Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 348801 |
| ensemblid | ENSG00000206535.8 |
| hgncid | 28014 |
| symbol | LNP1 |
| name | leukemia NUP98 fusion partner 1 |
| refseq_nuc | NM_001085451.2 |
| refseq_prot | NP_001078920.1 |
| ensembl_nuc | ENST00000383693.8 |
| ensembl_prot | ENSP00000373191.3 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 100401539 |
| end | 100456319 |
| strand | + |
| ver | v1.2 |
| region | chr3:100401539-100456319 |
| region5000 | chr3:100396539-100461319 |
| regionname0 | LNP1_chr3_100401539_100456319 |
| regionname5000 | LNP1_chr3_100396539_100461319 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 197 | 207 | 45 | 24 | 113 | 6 | 18 | 91 | LNP1_chr3_100396539_100461319 | LNP1 | MEHKD others(192): Show |
chr3 | 100396539 | 100461319 |
| a0002 | 1/0 | 178 | 191 | 45 | 48 | 67 | 6 | 24 | 49 | LNP1_chr3_100396539_100461319 | LNP1 | MEHKD others(173): Show |
chr3 | 100396539 | 100461319 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 591 | 206 | 44 | 24 | 113 | 6 | 18 | LNP1_chr3_100396539_100461319 | LNP1 | ATGGA others(586): Show |
chr3 | 100396539 | 100461319 | ||
| a0001c0004 | 0/0 | 591 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | ATGGA others(586): Show |
chr3 | 100396539 | 100461319 | ||
| a0002c0002 | 1/0 | 534 | 190 | 44 | 48 | 67 | 6 | 24 | LNP1_chr3_100396539_100461319 | LNP1 | ATGGA others(529): Show |
chr3 | 100396539 | 100461319 | ||
| a0002c0003 | 0/0 | 534 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | ATGGA others(529): Show |
chr3 | 100396539 | 100461319 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 1921 | 128 | 37 | 13 | 73 | 0 | 5 | LNP1_chr3_100396539_100461319 | LNP1 | AGTTT others(1916): Show |
chr3 | 100396539 | 100461319 |
| a0001c0001t0002 | 0/1 | 1921 | 63 | 0 | 9 | 36 | 6 | 11 | LNP1_chr3_100396539_100461319 | LNP1 | AGTTT others(1916): Show |
chr3 | 100396539 | 100461319 |
| a0001c0001t0003 | 0/0 | 1921 | 3 | 0 | 1 | 0 | 0 | 2 | LNP1_chr3_100396539_100461319 | LNP1 | AGTTT others(1916): Show |
chr3 | 100396539 | 100461319 |
| a0001c0001t0005 | 0/0 | 1921 | 7 | 7 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | AGTTT others(1916): Show |
chr3 | 100396539 | 100461319 |
| a0001c0001t0006 | 0/0 | 1921 | 4 | 0 | 0 | 4 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | AGTTT others(1916): Show |
chr3 | 100396539 | 100461319 |
| a0001c0001t0007 | 0/0 | 1921 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | AGTTT others(1916): Show |
chr3 | 100396539 | 100461319 |
| a0001c0004t0004 | 0/0 | 1921 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | AGTTT others(1916): Show |
chr3 | 100396539 | 100461319 |
| a0002c0002t0001 | 0/0 | 1864 | 104 | 23 | 22 | 47 | 1 | 11 | LNP1_chr3_100396539_100461319 | LNP1 | AGTTT others(1859): Show |
chr3 | 100396539 | 100461319 |
| a0002c0002t0002 | 0/0 | 1864 | 5 | 0 | 4 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | AGTTT others(1859): Show |
chr3 | 100396539 | 100461319 |
| a0002c0002t0003 | 1/0 | 1864 | 64 | 7 | 21 | 18 | 5 | 12 | LNP1_chr3_100396539_100461319 | LNP1 | AGTTT others(1859): Show |
chr3 | 100396539 | 100461319 |
| a0002c0002t0004 | 0/0 | 1864 | 11 | 10 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | AGTTT others(1859): Show |
chr3 | 100396539 | 100461319 |
| a0002c0002t0006 | 0/0 | 1864 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | AGTTT others(1859): Show |
chr3 | 100396539 | 100461319 |
| a0002c0002t0008 | 0/0 | 1864 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | AGTTT others(1859): Show |
chr3 | 100396539 | 100461319 |
| a0002c0002t0009 | 0/0 | 1864 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | AGTTT others(1859): Show |
chr3 | 100396539 | 100461319 |
| a0002c0002t0011 | 0/0 | 1864 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | AGTTT others(1859): Show |
chr3 | 100396539 | 100461319 |
| a0002c0002t0012 | 0/0 | 1864 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | AGTTT others(1859): Show |
chr3 | 100396539 | 100461319 |
| a0002c0002t0013 | 0/0 | 1864 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | AGTTT others(1859): Show |
chr3 | 100396539 | 100461319 |
| a0002c0003t0010 | 0/0 | 1864 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | AGTTT others(1859): Show |
chr3 | 100396539 | 100461319 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0001g0361 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0311 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0334 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0337 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0002g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0005g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0005g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0005g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0005g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0005g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0005g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0005g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0006g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0006g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0006g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0001t0007g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0001c0004t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0002g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0002g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0002g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0002g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0001 | 0/0 | 6 | 2 | 1 | 3 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0003 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0112 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0003g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0004g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0004g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0004g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0004g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0004g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0004g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0006g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0008g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0009g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0011g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0012g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0002t0013g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| a0002c0003t0010g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0299 | EUR | GBR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0326 | EUR | GBR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG00140 | hp1 | a0002 | c0002 | t0003 | g0082 | EUR | GBR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0334 | EUR | GBR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG00323 | hp1 | a0002 | c0002 | t0003 | g0089 | EUR | FIN | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG00323 | hp2 | a0002 | c0002 | t0001 | g0169 | EUR | FIN | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG00423 | hp1 | a0002 | c0002 | t0001 | g0250 | EAS | CHS | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0011 | EAS | CHS | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | CHS | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0347 | EAS | CHS | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0158 | EAS | CHS | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG00558 | hp1 | a0002 | c0002 | t0001 | g0049 | EAS | CHS | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | CHS | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG00609 | hp1 | a0002 | c0002 | t0001 | g0048 | EAS | CHS | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | CHS | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG00639 | hp1 | a0002 | c0002 | t0003 | g0099 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG00639 | hp2 | a0002 | c0002 | t0001 | g0179 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0018 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG00673 | hp2 | a0001 | c0001 | t0006 | g0016 | EAS | CHS | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0017 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG00735 | hp2 | a0002 | c0002 | t0002 | g0352 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0160 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0345 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0164 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0303 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0162 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01069 | hp2 | a0002 | c0002 | t0001 | g0287 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0157 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01070 | hp2 | a0002 | c0002 | t0003 | g0110 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0163 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01071 | hp2 | a0002 | c0002 | t0003 | g0003 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0100 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01074 | hp2 | a0001 | c0001 | t0007 | g0333 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01081 | hp1 | a0002 | c0002 | t0003 | g0121 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0297 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01099 | hp1 | a0002 | c0002 | t0004 | g0139 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01099 | hp2 | a0002 | c0002 | t0003 | g0105 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0037 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0313 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01167 | hp1 | a0002 | c0002 | t0003 | g0111 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0265 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0314 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01168 | hp2 | a0002 | c0002 | t0001 | g0171 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01169 | hp1 | a0002 | c0002 | t0001 | g0172 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01169 | hp2 | a0002 | c0002 | t0003 | g0003 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0177 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01175 | hp2 | a0002 | c0002 | t0003 | g0136 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01192 | hp1 | a0002 | c0002 | t0003 | g0093 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0319 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01243 | hp1 | a0002 | c0002 | t0001 | g0176 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0357 | AMR | PUR | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | CLM | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01255 | hp2 | a0002 | c0002 | t0003 | g0092 | AMR | CLM | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01257 | hp1 | a0002 | c0002 | t0003 | g0003 | AMR | CLM | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0151 | AMR | CLM | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01258 | hp1 | a0002 | c0002 | t0002 | g0294 | AMR | CLM | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0150 | AMR | CLM | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | CLM | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | CLM | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01358 | hp2 | a0002 | c0002 | t0003 | g0001 | AMR | CLM | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01361 | hp1 | a0002 | c0002 | t0003 | g0362 | AMR | CLM | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01361 | hp2 | a0002 | c0002 | t0002 | g0292 | AMR | CLM | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0155 | AMR | CLM | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | CLM | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01516 | hp1 | a0002 | c0002 | t0003 | g0116 | EUR | IBS | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0318 | EUR | IBS | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01928 | hp1 | a0002 | c0002 | t0003 | g0088 | AMR | PEL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01928 | hp2 | a0002 | c0002 | t0001 | g0053 | AMR | PEL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01934 | hp1 | a0002 | c0002 | t0003 | g0114 | AMR | PEL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01934 | hp2 | a0002 | c0002 | t0003 | g0090 | AMR | PEL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0361 | AMR | PEL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01943 | hp2 | a0002 | c0002 | t0003 | g0122 | AMR | PEL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PEL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01975 | hp1 | a0002 | c0002 | t0001 | g0233 | AMR | PEL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01975 | hp2 | a0002 | c0002 | t0003 | g0094 | AMR | PEL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01978 | hp1 | a0002 | c0002 | t0003 | g0118 | AMR | PEL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | PEL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0311 | AMR | PEL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01981 | hp2 | a0002 | c0002 | t0002 | g0330 | AMR | PEL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0050 | AMR | PEL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01993 | hp2 | a0002 | c0002 | t0003 | g0115 | AMR | PEL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0320 | AMR | PEL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02004 | hp2 | a0002 | c0002 | t0001 | g0270 | AMR | PEL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02015 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | KHV | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | KHV | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0237 | EAS | KHV | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0240 | EAS | KHV | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0349 | EAS | KHV | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0325 | EAS | KHV | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0278 | EAS | KHV | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02129 | hp1 | a0002 | c0002 | t0003 | g0108 | EAS | KHV | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0245 | EAS | KHV | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0026 | EAS | KHV | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02135 | hp2 | a0002 | c0002 | t0001 | g0174 | EAS | KHV | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02145 | hp1 | a0002 | c0002 | t0004 | g0076 | AFR | ACB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02145 | hp2 | a0002 | c0002 | t0001 | g0175 | AFR | ACB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02155 | hp1 | a0001 | c0001 | t0002 | g0322 | EAS | CDX | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02155 | hp2 | a0002 | c0002 | t0003 | g0124 | EAS | CDX | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02165 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | CDX | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02165 | hp2 | a0002 | c0002 | t0003 | g0106 | EAS | CDX | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02257 | hp2 | a0002 | c0002 | t0003 | g0135 | AFR | ACB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02258 | hp1 | a0002 | c0002 | t0003 | g0001 | AFR | ACB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0196 | AFR | ACB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02280 | hp1 | a0002 | c0002 | t0004 | g0140 | AFR | ACB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | ACB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PEL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02300 | hp2 | a0002 | c0002 | t0001 | g0189 | AMR | PEL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02523 | hp2 | a0002 | c0002 | t0001 | g0055 | EAS | KHV | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02602 | hp2 | a0002 | c0002 | t0001 | g0194 | SAS | PJL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02615 | hp1 | a0001 | c0004 | t0004 | g0193 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02615 | hp2 | a0002 | c0002 | t0008 | g0156 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02622 | hp2 | a0002 | c0002 | t0001 | g0280 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02630 | hp1 | a0002 | c0002 | t0003 | g0003 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0243 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02647 | hp2 | a0002 | c0002 | t0001 | g0264 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0310 | SAS | PJL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02683 | hp2 | a0002 | c0002 | t0003 | g0117 | SAS | PJL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02717 | hp1 | a0002 | c0002 | t0001 | g0259 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02717 | hp2 | a0002 | c0002 | t0004 | g0182 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02735 | hp1 | a0002 | c0002 | t0003 | g0101 | SAS | PJL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0023 | SAS | PJL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0302 | SAS | PJL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02738 | hp2 | a0002 | c0002 | t0003 | g0097 | SAS | PJL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0185 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02809 | hp2 | a0002 | c0002 | t0003 | g0001 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0241 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02886 | hp1 | a0002 | c0002 | t0001 | g0248 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0272 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02895 | hp2 | a0001 | c0001 | t0005 | g0286 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0356 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02897 | hp2 | a0001 | c0001 | t0005 | g0072 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0062 | AFR | ESN | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02965 | hp1 | a0002 | c0002 | t0001 | g0242 | AFR | ESN | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02965 | hp2 | a0002 | c0002 | t0004 | g0154 | AFR | ESN | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02970 | hp2 | a0002 | c0002 | t0003 | g0095 | AFR | ESN | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0263 | AFR | ESN | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0284 | AFR | ESN | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG03041 | hp1 | a0002 | c0002 | t0004 | g0075 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0187 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0358 | AFR | MSL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG03098 | hp2 | a0002 | c0002 | t0001 | g0148 | AFR | MSL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG03130 | hp1 | a0002 | c0002 | t0004 | g0166 | AFR | ESN | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0355 | AFR | ESN | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG03195 | hp1 | a0001 | c0001 | t0005 | g0281 | AFR | ESN | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG03195 | hp2 | a0002 | c0002 | t0009 | g0045 | AFR | ESN | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0285 | AFR | MSL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | MSL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | MSL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG03225 | hp2 | a0002 | c0002 | t0004 | g0074 | AFR | MSL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG03239 | hp1 | a0002 | c0002 | t0003 | g0107 | SAS | PJL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0293 | SAS | PJL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG03486 | hp1 | a0002 | c0002 | t0001 | g0260 | AFR | MSL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG03486 | hp2 | a0002 | c0003 | t0010 | g0195 | AFR | MSL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG03490 | hp1 | a0001 | c0001 | t0002 | g0315 | SAS | PJL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG03490 | hp2 | a0002 | c0002 | t0003 | g0125 | SAS | PJL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0331 | SAS | PJL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG03491 | hp2 | a0002 | c0002 | t0003 | g0129 | SAS | PJL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG03516 | hp1 | a0002 | c0002 | t0001 | g0236 | AFR | ESN | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0279 | AFR | GWD | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG03579 | hp1 | a0002 | c0002 | t0012 | g0291 | AFR | MSL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG03654 | hp1 | a0002 | c0002 | t0003 | g0126 | SAS | PJL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0047 | SAS | PJL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG03669 | hp1 | a0002 | c0002 | t0001 | g0161 | SAS | PJL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | STU | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG03688 | hp2 | a0002 | c0002 | t0003 | g0087 | SAS | STU | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG03704 | hp1 | a0002 | c0002 | t0001 | g0249 | SAS | PJL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0336 | SAS | PJL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG03831 | hp1 | a0002 | c0002 | t0003 | g0103 | SAS | BEB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG03831 | hp2 | a0002 | c0002 | t0002 | g0332 | SAS | BEB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG03834 | hp1 | a0002 | c0002 | t0001 | g0165 | SAS | BEB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG03834 | hp2 | a0002 | c0002 | t0001 | g0251 | SAS | BEB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG03927 | hp1 | a0001 | c0001 | t0003 | g0133 | SAS | BEB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | BEB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG03942 | hp1 | a0002 | c0002 | t0001 | g0232 | SAS | BEB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG03942 | hp2 | a0002 | c0002 | t0001 | g0152 | SAS | BEB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0134 | SAS | STU | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | STU | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0359 | SAS | BEB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG04184 | hp2 | a0002 | c0002 | t0001 | g0167 | SAS | BEB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0170 | SAS | STU | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0312 | SAS | STU | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG04204 | hp1 | a0002 | c0002 | t0003 | g0091 | SAS | STU | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0309 | SAS | STU | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0296 | SAS | STU | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG04228 | hp2 | a0002 | c0002 | t0003 | g0128 | SAS | STU | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18522 | hp1 | a0001 | c0001 | t0005 | g0283 | AFR | YRI | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18522 | hp2 | a0002 | c0002 | t0001 | g0017 | AFR | YRI | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | CHB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | CHB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | YRI | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18943 | hp1 | a0002 | c0002 | t0003 | g0119 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18943 | hp2 | a0002 | c0002 | t0001 | g0059 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18945 | hp2 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18946 | hp1 | a0001 | c0001 | t0002 | g0327 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18947 | hp1 | a0002 | c0002 | t0003 | g0083 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18949 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0350 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0346 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0342 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18953 | hp1 | a0002 | c0002 | t0001 | g0173 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18954 | hp2 | a0002 | c0002 | t0001 | g0277 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18956 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18957 | hp1 | a0002 | c0002 | t0001 | g0044 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18960 | hp2 | a0002 | c0002 | t0003 | g0104 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18961 | hp1 | a0002 | c0002 | t0003 | g0113 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18961 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0304 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18962 | hp2 | a0002 | c0002 | t0003 | g0084 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18964 | hp1 | a0002 | c0002 | t0003 | g0123 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0329 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18966 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0323 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18969 | hp1 | a0002 | c0002 | t0003 | g0131 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0324 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18973 | hp1 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18974 | hp1 | a0002 | c0002 | t0001 | g0178 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18977 | hp1 | a0002 | c0002 | t0001 | g0054 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18977 | hp2 | a0002 | c0002 | t0003 | g0120 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0340 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18978 | hp2 | a0001 | c0001 | t0006 | g0223 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0338 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18981 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18983 | hp2 | a0002 | c0002 | t0001 | g0052 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0335 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18986 | hp2 | a0002 | c0002 | t0001 | g0184 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18989 | hp1 | a0002 | c0002 | t0001 | g0043 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18990 | hp1 | a0002 | c0002 | t0003 | g0130 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18998 | hp2 | a0002 | c0002 | t0013 | g0096 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0343 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18999 | hp2 | a0002 | c0002 | t0001 | g0042 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19000 | hp1 | a0002 | c0002 | t0003 | g0085 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19002 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19003 | hp2 | a0002 | c0002 | t0001 | g0239 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0363 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0328 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19010 | hp1 | a0002 | c0002 | t0001 | g0180 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0360 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0348 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | LWK | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19030 | hp2 | a0002 | c0002 | t0004 | g0183 | AFR | LWK | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | LWK | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19043 | hp2 | a0002 | c0002 | t0011 | g0138 | AFR | LWK | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19057 | hp2 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0307 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19060 | hp2 | a0001 | c0001 | t0006 | g0222 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19065 | hp2 | a0002 | c0002 | t0001 | g0246 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0353 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19067 | hp1 | a0002 | c0002 | t0003 | g0001 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19072 | hp1 | a0002 | c0002 | t0001 | g0153 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0351 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19075 | hp2 | a0002 | c0002 | t0001 | g0034 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19077 | hp1 | a0002 | c0002 | t0003 | g0109 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0339 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19078 | hp2 | a0002 | c0002 | t0006 | g0224 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0341 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19084 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19084 | hp2 | a0002 | c0002 | t0001 | g0181 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19085 | hp2 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19086 | hp1 | a0002 | c0002 | t0003 | g0098 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19087 | hp2 | a0002 | c0002 | t0001 | g0168 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19240 | hp1 | a0002 | c0002 | t0004 | g0027 | AFR | YRI | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | YRI | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA20129 | hp1 | a0002 | c0002 | t0003 | g0137 | AFR | ASW | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0244 | AFR | ASW | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA20752 | hp1 | a0001 | c0001 | t0002 | g0316 | EUR | TSI | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA20752 | hp2 | a0002 | c0002 | t0003 | g0086 | EUR | TSI | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA20805 | hp1 | a0002 | c0002 | t0003 | g0132 | EUR | TSI | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0300 | EUR | TSI | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0344 | SAS | GIH | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA20905 | hp2 | a0002 | c0002 | t0003 | g0081 | SAS | GIH | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01123 | hp1 | a0002 | c0002 | t0003 | g0127 | AMR | CLM | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0321 | AMR | CLM | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02109 | hp1 | a0002 | c0002 | t0001 | g0262 | AFR | ACB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ACB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02559 | hp1 | a0001 | c0001 | t0005 | g0282 | AFR | ACB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG03471 | hp1 | a0002 | c0002 | t0001 | g0186 | AFR | MSL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG03471 | hp2 | a0002 | c0002 | t0004 | g0077 | AFR | MSL | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0354 | AFR | USA | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| HG06807 | hp2 | a0002 | c0002 | t0003 | g0102 | AFR | USA | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18955 | hp1 | a0001 | c0001 | t0006 | g0016 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | USA | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| NA20300 | hp2 | a0002 | c0002 | t0001 | g0261 | AFR | USA | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0337 | REF | REF | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0003 | g0112 | REF | REF | LNP1_chr3_100396539_100461319 | LNP1 | chr3 | 100396539 | 100461319 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:100451756 | A | ATCCTAGA others(50): Show |
1 | a0001 | 206 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(203): Show |
disruptive_inframe_insertion | MODERATE | c.221_222insGGAATTCC others(49): Show |
p.Gln74_Glu75insGluP others(53): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/4 | 1156/1864 | 222/537 | 74/178 | INFO_REALIGN_3_PRIME | chr3 | 100451756 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:100455788 | C | T | 1 | a0002c0003 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.399C>T | p.Ser133Ser | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 4/4 | 1333/1864 | 399/537 | 133/178 | chr3 | 100455788 | |||
| chr3:100455878 | G | A | 1 | a0001c0001 | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(202): Show |
synonymous_variant | LOW | c.489G>A | p.Glu163Glu | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 4/4 | 1423/1864 | 489/537 | 163/178 | chr3 | 100455878 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:100401637 | C | T | 2 | a0001c0001t0006 a0002c0002t0006 |
5 | HG00673.hp2 NA18955.hp1 NA18978.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-836C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/4 | 28093 | chr3 | 100401637 | ||||||
| chr3:100401879 | G | A | 2 | a0001c0001t0007 a0002c0002t0008 |
2 | HG01074.hp2 HG02615.hp2 |
5_prime_UTR_variant | MODIFIER | c.-594G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/4 | 27851 | chr3 | 100401879 | ||||||
| chr3:100402006 | G | A | 14 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(11): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(325): Show |
5_prime_UTR_variant | MODIFIER | c.-467G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/4 | 27724 | chr3 | 100402006 | ||||||
