Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 26577 |
| ensemblid | ENSG00000163710.9 |
| hgncid | 8739 |
| symbol | PCOLCE2 |
| name | procollagen C-endopeptidase enhancer 2 |
| refseq_nuc | NM_013363.4 |
| refseq_prot | NP_037495.1 |
| ensembl_nuc | ENST00000295992.8 |
| ensembl_prot | ENSP00000295992.3 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 142817874 |
| end | 142889083 |
| strand | - |
| ver | v1.2 |
| region | chr3:142817874-142889083 |
| region5000 | chr3:142812874-142894083 |
| regionname0 | PCOLCE2_chr3_142817874_142889083 |
| regionname5000 | PCOLCE2_chr3_142812874_142894083 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 415 | 311 | 83 | 56 | 121 | 12 | 37 | 85 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | MRGAN others(410): Show |
chr3 | 142812874 | 142894083 |
| a0002 | 0/0 | 415 | 18 | 3 | 4 | 10 | 1 | 0 | 6 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | MRGAN others(410): Show |
chr3 | 142812874 | 142894083 |
| a0003 | 0/0 | 415 | 10 | 0 | 6 | 0 | 3 | 1 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | MRGAN others(410): Show |
chr3 | 142812874 | 142894083 |
| a0004 | 0/0 | 415 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | MRGAN others(410): Show |
chr3 | 142812874 | 142894083 |
| a0005 | 0/0 | 415 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | MRGAN others(410): Show |
chr3 | 142812874 | 142894083 |
| a0006 | 0/0 | 415 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | MRGAN others(410): Show |
chr3 | 142812874 | 142894083 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1245 | 306 | 79 | 55 | 121 | 12 | 37 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | ATGAG others(1240): Show |
chr3 | 142812874 | 142894083 | ||
| a0001c0004 | 0/0 | 1245 | 4 | 4 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | ATGCG others(1240): Show |
chr3 | 142812874 | 142894083 | ||
| a0001c0007 | 0/0 | 1245 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | ATGAG others(1240): Show |
chr3 | 142812874 | 142894083 | ||
| a0002c0002 | 0/0 | 1245 | 18 | 3 | 4 | 10 | 1 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | ATGAG others(1240): Show |
chr3 | 142812874 | 142894083 | ||
| a0003c0003 | 0/0 | 1245 | 10 | 0 | 6 | 0 | 3 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | ATGAG others(1240): Show |
chr3 | 142812874 | 142894083 | ||
| a0004c0006 | 0/0 | 1245 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | ATGAG others(1240): Show |
chr3 | 142812874 | 142894083 | ||
| a0005c0005 | 0/0 | 1245 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | ATGAG others(1240): Show |
chr3 | 142812874 | 142894083 | ||
| a0006c0008 | 0/0 | 1245 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | ATGAG others(1240): Show |
chr3 | 142812874 | 142894083 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1896 | 160 | 48 | 27 | 55 | 8 | 20 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | GTATC others(1891): Show |
chr3 | 142812874 | 142894083 |
| a0001c0001t0002 | 0/0 | 1896 | 64 | 19 | 6 | 36 | 1 | 2 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | GTATC others(1891): Show |
chr3 | 142812874 | 142894083 |
| a0001c0001t0003 | 0/0 | 1918 | 33 | 7 | 13 | 6 | 1 | 6 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | GTATC others(1913): Show |
chr3 | 142812874 | 142894083 |
| a0001c0001t0004 | 0/0 | 1896 | 23 | 0 | 3 | 18 | 0 | 2 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | GTATC others(1891): Show |
chr3 | 142812874 | 142894083 |
| a0001c0001t0005 | 0/0 | 1918 | 9 | 2 | 3 | 0 | 2 | 2 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | GTATC others(1913): Show |
chr3 | 142812874 | 142894083 |
| a0001c0001t0006 | 0/0 | 1896 | 10 | 0 | 2 | 3 | 0 | 5 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | GTATC others(1891): Show |
chr3 | 142812874 | 142894083 |
| a0001c0001t0007 | 0/0 | 1896 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | GTATC others(1891): Show |
chr3 | 142812874 | 142894083 |
| a0001c0001t0008 | 0/0 | 1896 | 3 | 0 | 0 | 3 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | GTATC others(1891): Show |
chr3 | 142812874 | 142894083 |
| a0001c0001t0009 | 0/0 | 1918 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | GTATC others(1913): Show |
chr3 | 142812874 | 142894083 |
| a0001c0001t0010 | 0/0 | 1896 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | GTATC others(1891): Show |
chr3 | 142812874 | 142894083 |
| a0001c0001t0011 | 0/0 | 1896 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | GTATC others(1891): Show |
chr3 | 142812874 | 142894083 |
| a0001c0004t0001 | 0/0 | 1896 | 2 | 2 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | GTATC others(1891): Show |
chr3 | 142812874 | 142894083 |
| a0001c0004t0002 | 0/0 | 1896 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | GTATC others(1891): Show |
chr3 | 142812874 | 142894083 |
| a0001c0004t0007 | 0/0 | 1896 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | GTATC others(1891): Show |
chr3 | 142812874 | 142894083 |
| a0001c0007t0001 | 0/0 | 1896 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | GTATC others(1891): Show |
chr3 | 142812874 | 142894083 |
| a0002c0002t0001 | 0/0 | 1896 | 4 | 1 | 0 | 3 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | GTATC others(1891): Show |
chr3 | 142812874 | 142894083 |
| a0002c0002t0002 | 0/0 | 1896 | 6 | 1 | 0 | 4 | 1 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | GTATC others(1891): Show |
chr3 | 142812874 | 142894083 |
| a0002c0002t0004 | 0/0 | 1896 | 5 | 0 | 2 | 3 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | GTATC others(1891): Show |
chr3 | 142812874 | 142894083 |
| a0002c0002t0005 | 0/0 | 1918 | 2 | 0 | 2 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | GTATC others(1913): Show |
chr3 | 142812874 | 142894083 |
| a0002c0002t0007 | 0/0 | 1896 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | GTATC others(1891): Show |
chr3 | 142812874 | 142894083 |
| a0003c0003t0001 | 0/0 | 1896 | 5 | 0 | 4 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | GTATC others(1891): Show |
chr3 | 142812874 | 142894083 |
| a0003c0003t0003 | 0/0 | 1918 | 5 | 0 | 2 | 0 | 3 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | GTATC others(1913): Show |
chr3 | 142812874 | 142894083 |
| a0004c0006t0001 | 0/0 | 1896 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | GTATC others(1891): Show |
chr3 | 142812874 | 142894083 |
| a0005c0005t0001 | 0/0 | 1896 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | GTATC others(1891): Show |
chr3 | 142812874 | 142894083 |
| a0006c0008t0001 | 0/0 | 1896 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | GTATC others(1891): Show |
chr3 | 142812874 | 142894083 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0017 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0287 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0003g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0003g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0003g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0003g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0003g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0003g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0004g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0004g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0004g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0004g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0004g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0004g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0004g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0004g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0005g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0005g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0005g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0005g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0005g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0005g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0005g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0006g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0006g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0006g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0006g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0006g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0006g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0006g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0006g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0006g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0006g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0007g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0008g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0008g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0008g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0009g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0010g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0001t0011g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0004t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0004t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0004t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0004t0007g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0001c0007t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0002c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0002c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0002c0002t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0002c0002t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0002c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0002c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0002c0002t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0002c0002t0004g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0002c0002t0004g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0002c0002t0004g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0002c0002t0004g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0002c0002t0005g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0002c0002t0005g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0002c0002t0007g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0003c0003t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0003c0003t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0003c0003t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0003c0003t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0003c0003t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0003c0003t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0003c0003t0003g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0003c0003t0003g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0003c0003t0003g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0003c0003t0003g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0004c0006t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0005c0005t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| a0006c0008t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0310 | EUR | GBR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG00099 | hp2 | a0002 | c0002 | t0002 | g0197 | EUR | GBR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0288 | EUR | FIN | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG00280 | hp2 | a0001 | c0001 | t0003 | g0051 | EUR | FIN | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0118 | EUR | FIN | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG00323 | hp2 | a0001 | c0001 | t0002 | g0291 | EUR | FIN | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG00423 | hp1 | a0002 | c0002 | t0002 | g0132 | EAS | CHS | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG00423 | hp2 | a0001 | c0001 | t0004 | g0087 | EAS | CHS | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG00438 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | CHS | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | CHS | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | CHS | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG00544 | hp2 | a0002 | c0002 | t0004 | g0100 | EAS | CHS | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | CHS | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0292 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0028 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG00673 | hp1 | a0001 | c0001 | t0004 | g0097 | EAS | CHS | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0167 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG00738 | hp2 | a0003 | c0003 | t0003 | g0035 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0052 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01070 | hp1 | a0002 | c0002 | t0005 | g0041 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01070 | hp2 | a0001 | c0001 | t0003 | g0058 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01074 | hp1 | a0003 | c0003 | t0003 | g0053 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0313 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01081 | hp2 | a0001 | c0001 | t0006 | g0080 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01099 | hp2 | a0003 | c0003 | t0001 | g0259 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0284 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01109 | hp1 | a0001 | c0001 | t0003 | g0057 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01167 | hp2 | a0001 | c0001 | t0005 | g0002 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01168 | hp1 | a0003 | c0003 | t0001 | g0307 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0024 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01169 | hp1 | a0003 | c0003 | t0001 | g0271 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01169 | hp2 | a0001 | c0001 | t0005 | g0002 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0286 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0183 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01243 | hp2 | a0001 | c0001 | t0003 | g0031 | AMR | PUR | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01256 | hp1 | a0002 | c0002 | t0004 | g0004 | AMR | CLM | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01256 | hp2 | a0001 | c0001 | t0005 | g0032 | AMR | CLM | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | CLM | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01258 | hp1 | a0002 | c0002 | t0004 | g0004 | AMR | CLM | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | CLM | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01261 | hp2 | a0001 | c0001 | t0003 | g0048 | AMR | CLM | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0036 | AMR | CLM | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01346 | hp2 | a0002 | c0002 | t0005 | g0039 | AMR | CLM | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01361 | hp1 | a0003 | c0003 | t0001 | g0135 | AMR | CLM | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0306 | AMR | CLM | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0193 | AMR | CLM | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01496 | hp2 | a0001 | c0007 | t0001 | g0218 | AMR | CLM | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0258 | EUR | IBS | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01516 | hp1 | a0003 | c0003 | t0003 | g0054 | EUR | IBS | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | IBS | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | IBS | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01884 | hp1 | a0001 | c0001 | t0002 | g0195 | AFR | ACB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | ACB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0155 | AFR | ACB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0091 | AMR | PEL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01952 | hp1 | a0001 | c0001 | t0003 | g0043 | AMR | PEL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01952 | hp2 | a0001 | c0001 | t0006 | g0084 | AMR | PEL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01978 | hp1 | a0001 | c0001 | t0004 | g0092 | AMR | PEL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01978 | hp2 | a0001 | c0001 | t0010 | g0064 | AMR | PEL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0314 | AMR | PEL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | KHV | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0211 | EAS | KHV | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | KHV | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | ACB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0151 | AFR | ACB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02056 | hp1 | a0002 | c0002 | t0002 | g0227 | EAS | KHV | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | KHV | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | KHV | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | KHV | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0317 | EAS | KHV | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02074 | hp2 | a0001 | c0001 | t0004 | g0076 | EAS | KHV | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | KHV | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02080 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | KHV | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02083 | hp1 | a0001 | c0001 | t0004 | g0075 | EAS | KHV | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | KHV | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0275 | EAS | KHV | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | KHV | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0280 | EAS | KHV | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02135 | hp2 | a0001 | c0001 | t0004 | g0096 | EAS | KHV | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02148 | hp2 | a0001 | c0001 | t0003 | g0044 | AMR | PEL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02155 | hp1 | a0002 | c0002 | t0002 | g0205 | EAS | CDX | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | CDX | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CDX | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0303 | EAS | CDX | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02257 | hp1 | a0001 | c0004 | t0001 | g0322 | AFR | ACB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0033 | AFR | ACB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | ACB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0318 | AFR | ACB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02273 | hp1 | a0001 | c0001 | t0004 | g0071 | AMR | PEL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0253 | AMR | PEL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | ACB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0038 | AMR | PEL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PEL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0239 | AFR | ACB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02523 | hp2 | a0001 | c0001 | t0004 | g0095 | EAS | KHV | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02615 | hp2 | a0001 | c0001 | t0002 | g0146 | AFR | GWD | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0264 | AFR | GWD | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | GWD | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0240 | SAS | PJL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02735 | hp1 | a0001 | c0001 | t0006 | g0082 | SAS | PJL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0045 | SAS | PJL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02738 | hp2 | a0001 | c0001 | t0006 | g0066 | SAS | PJL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | GWD | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02896 | hp1 | a0001 | c0001 | t0003 | g0026 | AFR | GWD | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | GWD | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0152 | AFR | ESN | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02922 | hp2 | a0001 | c0004 | t0007 | g0321 | AFR | ESN | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0232 | AFR | ESN | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0124 | AFR | ESN | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | ESN | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02976 | hp1 | a0005 | c0005 | t0001 | g0244 | AFR | ESN | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0034 | SAS | PJL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG03017 | hp2 | a0001 | c0001 | t0006 | g0078 | SAS | PJL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | MSL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | MSL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ESN | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0140 | AFR | ESN | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | ESN | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | MSL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0255 | AFR | MSL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0025 | AFR | MSL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0149 | AFR | MSL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG03239 | hp1 | a0001 | c0001 | t0004 | g0070 | SAS | PJL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG03239 | hp2 | a0001 | c0001 | t0005 | g0040 | SAS | PJL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | MSL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | MSL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG03486 | hp1 | a0002 | c0002 | t0007 | g0139 | AFR | MSL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0194 | AFR | MSL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0047 | SAS | PJL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG03492 | hp1 | a0001 | c0001 | t0003 | g0003 | SAS | PJL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG03516 | hp1 | a0001 | c0001 | t0011 | g0101 | AFR | ESN | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0060 | AFR | ESN | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0221 | AFR | GWD | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG03579 | hp1 | a0001 | c0004 | t0002 | g0320 | AFR | MSL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0056 | AFR | MSL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0020 | SAS | PJL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG03710 | hp2 | a0003 | c0003 | t0001 | g0285 | SAS | PJL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0296 | SAS | BEB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG03927 | hp1 | a0001 | c0001 | t0005 | g0029 | SAS | BEB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | BEB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG03942 | hp1 | a0001 | c0001 | t0006 | g0067 | SAS | BEB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | BEB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0156 | SAS | STU | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0274 | SAS | STU | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG04199 | hp1 | a0001 | c0001 | t0004 | g0081 | SAS | STU | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG04199 | hp2 | a0001 | c0001 | t0006 | g0077 | SAS | STU | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | STU | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0185 | SAS | STU | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | CHB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | CHB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18747 | hp1 | a0001 | c0001 | t0004 | g0068 | EAS | CHB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | CHB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | YRI | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0265 | AFR | YRI | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18944 | hp2 | a0001 | c0001 | t0006 | g0086 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18946 | hp1 | a0006 | c0008 | t0001 | g0212 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18949 | hp1 | a0001 | c0001 | t0008 | g0316 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18950 | hp2 | a0002 | c0002 | t0004 | g0099 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18960 | hp1 | a0002 | c0002 | t0004 | g0098 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18960 | hp2 | a0001 | c0001 | t0004 | g0090 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18962 | hp1 | a0001 | c0001 | t0004 | g0085 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18971 | hp1 | a0001 | c0001 | t0004 | g0065 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18972 | hp1 | a0002 | c0002 | t0002 | g0302 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18979 | hp1 | a0001 | c0001 | t0004 | g0072 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18980 | hp1 | a0002 | c0002 | t0001 | g0111 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18980 | hp2 | a0001 | c0001 | t0006 | g0089 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18984 | hp1 | a0001 | c0001 | t0004 | g0088 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18984 | hp2 | a0001 | c0001 | t0008 | g0203 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18989 | hp1 | a0001 | c0001 | t0004 | g0074 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA19002 | hp2 | a0001 | c0001 | t0004 | g0083 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA19006 | hp2 | a0001 | c0001 | t0004 | g0094 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0312 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA19030 | hp1 | a0001 | c0001 | t0002 | g0254 | AFR | LWK | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0257 | AFR | LWK | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | LWK | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | LWK | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA19055 | hp2 | a0001 | c0001 | t0008 | g0315 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA19058 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA19058 | hp2 | a0001 | c0001 | t0006 | g0093 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA19062 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA19064 | hp2 | a0001 | c0001 | t0003 | g0046 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA19067 | hp2 | a0001 | c0001 | t0004 | g0069 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0169 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA19075 | hp1 | a0002 | c0002 | t0001 | g0170 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA19075 | hp2 | a0001 | c0001 | t0004 | g0079 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA19084 | hp1 | a0001 | c0001 | t0004 | g0073 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | YRI | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA19240 | hp2 | a0002 | c0002 | t0002 | g0142 | AFR | YRI | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0262 | AFR | ASW | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0144 | AFR | ASW | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA20752 | hp1 | a0001 | c0001 | t0005 | g0049 | EUR | TSI | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA20752 | hp2 | a0003 | c0003 | t0003 | g0063 | EUR | TSI | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA20805 | hp1 | a0001 | c0001 | t0005 | g0062 | EUR | TSI | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA20805 | hp2 | a0003 | c0003 | t0003 | g0050 | EUR | TSI | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | GIH | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | GIH | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | ACB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02109 | hp2 | a0004 | c0006 | t0001 | g0147 | AFR | ACB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02486 | hp1 | a0001 | c0001 | t0005 | g0055 | AFR | ACB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0061 | AFR | ACB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | MSL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG03471 | hp2 | a0001 | c0001 | t0007 | g0187 | AFR | MSL | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | USA | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| HG06807 | hp2 | a0001 | c0001 | t0009 | g0027 | AFR | USA | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA20300 | hp1 | a0001 | c0001 | t0003 | g0059 | AFR | USA | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | USA | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | LWK | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| NA21309 | hp2 | a0001 | c0004 | t0001 | g0323 | AFR | LWK | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0287 | REF | REF | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0017 | REF | REF | PCOLCE2_chr3_142812874_142894083 | PCOLCE2 | chr3 | 142812874 | 142894083 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:142820985 | G | A | 1 | a0006 | 1 | NA18946.hp1 | missense_variant | MODERATE | c.1010C>T | p.Ser337Leu | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/9 | 1197/1896 | 1010/1248 | 337/415 | chr3 | 142820985 | |||
