Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55825 |
| ensemblid | ENSG00000115425.14 |
| hgncid | 18281 |
| symbol | PECR |
| name | peroxisomal trans-2-enoyl-CoA reductase |
| refseq_nuc | NM_018441.6 |
| refseq_prot | NP_060911.2 |
| ensembl_nuc | ENST00000265322.8 |
| ensembl_prot | ENSP00000265322.7 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 216038388 |
| end | 216081809 |
| strand | - |
| ver | v1.2 |
| region | chr2:216038388-216081809 |
| region5000 | chr2:216033388-216086809 |
| regionname0 | PECR_chr2_216038388_216081809 |
| regionname5000 | PECR_chr2_216033388_216086809 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 303 | 297 | 71 | 64 | 121 | 15 | 24 | 83 | PECR_chr2_216033388_216086809 | PECR | MASWA others(298): Show |
chr2 | 216033388 | 216086809 |
| a0002 | 0/0 | 303 | 86 | 20 | 10 | 43 | 0 | 13 | 37 | PECR_chr2_216033388_216086809 | PECR | MASWA others(298): Show |
chr2 | 216033388 | 216086809 |
| a0003 | 0/0 | 303 | 3 | 0 | 1 | 1 | 0 | 1 | 1 | PECR_chr2_216033388_216086809 | PECR | MASWA others(298): Show |
chr2 | 216033388 | 216086809 |
| a0004 | 0/0 | 303 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | MASWA others(298): Show |
chr2 | 216033388 | 216086809 |
| a0005 | 0/0 | 303 | 2 | 1 | 0 | 0 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | MASWA others(298): Show |
chr2 | 216033388 | 216086809 |
| a0006 | 0/0 | 303 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | MASWA others(298): Show |
chr2 | 216033388 | 216086809 |
| a0007 | 0/0 | 303 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | MASWA others(298): Show |
chr2 | 216033388 | 216086809 |
| a0008 | 0/0 | 11 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | MWSLH others(6): Show |
chr2 | 216033388 | 216086809 |
| a0009 | 0/0 | 303 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | MASWA others(298): Show |
chr2 | 216033388 | 216086809 |
| a0010 | 0/0 | 303 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | MASWA others(298): Show |
chr2 | 216033388 | 216086809 |
| a0011 | 0/0 | 303 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | MASWA others(298): Show |
chr2 | 216033388 | 216086809 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 909 | 254 | 64 | 54 | 105 | 12 | 17 | PECR_chr2_216033388_216086809 | PECR | ATGGC others(904): Show |
chr2 | 216033388 | 216086809 | ||
| a0001c0003 | 0/0 | 909 | 39 | 3 | 10 | 16 | 3 | 7 | PECR_chr2_216033388_216086809 | PECR | ATGGC others(904): Show |
chr2 | 216033388 | 216086809 | ||
| a0001c0004 | 0/0 | 909 | 3 | 3 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | ATGGC others(904): Show |
chr2 | 216033388 | 216086809 | ||
| a0001c0011 | 0/0 | 909 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | ATGGC others(904): Show |
chr2 | 216033388 | 216086809 | ||
| a0002c0002 | 0/0 | 909 | 86 | 20 | 10 | 43 | 0 | 13 | PECR_chr2_216033388_216086809 | PECR | ATGGC others(904): Show |
chr2 | 216033388 | 216086809 | ||
| a0003c0006 | 0/0 | 909 | 2 | 0 | 1 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | ATGGC others(904): Show |
chr2 | 216033388 | 216086809 | ||
| a0003c0014 | 0/0 | 909 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | ATGGC others(904): Show |
chr2 | 216033388 | 216086809 | ||
| a0004c0005 | 0/0 | 909 | 2 | 2 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | ATGGC others(904): Show |
chr2 | 216033388 | 216086809 | ||
| a0005c0008 | 0/0 | 909 | 2 | 1 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | ATGGC others(904): Show |
chr2 | 216033388 | 216086809 | ||
| a0006c0009 | 0/0 | 909 | 2 | 2 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | ATGGC others(904): Show |
chr2 | 216033388 | 216086809 | ||
| a0007c0007 | 0/0 | 909 | 2 | 2 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | ATGGC others(904): Show |
chr2 | 216033388 | 216086809 | ||
| a0008c0010 | 0/0 | 909 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | ACGGC others(904): Show |
chr2 | 216033388 | 216086809 | ||
| a0009c0013 | 0/0 | 909 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | ATGGC others(904): Show |
chr2 | 216033388 | 216086809 | ||
| a0010c0012 | 0/0 | 909 | 1 | 0 | 0 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | ATGGC others(904): Show |
chr2 | 216033388 | 216086809 | ||
| a0011c0015 | 0/0 | 909 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | ATGGC others(904): Show |
chr2 | 216033388 | 216086809 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1867 | 217 | 37 | 47 | 103 | 11 | 17 | PECR_chr2_216033388_216086809 | PECR | GCCCG others(1862): Show |
chr2 | 216033388 | 216086809 |
| a0001c0001t0004 | 0/0 | 1867 | 19 | 15 | 3 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | GCCCG others(1862): Show |
chr2 | 216033388 | 216086809 |
| a0001c0001t0005 | 0/0 | 1867 | 10 | 10 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | GCCCG others(1862): Show |
chr2 | 216033388 | 216086809 |
| a0001c0001t0006 | 0/0 | 1867 | 2 | 2 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | GCCCG others(1862): Show |
chr2 | 216033388 | 216086809 |
| a0001c0001t0007 | 0/0 | 1867 | 3 | 0 | 3 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | GCCCG others(1862): Show |
chr2 | 216033388 | 216086809 |
| a0001c0001t0008 | 0/0 | 1867 | 3 | 0 | 1 | 2 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | GCCCG others(1862): Show |
chr2 | 216033388 | 216086809 |
| a0001c0003t0001 | 0/0 | 1867 | 2 | 0 | 0 | 2 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | GCCCG others(1862): Show |
chr2 | 216033388 | 216086809 |
| a0001c0003t0003 | 0/0 | 1867 | 37 | 3 | 10 | 14 | 3 | 7 | PECR_chr2_216033388_216086809 | PECR | GCCCG others(1862): Show |
chr2 | 216033388 | 216086809 |
| a0001c0004t0001 | 0/0 | 1867 | 3 | 3 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | GCCCG others(1862): Show |
chr2 | 216033388 | 216086809 |
| a0001c0011t0006 | 0/0 | 1867 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | GCCCG others(1862): Show |
chr2 | 216033388 | 216086809 |
| a0002c0002t0002 | 0/0 | 1867 | 85 | 20 | 9 | 43 | 0 | 13 | PECR_chr2_216033388_216086809 | PECR | GCCCG others(1862): Show |
chr2 | 216033388 | 216086809 |
| a0002c0002t0010 | 0/0 | 1867 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | GCCCG others(1862): Show |
chr2 | 216033388 | 216086809 |
| a0003c0006t0001 | 0/0 | 1867 | 2 | 0 | 1 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | GCCCG others(1862): Show |
chr2 | 216033388 | 216086809 |
| a0003c0014t0001 | 0/0 | 1867 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | GCCCG others(1862): Show |
chr2 | 216033388 | 216086809 |
| a0004c0005t0009 | 0/0 | 1867 | 2 | 2 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | GCCCG others(1862): Show |
chr2 | 216033388 | 216086809 |
| a0005c0008t0002 | 0/0 | 1867 | 2 | 1 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | GCCCG others(1862): Show |
chr2 | 216033388 | 216086809 |
| a0006c0009t0001 | 0/0 | 1867 | 2 | 2 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | GCCCG others(1862): Show |
chr2 | 216033388 | 216086809 |
| a0007c0007t0001 | 0/0 | 1867 | 2 | 2 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | GCCCG others(1862): Show |
chr2 | 216033388 | 216086809 |
| a0008c0010t0001 | 0/0 | 1867 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | GCCCG others(1862): Show |
chr2 | 216033388 | 216086809 |
| a0009c0013t0002 | 0/0 | 1867 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | GCCCG others(1862): Show |
chr2 | 216033388 | 216086809 |
| a0010c0012t0003 | 0/0 | 1867 | 1 | 0 | 0 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | GCCCG others(1862): Show |
chr2 | 216033388 | 216086809 |
| a0011c0015t0001 | 0/0 | 1867 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | GCCCG others(1862): Show |
chr2 | 216033388 | 216086809 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0013 | 1/0 | 2 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0262 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0001g0376 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0004g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0004g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0004g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0004g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0004g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0004g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0004g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0004g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0004g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0004g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0004g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0004g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0004g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0004g0365 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0004g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0005g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0005g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0005g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0005g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0005g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0005g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0005g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0005g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0005g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0005g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0006g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0006g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0007g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0007g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0007g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0008g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0008g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0001t0008g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0003t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0003t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0003t0003g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0003t0003g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0003t0003g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0003t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0003t0003g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0003t0003g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0003t0003g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0003t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0003t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0003t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0003t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0003t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0003t0003g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0003t0003g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0003t0003g0184 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0003t0003g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0003t0003g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0003t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0003t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0003t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0003t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0003t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0003t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0003t0003g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0003t0003g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0003t0003g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0003t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0003t0003g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0003t0003g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0003t0003g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0003t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0003t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0003t0003g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0003t0003g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0003t0003g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0004t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0004t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0004t0001g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0001c0011t0006g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0017 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0363 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0002g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0002c0002t0010g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0003c0006t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0003c0006t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0003c0014t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0004c0005t0009g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0004c0005t0009g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0005c0008t0002g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0005c0008t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0006c0009t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0007c0007t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0008c0010t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0009c0013t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0010c0012t0003g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| a0011c0015t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0033 | EUR | GBR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG00140 | hp2 | a0001 | c0003 | t0003 | g0098 | EUR | GBR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0084 | EUR | FIN | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0258 | EUR | FIN | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0292 | EUR | FIN | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0257 | EUR | FIN | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | CHS | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | CHS | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | CHS | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG00544 | hp2 | a0002 | c0002 | t0002 | g0026 | EAS | CHS | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG00597 | hp2 | a0002 | c0002 | t0002 | g0233 | EAS | CHS | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | CHS | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG00609 | hp2 | a0002 | c0002 | t0002 | g0105 | EAS | CHS | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | CHS | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0332 | EAS | CHS | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | CHS | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | CHS | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG00733 | hp1 | a0001 | c0003 | t0003 | g0182 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG00738 | hp2 | a0001 | c0003 | t0003 | g0023 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG00741 | hp1 | a0001 | c0003 | t0003 | g0186 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01070 | hp2 | a0002 | c0002 | t0010 | g0330 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01074 | hp1 | a0001 | c0003 | t0003 | g0076 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01106 | hp2 | a0001 | c0001 | t0007 | g0078 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0374 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01109 | hp2 | a0002 | c0002 | t0002 | g0321 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01167 | hp2 | a0001 | c0003 | t0003 | g0019 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01168 | hp1 | a0002 | c0002 | t0002 | g0217 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01169 | hp1 | a0002 | c0002 | t0002 | g0221 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01169 | hp2 | a0001 | c0003 | t0003 | g0019 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0376 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01243 | hp1 | a0002 | c0002 | t0002 | g0325 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01243 | hp2 | a0001 | c0003 | t0003 | g0199 | AMR | PUR | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01255 | hp1 | a0003 | c0006 | t0001 | g0226 | AMR | CLM | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01256 | hp2 | a0001 | c0003 | t0003 | g0202 | AMR | CLM | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | CLM | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | CLM | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | CLM | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01258 | hp2 | a0001 | c0003 | t0003 | g0201 | AMR | CLM | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01261 | hp1 | a0001 | c0001 | t0004 | g0256 | AMR | CLM | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01261 | hp2 | a0001 | c0001 | t0004 | g0366 | AMR | CLM | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01358 | hp1 | a0001 | c0003 | t0003 | g0183 | AMR | CLM | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01358 | hp2 | a0001 | c0001 | t0007 | g0079 | AMR | CLM | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01361 | hp1 | a0008 | c0010 | t0001 | g0021 | AMR | CLM | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | CLM | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01433 | hp1 | a0001 | c0001 | t0004 | g0365 | AMR | CLM | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | CLM | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01515 | hp1 | a0001 | c0001 | t0004 | g0260 | EUR | IBS | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01515 | hp2 | a0001 | c0003 | t0003 | g0184 | EUR | IBS | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0278 | EUR | IBS | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01517 | hp1 | a0001 | c0003 | t0003 | g0185 | EUR | IBS | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | IBS | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01884 | hp1 | a0002 | c0002 | t0002 | g0370 | AFR | ACB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01884 | hp2 | a0002 | c0002 | t0002 | g0357 | AFR | ACB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01891 | hp2 | a0001 | c0001 | t0005 | g0313 | AFR | ACB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PEL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PEL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0317 | AMR | PEL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01934 | hp2 | a0002 | c0002 | t0002 | g0331 | AMR | PEL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01943 | hp2 | a0001 | c0001 | t0007 | g0083 | AMR | PEL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01975 | hp1 | a0002 | c0002 | t0002 | g0338 | AMR | PEL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0343 | AMR | PEL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | PEL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | PEL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01993 | hp1 | a0002 | c0002 | t0002 | g0164 | AMR | PEL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0369 | AFR | ACB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02056 | hp2 | a0002 | c0002 | t0002 | g0096 | EAS | KHV | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02071 | hp1 | a0001 | c0003 | t0003 | g0012 | EAS | KHV | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | KHV | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | KHV | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | KHV | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02132 | hp1 | a0001 | c0003 | t0003 | g0190 | EAS | KHV | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | KHV | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02145 | hp1 | a0001 | c0001 | t0006 | g0103 | AFR | ACB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02145 | hp2 | a0001 | c0004 | t0001 | g0094 | AFR | ACB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | CDX | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | CDX | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | CDX | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CDX | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02257 | hp1 | a0001 | c0001 | t0004 | g0345 | AFR | ACB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02257 | hp2 | a0001 | c0001 | t0005 | g0311 | AFR | ACB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02258 | hp2 | a0002 | c0002 | t0002 | g0328 | AFR | ACB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0264 | AMR | PEL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02280 | hp2 | a0001 | c0001 | t0005 | g0378 | AFR | ACB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02293 | hp2 | a0001 | c0001 | t0008 | g0273 | AMR | PEL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02300 | hp1 | a0002 | c0002 | t0002 | g0165 | AMR | PEL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02451 | hp1 | a0001 | c0001 | t0005 | g0310 | AFR | ACB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0309 | AFR | ACB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02572 | hp1 | a0005 | c0008 | t0002 | g0315 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02572 | hp2 | a0002 | c0002 | t0002 | g0322 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0324 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02615 | hp2 | a0001 | c0001 | t0004 | g0351 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02622 | hp1 | a0001 | c0003 | t0003 | g0319 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02630 | hp1 | a0002 | c0002 | t0002 | g0207 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02630 | hp2 | a0002 | c0002 | t0002 | g0371 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0367 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02647 | hp2 | a0001 | c0004 | t0001 | g0093 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | PJL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02683 | hp2 | a0002 | c0002 | t0002 | g0187 | SAS | PJL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02717 | hp1 | a0001 | c0001 | t0005 | g0314 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02717 | hp2 | a0002 | c0002 | t0002 | g0359 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0056 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0352 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02735 | hp1 | a0001 | c0003 | t0003 | g0203 | SAS | PJL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0364 | SAS | PJL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02809 | hp1 | a0002 | c0002 | t0002 | g0361 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0327 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0347 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02818 | hp2 | a0001 | c0001 | t0005 | g0318 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0346 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02895 | hp2 | a0006 | c0009 | t0001 | g0020 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0304 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02897 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02897 | hp2 | a0006 | c0009 | t0001 | g0020 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | ESN | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | ESN | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | ESN | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ESN | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0312 | AFR | ESN | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02970 | hp2 | a0002 | c0002 | t0002 | g0329 | AFR | ESN | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ESN | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG03017 | hp1 | a0005 | c0008 | t0002 | g0253 | SAS | PJL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0306 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0356 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG03098 | hp1 | a0001 | c0001 | t0005 | g0307 | AFR | MSL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG03098 | hp2 | a0002 | c0002 | t0002 | g0320 | AFR | MSL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG03130 | hp2 | a0001 | c0001 | t0004 | g0155 | AFR | ESN | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0355 | AFR | ESN | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG03139 | hp2 | a0002 | c0002 | t0002 | g0358 | AFR | ESN | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG03195 | hp1 | a0001 | c0003 | t0003 | g0104 | AFR | ESN | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG03195 | hp2 | a0007 | c0007 | t0001 | g0001 | AFR | ESN | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0344 | AFR | MSL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | MSL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG03225 | hp1 | a0001 | c0001 | t0004 | g0157 | AFR | MSL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | MSL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG03486 | hp1 | a0002 | c0002 | t0002 | g0368 | AFR | MSL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG03486 | hp2 | a0004 | c0005 | t0009 | g0213 | AFR | MSL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG03492 | hp1 | a0001 | c0003 | t0003 | g0099 | SAS | PJL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ESN | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ESN | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG03540 | hp1 | a0002 | c0002 | t0002 | g0372 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0156 | AFR | GWD | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG03579 | hp1 | a0007 | c0007 | t0001 | g0001 | AFR | MSL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG03579 | hp2 | a0001 | c0011 | t0006 | g0375 | AFR | MSL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG03654 | hp2 | a0002 | c0002 | t0002 | g0363 | SAS | PJL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG03669 | hp1 | a0001 | c0003 | t0003 | g0200 | SAS | PJL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG03688 | hp1 | a0002 | c0002 | t0002 | g0066 | SAS | STU | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | STU | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG03704 | hp1 | a0002 | c0002 | t0002 | g0077 | SAS | PJL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG03704 | hp2 | a0002 | c0002 | t0002 | g0017 | SAS | PJL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG03710 | hp2 | a0001 | c0003 | t0003 | g0227 | SAS | PJL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG03831 | hp1 | a0002 | c0002 | t0002 | g0220 | SAS | BEB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | BEB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG03834 | hp1 | a0003 | c0006 | t0001 | g0218 | SAS | BEB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG03834 | hp2 | a0002 | c0002 | t0002 | g0230 | SAS | BEB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG03927 | hp1 | a0002 | c0002 | t0002 | g0234 | SAS | BEB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0289 | SAS | BEB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG03942 | hp1 | a0001 | c0003 | t0003 | g0295 | SAS | BEB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG03942 | hp2 | a0001 | c0003 | t0003 | g0097 | SAS | BEB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | STU | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | STU | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG04184 | hp1 | a0001 | c0003 | t0003 | g0204 | SAS | BEB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG04184 | hp2 | a0002 | c0002 | t0002 | g0242 | SAS | BEB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG04199 | hp1 | a0002 | c0002 | t0002 | g0250 | SAS | STU | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG04199 | hp2 | a0002 | c0002 | t0002 | g0228 | SAS | STU | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | STU | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG04204 | hp2 | a0002 | c0002 | t0002 | g0074 | SAS | STU | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | STU | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG04228 | hp2 | a0002 | c0002 | t0002 | g0240 | SAS | STU | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18522 | hp1 | a0001 | c0003 | t0003 | g0102 | AFR | YRI | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18522 | hp2 | a0002 | c0002 | t0002 | g0362 | AFR | YRI | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18612 | hp2 | a0002 | c0002 | t0002 | g0126 | EAS | CHB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CHB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18747 | hp2 | a0002 | c0002 | t0002 | g0118 | EAS | CHB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | YRI | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0215 | AFR | YRI | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18948 | hp1 | a0002 | c0002 | t0002 | g0225 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18948 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18952 | hp1 | a0001 | c0003 | t0003 | g0095 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18952 | hp2 | a0001 | c0003 | t0003 | g0188 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18953 | hp2 | a0002 | c0002 | t0002 | g0173 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18961 | hp1 | a0002 | c0002 | t0002 | g0112 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18962 | hp2 | a0002 | c0002 | t0002 | g0140 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18963 | hp1 | a0002 | c0002 | t0002 | g0231 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18964 | hp1 | a0001 | c0003 | t0003 | g0342 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18964 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18965 | hp1 | a0002 | c0002 | t0002 | g0243 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18967 | hp2 | a0002 | c0002 | t0002 | g0298 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18971 | hp2 | a0002 | c0002 | t0002 | g0166 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18974 | hp1 | a0002 | c0002 | t0002 | g0305 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18975 | hp1 | a0002 | c0002 | t0002 | g0241 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18978 | hp2 | a0002 | c0002 | t0002 | g0115 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18979 | hp1 | a0003 | c0014 | t0001 | g0244 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18980 | hp1 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18981 | hp1 | a0002 | c0002 | t0002 | g0316 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18981 | hp2 | a0002 | c0002 | t0002 | g0232 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18982 | hp1 | a0002 | c0002 | t0002 | g0198 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18983 | hp1 | a0001 | c0003 | t0001 | g0194 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18983 | hp2 | a0002 | c0002 | t0002 | g0251 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18984 | hp2 | a0001 | c0001 | t0008 | g0287 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18986 | hp1 | a0001 | c0003 | t0003 | g0147 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18990 | hp1 | a0001 | c0003 | t0003 | g0193 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18991 | hp2 | a0002 | c0002 | t0002 | g0151 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18998 | hp1 | a0001 | c0003 | t0003 | g0191 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18998 | hp2 | a0002 | c0002 | t0002 | g0133 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA19003 | hp2 | a0002 | c0002 | t0002 | g0006 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA19004 | hp1 | a0001 | c0003 | t0003 | g0012 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA19004 | hp2 | a0002 | c0002 | t0002 | g0153 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA19007 | hp1 | a0002 | c0002 | t0002 | g0017 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA19007 | hp2 | a0001 | c0003 | t0001 | g0197 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA19010 | hp2 | a0002 | c0002 | t0002 | g0334 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA19012 | hp1 | a0002 | c0002 | t0002 | g0167 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA19030 | hp1 | a0002 | c0002 | t0002 | g0360 | AFR | LWK | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA19030 | hp2 | a0002 | c0002 | t0002 | g0350 | AFR | LWK | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | LWK | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA19043 | hp2 | a0002 | c0002 | t0002 | g0354 | AFR | LWK | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0340 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA19056 | hp2 | a0002 | c0002 | t0002 | g0114 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA19058 | hp1 | a0001 | c0003 | t0003 | g0189 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA19058 | hp2 | a0009 | c0013 | t0002 | g0239 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA19063 | hp1 | a0001 | c0003 | t0003 | g0145 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA19063 | hp2 | a0002 | c0002 | t0002 | g0341 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA19064 | hp2 | a0002 | c0002 | t0002 | g0336 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA19065 | hp2 | a0002 | c0002 | t0002 | g0229 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA19066 | hp2 | a0002 | c0002 | t0002 | g0333 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA19067 | hp1 | a0002 | c0002 | t0002 | g0139 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA19067 | hp2 | a0001 | c0001 | t0008 | g0272 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA19070 | hp2 | a0002 | c0002 | t0002 | g0152 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA19082 | hp1 | a0002 | c0002 | t0002 | g0123 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA19083 | hp1 | a0001 | c0003 | t0003 | g0235 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA19083 | hp2 | a0001 | c0003 | t0003 | g0196 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA19085 | hp1 | a0002 | c0002 | t0002 | g0172 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA19086 | hp2 | a0002 | c0002 | t0002 | g0294 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0337 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA19089 | hp1 | a0001 | c0003 | t0003 | g0236 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA19089 | hp2 | a0002 | c0002 | t0002 | g0124 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA19090 | hp1 | a0002 | c0002 | t0002 | g0238 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA19240 | hp1 | a0002 | c0002 | t0002 | g0326 | AFR | YRI | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA19240 | hp2 | a0002 | c0002 | t0002 | g0349 | AFR | YRI | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA20129 | hp1 | a0001 | c0001 | t0006 | g0029 | AFR | ASW | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | ASW | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA20752 | hp1 | a0010 | c0012 | t0003 | g0211 | EUR | TSI | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0266 | EUR | TSI | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0180 | EUR | TSI | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0249 | EUR | TSI | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | GIH | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA20905 | hp2 | a0011 | c0015 | t0001 | g0252 | SAS | GIH | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG01123 | hp2 | a0002 | c0002 | t0002 | g0335 | AMR | CLM | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02109 | hp1 | a0004 | c0005 | t0009 | g0373 | AFR | ACB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0353 | AFR | ACB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0348 | AFR | ACB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | ACB | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0308 | AFR | MSL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0323 | AFR | MSL | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG06807 | hp1 | a0001 | c0004 | t0001 | g0377 | AFR | USA | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | USA | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | USA | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | USA | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA21309 | hp1 | a0002 | c0002 | t0002 | g0339 | AFR | LWK | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0262 | REF | REF | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0013 | REF | REF | PECR_chr2_216033388_216086809 | PECR | chr2 | 216033388 | 216086809 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:216039296 | A | T | 3 | a0002 a0005 a0009 |
89 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(86): Show |
missense_variant | MODERATE | c.891T>A | p.Phe297Leu | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 8/8 | 959/1867 | 891/912 | 297/303 | chr2 | 216039296 | |||
| chr2:216043934 | T | C | 2 | a0004 a0010 |
3 | HG02109.hp1 HG03486.hp2 NA20752.hp1 |
missense_variant | MODERATE | c.796A>G | p.Ser266Gly | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/8 | 864/1867 | 796/912 | 266/303 | chr2 | 216043934 | |||
| chr2:216051478 | T | C | 1 | a0010 | 1 | NA20752.hp1 | missense_variant | MODERATE | c.574A>G | p.Ser192Gly | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 5/8 | 642/1867 | 574/912 | 192/303 | chr2 | 216051478 | |||
| chr2:216058896 | C | G | 1 | a0007 | 2 | HG03195.hp2 HG03579.hp1 |
missense_variant&splice_region_variant | MODERATE | c.505G>C | p.Val169Leu | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/8 | 573/1867 | 505/912 | 169/303 | chr2 | 216058896 | |||
| chr2:216058956 | C | T | 3 | a0002 a0003 a0009 |
90 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(87): Show |
missense_variant | MODERATE | c.445G>A | p.Glu149Lys | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/8 | 513/1867 | 445/912 | 149/303 | chr2 | 216058956 | |||
| chr2:216065443 | A | C | 1 | a0009 | 1 | NA19058.hp2 | missense_variant | MODERATE | c.293T>G | p.Phe98Cys | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/8 | 361/1867 | 293/912 | 98/303 | chr2 | 216065443 | |||
| chr2:216066410 | T | G | 1 | a0011 | 1 | NA20905.hp2 | missense_variant | MODERATE | c.233A>C | p.Gln78Pro | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 2/8 | 301/1867 | 233/912 | 78/303 | chr2 | 216066410 | |||
| chr2:216081713 | T | C | 1 | a0006 | 2 | HG02895.hp2 HG02897.hp2 |
missense_variant | MODERATE | c.29A>G | p.Tyr10Cys | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/8 | 97/1867 | 29/912 | 10/303 | chr2 | 216081713 | |||
| chr2:216081740 | A | G | 1 | a0008 | 1 | HG01361.hp1 | start_lost | HIGH | c.2T>C | p.Met1? | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/8 | 70/1867 | 2/912 | 1/303 | chr2 | 216081740 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:216043956 | C | T | 2 | a0001c0003 a0003c0014 |
40 | HG00140.hp2 HG00733.hp1 HG00738.hp2 others(37): Show |
synonymous_variant | LOW | c.774G>A | p.Ser258Ser | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/8 | 842/1867 | 774/912 | 258/303 | chr2 | 216043956 | |||
| chr2:216066394 | A | G | 3 | a0001c0011 a0004c0005 a0010c0012 |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
synonymous_variant | LOW | c.249T>C | p.Asn83Asn | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 2/8 | 317/1867 | 249/912 | 83/303 | chr2 | 216066394 | |||
| chr2:216066460 | T | C | 1 | a0001c0004 | 3 | HG02145.hp2 HG02647.hp2 HG06807.hp1 |
synonymous_variant | LOW | c.183A>G | p.Glu61Glu | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 2/8 | 251/1867 | 183/912 | 61/303 | chr2 | 216066460 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:216038534 | A | C | 2 | a0001c0003t0003 a0010c0012t0003 |
38 | HG00140.hp2 HG00733.hp1 HG00738.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*741T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 8/8 | 741 | chr2 | 216038534 | ||||||
| chr2:216038554 | C | T | 2 | a0001c0001t0006 a0001c0011t0006 |
3 | HG02145.hp1 HG03579.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*721G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 8/8 | 721 | chr2 | 216038554 | ||||||
| chr2:216038555 | G | A | 1 | a0001c0001t0005 | 10 | HG01891.hp2 HG02257.hp2 HG02280.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*720C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 8/8 | 720 | chr2 | 216038555 | ||||||
| chr2:216038567 | G | A | 10 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0006 others(7): Show |
159 | HG00140.hp2 HG00544.hp2 HG00597.hp2 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*708C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 8/8 | 708 | chr2 | 216038567 | ||||||
| chr2:216038584 | A | T | 1 | a0001c0001t0008 | 3 | HG02293.hp2 NA18984.hp2 NA19067.hp2 |
3_prime_UTR_variant | MODIFIER | c.*691T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 8/8 | 691 | chr2 | 216038584 | ||||||
| chr2:216038632 | A | T | 1 | a0001c0001t0007 | 3 | HG01106.hp2 HG01358.hp2 HG01943.hp2 |
3_prime_UTR_variant | MODIFIER | c.*643T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 8/8 | 643 | chr2 | 216038632 | ||||||
| chr2:216038771 | C | T | 2 | a0001c0001t0006 a0001c0011t0006 |
3 | HG02145.hp1 HG03579.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*504G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 8/8 | 504 | chr2 | 216038771 | ||||||
| chr2:216039163 | T | C | 1 | a0002c0002t0010 | 1 | HG01070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*112A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 8/8 | 112 | chr2 | 216039163 | ||||||
| chr2:216039171 | A | C | 4 | a0002c0002t0002 a0002c0002t0010 a0005c0008t0002 others(1): Show |
89 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*104T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 8/8 | 104 | chr2 | 216039171 | ||||||
| chr2:216039247 | G | A | 1 | a0004c0005t0009 | 2 | HG02109.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*28C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 8/8 | 28 | chr2 | 216039247 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:216039676 | C | T | 53 | a0002c0002t0002g0006 a0002c0002t0002g0009 a0002c0002t0002g0066 others(50): Show |
55 | HG00597.hp2 HG00609.hp2 HG01168.hp1 others(52): Show |
intron_variant | MODIFIER | c.827-316G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216039676 | |||||||
| chr2:216039803 | T | C | 1 | a0001c0001t0001g0144 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.827-443A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216039803 | |||||||
| chr2:216039874 | T | G | 4 | a0001c0001t0004g0256 a0001c0001t0004g0260 a0001c0001t0004g0365 others(1): Show |
4 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.827-514A>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216039874 | |||||||
| chr2:216039997 | GCAT | G | 3 | a0001c0001t0006g0029 a0001c0001t0006g0103 a0001c0011t0006g0375 |
3 | HG02145.hp1 HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.827-640_827-638del others(3): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216039997 | |||||||
| chr2:216040116 | CAG | C | 4 | a0001c0001t0004g0256 a0001c0001t0004g0260 a0001c0001t0004g0365 others(1): Show |
4 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.827-758_827-757del others(2): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216040116 | |||||||
| chr2:216040137 | A | T | 7 | a0001c0001t0001g0154 a0001c0001t0001g0208 a0001c0001t0001g0209 others(4): Show |
7 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.827-777T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216040137 | |||||||
| chr2:216040153 | A | G | 10 | a0002c0002t0002g0320 a0002c0002t0002g0321 a0002c0002t0002g0322 others(7): Show |
10 | HG01109.hp2 HG01243.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.827-793T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216040153 | |||||||
| chr2:216040211 | G | C | 6 | a0002c0002t0002g0358 a0002c0002t0002g0359 a0002c0002t0002g0360 others(3): Show |
6 | HG02572.hp1 HG02717.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.827-851C>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216040211 | |||||||
| chr2:216040286 | A | G | 35 | a0001c0003t0003g0012 a0001c0003t0003g0019 a0001c0003t0003g0023 others(32): Show |
37 | HG00140.hp2 HG00733.hp1 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.827-926T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216040286 | |||||||
| chr2:216040293 | T | C | 289 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0008 others(286): Show |
304 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(301): Show |
intron_variant | MODIFIER | c.827-933A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216040293 | |||||||
| chr2:216040294 | G | A | 137 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(134): Show |
146 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.827-934C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216040294 | |||||||
| chr2:216040314 | G | A | 1 | a0001c0001t0001g0270 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.827-954C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216040314 | |||||||
| chr2:216040316 | G | A | 1 | a0001c0001t0001g0081 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.827-956C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216040316 | |||||||
| chr2:216040348 | G | A | 2 | a0001c0001t0001g0212 a0001c0001t0001g0214 |
2 | HG02886.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.827-988C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216040348 | |||||||
| chr2:216040403 | C | A | 40 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(37): Show |
43 | HG00140.hp2 HG00733.hp1 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.827-1043G>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216040403 | |||||||
| chr2:216040477 | T | C | 86 | a0002c0002t0002g0006 a0002c0002t0002g0009 a0002c0002t0002g0017 others(83): Show |
89 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.827-1117A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216040477 | |||||||
| chr2:216040511 | C | T | 4 | a0001c0001t0004g0256 a0001c0001t0004g0260 a0001c0001t0004g0365 others(1): Show |
4 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.827-1151G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216040511 | |||||||
| chr2:216040513 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.827-1153G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216040513 | |||||||
| chr2:216040547 | C | T | 137 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(134): Show |
146 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.827-1187G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216040547 | |||||||
| chr2:216040598 | G | A | 1 | a0002c0002t0002g0234 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.827-1238C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216040598 | |||||||
| chr2:216040634 | C | T | 86 | a0002c0002t0002g0006 a0002c0002t0002g0009 a0002c0002t0002g0017 others(83): Show |
89 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.827-1274G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216040634 | |||||||
| chr2:216040672 | T | C | 86 | a0002c0002t0002g0006 a0002c0002t0002g0009 a0002c0002t0002g0017 others(83): Show |
89 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.827-1312A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216040672 | |||||||
| chr2:216040957 | C | T | 86 | a0002c0002t0002g0006 a0002c0002t0002g0009 a0002c0002t0002g0017 others(83): Show |
89 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.827-1597G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216040957 | |||||||
| chr2:216040978 | T | C | 1 | a0001c0001t0001g0044 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.827-1618A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216040978 | |||||||
| chr2:216041005 | G | A | 86 | a0002c0002t0002g0006 a0002c0002t0002g0009 a0002c0002t0002g0017 others(83): Show |
89 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.827-1645C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216041005 | |||||||
| chr2:216041049 | C | T | 86 | a0002c0002t0002g0006 a0002c0002t0002g0009 a0002c0002t0002g0017 others(83): Show |
89 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.827-1689G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216041049 | |||||||
| chr2:216041083 | G | A | 86 | a0002c0002t0002g0006 a0002c0002t0002g0009 a0002c0002t0002g0017 others(83): Show |
89 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.827-1723C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216041083 | |||||||
| chr2:216041144 | C | T | 153 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(150): Show |
163 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.827-1784G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216041144 | |||||||
| chr2:216041145 | G | A | 1 | a0002c0002t0002g0228 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.827-1785C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216041145 | |||||||
| chr2:216041203 | AG | A | 6 | a0002c0002t0002g0358 a0002c0002t0002g0359 a0002c0002t0002g0360 others(3): Show |
6 | HG02572.hp1 HG02717.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.827-1844delC | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216041203 | |||||||
| chr2:216041204 | G | A | 80 | a0002c0002t0002g0006 a0002c0002t0002g0009 a0002c0002t0002g0017 others(77): Show |
83 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(80): Show |
intron_variant | MODIFIER | c.827-1844C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216041204 | |||||||
| chr2:216041299 | C | T | 1 | a0001c0001t0001g0271 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.827-1939G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216041299 | |||||||
| chr2:216041307 | T | C | 172 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(169): Show |
182 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.827-1947A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216041307 | |||||||
| chr2:216041508 | C | CTA | 48 | a0002c0002t0002g0006 a0002c0002t0002g0009 a0002c0002t0002g0066 others(45): Show |
50 | HG00597.hp2 HG00609.hp2 HG01168.hp1 others(47): Show |
intron_variant | MODIFIER | c.827-2150_827-2149d others(4): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216041508 | |||||||
| chr2:216041547 | C | T | 86 | a0002c0002t0002g0006 a0002c0002t0002g0009 a0002c0002t0002g0017 others(83): Show |
89 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.827-2187G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216041547 | |||||||
| chr2:216041570 | T | C | 25 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0096 others(22): Show |
26 | HG00544.hp2 HG01070.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.827-2210A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216041570 | |||||||
| chr2:216041604 | A | G | 6 | a0001c0001t0001g0109 a0001c0001t0001g0148 a0001c0001t0001g0160 others(3): Show |
6 | HG00438.hp2 HG00673.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.827-2244T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216041604 | |||||||
| chr2:216041671 | C | T | 3 | a0004c0005t0009g0213 a0004c0005t0009g0373 a0010c0012t0003g0211 |
3 | HG02109.hp1 HG03486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.826+2233G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216041671 | |||||||
| chr2:216041714 | C | G | 3 | a0004c0005t0009g0213 a0004c0005t0009g0373 a0010c0012t0003g0211 |
3 | HG02109.hp1 HG03486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.826+2190G>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216041714 | |||||||
| chr2:216041879 | G | C | 1 | a0001c0001t0004g0344 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.826+2025C>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216041879 | |||||||
| chr2:216041941 | C | T | 4 | a0001c0001t0004g0256 a0001c0001t0004g0260 a0001c0001t0004g0365 others(1): Show |
4 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+1963G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216041941 | |||||||
| chr2:216042157 | G | A | 1 | a0001c0001t0001g0038 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.826+1747C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042157 | |||||||
| chr2:216042369 | C | T | 24 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0096 others(21): Show |
25 | HG00544.hp2 HG01070.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.826+1535G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042369 | |||||||
| chr2:216042374 | A | C | 6 | a0002c0002t0002g0358 a0002c0002t0002g0359 a0002c0002t0002g0360 others(3): Show |
6 | HG02572.hp1 HG02717.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.826+1530T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042374 | |||||||
| chr2:216042475 | C | A | 270 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(267): Show |
284 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(281): Show |
intron_variant | MODIFIER | c.826+1429G>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042475 | |||||||
| chr2:216042495 | A | G | 7 | a0001c0001t0001g0154 a0001c0001t0001g0208 a0001c0001t0001g0209 others(4): Show |
7 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.826+1409T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042495 | |||||||
