0002g0044 a0001c0001t0002g0045 a0001c0001t0002g0046 others(6): Show |
9 | HG00423.hp2 HG00597.hp1 NA18942.hp1 others(6): Show |
intron_variant | MODIFIER | c.-153-5552C>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124903926 | |||||||
| chr7:124903972 | G | T | 80 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0036 others(77): Show |
83 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.-153-5598C>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124903972 | |||||||
| chr7:124904059 | A | G | 206 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(203): Show |
220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.-153-5685T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124904059 | |||||||
| chr7:124904230 | C | T | 1 | a0001c0002t0001g0193 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-153-5856G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124904230 | |||||||
| chr7:124904255 | T | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.-153-5881A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124904255 | |||||||
| chr7:124904267 | A | G | 1 | a0001c0001t0003g0179 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-153-5893T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124904267 | |||||||
| chr7:124904348 | A | C | 1 | a0001c0001t0001g0093 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-153-5974T>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124904348 | |||||||
| chr7:124904358 | C | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0097 others(90): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.-153-5984G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124904358 | |||||||
| chr7:124904415 | C | T | 1 | a0001c0001t0001g0222 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-153-6041G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124904415 | |||||||
| chr7:124904416 | G | A | 70 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0018 others(67): Show |
72 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.-153-6042C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124904416 | |||||||
| chr7:124904508 | A | G | 70 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0018 others(67): Show |
72 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.-153-6134T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124904508 | |||||||
| chr7:124904534 | A | G | 70 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0018 others(67): Show |
72 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.-153-6160T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124904534 | |||||||
| chr7:124904604 | C | T | 1 | a0001c0001t0001g0278 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-153-6230G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124904604 | |||||||
| chr7:124904643 | C | A | 5 | a0001c0001t0001g0007 a0001c0001t0001g0097 a0001c0001t0001g0098 others(2): Show |
6 | HG01361.hp1 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-153-6269G>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124904643 | |||||||
| chr7:124904644 | AG | A | 101 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0035 others(98): Show |
105 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.-153-6271delC | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124904644 | |||||||
| chr7:124904731 | A | G | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.-153-6357T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124904731 | |||||||
| chr7:124904933 | C | T | 3 | a0001c0001t0001g0100 a0001c0001t0001g0102 a0007c0009t0001g0101 |
3 | HG02895.hp2 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-153-6559G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124904933 | |||||||
| chr7:124904999 | C | G | 1 | a0001c0001t0003g0152 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-153-6625G>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124904999 | |||||||
| chr7:124905123 | T | C | 1 | a0001c0001t0002g0084 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-153-6749A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124905123 | |||||||
| chr7:124905172 | A | G | 16 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(13): Show |
16 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.-153-6798T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124905172 | |||||||
| chr7:124905217 | C | T | 5 | a0001c0001t0001g0008 a0001c0001t0001g0100 a0001c0001t0001g0102 others(2): Show |
6 | HG02717.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-153-6843G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124905217 | |||||||
| chr7:124905371 | G | A | 2 | a0001c0001t0003g0150 a0001c0001t0003g0173 |
2 | HG02698.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-153-6997C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124905371 | |||||||
| chr7:124905506 | T | C | 1 | a0001c0001t0006g0201 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-153-7132A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124905506 | |||||||
| chr7:124905641 | C | G | 1 | a0001c0001t0007g0096 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-153-7267G>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124905641 | |||||||
| chr7:124905691 | C | G | 2 | a0001c0001t0001g0035 a0003c0006t0009g0103 |
2 | HG02258.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-153-7317G>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124905691 | |||||||
| chr7:124905703 | T | C | 1 | a0001c0001t0002g0089 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-153-7329A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124905703 | |||||||
| chr7:124905828 | G | GAT | 5 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(2): Show |
5 | HG02055.hp2 HG02280.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.-153-7456_-153-745 others(6): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124905828 | |||||||
| chr7:124906007 | T | C | 190 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(187): Show |
203 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.-153-7633A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124906007 | |||||||
| chr7:124906078 | C | T | 1 | a0005c0012t0002g0039 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-153-7704G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124906078 | |||||||
| chr7:124906079 | G | A | 1 | a0001c0001t0002g0082 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-153-7705C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124906079 | |||||||
| chr7:124906125 | C | A | 1 | a0001c0001t0006g0201 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-153-7751G>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124906125 | |||||||
| chr7:124906125 | C | T | 3 | a0001c0001t0001g0100 a0001c0001t0001g0102 a0007c0009t0001g0101 |