| chr3:142823607 | G | T | 1 | a0003 | 10 | HG00738.hp2 HG01074.hp1 HG01099.hp2 others(7): Show |
missense_variant | MODERATE | c.874C>A | p.Pro292Thr | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/9 | 1061/1896 | 874/1248 | 292/415 | chr3 | 142823607 | |||
| chr3:142829718 | A | G | 2 | a0002 a0005 |
19 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(16): Show |
missense_variant | MODERATE | c.839T>C | p.Val280Ala | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/9 | 1026/1896 | 839/1248 | 280/415 | chr3 | 142829718 | |||
| chr3:142838825 | C | T | 1 | a0004 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.655G>A | p.Gly219Arg | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/9 | 842/1896 | 655/1248 | 219/415 | chr3 | 142838825 | |||
| chr3:142848403 | A | G | 1 | a0005 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.262T>C | p.Tyr88His | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/9 | 449/1896 | 262/1248 | 88/415 | chr3 | 142848403 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:142820939 | C | T | 1 | a0001c0007 | 1 | HG01496.hp2 | synonymous_variant | LOW | c.1056G>A | p.Ala352Ala | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/9 | 1243/1896 | 1056/1248 | 352/415 | chr3 | 142820939 | |||
| chr3:142888893 | T | G | 1 | a0001c0004 | 4 | HG02257.hp1 HG02922.hp2 HG03579.hp1 others(1): Show |
synonymous_variant | LOW | c.4A>C | p.Arg2Arg | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 1/9 | 191/1896 | 4/1248 | 2/415 | chr3 | 142888893 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:142818066 | C | T | 1 | a0001c0001t0010 | 1 | HG01978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*269G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 9/9 | 269 | chr3 | 142818066 | ||||||
| chr3:142818175 | G | A | 4 | a0001c0001t0007 a0001c0001t0009 a0001c0004t0007 others(1): Show |
4 | HG02922.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*160C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 9/9 | 160 | chr3 | 142818175 | ||||||
| chr3:142818196 | T | G | 1 | a0001c0001t0008 | 3 | NA18949.hp1 NA18984.hp2 NA19055.hp2 |
3_prime_UTR_variant | MODIFIER | c.*139A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 9/9 | 139 | chr3 | 142818196 | ||||||
| chr3:142818229 | C | G | 11 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(8): Show |
114 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*106G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 9/9 | 106 | chr3 | 142818229 | ||||||
| chr3:142888903 | G | T | 1 | a0001c0001t0011 | 1 | HG03516.hp1 | 5_prime_UTR_variant | MODIFIER | c.-7C>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 1/9 | 7 | chr3 | 142888903 | ||||||
| chr3:142888925 | C | T | 4 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0010 others(1): Show |
39 | HG00423.hp2 HG00544.hp2 HG00673.hp1 others(36): Show |
5_prime_UTR_variant | MODIFIER | c.-29G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 1/9 | 29 | chr3 | 142888925 | ||||||
| chr3:142888980 | C | CGCTCACA others(15): Show |
5 | a0001c0001t0003 a0001c0001t0005 a0001c0001t0009 others(2): Show |
50 | HG00280.hp2 HG00438.hp1 HG00642.hp1 others(47): Show |
5_prime_UTR_variant | MODIFIER | c.-106_-85dupCAGCGCT others(15): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 1/9 | 85 | chr3 | 142888980 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:142818531 | G | A | 2 | a0001c0001t0003g0034 a0001c0001t0006g0082 |
2 | HG02735.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1118-66C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142818531 | |||||||
| chr3:142818684 | G | C | 32 | a0001c0001t0001g0006 a0001c0001t0001g0117 a0001c0001t0001g0136 others(29): Show |
33 | HG00642.hp1 HG00735.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.1118-219C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142818684 | |||||||
| chr3:142818712 | C | G | 1 | a0001c0001t0001g0296 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1118-247G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142818712 | |||||||
| chr3:142818828 | C | T | 3 | a0001c0001t0002g0009 a0001c0001t0002g0196 a0001c0001t0002g0248 |
4 | NA18971.hp2 NA18972.hp2 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.1118-363G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142818828 | |||||||
| chr3:142818839 | G | A | 8 | a0001c0001t0001g0173 a0001c0001t0001g0251 a0001c0001t0001g0252 others(5): Show |
8 | HG02055.hp1 HG02109.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1118-374C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142818839 | |||||||
| chr3:142818897 | C | T | 10 | a0001c0001t0002g0102 a0001c0001t0002g0103 a0001c0001t0002g0116 others(7): Show |
10 | HG00673.hp1 HG00738.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1118-432G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142818897 | |||||||
| chr3:142818916 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1118-451C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142818916 | |||||||
| chr3:142818924 | G | A | 19 | a0001c0001t0002g0201 a0001c0001t0002g0207 a0001c0001t0002g0253 others(16): Show |
20 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(17): Show |
intron_variant | MODIFIER | c.1118-459C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142818924 | |||||||
| chr3:142818964 | T | C | 1 | a0001c0001t0001g0288 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1118-499A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142818964 | |||||||
| chr3:142818965 | G | C | 17 | a0001c0001t0002g0009 a0001c0001t0002g0106 a0001c0001t0002g0107 others(14): Show |
18 | HG01884.hp1 HG02027.hp1 HG02074.hp1 others(15): Show |
intron_variant | MODIFIER | c.1118-500C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142818965 | |||||||
| chr3:142819165 | G | A | 10 | a0001c0001t0002g0013 a0001c0001t0002g0140 a0001c0001t0002g0144 others(7): Show |
11 | HG02280.hp1 HG02451.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.1118-700C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142819165 | |||||||
| chr3:142819275 | T | C | 1 | a0001c0001t0002g0265 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1118-810A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142819275 | |||||||
| chr3:142819426 | G | A | 1 | a0001c0001t0003g0022 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1118-961C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142819426 | |||||||
| chr3:142819497 | A | T | 2 | a0001c0001t0001g0311 a0001c0004t0001g0322 |
2 | HG02257.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1118-1032T>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142819497 | |||||||
| chr3:142819554 | G | A | 1 | a0001c0001t0002g0195 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1118-1089C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142819554 | |||||||
| chr3:142819733 | C | A | 10 | a0001c0001t0002g0102 a0001c0001t0002g0103 a0001c0001t0002g0116 others(7): Show |
10 | HG00673.hp1 HG00738.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1117+1145G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142819733 | |||||||
| chr3:142819807 | G | A | 54 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0015 others(51): Show |
58 | HG00280.hp2 HG00597.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.1117+1071C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142819807 | |||||||
| chr3:142819962 | T | TTC | 10 | a0001c0001t0002g0102 a0001c0001t0002g0103 a0001c0001t0002g0116 others(7): Show |
10 | HG00673.hp1 HG00738.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1117+914_1117+915d others(4): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142819962 | |||||||
| chr3:142819980 | G | C | 1 | a0001c0001t0001g0190 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1117+898C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142819980 | |||||||
| chr3:142820107 | A | AT | 12 | a0001c0001t0001g0159 a0001c0001t0002g0013 a0001c0001t0002g0140 others(9): Show |
13 | HG02280.hp1 HG02451.hp1 HG02922.hp2 others(10): Show |
intron_variant | MODIFIER | c.1117+770dupA | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142820107 | |||||||
| chr3:142820107 | A | T | 4 | a0001c0001t0001g0012 a0001c0001t0001g0241 a0001c0001t0003g0038 others(1): Show |
5 | HG00280.hp2 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1117+771T>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142820107 | |||||||
| chr3:142820107 | AT | A | 26 | a0001c0001t0002g0124 a0001c0001t0002g0146 a0001c0001t0002g0149 others(23): Show |
27 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(24): Show |
intron_variant | MODIFIER | c.1117+770delA | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142820107 | |||||||
| chr3:142820121 | T | A | 5 | a0001c0001t0001g0251 a0001c0001t0001g0252 a0001c0001t0001g0318 others(2): Show |
5 | HG02055.hp1 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1117+757A>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142820121 | |||||||
| chr3:142820160 | C | A | 1 | a0001c0001t0001g0108 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1117+718G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142820160 | |||||||
| chr3:142820295 | C | T | 1 | a0001c0001t0001g0290 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1117+583G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142820295 | |||||||
| chr3:142820530 | C | T | 1 | a0001c0001t0002g0232 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1117+348G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142820530 | |||||||
| chr3:142820647 | C | T | 10 | a0001c0001t0002g0102 a0001c0001t0002g0103 a0001c0001t0002g0116 others(7): Show |
10 | HG00673.hp1 HG00738.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1117+231G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142820647 | |||||||
| chr3:142820687 | A | C | 11 | a0001c0001t0002g0120 a0001c0001t0002g0231 a0001c0001t0004g0071 others(8): Show |
11 | HG00423.hp2 HG01934.hp1 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.1117+191T>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142820687 | |||||||
| chr3:142820783 | G | A | 1 | a0002c0002t0002g0302 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1117+95C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 8/8 | chr3 | 142820783 | |||||||
| chr3:142821137 | A | G | 1 | a0001c0001t0003g0047 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.950-92T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142821137 | |||||||
| chr3:142821290 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.950-245C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142821290 | |||||||
| chr3:142821311 | C | G | 1 | a0001c0001t0001g0113 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.950-266G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142821311 | |||||||
| chr3:142821340 | CTTGA | C | 3 | a0001c0001t0001g0136 a0001c0001t0002g0146 a0001c0001t0002g0264 |
3 | HG02615.hp2 HG02622.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.950-299_950-296del others(4): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142821340 | |||||||
| chr3:142821351 | C | T | 22 | a0001c0001t0001g0136 a0001c0001t0002g0009 a0001c0001t0002g0106 others(19): Show |
23 | HG01884.hp1 HG02027.hp1 HG02074.hp1 others(20): Show |
intron_variant | MODIFIER | c.950-306G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142821351 | |||||||
| chr3:142821441 | G | A | 1 | a0001c0001t0002g0155 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.950-396C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142821441 | |||||||
| chr3:142821581 | G | C | 45 | a0001c0001t0001g0117 a0001c0001t0001g0136 a0001c0001t0001g0143 others(42): Show |
46 | HG00642.hp1 HG00735.hp1 HG01175.hp2 others(43): Show |
intron_variant | MODIFIER | c.950-536C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142821581 | |||||||
| chr3:142821609 | T | C | 4 | a0001c0001t0002g0270 a0002c0002t0004g0098 a0002c0002t0004g0099 others(1): Show |
4 | HG00544.hp2 NA18950.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.950-564A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142821609 | |||||||
| chr3:142821693 | C | CT | 10 | a0001c0001t0001g0226 a0001c0001t0002g0013 a0001c0001t0002g0140 others(7): Show |
11 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.950-649dupA | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142821693 | |||||||
| chr3:142821693 | CT | C | 78 | a0001c0001t0001g0220 a0001c0001t0002g0014 a0001c0001t0002g0018 others(75): Show |
83 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.950-649delA | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142821693 | |||||||
| chr3:142821781 | G | A | 23 | a0001c0001t0001g0136 a0001c0001t0001g0235 a0001c0001t0002g0009 others(20): Show |
24 | HG00735.hp1 HG01884.hp1 HG02027.hp1 others(21): Show |
intron_variant | MODIFIER | c.950-736C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142821781 | |||||||
| chr3:142821792 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.950-747G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142821792 | |||||||
| chr3:142821858 | G | C | 1 | a0001c0001t0001g0238 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.950-813C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142821858 | |||||||
| chr3:142821888 | G | C | 1 | a0001c0001t0002g0014 | 2 | NA18953.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.950-843C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142821888 | |||||||
| chr3:142821913 | T | G | 25 | a0001c0001t0001g0136 a0001c0001t0001g0235 a0001c0001t0002g0009 others(22): Show |
26 | HG00735.hp1 HG01884.hp1 HG02027.hp1 others(23): Show |
intron_variant | MODIFIER | c.950-868A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142821913 | |||||||
| chr3:142821916 | G | T | 39 | a0001c0001t0002g0018 a0001c0001t0002g0120 a0001c0001t0002g0156 others(36): Show |
41 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.950-871C>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142821916 | |||||||
| chr3:142821973 | A | T | 1 | a0001c0001t0005g0025 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.950-928T>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142821973 | |||||||
| chr3:142822031 | C | T | 1 | a0001c0001t0004g0087 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.950-986G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142822031 | |||||||
| chr3:142822066 | C | T | 9 | a0001c0001t0001g0226 a0001c0001t0002g0013 a0001c0001t0002g0140 others(6): Show |
10 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.950-1021G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142822066 | |||||||
| chr3:142822074 | C | A | 1 | a0001c0001t0003g0033 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.950-1029G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142822074 | |||||||
| chr3:142822122 | T | G | 10 | a0001c0001t0001g0226 a0001c0001t0002g0013 a0001c0001t0002g0140 others(7): Show |
11 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.950-1077A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142822122 | |||||||
| chr3:142822241 | C | T | 4 | a0001c0001t0001g0209 a0001c0001t0001g0246 a0001c0001t0003g0024 others(1): Show |
4 | HG01069.hp2 HG01070.hp2 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.950-1196G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142822241 | |||||||
| chr3:142822299 | A | G | 1 | a0001c0001t0001g0297 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.949+1233T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142822299 | |||||||
| chr3:142822672 | A | C | 20 | a0001c0001t0002g0201 a0001c0001t0002g0207 a0001c0001t0002g0253 others(17): Show |
22 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.949+860T>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142822672 | |||||||
| chr3:142822769 | G | A | 1 | a0001c0001t0010g0064 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.949+763C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142822769 | |||||||
| chr3:142822778 | A | G | 1 | a0001c0001t0002g0112 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.949+754T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142822778 | |||||||
| chr3:142822845 | T | C | 127 | a0001c0001t0001g0006 a0001c0001t0001g0117 a0001c0001t0001g0137 others(124): Show |
134 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.949+687A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142822845 | |||||||
| chr3:142823046 | A | C | 10 | a0001c0001t0001g0226 a0001c0001t0002g0013 a0001c0001t0002g0140 others(7): Show |
11 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.949+486T>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142823046 | |||||||
| chr3:142823159 | C | T | 10 | a0001c0001t0001g0226 a0001c0001t0002g0013 a0001c0001t0002g0140 others(7): Show |
11 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.949+373G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142823159 | |||||||
| chr3:142823192 | T | C | 143 | a0001c0001t0001g0006 a0001c0001t0001g0117 a0001c0001t0001g0137 others(140): Show |
151 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(148): Show |
intron_variant | MODIFIER | c.949+340A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142823192 | |||||||
| chr3:142823402 | C | A | 4 | a0001c0001t0005g0002 a0001c0001t0005g0032 a0001c0001t0005g0049 others(1): Show |
5 | HG01167.hp2 HG01169.hp2 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.949+130G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142823402 | |||||||
| chr3:142823439 | C | T | 1 | a0001c0001t0002g0183 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.949+93G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 7/8 | chr3 | 142823439 | |||||||
| chr3:142823644 | G | A | 1 | a0001c0001t0001g0282 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.866-29C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142823644 | |||||||
| chr3:142823823 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.866-208A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142823823 | |||||||
| chr3:142823841 | T | C | 127 | a0001c0001t0001g0006 a0001c0001t0001g0117 a0001c0001t0001g0137 others(124): Show |
134 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.866-226A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142823841 | |||||||
| chr3:142823899 | A | G | 86 | a0001c0001t0001g0173 a0001c0001t0001g0220 a0001c0001t0001g0251 others(83): Show |
91 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.866-284T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142823899 | |||||||
| chr3:142823914 | C | T | 2 | a0001c0001t0003g0003 a0001c0001t0003g0036 |
3 | HG01346.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.866-299G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142823914 | |||||||
| chr3:142823981 | T | C | 10 | a0001c0001t0001g0226 a0001c0001t0002g0013 a0001c0001t0002g0140 others(7): Show |
11 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.866-366A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142823981 | |||||||
| chr3:142824089 | T | C | 6 | a0001c0001t0001g0108 a0001c0001t0001g0159 a0001c0001t0001g0162 others(3): Show |
6 | NA18946.hp1 NA18947.hp2 NA19002.hp1 others(3): Show |
intron_variant | MODIFIER | c.866-474A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142824089 | |||||||
| chr3:142824125 | C | T | 2 | a0001c0001t0002g0124 a0001c0001t0002g0254 |
2 | HG02970.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.866-510G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142824125 | |||||||
| chr3:142824176 | AACTAAGA others(60): Show |
A | 4 | a0001c0001t0001g0125 a0001c0001t0006g0089 a0002c0002t0001g0169 others(1): Show |
4 | NA18980.hp2 NA19070.hp2 NA19075.hp1 others(1): Show |
intron_variant | MODIFIER | c.866-628_866-562del others(67): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142824176 | |||||||
| chr3:142824250 | C | T | 3 | a0001c0001t0002g0116 a0001c0001t0002g0219 a0001c0001t0002g0250 |
3 | NA18985.hp1 NA19012.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.866-635G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142824250 | |||||||
| chr3:142824264 | T | C | 1 | a0001c0001t0001g0215 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.866-649A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142824264 | |||||||
| chr3:142824411 | G | C | 3 | a0001c0001t0007g0187 a0001c0001t0009g0027 a0001c0004t0007g0321 |
3 | HG02922.hp2 HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.866-796C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142824411 | |||||||
| chr3:142824432 | G | A | 3 | a0001c0001t0001g0299 a0001c0001t0001g0301 a0001c0001t0001g0308 |
3 | HG02129.hp2 NA18973.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.866-817C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142824432 | |||||||
| chr3:142824457 | C | T | 1 | a0001c0001t0003g0030 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.866-842G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142824457 | |||||||
| chr3:142824491 | T | C | 2 | a0001c0001t0001g0190 a0001c0001t0006g0078 |
2 | HG03017.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.866-876A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142824491 | |||||||
| chr3:142824598 | T | C | 1 | a0001c0001t0005g0055 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.866-983A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142824598 | |||||||
| chr3:142824621 | C | CTGTTAAT others(6): Show |
10 | a0001c0001t0001g0226 a0001c0001t0002g0013 a0001c0001t0002g0140 others(7): Show |
11 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.866-1019_866-1007d others(15): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142824621 | |||||||
| chr3:142824664 | G | A | 84 | a0001c0001t0001g0173 a0001c0001t0001g0220 a0001c0001t0001g0251 others(81): Show |
88 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.866-1049C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142824664 | |||||||
| chr3:142824671 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.866-1056C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142824671 | |||||||
| chr3:142824679 | G | A | 7 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0157 others(4): Show |
7 | HG02015.hp1 HG02165.hp1 NA18948.hp2 others(4): Show |
intron_variant | MODIFIER | c.866-1064C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142824679 | |||||||
| chr3:142824726 | A | G | 10 | a0001c0001t0001g0226 a0001c0001t0002g0013 a0001c0001t0002g0140 others(7): Show |
11 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.866-1111T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142824726 | |||||||
| chr3:142824782 | G | C | 1 | a0001c0001t0005g0055 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.866-1167C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142824782 | |||||||
| chr3:142824809 | G | A | 9 | a0001c0001t0001g0126 a0001c0001t0001g0154 a0001c0001t0001g0178 others(6): Show |
9 | HG01243.hp1 HG01496.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.866-1194C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142824809 | |||||||
| chr3:142824816 | T | C | 127 | a0001c0001t0001g0006 a0001c0001t0001g0117 a0001c0001t0001g0137 others(124): Show |
134 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.866-1201A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142824816 | |||||||
| chr3:142824886 | T | C | 127 | a0001c0001t0001g0006 a0001c0001t0001g0117 a0001c0001t0001g0137 others(124): Show |
133 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.866-1271A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142824886 | |||||||
| chr3:142824930 | T | G | 87 | a0001c0001t0001g0173 a0001c0001t0001g0179 a0001c0001t0001g0180 others(84): Show |
91 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.866-1315A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142824930 | |||||||
| chr3:142824991 | A | T | 1 | a0001c0001t0002g0255 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.866-1376T>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142824991 | |||||||
| chr3:142825051 | A | T | 10 | a0001c0001t0001g0226 a0001c0001t0002g0013 a0001c0001t0002g0140 others(7): Show |
11 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.866-1436T>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142825051 | |||||||
| chr3:142825091 | A | T | 10 | a0001c0001t0001g0226 a0001c0001t0002g0013 a0001c0001t0002g0140 others(7): Show |
11 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.866-1476T>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142825091 | |||||||
| chr3:142825201 | G | A | 30 | a0001c0001t0002g0102 a0001c0001t0002g0103 a0001c0001t0002g0116 others(27): Show |
31 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.866-1586C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142825201 | |||||||
| chr3:142825295 | C | T | 1 | a0002c0002t0004g0099 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.866-1680G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142825295 | |||||||
| chr3:142825401 | G | A | 4 | a0001c0001t0001g0126 a0001c0001t0001g0154 a0001c0001t0001g0233 others(1): Show |
4 | HG01243.hp1 HG02723.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.866-1786C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142825401 | |||||||
| chr3:142825422 | G | A | 10 | a0001c0001t0001g0226 a0001c0001t0002g0013 a0001c0001t0002g0140 others(7): Show |
11 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.866-1807C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142825422 | |||||||
| chr3:142825564 | A | C | 10 | a0001c0001t0001g0226 a0001c0001t0002g0013 a0001c0001t0002g0140 others(7): Show |
11 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.866-1949T>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142825564 | |||||||
| chr3:142826005 | C | CT | 11 | a0001c0001t0001g0226 a0001c0001t0002g0013 a0001c0001t0002g0140 others(8): Show |
12 | HG00423.hp2 HG02258.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.866-2391dupA | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142826005 | |||||||
| chr3:142826124 | C | T | 1 | a0001c0001t0006g0078 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.866-2509G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142826124 | |||||||
| chr3:142826166 | G | A | 3 | a0001c0001t0001g0163 a0001c0001t0001g0277 a0001c0001t0006g0086 |
3 | NA18944.hp2 NA18953.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.866-2551C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142826166 | |||||||
| chr3:142826224 | G | A | 1 | a0001c0001t0003g0031 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.866-2609C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142826224 | |||||||
| chr3:142826229 | G | A | 2 | a0001c0001t0005g0029 a0001c0001t0005g0040 |
2 | HG03239.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.866-2614C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142826229 | |||||||
| chr3:142826244 | T | G | 1 | a0001c0001t0004g0071 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.866-2629A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142826244 | |||||||
| chr3:142826250 | A | G | 128 | a0001c0001t0001g0006 a0001c0001t0001g0117 a0001c0001t0001g0137 others(125): Show |
134 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.866-2635T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142826250 | |||||||
| chr3:142826272 | T | G | 128 | a0001c0001t0001g0006 a0001c0001t0001g0117 a0001c0001t0001g0137 others(125): Show |
134 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.866-2657A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142826272 | |||||||
| chr3:142826307 | G | A | 1 | a0001c0001t0001g0281 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.866-2692C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142826307 | |||||||