| chr2:216042535 | T | C | 1 | a0001c0001t0001g0089 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.826+1369A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042535 | |||||||
| chr2:216042543 | C | T | 3 | a0001c0003t0003g0188 a0001c0003t0003g0190 a0001c0003t0003g0191 |
3 | HG02132.hp1 NA18952.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.826+1361G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042543 | |||||||
| chr2:216042580 | C | A | 1 | a0001c0001t0001g0053 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.826+1324G>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042580 | |||||||
| chr2:216042599 | G | T | 244 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(241): Show |
257 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.826+1305C>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042599 | |||||||
| chr2:216042637 | C | T | 9 | a0001c0001t0004g0306 a0001c0001t0005g0307 a0001c0001t0005g0308 others(6): Show |
9 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.826+1267G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042637 | |||||||
| chr2:216042704 | C | A | 4 | a0001c0001t0001g0024 a0001c0001t0001g0033 a0001c0001t0001g0291 others(1): Show |
4 | HG00140.hp1 HG00323.hp1 HG00738.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+1200G>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042704 | |||||||
| chr2:216042789 | G | C | 266 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(263): Show |
280 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(277): Show |
intron_variant | MODIFIER | c.826+1115C>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042789 | |||||||
| chr2:216042906 | G | A | 260 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(257): Show |
274 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.826+998C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042906 | |||||||
| chr2:216042927 | T | TTA | 3 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0283 |
3 | HG02080.hp1 HG02080.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.826+975_826+976dup others(2): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042927 | |||||||
| chr2:216042949 | G | A | 1 | a0004c0005t0009g0373 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.826+955C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042949 | |||||||
| chr2:216042949 | G | GTGTATAT others(21): Show |
4 | a0001c0001t0004g0256 a0001c0001t0004g0260 a0001c0001t0004g0365 others(1): Show |
4 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+954_826+955ins others(28): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042949 | |||||||
| chr2:216042951 | G | GTA | 7 | a0001c0001t0001g0154 a0001c0001t0001g0208 a0001c0001t0001g0209 others(4): Show |
7 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.826+951_826+952dup others(2): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042951 | |||||||
| chr2:216042953 | A | G | 1 | a0004c0005t0009g0373 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.826+951T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042953 | |||||||
| chr2:216042964 | C | T | 14 | a0001c0001t0001g0154 a0001c0001t0001g0208 a0001c0001t0001g0209 others(11): Show |
14 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.826+940G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042964 | |||||||
| chr2:216042966 | C | CAT | 4 | a0002c0002t0002g0358 a0002c0002t0002g0359 a0002c0002t0002g0360 others(1): Show |
4 | HG02717.hp2 HG03139.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.826+936_826+937dup others(2): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042966 | |||||||
| chr2:216042966 | C | T | 3 | a0004c0005t0009g0213 a0004c0005t0009g0373 a0010c0012t0003g0211 |
3 | HG02109.hp1 HG03486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.826+938G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042966 | |||||||
| chr2:216042970 | C | T | 3 | a0004c0005t0009g0213 a0004c0005t0009g0373 a0010c0012t0003g0211 |
3 | HG02109.hp1 HG03486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.826+934G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042970 | |||||||
| chr2:216042971 | G | A | 132 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(129): Show |
140 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.826+933C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042971 | |||||||
| chr2:216042977 | G | A | 3 | a0004c0005t0009g0213 a0004c0005t0009g0373 a0010c0012t0003g0211 |
3 | HG02109.hp1 HG03486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.826+927C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042977 | |||||||
| chr2:216042979 | G | A | 14 | a0001c0001t0001g0154 a0001c0001t0001g0208 a0001c0001t0001g0209 others(11): Show |
14 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.826+925C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042979 | |||||||
| chr2:216042979 | G | GTA | 244 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(241): Show |
258 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.826+923_826+924dup others(2): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042979 | |||||||
| chr2:216042979 | G | GTATATAT others(23): Show |
2 | a0001c0004t0001g0093 a0001c0004t0001g0094 |
2 | HG02145.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.826+924_826+925ins others(30): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042979 | |||||||
| chr2:216042979 | G | GTATATAT others(51): Show |
2 | a0002c0002t0002g0133 a0002c0002t0002g0251 |
2 | NA18983.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.826+924_826+925ins others(58): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042979 | |||||||
| chr2:216042984 | T | C | 2 | a0004c0005t0009g0213 a0010c0012t0003g0211 |
2 | HG03486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.826+920A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042984 | |||||||
| chr2:216042988 | T | C | 3 | a0004c0005t0009g0213 a0004c0005t0009g0373 a0010c0012t0003g0211 |
3 | HG02109.hp1 HG03486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.826+916A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042988 | |||||||
| chr2:216042988 | T | TATATAC | 7 | a0001c0001t0001g0154 a0001c0001t0001g0208 a0001c0001t0001g0209 others(4): Show |
7 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.826+915_826+916ins others(6): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042988 | |||||||
| chr2:216042990 | T | C | 6 | a0001c0001t0004g0256 a0001c0001t0004g0260 a0001c0001t0004g0365 others(3): Show |
6 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.826+914A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042990 | |||||||
| chr2:216042990 | T | TAC | 11 | a0001c0001t0004g0306 a0001c0001t0005g0307 a0001c0001t0005g0308 others(8): Show |
11 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.826+912_826+913dup others(2): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042990 | |||||||
| chr2:216042994 | T | C | 1 | a0004c0005t0009g0373 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.826+910A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042994 | |||||||
| chr2:216042996 | C | T | 2 | a0004c0005t0009g0213 a0010c0012t0003g0211 |
2 | HG03486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.826+908G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042996 | |||||||
| chr2:216042997 | G | A | 1 | a0004c0005t0009g0373 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.826+907C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216042997 | |||||||
| chr2:216043003 | G | A | 1 | a0004c0005t0009g0373 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.826+901C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043003 | |||||||
| chr2:216043005 | G | A | 11 | a0001c0001t0001g0154 a0001c0001t0001g0208 a0001c0001t0001g0209 others(8): Show |
11 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.826+899C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043005 | |||||||
| chr2:216043007 | A | G | 3 | a0001c0003t0003g0189 a0001c0004t0001g0093 a0004c0005t0009g0373 |
3 | HG02109.hp1 HG02647.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.826+897T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043007 | |||||||
| chr2:216043016 | T | C | 4 | a0001c0001t0004g0256 a0001c0001t0004g0260 a0001c0001t0004g0365 others(1): Show |
4 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+888A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043016 | |||||||
| chr2:216043016 | T | TATACAC | 7 | a0001c0001t0001g0154 a0001c0001t0001g0208 a0001c0001t0001g0209 others(4): Show |
7 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.826+887_826+888ins others(6): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043016 | |||||||
| chr2:216043019 | A | G | 5 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0042 others(2): Show |
6 | NA18945.hp1 NA18961.hp2 NA19070.hp1 others(3): Show |
intron_variant | MODIFIER | c.826+885T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043019 | |||||||
| chr2:216043025 | G | A | 3 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 |
3 | HG02486.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.826+879C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043025 | |||||||
| chr2:216043025 | GTA | G | 7 | a0001c0001t0001g0154 a0001c0001t0001g0208 a0001c0001t0001g0209 others(4): Show |
7 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.826+877_826+878del others(2): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043025 | |||||||
| chr2:216043027 | A | ATATGTGT others(23): Show |
1 | a0001c0001t0005g0307 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.826+876_826+877ins others(30): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043027 | |||||||
| chr2:216043031 | A | G | 22 | a0001c0001t0001g0154 a0001c0001t0001g0208 a0001c0001t0001g0209 others(19): Show |
22 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(19): Show |
intron_variant | MODIFIER | c.826+873T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043031 | |||||||
| chr2:216043035 | A | G | 14 | a0001c0001t0001g0154 a0001c0001t0001g0208 a0001c0001t0001g0209 others(11): Show |
14 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.826+869T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043035 | |||||||
| chr2:216043035 | ATG | A | 218 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(215): Show |
230 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(227): Show |
intron_variant | MODIFIER | c.826+867_826+868del others(2): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043035 | |||||||
| chr2:216043037 | G | A | 7 | a0001c0001t0004g0256 a0001c0001t0004g0260 a0001c0001t0004g0365 others(4): Show |
7 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.826+867C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043037 | |||||||
| chr2:216043037 | G | GTATATAT others(23): Show |
20 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0039 others(17): Show |
22 | HG00280.hp2 HG00323.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.826+866_826+867ins others(30): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043037 | |||||||
| chr2:216043037 | G | GTATATAT others(23): Show |
8 | a0001c0001t0004g0306 a0001c0001t0005g0308 a0001c0001t0005g0310 others(5): Show |
8 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.826+866_826+867ins others(30): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043037 | |||||||
| chr2:216043039 | G | A | 4 | a0001c0001t0004g0256 a0001c0001t0004g0260 a0001c0001t0004g0365 others(1): Show |
4 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+865C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043039 | |||||||
| chr2:216043039 | GTA | G | 11 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(8): Show |
11 | HG02486.hp2 HG02572.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.826+863_826+864del others(2): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043039 | |||||||
| chr2:216043049 | ATACACAT others(3): Show |
A | 1 | a0004c0005t0009g0373 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.826+845_826+854del others(10): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043049 | |||||||
| chr2:216043052 | C | T | 7 | a0001c0001t0001g0154 a0001c0001t0001g0208 a0001c0001t0001g0209 others(4): Show |
7 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.826+852G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043052 | |||||||
| chr2:216043053 | A | G | 3 | a0001c0001t0005g0378 a0002c0002t0002g0333 a0002c0002t0002g0336 |
3 | HG02280.hp2 NA19064.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.826+851T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043053 | |||||||
| chr2:216043057 | ACG | A | 4 | a0001c0001t0004g0256 a0001c0001t0004g0260 a0001c0001t0004g0365 others(1): Show |
4 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+845_826+846del others(2): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043057 | |||||||
| chr2:216043059 | G | A | 7 | a0001c0001t0001g0154 a0001c0001t0001g0208 a0001c0001t0001g0209 others(4): Show |
7 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.826+845C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043059 | |||||||
| chr2:216043062 | T | C | 4 | a0001c0001t0004g0256 a0001c0001t0004g0260 a0001c0001t0004g0365 others(1): Show |
4 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+842A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043062 | |||||||
| chr2:216043063 | A | ACG | 7 | a0001c0001t0001g0154 a0001c0001t0001g0208 a0001c0001t0001g0209 others(4): Show |
7 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.826+840_826+841ins others(2): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043063 | |||||||
| chr2:216043063 | A | G | 4 | a0001c0001t0004g0256 a0001c0001t0004g0260 a0001c0001t0004g0365 others(1): Show |
4 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+841T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043063 | |||||||
| chr2:216043067 | G | A | 2 | a0004c0005t0009g0373 a0010c0012t0003g0211 |
2 | HG02109.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.826+837C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043067 | |||||||
| chr2:216043071 | G | A | 13 | a0001c0001t0001g0154 a0001c0001t0001g0208 a0001c0001t0001g0209 others(10): Show |
13 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(10): Show |
intron_variant | MODIFIER | c.826+833C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043071 | |||||||
| chr2:216043071 | G | GTA | 359 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(356): Show |
377 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(374): Show |
intron_variant | MODIFIER | c.826+831_826+832dup others(2): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043071 | |||||||
| chr2:216043071 | G | GTGTA | 5 | a0001c0001t0001g0004 a0001c0001t0001g0069 a0001c0001t0001g0086 others(2): Show |
5 | HG02486.hp2 HG02976.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.826+832_826+833ins others(4): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043071 | |||||||
| chr2:216043080 | T | C | 1 | a0004c0005t0009g0213 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.826+824A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043080 | |||||||
| chr2:216043083 | A | G | 6 | a0001c0001t0001g0059 a0001c0001t0001g0089 a0001c0001t0001g0195 others(3): Show |
6 | HG01081.hp1 HG02040.hp1 HG03834.hp1 others(3): Show |
intron_variant | MODIFIER | c.826+821T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043083 | |||||||
| chr2:216043084 | C | CACATATA others(19): Show |
7 | a0001c0001t0001g0154 a0001c0001t0001g0208 a0001c0001t0001g0209 others(4): Show |
7 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.826+819_826+820ins others(26): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043084 | |||||||
| chr2:216043086 | T | C | 11 | a0001c0001t0001g0154 a0001c0001t0001g0208 a0001c0001t0001g0209 others(8): Show |
11 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.826+818A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043086 | |||||||
| chr2:216043088 | C | T | 6 | a0001c0001t0004g0256 a0001c0001t0004g0260 a0001c0001t0004g0365 others(3): Show |
6 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.826+816G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043088 | |||||||
| chr2:216043089 | A | G | 3 | a0001c0001t0001g0195 a0002c0002t0002g0357 a0002c0002t0002g0372 |
3 | HG01884.hp2 HG03540.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.826+815T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043089 | |||||||
| chr2:216043090 | T | C | 9 | a0001c0001t0001g0154 a0001c0001t0001g0208 a0001c0001t0001g0209 others(6): Show |
9 | HG01975.hp2 HG02055.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.826+814A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043090 | |||||||
| chr2:216043091 | A | G | 2 | a0004c0005t0009g0213 a0004c0005t0009g0373 |
2 | HG02109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.826+813T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043091 | |||||||
| chr2:216043092 | T | C | 4 | a0001c0001t0004g0256 a0001c0001t0004g0260 a0001c0001t0004g0365 others(1): Show |
4 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+812A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043092 | |||||||
| chr2:216043093 | A | G | 4 | a0001c0001t0004g0256 a0001c0001t0004g0260 a0001c0001t0004g0365 others(1): Show |
4 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+811T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043093 | |||||||
| chr2:216043094 | T | C | 1 | a0010c0012t0003g0211 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.826+810A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043094 | |||||||
| chr2:216043095 | A | G | 3 | a0004c0005t0009g0213 a0004c0005t0009g0373 a0010c0012t0003g0211 |
3 | HG02109.hp1 HG03486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.826+809T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043095 | |||||||
| chr2:216043096 | T | C | 268 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(265): Show |
282 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.826+808A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043096 | |||||||
| chr2:216043097 | G | A | 1 | a0010c0012t0003g0211 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.826+807C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043097 | |||||||
| chr2:216043099 | A | G | 1 | a0010c0012t0003g0211 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.826+805T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043099 | |||||||
| chr2:216043101 | G | A | 4 | a0001c0001t0004g0256 a0001c0001t0004g0260 a0001c0001t0004g0365 others(1): Show |
4 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+803C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043101 | |||||||
| chr2:216043102 | C | T | 32 | a0001c0001t0001g0013 a0001c0001t0001g0028 a0001c0001t0001g0154 others(29): Show |
32 | HG00597.hp2 HG00642.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.826+802G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043102 | |||||||
| chr2:216043103 | G | A | 34 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0030 others(31): Show |
34 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(31): Show |
intron_variant | MODIFIER | c.826+801C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043103 | |||||||
| chr2:216043115 | A | ATTTT | 7 | a0001c0001t0001g0154 a0001c0001t0001g0208 a0001c0001t0001g0209 others(4): Show |
7 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.826+785_826+788dup others(4): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043115 | |||||||
| chr2:216043115 | A | T | 9 | a0001c0001t0004g0256 a0001c0001t0004g0260 a0001c0001t0004g0365 others(6): Show |
9 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.826+789T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043115 | |||||||
| chr2:216043117 | T | A | 8 | a0001c0001t0001g0135 a0001c0004t0001g0093 a0001c0004t0001g0094 others(5): Show |
8 | HG02109.hp1 HG02145.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.826+787A>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043117 | |||||||
| chr2:216043177 | G | A | 1 | a0001c0001t0001g0005 | 2 | NA18954.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.826+727C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043177 | |||||||
| chr2:216043198 | C | G | 7 | a0001c0001t0001g0154 a0001c0001t0001g0208 a0001c0001t0001g0209 others(4): Show |
7 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.826+706G>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043198 | |||||||
| chr2:216043284 | A | AT | 14 | a0001c0001t0001g0154 a0001c0001t0001g0208 a0001c0001t0001g0209 others(11): Show |
14 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.826+619dupA | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043284 | |||||||
| chr2:216043405 | C | T | 1 | a0001c0001t0004g0156 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.826+499G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043405 | |||||||
| chr2:216043504 | T | C | 3 | a0004c0005t0009g0213 a0004c0005t0009g0373 a0010c0012t0003g0211 |
3 | HG02109.hp1 HG03486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.826+400A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043504 | |||||||
| chr2:216043632 | C | T | 4 | a0001c0001t0004g0256 a0001c0001t0004g0260 a0001c0001t0004g0365 others(1): Show |
4 | HG01261.hp1 HG01261.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.826+272G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043632 | |||||||
| chr2:216043704 | C | T | 3 | a0004c0005t0009g0213 a0004c0005t0009g0373 a0010c0012t0003g0211 |
3 | HG02109.hp1 HG03486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.826+200G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043704 | |||||||
| chr2:216043711 | T | A | 3 | a0004c0005t0009g0213 a0004c0005t0009g0373 a0010c0012t0003g0211 |
3 | HG02109.hp1 HG03486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.826+193A>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 7/7 | chr2 | 216043711 | |||||||
| chr2:216044055 | T | A | 2 | a0002c0002t0002g0357 a0002c0002t0002g0372 |
2 | HG01884.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.715-40A>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216044055 | |||||||
| chr2:216044073 | G | A | 1 | a0001c0001t0001g0048 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.715-58C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216044073 | |||||||
| chr2:216044163 | A | T | 3 | a0001c0003t0003g0188 a0001c0003t0003g0190 a0001c0003t0003g0191 |
3 | HG02132.hp1 NA18952.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.715-148T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216044163 | |||||||
| chr2:216044187 | T | C | 273 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(270): Show |
287 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(284): Show |
intron_variant | MODIFIER | c.715-172A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216044187 | |||||||
| chr2:216044200 | C | G | 48 | a0002c0002t0002g0006 a0002c0002t0002g0009 a0002c0002t0002g0066 others(45): Show |
50 | HG00597.hp2 HG00609.hp2 HG01168.hp1 others(47): Show |
intron_variant | MODIFIER | c.715-185G>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216044200 | |||||||
| chr2:216044254 | G | A | 1 | a0009c0013t0002g0239 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.715-239C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216044254 | |||||||
| chr2:216044356 | T | G | 3 | a0004c0005t0009g0213 a0004c0005t0009g0373 a0010c0012t0003g0211 |
3 | HG02109.hp1 HG03486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.715-341A>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216044356 | |||||||
| chr2:216044484 | G | A | 3 | a0004c0005t0009g0213 a0004c0005t0009g0373 a0010c0012t0003g0211 |
3 | HG02109.hp1 HG03486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.715-469C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216044484 | |||||||
| chr2:216044571 | G | A | 3 | a0004c0005t0009g0213 a0004c0005t0009g0373 a0010c0012t0003g0211 |
3 | HG02109.hp1 HG03486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.715-556C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216044571 | |||||||
| chr2:216044613 | C | G | 3 | a0004c0005t0009g0213 a0004c0005t0009g0373 a0010c0012t0003g0211 |
3 | HG02109.hp1 HG03486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.715-598G>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216044613 | |||||||
| chr2:216044619 | G | T | 3 | a0004c0005t0009g0213 a0004c0005t0009g0373 a0010c0012t0003g0211 |
3 | HG02109.hp1 HG03486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.715-604C>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216044619 | |||||||
| chr2:216044628 | A | G | 3 | a0004c0005t0009g0213 a0004c0005t0009g0373 a0010c0012t0003g0211 |
3 | HG02109.hp1 HG03486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.715-613T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216044628 | |||||||
| chr2:216044645 | A | G | 273 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(270): Show |
287 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(284): Show |
intron_variant | MODIFIER | c.715-630T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216044645 | |||||||
| chr2:216044702 | AT | A | 3 | a0004c0005t0009g0213 a0004c0005t0009g0373 a0010c0012t0003g0211 |
3 | HG02109.hp1 HG03486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.715-688delA | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216044702 | |||||||
| chr2:216044712 | A | T | 3 | a0004c0005t0009g0213 a0004c0005t0009g0373 a0010c0012t0003g0211 |
3 | HG02109.hp1 HG03486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.715-697T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216044712 | |||||||
| chr2:216044725 | G | A | 1 | a0001c0003t0003g0196 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.715-710C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216044725 | |||||||
| chr2:216044792 | C | A | 7 | a0001c0001t0001g0154 a0001c0001t0001g0208 a0001c0001t0001g0209 others(4): Show |
7 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.715-777G>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216044792 | |||||||
| chr2:216044858 | G | A | 3 | a0004c0005t0009g0213 a0004c0005t0009g0373 a0010c0012t0003g0211 |
3 | HG02109.hp1 HG03486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.715-843C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216044858 | |||||||
| chr2:216045120 | G | T | 1 | a0001c0001t0001g0071 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.715-1105C>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216045120 | |||||||