| chr3:100402073 | A | G | 1 | a0002c0002t0013 | 1 | NA18998.hp2 | 5_prime_UTR_variant | MODIFIER | c.-400A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/4 | 27657 | chr3 | 100402073 | ||||||
| chr3:100402103 | A | G | 1 | a0001c0001t0005 | 7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-370A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/4 | chr3 | 100402103 | |||||||
| chr3:100402182 | G | A | 1 | a0002c0002t0009 | 1 | HG03195.hp2 | 5_prime_UTR_variant | MODIFIER | c.-291G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/4 | 27548 | chr3 | 100402182 | ||||||
| chr3:100402277 | G | A | 15 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(12): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(326): Show |
5_prime_UTR_variant | MODIFIER | c.-196G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/4 | 27453 | chr3 | 100402277 | ||||||
| chr3:100402296 | T | C | 3 | a0001c0001t0002 a0001c0001t0007 a0002c0002t0002 |
68 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(65): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-177T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/4 | chr3 | 100402296 | |||||||
| chr3:100402352 | T | C | 1 | a0002c0003t0010 | 1 | HG03486.hp2 | 5_prime_UTR_variant | MODIFIER | c.-121T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/4 | 27378 | chr3 | 100402352 | ||||||
| chr3:100456042 | A | G | 3 | a0001c0004t0004 a0002c0002t0004 a0002c0002t0008 |
13 | HG01099.hp1 HG02145.hp1 HG02280.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*116A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 4/4 | 116 | chr3 | 100456042 | ||||||
| chr3:100456115 | C | G | 1 | a0002c0002t0011 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*189C>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 4/4 | 189 | chr3 | 100456115 | ||||||
| chr3:100456206 | A | G | 1 | a0001c0001t0005 | 7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*280A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 4/4 | 280 | chr3 | 100456206 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:100402479 | T | A | 1 | a0002c0002t0001g0023 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-34+40T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100402479 | |||||||
| chr3:100402643 | AT | A | 62 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(59): Show |
75 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.-34+217delT | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100402643 | ||||||
| chr3:100402786 | A | C | 1 | a0001c0001t0002g0363 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-34+347A>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100402786 | |||||||
| chr3:100402789 | C | A | 1 | a0001c0001t0002g0363 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-34+350C>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100402789 | |||||||
| chr3:100402792 | T | A | 1 | a0001c0001t0002g0363 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-34+353T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100402792 | |||||||
| chr3:100402793 | T | A | 1 | a0001c0001t0002g0363 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-34+354T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100402793 | |||||||
| chr3:100403061 | A | G | 1 | a0002c0002t0003g0362 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-34+622A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100403061 | |||||||
| chr3:100403066 | C | T | 1 | a0001c0001t0001g0361 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-34+627C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100403066 | |||||||
| chr3:100403165 | C | T | 1 | a0001c0001t0001g0360 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-34+726C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100403165 | |||||||
| chr3:100403220 | T | C | 3 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 |
3 | NA18990.hp2 NA19058.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.-34+781T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100403220 | |||||||
| chr3:100403237 | C | T | 302 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(299): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(326): Show |
intron_variant | MODIFIER | c.-34+798C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100403237 | |||||||
| chr3:100403324 | G | A | 1 | a0002c0002t0011g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-34+885G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100403324 | |||||||
| chr3:100403412 | T | C | 1 | a0002c0002t0003g0081 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-34+973T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100403412 | |||||||
| chr3:100403995 | T | A | 2 | a0002c0002t0004g0139 a0002c0002t0004g0140 |
2 | HG01099.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.-34+1556T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100403995 | |||||||
| chr3:100404016 | T | C | 7 | a0001c0001t0001g0013 a0001c0001t0001g0141 a0001c0001t0001g0142 others(4): Show |
8 | HG02109.hp2 HG02280.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-34+1577T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100404016 | |||||||
| chr3:100404106 | C | T | 1 | a0001c0001t0002g0359 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-34+1667C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100404106 | |||||||
| chr3:100404489 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-34+2050T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100404489 | |||||||
| chr3:100404501 | C | T | 5 | a0001c0001t0001g0073 a0002c0002t0004g0074 a0002c0002t0004g0075 others(2): Show |
5 | HG02145.hp1 HG02486.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-34+2062C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100404501 | |||||||
| chr3:100404630 | G | A | 225 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(222): Show |
250 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(247): Show |
intron_variant | MODIFIER | c.-34+2191G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100404630 | |||||||
| chr3:100404747 | A | G | 1 | a0002c0002t0001g0287 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-34+2308A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100404747 | |||||||
| chr3:100404751 | C | T | 1 | a0002c0002t0003g0137 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-34+2312C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100404751 | |||||||
| chr3:100404790 | C | CG | 6 | a0001c0001t0005g0072 a0001c0001t0005g0281 a0001c0001t0005g0282 others(3): Show |
6 | HG02559.hp1 HG02897.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34+2351_-34+2352i others(3): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100404790 | |||||||
| chr3:100404791 | C | CT | 117 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(114): Show |
132 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(129): Show |
intron_variant | MODIFIER | c.-34+2369dupT | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100404791 | ||||||
| chr3:100404791 | C | CTT | 57 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(54): Show |
64 | HG00558.hp2 HG00597.hp1 HG00642.hp1 others(61): Show |
intron_variant | MODIFIER | c.-34+2368_-34+2369d others(4): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100404791 | ||||||
| chr3:100404791 | C | CTTT | 56 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0070 others(53): Show |
60 | HG00423.hp1 HG00438.hp1 HG00609.hp2 others(57): Show |
intron_variant | MODIFIER | c.-34+2367_-34+2369d others(5): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100404791 | ||||||
| chr3:100404791 | C | T | 7 | a0001c0001t0005g0072 a0001c0001t0005g0281 a0001c0001t0005g0282 others(4): Show |
7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-34+2352C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100404791 | |||||||
| chr3:100404896 | G | A | 2 | a0002c0002t0001g0150 a0002c0002t0001g0151 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-34+2457G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100404896 | |||||||
| chr3:100405029 | T | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-34+2590T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100405029 | |||||||
| chr3:100405249 | A | G | 7 | a0001c0001t0001g0013 a0001c0001t0001g0141 a0001c0001t0001g0142 others(4): Show |
8 | HG02109.hp2 HG02280.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-34+2810A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100405249 | |||||||
| chr3:100405268 | A | C | 108 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(105): Show |
119 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.-34+2829A>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100405268 | |||||||
| chr3:100405289 | C | A | 1 | a0001c0001t0001g0073 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-34+2850C>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100405289 | |||||||
| chr3:100405329 | T | C | 2 | a0001c0001t0001g0192 a0001c0004t0004g0193 |
2 | HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-34+2890T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100405329 | |||||||
| chr3:100405451 | C | T | 1 | a0002c0002t0001g0189 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-34+3012C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100405451 | |||||||
| chr3:100405534 | A | C | 225 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(222): Show |
250 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(247): Show |
intron_variant | MODIFIER | c.-34+3095A>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100405534 | |||||||
| chr3:100405654 | A | G | 1 | a0001c0001t0002g0350 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-34+3215A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100405654 | |||||||
| chr3:100405692 | C | G | 1 | a0002c0002t0001g0280 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-34+3253C>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100405692 | |||||||
| chr3:100405724 | C | T | 4 | a0001c0001t0002g0346 a0001c0001t0002g0347 a0001c0001t0002g0348 others(1): Show |
4 | HG00438.hp2 HG02074.hp1 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34+3285C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100405724 | |||||||
| chr3:100405803 | T | A | 1 | a0002c0002t0001g0232 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-34+3364T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100405803 | |||||||
| chr3:100405870 | A | G | 2 | a0001c0001t0003g0133 a0001c0001t0003g0134 |
2 | HG03927.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-34+3431A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100405870 | |||||||
| chr3:100406065 | C | T | 8 | a0001c0001t0001g0007 a0001c0001t0001g0225 a0001c0001t0001g0226 others(5): Show |
10 | HG00597.hp1 HG02027.hp2 HG02523.hp1 others(7): Show |
intron_variant | MODIFIER | c.-34+3626C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100406065 | |||||||