| chr3:142826596 | T | C | 10 | a0001c0001t0001g0226 a0001c0001t0002g0013 a0001c0001t0002g0140 others(7): Show |
11 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.866-2981A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142826596 | |||||||
| chr3:142826656 | C | T | 8 | a0001c0001t0001g0006 a0001c0001t0001g0137 a0001c0001t0001g0138 others(5): Show |
9 | HG01109.hp2 HG01891.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.865+3036G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142826656 | |||||||
| chr3:142826661 | C | T | 2 | a0001c0001t0001g0311 a0001c0004t0001g0322 |
2 | HG02257.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.865+3031G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142826661 | |||||||
| chr3:142826729 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.865+2963G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142826729 | |||||||
| chr3:142826802 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.865+2890G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142826802 | |||||||
| chr3:142826805 | T | G | 30 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0104 others(27): Show |
32 | HG00438.hp1 HG00639.hp2 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.865+2887A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142826805 | |||||||
| chr3:142827036 | T | C | 10 | a0001c0001t0001g0226 a0001c0001t0002g0013 a0001c0001t0002g0140 others(7): Show |
11 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.865+2656A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142827036 | |||||||
| chr3:142827092 | A | G | 2 | a0001c0001t0002g0146 a0001c0001t0002g0264 |
2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.865+2600T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142827092 | |||||||
| chr3:142827149 | G | A | 5 | a0001c0001t0002g0009 a0001c0001t0002g0124 a0001c0001t0002g0196 others(2): Show |
6 | HG02970.hp1 NA18971.hp2 NA18972.hp2 others(3): Show |
intron_variant | MODIFIER | c.865+2543C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142827149 | |||||||
| chr3:142827179 | C | G | 10 | a0001c0001t0001g0226 a0001c0001t0002g0013 a0001c0001t0002g0140 others(7): Show |
11 | HG02258.hp1 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.865+2513G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142827179 | |||||||
| chr3:142827211 | C | T | 4 | a0001c0001t0001g0126 a0001c0001t0001g0154 a0001c0001t0001g0233 others(1): Show |
4 | HG01243.hp1 HG02723.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.865+2481G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142827211 | |||||||
| chr3:142827212 | G | A | 2 | a0001c0001t0001g0258 a0001c0001t0003g0048 |
2 | HG01261.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.865+2480C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142827212 | |||||||
| chr3:142827512 | C | T | 139 | a0001c0001t0001g0006 a0001c0001t0001g0117 a0001c0001t0001g0118 others(136): Show |
146 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.865+2180G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142827512 | |||||||
| chr3:142827532 | C | T | 1 | a0001c0001t0001g0180 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.865+2160G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142827532 | |||||||
| chr3:142827538 | T | TAC | 4 | a0001c0001t0001g0226 a0001c0001t0007g0187 a0001c0001t0009g0027 others(1): Show |
4 | HG02258.hp1 HG02922.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.865+2152_865+2153d others(4): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142827538 | |||||||
| chr3:142827599 | G | A | 5 | a0001c0001t0001g0136 a0001c0001t0001g0226 a0001c0001t0007g0187 others(2): Show |
5 | HG02258.hp1 HG02922.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.865+2093C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142827599 | |||||||
| chr3:142827634 | C | T | 1 | a0001c0001t0002g0255 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.865+2058G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142827634 | |||||||
| chr3:142827901 | G | T | 32 | a0001c0001t0001g0123 a0001c0001t0001g0176 a0001c0001t0001g0177 others(29): Show |
33 | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(30): Show |
intron_variant | MODIFIER | c.865+1791C>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142827901 | |||||||
| chr3:142828041 | C | T | 1 | a0001c0001t0001g0243 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.865+1651G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142828041 | |||||||
| chr3:142828043 | C | T | 1 | a0001c0001t0003g0020 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.865+1649G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142828043 | |||||||
| chr3:142828274 | G | A | 1 | a0001c0001t0004g0091 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.865+1418C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142828274 | |||||||
| chr3:142828378 | A | G | 2 | a0001c0001t0001g0165 a0001c0001t0001g0199 |
2 | NA19055.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.865+1314T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142828378 | |||||||
| chr3:142828420 | T | C | 42 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0015 others(39): Show |
47 | HG00280.hp2 HG00642.hp2 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.865+1272A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142828420 | |||||||
| chr3:142828552 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.865+1140C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142828552 | |||||||
| chr3:142828575 | C | T | 156 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0010 others(153): Show |
167 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.865+1117G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142828575 | |||||||
| chr3:142828588 | G | A | 1 | a0001c0001t0003g0003 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.865+1104C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142828588 | |||||||
| chr3:142828645 | C | G | 1 | a0001c0001t0002g0265 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.865+1047G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142828645 | |||||||
| chr3:142828720 | G | A | 10 | a0001c0001t0001g0143 a0001c0001t0001g0174 a0001c0001t0001g0175 others(7): Show |
10 | HG02257.hp2 HG02280.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.865+972C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142828720 | |||||||
| chr3:142828828 | T | C | 1 | a0001c0001t0001g0220 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.865+864A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142828828 | |||||||
| chr3:142828834 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.865+858C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142828834 | |||||||
| chr3:142828911 | T | C | 46 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0015 others(43): Show |
51 | HG00280.hp2 HG00642.hp2 HG01069.hp2 others(48): Show |
intron_variant | MODIFIER | c.865+781A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142828911 | |||||||
| chr3:142828957 | A | G | 1 | a0001c0001t0002g0265 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.865+735T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142828957 | |||||||
| chr3:142829110 | C | G | 1 | a0001c0001t0002g0265 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.865+582G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142829110 | |||||||
| chr3:142829113 | C | G | 115 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(112): Show |
123 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.865+579G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142829113 | |||||||
| chr3:142829161 | C | G | 1 | a0001c0001t0002g0265 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.865+531G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142829161 | |||||||
| chr3:142829193 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.865+499G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142829193 | |||||||
| chr3:142829227 | AAAAT | A | 113 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(110): Show |
121 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.865+461_865+464del others(4): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142829227 | |||||||
| chr3:142829281 | C | CA | 35 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0117 others(32): Show |
37 | HG00323.hp1 HG00738.hp2 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.865+410dupT | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142829281 | |||||||
| chr3:142829512 | C | T | 115 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(112): Show |
123 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.865+180G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142829512 | |||||||
| chr3:142829622 | TTTC | T | 7 | a0001c0001t0001g0182 a0001c0001t0001g0235 a0001c0001t0001g0249 others(4): Show |
7 | HG00735.hp1 HG01175.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.865+67_865+69delGA others(1): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 6/8 | chr3 | 142829622 | |||||||
| chr3:142829899 | T | C | 1 | a0001c0001t0001g0301 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.711-53A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142829899 | |||||||
| chr3:142830633 | T | C | 1 | a0001c0001t0005g0055 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.711-787A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142830633 | |||||||
| chr3:142830707 | C | T | 1 | a0005c0005t0001g0244 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.711-861G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142830707 | |||||||
| chr3:142831023 | G | A | 6 | a0001c0001t0001g0108 a0001c0001t0001g0110 a0001c0001t0002g0106 others(3): Show |
6 | HG00597.hp1 HG02027.hp1 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.711-1177C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142831023 | |||||||
| chr3:142831042 | G | A | 1 | a0001c0001t0002g0275 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.711-1196C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142831042 | |||||||
| chr3:142831243 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.711-1397A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142831243 | |||||||
| chr3:142831306 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.711-1460C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142831306 | |||||||
| chr3:142831513 | G | A | 5 | a0001c0001t0001g0182 a0001c0001t0001g0235 a0001c0001t0001g0311 others(2): Show |
5 | HG00735.hp1 HG01175.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.711-1667C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142831513 | |||||||
| chr3:142831674 | A | C | 1 | a0002c0002t0002g0132 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.711-1828T>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142831674 | |||||||
| chr3:142832095 | A | G | 1 | a0001c0001t0001g0226 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.711-2249T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142832095 | |||||||
| chr3:142832140 | C | T | 1 | a0001c0001t0002g0149 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.711-2294G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142832140 | |||||||
| chr3:142832229 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.711-2383C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142832229 | |||||||
| chr3:142832256 | T | C | 1 | a0003c0003t0003g0035 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.711-2410A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142832256 | |||||||
| chr3:142832296 | T | G | 4 | a0001c0001t0001g0182 a0001c0001t0001g0311 a0001c0001t0005g0055 others(1): Show |
4 | HG01175.hp2 HG02257.hp1 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.711-2450A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142832296 | |||||||
| chr3:142832342 | C | T | 4 | a0001c0001t0001g0242 a0001c0001t0003g0003 a0001c0001t0003g0036 others(1): Show |
5 | HG01346.hp1 HG02080.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.711-2496G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142832342 | |||||||
| chr3:142832414 | G | A | 23 | a0001c0001t0002g0140 a0001c0001t0002g0151 a0001c0001t0002g0167 others(20): Show |
24 | HG00099.hp2 HG00423.hp1 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.711-2568C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142832414 | |||||||
| chr3:142832514 | C | T | 2 | a0002c0002t0001g0152 a0002c0002t0002g0142 |
2 | HG02922.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.711-2668G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142832514 | |||||||
| chr3:142832549 | A | G | 1 | a0001c0001t0001g0242 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.711-2703T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142832549 | |||||||
| chr3:142832681 | G | T | 6 | a0001c0001t0001g0182 a0001c0001t0001g0235 a0001c0001t0001g0311 others(3): Show |
6 | HG00735.hp1 HG01175.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.711-2835C>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142832681 | |||||||
| chr3:142832722 | C | T | 1 | a0001c0001t0004g0081 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.711-2876G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142832722 | |||||||
| chr3:142832753 | CA | C | 41 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0015 others(38): Show |
45 | HG00280.hp2 HG00642.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.711-2908delT | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142832753 | |||||||
| chr3:142832955 | A | C | 1 | a0001c0001t0002g0151 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.711-3109T>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142832955 | |||||||
| chr3:142833008 | A | G | 50 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(47): Show |
53 | HG00323.hp1 HG00735.hp1 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.711-3162T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142833008 | |||||||
| chr3:142833095 | C | G | 1 | a0001c0001t0002g0309 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.711-3249G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142833095 | |||||||
| chr3:142833159 | G | T | 2 | a0001c0001t0001g0220 a0001c0001t0001g0249 |
2 | HG02109.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.711-3313C>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142833159 | |||||||
| chr3:142833182 | T | C | 50 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(47): Show |
53 | HG00323.hp1 HG00735.hp1 HG00738.hp2 others(50): Show |
intron_variant | MODIFIER | c.711-3336A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142833182 | |||||||
| chr3:142833384 | A | G | 114 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(111): Show |
122 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.711-3538T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142833384 | |||||||
| chr3:142833481 | CT | C | 45 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0015 others(42): Show |
49 | HG00280.hp2 HG00642.hp2 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.711-3636delA | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142833481 | |||||||
| chr3:142833790 | G | T | 89 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(86): Show |
96 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.711-3944C>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142833790 | |||||||
| chr3:142833816 | T | C | 1 | a0001c0001t0001g0281 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.711-3970A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142833816 | |||||||
| chr3:142834161 | C | T | 1 | a0002c0002t0004g0099 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.711-4315G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142834161 | |||||||
| chr3:142834166 | T | G | 1 | a0001c0001t0002g0265 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.711-4320A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142834166 | |||||||
| chr3:142834247 | C | A | 2 | a0001c0001t0008g0315 a0001c0001t0008g0316 |
2 | NA18949.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.711-4401G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142834247 | |||||||
| chr3:142834253 | C | T | 1 | a0002c0002t0004g0099 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.711-4407G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142834253 | |||||||
| chr3:142834336 | G | T | 1 | a0001c0001t0004g0070 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.710+4434C>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142834336 | |||||||
| chr3:142834471 | T | C | 1 | a0003c0003t0001g0259 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.710+4299A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142834471 | |||||||
| chr3:142834594 | A | G | 1 | a0001c0001t0002g0149 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.710+4176T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142834594 | |||||||
| chr3:142834828 | T | C | 2 | a0001c0001t0001g0136 a0001c0001t0002g0146 |
2 | HG02615.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.710+3942A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142834828 | |||||||
| chr3:142834830 | G | A | 1 | a0001c0001t0001g0247 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.710+3940C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142834830 | |||||||
| chr3:142835004 | C | T | 1 | a0001c0001t0002g0255 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.710+3766G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142835004 | |||||||
| chr3:142835159 | T | G | 2 | a0001c0001t0004g0075 a0001c0001t0004g0076 |
2 | HG02074.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.710+3611A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142835159 | |||||||
| chr3:142835194 | T | G | 15 | a0001c0001t0001g0108 a0001c0001t0001g0110 a0001c0001t0001g0213 others(12): Show |
16 | HG00597.hp1 HG02027.hp1 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.710+3576A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142835194 | |||||||
| chr3:142835238 | T | G | 2 | a0001c0001t0001g0220 a0001c0001t0001g0249 |
2 | HG02109.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.710+3532A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142835238 | |||||||
| chr3:142835308 | T | C | 41 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0015 others(38): Show |
45 | HG00280.hp2 HG00642.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.710+3462A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142835308 | |||||||
| chr3:142835311 | A | T | 1 | a0001c0001t0001g0188 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.710+3459T>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142835311 | |||||||
| chr3:142835333 | T | C | 34 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(31): Show |
37 | HG00323.hp1 HG00738.hp2 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.710+3437A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142835333 | |||||||
| chr3:142835516 | A | T | 89 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(86): Show |
96 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.710+3254T>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142835516 | |||||||
| chr3:142835517 | A | G | 111 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(108): Show |
120 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.710+3253T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142835517 | |||||||
| chr3:142835614 | A | G | 88 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(85): Show |
95 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(92): Show |
intron_variant | MODIFIER | c.710+3156T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142835614 | |||||||
| chr3:142835627 | T | C | 76 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(73): Show |
83 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.710+3143A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142835627 | |||||||
| chr3:142835732 | T | C | 1 | a0001c0001t0008g0316 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.710+3038A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142835732 | |||||||
| chr3:142835815 | T | A | 111 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(108): Show |
120 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.710+2955A>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142835815 | |||||||
| chr3:142835893 | C | A | 6 | a0002c0002t0001g0111 a0002c0002t0001g0169 a0002c0002t0001g0170 others(3): Show |
6 | HG00544.hp2 NA18950.hp2 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.710+2877G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142835893 | |||||||
| chr3:142835893 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.710+2877G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142835893 | |||||||
| chr3:142836001 | A | AT | 75 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(72): Show |
82 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.710+2768dupA | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142836001 | |||||||
| chr3:142836121 | T | G | 2 | a0001c0001t0001g0220 a0001c0001t0001g0249 |
2 | HG02109.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.710+2649A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142836121 | |||||||
| chr3:142836133 | G | A | 1 | a0001c0001t0002g0140 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.710+2637C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142836133 | |||||||
| chr3:142836151 | C | A | 75 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(72): Show |
82 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.710+2619G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142836151 | |||||||
| chr3:142836175 | C | T | 88 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(85): Show |
95 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(92): Show |
intron_variant | MODIFIER | c.710+2595G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142836175 | |||||||
| chr3:142836329 | T | G | 1 | a0001c0001t0003g0061 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.710+2441A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142836329 | |||||||
| chr3:142836386 | G | A | 75 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(72): Show |
82 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.710+2384C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142836386 | |||||||
| chr3:142836504 | G | A | 1 | a0001c0001t0001g0008 | 2 | HG03831.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.710+2266C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142836504 | |||||||
| chr3:142836573 | T | C | 1 | a0001c0001t0001g0141 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.710+2197A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142836573 | |||||||
| chr3:142836578 | T | C | 2 | a0001c0001t0001g0235 a0001c0001t0011g0101 |
2 | HG00735.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.710+2192A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142836578 | |||||||
| chr3:142836649 | T | C | 1 | a0001c0001t0002g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.710+2121A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142836649 | |||||||
| chr3:142836699 | G | A | 9 | a0001c0001t0001g0143 a0001c0001t0001g0154 a0001c0001t0001g0178 others(6): Show |
9 | HG01243.hp1 HG01496.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.710+2071C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142836699 | |||||||
| chr3:142837004 | A | G | 41 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0015 others(38): Show |
45 | HG00280.hp2 HG00642.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.710+1766T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142837004 | |||||||
| chr3:142837006 | G | A | 1 | a0001c0001t0001g0161 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.710+1764C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142837006 | |||||||
| chr3:142837099 | C | T | 1 | a0001c0001t0002g0155 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.710+1671G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142837099 | |||||||
| chr3:142837364 | G | A | 2 | a0001c0001t0001g0136 a0001c0001t0002g0146 |
2 | HG02615.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.710+1406C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142837364 | |||||||
| chr3:142837453 | C | CTTAATA | 88 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(85): Show |
95 | HG00280.hp2 HG00323.hp1 HG00642.hp2 others(92): Show |
intron_variant | MODIFIER | c.710+1316_710+1317i others(8): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142837453 | |||||||
| chr3:142837513 | C | T | 41 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0015 others(38): Show |
45 | HG00280.hp2 HG00642.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.710+1257G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142837513 | |||||||
| chr3:142837557 | A | G | 41 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0015 others(38): Show |
45 | HG00280.hp2 HG00642.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.710+1213T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142837557 | |||||||
| chr3:142837576 | GA | G | 6 | a0001c0001t0002g0245 a0001c0001t0002g0309 a0001c0001t0004g0083 others(3): Show |
6 | HG00597.hp2 HG02135.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.710+1193delT | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142837576 | |||||||
| chr3:142837741 | T | C | 1 | a0001c0001t0002g0270 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.710+1029A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142837741 | |||||||
| chr3:142837748 | G | A | 41 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0015 others(38): Show |
45 | HG00280.hp2 HG00642.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.710+1022C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142837748 | |||||||
| chr3:142838247 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.710+523T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142838247 | |||||||
| chr3:142838392 | T | G | 1 | a0001c0001t0001g0313 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.710+378A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142838392 | |||||||
| chr3:142838565 | T | C | 4 | a0001c0001t0002g0102 a0001c0001t0002g0103 a0001c0001t0002g0184 others(1): Show |
4 | HG00673.hp1 HG02132.hp2 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.710+205A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 5/8 | chr3 | 142838565 | |||||||
| chr3:142839002 | C | T | 1 | a0001c0001t0005g0055 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.574-96G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142839002 | |||||||
| chr3:142839064 | T | TA | 6 | a0001c0001t0001g0006 a0001c0001t0001g0150 a0001c0001t0001g0243 others(3): Show |
7 | HG01891.hp1 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.574-159dupT | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142839064 | |||||||
| chr3:142839312 | T | C | 3 | a0001c0001t0008g0203 a0001c0001t0008g0315 a0001c0001t0008g0316 |
3 | NA18949.hp1 NA18984.hp2 NA19055.hp2 |
intron_variant | MODIFIER | c.574-406A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142839312 | |||||||
| chr3:142839315 | AT | A | 8 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0182 others(5): Show |
8 | HG01109.hp2 HG01167.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.574-410delA | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142839315 | |||||||
| chr3:142839464 | C | T | 3 | a0001c0001t0004g0068 a0001c0001t0004g0069 a0001c0001t0004g0074 |
3 | NA18747.hp1 NA18989.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.574-558G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142839464 | |||||||
| chr3:142839501 | C | T | 4 | a0001c0001t0001g0182 a0001c0001t0001g0235 a0001c0001t0001g0311 others(1): Show |
4 | HG00735.hp1 HG01175.hp2 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.574-595G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142839501 | |||||||
| chr3:142839742 | T | G | 1 | a0001c0001t0001g0281 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.574-836A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142839742 | |||||||