| chr2:216045149 | C | G | 1 | a0001c0011t0006g0375 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.715-1134G>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216045149 | |||||||
| chr2:216045164 | C | T | 1 | a0001c0001t0004g0056 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.715-1149G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216045164 | |||||||
| chr2:216045179 | A | G | 2 | a0001c0001t0001g0136 a0001c0001t0001g0141 |
2 | NA18949.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.715-1164T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216045179 | |||||||
| chr2:216045273 | C | T | 137 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(134): Show |
146 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.715-1258G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216045273 | |||||||
| chr2:216045308 | G | A | 1 | a0002c0002t0002g0077 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.715-1293C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216045308 | |||||||
| chr2:216045373 | C | T | 1 | a0001c0001t0006g0103 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.715-1358G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216045373 | |||||||
| chr2:216045454 | A | T | 91 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(88): Show |
97 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.715-1439T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216045454 | |||||||
| chr2:216045490 | C | T | 9 | a0001c0001t0001g0016 a0001c0001t0001g0043 a0001c0001t0001g0101 others(6): Show |
10 | HG01106.hp2 HG01175.hp2 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.715-1475G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216045490 | |||||||
| chr2:216045570 | T | A | 3 | a0004c0005t0009g0213 a0004c0005t0009g0373 a0010c0012t0003g0211 |
3 | HG02109.hp1 HG03486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.715-1555A>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216045570 | |||||||
| chr2:216045747 | G | C | 3 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 |
3 | NA18990.hp2 NA18993.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.715-1732C>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216045747 | |||||||
| chr2:216045893 | A | T | 1 | a0001c0003t0003g0019 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.715-1878T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216045893 | |||||||
| chr2:216046015 | A | G | 4 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0223 others(1): Show |
4 | HG01346.hp1 HG02040.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.715-2000T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046015 | |||||||
| chr2:216046039 | T | C | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.715-2024A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046039 | |||||||
| chr2:216046048 | A | G | 1 | a0001c0001t0001g0100 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.715-2033T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046048 | |||||||
| chr2:216046101 | CA | C | 9 | a0001c0001t0001g0178 a0001c0001t0001g0343 a0001c0001t0004g0260 others(6): Show |
9 | HG01261.hp2 HG01433.hp1 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.715-2087delT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046101 | |||||||
| chr2:216046276 | GTA | G | 69 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 others(66): Show |
73 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.715-2263_715-2262d others(4): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046276 | |||||||
| chr2:216046277 | T | TATATATA others(7): Show |
1 | a0002c0002t0002g0105 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.715-2263_715-2262i others(16): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046277 | |||||||
| chr2:216046283 | T | TATACATA others(1): Show |
6 | a0002c0002t0002g0238 a0002c0002t0002g0241 a0002c0002t0002g0243 others(3): Show |
6 | HG01884.hp1 HG02630.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.715-2269_715-2268i others(10): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046283 | |||||||
| chr2:216046285 | T | TAC | 79 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0024 others(76): Show |
83 | HG00544.hp2 HG00738.hp1 HG01070.hp2 others(80): Show |
intron_variant | MODIFIER | c.715-2271_715-2270i others(4): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046285 | |||||||
| chr2:216046285 | T | TACATAC | 40 | a0001c0001t0001g0353 a0001c0001t0004g0056 a0002c0002t0002g0006 others(37): Show |
42 | HG00597.hp2 HG01168.hp1 HG01169.hp1 others(39): Show |
intron_variant | MODIFIER | c.715-2271_715-2270i others(8): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046285 | |||||||
| chr2:216046287 | T | C | 70 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0015 others(67): Show |
73 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.715-2272A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046287 | |||||||
| chr2:216046289 | C | CAT | 22 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0096 others(19): Show |
23 | HG00544.hp2 HG01070.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.715-2276_715-2275d others(4): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046289 | |||||||
| chr2:216046289 | C | T | 119 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0015 others(116): Show |
124 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.715-2274G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046289 | |||||||
| chr2:216046291 | T | C | 69 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0015 others(66): Show |
72 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.715-2276A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046291 | |||||||
| chr2:216046293 | C | T | 199 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(196): Show |
208 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(205): Show |
intron_variant | MODIFIER | c.715-2278G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046293 | |||||||
| chr2:216046302 | A | T | 1 | a0001c0011t0006g0375 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.715-2287T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046302 | |||||||
| chr2:216046304 | A | T | 2 | a0001c0011t0006g0375 a0004c0005t0009g0373 |
2 | HG02109.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.715-2289T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046304 | |||||||
| chr2:216046306 | A | T | 2 | a0001c0011t0006g0375 a0004c0005t0009g0373 |
2 | HG02109.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.715-2291T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046306 | |||||||
| chr2:216046308 | A | T | 3 | a0001c0001t0001g0209 a0001c0011t0006g0375 a0004c0005t0009g0373 |
3 | HG02109.hp1 HG02280.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.715-2293T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046308 | |||||||
| chr2:216046310 | A | AT | 9 | a0001c0001t0001g0087 a0001c0001t0001g0212 a0001c0003t0003g0147 others(6): Show |
10 | HG01256.hp2 HG02132.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.715-2296dupA | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046310 | |||||||
| chr2:216046310 | A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0101 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.715-2296_715-2295i others(17): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046310 | |||||||
| chr2:216046310 | A | ATATATAT others(5): Show |
3 | a0001c0001t0001g0016 a0001c0001t0001g0323 a0001c0001t0001g0324 |
4 | HG02615.hp1 HG02976.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.715-2296_715-2295i others(14): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046310 | |||||||
| chr2:216046310 | A | ATATT | 8 | a0001c0001t0004g0018 a0001c0001t0004g0156 a0001c0001t0004g0157 others(5): Show |
8 | HG02486.hp1 HG02615.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.715-2296_715-2295i others(6): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046310 | |||||||
| chr2:216046310 | A | ATT | 32 | a0001c0001t0004g0366 a0001c0001t0006g0103 a0001c0003t0001g0194 others(29): Show |
34 | HG00140.hp2 HG00733.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.715-2297_715-2296d others(4): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046310 | |||||||
| chr2:216046310 | A | G | 1 | a0001c0011t0006g0375 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.715-2295T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046310 | |||||||
| chr2:216046310 | A | T | 18 | a0001c0001t0001g0002 a0001c0001t0001g0036 a0001c0001t0001g0040 others(15): Show |
19 | HG00280.hp1 HG00609.hp1 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.715-2295T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046310 | |||||||
| chr2:216046310 | AT | A | 12 | a0001c0001t0001g0058 a0001c0001t0001g0064 a0001c0001t0001g0121 others(9): Show |
12 | HG01891.hp2 HG02015.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.715-2296delA | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046310 | |||||||
| chr2:216046311 | T | TA | 31 | a0001c0001t0001g0005 a0001c0001t0001g0086 a0001c0001t0001g0088 others(28): Show |
33 | HG00280.hp2 HG01099.hp1 HG02145.hp2 others(30): Show |
intron_variant | MODIFIER | c.715-2297_715-2296i others(3): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046311 | |||||||
| chr2:216046311 | T | TATATA | 3 | a0002c0002t0002g0228 a0002c0002t0002g0234 a0002c0002t0002g0363 |
3 | HG03654.hp2 HG03927.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.715-2297_715-2296i others(7): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046311 | |||||||
| chr2:216046312 | T | A | 120 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0010 others(117): Show |
127 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(124): Show |
intron_variant | MODIFIER | c.715-2297A>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046312 | |||||||
| chr2:216046313 | T | A | 25 | a0001c0001t0001g0064 a0001c0001t0001g0086 a0001c0001t0001g0088 others(22): Show |
26 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(23): Show |
intron_variant | MODIFIER | c.715-2298A>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046313 | |||||||
| chr2:216046313 | T | G | 1 | a0004c0005t0009g0373 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.715-2298A>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046313 | |||||||
| chr2:216046314 | T | A | 10 | a0001c0001t0001g0131 a0001c0001t0001g0180 a0001c0001t0001g0261 others(7): Show |
10 | HG00609.hp2 HG02080.hp1 HG02155.hp1 others(7): Show |
intron_variant | MODIFIER | c.715-2299A>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046314 | |||||||
| chr2:216046314 | T | G | 1 | a0001c0011t0006g0375 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.715-2299A>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046314 | |||||||
| chr2:216046315 | T | A | 6 | a0001c0001t0004g0306 a0001c0001t0005g0307 a0001c0001t0005g0311 others(3): Show |
6 | HG01891.hp2 HG02257.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.715-2300A>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046315 | |||||||
| chr2:216046318 | T | G | 2 | a0001c0011t0006g0375 a0004c0005t0009g0373 |
2 | HG02109.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.715-2303A>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046318 | |||||||
| chr2:216046323 | T | G | 2 | a0001c0011t0006g0375 a0004c0005t0009g0373 |
2 | HG02109.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.715-2308A>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046323 | |||||||
| chr2:216046323 | T | TTTTTGTT others(3): Show |
1 | a0010c0012t0003g0211 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.715-2309_715-2308i others(12): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046323 | |||||||
| chr2:216046339 | G | A | 85 | a0001c0001t0006g0103 a0002c0002t0002g0006 a0002c0002t0002g0009 others(82): Show |
88 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.715-2324C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046339 | |||||||
| chr2:216046500 | C | T | 1 | a0001c0003t0003g0295 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.715-2485G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046500 | |||||||
| chr2:216046510 | C | T | 1 | a0002c0002t0010g0330 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.715-2495G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046510 | |||||||
| chr2:216046617 | A | C | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.715-2602T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046617 | |||||||
| chr2:216046674 | A | G | 5 | a0001c0001t0001g0043 a0001c0001t0001g0376 a0001c0001t0007g0078 others(2): Show |
5 | HG01106.hp2 HG01175.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.714+2589T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046674 | |||||||
| chr2:216046759 | T | C | 2 | a0001c0001t0001g0223 a0001c0001t0001g0237 |
2 | HG02040.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.714+2504A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046759 | |||||||
| chr2:216046922 | C | T | 3 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 |
3 | HG02486.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.714+2341G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216046922 | |||||||
| chr2:216047118 | T | C | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+2145A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216047118 | |||||||
| chr2:216047259 | A | AG | 3 | a0001c0001t0004g0260 a0001c0001t0004g0365 a0001c0001t0004g0366 |
3 | HG01261.hp2 HG01433.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.714+2003dupC | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216047259 | |||||||
| chr2:216047260 | G | GAA | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+2002_714+2003i others(4): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216047260 | |||||||
| chr2:216047261 | G | A | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+2002C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216047261 | |||||||
| chr2:216047261 | G | GA | 260 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(257): Show |
273 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(270): Show |
intron_variant | MODIFIER | c.714+2001dupT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216047261 | |||||||
| chr2:216047512 | C | A | 1 | a0002c0002t0002g0372 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.714+1751G>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216047512 | |||||||
| chr2:216047719 | C | T | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+1544G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216047719 | |||||||
| chr2:216047756 | CA | C | 86 | a0002c0002t0002g0006 a0002c0002t0002g0009 a0002c0002t0002g0017 others(83): Show |
89 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.714+1506delT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216047756 | |||||||
| chr2:216047781 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.714+1482C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216047781 | |||||||
| chr2:216047810 | A | ATAAAT | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+1452_714+1453i others(7): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216047810 | |||||||
| chr2:216047827 | G | A | 3 | a0001c0001t0004g0260 a0001c0001t0004g0365 a0001c0001t0004g0366 |
3 | HG01261.hp2 HG01433.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.714+1436C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216047827 | |||||||
| chr2:216047842 | T | C | 7 | a0001c0001t0001g0154 a0001c0001t0001g0208 a0001c0001t0001g0209 others(4): Show |
7 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.714+1421A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216047842 | |||||||
| chr2:216047897 | T | C | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+1366A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216047897 | |||||||
| chr2:216047983 | A | AT | 14 | a0001c0001t0001g0041 a0001c0001t0004g0260 a0001c0001t0004g0306 others(11): Show |
14 | HG01261.hp2 HG01433.hp1 HG01515.hp1 others(11): Show |
intron_variant | MODIFIER | c.714+1279dupA | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216047983 | |||||||
| chr2:216047983 | AT | A | 79 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0015 others(76): Show |
83 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.714+1279delA | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216047983 | |||||||
| chr2:216048013 | T | G | 1 | a0001c0001t0001g0033 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.714+1250A>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048013 | |||||||
| chr2:216048057 | C | CTTTTCTT | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+1199_714+1205d others(9): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048057 | |||||||
| chr2:216048067 | C | T | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+1196G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048067 | |||||||
| chr2:216048075 | T | A | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+1188A>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048075 | |||||||
| chr2:216048107 | C | T | 3 | a0001c0001t0004g0260 a0001c0001t0004g0365 a0001c0001t0004g0366 |
3 | HG01261.hp2 HG01433.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.714+1156G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048107 | |||||||
| chr2:216048131 | G | A | 1 | a0001c0001t0005g0378 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.714+1132C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048131 | |||||||
| chr2:216048133 | G | A | 10 | a0001c0001t0001g0154 a0001c0001t0001g0208 a0001c0001t0001g0209 others(7): Show |
10 | HG01261.hp2 HG01433.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.714+1130C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048133 | |||||||
| chr2:216048135 | T | C | 5 | a0001c0001t0004g0348 a0001c0011t0006g0375 a0004c0005t0009g0213 others(2): Show |
5 | HG02109.hp1 HG02486.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.714+1128A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048135 | |||||||
| chr2:216048187 | G | C | 2 | a0002c0002t0002g0126 a0002c0002t0002g0232 |
2 | NA18612.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.714+1076C>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048187 | |||||||
| chr2:216048221 | T | C | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+1042A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048221 | |||||||
| chr2:216048235 | C | T | 13 | a0001c0001t0004g0306 a0001c0001t0005g0307 a0001c0001t0005g0308 others(10): Show |
13 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.714+1028G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048235 | |||||||
| chr2:216048277 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.714+986C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048277 | |||||||
| chr2:216048311 | G | A | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+952C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048311 | |||||||
| chr2:216048326 | C | T | 3 | a0001c0001t0007g0078 a0001c0001t0007g0079 a0001c0001t0007g0083 |
3 | HG01106.hp2 HG01358.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.714+937G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048326 | |||||||
| chr2:216048333 | C | T | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+930G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048333 | |||||||
| chr2:216048344 | G | C | 5 | a0001c0001t0001g0043 a0001c0001t0001g0376 a0001c0001t0007g0078 others(2): Show |
5 | HG01106.hp2 HG01175.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.714+919C>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048344 | |||||||
| chr2:216048366 | C | T | 15 | a0001c0001t0001g0352 a0001c0001t0001g0353 a0001c0001t0004g0018 others(12): Show |
16 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.714+897G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048366 | |||||||
| chr2:216048368 | C | A | 1 | a0002c0002t0002g0322 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.714+895G>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048368 | |||||||
| chr2:216048384 | TA | T | 226 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0015 others(223): Show |
237 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.714+878delT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048384 | |||||||
| chr2:216048384 | TAA | T | 32 | a0001c0001t0001g0087 a0001c0001t0001g0100 a0001c0001t0001g0148 others(29): Show |
33 | HG00323.hp1 HG00323.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.714+877_714+878del others(2): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048384 | |||||||
| chr2:216048441 | G | A | 2 | a0001c0001t0001g0278 a0001c0001t0001g0289 |
2 | HG01516.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.714+822C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048441 | |||||||
| chr2:216048464 | C | T | 2 | a0002c0002t0002g0357 a0002c0002t0002g0372 |
2 | HG01884.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.714+799G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048464 | |||||||
| chr2:216048485 | G | GT | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+777dupA | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048485 | |||||||
| chr2:216048584 | T | C | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+679A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048584 | |||||||
| chr2:216048625 | G | C | 4 | a0001c0001t0001g0016 a0001c0001t0001g0101 a0001c0001t0001g0323 others(1): Show |
5 | HG02055.hp2 HG02615.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.714+638C>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048625 | |||||||
| chr2:216048645 | A | G | 272 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(269): Show |
285 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(282): Show |
intron_variant | MODIFIER | c.714+618T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048645 | |||||||
| chr2:216048650 | C | T | 2 | a0001c0001t0001g0212 a0001c0001t0001g0214 |
2 | HG02886.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.714+613G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048650 | |||||||
| chr2:216048730 | G | A | 15 | a0001c0001t0001g0008 a0001c0001t0001g0108 a0001c0001t0001g0122 others(12): Show |
16 | HG00733.hp1 HG00738.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.714+533C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048730 | |||||||
| chr2:216048843 | C | CA | 41 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0022 others(38): Show |
43 | HG00558.hp2 HG00642.hp1 HG01175.hp1 others(40): Show |
intron_variant | MODIFIER | c.714+419dupT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048843 | |||||||
| chr2:216048843 | C | CAA | 11 | a0001c0001t0001g0061 a0001c0001t0001g0065 a0001c0001t0001g0070 others(8): Show |
11 | HG00642.hp2 HG01891.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.714+418_714+419dup others(2): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048843 | |||||||
| chr2:216048843 | CA | C | 170 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(167): Show |
181 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.714+419delT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048843 | |||||||
| chr2:216048865 | A | G | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+398T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048865 | |||||||
| chr2:216048869 | G | A | 24 | a0001c0001t0001g0352 a0001c0001t0001g0353 a0001c0001t0004g0018 others(21): Show |
25 | HG01891.hp2 HG02109.hp2 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.714+394C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048869 | |||||||
| chr2:216048888 | G | C | 1 | a0001c0001t0006g0103 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.714+375C>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048888 | |||||||
| chr2:216048957 | A | G | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+306T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216048957 | |||||||
| chr2:216049064 | A | G | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+199T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216049064 | |||||||
| chr2:216049090 | G | C | 9 | a0001c0001t0001g0016 a0001c0001t0001g0043 a0001c0001t0001g0101 others(6): Show |
10 | HG01106.hp2 HG01175.hp2 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.714+173C>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216049090 | |||||||
| chr2:216049185 | G | A | 1 | a0001c0001t0001g0337 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.714+78C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 6/7 | chr2 | 216049185 | |||||||
| chr2:216049763 | C | T | 3 | a0001c0001t0001g0180 a0001c0001t0001g0261 a0001c0001t0001g0266 |
3 | HG03831.hp2 NA20752.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.604-390G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 5/7 | chr2 | 216049763 | |||||||
| chr2:216049947 | G | A | 15 | a0001c0001t0001g0352 a0001c0001t0001g0353 a0001c0001t0004g0018 others(12): Show |
16 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.604-574C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 5/7 | chr2 | 216049947 | |||||||
| chr2:216050018 | G | C | 1 | a0002c0002t0002g0322 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.604-645C>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 5/7 | chr2 | 216050018 | |||||||
| chr2:216050155 | G | A | 1 | a0001c0001t0004g0351 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.604-782C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 5/7 | chr2 | 216050155 | |||||||
| chr2:216050197 | A | G | 273 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(270): Show |
286 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(283): Show |
intron_variant | MODIFIER | c.604-824T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 5/7 | chr2 | 216050197 | |||||||
| chr2:216050303 | G | A | 3 | a0001c0003t0003g0184 a0001c0003t0003g0185 a0005c0008t0002g0253 |
3 | HG01515.hp2 HG01517.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.604-930C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 5/7 | chr2 | 216050303 | |||||||
| chr2:216050416 | T | C | 1 | a0001c0001t0001g0374 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.603+1033A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 5/7 | chr2 | 216050416 | |||||||
| chr2:216050858 | G | A | 1 | a0002c0002t0002g0153 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.603+591C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 5/7 | chr2 | 216050858 | |||||||
| chr2:216050899 | T | TA | 13 | a0001c0001t0001g0050 a0001c0001t0001g0055 a0001c0001t0001g0101 others(10): Show |