| chr3:100406201 | G | A | 4 | a0002c0002t0001g0017 a0002c0002t0001g0148 a0002c0002t0001g0233 others(1): Show |
5 | HG00735.hp1 HG01975.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-34+3762G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100406201 | |||||||
| chr3:100406217 | C | T | 2 | a0001c0001t0001g0192 a0001c0004t0004g0193 |
2 | HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-34+3778C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100406217 | |||||||
| chr3:100406243 | C | A | 2 | a0002c0002t0001g0008 a0002c0002t0001g0026 |
3 | HG02132.hp2 NA18747.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.-34+3804C>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100406243 | |||||||
| chr3:100406463 | G | T | 1 | a0001c0001t0002g0345 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-34+4024G>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100406463 | |||||||
| chr3:100406484 | A | C | 1 | a0002c0002t0001g0279 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-34+4045A>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100406484 | |||||||
| chr3:100406607 | T | A | 6 | a0001c0001t0001g0073 a0002c0002t0004g0027 a0002c0002t0004g0074 others(3): Show |
6 | HG02145.hp1 HG02486.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.-34+4168T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100406607 | |||||||
| chr3:100406637 | C | T | 1 | a0002c0002t0003g0132 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-34+4198C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100406637 | |||||||
| chr3:100406650 | T | C | 4 | a0001c0001t0001g0013 a0001c0001t0001g0141 a0001c0001t0001g0142 others(1): Show |
5 | HG02109.hp2 HG02630.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-34+4211T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100406650 | |||||||
| chr3:100406657 | C | T | 7 | a0001c0001t0005g0072 a0001c0001t0005g0281 a0001c0001t0005g0282 others(4): Show |
7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-34+4218C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100406657 | |||||||
| chr3:100406679 | T | C | 2 | a0001c0001t0001g0234 a0001c0001t0001g0235 |
2 | HG02015.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.-34+4240T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100406679 | |||||||
| chr3:100406855 | A | G | 1 | a0002c0002t0001g0278 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-34+4416A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100406855 | |||||||
| chr3:100406934 | C | T | 1 | a0001c0001t0002g0344 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-34+4495C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100406934 | |||||||
| chr3:100406982 | T | A | 2 | a0002c0002t0001g0196 a0002c0002t0001g0236 |
2 | HG02258.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-34+4543T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100406982 | |||||||
| chr3:100407171 | G | A | 6 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0029 others(3): Show |
8 | NA18945.hp1 NA18965.hp2 NA18988.hp1 others(5): Show |
intron_variant | MODIFIER | c.-34+4732G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100407171 | |||||||
| chr3:100407369 | G | C | 2 | a0001c0001t0001g0197 a0001c0001t0001g0198 |
2 | NA18988.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.-34+4930G>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100407369 | |||||||
| chr3:100407405 | A | G | 7 | a0001c0001t0005g0072 a0001c0001t0005g0281 a0001c0001t0005g0282 others(4): Show |
7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-34+4966A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100407405 | |||||||
| chr3:100407435 | A | T | 1 | a0002c0002t0001g0277 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-34+4996A>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100407435 | |||||||
| chr3:100407448 | A | G | 4 | a0001c0001t0001g0013 a0001c0001t0001g0141 a0001c0001t0001g0142 others(1): Show |
5 | HG02109.hp2 HG02630.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.-34+5009A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100407448 | |||||||
| chr3:100407477 | G | A | 39 | a0001c0001t0001g0361 a0002c0002t0001g0023 a0002c0002t0001g0150 others(36): Show |
39 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.-34+5038G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100407477 | |||||||
| chr3:100407672 | A | G | 1 | a0001c0001t0001g0032 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-34+5233A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100407672 | |||||||
| chr3:100407715 | G | C | 1 | a0001c0001t0001g0199 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-34+5276G>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100407715 | |||||||
| chr3:100408143 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-34+5704C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100408143 | |||||||
| chr3:100408239 | A | G | 1 | a0002c0002t0001g0062 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-34+5800A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100408239 | |||||||
| chr3:100408397 | C | T | 108 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(105): Show |
119 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.-34+5958C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100408397 | |||||||
| chr3:100408417 | G | A | 108 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(105): Show |
119 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.-34+5978G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100408417 | |||||||
| chr3:100408521 | G | T | 1 | a0001c0001t0001g0146 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-34+6082G>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100408521 | |||||||
| chr3:100408575 | A | T | 38 | a0001c0001t0001g0361 a0002c0002t0001g0023 a0002c0002t0001g0150 others(35): Show |
38 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.-34+6136A>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100408575 | |||||||
| chr3:100408675 | A | C | 2 | a0002c0002t0004g0139 a0002c0002t0004g0140 |
2 | HG01099.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.-34+6236A>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100408675 | |||||||
| chr3:100408696 | C | T | 9 | a0001c0001t0001g0022 a0001c0001t0001g0354 a0001c0001t0001g0355 others(6): Show |
10 | HG01099.hp1 HG01243.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.-34+6257C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100408696 | |||||||
| chr3:100408796 | C | T | 1 | a0002c0002t0003g0081 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-34+6357C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100408796 | |||||||
| chr3:100408797 | G | A | 2 | a0001c0001t0002g0288 a0001c0001t0002g0289 |
2 | NA18955.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.-34+6358G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100408797 | |||||||
| chr3:100408833 | G | A | 2 | a0001c0001t0001g0192 a0001c0004t0004g0193 |
2 | HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-34+6394G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100408833 | |||||||
| chr3:100408993 | G | A | 2 | a0002c0002t0003g0081 a0002c0002t0003g0082 |
2 | HG00140.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-34+6554G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100408993 | |||||||
| chr3:100409104 | T | C | 1 | a0001c0001t0002g0290 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-34+6665T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409104 | |||||||
| chr3:100409129 | G | A | 3 | a0002c0002t0003g0083 a0002c0002t0003g0084 a0002c0002t0003g0085 |
3 | NA18947.hp1 NA18962.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.-34+6690G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409129 | |||||||
| chr3:100409169 | G | A | 2 | a0001c0001t0001g0033 a0002c0002t0001g0034 |
2 | NA19063.hp1 NA19075.hp2 |
intron_variant | MODIFIER | c.-34+6730G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409169 | |||||||
| chr3:100409538 | C | A | 7 | a0001c0001t0005g0072 a0001c0001t0005g0281 a0001c0001t0005g0282 others(4): Show |
7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-34+7099C>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409538 | |||||||
| chr3:100409540 | C | A | 11 | a0001c0001t0001g0063 a0001c0001t0001g0067 a0001c0001t0005g0072 others(8): Show |
11 | HG02055.hp2 HG02559.hp1 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.-34+7101C>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409540 | |||||||
| chr3:100409542 | C | A | 207 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(204): Show |
229 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(226): Show |
intron_variant | MODIFIER | c.-34+7103C>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409542 | |||||||
| chr3:100409544 | A | C | 6 | a0001c0001t0002g0338 a0001c0001t0002g0339 a0001c0001t0002g0340 others(3): Show |
6 | NA18951.hp2 NA18978.hp1 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.-34+7105A>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409544 | |||||||
| chr3:100409553 | TAC | T | 3 | a0001c0001t0001g0022 a0001c0001t0001g0357 a0001c0001t0001g0358 |
4 | HG01243.hp2 HG02055.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-34+7116_-34+7117d others(4): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100409553 | ||||||
| chr3:100409553 | TACATACA others(5): Show |
T | 1 | a0002c0003t0010g0195 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-34+7118_-34+7129d others(14): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100409553 | ||||||
| chr3:100409557 | T | TAC | 11 | a0001c0001t0003g0133 a0002c0002t0003g0087 a0002c0002t0003g0088 others(8): Show |
11 | HG00639.hp1 HG01175.hp2 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.-34+7152_-34+7153d others(4): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100409557 | ||||||
| chr3:100409557 | TAC | T | 34 | a0001c0001t0002g0334 a0001c0001t0007g0333 a0001c0004t0004g0193 others(31): Show |
34 | HG00140.hp2 HG00323.hp2 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.-34+7152_-34+7153d others(4): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100409557 | ||||||
| chr3:100409557 | TACAC | T | 7 | a0001c0001t0002g0290 a0001c0001t0002g0335 a0001c0001t0002g0336 others(4): Show |
7 | HG02602.hp2 HG02717.hp2 HG03704.hp2 others(4): Show |
intron_variant | MODIFIER | c.-34+7150_-34+7153d others(6): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100409557 | ||||||
| chr3:100409557 | TACACAC | T | 4 | a0002c0002t0001g0017 a0002c0002t0001g0148 a0002c0002t0001g0233 others(1): Show |
5 | HG00735.hp1 HG01975.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-34+7148_-34+7153d others(8): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100409557 | ||||||
| chr3:100409559 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-34+7120C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409559 | |||||||