3 | HG02895.hp2 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-153-7751G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124906125 | |||||||
| chr7:124906234 | T | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.-153-7860A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124906234 | |||||||
| chr7:124906309 | G | A | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.-153-7935C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124906309 | |||||||
| chr7:124906361 | C | A | 1 | a0001c0001t0003g0186 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-153-7987G>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124906361 | |||||||
| chr7:124906455 | C | A | 1 | a0001c0001t0002g0083 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-153-8081G>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124906455 | |||||||
| chr7:124906478 | G | A | 94 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0097 others(91): Show |
103 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.-153-8104C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124906478 | |||||||
| chr7:124906558 | C | T | 1 | a0001c0001t0003g0133 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-153-8184G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124906558 | |||||||
| chr7:124906570 | G | A | 1 | a0001c0001t0001g0305 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-153-8196C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124906570 | |||||||
| chr7:124906578 | T | C | 1 | a0001c0001t0001g0306 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-153-8204A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124906578 | |||||||
| chr7:124906589 | G | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.-153-8215C>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124906589 | |||||||
| chr7:124906604 | G | A | 1 | a0001c0001t0003g0183 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-153-8230C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124906604 | |||||||
| chr7:124906791 | A | G | 6 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0242 others(3): Show |
6 | HG01496.hp2 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-153-8417T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124906791 | |||||||
| chr7:124906895 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-153-8521A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124906895 | |||||||
| chr7:124907261 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-154+8313C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124907261 | |||||||
| chr7:124907339 | T | G | 6 | a0001c0001t0001g0240 a0001c0001t0001g0241 a0001c0001t0001g0242 others(3): Show |
6 | HG01496.hp2 HG02258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.-154+8235A>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124907339 | |||||||
| chr7:124907455 | C | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 |
3 | HG01099.hp2 HG01943.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-154+8119G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124907455 | |||||||
| chr7:124907457 | A | G | 2 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
2 | HG00597.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.-154+8117T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124907457 | |||||||
| chr7:124907490 | GT | G | 80 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0036 others(77): Show |
83 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.-154+8083delA | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124907490 | |||||||
| chr7:124907537 | C | T | 6 | a0001c0001t0001g0008 a0001c0001t0001g0100 a0001c0001t0001g0102 others(3): Show |
7 | HG02717.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-154+8037G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124907537 | |||||||
| chr7:124907565 | A | G | 1 | a0001c0001t0002g0086 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-154+8009T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124907565 | |||||||
| chr7:124908110 | G | T | 1 | a0001c0001t0001g0214 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-154+7464C>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124908110 | |||||||
| chr7:124908342 | A | G | 1 | a0001c0001t0006g0201 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-154+7232T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124908342 | |||||||
| chr7:124908403 | A | C | 1 | a0001c0001t0001g0122 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-154+7171T>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124908403 | |||||||
| chr7:124908422 | A | C | 1 | a0001c0001t0002g0043 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-154+7152T>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124908422 | |||||||
| chr7:124908583 | A | G | 5 | a0001c0001t0001g0007 a0001c0001t0001g0097 a0001c0001t0001g0098 others(2): Show |
6 | HG01361.hp1 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-154+6991T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124908583 | |||||||
| chr7:124908620 | ACATAT | A | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.-154+6949_-154+695 others(9): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124908620 | |||||||
| chr7:124908642 | A | G | 16 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(13): Show |
16 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.-154+6932T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124908642 | |||||||
| chr7:124908836 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-154+6738C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124908836 | |||||||
| chr7:124909020 | CCAAATCT others(14): Show |
C | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | HG02074.hp1 NA18747.hp2 |
intron_variant | MODIFIER | c.-154+6533_-154+655 others(25): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124909020 | |||||||
| chr7:124909053 | C | T | 5 | a0001c0001t0001g0007 a0001c0001t0001g0097 a0001c0001t0001g0098 others(2): Show |
6 | HG01361.hp1 HG02486.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.-154+6521G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124909053 | |||||||
| chr7:124909092 | G | A | 1 | a0001c0001t0003g0184 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-154+6482C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124909092 | |||||||
| chr7:124909104 | T | C | 1 | a0001c0001t0001g0008 | 2 | HG02717.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-154+6470A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124909104 | |||||||
| chr7:124909279 | T | A | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.-154+6295A>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124909279 | |||||||
| chr7:124909519 | T | C | 101 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0035 others(98): Show |
105 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.-154+6055A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124909519 | |||||||