13 | HG00423.hp2 HG01175.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.603+549dupT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 5/7 | chr2 | 216050899 | |||||||
| chr2:216050899 | TA | T | 11 | a0001c0001t0001g0052 a0001c0001t0001g0265 a0001c0001t0004g0306 others(8): Show |
11 | HG01168.hp2 HG01257.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.603+549delT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 5/7 | chr2 | 216050899 | |||||||
| chr2:216051084 | G | A | 1 | a0001c0003t0003g0203 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.603+365C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 5/7 | chr2 | 216051084 | |||||||
| chr2:216051095 | G | A | 9 | a0001c0001t0001g0016 a0001c0001t0001g0043 a0001c0001t0001g0101 others(6): Show |
10 | HG01106.hp2 HG01175.hp2 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.603+354C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 5/7 | chr2 | 216051095 | |||||||
| chr2:216051099 | A | C | 1 | a0001c0001t0001g0070 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.603+350T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 5/7 | chr2 | 216051099 | |||||||
| chr2:216051115 | A | G | 263 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(260): Show |
276 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.603+334T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 5/7 | chr2 | 216051115 | |||||||
| chr2:216051275 | C | G | 1 | a0001c0001t0001g0264 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.603+174G>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 5/7 | chr2 | 216051275 | |||||||
| chr2:216051281 | C | CAAA | 6 | a0001c0001t0001g0154 a0001c0001t0001g0208 a0001c0001t0001g0209 others(3): Show |
6 | HG01975.hp2 HG02280.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.603+165_603+167dup others(3): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 5/7 | chr2 | 216051281 | |||||||
| chr2:216051281 | CA | C | 110 | a0001c0001t0001g0016 a0001c0001t0001g0022 a0001c0001t0001g0030 others(107): Show |
114 | HG00597.hp2 HG00609.hp2 HG01070.hp1 others(111): Show |
intron_variant | MODIFIER | c.603+167delT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 5/7 | chr2 | 216051281 | |||||||
| chr2:216051281 | CAA | C | 79 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0086 others(76): Show |
85 | HG00140.hp2 HG00733.hp1 HG00738.hp2 others(82): Show |
intron_variant | MODIFIER | c.603+166_603+167del others(2): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 5/7 | chr2 | 216051281 | |||||||
| chr2:216051281 | CAAA | C | 76 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0015 others(73): Show |
80 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.603+165_603+167del others(3): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 5/7 | chr2 | 216051281 | |||||||
| chr2:216051299 | A | G | 3 | a0001c0001t0001g0158 a0001c0001t0004g0306 a0001c0001t0005g0318 |
3 | HG02818.hp2 HG03041.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.603+150T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 5/7 | chr2 | 216051299 | |||||||
| chr2:216051813 | A | G | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.507-268T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216051813 | |||||||
| chr2:216051962 | G | A | 1 | a0002c0002t0002g0066 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.507-417C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216051962 | |||||||
| chr2:216052034 | A | G | 7 | a0001c0001t0001g0154 a0001c0001t0001g0208 a0001c0001t0001g0209 others(4): Show |
7 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.507-489T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216052034 | |||||||
| chr2:216052051 | T | C | 1 | a0001c0001t0001g0069 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.507-506A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216052051 | |||||||
| chr2:216052058 | T | C | 272 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(269): Show |
285 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(282): Show |
intron_variant | MODIFIER | c.507-513A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216052058 | |||||||
| chr2:216052075 | G | A | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.507-530C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216052075 | |||||||
| chr2:216052100 | C | T | 1 | a0001c0001t0005g0307 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.507-555G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216052100 | |||||||
| chr2:216052101 | G | A | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.507-556C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216052101 | |||||||
| chr2:216052218 | T | C | 1 | a0002c0002t0002g0294 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.507-673A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216052218 | |||||||
| chr2:216052287 | A | G | 3 | a0001c0001t0001g0160 a0001c0001t0001g0161 a0001c0001t0001g0162 |
3 | NA18990.hp2 NA18993.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.507-742T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216052287 | |||||||
| chr2:216052572 | T | C | 1 | a0002c0002t0002g0187 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.507-1027A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216052572 | |||||||
| chr2:216052575 | T | C | 3 | a0001c0001t0001g0352 a0001c0001t0006g0029 a0001c0001t0006g0103 |
3 | HG02145.hp1 HG02723.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.507-1030A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216052575 | |||||||
| chr2:216052635 | C | T | 1 | a0002c0002t0010g0330 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.507-1090G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216052635 | |||||||
| chr2:216052646 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.507-1101C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216052646 | |||||||
| chr2:216052675 | T | G | 9 | a0001c0001t0004g0306 a0001c0001t0005g0307 a0001c0001t0005g0308 others(6): Show |
9 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.507-1130A>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216052675 | |||||||
| chr2:216052823 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.507-1278G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216052823 | |||||||
| chr2:216052832 | C | G | 2 | a0002c0002t0002g0359 a0002c0002t0002g0360 |
2 | HG02717.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.507-1287G>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216052832 | |||||||
| chr2:216052841 | C | G | 2 | a0001c0001t0001g0352 a0001c0001t0006g0103 |
2 | HG02145.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.507-1296G>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216052841 | |||||||
| chr2:216052891 | T | C | 2 | a0001c0001t0001g0223 a0001c0001t0001g0237 |
2 | HG02040.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.507-1346A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216052891 | |||||||
| chr2:216052922 | C | G | 1 | a0001c0001t0001g0091 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.507-1377G>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216052922 | |||||||
| chr2:216052986 | T | C | 9 | a0001c0001t0004g0306 a0001c0001t0005g0307 a0001c0001t0005g0308 others(6): Show |
9 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.507-1441A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216052986 | |||||||
| chr2:216053080 | C | T | 3 | a0001c0001t0001g0032 a0001c0001t0001g0038 a0001c0001t0001g0041 |
3 | NA18960.hp1 NA18980.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.507-1535G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216053080 | |||||||
| chr2:216053103 | C | T | 3 | a0001c0004t0001g0093 a0001c0004t0001g0094 a0001c0004t0001g0377 |
3 | HG02145.hp2 HG02647.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.507-1558G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216053103 | |||||||
| chr2:216053236 | A | ATTTTG | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.507-1696_507-1692d others(7): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216053236 | |||||||
| chr2:216053236 | ATTTTG | A | 15 | a0001c0001t0004g0306 a0001c0001t0005g0307 a0001c0001t0005g0308 others(12): Show |
15 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.507-1696_507-1692d others(7): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216053236 | |||||||
| chr2:216053446 | G | A | 249 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(246): Show |
262 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.507-1901C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216053446 | |||||||
| chr2:216054284 | T | C | 1 | a0002c0002t0002g0240 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.507-2739A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216054284 | |||||||
| chr2:216054306 | A | G | 2 | a0001c0001t0001g0277 a0001c0001t0001g0296 |
2 | HG00438.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.507-2761T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216054306 | |||||||
| chr2:216054339 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.507-2794C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216054339 | |||||||
| chr2:216054364 | T | C | 87 | a0002c0002t0002g0006 a0002c0002t0002g0009 a0002c0002t0002g0017 others(84): Show |
90 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.507-2819A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216054364 | |||||||
| chr2:216054371 | C | CT | 8 | a0001c0001t0001g0039 a0001c0001t0001g0042 a0001c0001t0001g0057 others(5): Show |
8 | HG00609.hp1 HG00741.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.507-2827dupA | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216054371 | |||||||
| chr2:216054371 | CT | C | 238 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(235): Show |
251 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.507-2827delA | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216054371 | |||||||
| chr2:216054371 | CTTTTTTT | C | 7 | a0001c0001t0001g0154 a0001c0001t0001g0208 a0001c0001t0001g0209 others(4): Show |
7 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.507-2833_507-2827d others(9): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216054371 | |||||||
| chr2:216054371 | CTTTTTTT others(2): Show |
C | 9 | a0001c0001t0004g0306 a0001c0001t0005g0307 a0001c0001t0005g0308 others(6): Show |
9 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.507-2835_507-2827d others(11): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216054371 | |||||||
| chr2:216054670 | T | C | 87 | a0002c0002t0002g0006 a0002c0002t0002g0009 a0002c0002t0002g0017 others(84): Show |
90 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.507-3125A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216054670 | |||||||
| chr2:216054682 | A | G | 1 | a0002c0002t0002g0220 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.507-3137T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216054682 | |||||||
| chr2:216054748 | T | C | 1 | a0002c0002t0002g0363 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.507-3203A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216054748 | |||||||
| chr2:216054749 | T | G | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.507-3204A>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216054749 | |||||||
| chr2:216054888 | G | A | 2 | a0001c0001t0001g0175 a0001c0001t0001g0176 |
2 | NA19003.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.507-3343C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216054888 | |||||||
| chr2:216054980 | C | A | 1 | a0002c0002t0002g0234 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.507-3435G>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216054980 | |||||||
| chr2:216054984 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.507-3439G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216054984 | |||||||
| chr2:216055113 | C | CA | 6 | a0001c0001t0001g0055 a0001c0001t0001g0071 a0001c0001t0008g0273 others(3): Show |
6 | HG01981.hp2 HG02293.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.507-3569dupT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216055113 | |||||||
| chr2:216055113 | C | CAA | 8 | a0001c0001t0001g0154 a0001c0001t0001g0208 a0001c0001t0001g0209 others(5): Show |
8 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.507-3570_507-3569d others(4): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216055113 | |||||||
| chr2:216055115 | A | G | 1 | a0001c0001t0001g0212 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.507-3570T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216055115 | |||||||
| chr2:216055146 | A | T | 1 | a0001c0001t0005g0215 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.507-3601T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216055146 | |||||||
| chr2:216055375 | T | C | 249 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(246): Show |
262 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.506+3520A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216055375 | |||||||
| chr2:216055403 | C | G | 136 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(133): Show |
144 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(141): Show |
intron_variant | MODIFIER | c.506+3492G>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216055403 | |||||||
| chr2:216055423 | A | G | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.506+3472T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216055423 | |||||||
| chr2:216055433 | A | G | 268 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(265): Show |
281 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.506+3462T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216055433 | |||||||
| chr2:216055434 | T | C | 1 | a0001c0001t0005g0378 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.506+3461A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216055434 | |||||||
| chr2:216055437 | CA | C | 257 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(254): Show |
270 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.506+3457delT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216055437 | |||||||
| chr2:216055441 | AAAAAAAA others(2): Show |
A | 10 | a0001c0001t0001g0154 a0001c0001t0001g0208 a0001c0001t0001g0209 others(7): Show |
10 | HG01261.hp2 HG01433.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.506+3445_506+3453d others(11): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216055441 | |||||||
| chr2:216055443 | A | C | 87 | a0002c0002t0002g0006 a0002c0002t0002g0009 a0002c0002t0002g0017 others(84): Show |
90 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.506+3452T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216055443 | |||||||
| chr2:216055462 | A | C | 17 | a0001c0001t0001g0138 a0001c0001t0001g0280 a0001c0001t0001g0353 others(14): Show |
19 | HG00423.hp2 HG02109.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.506+3433T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216055462 | |||||||
| chr2:216055500 | A | C | 2 | a0001c0001t0004g0306 a0001c0001t0005g0318 |
2 | HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.506+3395T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216055500 | |||||||
| chr2:216055530 | GACA | G | 10 | a0001c0001t0001g0154 a0001c0001t0001g0208 a0001c0001t0001g0209 others(7): Show |
10 | HG01261.hp2 HG01433.hp1 HG01515.hp1 others(7): Show |
intron_variant | MODIFIER | c.506+3362_506+3364d others(5): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216055530 | |||||||
| chr2:216055859 | G | T | 1 | a0001c0001t0001g0135 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.506+3036C>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216055859 | |||||||
| chr2:216055992 | C | T | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.506+2903G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216055992 | |||||||
| chr2:216056116 | A | G | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.506+2779T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216056116 | |||||||
| chr2:216056119 | C | G | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.506+2776G>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216056119 | |||||||
| chr2:216056342 | C | T | 5 | a0001c0001t0001g0043 a0001c0001t0001g0376 a0001c0001t0007g0078 others(2): Show |
5 | HG01106.hp2 HG01175.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.506+2553G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216056342 | |||||||
| chr2:216056467 | T | A | 4 | a0001c0003t0003g0097 a0001c0003t0003g0182 a0001c0003t0003g0183 others(1): Show |
4 | HG00733.hp1 HG00741.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.506+2428A>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216056467 | |||||||
| chr2:216056550 | G | A | 249 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(246): Show |
262 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.506+2345C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216056550 | |||||||
| chr2:216056585 | G | A | 2 | a0001c0001t0006g0029 a0001c0001t0006g0103 |
2 | HG02145.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.506+2310C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216056585 | |||||||
| chr2:216056599 | C | T | 272 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(269): Show |
285 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(282): Show |
intron_variant | MODIFIER | c.506+2296G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216056599 | |||||||
| chr2:216056697 | G | A | 4 | a0001c0001t0001g0290 a0001c0001t0001g0301 a0001c0001t0001g0302 others(1): Show |
4 | HG00609.hp1 HG00673.hp1 HG02040.hp1 others(1): Show |
intron_variant | MODIFIER | c.506+2198C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216056697 | |||||||
| chr2:216056721 | CAGAAAAA others(4): Show |
C | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.506+2163_506+2173d others(13): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216056721 | |||||||
| chr2:216056723 | G | GA | 90 | a0001c0001t0001g0041 a0001c0001t0001g0130 a0001c0001t0004g0260 others(87): Show |
93 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.506+2171dupT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216056723 | |||||||
| chr2:216056796 | G | A | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.506+2099C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216056796 | |||||||
| chr2:216056821 | T | C | 6 | a0001c0001t0001g0278 a0001c0001t0001g0289 a0001c0011t0006g0375 others(3): Show |
6 | HG01516.hp2 HG02109.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.506+2074A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216056821 | |||||||
| chr2:216056889 | A | C | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.506+2006T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216056889 | |||||||
| chr2:216056895 | C | G | 1 | a0001c0001t0001g0047 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.506+2000G>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216056895 | |||||||
| chr2:216056897 | G | T | 1 | a0001c0001t0007g0078 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.506+1998C>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216056897 | |||||||
| chr2:216056909 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.506+1986C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216056909 | |||||||
| chr2:216056938 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.506+1957A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216056938 | |||||||
| chr2:216057031 | T | C | 1 | a0001c0011t0006g0375 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.506+1864A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216057031 | |||||||
| chr2:216057168 | C | T | 1 | a0001c0001t0001g0353 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.506+1727G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216057168 | |||||||
| chr2:216057206 | A | C | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.506+1689T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216057206 | |||||||
| chr2:216057235 | C | T | 2 | a0001c0001t0001g0015 a0001c0001t0001g0279 |
3 | HG02015.hp2 HG02129.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.506+1660G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216057235 | |||||||
| chr2:216057489 | G | T | 19 | a0001c0001t0001g0353 a0001c0001t0004g0018 a0001c0001t0004g0056 others(16): Show |
20 | HG02109.hp1 HG02109.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.506+1406C>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216057489 | |||||||
| chr2:216057512 | A | G | 9 | a0001c0001t0004g0306 a0001c0001t0005g0307 a0001c0001t0005g0308 others(6): Show |
9 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.506+1383T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216057512 | |||||||
| chr2:216057636 | G | T | 1 | a0002c0002t0002g0358 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.506+1259C>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216057636 | |||||||
| chr2:216057869 | T | C | 3 | a0001c0001t0001g0100 a0001c0001t0001g0257 a0001c0001t0001g0258 |
3 | HG00280.hp2 HG00323.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.506+1026A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216057869 | |||||||
| chr2:216058042 | A | T | 1 | a0001c0001t0001g0159 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.506+853T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216058042 | |||||||
| chr2:216058084 | T | C | 1 | a0001c0001t0004g0351 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.506+811A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216058084 | |||||||
| chr2:216058152 | C | T | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.506+743G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216058152 | |||||||
| chr2:216058182 | T | A | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.506+713A>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216058182 | |||||||
| chr2:216058386 | G | C | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.506+509C>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216058386 | |||||||
| chr2:216058410 | G | A | 3 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 |
3 | HG02486.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.506+485C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216058410 | |||||||
| chr2:216058478 | A | T | 1 | a0002c0002t0002g0320 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.506+417T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216058478 | |||||||
| chr2:216058574 | T | C | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.506+321A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216058574 | |||||||
| chr2:216058830 | A | C | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.506+65T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 4/7 | chr2 | 216058830 | |||||||
| chr2:216059166 | T | C | 4 | a0001c0001t0001g0121 a0001c0001t0001g0134 a0001c0001t0001g0137 others(1): Show |
4 | NA18941.hp2 NA18957.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.425-190A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216059166 | |||||||
| chr2:216059222 | C | T | 9 | a0001c0001t0001g0014 a0001c0001t0001g0113 a0001c0001t0001g0121 others(6): Show |
10 | NA18941.hp2 NA18949.hp1 NA18957.hp1 others(7): Show |
intron_variant | MODIFIER | c.425-246G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216059222 | |||||||
| chr2:216059301 | G | T | 3 | a0001c0001t0004g0260 a0001c0001t0004g0365 a0001c0001t0004g0366 |
3 | HG01261.hp2 HG01433.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.425-325C>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216059301 | |||||||
| chr2:216059351 | C | T | 1 | a0002c0002t0002g0133 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.425-375G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216059351 | |||||||
| chr2:216059416 | T | A | 87 | a0002c0002t0002g0006 a0002c0002t0002g0009 a0002c0002t0002g0017 others(84): Show |
90 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.425-440A>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216059416 | |||||||
| chr2:216059424 | T | C | 87 | a0002c0002t0002g0006 a0002c0002t0002g0009 a0002c0002t0002g0017 others(84): Show |
90 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.425-448A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216059424 | |||||||
| chr2:216059442 | C | T | 7 | a0001c0001t0001g0154 a0001c0001t0001g0208 a0001c0001t0001g0209 others(4): Show |
7 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.425-466G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216059442 | |||||||
| chr2:216059537 | T | C | 3 | a0001c0001t0001g0352 a0001c0001t0006g0029 a0001c0001t0006g0103 |
3 | HG02145.hp1 HG02723.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.425-561A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216059537 | |||||||
| chr2:216059617 | C | G | 3 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 |
3 | HG02486.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.425-641G>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216059617 | |||||||
| chr2:216059769 | C | T | 2 | a0001c0004t0001g0093 a0001c0004t0001g0094 |
2 | HG02145.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.425-793G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216059769 | |||||||
| chr2:216059922 | T | C | 3 | a0001c0001t0001g0100 a0001c0001t0001g0257 a0001c0001t0001g0258 |
3 | HG00280.hp2 HG00323.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.425-946A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216059922 | |||||||
| chr2:216060049 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.425-1073G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216060049 | |||||||
| chr2:216060244 | C | T | 91 | a0001c0011t0006g0375 a0002c0002t0002g0006 a0002c0002t0002g0009 others(88): Show |
94 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.425-1268G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216060244 | |||||||
| chr2:216060248 | C | T | 91 | a0001c0011t0006g0375 a0002c0002t0002g0006 a0002c0002t0002g0009 others(88): Show |
94 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.425-1272G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216060248 | |||||||
| chr2:216060280 | T | C | 4 | a0001c0001t0001g0245 a0001c0001t0001g0246 a0001c0001t0001g0247 others(1): Show |
4 | NA18943.hp1 NA18969.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.425-1304A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216060280 | |||||||
| chr2:216060371 | A | C | 7 | a0001c0001t0001g0154 a0001c0001t0001g0208 a0001c0001t0001g0209 others(4): Show |