| chr3:100409561 | C | T | 3 | a0001c0001t0001g0022 a0001c0001t0001g0357 a0001c0001t0001g0358 |
4 | HG01243.hp2 HG02055.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-34+7122C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409561 | |||||||
| chr3:100409563 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-34+7124C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409563 | |||||||
| chr3:100409567 | C | T | 1 | a0002c0003t0010g0195 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-34+7128C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409567 | |||||||
| chr3:100409571 | C | T | 1 | a0002c0003t0010g0195 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-34+7132C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409571 | |||||||
| chr3:100409576 | A | G | 1 | a0001c0001t0002g0349 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-34+7137A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409576 | |||||||
| chr3:100409587 | CACACAT | C | 6 | a0002c0002t0001g0185 a0002c0002t0001g0186 a0002c0002t0001g0187 others(3): Show |
6 | HG01099.hp1 HG02280.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-34+7150_-34+7155d others(8): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100409587 | ||||||
| chr3:100409589 | C | T | 62 | a0001c0001t0001g0192 a0001c0001t0001g0219 a0001c0001t0001g0221 others(59): Show |
63 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(60): Show |
intron_variant | MODIFIER | c.-34+7150C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409589 | |||||||
| chr3:100409589 | CACAT | C | 3 | a0001c0001t0001g0354 a0001c0001t0001g0355 a0001c0001t0001g0356 |
3 | HG02896.hp1 HG03139.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-34+7152_-34+7155d others(6): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100409589 | ||||||
| chr3:100409591 | C | T | 160 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(157): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.-34+7152C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409591 | |||||||
| chr3:100409591 | CAT | C | 3 | a0001c0001t0001g0022 a0001c0001t0001g0357 a0002c0002t0003g0113 |
4 | HG01243.hp2 HG02055.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-34+7167_-34+7168d others(4): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100409591 | ||||||
| chr3:100409593 | T | C | 25 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0024 others(22): Show |
27 | HG00639.hp1 HG01074.hp1 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.-34+7154T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409593 | |||||||
| chr3:100409595 | T | C | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-34+7156T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409595 | |||||||
| chr3:100409601 | TATA | T | 5 | a0001c0001t0002g0331 a0001c0001t0002g0345 a0001c0001t0002g0348 others(2): Show |
5 | HG00738.hp2 HG01981.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.-34+7163_-34+7165d others(5): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409601 | |||||||
| chr3:100409602 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-34+7163A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409602 | |||||||
| chr3:100409603 | TATA | T | 53 | a0001c0001t0002g0021 a0001c0001t0002g0288 a0001c0001t0002g0289 others(50): Show |
54 | HG00099.hp1 HG00099.hp2 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.-34+7165_-34+7167d others(5): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409603 | |||||||
| chr3:100409604 | A | G | 37 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0029 others(34): Show |
48 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.-34+7165A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409604 | |||||||
| chr3:100409605 | TA | T | 5 | a0001c0001t0002g0329 a0001c0001t0002g0347 a0002c0002t0001g0017 others(2): Show |
6 | HG00438.hp2 HG00735.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.-34+7167delA | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409605 | |||||||
| chr3:100409606 | A | ATATATTT | 5 | a0001c0001t0001g0013 a0001c0001t0001g0141 a0001c0001t0001g0142 others(2): Show |
6 | HG02109.hp2 HG02630.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34+7168_-34+7169i others(9): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100409606 | ||||||
| chr3:100409606 | A | G | 17 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0035 others(14): Show |
19 | HG01106.hp1 HG01952.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.-34+7167A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409606 | |||||||
| chr3:100409606 | A | T | 14 | a0001c0001t0002g0331 a0001c0001t0002g0345 a0001c0001t0002g0348 others(11): Show |
14 | HG00323.hp1 HG00738.hp2 HG01255.hp2 others(11): Show |
intron_variant | MODIFIER | c.-34+7167A>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409606 | |||||||
| chr3:100409606 | AT | A | 133 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(130): Show |
152 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(149): Show |
intron_variant | MODIFIER | c.-34+7181delT | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100409606 | ||||||
| chr3:100409606 | ATTT | A | 11 | a0001c0001t0001g0061 a0001c0001t0001g0216 a0001c0001t0001g0219 others(8): Show |
11 | HG02257.hp1 HG02559.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.-34+7179_-34+7181d others(5): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100409606 | ||||||
| chr3:100409607 | T | TA | 29 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0019 others(26): Show |
33 | HG00438.hp1 HG00609.hp2 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.-34+7168_-34+7169i others(3): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409607 | |||||||
| chr3:100409608 | T | A | 48 | a0001c0001t0001g0192 a0001c0001t0001g0354 a0001c0001t0001g0355 others(45): Show |
48 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.-34+7169T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409608 | |||||||
| chr3:100409609 | T | A | 146 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(143): Show |
169 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(166): Show |
intron_variant | MODIFIER | c.-34+7170T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409609 | |||||||
| chr3:100409610 | T | A | 4 | a0002c0002t0001g0155 a0002c0002t0001g0158 a0002c0002t0001g0159 others(1): Show |
4 | HG00544.hp2 HG01496.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34+7171T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409610 | |||||||
| chr3:100409611 | T | A | 7 | a0001c0001t0005g0072 a0001c0001t0005g0281 a0001c0001t0005g0282 others(4): Show |
7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-34+7172T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409611 | |||||||
| chr3:100409613 | T | A | 6 | a0001c0001t0005g0072 a0001c0001t0005g0281 a0001c0001t0005g0282 others(3): Show |
6 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.-34+7174T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409613 | |||||||
| chr3:100409751 | T | G | 1 | a0001c0001t0001g0265 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-34+7312T>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409751 | |||||||
| chr3:100409844 | C | G | 47 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(44): Show |
60 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.-34+7405C>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409844 | |||||||
| chr3:100409865 | G | A | 19 | a0001c0001t0001g0238 a0001c0001t0001g0247 a0002c0002t0001g0018 others(16): Show |
20 | HG00423.hp1 HG00642.hp2 HG02027.hp1 others(17): Show |
intron_variant | MODIFIER | c.-34+7426G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409865 | |||||||
| chr3:100409883 | C | A | 1 | a0001c0001t0003g0133 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-34+7444C>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100409883 | |||||||
| chr3:100409956 | C | CATCT | 76 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0061 others(73): Show |
79 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.-34+7559_-34+7562d others(6): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100409956 | ||||||
| chr3:100409956 | C | CATCTATC others(1): Show |
3 | a0001c0001t0002g0326 a0002c0002t0001g0181 a0002c0002t0003g0128 |
3 | HG00099.hp2 HG04228.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.-34+7555_-34+7562d others(10): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100409956 | ||||||
| chr3:100409956 | C | CATCTATC others(5): Show |
3 | a0002c0002t0001g0196 a0002c0002t0001g0236 a0002c0002t0003g0129 |
3 | HG02258.hp2 HG03491.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-34+7551_-34+7562d others(14): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100409956 | ||||||
| chr3:100409956 | C | CATCTATC others(9): Show |
3 | a0001c0001t0001g0258 a0001c0001t0002g0327 a0001c0001t0002g0328 |
3 | HG01346.hp1 NA18946.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.-34+7547_-34+7562d others(18): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100409956 | ||||||
| chr3:100409956 | CATCT | C | 30 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0028 others(27): Show |
33 | HG00738.hp1 HG01069.hp1 HG01071.hp1 others(30): Show |
intron_variant | MODIFIER | c.-34+7559_-34+7562d others(6): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100409956 | ||||||
| chr3:100409956 | CATCTATC others(1): Show |
C | 9 | a0001c0001t0001g0007 a0001c0001t0001g0225 a0001c0001t0001g0226 others(6): Show |
11 | HG00597.hp1 HG01361.hp2 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.-34+7555_-34+7562d others(10): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100409956 | ||||||
| chr3:100410046 | C | G | 1 | a0002c0002t0011g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-34+7607C>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100410046 | |||||||
| chr3:100410155 | G | A | 19 | a0001c0001t0001g0238 a0001c0001t0001g0247 a0002c0002t0001g0018 others(16): Show |
20 | HG00423.hp1 HG00642.hp2 HG02027.hp1 others(17): Show |
intron_variant | MODIFIER | c.-34+7716G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100410155 | |||||||
| chr3:100410282 | T | A | 57 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(54): Show |
70 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.-34+7843T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100410282 | |||||||
| chr3:100410365 | TAAA | T | 115 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(112): Show |
127 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.-34+7927_-34+7929d others(5): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100410365 | |||||||
| chr3:100410524 | T | C | 59 | a0001c0001t0002g0021 a0001c0001t0002g0288 a0001c0001t0002g0289 others(56): Show |
60 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(57): Show |