| chr7:124909677 | G | A | 1 | a0001c0002t0001g0193 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-154+5897C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124909677 | |||||||
| chr7:124909818 | G | A | 1 | a0001c0001t0006g0201 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-154+5756C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124909818 | |||||||
| chr7:124909922 | C | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.-154+5652G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124909922 | |||||||
| chr7:124910052 | C | T | 5 | a0001c0001t0001g0008 a0001c0001t0001g0100 a0001c0001t0001g0102 others(2): Show |
6 | HG02717.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-154+5522G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124910052 | |||||||
| chr7:124910079 | A | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0097 others(90): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.-154+5495T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124910079 | |||||||
| chr7:124910342 | T | G | 1 | a0001c0001t0001g0105 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-154+5232A>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124910342 | |||||||
| chr7:124910381 | T | C | 1 | a0001c0001t0006g0201 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-154+5193A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124910381 | |||||||
| chr7:124910472 | C | T | 80 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0036 others(77): Show |
83 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.-154+5102G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124910472 | |||||||
| chr7:124910634 | A | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0097 others(90): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.-154+4940T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124910634 | |||||||
| chr7:124910764 | T | C | 3 | a0001c0001t0001g0100 a0001c0001t0001g0102 a0007c0009t0001g0101 |
3 | HG02895.hp2 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-154+4810A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124910764 | |||||||
| chr7:124910859 | A | C | 1 | a0001c0011t0001g0275 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.-154+4715T>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124910859 | |||||||
| chr7:124910896 | C | G | 2 | a0001c0001t0001g0106 a0001c0001t0001g0118 |
2 | HG03688.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-154+4678G>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124910896 | |||||||
| chr7:124911122 | T | C | 1 | a0001c0001t0001g0246 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.-154+4452A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124911122 | |||||||
| chr7:124911180 | C | G | 1 | a0001c0002t0001g0194 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-154+4394G>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124911180 | |||||||
| chr7:124911256 | T | C | 5 | a0001c0001t0001g0008 a0001c0001t0001g0100 a0001c0001t0001g0102 others(2): Show |
6 | HG02717.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-154+4318A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124911256 | |||||||
| chr7:124911264 | G | C | 5 | a0001c0001t0001g0008 a0001c0001t0001g0100 a0001c0001t0001g0102 others(2): Show |
6 | HG02717.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-154+4310C>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124911264 | |||||||
| chr7:124911355 | T | C | 1 | a0001c0001t0001g0255 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-154+4219A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124911355 | |||||||
| chr7:124911411 | G | T | 3 | a0001c0001t0001g0100 a0001c0001t0001g0102 a0007c0009t0001g0101 |
3 | HG02895.hp2 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-154+4163C>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124911411 | |||||||
| chr7:124911443 | C | T | 4 | a0001c0001t0001g0271 a0001c0001t0001g0272 a0001c0001t0001g0273 others(1): Show |
4 | NA19002.hp2 NA19012.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.-154+4131G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124911443 | |||||||
| chr7:124911603 | C | T | 3 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 |
3 | HG01099.hp2 HG01943.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-154+3971G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124911603 | |||||||
| chr7:124911672 | T | C | 1 | a0001c0001t0002g0085 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-154+3902A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124911672 | |||||||
| chr7:124911815 | G | A | 10 | a0001c0001t0001g0211 a0001c0001t0001g0212 a0001c0001t0001g0247 others(7): Show |
10 | HG00621.hp2 HG01516.hp2 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.-154+3759C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124911815 | |||||||
| chr7:124911855 | C | T | 8 | a0001c0001t0001g0016 a0001c0001t0001g0319 a0001c0001t0001g0320 others(5): Show |
9 | HG02486.hp1 HG02818.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.-154+3719G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124911855 | |||||||
| chr7:124911871 | T | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.-154+3703A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124911871 | |||||||
| chr7:124912166 | G | T | 2 | a0001c0001t0001g0106 a0001c0001t0001g0118 |
2 | HG03688.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-154+3408C>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124912166 | |||||||
| chr7:124912249 | GA | G | 7 | a0001c0001t0001g0319 a0001c0001t0001g0320 a0001c0001t0001g0321 others(4): Show |
7 | HG01255.hp2 HG02486.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.-154+3324delT | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124912249 | |||||||
| chr7:124912250 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-154+3324T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124912250 | |||||||
| chr7:124912266 | G | A | 2 | a0001c0001t0003g0011 a0001c0001t0003g0174 |
3 | NA18965.hp2 NA18985.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.-154+3308C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124912266 | |||||||
| chr7:124912339 | T | C | 1 | a0001c0001t0001g0254 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-154+3235A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124912339 | |||||||
| chr7:124912393 | T | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.-154+3181A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124912393 | |||||||
| chr7:124912728 | G | A | 5 | a0001c0001t0001g0008 a0001c0001t0001g0100 a0001c0001t0001g0102 others(2): Show |
6 | HG02717.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-154+2846C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124912728 | |||||||