7 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.425-1395T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216060371 | |||||||
| chr2:216060479 | G | C | 91 | a0001c0011t0006g0375 a0002c0002t0002g0006 a0002c0002t0002g0009 others(88): Show |
94 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.425-1503C>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216060479 | |||||||
| chr2:216060528 | G | A | 2 | a0002c0002t0002g0357 a0002c0002t0002g0372 |
2 | HG01884.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.425-1552C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216060528 | |||||||
| chr2:216060539 | A | G | 91 | a0001c0011t0006g0375 a0002c0002t0002g0006 a0002c0002t0002g0009 others(88): Show |
94 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.425-1563T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216060539 | |||||||
| chr2:216060608 | G | C | 7 | a0001c0001t0001g0154 a0001c0001t0001g0208 a0001c0001t0001g0209 others(4): Show |
7 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.425-1632C>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216060608 | |||||||
| chr2:216060613 | T | C | 1 | a0001c0011t0006g0375 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.425-1637A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216060613 | |||||||
| chr2:216060742 | C | T | 1 | a0001c0001t0008g0287 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.425-1766G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216060742 | |||||||
| chr2:216060743 | A | C | 1 | a0001c0001t0008g0287 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.425-1767T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216060743 | |||||||
| chr2:216060755 | T | A | 1 | a0001c0001t0008g0287 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.425-1779A>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216060755 | |||||||
| chr2:216060766 | C | T | 1 | a0001c0001t0008g0287 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.425-1790G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216060766 | |||||||
| chr2:216060771 | A | C | 1 | a0001c0001t0008g0287 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.425-1795T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216060771 | |||||||
| chr2:216060818 | A | T | 1 | a0001c0001t0008g0287 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.425-1842T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216060818 | |||||||
| chr2:216060837 | A | T | 1 | a0001c0001t0008g0287 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.425-1861T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216060837 | |||||||
| chr2:216060843 | A | T | 1 | a0001c0001t0008g0287 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.425-1867T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216060843 | |||||||
| chr2:216060845 | A | C | 1 | a0001c0001t0008g0287 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.425-1869T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216060845 | |||||||
| chr2:216060874 | GA | G | 91 | a0001c0011t0006g0375 a0002c0002t0002g0006 a0002c0002t0002g0009 others(88): Show |
94 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.425-1899delT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216060874 | |||||||
| chr2:216060921 | TAATA | T | 8 | a0001c0001t0001g0016 a0001c0001t0001g0043 a0001c0001t0001g0101 others(5): Show |
9 | HG01106.hp2 HG01175.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.425-1949_425-1946d others(6): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216060921 | |||||||
| chr2:216061092 | G | A | 7 | a0001c0001t0001g0154 a0001c0001t0001g0208 a0001c0001t0001g0209 others(4): Show |
7 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.425-2116C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061092 | |||||||
| chr2:216061129 | C | CA | 14 | a0001c0001t0001g0004 a0001c0001t0001g0039 a0001c0001t0001g0040 others(11): Show |
14 | HG00423.hp1 HG01891.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.425-2154dupT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061129 | |||||||
| chr2:216061129 | CA | C | 50 | a0001c0001t0001g0010 a0001c0001t0001g0030 a0001c0001t0001g0100 others(47): Show |
50 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.425-2154delT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061129 | |||||||
| chr2:216061129 | CAA | C | 203 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0015 others(200): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.425-2155_425-2154d others(4): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061129 | |||||||
| chr2:216061129 | CAAA | C | 14 | a0001c0001t0001g0010 a0001c0001t0001g0214 a0001c0001t0001g0352 others(11): Show |
14 | HG01515.hp1 HG01891.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.425-2156_425-2154d others(5): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061129 | |||||||
| chr2:216061131 | A | C | 2 | a0001c0011t0006g0375 a0004c0005t0009g0213 |
2 | HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.425-2155T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061131 | |||||||
| chr2:216061132 | A | C | 2 | a0004c0005t0009g0373 a0010c0012t0003g0211 |
2 | HG02109.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.425-2156T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061132 | |||||||
| chr2:216061188 | T | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0107 a0001c0001t0001g0146 |
4 | HG00639.hp1 HG01123.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.425-2212A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061188 | |||||||
| chr2:216061258 | G | A | 1 | a0001c0001t0004g0018 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.425-2282C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061258 | |||||||
| chr2:216061263 | G | A | 1 | a0001c0001t0001g0041 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.425-2287C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061263 | |||||||
| chr2:216061276 | C | T | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.425-2300G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061276 | |||||||
| chr2:216061311 | C | CA | 35 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0022 others(32): Show |
37 | HG00423.hp1 HG00642.hp1 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.425-2336dupT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061311 | |||||||
| chr2:216061311 | C | CAA | 6 | a0001c0001t0001g0039 a0001c0001t0001g0046 a0001c0001t0001g0072 others(3): Show |
6 | HG01891.hp1 HG02922.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.425-2337_425-2336d others(4): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061311 | |||||||
| chr2:216061311 | CA | C | 9 | a0001c0001t0001g0062 a0001c0001t0001g0091 a0001c0001t0004g0309 others(6): Show |
9 | HG01167.hp1 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.425-2336delT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061311 | |||||||
| chr2:216061311 | CAA | C | 9 | a0001c0001t0001g0208 a0001c0001t0001g0367 a0001c0001t0004g0306 others(6): Show |
9 | HG01891.hp2 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.425-2337_425-2336d others(4): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061311 | |||||||
| chr2:216061311 | CAAA | C | 21 | a0001c0001t0001g0154 a0001c0001t0001g0162 a0001c0001t0001g0175 others(18): Show |
23 | HG01167.hp2 HG01169.hp2 HG01975.hp2 others(20): Show |
intron_variant | MODIFIER | c.425-2338_425-2336d others(5): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061311 | |||||||
| chr2:216061311 | CAAAA | C | 65 | a0001c0001t0001g0008 a0001c0001t0001g0024 a0001c0001t0001g0088 others(62): Show |
67 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(64): Show |
intron_variant | MODIFIER | c.425-2339_425-2336d others(6): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061311 | |||||||
| chr2:216061311 | CAAAAA | C | 76 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0015 others(73): Show |
82 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.425-2340_425-2336d others(7): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061311 | |||||||
| chr2:216061311 | CAAAAAAA | C | 6 | a0002c0002t0002g0066 a0002c0002t0002g0123 a0002c0002t0002g0233 others(3): Show |
6 | HG00597.hp2 HG01255.hp1 HG03688.hp1 others(3): Show |
intron_variant | MODIFIER | c.425-2342_425-2336d others(9): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061311 | |||||||
| chr2:216061311 | CAAAAAAA others(1): Show |
C | 47 | a0001c0011t0006g0375 a0002c0002t0002g0006 a0002c0002t0002g0009 others(44): Show |
49 | HG00609.hp2 HG01168.hp1 HG01169.hp1 others(46): Show |
intron_variant | MODIFIER | c.425-2343_425-2336d others(10): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061311 | |||||||
| chr2:216061311 | CAAAAAAA others(2): Show |
C | 34 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0077 others(31): Show |
35 | HG00544.hp2 HG01109.hp2 HG01123.hp2 others(32): Show |
intron_variant | MODIFIER | c.425-2344_425-2336d others(11): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061311 | |||||||
| chr2:216061311 | CAAAAAAA others(3): Show |
C | 4 | a0002c0002t0002g0173 a0002c0002t0002g0368 a0002c0002t0002g0370 others(1): Show |
4 | HG01070.hp2 HG01884.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.425-2345_425-2336d others(12): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061311 | |||||||
| chr2:216061311 | CAAAAAAA others(6): Show |
C | 2 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
2 | HG00280.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.425-2348_425-2336d others(15): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061311 | |||||||
| chr2:216061334 | AAAAAAAA others(3): Show |
A | 3 | a0001c0001t0004g0260 a0001c0001t0004g0365 a0001c0001t0004g0366 |
3 | HG01261.hp2 HG01433.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.425-2368_425-2359d others(12): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061334 | |||||||
| chr2:216061343 | A | C | 1 | a0001c0001t0001g0214 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.425-2367T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061343 | |||||||
| chr2:216061348 | C | G | 87 | a0002c0002t0002g0006 a0002c0002t0002g0009 a0002c0002t0002g0017 others(84): Show |
90 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.425-2372G>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061348 | |||||||
| chr2:216061349 | C | T | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.425-2373G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061349 | |||||||
| chr2:216061491 | G | A | 9 | a0001c0001t0004g0306 a0001c0001t0005g0307 a0001c0001t0005g0308 others(6): Show |
9 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.425-2515C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061491 | |||||||
| chr2:216061790 | T | C | 1 | a0001c0003t0003g0076 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.425-2814A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061790 | |||||||
| chr2:216061897 | G | T | 1 | a0001c0003t0003g0076 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.425-2921C>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061897 | |||||||
| chr2:216061955 | C | T | 2 | a0001c0001t0001g0352 a0001c0001t0006g0103 |
2 | HG02145.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.425-2979G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061955 | |||||||
| chr2:216061970 | A | ATGTG | 86 | a0002c0002t0002g0006 a0002c0002t0002g0009 a0002c0002t0002g0017 others(83): Show |
89 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.425-2998_425-2995d others(6): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061970 | |||||||
| chr2:216061970 | A | ATGTGTGT others(3): Show |
3 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 |
3 | HG02109.hp1 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.425-3004_425-2995d others(12): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061970 | |||||||
| chr2:216061970 | A | ATGTGTGT others(7): Show |
1 | a0010c0012t0003g0211 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.425-3008_425-2995d others(16): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216061970 | |||||||
| chr2:216062040 | A | C | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.425-3064T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216062040 | |||||||
| chr2:216062045 | G | A | 91 | a0001c0011t0006g0375 a0002c0002t0002g0006 a0002c0002t0002g0009 others(88): Show |
94 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.425-3069C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216062045 | |||||||
| chr2:216062052 | A | AT | 8 | a0001c0001t0001g0055 a0001c0001t0001g0160 a0001c0001t0001g0340 others(5): Show |
8 | HG01891.hp2 HG01981.hp2 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.425-3077dupA | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216062052 | |||||||
| chr2:216062125 | A | C | 3 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 |
3 | HG02486.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.425-3149T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216062125 | |||||||
| chr2:216062236 | G | C | 1 | a0001c0001t0001g0150 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.424+3076C>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216062236 | |||||||
| chr2:216062297 | C | T | 11 | a0001c0001t0001g0005 a0001c0001t0001g0058 a0001c0001t0001g0089 others(8): Show |
12 | HG02015.hp1 HG02083.hp1 HG02155.hp2 others(9): Show |
intron_variant | MODIFIER | c.424+3015G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216062297 | |||||||
| chr2:216062441 | G | A | 87 | a0002c0002t0002g0006 a0002c0002t0002g0009 a0002c0002t0002g0017 others(84): Show |
90 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.424+2871C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216062441 | |||||||
| chr2:216062498 | T | A | 1 | a0001c0001t0001g0132 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.424+2814A>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216062498 | |||||||
| chr2:216062543 | T | C | 9 | a0001c0001t0004g0306 a0001c0001t0005g0307 a0001c0001t0005g0308 others(6): Show |
9 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.424+2769A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216062543 | |||||||
| chr2:216062639 | G | A | 5 | a0002c0002t0002g0105 a0002c0002t0002g0238 a0002c0002t0002g0241 others(2): Show |
5 | HG00609.hp2 NA18965.hp1 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.424+2673C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216062639 | |||||||
| chr2:216062724 | C | T | 85 | a0002c0002t0002g0006 a0002c0002t0002g0009 a0002c0002t0002g0017 others(82): Show |
88 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.424+2588G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216062724 | |||||||
| chr2:216062869 | C | T | 3 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 |
3 | HG02486.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.424+2443G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216062869 | |||||||
| chr2:216063075 | T | C | 85 | a0002c0002t0002g0006 a0002c0002t0002g0009 a0002c0002t0002g0017 others(82): Show |
88 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.424+2237A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216063075 | |||||||
| chr2:216063107 | TA | T | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+2204delT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216063107 | |||||||
| chr2:216063142 | A | C | 9 | a0001c0001t0004g0306 a0001c0001t0005g0307 a0001c0001t0005g0308 others(6): Show |
9 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.424+2170T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216063142 | |||||||
| chr2:216063225 | G | A | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+2087C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216063225 | |||||||
| chr2:216063239 | C | T | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+2073G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216063239 | |||||||
| chr2:216063243 | T | C | 1 | a0002c0002t0002g0322 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.424+2069A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216063243 | |||||||
| chr2:216063444 | C | T | 9 | a0001c0001t0004g0306 a0001c0001t0005g0307 a0001c0001t0005g0308 others(6): Show |
9 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.424+1868G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216063444 | |||||||
| chr2:216063532 | T | C | 91 | a0001c0011t0006g0375 a0002c0002t0002g0006 a0002c0002t0002g0009 others(88): Show |
94 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.424+1780A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216063532 | |||||||
| chr2:216063719 | T | A | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+1593A>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216063719 | |||||||
| chr2:216063732 | T | G | 2 | a0001c0001t0001g0352 a0001c0001t0006g0103 |
2 | HG02145.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.424+1580A>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216063732 | |||||||
| chr2:216063819 | G | T | 1 | a0001c0001t0001g0286 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.424+1493C>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216063819 | |||||||
| chr2:216063827 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.424+1485G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216063827 | |||||||
| chr2:216063889 | T | C | 1 | a0001c0001t0001g0034 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.424+1423A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216063889 | |||||||
| chr2:216063914 | G | A | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+1398C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216063914 | |||||||
| chr2:216063925 | G | A | 8 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0277 others(5): Show |
8 | HG00438.hp1 HG00544.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.424+1387C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216063925 | |||||||
| chr2:216063968 | G | A | 4 | a0001c0001t0004g0018 a0001c0001t0004g0155 a0001c0001t0004g0156 others(1): Show |
5 | HG02896.hp1 HG02897.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+1344C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216063968 | |||||||
| chr2:216063990 | G | A | 1 | a0001c0001t0001g0278 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.424+1322C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216063990 | |||||||
| chr2:216064042 | T | C | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+1270A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216064042 | |||||||
| chr2:216064138 | C | T | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+1174G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216064138 | |||||||
| chr2:216064147 | C | T | 113 | a0001c0001t0001g0154 a0001c0001t0001g0208 a0001c0001t0001g0209 others(110): Show |
116 | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(113): Show |
intron_variant | MODIFIER | c.424+1165G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216064147 | |||||||
| chr2:216064201 | A | T | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+1111T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216064201 | |||||||
| chr2:216064243 | A | T | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+1069T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216064243 | |||||||
| chr2:216064336 | C | T | 8 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0045 others(5): Show |
8 | HG02109.hp1 HG03486.hp2 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.424+976G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216064336 | |||||||
| chr2:216064399 | C | T | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+913G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216064399 | |||||||
| chr2:216064557 | T | G | 1 | a0001c0003t0003g0204 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.424+755A>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216064557 | |||||||
| chr2:216064560 | C | T | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.424+752G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216064560 | |||||||
| chr2:216064885 | T | G | 1 | a0001c0001t0001g0337 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.424+427A>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216064885 | |||||||
| chr2:216065228 | G | A | 5 | a0001c0001t0001g0063 a0001c0001t0001g0064 a0001c0001t0001g0065 others(2): Show |
5 | HG02559.hp2 HG02965.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+84C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 3/7 | chr2 | 216065228 | |||||||
| chr2:216065523 | C | T | 1 | a0001c0003t0003g0235 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.259-46G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 2/7 | chr2 | 216065523 | |||||||
| chr2:216065761 | C | T | 5 | a0001c0003t0003g0012 a0001c0003t0003g0188 a0001c0003t0003g0189 others(2): Show |
6 | HG02071.hp1 HG02132.hp1 NA18952.hp2 others(3): Show |
intron_variant | MODIFIER | c.259-284G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 2/7 | chr2 | 216065761 | |||||||
| chr2:216065765 | T | C | 2 | a0001c0001t0001g0084 a0001c0001t0001g0085 |
2 | HG00280.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.259-288A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 2/7 | chr2 | 216065765 | |||||||
| chr2:216065852 | C | T | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.259-375G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 2/7 | chr2 | 216065852 | |||||||
| chr2:216065942 | C | T | 266 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(263): Show |
279 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(276): Show |
intron_variant | MODIFIER | c.258+443G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 2/7 | chr2 | 216065942 | |||||||
| chr2:216065943 | G | A | 7 | a0001c0001t0001g0154 a0001c0001t0001g0208 a0001c0001t0001g0209 others(4): Show |
7 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.258+442C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 2/7 | chr2 | 216065943 | |||||||
| chr2:216065952 | C | T | 2 | a0002c0002t0002g0228 a0002c0002t0002g0234 |
2 | HG03927.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.258+433G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 2/7 | chr2 | 216065952 | |||||||
| chr2:216065961 | G | T | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+424C>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 2/7 | chr2 | 216065961 | |||||||
| chr2:216065967 | T | C | 6 | a0001c0001t0001g0109 a0001c0001t0001g0148 a0001c0001t0001g0160 others(3): Show |
6 | HG00438.hp2 HG00673.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.258+418A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 2/7 | chr2 | 216065967 | |||||||
| chr2:216066059 | G | A | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+326C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 2/7 | chr2 | 216066059 | |||||||
| chr2:216066075 | T | C | 1 | a0001c0011t0006g0375 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.258+310A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 2/7 | chr2 | 216066075 | |||||||
| chr2:216066125 | AAAAAAT | A | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+254_258+259del others(6): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 2/7 | chr2 | 216066125 | |||||||
| chr2:216066151 | T | TA | 4 | a0001c0004t0001g0093 a0001c0004t0001g0094 a0001c0004t0001g0377 others(1): Show |
5 | HG02145.hp2 HG02647.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.258+233dupT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 2/7 | chr2 | 216066151 | |||||||
| chr2:216066216 | T | G | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+169A>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 2/7 | chr2 | 216066216 | |||||||
| chr2:216066222 | G | A | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.258+163C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 2/7 | chr2 | 216066222 | |||||||
| chr2:216066537 | AGAACAAA others(59): Show |
A | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.125-85_125-20delCC others(64): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216066537 | |||||||
| chr2:216066633 | C | A | 2 | a0001c0001t0001g0352 a0001c0001t0006g0103 |
2 | HG02145.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.125-115G>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216066633 | |||||||
| chr2:216066865 | A | G | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.125-347T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216066865 | |||||||
| chr2:216066897 | G | C | 4 | a0001c0004t0001g0093 a0001c0004t0001g0094 a0001c0004t0001g0377 others(1): Show |
5 | HG02145.hp2 HG02647.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.125-379C>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216066897 | |||||||
| chr2:216067004 | T | C | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.125-486A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216067004 | |||||||
| chr2:216067059 | T | C | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.125-541A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216067059 | |||||||
| chr2:216067065 | C | G | 25 | a0002c0002t0002g0017 a0002c0002t0002g0026 a0002c0002t0002g0096 others(22): Show |
26 | HG00544.hp2 HG01070.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.125-547G>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216067065 | |||||||
| chr2:216067184 | T | TTGCCCAG others(4): Show |
1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-677_125-667dup others(11): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216067184 | |||||||
| chr2:216067213 | C | G | 1 | a0001c0001t0001g0044 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.125-695G>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216067213 | |||||||
| chr2:216067221 | G | A | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.125-703C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216067221 | |||||||
| chr2:216067235 | T | A | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.125-717A>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216067235 | |||||||
| chr2:216067369 | GCCCACCA others(7): Show |
G | 1 | a0001c0001t0001g0158 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.125-865_125-852del others(14): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216067369 | |||||||
| chr2:216067447 | C | G | 3 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 |
3 | HG02486.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.125-929G>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216067447 | |||||||