| chr3:142839867 | T | C | 1 | a0001c0001t0001g0208 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.574-961A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142839867 | |||||||
| chr3:142839973 | G | T | 1 | a0001c0001t0004g0083 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.574-1067C>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142839973 | |||||||
| chr3:142840195 | C | T | 40 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0015 others(37): Show |
44 | HG00280.hp2 HG00642.hp2 HG01069.hp2 others(41): Show |
intron_variant | MODIFIER | c.574-1289G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142840195 | |||||||
| chr3:142840319 | A | G | 2 | a0001c0001t0001g0126 a0001c0001t0006g0082 |
2 | HG02735.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.574-1413T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142840319 | |||||||
| chr3:142840379 | C | T | 62 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0015 others(59): Show |
68 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.574-1473G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142840379 | |||||||
| chr3:142840689 | T | C | 4 | a0001c0001t0001g0242 a0001c0001t0003g0003 a0001c0001t0003g0036 others(1): Show |
5 | HG01346.hp1 HG02080.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.574-1783A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142840689 | |||||||
| chr3:142840691 | T | C | 1 | a0001c0001t0004g0073 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.574-1785A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142840691 | |||||||
| chr3:142840762 | C | T | 2 | a0001c0001t0001g0226 a0001c0001t0002g0255 |
2 | HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.574-1856G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142840762 | |||||||
| chr3:142840846 | C | T | 5 | a0001c0001t0001g0145 a0001c0001t0002g0144 a0001c0001t0002g0239 others(2): Show |
5 | HG02451.hp1 HG02965.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.574-1940G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142840846 | |||||||
| chr3:142840944 | G | A | 1 | a0001c0001t0002g0254 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.573+1980C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142840944 | |||||||
| chr3:142841024 | G | A | 1 | a0001c0001t0005g0055 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.573+1900C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142841024 | |||||||
| chr3:142841029 | C | T | 3 | a0001c0001t0001g0160 a0001c0001t0001g0210 a0001c0001t0006g0084 |
3 | HG01257.hp1 HG01952.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.573+1895G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142841029 | |||||||
| chr3:142841074 | C | CA | 84 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(81): Show |
92 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.573+1849dupT | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142841074 | |||||||
| chr3:142841125 | A | T | 2 | a0001c0001t0001g0136 a0001c0001t0002g0146 |
2 | HG02615.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.573+1799T>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142841125 | |||||||
| chr3:142841210 | G | A | 72 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(69): Show |
79 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.573+1714C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142841210 | |||||||
| chr3:142841225 | C | A | 8 | a0002c0002t0001g0111 a0002c0002t0001g0169 a0002c0002t0001g0170 others(5): Show |
8 | HG00544.hp2 HG02056.hp1 NA18950.hp2 others(5): Show |
intron_variant | MODIFIER | c.573+1699G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142841225 | |||||||
| chr3:142841335 | A | T | 42 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0015 others(39): Show |
46 | HG00280.hp2 HG00642.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.573+1589T>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142841335 | |||||||
| chr3:142841523 | G | C | 1 | a0001c0001t0001g0012 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.573+1401C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142841523 | |||||||
| chr3:142841551 | T | A | 1 | a0001c0001t0001g0220 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.573+1373A>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142841551 | |||||||
| chr3:142841555 | ATTACT | A | 4 | a0001c0001t0002g0151 a0001c0001t0002g0167 a0001c0001t0002g0264 others(1): Show |
4 | HG00738.hp1 HG02055.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.573+1364_573+1368d others(7): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142841555 | |||||||
| chr3:142842000 | A | G | 1 | a0001c0001t0001g0213 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.573+924T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142842000 | |||||||
| chr3:142842037 | A | C | 2 | a0001c0001t0001g0136 a0001c0001t0002g0146 |
2 | HG02615.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.573+887T>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142842037 | |||||||
| chr3:142842103 | C | G | 1 | a0001c0001t0002g0312 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.573+821G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142842103 | |||||||
| chr3:142842149 | G | C | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | HG01109.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.573+775C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142842149 | |||||||
| chr3:142842285 | T | A | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | HG01109.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.573+639A>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142842285 | |||||||
| chr3:142842353 | A | G | 94 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(91): Show |
102 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.573+571T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142842353 | |||||||
| chr3:142842517 | C | G | 1 | a0001c0001t0001g0235 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.573+407G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142842517 | |||||||
| chr3:142842654 | G | A | 42 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0015 others(39): Show |
46 | HG00280.hp2 HG00642.hp2 HG01069.hp2 others(43): Show |
intron_variant | MODIFIER | c.573+270C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142842654 | |||||||
| chr3:142842739 | C | CA | 7 | a0001c0001t0001g0136 a0001c0001t0001g0182 a0001c0001t0001g0235 others(4): Show |
7 | HG00735.hp1 HG01175.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.573+184dupT | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142842739 | |||||||
| chr3:142842739 | C | CAA | 22 | a0001c0001t0001g0005 a0001c0001t0002g0140 a0001c0001t0002g0151 others(19): Show |
24 | HG00099.hp2 HG00544.hp2 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.573+183_573+184dup others(2): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142842739 | |||||||
| chr3:142842760 | G | C | 1 | a0001c0001t0005g0055 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.573+164C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142842760 | |||||||
| chr3:142842791 | A | G | 1 | a0001c0001t0001g0165 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.573+133T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 4/8 | chr3 | 142842791 | |||||||
| chr3:142843111 | G | A | 2 | a0001c0001t0003g0034 a0003c0003t0001g0135 |
2 | HG01361.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.449-63C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142843111 | |||||||
| chr3:142843291 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.449-243G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142843291 | |||||||
| chr3:142843312 | T | C | 1 | a0001c0001t0002g0239 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.449-264A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142843312 | |||||||
| chr3:142843646 | A | G | 1 | a0001c0001t0001g0235 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.449-598T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142843646 | |||||||
| chr3:142843841 | C | A | 2 | a0001c0001t0003g0034 a0003c0003t0001g0135 |
2 | HG01361.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.449-793G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142843841 | |||||||
| chr3:142843879 | T | C | 1 | a0001c0001t0002g0265 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.449-831A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142843879 | |||||||
| chr3:142843968 | T | G | 1 | a0001c0001t0004g0090 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.449-920A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142843968 | |||||||
| chr3:142844205 | A | G | 1 | a0001c0001t0011g0101 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.449-1157T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142844205 | |||||||
| chr3:142844265 | C | T | 1 | a0001c0001t0002g0239 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.449-1217G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142844265 | |||||||
| chr3:142844335 | T | C | 1 | a0001c0001t0002g0265 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.449-1287A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142844335 | |||||||
| chr3:142844395 | T | C | 1 | a0001c0001t0005g0055 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.449-1347A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142844395 | |||||||
| chr3:142844452 | G | A | 1 | a0001c0001t0002g0265 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.449-1404C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142844452 | |||||||
| chr3:142844472 | T | C | 6 | a0001c0001t0001g0008 a0001c0001t0001g0122 a0001c0001t0001g0272 others(3): Show |
7 | HG01884.hp2 HG02735.hp2 HG03710.hp1 others(4): Show |
intron_variant | MODIFIER | c.449-1424A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142844472 | |||||||
| chr3:142844631 | C | G | 1 | a0001c0001t0001g0267 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.449-1583G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142844631 | |||||||
| chr3:142844958 | AGAC | A | 3 | a0001c0001t0001g0006 a0001c0001t0001g0150 a0001c0001t0003g0056 |
4 | HG01891.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.449-1913_449-1911d others(5): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142844958 | |||||||
| chr3:142844966 | T | C | 41 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0015 others(38): Show |
45 | HG00280.hp2 HG00642.hp2 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.449-1918A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142844966 | |||||||
| chr3:142845164 | G | A | 1 | a0001c0001t0005g0055 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.449-2116C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142845164 | |||||||
| chr3:142845482 | T | C | 52 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0015 others(49): Show |
56 | HG00280.hp2 HG00642.hp2 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.449-2434A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142845482 | |||||||
| chr3:142845578 | T | G | 1 | a0001c0001t0003g0022 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.449-2530A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142845578 | |||||||
| chr3:142845619 | C | T | 1 | a0001c0001t0001g0008 | 2 | HG03831.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.449-2571G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142845619 | |||||||
| chr3:142845739 | C | T | 1 | a0001c0001t0001g0313 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.448+2478G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142845739 | |||||||
| chr3:142845755 | A | G | 25 | a0001c0001t0001g0141 a0001c0001t0001g0154 a0001c0001t0001g0171 others(22): Show |
26 | HG00642.hp1 HG00735.hp1 HG01175.hp2 others(23): Show |
intron_variant | MODIFIER | c.448+2462T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142845755 | |||||||
| chr3:142845762 | G | C | 7 | a0001c0001t0001g0117 a0001c0001t0001g0136 a0001c0001t0001g0226 others(4): Show |
7 | HG02258.hp1 HG02615.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.448+2455C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142845762 | |||||||
| chr3:142845778 | C | T | 3 | a0001c0001t0002g0155 a0001c0001t0002g0239 a0001c0001t0002g0257 |
3 | HG01891.hp2 HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.448+2439G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142845778 | |||||||
| chr3:142845804 | G | A | 8 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0189 others(5): Show |
8 | HG02015.hp1 HG02165.hp1 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.448+2413C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142845804 | |||||||
| chr3:142845866 | T | G | 1 | a0001c0001t0001g0263 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.448+2351A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142845866 | |||||||
| chr3:142845867 | T | C | 1 | a0001c0001t0001g0263 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.448+2350A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142845867 | |||||||
| chr3:142845868 | G | C | 1 | a0001c0001t0001g0263 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.448+2349C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142845868 | |||||||
| chr3:142845870 | G | C | 1 | a0001c0001t0001g0263 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.448+2347C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142845870 | |||||||
| chr3:142845874 | T | G | 1 | a0001c0001t0001g0263 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.448+2343A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142845874 | |||||||
| chr3:142845875 | T | A | 1 | a0001c0001t0001g0263 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.448+2342A>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142845875 | |||||||
| chr3:142845876 | G | T | 1 | a0001c0001t0001g0263 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.448+2341C>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142845876 | |||||||
| chr3:142845877 | A | T | 1 | a0001c0001t0001g0263 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.448+2340T>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142845877 | |||||||
| chr3:142845952 | T | G | 2 | a0001c0001t0002g0232 a0001c0004t0001g0322 |
2 | HG02257.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.448+2265A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142845952 | |||||||
| chr3:142846011 | G | A | 64 | a0001c0001t0001g0011 a0001c0001t0001g0118 a0001c0001t0001g0143 others(61): Show |
69 | HG00099.hp2 HG00323.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.448+2206C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142846011 | |||||||
| chr3:142846060 | T | G | 1 | a0001c0001t0002g0155 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.448+2157A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142846060 | |||||||
| chr3:142846230 | G | T | 3 | a0001c0001t0001g0117 a0001c0001t0001g0182 a0001c0001t0001g0311 |
3 | HG01175.hp2 NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.448+1987C>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142846230 | |||||||
| chr3:142846257 | G | A | 3 | a0001c0001t0001g0117 a0001c0001t0001g0182 a0001c0001t0001g0311 |
3 | HG01175.hp2 NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.448+1960C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142846257 | |||||||
| chr3:142846286 | C | T | 7 | a0001c0001t0001g0117 a0001c0001t0001g0154 a0001c0001t0001g0182 others(4): Show |
7 | HG01175.hp2 HG02723.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.448+1931G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142846286 | |||||||
| chr3:142846288 | T | C | 1 | a0001c0001t0002g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.448+1929A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142846288 | |||||||
| chr3:142846313 | T | G | 5 | a0001c0001t0001g0136 a0001c0001t0001g0182 a0001c0001t0001g0311 others(2): Show |
5 | HG01175.hp2 HG02559.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.448+1904A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142846313 | |||||||
| chr3:142846678 | T | G | 1 | a0001c0001t0002g0293 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.448+1539A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142846678 | |||||||
| chr3:142846723 | T | C | 93 | a0001c0001t0001g0119 a0001c0001t0001g0143 a0001c0001t0001g0159 others(90): Show |
97 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.448+1494A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142846723 | |||||||
| chr3:142846728 | C | T | 1 | a0001c0001t0001g0164 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.448+1489G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142846728 | |||||||
| chr3:142846778 | T | C | 1 | a0001c0001t0001g0235 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.448+1439A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142846778 | |||||||
| chr3:142846952 | C | T | 1 | a0001c0001t0001g0263 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.448+1265G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142846952 | |||||||
| chr3:142846996 | C | T | 1 | a0001c0001t0001g0284 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.448+1221G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142846996 | |||||||
| chr3:142847482 | T | C | 5 | a0001c0001t0001g0109 a0001c0001t0001g0206 a0001c0001t0001g0289 others(2): Show |
5 | HG00438.hp2 HG02083.hp2 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.448+735A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142847482 | |||||||
| chr3:142847495 | G | A | 110 | a0001c0001t0001g0005 a0001c0001t0001g0118 a0001c0001t0001g0119 others(107): Show |
117 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.448+722C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142847495 | |||||||
| chr3:142847533 | G | GTA | 2 | a0001c0001t0002g0018 a0001c0001t0002g0303 |
3 | HG02056.hp2 HG02071.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.448+682_448+683dup others(2): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142847533 | |||||||
| chr3:142847541 | A | G | 1 | a0002c0002t0005g0041 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.448+676T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142847541 | |||||||
| chr3:142847750 | TG | T | 39 | a0001c0001t0001g0104 a0001c0001t0001g0114 a0001c0001t0001g0115 others(36): Show |
40 | HG00642.hp2 HG00673.hp1 HG00735.hp1 others(37): Show |
intron_variant | MODIFIER | c.448+466delC | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142847750 | |||||||
| chr3:142847762 | T | C | 176 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0104 others(173): Show |
185 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.448+455A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142847762 | |||||||
| chr3:142847834 | G | C | 176 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0104 others(173): Show |
185 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.448+383C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142847834 | |||||||
| chr3:142847989 | T | C | 1 | a0001c0001t0005g0032 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.448+228A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142847989 | |||||||
| chr3:142847999 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.448+218G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142847999 | |||||||
| chr3:142848004 | T | C | 4 | a0001c0001t0001g0171 a0001c0001t0001g0243 a0001c0001t0001g0261 others(1): Show |
4 | HG00738.hp1 HG02895.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.448+213A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142848004 | |||||||
| chr3:142848132 | A | T | 1 | a0001c0001t0002g0106 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.448+85T>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142848132 | |||||||
| chr3:142848188 | T | C | 34 | a0001c0001t0001g0104 a0001c0001t0001g0114 a0001c0001t0001g0115 others(31): Show |
35 | HG00642.hp2 HG00673.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.448+29A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 3/8 | chr3 | 142848188 | |||||||
| chr3:142848485 | G | A | 175 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0104 others(172): Show |
184 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.193-13C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142848485 | |||||||
| chr3:142848589 | C | G | 2 | a0001c0001t0001g0154 a0001c0001t0002g0155 |
2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.193-117G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142848589 | |||||||
| chr3:142848687 | G | T | 3 | a0002c0002t0001g0152 a0002c0002t0002g0142 a0002c0002t0007g0139 |
3 | HG02922.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.193-215C>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142848687 | |||||||
| chr3:142848741 | G | A | 176 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0104 others(173): Show |
185 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.193-269C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142848741 | |||||||
| chr3:142848760 | G | A | 1 | a0001c0001t0001g0267 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.193-288C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142848760 | |||||||
| chr3:142848803 | C | T | 29 | a0001c0001t0001g0005 a0001c0001t0001g0118 a0001c0001t0001g0145 others(26): Show |
32 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.193-331G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142848803 | |||||||
| chr3:142848882 | A | G | 176 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0104 others(173): Show |
185 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.193-410T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142848882 | |||||||
| chr3:142848920 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.193-448C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142848920 | |||||||
| chr3:142849069 | C | T | 1 | a0001c0001t0002g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.193-597G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142849069 | |||||||
| chr3:142849078 | G | A | 1 | a0001c0001t0001g0294 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.193-606C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142849078 | |||||||
| chr3:142849084 | C | T | 176 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0104 others(173): Show |
185 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.193-612G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142849084 | |||||||
| chr3:142849091 | T | C | 5 | a0001c0001t0002g0312 a0001c0001t0004g0079 a0001c0001t0008g0203 others(2): Show |
5 | NA18949.hp1 NA18984.hp2 NA19012.hp1 others(2): Show |
intron_variant | MODIFIER | c.193-619A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142849091 | |||||||
| chr3:142849101 | C | T | 1 | a0001c0001t0002g0254 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.193-629G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142849101 | |||||||
| chr3:142849139 | C | T | 3 | a0001c0001t0001g0125 a0001c0001t0001g0297 a0001c0001t0002g0116 |
3 | NA19012.hp2 NA19074.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.193-667G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142849139 | |||||||
| chr3:142849152 | CA | C | 175 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0104 others(172): Show |
184 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.193-681delT | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142849152 | |||||||
| chr3:142849262 | A | C | 1 | a0002c0002t0002g0142 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.193-790T>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142849262 | |||||||
| chr3:142849306 | T | A | 2 | a0001c0001t0002g0151 a0001c0001t0005g0055 |
2 | HG02055.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.193-834A>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142849306 | |||||||
| chr3:142849314 | C | G | 1 | a0001c0001t0002g0116 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.193-842G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142849314 | |||||||
| chr3:142849320 | T | C | 7 | a0001c0001t0001g0143 a0001c0001t0001g0178 a0001c0001t0001g0208 others(4): Show |
7 | HG01496.hp2 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.193-848A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142849320 | |||||||
| chr3:142849551 | G | A | 1 | a0002c0002t0007g0139 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.193-1079C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142849551 | |||||||
| chr3:142849886 | C | T | 7 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0001c0001t0001g0251 others(4): Show |
7 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.193-1414G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142849886 | |||||||
| chr3:142849950 | T | A | 1 | a0001c0001t0002g0255 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.193-1478A>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142849950 | |||||||
| chr3:142850105 | A | G | 1 | a0001c0001t0002g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.193-1633T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142850105 | |||||||
| chr3:142850151 | A | G | 176 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0104 others(173): Show |
185 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.193-1679T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142850151 | |||||||
| chr3:142850172 | GTTT | G | 37 | a0001c0001t0001g0104 a0001c0001t0001g0114 a0001c0001t0001g0115 others(34): Show |
38 | HG00642.hp2 HG00673.hp1 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.193-1703_193-1701d others(5): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142850172 | |||||||
| chr3:142850179 | G | C | 1 | a0001c0001t0002g0291 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.193-1707C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142850179 | |||||||
| chr3:142850305 | C | A | 1 | a0001c0001t0002g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.193-1833G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142850305 | |||||||
| chr3:142850414 | G | C | 3 | a0001c0001t0001g0143 a0001c0001t0001g0208 a0001c0001t0001g0229 |
3 | HG02886.hp1 HG03041.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.193-1942C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142850414 | |||||||
| chr3:142850534 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.193-2062C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142850534 | |||||||
| chr3:142850758 | A | G | 176 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0104 others(173): Show |
185 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.193-2286T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142850758 | |||||||
| chr3:142850808 | G | T | 1 | a0001c0001t0010g0064 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.193-2336C>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142850808 | |||||||
| chr3:142850812 | A | ACT | 176 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0104 others(173): Show |
185 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.193-2341_193-2340i others(4): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142850812 | |||||||
| chr3:142850875 | T | G | 3 | a0001c0001t0001g0173 a0001c0001t0002g0262 a0004c0006t0001g0147 |
3 | HG02109.hp2 HG02976.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.193-2403A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142850875 | |||||||
| chr3:142850964 | G | A | 6 | a0001c0001t0001g0006 a0001c0001t0001g0150 a0001c0001t0001g0267 others(3): Show |
7 | HG01891.hp1 HG02630.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.193-2492C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142850964 | |||||||
| chr3:142851023 | A | G | 1 | a0001c0001t0001g0157 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.193-2551T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142851023 | |||||||
| chr3:142851060 | T | C | 1 | a0001c0001t0002g0264 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.193-2588A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142851060 | |||||||
| chr3:142851092 | T | C | 1 | a0001c0001t0003g0037 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.193-2620A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142851092 | |||||||