intron_variant | MODIFIER | c.-34+8085T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100410524 | |||||||
| chr3:100410654 | G | A | 1 | a0002c0002t0001g0272 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-34+8215G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100410654 | |||||||
| chr3:100410866 | C | G | 58 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(55): Show |
71 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.-34+8427C>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100410866 | |||||||
| chr3:100410887 | A | G | 1 | a0002c0002t0001g0180 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-34+8448A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100410887 | |||||||
| chr3:100411039 | C | A | 1 | a0002c0002t0012g0291 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-34+8600C>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100411039 | |||||||
| chr3:100411072 | C | T | 7 | a0001c0001t0001g0013 a0001c0001t0001g0141 a0001c0001t0001g0142 others(4): Show |
8 | HG02109.hp2 HG02280.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-34+8633C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100411072 | |||||||
| chr3:100411109 | A | T | 3 | a0002c0002t0001g0185 a0002c0002t0001g0186 a0002c0002t0001g0187 |
3 | HG02809.hp1 HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-34+8670A>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100411109 | |||||||
| chr3:100411169 | A | G | 1 | a0001c0001t0001g0144 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-34+8730A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100411169 | |||||||
| chr3:100411426 | G | A | 108 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(105): Show |
119 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(116): Show |
intron_variant | MODIFIER | c.-34+8987G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100411426 | |||||||
| chr3:100411604 | G | A | 1 | a0002c0003t0010g0195 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-34+9165G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100411604 | |||||||
| chr3:100411779 | C | T | 1 | a0002c0002t0001g0060 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-34+9340C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100411779 | |||||||
| chr3:100411865 | A | G | 1 | a0002c0002t0001g0244 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-34+9426A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100411865 | |||||||
| chr3:100411888 | G | A | 1 | a0001c0001t0001g0202 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-34+9449G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100411888 | |||||||
| chr3:100412001 | G | C | 2 | a0002c0002t0001g0164 a0002c0002t0001g0165 |
2 | HG00741.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.-34+9562G>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100412001 | |||||||
| chr3:100412002 | A | G | 3 | a0001c0001t0001g0022 a0001c0001t0001g0357 a0001c0001t0001g0358 |
4 | HG01243.hp2 HG02055.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-34+9563A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100412002 | |||||||
| chr3:100412030 | A | G | 1 | a0001c0001t0002g0345 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-34+9591A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100412030 | |||||||
| chr3:100412044 | G | A | 1 | a0001c0001t0001g0252 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-34+9605G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100412044 | |||||||
| chr3:100412294 | G | A | 1 | a0001c0001t0001g0190 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-34+9855G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100412294 | |||||||
| chr3:100412394 | C | T | 111 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(108): Show |
123 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(120): Show |
intron_variant | MODIFIER | c.-34+9955C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100412394 | |||||||
| chr3:100412401 | T | G | 1 | a0001c0001t0002g0338 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-34+9962T>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100412401 | |||||||
| chr3:100412935 | C | T | 2 | a0001c0001t0002g0353 a0002c0002t0002g0332 |
2 | HG03831.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.-34+10496C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100412935 | |||||||
| chr3:100413053 | A | G | 67 | a0001c0001t0002g0021 a0001c0001t0002g0288 a0001c0001t0002g0289 others(64): Show |
68 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(65): Show |
intron_variant | MODIFIER | c.-34+10614A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100413053 | |||||||
| chr3:100413076 | C | T | 25 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0070 others(22): Show |
27 | HG00438.hp1 HG00597.hp2 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.-34+10637C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100413076 | |||||||
| chr3:100413077 | G | A | 2 | a0001c0001t0001g0188 a0002c0003t0010g0195 |
2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-34+10638G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100413077 | |||||||
| chr3:100413110 | C | A | 1 | a0002c0002t0004g0183 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-34+10671C>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100413110 | |||||||
| chr3:100413132 | C | G | 67 | a0001c0001t0002g0021 a0001c0001t0002g0288 a0001c0001t0002g0289 others(64): Show |
68 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(65): Show |
intron_variant | MODIFIER | c.-34+10693C>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100413132 | |||||||
| chr3:100413254 | G | A | 4 | a0002c0002t0004g0074 a0002c0002t0004g0075 a0002c0002t0004g0076 others(1): Show |
4 | HG02145.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34+10815G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100413254 | |||||||
| chr3:100413720 | T | A | 7 | a0001c0001t0001g0013 a0001c0001t0001g0141 a0001c0001t0001g0142 others(4): Show |
8 | HG02109.hp2 HG02280.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-34+11281T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100413720 | |||||||
| chr3:100413830 | A | G | 1 | a0002c0002t0003g0127 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-34+11391A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100413830 | |||||||
| chr3:100413845 | G | A | 1 | a0002c0002t0003g0106 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-34+11406G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100413845 | |||||||
| chr3:100413873 | A | T | 8 | a0002c0002t0003g0086 a0002c0002t0003g0088 a0002c0002t0003g0090 others(5): Show |
8 | HG01192.hp1 HG01255.hp2 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.-34+11434A>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100413873 | |||||||
| chr3:100414053 | G | C | 39 | a0001c0001t0001g0361 a0002c0002t0001g0023 a0002c0002t0001g0150 others(36): Show |
39 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(36): Show |
intron_variant | MODIFIER | c.-34+11614G>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100414053 | |||||||
| chr3:100414161 | C | T | 3 | a0001c0001t0002g0309 a0001c0001t0002g0310 a0001c0001t0002g0311 |
3 | HG01981.hp1 HG02683.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-34+11722C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100414161 | |||||||
| chr3:100414449 | A | G | 2 | a0001c0001t0001g0188 a0002c0003t0010g0195 |
2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-34+12010A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100414449 | |||||||
| chr3:100414462 | G | A | 2 | a0002c0002t0001g0158 a0002c0002t0001g0159 |
2 | HG00544.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.-34+12023G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100414462 | |||||||
| chr3:100414465 | T | G | 1 | a0002c0002t0003g0107 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-34+12026T>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100414465 | |||||||
| chr3:100414546 | TA | T | 8 | a0001c0001t0001g0033 a0002c0002t0001g0178 a0002c0002t0001g0179 others(5): Show |
8 | HG00639.hp2 HG01081.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.-34+12122delA | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100414546 | ||||||
| chr3:100414792 | G | A | 45 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(42): Show |
52 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.-34+12353G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100414792 | |||||||
| chr3:100414899 | C | T | 4 | a0001c0001t0001g0354 a0001c0001t0001g0355 a0001c0001t0001g0356 others(1): Show |
4 | HG02896.hp1 HG03139.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-34+12460C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100414899 | |||||||
| chr3:100415009 | G | A | 1 | a0001c0004t0004g0193 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-34+12570G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100415009 | |||||||
| chr3:100415133 | G | T | 34 | a0001c0001t0001g0361 a0002c0002t0001g0023 a0002c0002t0001g0150 others(31): Show |
34 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.-34+12694G>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100415133 | |||||||
| chr3:100415356 | T | G | 7 | a0001c0001t0001g0013 a0001c0001t0001g0141 a0001c0001t0001g0142 others(4): Show |
8 | HG02109.hp2 HG02280.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-34+12917T>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100415356 | |||||||
| chr3:100415391 | A | G | 2 | a0001c0001t0001g0192 a0001c0004t0004g0193 |
2 | HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-34+12952A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100415391 | |||||||
| chr3:100415499 | A | T | 1 | a0001c0001t0001g0192 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-34+13060A>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100415499 | |||||||
| chr3:100415675 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-34+13236C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100415675 | |||||||
| chr3:100415758 | A | G | 9 | a0001c0001t0001g0354 a0001c0001t0001g0355 a0001c0001t0001g0356 others(6): Show |
9 | HG01099.hp1 HG02280.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-34+13319A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100415758 | |||||||
| chr3:100415829 | C | T | 1 | a0001c0001t0001g0228 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-34+13390C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100415829 | |||||||
| chr3:100415943 | C | T | 2 | a0001c0001t0002g0307 a0001c0001t0002g0308 |
2 | NA18980.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.-34+13504C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100415943 | |||||||
| chr3:100416101 | A | G | 2 | a0001c0001t0001g0354 a0001c0001t0001g0356 |
2 | HG02896.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-33-13596A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100416101 | |||||||