| chr2:216067563 | CT | C | 25 | a0001c0001t0001g0010 a0001c0001t0001g0106 a0001c0001t0001g0107 others(22): Show |
26 | HG00438.hp2 HG00621.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.125-1046delA | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216067563 | |||||||
| chr2:216067589 | A | G | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.125-1071T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216067589 | |||||||
| chr2:216067605 | G | A | 162 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(159): Show |
172 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.125-1087C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216067605 | |||||||
| chr2:216067625 | C | T | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.125-1107G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216067625 | |||||||
| chr2:216067993 | C | T | 7 | a0001c0001t0001g0154 a0001c0001t0001g0208 a0001c0001t0001g0209 others(4): Show |
7 | HG01975.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.125-1475G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216067993 | |||||||
| chr2:216067996 | A | T | 2 | a0001c0004t0001g0093 a0001c0004t0001g0094 |
2 | HG02145.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.125-1478T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216067996 | |||||||
| chr2:216067999 | C | A | 6 | a0002c0002t0002g0105 a0002c0002t0002g0238 a0002c0002t0002g0240 others(3): Show |
6 | HG00609.hp2 HG04228.hp2 NA18965.hp1 others(3): Show |
intron_variant | MODIFIER | c.125-1481G>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216067999 | |||||||
| chr2:216068155 | A | T | 1 | a0001c0001t0001g0171 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.125-1637T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216068155 | |||||||
| chr2:216068156 | G | A | 5 | a0002c0002t0002g0006 a0002c0002t0002g0112 a0002c0002t0002g0114 others(2): Show |
6 | NA18948.hp2 NA18961.hp1 NA18978.hp2 others(3): Show |
intron_variant | MODIFIER | c.125-1638C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216068156 | |||||||
| chr2:216068221 | A | G | 4 | a0001c0001t0001g0024 a0001c0001t0001g0033 a0001c0001t0001g0291 others(1): Show |
4 | HG00140.hp1 HG00323.hp1 HG00738.hp1 others(1): Show |
intron_variant | MODIFIER | c.125-1703T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216068221 | |||||||
| chr2:216068225 | C | CA | 49 | a0001c0001t0001g0032 a0001c0001t0001g0038 a0001c0001t0001g0039 others(46): Show |
49 | HG00423.hp1 HG00609.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.125-1708dupT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216068225 | |||||||
| chr2:216068225 | CA | C | 128 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0015 others(125): Show |
135 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(132): Show |
intron_variant | MODIFIER | c.125-1708delT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216068225 | |||||||
| chr2:216068225 | CAA | C | 25 | a0001c0001t0001g0016 a0001c0001t0001g0101 a0001c0001t0001g0154 others(22): Show |
27 | HG01975.hp2 HG02055.hp1 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.125-1709_125-1708d others(4): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216068225 | |||||||
| chr2:216068250 | C | T | 1 | a0001c0001t0001g0120 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.125-1732G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216068250 | |||||||
| chr2:216068701 | G | A | 9 | a0001c0001t0004g0306 a0001c0001t0005g0307 a0001c0001t0005g0308 others(6): Show |
9 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.125-2183C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216068701 | |||||||
| chr2:216068748 | C | T | 9 | a0001c0001t0004g0306 a0001c0001t0005g0307 a0001c0001t0005g0308 others(6): Show |
9 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.125-2230G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216068748 | |||||||
| chr2:216068769 | C | G | 3 | a0001c0001t0004g0260 a0001c0001t0004g0365 a0001c0001t0004g0366 |
3 | HG01261.hp2 HG01433.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.125-2251G>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216068769 | |||||||
| chr2:216068804 | A | AT | 16 | a0001c0001t0001g0025 a0001c0001t0001g0035 a0001c0001t0001g0036 others(13): Show |
16 | HG00673.hp1 HG01261.hp2 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.125-2287dupA | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216068804 | |||||||
| chr2:216068804 | AT | A | 226 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(223): Show |
238 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(235): Show |
intron_variant | MODIFIER | c.125-2287delA | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216068804 | |||||||
| chr2:216068804 | ATT | A | 16 | a0001c0001t0001g0148 a0001c0001t0001g0214 a0001c0001t0001g0288 others(13): Show |
17 | HG01256.hp2 HG02109.hp2 HG02300.hp1 others(14): Show |
intron_variant | MODIFIER | c.125-2288_125-2287d others(4): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216068804 | |||||||
| chr2:216068804 | ATTTTTTT others(6): Show |
A | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.125-2299_125-2287d others(15): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216068804 | |||||||
| chr2:216068890 | T | C | 1 | a0001c0001t0006g0029 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.125-2372A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216068890 | |||||||
| chr2:216068904 | C | CAGATCTC others(7): Show |
1 | a0001c0001t0001g0158 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.125-2400_125-2387d others(16): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216068904 | |||||||
| chr2:216068953 | G | A | 4 | a0001c0011t0006g0375 a0004c0005t0009g0213 a0004c0005t0009g0373 others(1): Show |
4 | HG02109.hp1 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.125-2435C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216068953 | |||||||
| chr2:216069069 | C | T | 273 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(270): Show |
286 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(283): Show |
intron_variant | MODIFIER | c.125-2551G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069069 | |||||||
| chr2:216069139 | C | T | 14 | a0001c0001t0004g0306 a0001c0001t0005g0307 a0001c0001t0005g0308 others(11): Show |
14 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.125-2621G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069139 | |||||||
| chr2:216069173 | G | T | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-2655C>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069173 | |||||||
| chr2:216069174 | C | G | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-2656G>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069174 | |||||||
| chr2:216069175 | A | C | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-2657T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069175 | |||||||
| chr2:216069195 | C | T | 1 | a0001c0001t0005g0378 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.125-2677G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069195 | |||||||
| chr2:216069197 | A | C | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-2679T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069197 | |||||||
| chr2:216069199 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-2681G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069199 | |||||||
| chr2:216069318 | G | T | 1 | a0001c0001t0001g0011 | 2 | HG00558.hp1 HG00597.hp1 |
intron_variant | MODIFIER | c.125-2800C>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069318 | |||||||
| chr2:216069339 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-2821G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069339 | |||||||
| chr2:216069348 | C | A | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-2830G>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069348 | |||||||
| chr2:216069359 | A | T | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-2841T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069359 | |||||||
| chr2:216069366 | A | T | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-2848T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069366 | |||||||
| chr2:216069370 | A | T | 1 | a0002c0002t0002g0124 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.125-2852T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069370 | |||||||
| chr2:216069392 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-2874G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069392 | |||||||
| chr2:216069397 | G | A | 1 | a0001c0011t0006g0375 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.125-2879C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069397 | |||||||
| chr2:216069397 | G | C | 80 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(77): Show |
85 | HG00280.hp1 HG00423.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.125-2879C>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069397 | |||||||
| chr2:216069401 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-2883C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069401 | |||||||
| chr2:216069403 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-2885G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069403 | |||||||
| chr2:216069404 | T | A | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-2886A>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069404 | |||||||
| chr2:216069413 | A | G | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-2895T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069413 | |||||||
| chr2:216069453 | T | G | 2 | a0002c0002t0002g0357 a0002c0002t0002g0372 |
2 | HG01884.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.125-2935A>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069453 | |||||||
| chr2:216069474 | T | A | 2 | a0002c0002t0002g0357 a0002c0002t0002g0372 |
2 | HG01884.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.125-2956A>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069474 | |||||||
| chr2:216069514 | C | T | 2 | a0002c0002t0002g0357 a0002c0002t0002g0372 |
2 | HG01884.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.125-2996G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069514 | |||||||
| chr2:216069574 | G | A | 1 | a0001c0001t0001g0090 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.125-3056C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069574 | |||||||
| chr2:216069693 | T | G | 1 | a0004c0005t0009g0213 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.125-3175A>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069693 | |||||||
| chr2:216069706 | G | C | 3 | a0001c0004t0001g0093 a0001c0004t0001g0094 a0001c0004t0001g0377 |
3 | HG02145.hp2 HG02647.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.125-3188C>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069706 | |||||||
| chr2:216069734 | G | A | 29 | a0001c0001t0001g0016 a0001c0001t0001g0062 a0001c0001t0001g0101 others(26): Show |
33 | HG01167.hp1 HG01167.hp2 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.125-3216C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069734 | |||||||
| chr2:216069765 | T | G | 36 | a0001c0001t0001g0016 a0001c0001t0001g0063 a0001c0001t0001g0064 others(33): Show |
40 | HG01167.hp2 HG01169.hp2 HG01261.hp2 others(37): Show |
intron_variant | MODIFIER | c.125-3247A>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069765 | |||||||
| chr2:216069808 | C | T | 322 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(319): Show |
339 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(336): Show |
intron_variant | MODIFIER | c.125-3290G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069808 | |||||||
| chr2:216069830 | G | A | 1 | a0001c0001t0001g0291 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.125-3312C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069830 | |||||||
| chr2:216069900 | C | T | 1 | a0001c0001t0001g0042 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.125-3382G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069900 | |||||||
| chr2:216069934 | C | CA | 10 | a0001c0001t0001g0040 a0001c0001t0001g0067 a0001c0001t0001g0082 others(7): Show |
10 | HG01175.hp1 NA18943.hp1 NA18962.hp1 others(7): Show |
intron_variant | MODIFIER | c.125-3417dupT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069934 | |||||||
| chr2:216069934 | CAAA | C | 156 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0015 others(153): Show |
164 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(161): Show |
intron_variant | MODIFIER | c.125-3419_125-3417d others(5): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069934 | |||||||
| chr2:216069934 | CAAAA | C | 6 | a0001c0001t0001g0179 a0001c0001t0004g0365 a0001c0001t0004g0366 others(3): Show |
7 | HG00544.hp1 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.125-3420_125-3417d others(6): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069934 | |||||||
| chr2:216069979 | T | C | 1 | a0002c0002t0002g0234 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.125-3461A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216069979 | |||||||
| chr2:216070011 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3493C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070011 | |||||||
| chr2:216070012 | A | G | 1 | a0001c0001t0005g0378 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.125-3494T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070012 | |||||||
| chr2:216070012 | A | T | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3494T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070012 | |||||||
| chr2:216070014 | C | T | 1 | a0002c0002t0002g0105 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.125-3496G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070014 | |||||||
| chr2:216070020 | A | T | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3502T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070020 | |||||||
| chr2:216070035 | A | T | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3517T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070035 | |||||||
| chr2:216070038 | A | T | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3520T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070038 | |||||||
| chr2:216070046 | A | G | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3528T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070046 | |||||||
| chr2:216070061 | T | C | 57 | a0001c0001t0001g0016 a0001c0001t0001g0068 a0001c0001t0001g0086 others(54): Show |
61 | HG01167.hp2 HG01169.hp2 HG01243.hp1 others(58): Show |
intron_variant | MODIFIER | c.125-3543A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070061 | |||||||
| chr2:216070071 | A | T | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3553T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070071 | |||||||
| chr2:216070073 | A | G | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3555T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070073 | |||||||
| chr2:216070076 | A | T | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3558T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070076 | |||||||
| chr2:216070078 | A | T | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3560T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070078 | |||||||
| chr2:216070079 | A | G | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3561T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070079 | |||||||
| chr2:216070082 | T | G | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3564A>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070082 | |||||||
| chr2:216070083 | A | T | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3565T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070083 | |||||||
| chr2:216070088 | A | G | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3570T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070088 | |||||||
| chr2:216070093 | A | T | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3575T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070093 | |||||||
| chr2:216070140 | AAC | A | 3 | a0001c0001t0006g0029 a0001c0003t0003g0235 a0005c0008t0002g0315 |
3 | HG02572.hp1 NA19083.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.125-3624_125-3623d others(4): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070140 | |||||||
| chr2:216070176 | T | A | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3658A>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070176 | |||||||
| chr2:216070308 | A | C | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3790T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070308 | |||||||
| chr2:216070308 | A | G | 1 | a0001c0001t0001g0337 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.125-3790T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070308 | |||||||
| chr2:216070309 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3791G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070309 | |||||||
| chr2:216070316 | C | G | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3798G>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070316 | |||||||
| chr2:216070323 | C | A | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3805G>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070323 | |||||||
| chr2:216070324 | A | T | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3806T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070324 | |||||||
| chr2:216070325 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3807G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070325 | |||||||
| chr2:216070327 | A | T | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3809T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070327 | |||||||
| chr2:216070328 | T | C | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3810A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070328 | |||||||
| chr2:216070329 | T | A | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3811A>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070329 | |||||||
| chr2:216070331 | T | G | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3813A>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070331 | |||||||
| chr2:216070334 | G | C | 58 | a0001c0001t0001g0323 a0001c0001t0001g0324 a0001c0001t0001g0327 others(55): Show |
62 | HG00544.hp2 HG00621.hp2 HG01070.hp2 others(59): Show |
intron_variant | MODIFIER | c.125-3816C>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070334 | |||||||
| chr2:216070335 | A | T | 58 | a0001c0001t0001g0323 a0001c0001t0001g0324 a0001c0001t0001g0327 others(55): Show |
62 | HG00544.hp2 HG00621.hp2 HG01070.hp2 others(59): Show |
intron_variant | MODIFIER | c.125-3817T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070335 | |||||||
| chr2:216070336 | A | C | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3818T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070336 | |||||||
| chr2:216070343 | A | G | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3825T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070343 | |||||||
| chr2:216070344 | A | T | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3826T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070344 | |||||||
| chr2:216070345 | T | G | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3827A>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070345 | |||||||
| chr2:216070347 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3829G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070347 | |||||||
| chr2:216070349 | C | A | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3831G>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070349 | |||||||
| chr2:216070350 | A | C | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3832T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070350 | |||||||
| chr2:216070361 | A | G | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3843T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070361 | |||||||
| chr2:216070363 | C | A | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3845G>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070363 | |||||||
| chr2:216070376 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3858C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070376 | |||||||
| chr2:216070377 | C | G | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3859G>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070377 | |||||||
| chr2:216070382 | C | A | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3864G>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070382 | |||||||
| chr2:216070383 | A | G | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3865T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070383 | |||||||
| chr2:216070386 | A | G | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3868T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070386 | |||||||
| chr2:216070390 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3872G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070390 | |||||||
| chr2:216070391 | A | G | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3873T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070391 | |||||||
| chr2:216070393 | C | A | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3875G>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070393 | |||||||
| chr2:216070394 | A | T | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3876T>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070394 | |||||||
| chr2:216070395 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3877C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070395 | |||||||
| chr2:216070396 | A | G | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3878T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070396 | |||||||
| chr2:216070398 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3880G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070398 | |||||||
| chr2:216070400 | T | G | 1 | a0001c0001t0001g0179 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.125-3882A>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070400 | |||||||
| chr2:216070458 | T | A | 29 | a0001c0001t0001g0323 a0001c0001t0001g0324 a0001c0001t0001g0327 others(26): Show |
30 | HG00544.hp2 HG00621.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.125-3940A>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070458 | |||||||
| chr2:216070532 | G | A | 3 | a0001c0003t0003g0098 a0001c0003t0003g0099 a0001c0003t0003g0227 |
3 | HG00140.hp2 HG03492.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.125-4014C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070532 | |||||||
| chr2:216070585 | C | T | 1 | a0001c0001t0001g0317 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.125-4067G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070585 | |||||||
| chr2:216070665 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.125-4147C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070665 | |||||||
| chr2:216070700 | T | C | 29 | a0001c0001t0001g0323 a0001c0001t0001g0324 a0001c0001t0001g0327 others(26): Show |
30 | HG00544.hp2 HG00621.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.125-4182A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070700 | |||||||
| chr2:216070867 | C | T | 1 | a0001c0011t0006g0375 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.125-4349G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070867 | |||||||
| chr2:216070876 | G | A | 1 | a0001c0001t0001g0337 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.125-4358C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070876 | |||||||
| chr2:216070953 | C | T | 36 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0024 others(33): Show |
39 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.125-4435G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216070953 | |||||||
| chr2:216071252 | G | C | 1 | a0001c0001t0001g0212 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.125-4734C>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216071252 | |||||||
| chr2:216071445 | C | CA | 4 | a0001c0001t0001g0100 a0001c0001t0006g0103 a0001c0003t0003g0102 others(1): Show |
4 | HG01099.hp1 HG02145.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.125-4928dupT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216071445 | |||||||
| chr2:216071449 | G | A | 215 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0010 others(212): Show |
227 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.125-4931C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216071449 | |||||||
| chr2:216071707 | G | C | 31 | a0001c0001t0001g0343 a0001c0001t0001g0352 a0001c0001t0001g0353 others(28): Show |
34 | HG01167.hp2 HG01169.hp2 HG01261.hp2 others(31): Show |
intron_variant | MODIFIER | c.125-5189C>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216071707 | |||||||
| chr2:216071928 | A | G | 30 | a0001c0001t0001g0323 a0001c0001t0001g0324 a0001c0001t0001g0327 others(27): Show |
31 | HG00544.hp2 HG00621.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.125-5410T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216071928 | |||||||
| chr2:216071935 | A | G | 1 | a0001c0011t0006g0375 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.125-5417T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216071935 | |||||||
| chr2:216072036 | C | T | 1 | a0002c0002t0002g0220 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.125-5518G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216072036 | |||||||
| chr2:216072130 | A | C | 4 | a0001c0001t0004g0365 a0001c0001t0004g0366 a0001c0003t0003g0019 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.125-5612T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216072130 | |||||||
| chr2:216072143 | C | T | 1 | a0001c0001t0004g0256 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.125-5625G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216072143 | |||||||
| chr2:216072317 | C | T | 1 | a0001c0011t0006g0375 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.125-5799G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216072317 | |||||||
| chr2:216072466 | C | A | 31 | a0001c0001t0001g0343 a0001c0001t0001g0352 a0001c0001t0001g0353 others(28): Show |
34 | HG01167.hp2 HG01169.hp2 HG01261.hp2 others(31): Show |
intron_variant | MODIFIER | c.125-5948G>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216072466 | |||||||
| chr2:216072761 | A | G | 2 | a0002c0002t0002g0372 a0004c0005t0009g0373 |