| chr3:142851122 | G | C | 1 | a0001c0001t0002g0216 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.193-2650C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142851122 | |||||||
| chr3:142851201 | T | C | 4 | a0001c0001t0001g0006 a0001c0001t0001g0150 a0001c0001t0002g0140 others(1): Show |
5 | HG01891.hp1 HG02895.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.193-2729A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142851201 | |||||||
| chr3:142851541 | A | T | 8 | a0001c0001t0001g0171 a0001c0001t0001g0179 a0001c0001t0001g0180 others(5): Show |
8 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.193-3069T>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142851541 | |||||||
| chr3:142851578 | A | G | 2 | a0001c0001t0001g0222 a0001c0001t0001g0223 |
2 | HG03704.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.193-3106T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142851578 | |||||||
| chr3:142851596 | G | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0263 |
2 | HG00323.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.193-3124C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142851596 | |||||||
| chr3:142851619 | G | T | 2 | a0002c0002t0002g0142 a0002c0002t0007g0139 |
2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.193-3147C>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142851619 | |||||||
| chr3:142851749 | C | T | 2 | a0001c0001t0001g0263 a0001c0001t0002g0156 |
2 | HG03453.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.193-3277G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142851749 | |||||||
| chr3:142851989 | G | C | 3 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 |
3 | HG02280.hp2 HG03130.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.193-3517C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142851989 | |||||||
| chr3:142852112 | T | C | 2 | a0001c0001t0001g0267 a0001c0001t0002g0254 |
2 | HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.193-3640A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142852112 | |||||||
| chr3:142852222 | A | G | 1 | a0001c0001t0001g0247 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.193-3750T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142852222 | |||||||
| chr3:142852245 | A | G | 44 | a0001c0001t0001g0104 a0001c0001t0001g0114 a0001c0001t0001g0115 others(41): Show |
45 | HG00642.hp2 HG00673.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.193-3773T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142852245 | |||||||
| chr3:142852276 | C | T | 1 | a0001c0001t0001g0249 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.193-3804G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142852276 | |||||||
| chr3:142852355 | G | A | 1 | a0001c0001t0001g0319 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.193-3883C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142852355 | |||||||
| chr3:142852421 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.193-3949A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142852421 | |||||||
| chr3:142852533 | A | G | 1 | a0001c0001t0001g0175 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.193-4061T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142852533 | |||||||
| chr3:142852647 | A | ATG | 11 | a0001c0001t0001g0006 a0001c0001t0001g0150 a0001c0001t0001g0190 others(8): Show |
12 | HG01891.hp1 HG02074.hp2 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.193-4177_193-4176d others(4): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142852647 | |||||||
| chr3:142852647 | A | ATGTG | 6 | a0001c0001t0001g0117 a0001c0001t0001g0175 a0001c0001t0002g0149 others(3): Show |
6 | HG02055.hp2 HG02486.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.193-4179_193-4176d others(6): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142852647 | |||||||
| chr3:142852647 | A | ATGTGTG | 3 | a0001c0001t0001g0154 a0001c0001t0001g0266 a0001c0001t0002g0155 |
3 | HG01891.hp2 HG02723.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.193-4181_193-4176d others(8): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142852647 | |||||||
| chr3:142852647 | ATG | A | 45 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0010 others(42): Show |
53 | HG00639.hp2 HG00673.hp2 HG01081.hp1 others(50): Show |
intron_variant | MODIFIER | c.193-4177_193-4176d others(4): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142852647 | |||||||
| chr3:142852647 | ATGTG | A | 5 | a0001c0001t0001g0267 a0001c0001t0002g0254 a0001c0001t0002g0275 others(2): Show |
5 | HG02132.hp1 HG02630.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.193-4179_193-4176d others(6): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142852647 | |||||||
| chr3:142852717 | A | G | 2 | a0002c0002t0002g0142 a0002c0002t0007g0139 |
2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.193-4245T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142852717 | |||||||
| chr3:142852725 | T | G | 2 | a0002c0002t0002g0142 a0002c0002t0007g0139 |
2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.193-4253A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142852725 | |||||||
| chr3:142852787 | T | C | 169 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0104 others(166): Show |
178 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.193-4315A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142852787 | |||||||
| chr3:142852791 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.193-4319G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142852791 | |||||||
| chr3:142852844 | C | T | 1 | a0001c0001t0004g0081 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.193-4372G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142852844 | |||||||
| chr3:142852932 | G | A | 2 | a0002c0002t0002g0142 a0002c0002t0007g0139 |
2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.193-4460C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142852932 | |||||||
| chr3:142853101 | T | TA | 36 | a0001c0001t0001g0104 a0001c0001t0001g0114 a0001c0001t0001g0117 others(33): Show |
37 | HG00642.hp2 HG00673.hp1 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.193-4630dupT | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142853101 | |||||||
| chr3:142853101 | TA | T | 8 | a0001c0001t0001g0176 a0001c0001t0001g0199 a0001c0001t0001g0215 others(5): Show |
8 | HG01496.hp1 HG01993.hp1 HG02735.hp1 others(5): Show |
intron_variant | MODIFIER | c.193-4630delT | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142853101 | |||||||
| chr3:142853139 | C | T | 9 | a0001c0001t0001g0117 a0001c0001t0001g0154 a0001c0001t0001g0175 others(6): Show |
9 | HG01891.hp2 HG02055.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.193-4667G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142853139 | |||||||
| chr3:142853214 | T | C | 2 | a0001c0001t0001g0182 a0001c0001t0001g0311 |
2 | HG01175.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.193-4742A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142853214 | |||||||
| chr3:142853334 | C | T | 1 | a0001c0001t0002g0221 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.193-4862G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142853334 | |||||||
| chr3:142853422 | T | C | 1 | a0001c0001t0001g0235 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.193-4950A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142853422 | |||||||
| chr3:142853456 | T | C | 2 | a0001c0001t0001g0267 a0001c0001t0002g0254 |
2 | HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.193-4984A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142853456 | |||||||
| chr3:142853624 | A | G | 2 | a0001c0001t0001g0182 a0001c0001t0001g0311 |
2 | HG01175.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.193-5152T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142853624 | |||||||
| chr3:142853745 | C | T | 6 | a0001c0001t0002g0231 a0001c0001t0004g0085 a0001c0001t0004g0087 others(3): Show |
6 | HG00423.hp2 NA18960.hp2 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.193-5273G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142853745 | |||||||
| chr3:142853752 | T | A | 1 | a0001c0001t0001g0171 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.193-5280A>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142853752 | |||||||
| chr3:142853773 | C | T | 2 | a0001c0001t0001g0192 a0001c0001t0002g0124 |
2 | HG02622.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.193-5301G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142853773 | |||||||
| chr3:142854078 | C | T | 167 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0104 others(164): Show |
176 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.193-5606G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142854078 | |||||||
| chr3:142854166 | C | T | 1 | a0001c0001t0001g0220 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.193-5694G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142854166 | |||||||
| chr3:142854208 | C | CAT | 181 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0104 others(178): Show |
190 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.193-5737_193-5736i others(4): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142854208 | |||||||
| chr3:142854209 | G | A | 1 | a0001c0001t0001g0283 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.193-5737C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142854209 | |||||||
| chr3:142854262 | A | T | 2 | a0001c0001t0001g0263 a0001c0001t0002g0156 |
2 | HG03453.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.193-5790T>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142854262 | |||||||
| chr3:142854321 | C | T | 167 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0104 others(164): Show |
176 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.193-5849G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142854321 | |||||||
| chr3:142854329 | AGTTGATC others(18): Show |
A | 169 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0104 others(166): Show |
178 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.193-5882_193-5858d others(27): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142854329 | |||||||
| chr3:142854486 | A | G | 1 | a0001c0001t0002g0112 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.193-6014T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142854486 | |||||||
| chr3:142854532 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.193-6060A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142854532 | |||||||
| chr3:142854613 | C | A | 44 | a0001c0001t0001g0104 a0001c0001t0001g0114 a0001c0001t0001g0115 others(41): Show |
45 | HG00642.hp2 HG00673.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.193-6141G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142854613 | |||||||
| chr3:142854651 | G | A | 44 | a0001c0001t0001g0104 a0001c0001t0001g0114 a0001c0001t0001g0115 others(41): Show |
45 | HG00642.hp2 HG00673.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.193-6179C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142854651 | |||||||
| chr3:142854688 | C | T | 115 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0118 others(112): Show |
123 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.193-6216G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142854688 | |||||||
| chr3:142854695 | G | A | 7 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(4): Show |
7 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.193-6223C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142854695 | |||||||
| chr3:142854947 | T | C | 115 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0118 others(112): Show |
123 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.193-6475A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142854947 | |||||||
| chr3:142855019 | G | T | 1 | a0001c0001t0001g0300 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.193-6547C>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142855019 | |||||||
| chr3:142855033 | G | A | 1 | a0001c0001t0002g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.193-6561C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142855033 | |||||||
| chr3:142855281 | G | A | 1 | a0001c0001t0001g0266 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.193-6809C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142855281 | |||||||
| chr3:142855325 | C | T | 115 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0118 others(112): Show |
123 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.193-6853G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142855325 | |||||||
| chr3:142855326 | G | A | 1 | a0001c0001t0002g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.193-6854C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142855326 | |||||||
| chr3:142855340 | T | TA | 168 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0104 others(165): Show |
177 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.193-6869dupT | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142855340 | |||||||
| chr3:142855345 | T | A | 169 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0104 others(166): Show |
178 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.193-6873A>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142855345 | |||||||
| chr3:142855353 | C | T | 5 | a0001c0001t0001g0160 a0001c0001t0001g0164 a0001c0001t0001g0210 others(2): Show |
5 | HG01192.hp2 HG01257.hp1 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.193-6881G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142855353 | |||||||
| chr3:142855354 | A | G | 159 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0104 others(156): Show |
168 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.193-6882T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142855354 | |||||||
| chr3:142855439 | G | A | 1 | a0001c0001t0002g0239 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.193-6967C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142855439 | |||||||
| chr3:142855463 | G | A | 1 | a0001c0001t0002g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.193-6991C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142855463 | |||||||
| chr3:142855614 | G | A | 159 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0104 others(156): Show |
168 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.193-7142C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142855614 | |||||||
| chr3:142855705 | A | C | 163 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0104 others(160): Show |
172 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.193-7233T>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142855705 | |||||||
| chr3:142855727 | C | T | 2 | a0001c0001t0001g0263 a0001c0001t0002g0156 |
2 | HG03453.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.193-7255G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142855727 | |||||||
| chr3:142855787 | A | G | 115 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0118 others(112): Show |
123 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.193-7315T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142855787 | |||||||
| chr3:142856086 | C | T | 3 | a0001c0001t0001g0194 a0001c0001t0002g0195 a0001c0001t0003g0033 |
3 | HG01884.hp1 HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.193-7614G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142856086 | |||||||
| chr3:142856200 | C | T | 2 | a0002c0002t0002g0142 a0002c0002t0007g0139 |
2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.193-7728G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142856200 | |||||||
| chr3:142856203 | T | G | 1 | a0001c0001t0001g0263 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.193-7731A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142856203 | |||||||
| chr3:142856371 | T | C | 169 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0104 others(166): Show |
178 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.193-7899A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142856371 | |||||||
| chr3:142856718 | G | A | 1 | a0001c0001t0002g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.193-8246C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142856718 | |||||||
| chr3:142856758 | C | T | 1 | a0001c0001t0002g0240 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.193-8286G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142856758 | |||||||
| chr3:142856840 | A | G | 1 | a0001c0001t0002g0239 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.193-8368T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142856840 | |||||||
| chr3:142856892 | CT | C | 50 | a0001c0001t0001g0104 a0001c0001t0001g0114 a0001c0001t0001g0115 others(47): Show |
50 | HG00642.hp2 HG00673.hp1 HG00741.hp1 others(47): Show |
intron_variant | MODIFIER | c.193-8421delA | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142856892 | |||||||
| chr3:142856992 | C | T | 2 | a0002c0002t0002g0142 a0002c0002t0007g0139 |
2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.193-8520G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142856992 | |||||||
| chr3:142857048 | CTCTATAG others(3): Show |
C | 3 | a0001c0001t0001g0175 a0001c0001t0002g0149 a0001c0001t0002g0255 |
3 | HG03041.hp2 HG03209.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.193-8586_193-8577d others(12): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142857048 | |||||||
| chr3:142857053 | T | C | 2 | a0002c0002t0002g0142 a0002c0002t0007g0139 |
2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.193-8581A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142857053 | |||||||
| chr3:142857054 | A | G | 2 | a0001c0001t0002g0264 a0001c0001t0002g0265 |
2 | HG02622.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.193-8582T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142857054 | |||||||
| chr3:142857059 | G | C | 3 | a0001c0001t0001g0175 a0001c0001t0002g0149 a0001c0001t0002g0255 |
3 | HG03041.hp2 HG03209.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.193-8587C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142857059 | |||||||
| chr3:142857166 | C | G | 1 | a0001c0001t0001g0263 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.193-8694G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142857166 | |||||||
| chr3:142857412 | C | T | 169 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0104 others(166): Show |
178 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.193-8940G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142857412 | |||||||
| chr3:142857440 | T | C | 2 | a0002c0002t0002g0142 a0002c0002t0007g0139 |
2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.193-8968A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142857440 | |||||||
| chr3:142857593 | A | G | 4 | a0001c0001t0003g0047 a0001c0001t0003g0048 a0001c0001t0005g0049 others(1): Show |
4 | HG01261.hp2 HG03490.hp2 NA20752.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-9121T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142857593 | |||||||
| chr3:142857613 | C | T | 169 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0104 others(166): Show |
178 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.193-9141G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142857613 | |||||||
| chr3:142857637 | G | A | 4 | a0001c0001t0003g0023 a0001c0001t0003g0026 a0001c0001t0005g0025 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-9165C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142857637 | |||||||
| chr3:142857689 | C | T | 1 | a0001c0001t0001g0294 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.193-9217G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142857689 | |||||||
| chr3:142857706 | T | C | 1 | a0001c0001t0004g0070 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.193-9234A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142857706 | |||||||
| chr3:142857875 | C | T | 1 | a0001c0001t0002g0309 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.193-9403G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142857875 | |||||||
| chr3:142857905 | C | G | 1 | a0001c0001t0002g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.193-9433G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142857905 | |||||||
| chr3:142857912 | A | C | 169 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0104 others(166): Show |
178 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(175): Show |
intron_variant | MODIFIER | c.193-9440T>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142857912 | |||||||
| chr3:142857958 | C | A | 1 | a0001c0001t0001g0318 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.193-9486G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142857958 | |||||||
| chr3:142858539 | T | C | 1 | a0001c0001t0003g0021 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.193-10067A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142858539 | |||||||
| chr3:142858657 | T | C | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | HG01109.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.193-10185A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142858657 | |||||||
| chr3:142858735 | A | ATG | 110 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0117 others(107): Show |
117 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.193-10265_193-1026 others(6): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142858735 | |||||||
| chr3:142858735 | A | ATGTG | 3 | a0001c0001t0001g0267 a0001c0001t0002g0254 a0002c0002t0004g0098 |
3 | HG02630.hp1 NA18960.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.193-10267_193-1026 others(8): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142858735 | |||||||
| chr3:142858735 | A | G | 1 | a0001c0001t0002g0317 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.193-10263T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142858735 | |||||||
| chr3:142858750 | T | TGC | 29 | a0001c0001t0001g0143 a0001c0001t0001g0166 a0001c0001t0001g0178 others(26): Show |
31 | HG00280.hp2 HG00639.hp1 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.193-10279_193-1027 others(6): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142858750 | |||||||
| chr3:142858780 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.193-10308C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142858780 | |||||||
| chr3:142858870 | C | T | 2 | a0001c0001t0002g0239 a0001c0001t0002g0257 |
2 | HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.193-10398G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142858870 | |||||||
| chr3:142858939 | C | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0161 a0001c0001t0001g0217 |
4 | HG00673.hp2 NA18942.hp2 NA18949.hp2 others(1): Show |
intron_variant | MODIFIER | c.193-10467G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142858939 | |||||||
| chr3:142859014 | C | T | 14 | a0001c0001t0001g0117 a0001c0001t0001g0154 a0001c0001t0001g0175 others(11): Show |
14 | HG01891.hp2 HG02055.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.193-10542G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142859014 | |||||||
| chr3:142859069 | T | C | 1 | a0001c0001t0004g0083 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.193-10597A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142859069 | |||||||
| chr3:142859078 | T | C | 1 | a0001c0001t0001g0166 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.193-10606A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142859078 | |||||||
| chr3:142859101 | C | T | 3 | a0001c0001t0001g0127 a0001c0001t0001g0267 a0001c0001t0002g0254 |
3 | HG00642.hp2 HG02630.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.193-10629G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142859101 | |||||||
| chr3:142859102 | G | A | 27 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0015 others(24): Show |
31 | HG00438.hp1 HG00673.hp2 HG01515.hp1 others(28): Show |
intron_variant | MODIFIER | c.193-10630C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142859102 | |||||||
| chr3:142859116 | G | A | 113 | a0001c0001t0001g0005 a0001c0001t0001g0118 a0001c0001t0001g0119 others(110): Show |
121 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.193-10644C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142859116 | |||||||
| chr3:142859252 | G | A | 4 | a0001c0001t0001g0141 a0001c0001t0001g0263 a0002c0002t0002g0142 others(1): Show |
4 | HG02615.hp1 HG03453.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-10780C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142859252 | |||||||
| chr3:142859466 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.193-10994A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142859466 | |||||||
| chr3:142859564 | G | GT | 6 | a0001c0001t0001g0263 a0001c0001t0002g0265 a0001c0001t0003g0023 others(3): Show |
6 | HG02896.hp1 HG02897.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.193-11093dupA | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142859564 | |||||||
| chr3:142859714 | C | T | 33 | a0001c0001t0001g0104 a0001c0001t0001g0114 a0001c0001t0001g0115 others(30): Show |
33 | HG00642.hp2 HG00673.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.193-11242G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142859714 | |||||||
| chr3:142859778 | G | A | 3 | a0001c0001t0001g0141 a0002c0002t0002g0142 a0002c0002t0007g0139 |
3 | HG02615.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.193-11306C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142859778 | |||||||
| chr3:142859850 | A | G | 9 | a0001c0001t0001g0117 a0001c0001t0001g0154 a0001c0001t0001g0175 others(6): Show |
9 | HG01891.hp2 HG02055.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.193-11378T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142859850 | |||||||
| chr3:142859855 | T | C | 5 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0130 others(2): Show |
5 | HG02451.hp2 HG02559.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.193-11383A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142859855 | |||||||
| chr3:142859944 | T | C | 1 | a0001c0001t0001g0267 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.193-11472A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142859944 | |||||||
| chr3:142859962 | A | G | 118 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0118 others(115): Show |
127 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.193-11490T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142859962 | |||||||
| chr3:142860055 | T | TA | 9 | a0001c0001t0001g0117 a0001c0001t0001g0154 a0001c0001t0001g0175 others(6): Show |
9 | HG01891.hp2 HG02055.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.193-11584dupT | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142860055 | |||||||
| chr3:142860111 | A | G | 1 | a0001c0001t0003g0052 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.193-11639T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142860111 | |||||||
| chr3:142860149 | G | A | 1 | a0001c0001t0003g0045 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.193-11677C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142860149 | |||||||
| chr3:142860370 | T | A | 1 | a0001c0001t0001g0286 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.193-11898A>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142860370 | |||||||
| chr3:142860388 | A | T | 182 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0104 others(179): Show |
191 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(188): Show |
intron_variant | MODIFIER | c.193-11916T>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142860388 | |||||||
| chr3:142860403 | T | C | 9 | a0001c0001t0001g0117 a0001c0001t0001g0154 a0001c0001t0001g0175 others(6): Show |
9 | HG01891.hp2 HG02055.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.193-11931A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142860403 | |||||||
| chr3:142860425 | T | TTTG | 5 | a0001c0001t0001g0226 a0001c0001t0001g0263 a0001c0001t0002g0013 others(2): Show |
6 | HG00642.hp1 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.193-11956_193-1195 others(7): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142860425 | |||||||
| chr3:142860425 | TTTG | T | 15 | a0001c0001t0001g0117 a0001c0001t0001g0154 a0001c0001t0001g0175 others(12): Show |