| chr7:124912748 | C | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.-154+2826G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124912748 | |||||||
| chr7:124912826 | G | A | 93 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0097 others(90): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.-154+2748C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124912826 | |||||||
| chr7:124912918 | T | C | 1 | a0001c0001t0001g0307 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-154+2656A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124912918 | |||||||
| chr7:124912939 | C | T | 6 | a0001c0001t0001g0006 a0001c0001t0001g0091 a0001c0001t0001g0092 others(3): Show |
7 | HG02257.hp2 HG02622.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.-154+2635G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124912939 | |||||||
| chr7:124912953 | A | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.-154+2621T>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124912953 | |||||||
| chr7:124912988 | C | T | 1 | a0001c0001t0006g0201 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-154+2586G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124912988 | |||||||
| chr7:124913117 | T | G | 2 | a0001c0001t0002g0084 a0001c0001t0002g0085 |
2 | HG00140.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-154+2457A>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124913117 | |||||||
| chr7:124913124 | A | T | 1 | a0001c0001t0001g0105 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-154+2450T>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124913124 | |||||||
| chr7:124913292 | A | T | 2 | a0001c0001t0002g0031 a0001c0001t0002g0032 |
2 | NA18940.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.-154+2282T>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124913292 | |||||||
| chr7:124913349 | A | G | 2 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
2 | HG02647.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.-154+2225T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124913349 | |||||||
| chr7:124913577 | T | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0097 others(90): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.-154+1997A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124913577 | |||||||
| chr7:124913736 | AT | A | 93 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0097 others(90): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.-154+1837delA | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124913736 | |||||||
| chr7:124913939 | T | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0097 others(90): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.-154+1635A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124913939 | |||||||
| chr7:124914003 | T | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.-154+1571A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124914003 | |||||||
| chr7:124914136 | G | GA | 103 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0035 others(100): Show |
107 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.-154+1437dupT | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124914136 | |||||||
| chr7:124914136 | G | GAA | 89 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0098 others(86): Show |
98 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.-154+1436_-154+143 others(6): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124914136 | |||||||
| chr7:124914136 | GA | G | 11 | a0001c0001t0001g0016 a0001c0001t0001g0220 a0001c0001t0001g0221 others(8): Show |
12 | HG02486.hp1 HG02818.hp1 HG02895.hp1 others(9): Show |
intron_variant | MODIFIER | c.-154+1437delT | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124914136 | |||||||
| chr7:124914213 | C | A | 101 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0035 others(98): Show |
105 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(102): Show |
intron_variant | MODIFIER | c.-154+1361G>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124914213 | |||||||
| chr7:124914236 | G | A | 1 | a0001c0001t0002g0086 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.-154+1338C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124914236 | |||||||
| chr7:124914310 | C | T | 70 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0018 others(67): Show |
72 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.-154+1264G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124914310 | |||||||
| chr7:124914408 | C | A | 1 | a0001c0001t0003g0191 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-154+1166G>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124914408 | |||||||
| chr7:124914477 | A | G | 8 | a0001c0001t0001g0016 a0001c0001t0001g0319 a0001c0001t0001g0320 others(5): Show |
9 | HG02486.hp1 HG02818.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.-154+1097T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124914477 | |||||||
| chr7:124914640 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-154+934G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124914640 | |||||||
| chr7:124914873 | C | T | 203 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(200): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.-154+701G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124914873 | |||||||
| chr7:124915052 | C | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0105 |
3 | HG02717.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-154+522G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124915052 | |||||||
| chr7:124915106 | C | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0097 others(90): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.-154+468G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124915106 | |||||||
| chr7:124915225 | C | A | 5 | a0001c0001t0001g0008 a0001c0001t0001g0100 a0001c0001t0001g0102 others(2): Show |
6 | HG02717.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-154+349G>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124915225 | |||||||
| chr7:124915263 | A | C | 1 | a0001c0001t0001g0203 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-154+311T>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 3/18 | chr7 | 124915263 | |||||||
| chr7:124915746 | T | G | 1 | a0001c0001t0001g0131 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-226-100A>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124915746 | |||||||
| chr7:124915801 | T | C | 203 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(200): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.-226-155A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124915801 | |||||||
| chr7:124915995 | A | T | 1 | a0001c0001t0003g0191 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-226-349T>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124915995 | |||||||