2 | HG02109.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.125-6243T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216072761 | |||||||
| chr2:216073191 | A | C | 1 | a0001c0001t0001g0041 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.125-6673T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216073191 | |||||||
| chr2:216073211 | T | C | 1 | a0001c0001t0005g0378 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.125-6693A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216073211 | |||||||
| chr2:216073398 | C | T | 1 | a0001c0001t0001g0141 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.125-6880G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216073398 | |||||||
| chr2:216073760 | C | T | 1 | a0001c0003t0003g0019 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.125-7242G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216073760 | |||||||
| chr2:216074270 | C | A | 1 | a0001c0001t0001g0055 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.124+7348G>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074270 | |||||||
| chr2:216074300 | A | G | 1 | a0006c0009t0001g0020 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.124+7318T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074300 | |||||||
| chr2:216074345 | A | G | 1 | a0004c0005t0009g0373 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.124+7273T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074345 | |||||||
| chr2:216074441 | AAAAAGAA others(2): Show |
A | 33 | a0001c0001t0001g0027 a0001c0001t0001g0088 a0001c0001t0001g0343 others(30): Show |
36 | HG01167.hp2 HG01169.hp2 HG01261.hp2 others(33): Show |
intron_variant | MODIFIER | c.124+7168_124+7176d others(11): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074441 | |||||||
| chr2:216074466 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.124+7152T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074466 | |||||||
| chr2:216074470 | A | G | 1 | a0001c0001t0001g0087 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.124+7148T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074470 | |||||||
| chr2:216074474 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.124+7144C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074474 | |||||||
| chr2:216074478 | G | A | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | HG02486.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.124+7140C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074478 | |||||||
| chr2:216074480 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.124+7138C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074480 | |||||||
| chr2:216074485 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.124+7133T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074485 | |||||||
| chr2:216074488 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.124+7130C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074488 | |||||||
| chr2:216074489 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.124+7129T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074489 | |||||||
| chr2:216074492 | A | G | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | HG02486.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.124+7126T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074492 | |||||||
| chr2:216074493 | A | AAAGG | 72 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0028 others(69): Show |
73 | HG00140.hp2 HG00280.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.124+7121_124+7124d others(6): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074493 | |||||||
| chr2:216074493 | A | AAAGGAAG others(1): Show |
55 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0008 others(52): Show |
61 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.124+7117_124+7124d others(10): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074493 | |||||||
| chr2:216074493 | A | AAAGGAAG others(5): Show |
36 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0014 others(33): Show |
39 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(36): Show |
intron_variant | MODIFIER | c.124+7113_124+7124d others(14): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074493 | |||||||
| chr2:216074493 | A | AAAGGAAG others(9): Show |
8 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0121 others(5): Show |
8 | HG01934.hp1 HG01943.hp1 HG04115.hp2 others(5): Show |
intron_variant | MODIFIER | c.124+7109_124+7124d others(18): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074493 | |||||||
| chr2:216074493 | A | AAAGGAAG others(13): Show |
7 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0003t0003g0095 others(4): Show |
8 | HG00558.hp2 NA18747.hp2 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.124+7105_124+7124d others(22): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074493 | |||||||
| chr2:216074493 | A | G | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | HG02486.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.124+7125T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074493 | |||||||
| chr2:216074493 | AAAGG | A | 26 | a0001c0001t0001g0004 a0001c0001t0001g0022 a0001c0001t0001g0030 others(23): Show |
27 | HG00609.hp2 HG00733.hp2 HG01081.hp2 others(24): Show |
intron_variant | MODIFIER | c.124+7121_124+7124d others(6): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074493 | |||||||
| chr2:216074493 | AAAGGAAG others(1): Show |
A | 17 | a0001c0001t0001g0024 a0001c0001t0001g0073 a0001c0001t0001g0075 others(14): Show |
18 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(15): Show |
intron_variant | MODIFIER | c.124+7117_124+7124d others(10): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074493 | |||||||
| chr2:216074493 | AAAGGAAG others(5): Show |
A | 45 | a0001c0001t0001g0015 a0001c0001t0001g0178 a0001c0001t0001g0179 others(42): Show |
48 | HG00323.hp1 HG00423.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.124+7113_124+7124d others(14): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074493 | |||||||
| chr2:216074493 | AAAGGAAG others(9): Show |
A | 19 | a0001c0001t0001g0343 a0001c0001t0001g0352 a0001c0001t0001g0353 others(16): Show |
19 | HG01884.hp2 HG01975.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.124+7109_124+7124d others(18): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074493 | |||||||
| chr2:216074493 | AAAGGAAG others(13): Show |
A | 1 | a0001c0001t0005g0378 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.124+7105_124+7124d others(22): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074493 | |||||||
| chr2:216074497 | GAAGGAAG others(37): Show |
G | 1 | a0001c0001t0006g0029 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.124+7077_124+7120d others(46): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074497 | |||||||
| chr2:216074517 | G | A | 1 | a0002c0002t0002g0372 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.124+7101C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074517 | |||||||
| chr2:216074517 | GAAGGAAG others(17): Show |
G | 29 | a0001c0001t0001g0323 a0001c0001t0001g0324 a0001c0001t0001g0327 others(26): Show |
30 | HG00544.hp2 HG00621.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.124+7077_124+7100d others(26): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074517 | |||||||
| chr2:216074525 | G | A | 1 | a0002c0002t0002g0372 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.124+7093C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074525 | |||||||
| chr2:216074529 | GAAGGAAG others(5): Show |
G | 1 | a0002c0002t0002g0372 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.124+7077_124+7088d others(14): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074529 | |||||||
| chr2:216074537 | G | A | 2 | a0002c0002t0002g0217 a0002c0002t0002g0221 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.124+7081C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074537 | |||||||
| chr2:216074541 | A | G | 4 | a0002c0002t0002g0164 a0002c0002t0002g0217 a0002c0002t0002g0221 others(1): Show |
4 | HG01168.hp1 HG01169.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.124+7077T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074541 | |||||||
| chr2:216074545 | G | A | 29 | a0001c0001t0001g0323 a0001c0001t0001g0324 a0001c0001t0001g0327 others(26): Show |
30 | HG00544.hp2 HG00621.hp2 HG01070.hp2 others(27): Show |
intron_variant | MODIFIER | c.124+7073C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074545 | |||||||
| chr2:216074634 | G | T | 10 | a0001c0001t0004g0306 a0001c0001t0004g0309 a0001c0001t0005g0307 others(7): Show |
10 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.124+6984C>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074634 | |||||||
| chr2:216074667 | T | C | 1 | a0001c0003t0003g0204 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.124+6951A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074667 | |||||||
| chr2:216074680 | G | T | 1 | a0001c0003t0003g0204 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.124+6938C>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074680 | |||||||
| chr2:216074885 | G | A | 1 | a0011c0015t0001g0252 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.124+6733C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216074885 | |||||||
| chr2:216075659 | C | T | 1 | a0001c0003t0003g0076 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.124+5959G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216075659 | |||||||
| chr2:216075693 | T | C | 30 | a0001c0001t0001g0343 a0001c0001t0001g0352 a0001c0001t0001g0353 others(27): Show |
33 | HG01167.hp2 HG01169.hp2 HG01261.hp2 others(30): Show |
intron_variant | MODIFIER | c.124+5925A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216075693 | |||||||
| chr2:216075976 | C | T | 1 | a0001c0011t0006g0375 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.124+5642G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216075976 | |||||||
| chr2:216076038 | A | G | 3 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 |
3 | HG02486.hp2 HG02976.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.124+5580T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216076038 | |||||||
| chr2:216076209 | T | C | 1 | a0001c0003t0003g0099 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.124+5409A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216076209 | |||||||
| chr2:216076274 | C | A | 30 | a0001c0001t0001g0343 a0001c0001t0001g0352 a0001c0001t0001g0353 others(27): Show |
33 | HG01167.hp2 HG01169.hp2 HG01261.hp2 others(30): Show |
intron_variant | MODIFIER | c.124+5344G>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216076274 | |||||||
| chr2:216076278 | C | T | 2 | a0002c0002t0002g0328 a0002c0002t0002g0329 |
2 | HG02258.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.124+5340G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216076278 | |||||||
| chr2:216076404 | G | A | 28 | a0001c0001t0001g0323 a0001c0001t0001g0324 a0001c0001t0001g0327 others(25): Show |
29 | HG00544.hp2 HG00621.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.124+5214C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216076404 | |||||||
| chr2:216076456 | G | A | 1 | a0005c0008t0002g0315 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.124+5162C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216076456 | |||||||
| chr2:216076463 | A | G | 1 | a0001c0001t0001g0113 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.124+5155T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216076463 | |||||||
| chr2:216076505 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.124+5113A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216076505 | |||||||
| chr2:216076518 | T | G | 29 | a0001c0001t0001g0343 a0001c0001t0001g0352 a0001c0001t0001g0353 others(26): Show |
32 | HG01167.hp2 HG01169.hp2 HG01261.hp2 others(29): Show |
intron_variant | MODIFIER | c.124+5100A>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216076518 | |||||||
| chr2:216076707 | C | T | 1 | a0002c0002t0002g0112 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.124+4911G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216076707 | |||||||
| chr2:216076750 | C | A | 2 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
2 | HG02129.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.124+4868G>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216076750 | |||||||
| chr2:216076751 | T | C | 2 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
2 | HG02129.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.124+4867A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216076751 | |||||||
| chr2:216076766 | C | T | 30 | a0001c0001t0001g0343 a0001c0001t0001g0352 a0001c0001t0001g0353 others(27): Show |
33 | HG01167.hp2 HG01169.hp2 HG01261.hp2 others(30): Show |
intron_variant | MODIFIER | c.124+4852G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216076766 | |||||||
| chr2:216077000 | C | CA | 144 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0010 others(141): Show |
154 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(151): Show |
intron_variant | MODIFIER | c.124+4617dupT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216077000 | |||||||
| chr2:216077047 | G | A | 1 | a0001c0001t0001g0174 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.124+4571C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216077047 | |||||||
| chr2:216077100 | T | C | 1 | a0002c0002t0002g0316 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.124+4518A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216077100 | |||||||
| chr2:216077141 | G | T | 29 | a0001c0001t0001g0343 a0001c0001t0001g0352 a0001c0001t0001g0353 others(26): Show |
32 | HG01167.hp2 HG01169.hp2 HG01261.hp2 others(29): Show |
intron_variant | MODIFIER | c.124+4477C>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216077141 | |||||||
| chr2:216077150 | G | A | 1 | a0001c0011t0006g0375 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.124+4468C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216077150 | |||||||
| chr2:216077322 | C | T | 4 | a0001c0001t0004g0365 a0001c0001t0004g0366 a0001c0003t0003g0019 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.124+4296G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216077322 | |||||||
| chr2:216077329 | AC | A | 252 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0010 others(249): Show |
267 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(264): Show |
intron_variant | MODIFIER | c.124+4288delG | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216077329 | |||||||
| chr2:216077398 | T | A | 1 | a0001c0011t0006g0375 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.124+4220A>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216077398 | |||||||
| chr2:216077431 | C | T | 26 | a0001c0001t0001g0343 a0001c0001t0001g0352 a0001c0001t0001g0353 others(23): Show |
28 | HG01167.hp2 HG01169.hp2 HG01261.hp2 others(25): Show |
intron_variant | MODIFIER | c.124+4187G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216077431 | |||||||
| chr2:216077432 | G | A | 2 | a0001c0001t0001g0175 a0001c0001t0001g0176 |
2 | NA19003.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.124+4186C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216077432 | |||||||
| chr2:216077529 | C | T | 10 | a0001c0001t0004g0306 a0001c0001t0004g0309 a0001c0001t0005g0307 others(7): Show |
10 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.124+4089G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216077529 | |||||||
| chr2:216077715 | A | G | 30 | a0001c0001t0001g0343 a0001c0001t0001g0352 a0001c0001t0001g0353 others(27): Show |
33 | HG01167.hp2 HG01169.hp2 HG01261.hp2 others(30): Show |
intron_variant | MODIFIER | c.124+3903T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216077715 | |||||||
| chr2:216077723 | C | T | 1 | a0001c0001t0005g0307 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.124+3895G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216077723 | |||||||
| chr2:216077794 | A | G | 1 | a0001c0004t0001g0377 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.124+3824T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216077794 | |||||||
| chr2:216077806 | C | CA | 20 | a0001c0001t0001g0025 a0001c0001t0001g0080 a0001c0001t0001g0081 others(17): Show |
20 | HG01106.hp2 HG01175.hp1 HG01256.hp2 others(17): Show |
intron_variant | MODIFIER | c.124+3811dupT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216077806 | |||||||
| chr2:216077806 | CA | C | 109 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0010 others(106): Show |
116 | HG00438.hp2 HG00544.hp2 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.124+3811delT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216077806 | |||||||
| chr2:216077806 | CAA | C | 11 | a0001c0001t0001g0323 a0001c0001t0001g0324 a0001c0001t0001g0327 others(8): Show |
11 | HG01109.hp2 HG01243.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.124+3810_124+3811d others(4): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216077806 | |||||||
| chr2:216077927 | G | A | 10 | a0001c0001t0004g0306 a0001c0001t0004g0309 a0001c0001t0005g0307 others(7): Show |
10 | HG01891.hp2 HG02257.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.124+3691C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216077927 | |||||||
| chr2:216078020 | T | TA | 110 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0010 others(107): Show |
117 | HG00544.hp2 HG00558.hp2 HG00621.hp2 others(114): Show |
intron_variant | MODIFIER | c.124+3597dupT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216078020 | |||||||
| chr2:216078167 | G | A | 7 | a0002c0002t0002g0357 a0002c0002t0002g0358 a0002c0002t0002g0359 others(4): Show |
7 | HG01884.hp2 HG02109.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.124+3451C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216078167 | |||||||
| chr2:216078200 | G | C | 2 | a0002c0002t0002g0372 a0004c0005t0009g0373 |
2 | HG02109.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.124+3418C>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216078200 | |||||||
| chr2:216078309 | G | A | 219 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(216): Show |
228 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.124+3309C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216078309 | |||||||
| chr2:216078419 | T | C | 88 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0010 others(85): Show |
94 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(91): Show |
intron_variant | MODIFIER | c.124+3199A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216078419 | |||||||
| chr2:216078552 | T | C | 50 | a0001c0001t0001g0011 a0001c0001t0001g0024 a0001c0001t0001g0025 others(47): Show |
52 | HG00280.hp1 HG00558.hp1 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.124+3066A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216078552 | |||||||
| chr2:216078567 | G | A | 40 | a0001c0001t0001g0011 a0001c0001t0001g0024 a0001c0001t0001g0025 others(37): Show |
42 | HG00558.hp1 HG00597.hp1 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.124+3051C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216078567 | |||||||
| chr2:216078568 | A | C | 3 | a0001c0004t0001g0093 a0001c0004t0001g0094 a0007c0007t0001g0001 |
4 | HG02145.hp2 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.124+3050T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216078568 | |||||||
| chr2:216078577 | A | G | 138 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0010 others(135): Show |
146 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(143): Show |
intron_variant | MODIFIER | c.124+3041T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216078577 | |||||||
| chr2:216078683 | T | C | 3 | a0001c0001t0001g0301 a0001c0001t0001g0302 a0001c0001t0001g0303 |
3 | HG00609.hp1 HG00673.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.124+2935A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216078683 | |||||||
| chr2:216078721 | T | G | 14 | a0001c0001t0001g0016 a0001c0001t0001g0086 a0001c0001t0001g0087 others(11): Show |
15 | HG01975.hp2 HG02055.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.124+2897A>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216078721 | |||||||
| chr2:216078998 | T | G | 1 | a0001c0004t0001g0377 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.124+2620A>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216078998 | |||||||
| chr2:216079151 | C | CT | 35 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0343 others(32): Show |
36 | HG00140.hp2 HG01099.hp1 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.124+2466dupA | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216079151 | |||||||
| chr2:216079151 | CT | C | 17 | a0001c0001t0001g0340 a0001c0001t0004g0306 a0001c0001t0004g0309 others(14): Show |
17 | HG01891.hp2 HG02145.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.124+2466delA | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216079151 | |||||||
| chr2:216079179 | T | G | 1 | a0002c0002t0002g0316 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.124+2439A>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216079179 | |||||||
| chr2:216079182 | A | AT | 13 | a0001c0001t0001g0343 a0001c0001t0004g0344 a0001c0001t0004g0345 others(10): Show |
13 | HG01975.hp2 HG02056.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.124+2435dupA | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216079182 | |||||||
| chr2:216079490 | C | A | 31 | a0001c0001t0001g0317 a0001c0001t0001g0323 a0001c0001t0001g0324 others(28): Show |
33 | HG00544.hp2 HG00621.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.124+2128G>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216079490 | |||||||
| chr2:216079517 | G | A | 1 | a0001c0003t0003g0342 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.124+2101C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216079517 | |||||||
| chr2:216079583 | A | G | 1 | a0001c0004t0001g0377 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.124+2035T>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216079583 | |||||||
| chr2:216079657 | G | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0089 a0001c0001t0001g0090 others(1): Show |
5 | NA18954.hp2 NA18975.hp2 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.124+1961C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216079657 | |||||||
| chr2:216079662 | C | T | 4 | a0001c0001t0001g0369 a0002c0002t0002g0368 a0002c0002t0002g0370 others(1): Show |
4 | HG01884.hp1 HG02055.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.124+1956G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216079662 | |||||||
| chr2:216079747 | C | A | 1 | a0001c0001t0001g0092 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.124+1871G>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216079747 | |||||||
| chr2:216079756 | C | T | 76 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(73): Show |
81 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.124+1862G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216079756 | |||||||
| chr2:216079757 | G | A | 28 | a0001c0001t0001g0343 a0001c0001t0001g0352 a0001c0001t0001g0353 others(25): Show |
29 | HG01884.hp1 HG01884.hp2 HG01975.hp2 others(26): Show |
intron_variant | MODIFIER | c.124+1861C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216079757 | |||||||
| chr2:216079797 | C | T | 1 | a0002c0002t0002g0368 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.124+1821G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216079797 | |||||||
| chr2:216079863 | C | T | 74 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(71): Show |
79 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.124+1755G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216079863 | |||||||
| chr2:216079955 | T | C | 1 | a0002c0002t0002g0363 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.124+1663A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216079955 | |||||||
| chr2:216079981 | C | CA | 5 | a0001c0001t0001g0364 a0001c0001t0004g0365 a0001c0001t0004g0366 others(2): Show |
6 | HG01167.hp2 HG01169.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.124+1636dupT | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216079981 | |||||||
| chr2:216080113 | G | A | 1 | a0001c0001t0001g0367 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.124+1505C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216080113 | |||||||
| chr2:216080133 | G | A | 7 | a0001c0001t0001g0369 a0001c0001t0005g0378 a0002c0002t0002g0368 others(4): Show |
7 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.124+1485C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216080133 | |||||||
| chr2:216080230 | C | T | 1 | a0001c0001t0001g0027 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.124+1388G>A | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216080230 | |||||||
| chr2:216080706 | G | C | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG00738.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.124+912C>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216080706 | |||||||
| chr2:216080962 | C | G | 1 | a0002c0002t0002g0026 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.124+656G>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216080962 | |||||||
| chr2:216080980 | A | C | 2 | a0001c0004t0001g0377 a0001c0011t0006g0375 |
2 | HG03579.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.124+638T>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216080980 | |||||||
| chr2:216081106 | T | C | 1 | a0001c0001t0001g0374 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.124+512A>G | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216081106 | |||||||
| chr2:216081137 | T | G | 1 | a0001c0011t0006g0375 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.124+481A>C | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216081137 | |||||||
| chr2:216081226 | G | A | 1 | a0001c0001t0001g0376 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.124+392C>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216081226 | |||||||
| chr2:216081230 | GACTC | G | 4 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0025 others(1): Show |
4 | HG00738.hp1 HG00738.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.124+384_124+387del others(4): Show |
PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216081230 | |||||||
| chr2:216081326 | T | A | 2 | a0001c0001t0005g0378 a0001c0004t0001g0377 |
2 | HG02280.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.124+292A>T | PECR | ENSG00000115425.14 | transcript | ENST00000265322.8 | protein_coding | 1/7 | chr2 | 216081326 |