15 | HG01891.hp2 HG02055.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.193-11956_193-1195 others(7): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142860425 | |||||||
| chr3:142860494 | T | C | 310 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(307): Show |
328 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(325): Show |
intron_variant | MODIFIER | c.193-12022A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142860494 | |||||||
| chr3:142860554 | G | A | 4 | a0001c0001t0003g0023 a0001c0001t0003g0026 a0001c0001t0005g0025 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-12082C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142860554 | |||||||
| chr3:142860560 | C | A | 2 | a0001c0001t0001g0289 a0001c0001t0001g0295 |
2 | HG00438.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.193-12088G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142860560 | |||||||
| chr3:142860565 | C | T | 2 | a0001c0001t0001g0182 a0001c0001t0001g0311 |
2 | HG01175.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.193-12093G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142860565 | |||||||
| chr3:142860669 | A | G | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | HG01109.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.193-12197T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142860669 | |||||||
| chr3:142861102 | C | A | 117 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0118 others(114): Show |
126 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.193-12630G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142861102 | |||||||
| chr3:142861242 | G | C | 137 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0117 others(134): Show |
146 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.193-12770C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142861242 | |||||||
| chr3:142861480 | T | TATCTTCC | 17 | a0001c0001t0001g0117 a0001c0001t0001g0154 a0001c0001t0001g0175 others(14): Show |
17 | HG01891.hp2 HG02055.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.193-13009_193-1300 others(11): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142861480 | |||||||
| chr3:142861541 | CTTG | C | 9 | a0001c0001t0001g0117 a0001c0001t0001g0154 a0001c0001t0001g0175 others(6): Show |
9 | HG01891.hp2 HG02055.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.193-13072_193-1307 others(7): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142861541 | |||||||
| chr3:142861615 | C | T | 1 | a0001c0001t0002g0167 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.193-13143G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142861615 | |||||||
| chr3:142861626 | A | C | 1 | a0001c0001t0002g0254 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.193-13154T>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142861626 | |||||||
| chr3:142861655 | CT | C | 121 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0118 others(118): Show |
130 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.193-13184delA | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142861655 | |||||||
| chr3:142862055 | G | A | 2 | a0001c0001t0002g0239 a0001c0001t0002g0257 |
2 | HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.193-13583C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142862055 | |||||||
| chr3:142862123 | G | A | 56 | a0001c0001t0001g0104 a0001c0001t0001g0114 a0001c0001t0001g0115 others(53): Show |
56 | HG00642.hp2 HG00673.hp1 HG00741.hp1 others(53): Show |
intron_variant | MODIFIER | c.193-13651C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142862123 | |||||||
| chr3:142862471 | T | G | 55 | a0001c0001t0001g0104 a0001c0001t0001g0114 a0001c0001t0001g0115 others(52): Show |
55 | HG00642.hp2 HG00673.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.193-13999A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142862471 | |||||||
| chr3:142862494 | A | G | 3 | a0001c0001t0001g0141 a0002c0002t0002g0142 a0002c0002t0007g0139 |
3 | HG02615.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.193-14022T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142862494 | |||||||
| chr3:142862500 | T | C | 21 | a0001c0001t0001g0005 a0001c0001t0001g0118 a0001c0001t0001g0145 others(18): Show |
24 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.193-14028A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142862500 | |||||||
| chr3:142862580 | C | T | 2 | a0001c0001t0001g0194 a0001c0001t0002g0255 |
2 | HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.193-14108G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142862580 | |||||||
| chr3:142862651 | G | C | 20 | a0001c0001t0001g0005 a0001c0001t0001g0118 a0001c0001t0001g0145 others(17): Show |
23 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.193-14179C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142862651 | |||||||
| chr3:142862757 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.193-14285C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142862757 | |||||||
| chr3:142862772 | A | G | 1 | a0001c0001t0001g0160 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.193-14300T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142862772 | |||||||
| chr3:142862948 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.193-14476C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142862948 | |||||||
| chr3:142863000 | G | A | 4 | a0001c0001t0001g0189 a0001c0001t0001g0236 a0001c0001t0001g0237 others(1): Show |
4 | NA18944.hp1 NA18961.hp2 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-14528C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142863000 | |||||||
| chr3:142863055 | T | G | 1 | a0001c0001t0001g0267 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.193-14583A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142863055 | |||||||
| chr3:142863060 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0002g0253 |
3 | HG01433.hp2 HG01993.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.193-14588G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142863060 | |||||||
| chr3:142863096 | CA | C | 221 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0010 others(218): Show |
235 | HG00280.hp2 HG00323.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.193-14625delT | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142863096 | |||||||
| chr3:142863096 | CAA | C | 20 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(17): Show |
20 | HG00438.hp2 HG01884.hp1 HG01993.hp1 others(17): Show |
intron_variant | MODIFIER | c.193-14626_193-1462 others(6): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142863096 | |||||||
| chr3:142863096 | CAAA | C | 52 | a0001c0001t0001g0005 a0001c0001t0001g0104 a0001c0001t0001g0114 others(49): Show |
55 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.193-14627_193-1462 others(7): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142863096 | |||||||
| chr3:142863211 | T | TA | 4 | a0001c0001t0001g0209 a0001c0001t0001g0246 a0001c0001t0003g0024 others(1): Show |
4 | HG01069.hp2 HG01168.hp2 HG01261.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-14740dupT | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142863211 | |||||||
| chr3:142863252 | G | C | 5 | a0001c0001t0001g0160 a0001c0001t0001g0210 a0001c0001t0002g0183 others(2): Show |
5 | HG01192.hp2 HG01257.hp1 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.193-14780C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142863252 | |||||||
| chr3:142863535 | C | T | 1 | a0001c0001t0001g0313 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.193-15063G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142863535 | |||||||
| chr3:142863537 | T | G | 3 | a0001c0001t0001g0182 a0001c0001t0001g0311 a0001c0001t0002g0156 |
3 | HG01175.hp2 HG04115.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.193-15065A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142863537 | |||||||
| chr3:142863584 | T | C | 12 | a0001c0001t0001g0117 a0001c0001t0001g0154 a0001c0001t0001g0252 others(9): Show |
12 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.193-15112A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142863584 | |||||||
| chr3:142863688 | G | A | 2 | a0001c0001t0002g0193 a0001c0001t0002g0232 |
2 | HG01433.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.193-15216C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142863688 | |||||||
| chr3:142863797 | T | C | 90 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0104 others(87): Show |
94 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(91): Show |
intron_variant | MODIFIER | c.193-15325A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142863797 | |||||||
| chr3:142863888 | A | C | 1 | a0001c0001t0001g0267 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.193-15416T>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142863888 | |||||||
| chr3:142863984 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.193-15512G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142863984 | |||||||
| chr3:142863985 | G | A | 68 | a0001c0001t0001g0005 a0001c0001t0001g0104 a0001c0001t0001g0114 others(65): Show |
71 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.193-15513C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142863985 | |||||||
| chr3:142863999 | G | GA | 67 | a0001c0001t0001g0005 a0001c0001t0001g0104 a0001c0001t0001g0114 others(64): Show |
70 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.193-15528dupT | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142863999 | |||||||
| chr3:142864057 | G | A | 1 | a0001c0001t0004g0092 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.193-15585C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142864057 | |||||||
| chr3:142864147 | A | G | 2 | a0001c0001t0002g0264 a0001c0001t0002g0265 |
2 | HG02622.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.193-15675T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142864147 | |||||||
| chr3:142864336 | TGA | T | 7 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(4): Show |
7 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.193-15866_193-1586 others(6): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142864336 | |||||||
| chr3:142864406 | C | A | 1 | a0001c0001t0002g0219 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.193-15934G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142864406 | |||||||
| chr3:142864407 | A | G | 1 | a0001c0001t0002g0219 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.193-15935T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142864407 | |||||||
| chr3:142864582 | G | A | 1 | a0001c0001t0001g0297 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.193-16110C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142864582 | |||||||
| chr3:142864938 | T | C | 1 | a0001c0001t0006g0093 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.193-16466A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142864938 | |||||||
| chr3:142865145 | C | T | 3 | a0001c0001t0001g0263 a0001c0001t0002g0239 a0001c0001t0002g0257 |
3 | HG02451.hp1 HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.193-16673G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142865145 | |||||||
| chr3:142865210 | G | A | 6 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0145 others(3): Show |
6 | HG01109.hp2 HG02486.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.193-16738C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142865210 | |||||||
| chr3:142865319 | G | GT | 9 | a0001c0001t0001g0006 a0001c0001t0001g0171 a0001c0001t0001g0233 others(6): Show |
10 | HG00735.hp1 HG00738.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.193-16848dupA | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142865319 | |||||||
| chr3:142865365 | C | T | 3 | a0001c0001t0001g0263 a0001c0001t0002g0239 a0001c0001t0002g0257 |
3 | HG02451.hp1 HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.193-16893G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142865365 | |||||||
| chr3:142865367 | G | C | 1 | a0001c0001t0001g0174 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.193-16895C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142865367 | |||||||
| chr3:142865452 | AGAGT | A | 11 | a0001c0001t0001g0117 a0001c0001t0001g0154 a0001c0001t0001g0252 others(8): Show |
11 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.193-16984_193-1698 others(8): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142865452 | |||||||
| chr3:142865747 | T | C | 10 | a0001c0001t0001g0104 a0001c0001t0001g0158 a0001c0001t0001g0190 others(7): Show |
10 | HG00673.hp1 HG02132.hp2 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.193-17275A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142865747 | |||||||
| chr3:142865778 | G | A | 17 | a0001c0001t0001g0005 a0001c0001t0001g0118 a0001c0001t0002g0140 others(14): Show |
20 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.193-17306C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142865778 | |||||||
| chr3:142866107 | T | G | 3 | a0001c0001t0001g0121 a0001c0001t0001g0288 a0001c0001t0001g0296 |
3 | HG00280.hp1 HG01069.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.193-17635A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142866107 | |||||||
| chr3:142866206 | G | A | 1 | a0001c0001t0001g0117 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.193-17734C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142866206 | |||||||
| chr3:142866399 | T | A | 20 | a0001c0001t0001g0005 a0001c0001t0001g0118 a0001c0001t0001g0263 others(17): Show |
23 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.193-17927A>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142866399 | |||||||
| chr3:142866467 | A | G | 1 | a0001c0001t0001g0202 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.193-17995T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142866467 | |||||||
| chr3:142866515 | A | G | 1 | a0001c0001t0001g0263 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.193-18043T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142866515 | |||||||
| chr3:142866662 | T | C | 3 | a0001c0001t0001g0263 a0001c0001t0002g0239 a0001c0001t0002g0257 |
3 | HG02451.hp1 HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.193-18190A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142866662 | |||||||
| chr3:142866690 | A | G | 3 | a0001c0001t0001g0136 a0001c0001t0003g0060 a0001c0001t0003g0061 |
3 | HG02559.hp1 HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.193-18218T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142866690 | |||||||
| chr3:142866850 | T | C | 1 | a0001c0001t0001g0263 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.193-18378A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142866850 | |||||||
| chr3:142866854 | C | T | 20 | a0001c0001t0001g0005 a0001c0001t0001g0118 a0001c0001t0001g0263 others(17): Show |
23 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.193-18382G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142866854 | |||||||
| chr3:142866874 | T | C | 1 | a0006c0008t0001g0212 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.193-18402A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142866874 | |||||||
| chr3:142866896 | C | T | 7 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(4): Show |
7 | HG01884.hp1 HG02257.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.193-18424G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142866896 | |||||||
| chr3:142866946 | T | A | 20 | a0001c0001t0001g0005 a0001c0001t0001g0118 a0001c0001t0001g0263 others(17): Show |
23 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.193-18474A>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142866946 | |||||||
| chr3:142866948 | T | C | 29 | a0001c0001t0001g0104 a0001c0001t0001g0114 a0001c0001t0001g0115 others(26): Show |
29 | HG00642.hp2 HG00673.hp1 HG00741.hp1 others(26): Show |
intron_variant | MODIFIER | c.193-18476A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142866948 | |||||||
| chr3:142866960 | T | C | 83 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0104 others(80): Show |
87 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.193-18488A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142866960 | |||||||
| chr3:142867219 | T | C | 4 | a0001c0001t0001g0105 a0001c0001t0001g0305 a0001c0001t0002g0196 others(1): Show |
4 | HG00544.hp1 HG02074.hp1 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-18747A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142867219 | |||||||
| chr3:142867292 | T | C | 2 | a0001c0001t0002g0264 a0001c0001t0002g0265 |
2 | HG02622.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.193-18820A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142867292 | |||||||
| chr3:142867299 | C | A | 1 | a0001c0001t0001g0110 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.193-18827G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142867299 | |||||||
| chr3:142867327 | C | T | 1 | a0003c0003t0003g0053 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.193-18855G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142867327 | |||||||
| chr3:142867343 | C | A | 17 | a0001c0001t0001g0005 a0001c0001t0001g0118 a0001c0001t0002g0140 others(14): Show |
20 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.193-18871G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142867343 | |||||||
| chr3:142867434 | A | G | 1 | a0001c0001t0002g0260 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.193-18962T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142867434 | |||||||
| chr3:142867476 | T | A | 3 | a0001c0001t0001g0215 a0001c0001t0001g0290 a0001c0001t0002g0291 |
3 | HG00323.hp2 HG01496.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.193-19004A>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142867476 | |||||||
| chr3:142867508 | C | T | 5 | a0001c0001t0001g0006 a0001c0001t0001g0150 a0001c0001t0001g0171 others(2): Show |
6 | HG00738.hp1 HG01891.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.193-19036G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142867508 | |||||||
| chr3:142867628 | C | A | 3 | a0001c0001t0001g0263 a0001c0001t0002g0239 a0001c0001t0002g0257 |
3 | HG02451.hp1 HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.193-19156G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142867628 | |||||||
| chr3:142867636 | G | A | 3 | a0001c0001t0001g0213 a0001c0001t0002g0009 a0001c0001t0002g0248 |
4 | NA18972.hp2 NA18973.hp1 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.193-19164C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142867636 | |||||||
| chr3:142867653 | CACA | C | 17 | a0001c0001t0001g0005 a0001c0001t0001g0118 a0001c0001t0002g0140 others(14): Show |
20 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.193-19184_193-1918 others(7): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142867653 | |||||||
| chr3:142867714 | T | G | 2 | a0001c0001t0005g0049 a0003c0003t0003g0050 |
2 | NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.193-19242A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142867714 | |||||||
| chr3:142867909 | C | T | 19 | a0001c0001t0001g0005 a0001c0001t0001g0118 a0001c0001t0001g0263 others(16): Show |
22 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.193-19437G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142867909 | |||||||
| chr3:142867955 | T | C | 1 | a0001c0007t0001g0218 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.193-19483A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142867955 | |||||||
| chr3:142868019 | C | T | 20 | a0001c0001t0001g0005 a0001c0001t0001g0118 a0001c0001t0001g0263 others(17): Show |
23 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.193-19547G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142868019 | |||||||
| chr3:142868145 | C | T | 1 | a0001c0001t0001g0272 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.192+19524G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142868145 | |||||||
| chr3:142868202 | G | C | 1 | a0001c0001t0002g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.192+19467C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142868202 | |||||||
| chr3:142868217 | C | T | 20 | a0001c0001t0001g0005 a0001c0001t0001g0118 a0001c0001t0001g0263 others(17): Show |
23 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.192+19452G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142868217 | |||||||
| chr3:142868484 | A | G | 1 | a0001c0001t0002g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.192+19185T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142868484 | |||||||
| chr3:142868497 | G | A | 1 | a0001c0001t0003g0023 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.192+19172C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142868497 | |||||||
| chr3:142868661 | G | A | 2 | a0001c0001t0002g0264 a0001c0001t0002g0265 |
2 | HG02622.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.192+19008C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142868661 | |||||||
| chr3:142868731 | C | T | 20 | a0001c0001t0001g0005 a0001c0001t0001g0118 a0001c0001t0001g0263 others(17): Show |
23 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.192+18938G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142868731 | |||||||
| chr3:142868735 | C | T | 1 | a0001c0001t0001g0117 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.192+18934G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142868735 | |||||||
| chr3:142868790 | G | A | 17 | a0001c0001t0001g0005 a0001c0001t0001g0118 a0001c0001t0002g0140 others(14): Show |
20 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.192+18879C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142868790 | |||||||
| chr3:142868978 | G | A | 2 | a0001c0001t0002g0239 a0001c0001t0002g0257 |
2 | HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.192+18691C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142868978 | |||||||
| chr3:142869019 | C | T | 2 | a0001c0001t0002g0239 a0001c0001t0002g0257 |
2 | HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.192+18650G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142869019 | |||||||
| chr3:142869030 | G | A | 1 | a0001c0001t0001g0289 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.192+18639C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142869030 | |||||||
| chr3:142869108 | G | C | 1 | a0001c0001t0001g0294 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.192+18561C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142869108 | |||||||
| chr3:142869183 | C | T | 1 | a0001c0001t0002g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.192+18486G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142869183 | |||||||
| chr3:142869184 | G | A | 28 | a0001c0001t0001g0104 a0001c0001t0001g0114 a0001c0001t0001g0115 others(25): Show |
28 | HG00642.hp2 HG00673.hp1 HG00741.hp1 others(25): Show |
intron_variant | MODIFIER | c.192+18485C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142869184 | |||||||
| chr3:142869207 | T | C | 20 | a0001c0001t0001g0005 a0001c0001t0001g0118 a0001c0001t0001g0263 others(17): Show |
23 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.192+18462A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142869207 | |||||||
| chr3:142869216 | G | A | 3 | a0001c0001t0001g0141 a0002c0002t0002g0142 a0002c0002t0007g0139 |
3 | HG02615.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.192+18453C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142869216 | |||||||
| chr3:142869239 | C | T | 2 | a0001c0001t0001g0299 a0001c0001t0001g0308 |
2 | NA18973.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.192+18430G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142869239 | |||||||
| chr3:142869245 | C | T | 1 | a0002c0002t0005g0039 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.192+18424G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142869245 | |||||||
| chr3:142869302 | C | A | 2 | a0001c0001t0001g0016 a0001c0001t0001g0172 |
3 | HG01515.hp1 HG01517.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.192+18367G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142869302 | |||||||
| chr3:142869382 | G | T | 40 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(37): Show |
43 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.192+18287C>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142869382 | |||||||
| chr3:142869419 | C | A | 2 | a0001c0001t0001g0182 a0001c0001t0001g0311 |
2 | HG01175.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.192+18250G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142869419 | |||||||
| chr3:142869525 | G | T | 4 | a0001c0001t0003g0023 a0001c0001t0003g0026 a0001c0001t0005g0025 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.192+18144C>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142869525 | |||||||
| chr3:142869564 | C | T | 4 | a0001c0001t0001g0019 a0001c0001t0001g0279 a0001c0001t0001g0313 others(1): Show |
5 | HG00639.hp2 HG01081.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.192+18105G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142869564 | |||||||
| chr3:142869625 | G | T | 2 | a0001c0001t0002g0239 a0001c0001t0002g0257 |
2 | HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.192+18044C>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142869625 | |||||||
| chr3:142869932 | A | G | 1 | a0001c0001t0001g0267 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.192+17737T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142869932 | |||||||
| chr3:142870131 | A | G | 20 | a0001c0001t0001g0005 a0001c0001t0001g0118 a0001c0001t0001g0263 others(17): Show |
23 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.192+17538T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142870131 | |||||||
| chr3:142870171 | C | T | 3 | a0002c0002t0004g0004 a0002c0002t0005g0039 a0002c0002t0005g0041 |
4 | HG01070.hp1 HG01256.hp1 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.192+17498G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142870171 | |||||||
| chr3:142870299 | T | C | 2 | a0001c0001t0002g0239 a0001c0001t0002g0257 |
2 | HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.192+17370A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142870299 | |||||||
| chr3:142870310 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.192+17359G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142870310 | |||||||
| chr3:142870483 | T | C | 1 | a0001c0001t0002g0102 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.192+17186A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142870483 | |||||||
| chr3:142870489 | G | A | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | HG01109.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.192+17180C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142870489 | |||||||
| chr3:142870492 | A | G | 20 | a0001c0001t0001g0005 a0001c0001t0001g0118 a0001c0001t0001g0263 others(17): Show |
23 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.192+17177T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142870492 | |||||||
| chr3:142870598 | T | C | 2 | a0001c0001t0001g0157 a0001c0001t0006g0084 |
2 | HG01952.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.192+17071A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142870598 | |||||||
| chr3:142870706 | A | AT | 23 | a0001c0001t0001g0006 a0001c0001t0001g0129 a0001c0001t0001g0131 others(20): Show |
24 | HG00280.hp2 HG00738.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.192+16962dupA | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142870706 | |||||||
| chr3:142870706 | A | ATT | 41 | a0001c0001t0001g0005 a0001c0001t0001g0104 a0001c0001t0001g0114 others(38): Show |
44 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(41): Show |
intron_variant | MODIFIER | c.192+16961_192+1696 others(6): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142870706 | |||||||
| chr3:142870706 | A | ATTT | 8 | a0001c0001t0001g0117 a0001c0001t0001g0263 a0001c0001t0001g0267 others(5): Show |
8 | HG02451.hp1 HG02630.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.192+16960_192+1696 others(7): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142870706 | |||||||
| chr3:142870706 | A | ATTTT | 14 | a0001c0001t0001g0154 a0001c0001t0001g0182 a0001c0001t0001g0252 others(11): Show |