| chr7:124916202 | T | C | 1 | a0001c0001t0002g0087 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-226-556A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124916202 | |||||||
| chr7:124916419 | A | G | 2 | a0001c0001t0001g0008 a0001c0001t0001g0105 |
3 | HG02717.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-226-773T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124916419 | |||||||
| chr7:124916511 | G | C | 4 | a0001c0001t0001g0007 a0001c0001t0001g0097 a0001c0001t0001g0098 others(1): Show |
5 | HG01361.hp1 HG02572.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-226-865C>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124916511 | |||||||
| chr7:124916532 | T | A | 8 | a0001c0001t0001g0016 a0001c0001t0001g0319 a0001c0001t0001g0320 others(5): Show |
9 | HG02486.hp1 HG02818.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.-226-886A>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124916532 | |||||||
| chr7:124916605 | A | G | 70 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0018 others(67): Show |
72 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.-226-959T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124916605 | |||||||
| chr7:124916836 | C | T | 3 | a0001c0001t0001g0100 a0001c0001t0001g0102 a0007c0009t0001g0101 |
3 | HG02895.hp2 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-226-1190G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124916836 | |||||||
| chr7:124916971 | C | CA | 10 | a0001c0001t0001g0008 a0001c0001t0003g0140 a0001c0002t0001g0193 others(7): Show |
11 | HG00639.hp2 HG01433.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.-226-1326dupT | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124916971 | |||||||
| chr7:124917389 | G | A | 1 | a0001c0001t0001g0255 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-226-1743C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124917389 | |||||||
| chr7:124917495 | A | G | 80 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0036 others(77): Show |
83 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.-226-1849T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124917495 | |||||||
| chr7:124917539 | C | T | 5 | a0001c0001t0002g0033 a0001c0001t0002g0040 a0001c0001t0002g0041 others(2): Show |
5 | HG00609.hp1 HG00621.hp1 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.-226-1893G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124917539 | |||||||
| chr7:124917558 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-226-1912G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124917558 | |||||||
| chr7:124917654 | A | T | 2 | a0001c0001t0001g0268 a0001c0001t0001g0269 |
2 | NA18957.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.-226-2008T>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124917654 | |||||||
| chr7:124917657 | A | T | 324 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(321): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.-226-2011T>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124917657 | |||||||
| chr7:124917712 | C | T | 8 | a0001c0001t0001g0016 a0001c0001t0001g0319 a0001c0001t0001g0320 others(5): Show |
9 | HG02486.hp1 HG02818.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.-226-2066G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124917712 | |||||||
| chr7:124917861 | A | G | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.-226-2215T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124917861 | |||||||
| chr7:124917889 | C | T | 6 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0216 others(3): Show |
6 | HG00323.hp2 HG01358.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.-226-2243G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124917889 | |||||||
| chr7:124917934 | G | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0097 others(90): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.-226-2288C>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124917934 | |||||||
| chr7:124918285 | T | C | 203 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(200): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.-226-2639A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124918285 | |||||||
| chr7:124918373 | G | C | 1 | a0001c0001t0001g0308 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-226-2727C>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124918373 | |||||||
| chr7:124918531 | T | G | 1 | a0001c0001t0001g0117 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-226-2885A>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124918531 | |||||||
| chr7:124918612 | A | G | 1 | a0001c0001t0008g0261 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-226-2966T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124918612 | |||||||
| chr7:124918782 | G | A | 88 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0123 others(85): Show |
96 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.-226-3136C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124918782 | |||||||
| chr7:124918802 | G | A | 1 | a0001c0001t0001g0256 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-226-3156C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124918802 | |||||||
| chr7:124918871 | G | C | 1 | a0001c0001t0001g0256 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-226-3225C>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124918871 | |||||||
| chr7:124919032 | T | C | 1 | a0001c0001t0003g0175 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-226-3386A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124919032 | |||||||
| chr7:124919186 | G | A | 1 | a0001c0003t0001g0309 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-226-3540C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124919186 | |||||||
| chr7:124919259 | G | A | 1 | a0001c0001t0001g0324 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-226-3613C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124919259 | |||||||
| chr7:124919280 | A | C | 3 | a0001c0001t0001g0100 a0001c0001t0001g0102 a0007c0009t0001g0101 |
3 | HG02895.hp2 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-226-3634T>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124919280 | |||||||
| chr7:124919294 | T | C | 3 | a0001c0001t0001g0100 a0001c0001t0001g0102 a0007c0009t0001g0101 |
3 | HG02895.hp2 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-226-3648A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124919294 | |||||||
| chr7:124919474 | T | C | 1 | a0001c0001t0001g0257 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-226-3828A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124919474 | |||||||
| chr7:124919601 | AAC | A | 2 | a0001c0001t0003g0002 a0001c0001t0003g0176 |
4 | HG00423.hp1 HG02040.hp2 NA18939.hp2 others(1): Show |
intron_variant | MODIFIER | c.-226-3957_-226-395 others(6): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124919601 | |||||||
| chr7:124919840 | C | T | 1 | a0001c0001t0002g0038 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-226-4194G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124919840 | |||||||
| chr7:124919897 | C | T | 1 | a0001c0001t0002g0037 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-226-4251G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124919897 | |||||||
| chr7:124919975 | TACTACCT others(28): Show |
T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0097 others(90): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.-226-4364_-226-433 others(39): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124919975 | |||||||
| chr7:124920012 | C | A | 3 | a0001c0001t0001g0092 a0001c0001t0001g0093 a0001c0001t0001g0094 |
3 | HG02622.hp2 HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-226-4366G>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124920012 | |||||||
| chr7:124920097 | T | C | 9 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0036 others(6): Show |
10 | HG02257.hp2 HG02258.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.-226-4451A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124920097 | |||||||
| chr7:124920231 | C | G | 8 | a0001c0001t0003g0022 a0001c0001t0003g0142 a0001c0001t0003g0144 others(5): Show |
8 | HG01070.hp2 HG01261.hp2 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.-226-4585G>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124920231 | |||||||
| chr7:124920331 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-226-4685G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124920331 | |||||||
| chr7:124920462 | C | T | 1 | a0002c0005t0001g0213 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-226-4816G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124920462 | |||||||
| chr7:124920463 | G | A | 1 | a0001c0001t0001g0095 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-226-4817C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124920463 | |||||||
| chr7:124920666 | CT | C | 196 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(193): Show |
209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.-226-5021delA | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124920666 | |||||||
| chr7:124920795 | T | C | 3 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 |
3 | HG01099.hp2 HG01943.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-226-5149A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124920795 | |||||||
| chr7:124920938 | A | T | 18 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(15): Show |
18 | HG00438.hp1 HG01884.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.-226-5292T>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124920938 | |||||||
| chr7:124920939 | T | A | 2 | a0001c0001t0003g0177 a0001c0001t0003g0178 |
2 | HG02293.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.-226-5293A>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124920939 | |||||||
| chr7:124921005 | A | G | 324 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(321): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.-226-5359T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124921005 | |||||||
| chr7:124921061 | C | G | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.-226-5415G>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124921061 | |||||||
| chr7:124921078 | C | T | 1 | a0001c0001t0003g0143 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-226-5432G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124921078 | |||||||
| chr7:124921151 | G | A | 1 | a0001c0001t0001g0260 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-226-5505C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124921151 | |||||||
| chr7:124921154 | A | G | 203 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(200): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.-226-5508T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124921154 | |||||||
| chr7:124921316 | A | C | 1 | a0001c0001t0003g0186 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-226-5670T>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124921316 | |||||||
| chr7:124921528 | C | CAAAT | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.-226-5883_-226-588 others(8): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124921528 | |||||||
| chr7:124921736 | T | G | 70 | a0001c0001t0002g0005 a0001c0001t0002g0017 a0001c0001t0002g0018 others(67): Show |
72 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.-226-6090A>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124921736 | |||||||
| chr7:124921828 | T | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.-226-6182A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124921828 | |||||||
| chr7:124921832 | C | T | 1 | a0001c0001t0002g0034 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-226-6186G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124921832 | |||||||
| chr7:124922232 | T | C | 6 | a0001c0001t0003g0179 a0001c0001t0003g0180 a0001c0001t0003g0181 others(3): Show |
6 | HG02129.hp1 HG02155.hp2 HG02523.hp1 others(3): Show |
intron_variant | MODIFIER | c.-227+6583A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124922232 | |||||||
| chr7:124922242 | T | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0097 others(90): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.-227+6573A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124922242 | |||||||
| chr7:124922247 | A | G | 195 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(192): Show |
208 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(205): Show |
intron_variant | MODIFIER | c.-227+6568T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124922247 | |||||||
| chr7:124922461 | T | C | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.-227+6354A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124922461 | |||||||
| chr7:124922575 | T | C | 2 | a0001c0001t0001g0008 a0001c0002t0001g0185 |
3 | HG02559.hp2 HG02717.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-227+6240A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124922575 | |||||||
| chr7:124922641 | A | C | 79 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0036 others(76): Show |
82 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.-227+6174T>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124922641 | |||||||
| chr7:124922645 | C | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0097 others(90): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.-227+6170G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124922645 | |||||||
| chr7:124922683 | A | G | 1 | a0001c0001t0002g0033 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-227+6132T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124922683 | |||||||