14 | HG01175.hp2 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.192+16959_192+1696 others(8): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142870706 | |||||||
| chr3:142870784 | C | T | 17 | a0001c0001t0001g0005 a0001c0001t0001g0118 a0001c0001t0002g0140 others(14): Show |
20 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.192+16885G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142870784 | |||||||
| chr3:142871082 | C | G | 2 | a0001c0001t0001g0182 a0001c0001t0001g0311 |
2 | HG01175.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.192+16587G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142871082 | |||||||
| chr3:142871154 | C | T | 6 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0145 others(3): Show |
6 | HG01109.hp2 HG02486.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.192+16515G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142871154 | |||||||
| chr3:142871186 | C | G | 5 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(2): Show |
5 | NA18944.hp2 NA18947.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.192+16483G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142871186 | |||||||
| chr3:142871383 | T | C | 1 | a0001c0001t0004g0081 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.192+16286A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142871383 | |||||||
| chr3:142871519 | G | C | 14 | a0001c0001t0002g0018 a0001c0001t0002g0120 a0001c0001t0002g0231 others(11): Show |
15 | HG00423.hp2 HG01934.hp1 HG01978.hp1 others(12): Show |
intron_variant | MODIFIER | c.192+16150C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142871519 | |||||||
| chr3:142871543 | G | C | 40 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(37): Show |
43 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.192+16126C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142871543 | |||||||
| chr3:142871671 | C | T | 2 | a0001c0001t0002g0264 a0001c0001t0002g0265 |
2 | HG02622.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.192+15998G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142871671 | |||||||
| chr3:142871675 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.192+15994T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142871675 | |||||||
| chr3:142871819 | C | T | 90 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0104 others(87): Show |
94 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(91): Show |
intron_variant | MODIFIER | c.192+15850G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142871819 | |||||||
| chr3:142871832 | G | A | 2 | a0001c0001t0002g0264 a0001c0001t0002g0265 |
2 | HG02622.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.192+15837C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142871832 | |||||||
| chr3:142871877 | T | G | 2 | a0001c0001t0001g0182 a0001c0001t0001g0311 |
2 | HG01175.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.192+15792A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142871877 | |||||||
| chr3:142872252 | A | G | 1 | a0001c0001t0002g0149 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.192+15417T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142872252 | |||||||
| chr3:142872332 | G | A | 1 | a0001c0001t0001g0130 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.192+15337C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142872332 | |||||||
| chr3:142872392 | T | C | 2 | a0001c0001t0002g0239 a0001c0001t0002g0257 |
2 | HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.192+15277A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142872392 | |||||||
| chr3:142872455 | C | A | 17 | a0001c0001t0001g0005 a0001c0001t0001g0118 a0001c0001t0002g0140 others(14): Show |
20 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.192+15214G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142872455 | |||||||
| chr3:142872685 | C | T | 19 | a0001c0001t0001g0117 a0001c0001t0001g0154 a0001c0001t0001g0182 others(16): Show |
19 | HG01175.hp2 HG01891.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.192+14984G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142872685 | |||||||
| chr3:142872701 | C | T | 1 | a0001c0007t0001g0218 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.192+14968G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142872701 | |||||||
| chr3:142872728 | C | T | 11 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0015 others(8): Show |
14 | HG00438.hp1 HG00673.hp2 HG01952.hp1 others(11): Show |
intron_variant | MODIFIER | c.192+14941G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142872728 | |||||||
| chr3:142872778 | T | C | 1 | a0001c0001t0001g0263 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.192+14891A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142872778 | |||||||
| chr3:142872873 | T | C | 1 | a0001c0001t0001g0263 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.192+14796A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142872873 | |||||||
| chr3:142872889 | A | C | 2 | a0001c0001t0002g0239 a0001c0001t0002g0257 |
2 | HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.192+14780T>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142872889 | |||||||
| chr3:142873023 | T | C | 1 | a0001c0001t0002g0214 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.192+14646A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142873023 | |||||||
| chr3:142873114 | T | C | 40 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(37): Show |
43 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.192+14555A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142873114 | |||||||
| chr3:142873166 | C | T | 1 | a0001c0001t0006g0082 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.192+14503G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142873166 | |||||||
| chr3:142873177 | T | A | 1 | a0001c0001t0001g0143 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.192+14492A>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142873177 | |||||||
| chr3:142873283 | T | A | 1 | a0001c0001t0002g0303 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.192+14386A>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142873283 | |||||||
| chr3:142873332 | G | T | 1 | a0001c0001t0006g0066 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.192+14337C>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142873332 | |||||||
| chr3:142873347 | C | T | 2 | a0001c0001t0001g0157 a0001c0001t0006g0084 |
2 | HG01952.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.192+14322G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142873347 | |||||||
| chr3:142873355 | T | G | 3 | a0001c0001t0001g0215 a0001c0001t0001g0290 a0001c0001t0002g0291 |
3 | HG00323.hp2 HG01496.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.192+14314A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142873355 | |||||||
| chr3:142873367 | C | T | 21 | a0001c0001t0001g0005 a0001c0001t0001g0118 a0001c0001t0001g0263 others(18): Show |
24 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.192+14302G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142873367 | |||||||
| chr3:142873375 | T | C | 2 | a0001c0001t0002g0239 a0001c0001t0002g0257 |
2 | HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.192+14294A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142873375 | |||||||
| chr3:142873393 | C | CA | 11 | a0001c0001t0001g0104 a0001c0001t0001g0141 a0001c0001t0001g0238 others(8): Show |
11 | HG00642.hp1 HG02074.hp2 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.192+14275dupT | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142873393 | |||||||
| chr3:142873407 | A | G | 2 | a0001c0001t0001g0182 a0001c0001t0001g0311 |
2 | HG01175.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.192+14262T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142873407 | |||||||
| chr3:142873418 | T | A | 7 | a0001c0001t0001g0122 a0001c0001t0001g0127 a0001c0001t0001g0128 others(4): Show |
7 | HG00642.hp2 HG02451.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.192+14251A>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142873418 | |||||||
| chr3:142873424 | A | T | 17 | a0001c0001t0001g0005 a0001c0001t0001g0118 a0001c0001t0002g0140 others(14): Show |
20 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.192+14245T>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142873424 | |||||||
| chr3:142873539 | G | A | 6 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0145 others(3): Show |
6 | HG01109.hp2 HG02486.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.192+14130C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142873539 | |||||||
| chr3:142873714 | C | T | 21 | a0001c0001t0001g0005 a0001c0001t0001g0118 a0001c0001t0001g0263 others(18): Show |
24 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.192+13955G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142873714 | |||||||
| chr3:142873781 | G | T | 3 | a0001c0001t0001g0263 a0001c0001t0002g0239 a0001c0001t0002g0257 |
3 | HG02451.hp1 HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.192+13888C>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142873781 | |||||||
| chr3:142873786 | T | C | 1 | a0001c0001t0002g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.192+13883A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142873786 | |||||||
| chr3:142873825 | C | T | 1 | a0001c0001t0001g0296 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.192+13844G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142873825 | |||||||
| chr3:142873925 | C | T | 5 | a0001c0001t0005g0062 a0003c0003t0001g0259 a0003c0003t0003g0053 others(2): Show |
5 | HG01074.hp1 HG01099.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.192+13744G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142873925 | |||||||
| chr3:142873998 | G | C | 3 | a0001c0001t0001g0263 a0001c0001t0002g0239 a0001c0001t0002g0257 |
3 | HG02451.hp1 HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.192+13671C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142873998 | |||||||
| chr3:142874169 | G | A | 4 | a0001c0001t0003g0023 a0001c0001t0003g0026 a0001c0001t0005g0025 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.192+13500C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142874169 | |||||||
| chr3:142874207 | T | A | 1 | a0001c0001t0002g0140 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.192+13462A>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142874207 | |||||||
| chr3:142874265 | G | T | 1 | a0001c0001t0001g0200 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.192+13404C>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142874265 | |||||||
| chr3:142874345 | A | G | 1 | a0001c0001t0001g0266 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.192+13324T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142874345 | |||||||
| chr3:142874428 | C | T | 2 | a0001c0001t0003g0060 a0001c0001t0003g0061 |
2 | HG02559.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.192+13241G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142874428 | |||||||
| chr3:142874429 | G | A | 1 | a0001c0001t0001g0263 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.192+13240C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142874429 | |||||||
| chr3:142874548 | T | C | 17 | a0001c0001t0001g0166 a0001c0001t0001g0242 a0001c0001t0002g0292 others(14): Show |
19 | HG00280.hp2 HG00639.hp1 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.192+13121A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142874548 | |||||||
| chr3:142874853 | G | A | 1 | a0001c0001t0006g0084 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.192+12816C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142874853 | |||||||
| chr3:142875113 | T | C | 7 | a0001c0001t0005g0002 a0001c0001t0005g0032 a0001c0001t0005g0062 others(4): Show |
8 | HG01074.hp1 HG01099.hp2 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.192+12556A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142875113 | |||||||
| chr3:142875224 | C | A | 3 | a0001c0001t0001g0263 a0001c0001t0002g0239 a0001c0001t0002g0257 |
3 | HG02451.hp1 HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.192+12445G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142875224 | |||||||
| chr3:142875326 | C | T | 1 | a0001c0001t0002g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.192+12343G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142875326 | |||||||
| chr3:142875443 | T | C | 12 | a0001c0001t0001g0117 a0001c0001t0001g0154 a0001c0001t0001g0252 others(9): Show |
12 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.192+12226A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142875443 | |||||||
| chr3:142875445 | A | C | 2 | a0002c0002t0001g0169 a0002c0002t0001g0170 |
2 | NA19070.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.192+12224T>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142875445 | |||||||
| chr3:142875474 | T | TGG | 3 | a0001c0001t0001g0263 a0001c0001t0002g0239 a0001c0001t0002g0257 |
3 | HG02451.hp1 HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.192+12194_192+1219 others(6): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142875474 | |||||||
| chr3:142875669 | C | G | 1 | a0001c0001t0001g0261 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.192+12000G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142875669 | |||||||
| chr3:142876097 | C | T | 3 | a0001c0001t0001g0263 a0001c0001t0002g0239 a0001c0001t0002g0257 |
3 | HG02451.hp1 HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.192+11572G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142876097 | |||||||
| chr3:142876144 | T | C | 1 | a0001c0001t0002g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.192+11525A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142876144 | |||||||
| chr3:142876317 | G | A | 1 | a0001c0001t0002g0167 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.192+11352C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142876317 | |||||||
| chr3:142876327 | C | T | 43 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(40): Show |
46 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.192+11342G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142876327 | |||||||
| chr3:142876356 | GAGGT | G | 20 | a0001c0001t0001g0005 a0001c0001t0001g0118 a0001c0001t0001g0263 others(17): Show |
23 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.192+11309_192+1131 others(8): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142876356 | |||||||
| chr3:142876444 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.192+11225C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142876444 | |||||||
| chr3:142876538 | G | C | 1 | a0001c0001t0002g0216 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.192+11131C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142876538 | |||||||
| chr3:142876657 | C | T | 20 | a0001c0001t0001g0005 a0001c0001t0001g0118 a0001c0001t0001g0263 others(17): Show |
23 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.192+11012G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142876657 | |||||||
| chr3:142876950 | C | T | 20 | a0001c0001t0001g0005 a0001c0001t0001g0118 a0001c0001t0001g0263 others(17): Show |
23 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.192+10719G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142876950 | |||||||
| chr3:142876985 | C | G | 12 | a0001c0001t0001g0117 a0001c0001t0001g0154 a0001c0001t0001g0252 others(9): Show |
12 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.192+10684G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142876985 | |||||||
| chr3:142876992 | T | C | 20 | a0001c0001t0001g0005 a0001c0001t0001g0118 a0001c0001t0001g0263 others(17): Show |
23 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.192+10677A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142876992 | |||||||
| chr3:142877015 | T | A | 40 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(37): Show |
43 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.192+10654A>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142877015 | |||||||
| chr3:142877205 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.192+10464G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142877205 | |||||||
| chr3:142877219 | C | T | 1 | a0001c0001t0001g0199 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.192+10450G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142877219 | |||||||
| chr3:142877338 | T | C | 2 | a0001c0001t0002g0193 a0001c0001t0002g0232 |
2 | HG01433.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.192+10331A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142877338 | |||||||
| chr3:142877370 | C | G | 40 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(37): Show |
43 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(40): Show |
intron_variant | MODIFIER | c.192+10299G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142877370 | |||||||
| chr3:142877634 | T | A | 2 | a0001c0001t0002g0292 a0001c0001t0003g0038 |
2 | HG00639.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.192+10035A>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142877634 | |||||||
| chr3:142877637 | C | A | 1 | a0001c0001t0003g0030 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.192+10032G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142877637 | |||||||
| chr3:142877818 | A | T | 2 | a0001c0001t0002g0239 a0001c0001t0002g0257 |
2 | HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.192+9851T>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142877818 | |||||||
| chr3:142877834 | C | T | 4 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0274 others(1): Show |
4 | HG01884.hp2 HG02735.hp2 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.192+9835G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142877834 | |||||||
| chr3:142877933 | G | T | 20 | a0001c0001t0001g0005 a0001c0001t0001g0118 a0001c0001t0001g0263 others(17): Show |
23 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.192+9736C>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142877933 | |||||||
| chr3:142878081 | A | T | 72 | a0001c0001t0001g0005 a0001c0001t0001g0104 a0001c0001t0001g0114 others(69): Show |
75 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.192+9588T>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142878081 | |||||||
| chr3:142878365 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.192+9304G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142878365 | |||||||
| chr3:142878662 | T | C | 88 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0104 others(85): Show |
92 | HG00099.hp2 HG00323.hp1 HG00642.hp2 others(89): Show |
intron_variant | MODIFIER | c.192+9007A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142878662 | |||||||
| chr3:142878721 | G | C | 1 | a0001c0001t0001g0295 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.192+8948C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142878721 | |||||||
| chr3:142878852 | C | CA | 25 | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0001g0154 others(22): Show |
25 | HG00735.hp1 HG01243.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.192+8816dupT | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142878852 | |||||||
| chr3:142879125 | C | T | 18 | a0001c0001t0001g0005 a0001c0001t0001g0118 a0001c0001t0003g0001 others(15): Show |
21 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.192+8544G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142879125 | |||||||
| chr3:142879290 | G | T | 43 | a0001c0001t0001g0005 a0001c0001t0001g0117 a0001c0001t0001g0118 others(40): Show |
46 | HG00099.hp2 HG00323.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.192+8379C>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142879290 | |||||||
| chr3:142879307 | C | T | 3 | a0001c0001t0001g0145 a0001c0001t0002g0144 a0001c0001t0002g0146 |
3 | HG02615.hp2 HG02965.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.192+8362G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142879307 | |||||||
| chr3:142879372 | G | C | 1 | a0001c0001t0001g0173 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.192+8297C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142879372 | |||||||
| chr3:142879421 | C | A | 1 | a0001c0001t0002g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.192+8248G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142879421 | |||||||
| chr3:142879691 | C | T | 1 | a0001c0001t0001g0311 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.192+7978G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142879691 | |||||||
| chr3:142879720 | G | A | 4 | a0001c0001t0001g0189 a0001c0001t0001g0236 a0001c0001t0001g0237 others(1): Show |
4 | NA18944.hp1 NA18961.hp2 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.192+7949C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142879720 | |||||||
| chr3:142879724 | C | A | 21 | a0001c0001t0001g0141 a0001c0001t0001g0145 a0001c0001t0001g0171 others(18): Show |
21 | HG02109.hp2 HG02257.hp1 HG02615.hp1 others(18): Show |
intron_variant | MODIFIER | c.192+7945G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142879724 | |||||||
| chr3:142879725 | T | C | 12 | a0001c0001t0001g0117 a0001c0001t0001g0154 a0001c0001t0001g0252 others(9): Show |
12 | HG01891.hp2 HG02055.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.192+7944A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142879725 | |||||||
| chr3:142879736 | G | A | 150 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(147): Show |
164 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(161): Show |
intron_variant | MODIFIER | c.192+7933C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142879736 | |||||||
| chr3:142879740 | A | C | 1 | a0001c0001t0004g0095 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.192+7929T>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142879740 | |||||||
| chr3:142879740 | A | T | 1 | a0001c0001t0001g0198 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.192+7929T>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142879740 | |||||||
| chr3:142879765 | C | G | 4 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(1): Show |
4 | HG02280.hp2 HG02976.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.192+7904G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142879765 | |||||||
| chr3:142879785 | C | T | 1 | a0001c0001t0002g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.192+7884G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142879785 | |||||||
| chr3:142879796 | C | T | 4 | a0001c0001t0004g0075 a0001c0001t0004g0076 a0001c0001t0005g0062 others(1): Show |
4 | HG02074.hp2 HG02083.hp1 NA20752.hp2 others(1): Show |
intron_variant | MODIFIER | c.192+7873G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142879796 | |||||||
| chr3:142879797 | G | A | 3 | a0001c0001t0002g0018 a0001c0001t0002g0156 a0001c0001t0002g0303 |
4 | HG02056.hp2 HG02071.hp2 HG02165.hp2 others(1): Show |
intron_variant | MODIFIER | c.192+7872C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142879797 | |||||||
| chr3:142879798 | C | T | 6 | a0001c0001t0002g0018 a0001c0001t0002g0156 a0001c0001t0002g0303 others(3): Show |
8 | HG00099.hp2 HG00735.hp2 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.192+7871G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142879798 | |||||||
| chr3:142879805 | TA | T | 9 | a0001c0001t0001g0141 a0001c0001t0002g0018 a0001c0001t0002g0156 others(6): Show |
11 | HG00099.hp2 HG00735.hp2 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.192+7863delT | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142879805 | |||||||
| chr3:142879830 | C | T | 3 | a0001c0001t0001g0182 a0001c0001t0001g0311 a0001c0001t0002g0275 |
3 | HG01175.hp2 HG02132.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.192+7839G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142879830 | |||||||
| chr3:142879970 | C | CA | 8 | a0001c0001t0001g0166 a0001c0001t0001g0185 a0001c0001t0001g0238 others(5): Show |
8 | HG02027.hp2 HG02602.hp1 HG03831.hp2 others(5): Show |
intron_variant | MODIFIER | c.192+7698dupT | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142879970 | |||||||
| chr3:142879970 | CA | C | 13 | a0001c0001t0001g0105 a0001c0001t0001g0305 a0001c0001t0002g0196 others(10): Show |
13 | HG00544.hp1 HG02074.hp1 HG02129.hp1 others(10): Show |
intron_variant | MODIFIER | c.192+7698delT | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142879970 | |||||||
| chr3:142879970 | CAA | C | 33 | a0001c0001t0001g0006 a0001c0001t0001g0137 a0001c0001t0001g0138 others(30): Show |
34 | HG01109.hp2 HG01433.hp1 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.192+7697_192+7698d others(4): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142879970 | |||||||
| chr3:142879970 | CAAA | C | 37 | a0001c0001t0001g0104 a0001c0001t0001g0114 a0001c0001t0001g0115 others(34): Show |
37 | HG00642.hp2 HG00673.hp1 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.192+7696_192+7698d others(5): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142879970 | |||||||
| chr3:142880043 | C | T | 1 | a0001c0001t0001g0297 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.192+7626G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142880043 | |||||||
| chr3:142880050 | C | G | 9 | a0001c0001t0003g0023 a0001c0001t0003g0026 a0001c0001t0005g0025 others(6): Show |
9 | HG02257.hp1 HG02896.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.192+7619G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142880050 | |||||||
| chr3:142880061 | C | A | 3 | a0001c0001t0001g0261 a0001c0001t0002g0264 a0001c0001t0002g0265 |
3 | HG02622.hp2 HG02895.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.192+7608G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142880061 | |||||||
| chr3:142880107 | A | G | 1 | a0001c0001t0002g0264 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.192+7562T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142880107 | |||||||
| chr3:142880146 | C | T | 13 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0145 others(10): Show |
13 | HG01109.hp2 HG02109.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.192+7523G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142880146 | |||||||
| chr3:142880233 | T | C | 2 | a0001c0001t0002g0239 a0001c0001t0002g0257 |
2 | HG02451.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.192+7436A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142880233 | |||||||
| chr3:142880238 | T | TA | 8 | a0001c0001t0001g0179 a0001c0001t0001g0180 a0001c0001t0001g0181 others(5): Show |
8 | HG01175.hp2 HG02280.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.192+7430dupT | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142880238 | |||||||
| chr3:142880238 | TA | T | 19 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0143 others(16): Show |
20 | HG01109.hp2 HG01167.hp2 HG01169.hp2 others(17): Show |
intron_variant | MODIFIER | c.192+7430delT | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142880238 | |||||||
| chr3:142880274 | T | C | 10 | a0001c0001t0001g0136 a0001c0001t0001g0145 a0001c0001t0001g0148 others(7): Show |
10 | HG02109.hp2 HG02451.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.192+7395A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142880274 | |||||||
| chr3:142880282 | T | G | 1 | a0001c0001t0002g0257 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.192+7387A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142880282 | |||||||
| chr3:142880332 | A | T | 3 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0171 |
3 | HG01109.hp2 HG02486.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.192+7337T>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142880332 | |||||||
| chr3:142880406 | AC | A | 17 | a0001c0001t0001g0115 a0001c0001t0001g0122 a0001c0001t0001g0123 others(14): Show |
17 | HG00642.hp2 HG01243.hp2 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.192+7262delG | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142880406 | |||||||
| chr3:142880443 | C | T | 62 | a0001c0001t0001g0006 a0001c0001t0001g0114 a0001c0001t0001g0115 others(59): Show |
63 | HG00642.hp1 HG00642.hp2 HG00741.hp1 others(60): Show |
intron_variant | MODIFIER | c.192+7226G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142880443 | |||||||