| chr7:124923037 | C | CA | 6 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 others(3): Show |
6 | HG00099.hp2 HG01070.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.-227+5777dupT | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124923037 | |||||||
| chr7:124923055 | C | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0105 |
3 | HG02717.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-227+5760G>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124923055 | |||||||
| chr7:124923164 | T | A | 8 | a0001c0001t0001g0016 a0001c0001t0001g0319 a0001c0001t0001g0320 others(5): Show |
9 | HG02486.hp1 HG02818.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.-227+5651A>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124923164 | |||||||
| chr7:124923257 | A | T | 3 | a0001c0001t0001g0100 a0001c0001t0001g0102 a0007c0009t0001g0101 |
3 | HG02895.hp2 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-227+5558T>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124923257 | |||||||
| chr7:124923286 | T | G | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.-227+5529A>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124923286 | |||||||
| chr7:124923290 | T | C | 1 | a0001c0001t0001g0310 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-227+5525A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124923290 | |||||||
| chr7:124923342 | C | T | 1 | a0003c0006t0009g0103 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-227+5473G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124923342 | |||||||
| chr7:124923548 | C | T | 2 | a0001c0001t0001g0211 a0001c0001t0001g0212 |
2 | HG01516.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.-227+5267G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124923548 | |||||||
| chr7:124923886 | T | C | 5 | a0001c0001t0003g0012 a0001c0001t0003g0186 a0001c0001t0003g0187 others(2): Show |
6 | NA18972.hp2 NA18974.hp2 NA19007.hp2 others(3): Show |
intron_variant | MODIFIER | c.-227+4929A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124923886 | |||||||
| chr7:124923889 | TCAAACAA others(1): Show |
T | 16 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(13): Show |
16 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.-227+4918_-227+492 others(12): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124923889 | |||||||
| chr7:124924003 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-227+4812C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124924003 | |||||||
| chr7:124924122 | C | A | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.-227+4693G>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124924122 | |||||||
| chr7:124924156 | C | CA | 191 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(188): Show |
203 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.-227+4658dupT | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124924156 | |||||||
| chr7:124924156 | CA | C | 13 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0100 others(10): Show |
15 | HG02486.hp1 HG02717.hp2 HG02818.hp1 others(12): Show |
intron_variant | MODIFIER | c.-227+4658delT | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124924156 | |||||||
| chr7:124924170 | C | A | 1 | a0001c0001t0001g0118 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-227+4645G>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124924170 | |||||||
| chr7:124924392 | T | C | 1 | a0001c0001t0002g0089 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-227+4423A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124924392 | |||||||
| chr7:124924514 | C | CAGAT | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.-227+4297_-227+430 others(8): Show |
POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124924514 | |||||||
| chr7:124924591 | T | C | 55 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0203 others(52): Show |
57 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.-227+4224A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124924591 | |||||||
| chr7:124924697 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-227+4118G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124924697 | |||||||
| chr7:124924864 | G | T | 3 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 |
3 | HG01175.hp2 HG02129.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.-227+3951C>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124924864 | |||||||
| chr7:124924865 | A | G | 3 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 |
3 | HG01175.hp2 HG02129.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.-227+3950T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124924865 | |||||||
| chr7:124924920 | T | G | 1 | a0001c0001t0002g0090 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-227+3895A>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124924920 | |||||||
| chr7:124925064 | T | C | 1 | a0001c0001t0001g0315 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-227+3751A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124925064 | |||||||
| chr7:124925093 | A | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0097 others(90): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.-227+3722T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124925093 | |||||||
| chr7:124925180 | T | C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0105 |
3 | HG02717.hp2 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-227+3635A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124925180 | |||||||
| chr7:124925199 | T | C | 6 | a0001c0001t0001g0006 a0001c0001t0001g0091 a0001c0001t0001g0092 others(3): Show |
7 | HG02257.hp2 HG02622.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.-227+3616A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124925199 | |||||||
| chr7:124925400 | C | T | 3 | a0001c0001t0001g0100 a0001c0001t0001g0102 a0007c0009t0001g0101 |
3 | HG02895.hp2 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-227+3415G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124925400 | |||||||
| chr7:124925404 | C | G | 1 | a0001c0001t0006g0201 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-227+3411G>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124925404 | |||||||
| chr7:124925441 | C | T | 6 | a0001c0001t0003g0135 a0001c0001t0003g0136 a0001c0001t0003g0137 others(3): Show |
6 | NA18969.hp2 NA18973.hp2 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.-227+3374G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124925441 | |||||||
| chr7:124926059 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-227+2756C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124926059 | |||||||
| chr7:124926203 | A | G | 1 | a0001c0001t0001g0207 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-227+2612T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124926203 | |||||||
| chr7:124926331 | A | G | 2 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
2 | NA18950.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.-227+2484T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124926331 | |||||||
| chr7:124926686 | G | A | 3 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 |
3 | HG02647.hp1 HG02896.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-227+2129C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124926686 | |||||||
| chr7:124926989 | C | A | 1 | a0001c0001t0001g0316 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-227+1826G>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124926989 | |||||||
| chr7:124927069 | C | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(191): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.-227+1746G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124927069 | |||||||
| chr7:124927187 | T | G | 1 | a0001c0001t0003g0191 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-227+1628A>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124927187 | |||||||
| chr7:124927256 | A | T | 1 | a0001c0001t0003g0134 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-227+1559T>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124927256 | |||||||
| chr7:124927541 | C | T | 2 | a0001c0001t0002g0031 a0001c0001t0002g0032 |
2 | NA18940.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.-227+1274G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124927541 | |||||||
| chr7:124927543 | T | G | 1 | a0001c0001t0001g0317 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-227+1272A>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124927543 | |||||||
| chr7:124927838 | A | T | 4 | a0001c0001t0001g0013 a0001c0001t0001g0203 a0001c0001t0001g0204 others(1): Show |
5 | HG00544.hp2 HG02523.hp2 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.-227+977T>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124927838 | |||||||
| chr7:124927846 | C | T | 1 | a0001c0001t0003g0133 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-227+969G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124927846 | |||||||
| chr7:124927991 | T | C | 1 | a0001c0001t0001g0318 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-227+824A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124927991 | |||||||
| chr7:124928012 | G | C | 8 | a0001c0001t0001g0016 a0001c0001t0001g0319 a0001c0001t0001g0320 others(5): Show |
9 | HG02486.hp1 HG02818.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.-227+803C>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124928012 | |||||||
| chr7:124928106 | T | C | 16 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 others(13): Show |
16 | HG01884.hp1 HG02055.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.-227+709A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124928106 | |||||||
| chr7:124928334 | C | A | 1 | a0001c0001t0006g0201 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-227+481G>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124928334 | |||||||
| chr7:124928397 | A | C | 1 | a0001c0001t0002g0030 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-227+418T>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124928397 | |||||||
| chr7:124928413 | C | T | 93 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0097 others(90): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.-227+402G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124928413 | |||||||
| chr7:124928454 | T | G | 8 | a0001c0001t0001g0016 a0001c0001t0001g0319 a0001c0001t0001g0320 others(5): Show |
9 | HG02486.hp1 HG02818.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.-227+361A>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124928454 | |||||||
| chr7:124928656 | A | G | 13 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0123 others(10): Show |
15 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(12): Show |
intron_variant | MODIFIER | c.-227+159T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 2/18 | chr7 | 124928656 | |||||||
| chr7:124929324 | G | GT | 79 | a0001c0001t0001g0006 a0001c0001t0001g0035 a0001c0001t0001g0036 others(76): Show |
82 | HG00140.hp1 HG00423.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.-411-326dupA | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 1/18 | chr7 | 124929324 | |||||||
| chr7:124929328 | T | C | 87 | a0001c0001t0001g0001 a0001c0001t0001g0122 a0001c0001t0001g0123 others(84): Show |
95 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.-411-329A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 1/18 | chr7 | 124929328 | |||||||
| chr7:124929360 | A | G | 6 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 others(3): Show |
6 | HG02015.hp1 HG02056.hp2 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.-411-361T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 1/18 | chr7 | 124929360 | |||||||
| chr7:124929361 | T | C | 9 | a0001c0001t0001g0192 a0001c0002t0001g0193 a0001c0002t0001g0194 others(6): Show |
9 | HG00639.hp2 HG01433.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-411-362A>G | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 1/18 | chr7 | 124929361 | |||||||
| chr7:124929364 | A | G | 196 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(193): Show |
209 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(206): Show |
intron_variant | MODIFIER | c.-411-365T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 1/18 | chr7 | 124929364 | |||||||
| chr7:124929369 | C | T | 1 | a0001c0001t0003g0023 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-411-370G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 1/18 | chr7 | 124929369 | |||||||
| chr7:124929568 | A | G | 1 | a0001c0001t0003g0022 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-412+226T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 1/18 | chr7 | 124929568 | |||||||
| chr7:124929601 | A | G | 3 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0021 |
3 | HG01099.hp2 HG01943.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-412+193T>C | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 1/18 | chr7 | 124929601 | |||||||
| chr7:124929749 | G | A | 1 | a0001c0001t0001g0326 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.-412+45C>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 1/18 | chr7 | 124929749 | |||||||
| chr7:124929750 | C | A | 2 | a0001c0001t0002g0017 a0001c0001t0002g0018 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-412+44G>T | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 1/18 | chr7 | 124929750 | |||||||
| chr7:124929758 | C | T | 2 | a0001c0001t0002g0017 a0001c0001t0002g0018 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.-412+36G>A | POT1 | ENSG00000128513.16 | transcript | ENST00000357628.8 | protein_coding | 1/18 | chr7 | 124929758 |