| chr3:142880464 | A | C | 2 | a0001c0001t0001g0154 a0001c0001t0002g0155 |
2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.192+7205T>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142880464 | |||||||
| chr3:142880522 | A | G | 1 | a0001c0001t0001g0261 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.192+7147T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142880522 | |||||||
| chr3:142880581 | T | C | 50 | a0001c0001t0001g0015 a0001c0001t0001g0119 a0001c0001t0001g0136 others(47): Show |
53 | HG00423.hp2 HG00597.hp2 HG01099.hp1 others(50): Show |
intron_variant | MODIFIER | c.192+7088A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142880581 | |||||||
| chr3:142880593 | C | T | 38 | a0001c0001t0001g0015 a0001c0001t0001g0119 a0001c0001t0001g0136 others(35): Show |
41 | HG00423.hp2 HG00597.hp2 HG01099.hp1 others(38): Show |
intron_variant | MODIFIER | c.192+7076G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142880593 | |||||||
| chr3:142880760 | C | T | 1 | a0001c0001t0003g0030 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.192+6909G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142880760 | |||||||
| chr3:142880811 | C | T | 1 | a0001c0001t0003g0001 | 2 | HG00735.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.192+6858G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142880811 | |||||||
| chr3:142880846 | A | G | 23 | a0001c0001t0001g0005 a0001c0001t0001g0118 a0001c0001t0001g0136 others(20): Show |
25 | HG00323.hp1 HG00642.hp1 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.192+6823T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142880846 | |||||||
| chr3:142880978 | C | T | 266 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(263): Show |
283 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(280): Show |
intron_variant | MODIFIER | c.192+6691G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142880978 | |||||||
| chr3:142881235 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.192+6434G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142881235 | |||||||
| chr3:142881245 | T | C | 272 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(269): Show |
289 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.192+6424A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142881245 | |||||||
| chr3:142881410 | A | G | 62 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0114 others(59): Show |
65 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.192+6259T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142881410 | |||||||
| chr3:142881558 | A | C | 1 | a0001c0001t0002g0184 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.192+6111T>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142881558 | |||||||
| chr3:142881614 | A | G | 1 | a0001c0001t0001g0136 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.192+6055T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142881614 | |||||||
| chr3:142881646 | T | G | 2 | a0001c0001t0001g0143 a0001c0001t0001g0263 |
2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.192+6023A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142881646 | |||||||
| chr3:142881764 | T | TA | 10 | a0001c0001t0001g0136 a0001c0001t0001g0299 a0001c0001t0001g0300 others(7): Show |
11 | HG02056.hp2 HG02071.hp2 HG02129.hp2 others(8): Show |
intron_variant | MODIFIER | c.192+5904dupT | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142881764 | |||||||
| chr3:142881827 | G | A | 38 | a0001c0001t0001g0015 a0001c0001t0001g0242 a0001c0001t0004g0065 others(35): Show |
40 | HG00423.hp2 HG00544.hp2 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.192+5842C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142881827 | |||||||
| chr3:142881833 | C | T | 59 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0114 others(56): Show |
62 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.192+5836G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142881833 | |||||||
| chr3:142881882 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.192+5787C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142881882 | |||||||
| chr3:142882141 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.192+5528G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142882141 | |||||||
| chr3:142882193 | C | A | 2 | a0001c0001t0001g0141 a0002c0002t0002g0142 |
2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.192+5476G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142882193 | |||||||
| chr3:142882199 | T | TA | 114 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0104 others(111): Show |
120 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.192+5469dupT | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142882199 | |||||||
| chr3:142882226 | G | C | 1 | a0001c0001t0002g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.192+5443C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142882226 | |||||||
| chr3:142882417 | T | A | 122 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0104 others(119): Show |
128 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.192+5252A>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142882417 | |||||||
| chr3:142882453 | G | A | 2 | a0001c0001t0001g0243 a0005c0005t0001g0244 |
2 | HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.192+5216C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142882453 | |||||||
| chr3:142882587 | A | ATTATTAT others(17): Show |
1 | a0002c0002t0002g0142 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.192+5081_192+5082i others(26): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142882587 | |||||||
| chr3:142882587 | A | ATTATTAT others(27): Show |
1 | a0001c0001t0001g0141 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.192+5081_192+5082i others(36): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142882587 | |||||||
| chr3:142882589 | A | T | 2 | a0001c0001t0001g0141 a0002c0002t0002g0142 |
2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.192+5080T>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142882589 | |||||||
| chr3:142882590 | C | T | 3 | a0001c0001t0001g0136 a0001c0001t0001g0141 a0002c0002t0002g0142 |
3 | HG02615.hp1 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.192+5079G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142882590 | |||||||
| chr3:142882594 | A | T | 2 | a0001c0001t0001g0141 a0002c0002t0002g0142 |
2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.192+5075T>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142882594 | |||||||
| chr3:142882599 | A | C | 2 | a0001c0001t0001g0141 a0002c0002t0002g0142 |
2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.192+5070T>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142882599 | |||||||
| chr3:142882601 | A | G | 2 | a0001c0001t0001g0141 a0002c0002t0002g0142 |
2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.192+5068T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142882601 | |||||||
| chr3:142882602 | G | A | 2 | a0001c0001t0001g0141 a0002c0002t0002g0142 |
2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.192+5067C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142882602 | |||||||
| chr3:142882603 | G | T | 1 | a0001c0001t0001g0157 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.192+5066C>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142882603 | |||||||
| chr3:142882608 | A | G | 2 | a0001c0001t0001g0141 a0002c0002t0002g0142 |
2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.192+5061T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142882608 | |||||||
| chr3:142882615 | C | T | 1 | a0001c0001t0002g0183 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.192+5054G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142882615 | |||||||
| chr3:142882616 | G | A | 3 | a0001c0001t0003g0059 a0001c0001t0003g0060 a0001c0001t0003g0061 |
3 | HG02559.hp1 HG03516.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.192+5053C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142882616 | |||||||
| chr3:142882622 | C | G | 2 | a0001c0001t0001g0141 a0002c0002t0002g0142 |
2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.192+5047G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142882622 | |||||||
| chr3:142882943 | G | A | 4 | a0001c0001t0001g0143 a0001c0001t0001g0154 a0001c0001t0001g0263 others(1): Show |
4 | HG01891.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.192+4726C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142882943 | |||||||
| chr3:142883124 | T | C | 1 | a0001c0001t0003g0056 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.192+4545A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142883124 | |||||||
| chr3:142883130 | G | A | 59 | a0001c0001t0001g0005 a0001c0001t0001g0114 a0001c0001t0001g0115 others(56): Show |
61 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.192+4539C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142883130 | |||||||
| chr3:142883156 | G | A | 1 | a0002c0002t0001g0152 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.192+4513C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142883156 | |||||||
| chr3:142883198 | C | CA | 30 | a0001c0001t0001g0006 a0001c0001t0001g0136 a0001c0001t0001g0137 others(27): Show |
31 | HG00544.hp1 HG00597.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.192+4470dupT | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142883198 | |||||||
| chr3:142883198 | C | CAA | 56 | a0001c0001t0001g0005 a0001c0001t0001g0114 a0001c0001t0001g0115 others(53): Show |
58 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.192+4469_192+4470d others(4): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142883198 | |||||||
| chr3:142883198 | CA | C | 49 | a0001c0001t0001g0141 a0001c0001t0001g0258 a0001c0001t0003g0001 others(46): Show |
52 | HG00280.hp2 HG00438.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.192+4470delT | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142883198 | |||||||
| chr3:142883198 | CAAAAA | C | 10 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0108 others(7): Show |
10 | HG00597.hp1 HG02083.hp2 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.192+4466_192+4470d others(7): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142883198 | |||||||
| chr3:142883363 | C | G | 61 | a0001c0001t0001g0005 a0001c0001t0001g0114 a0001c0001t0001g0115 others(58): Show |
63 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.192+4306G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142883363 | |||||||
| chr3:142883393 | C | T | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | HG01109.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.192+4276G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142883393 | |||||||
| chr3:142883402 | T | G | 1 | a0001c0001t0002g0253 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.192+4267A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142883402 | |||||||
| chr3:142883426 | T | C | 59 | a0001c0001t0001g0005 a0001c0001t0001g0114 a0001c0001t0001g0115 others(56): Show |
61 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.192+4243A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142883426 | |||||||
| chr3:142883598 | T | C | 12 | a0001c0001t0001g0006 a0001c0001t0001g0145 a0001c0001t0001g0148 others(9): Show |
13 | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.192+4071A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142883598 | |||||||
| chr3:142883625 | G | C | 1 | a0001c0001t0001g0136 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.192+4044C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142883625 | |||||||
| chr3:142883709 | A | AC | 63 | a0001c0001t0001g0005 a0001c0001t0001g0114 a0001c0001t0001g0115 others(60): Show |
65 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.192+3959_192+3960i others(3): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142883709 | |||||||
| chr3:142883711 | A | C | 18 | a0001c0001t0001g0008 a0001c0001t0001g0171 a0001c0001t0001g0172 others(15): Show |
19 | HG00738.hp1 HG01175.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.192+3958T>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142883711 | |||||||
| chr3:142883822 | G | C | 2 | a0001c0001t0003g0060 a0001c0001t0003g0061 |
2 | HG02559.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.192+3847C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142883822 | |||||||
| chr3:142883824 | C | T | 47 | a0001c0001t0001g0153 a0001c0001t0001g0258 a0001c0001t0003g0001 others(44): Show |
50 | HG00280.hp2 HG00438.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.192+3845G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142883824 | |||||||
| chr3:142883858 | C | T | 63 | a0001c0001t0001g0005 a0001c0001t0001g0114 a0001c0001t0001g0115 others(60): Show |
65 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.192+3811G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142883858 | |||||||
| chr3:142883893 | A | G | 4 | a0001c0004t0001g0322 a0001c0004t0001g0323 a0001c0004t0002g0320 others(1): Show |
4 | HG02257.hp1 HG02922.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.192+3776T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142883893 | |||||||
| chr3:142883902 | C | T | 63 | a0001c0001t0001g0005 a0001c0001t0001g0114 a0001c0001t0001g0115 others(60): Show |
65 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.192+3767G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142883902 | |||||||
| chr3:142883911 | C | T | 2 | a0001c0001t0001g0141 a0002c0002t0002g0142 |
2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.192+3758G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142883911 | |||||||
| chr3:142883950 | G | C | 1 | a0001c0001t0001g0310 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.192+3719C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142883950 | |||||||
| chr3:142883971 | T | C | 2 | a0001c0001t0001g0141 a0002c0002t0002g0142 |
2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.192+3698A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142883971 | |||||||
| chr3:142884193 | T | C | 1 | a0001c0001t0001g0143 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.192+3476A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142884193 | |||||||
| chr3:142884210 | G | A | 1 | a0001c0001t0002g0254 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.192+3459C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142884210 | |||||||
| chr3:142884268 | G | A | 63 | a0001c0001t0001g0005 a0001c0001t0001g0114 a0001c0001t0001g0115 others(60): Show |
65 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.192+3401C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142884268 | |||||||
| chr3:142884312 | C | A | 9 | a0001c0001t0004g0085 a0001c0001t0004g0087 a0001c0001t0004g0088 others(6): Show |
9 | HG00423.hp2 HG01934.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.192+3357G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142884312 | |||||||
| chr3:142884386 | C | T | 17 | a0001c0001t0001g0006 a0001c0001t0001g0143 a0001c0001t0001g0145 others(14): Show |
18 | HG01891.hp1 HG01891.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.192+3283G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142884386 | |||||||
| chr3:142884458 | C | G | 2 | a0001c0001t0003g0021 a0001c0001t0003g0022 |
2 | NA18948.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.192+3211G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142884458 | |||||||
| chr3:142884560 | T | A | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | HG01109.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.192+3109A>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142884560 | |||||||
| chr3:142884628 | T | C | 266 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(263): Show |
282 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(279): Show |
intron_variant | MODIFIER | c.192+3041A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142884628 | |||||||
| chr3:142884858 | A | G | 1 | a0001c0001t0001g0311 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.192+2811T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142884858 | |||||||
| chr3:142884928 | T | C | 3 | a0001c0001t0001g0256 a0001c0001t0002g0255 a0001c0001t0002g0257 |
3 | HG03195.hp2 HG03209.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.192+2741A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142884928 | |||||||
| chr3:142884950 | G | A | 1 | a0003c0003t0001g0135 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.192+2719C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142884950 | |||||||
| chr3:142885019 | T | A | 47 | a0001c0001t0001g0153 a0001c0001t0001g0258 a0001c0001t0003g0001 others(44): Show |
50 | HG00280.hp2 HG00438.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.192+2650A>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142885019 | |||||||
| chr3:142885021 | TA | T | 47 | a0001c0001t0001g0153 a0001c0001t0001g0258 a0001c0001t0003g0001 others(44): Show |
50 | HG00280.hp2 HG00438.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.192+2647delT | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142885021 | |||||||
| chr3:142885023 | A | T | 47 | a0001c0001t0001g0153 a0001c0001t0001g0258 a0001c0001t0003g0001 others(44): Show |
50 | HG00280.hp2 HG00438.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.192+2646T>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142885023 | |||||||
| chr3:142885062 | T | A | 4 | a0001c0004t0001g0322 a0001c0004t0001g0323 a0001c0004t0002g0320 others(1): Show |
4 | HG02257.hp1 HG02922.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.192+2607A>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142885062 | |||||||
| chr3:142885073 | A | G | 128 | a0001c0001t0001g0005 a0001c0001t0001g0104 a0001c0001t0001g0105 others(125): Show |
133 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.192+2596T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142885073 | |||||||
| chr3:142885086 | G | A | 1 | a0001c0001t0001g0136 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.192+2583C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142885086 | |||||||
| chr3:142885156 | A | G | 3 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0002g0270 |
3 | NA18982.hp1 NA19081.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.192+2513T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142885156 | |||||||
| chr3:142885185 | G | C | 269 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(266): Show |
285 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.192+2484C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142885185 | |||||||
| chr3:142885295 | A | G | 115 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0010 others(112): Show |
125 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(122): Show |
intron_variant | MODIFIER | c.192+2374T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142885295 | |||||||
| chr3:142885634 | G | A | 206 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(203): Show |
220 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.192+2035C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142885634 | |||||||
| chr3:142885684 | T | A | 3 | a0001c0001t0003g0059 a0001c0001t0003g0060 a0001c0001t0003g0061 |
3 | HG02559.hp1 HG03516.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.192+1985A>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142885684 | |||||||
| chr3:142885745 | A | G | 254 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(251): Show |
269 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.192+1924T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142885745 | |||||||
| chr3:142885965 | C | A | 4 | a0001c0004t0001g0322 a0001c0004t0001g0323 a0001c0004t0002g0320 others(1): Show |
4 | HG02257.hp1 HG02922.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.192+1704G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142885965 | |||||||
| chr3:142886005 | A | T | 1 | a0001c0001t0001g0168 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.192+1664T>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142886005 | |||||||
| chr3:142886054 | C | T | 42 | a0001c0001t0004g0065 a0001c0001t0004g0068 a0001c0001t0004g0069 others(39): Show |
43 | HG00423.hp2 HG00544.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.192+1615G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142886054 | |||||||
| chr3:142886145 | T | C | 1 | a0001c0001t0002g0312 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.192+1524A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142886145 | |||||||
| chr3:142886220 | G | T | 1 | a0001c0001t0002g0167 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.192+1449C>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142886220 | |||||||
| chr3:142886304 | T | C | 48 | a0001c0001t0001g0153 a0001c0001t0003g0001 a0001c0001t0003g0003 others(45): Show |
51 | HG00280.hp2 HG00438.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.192+1365A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142886304 | |||||||
| chr3:142886365 | T | C | 2 | a0001c0001t0001g0016 a0003c0003t0001g0259 |
3 | HG01099.hp2 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.192+1304A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142886365 | |||||||
| chr3:142886375 | T | TAAAACAC others(305): Show |
1 | a0001c0001t0001g0143 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.192+1293_192+1294i others(314): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142886375 | |||||||
| chr3:142886375 | T | TAAAACAC others(311): Show |
1 | a0001c0001t0001g0137 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.192+1293_192+1294i others(320): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142886375 | |||||||
| chr3:142886375 | T | TAAAACAC others(312): Show |
1 | a0001c0001t0001g0138 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.192+1293_192+1294i others(321): Show |
PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142886375 | |||||||
| chr3:142886391 | C | T | 255 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(252): Show |
270 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.192+1278G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142886391 | |||||||
| chr3:142886478 | C | A | 1 | a0001c0001t0001g0267 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.192+1191G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142886478 | |||||||
| chr3:142886548 | C | T | 42 | a0001c0001t0004g0065 a0001c0001t0004g0068 a0001c0001t0004g0069 others(39): Show |
43 | HG00423.hp2 HG00544.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.192+1121G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142886548 | |||||||
| chr3:142886593 | A | G | 1 | a0001c0001t0003g0020 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.192+1076T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142886593 | |||||||
| chr3:142886607 | A | T | 2 | a0001c0001t0001g0114 a0001c0001t0001g0115 |
2 | HG00741.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.192+1062T>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142886607 | |||||||
| chr3:142886714 | G | A | 48 | a0001c0001t0001g0153 a0001c0001t0003g0001 a0001c0001t0003g0003 others(45): Show |
51 | HG00280.hp2 HG00438.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.192+955C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142886714 | |||||||
| chr3:142886716 | T | C | 1 | a0001c0001t0001g0136 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.192+953A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142886716 | |||||||
| chr3:142886938 | C | T | 270 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(267): Show |
286 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(283): Show |
intron_variant | MODIFIER | c.192+731G>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142886938 | |||||||
| chr3:142886996 | T | C | 5 | a0001c0001t0001g0019 a0001c0001t0001g0313 a0001c0001t0001g0314 others(2): Show |
6 | HG00639.hp2 HG01081.hp1 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.192+673A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142886996 | |||||||
| chr3:142887156 | A | AC | 116 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0010 others(113): Show |
126 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(123): Show |
intron_variant | MODIFIER | c.192+512dupG | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142887156 | |||||||
| chr3:142887220 | G | A | 2 | a0001c0001t0005g0062 a0003c0003t0003g0063 |
2 | NA20752.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.192+449C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142887220 | |||||||
| chr3:142887228 | T | A | 2 | a0001c0001t0001g0154 a0001c0001t0002g0155 |
2 | HG01891.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.192+441A>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142887228 | |||||||
| chr3:142887319 | C | A | 8 | a0001c0001t0004g0094 a0001c0001t0004g0095 a0001c0001t0004g0096 others(5): Show |
8 | HG00544.hp2 HG00673.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.192+350G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142887319 | |||||||
| chr3:142887489 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.192+180C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142887489 | |||||||
| chr3:142887574 | C | G | 2 | a0001c0001t0002g0140 a0002c0002t0007g0139 |
2 | HG03130.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.192+95G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142887574 | |||||||
| chr3:142887643 | A | G | 2 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
2 | HG01109.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.192+26T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142887643 | |||||||
| chr3:142887651 | T | C | 2 | a0001c0001t0001g0318 a0001c0001t0001g0319 |
2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.192+18A>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 2/8 | chr3 | 142887651 | |||||||
| chr3:142887865 | T | G | 1 | a0001c0001t0002g0156 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.84-88A>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 1/8 | chr3 | 142887865 | |||||||
| chr3:142888071 | A | T | 11 | a0001c0001t0001g0007 a0001c0001t0001g0157 a0001c0001t0001g0158 others(8): Show |
12 | HG00673.hp2 HG02602.hp1 NA18942.hp2 others(9): Show |
intron_variant | MODIFIER | c.84-294T>A | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 1/8 | chr3 | 142888071 | |||||||
| chr3:142888100 | G | C | 117 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0010 others(114): Show |
127 | HG00099.hp2 HG00597.hp2 HG00673.hp2 others(124): Show |
intron_variant | MODIFIER | c.84-323C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 1/8 | chr3 | 142888100 | |||||||
| chr3:142888425 | G | C | 1 | a0001c0001t0002g0262 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.83+389C>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 1/8 | chr3 | 142888425 | |||||||
| chr3:142888430 | A | G | 26 | a0001c0001t0001g0005 a0001c0001t0001g0114 a0001c0001t0001g0115 others(23): Show |
27 | HG00323.hp1 HG00423.hp1 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.83+384T>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 1/8 | chr3 | 142888430 | |||||||
| chr3:142888454 | A | C | 12 | a0001c0001t0001g0104 a0001c0001t0001g0105 a0001c0001t0001g0108 others(9): Show |
12 | HG00597.hp1 HG02083.hp2 HG02129.hp1 others(9): Show |
intron_variant | MODIFIER | c.83+360T>G | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 1/8 | chr3 | 142888454 | |||||||
| chr3:142888515 | C | A | 1 | a0001c0001t0002g0317 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.83+299G>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 1/8 | chr3 | 142888515 | |||||||
| chr3:142888645 | C | G | 265 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(262): Show |
281 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(278): Show |
intron_variant | MODIFIER | c.83+169G>C | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 1/8 | chr3 | 142888645 | |||||||
| chr3:142888646 | G | A | 2 | a0001c0001t0001g0318 a0001c0001t0001g0319 |
2 | HG02258.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.83+168C>T | PCOLCE2 | ENSG00000163710.9 | transcript | ENST00000295992.8 | protein_coding | 1/8 | chr3 | 142888646 |