| chr3:100416114 | A | T | 2 | a0001c0001t0001g0188 a0002c0003t0010g0195 |
2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-33-13583A>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100416114 | |||||||
| chr3:100416158 | G | A | 4 | a0002c0002t0001g0017 a0002c0002t0001g0148 a0002c0002t0001g0233 others(1): Show |
5 | HG00735.hp1 HG01975.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-33-13539G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100416158 | |||||||
| chr3:100416181 | AT | A | 3 | a0001c0001t0001g0013 a0001c0001t0001g0141 a0001c0001t0001g0143 |
4 | HG02109.hp2 HG02630.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-33-13514delT | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100416181 | ||||||
| chr3:100416406 | C | G | 1 | a0001c0001t0001g0080 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-33-13291C>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100416406 | |||||||
| chr3:100416467 | T | C | 2 | a0001c0001t0002g0296 a0001c0001t0002g0317 |
2 | HG04228.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.-33-13230T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100416467 | |||||||
| chr3:100416594 | CTT | C | 68 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0056 others(65): Show |
74 | HG00544.hp1 HG00558.hp2 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.-33-13098_-33-1309 others(6): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100416594 | ||||||
| chr3:100416597 | T | G | 1 | a0001c0001t0002g0318 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-33-13100T>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100416597 | |||||||
| chr3:100416597 | T | TG | 5 | a0001c0001t0001g0266 a0002c0002t0001g0155 a0002c0002t0001g0158 others(2): Show |
5 | HG00544.hp2 HG00738.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.-33-13100_-33-1309 others(5): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100416597 | |||||||
| chr3:100416597 | T | TTG | 31 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0071 others(28): Show |
33 | HG00609.hp2 HG00673.hp1 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.-33-13099_-33-1309 others(6): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100416597 | ||||||
| chr3:100416597 | T | TTGTG | 11 | a0001c0001t0001g0252 a0001c0001t0001g0271 a0001c0001t0002g0021 others(8): Show |
12 | HG00735.hp2 HG01496.hp2 HG02004.hp2 others(9): Show |
intron_variant | MODIFIER | c.-33-13099_-33-1309 others(8): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100416597 | ||||||
| chr3:100416597 | T | TTGTGTGT others(3): Show |
1 | a0002c0002t0001g0181 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-33-13099_-33-1309 others(14): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100416597 | ||||||
| chr3:100416597 | TTTTG | T | 36 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0201 others(33): Show |
40 | HG00099.hp1 HG00099.hp2 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.-33-13098_-33-1309 others(8): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100416597 | ||||||
| chr3:100416597 | TTTTGTG | T | 44 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0028 others(41): Show |
51 | HG00140.hp2 HG00558.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.-33-13098_-33-1309 others(10): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100416597 | ||||||
| chr3:100416597 | TTTTGTGT others(1): Show |
T | 23 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0024 others(20): Show |
26 | HG00423.hp2 HG01106.hp1 HG01192.hp2 others(23): Show |
intron_variant | MODIFIER | c.-33-13098_-33-1309 others(12): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100416597 | ||||||
| chr3:100416597 | TTTTGTGT others(3): Show |
T | 2 | a0001c0001t0001g0192 a0001c0004t0004g0193 |
2 | HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-33-13098_-33-1308 others(14): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100416597 | ||||||
| chr3:100416597 | TTTTGTGT others(7): Show |
T | 1 | a0001c0001t0001g0038 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-33-13098_-33-1308 others(18): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100416597 | ||||||
| chr3:100416597 | TTTTGTGT others(9): Show |
T | 1 | a0001c0001t0002g0297 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-33-13098_-33-1308 others(20): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100416597 | ||||||
| chr3:100416599 | T | G | 131 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0019 others(128): Show |
138 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.-33-13098T>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100416599 | |||||||
| chr3:100416599 | T | TTG | 4 | a0001c0001t0003g0133 a0002c0002t0003g0114 a0002c0002t0003g0122 others(1): Show |
4 | HG01934.hp1 HG01943.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.-33-13051_-33-1305 others(6): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100416599 | ||||||
| chr3:100416599 | T | TTGTG | 3 | a0001c0001t0003g0134 a0002c0002t0003g0081 a0002c0002t0003g0091 |
3 | HG04115.hp1 HG04204.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-33-13053_-33-1305 others(8): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100416599 | ||||||
| chr3:100416599 | T | TTTTTTGT others(3): Show |
1 | a0001c0001t0003g0100 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-33-13097_-33-1309 others(14): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100416599 | ||||||
| chr3:100416599 | TTG | T | 6 | a0002c0002t0003g0089 a0002c0002t0003g0090 a0002c0002t0003g0095 others(3): Show |
6 | HG00323.hp1 HG01361.hp1 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.-33-13051_-33-1305 others(6): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100416599 | ||||||
| chr3:100416599 | TTGTG | T | 16 | a0002c0002t0003g0083 a0002c0002t0003g0084 a0002c0002t0003g0085 others(13): Show |
16 | HG01099.hp2 HG01192.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.-33-13053_-33-1305 others(8): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100416599 | ||||||
| chr3:100416599 | TTGTGTGT others(7): Show |
T | 1 | a0002c0002t0003g0106 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-33-13063_-33-1305 others(18): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100416599 | ||||||
| chr3:100416601 | G | T | 3 | a0002c0002t0003g0116 a0002c0002t0003g0123 a0002c0002t0003g0126 |
3 | HG01516.hp1 HG03654.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.-33-13096G>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100416601 | |||||||
| chr3:100416603 | G | T | 1 | a0002c0002t0003g0362 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-33-13094G>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100416603 | |||||||
| chr3:100416605 | G | T | 1 | a0002c0002t0003g0093 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-33-13092G>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100416605 | |||||||
| chr3:100416718 | AT | A | 118 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(115): Show |
129 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.-33-12964delT | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100416718 | ||||||
| chr3:100416718 | ATT | A | 58 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(55): Show |
72 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.-33-12965_-33-1296 others(6): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100416718 | ||||||
| chr3:100416732 | TTA | T | 38 | a0001c0001t0001g0361 a0002c0002t0001g0023 a0002c0002t0001g0150 others(35): Show |
38 | HG00323.hp2 HG00544.hp2 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.-33-12964_-33-1296 others(6): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100416732 | |||||||
| chr3:100416734 | A | G | 1 | a0002c0003t0010g0195 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-33-12963A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100416734 | |||||||
| chr3:100416780 | T | C | 184 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(181): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.-33-12917T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100416780 | |||||||
| chr3:100416849 | C | T | 2 | a0001c0001t0001g0192 a0001c0004t0004g0193 |
2 | HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-33-12848C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100416849 | |||||||
| chr3:100416887 | C | T | 14 | a0001c0001t0001g0361 a0002c0002t0001g0023 a0002c0002t0001g0155 others(11): Show |
14 | HG00639.hp2 HG00741.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.-33-12810C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100416887 | |||||||
| chr3:100417020 | T | G | 3 | a0001c0001t0005g0281 a0001c0001t0005g0282 a0001c0001t0005g0284 |
3 | HG02559.hp1 HG02976.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-33-12677T>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100417020 | |||||||
| chr3:100417128 | A | G | 1 | a0002c0002t0001g0270 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.-33-12569A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100417128 | |||||||
| chr3:100417158 | CA | C | 3 | a0002c0002t0001g0185 a0002c0002t0001g0186 a0002c0002t0001g0187 |
3 | HG02809.hp1 HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.-33-12534delA | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100417158 | ||||||
| chr3:100417316 | C | T | 2 | a0001c0001t0001g0188 a0002c0003t0010g0195 |
2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-33-12381C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100417316 | |||||||
| chr3:100417371 | C | CT | 249 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(246): Show |
280 | HG00140.hp1 HG00323.hp1 HG00423.hp1 others(277): Show |
intron_variant | MODIFIER | c.-33-12304dupT | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100417371 | ||||||
| chr3:100417371 | C | CTT | 13 | a0001c0001t0001g0031 a0001c0001t0001g0227 a0001c0001t0001g0253 others(10): Show |
13 | HG01099.hp1 HG02257.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.-33-12305_-33-1230 others(6): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100417371 | ||||||
| chr3:100417371 | CT | C | 6 | a0001c0001t0002g0314 a0001c0001t0002g0339 a0001c0001t0002g0351 others(3): Show |
6 | HG00639.hp1 HG01070.hp2 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.-33-12304delT | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100417371 | ||||||
| chr3:100417371 | CTTTTTTT others(3): Show |
C | 1 | a0002c0002t0006g0224 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-33-12313_-33-1230 others(14): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100417371 | ||||||
| chr3:100417525 | G | A | 1 | a0002c0002t0001g0237 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-33-12172G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100417525 | |||||||
| chr3:100417800 | A | G | 66 | a0001c0001t0002g0021 a0001c0001t0002g0288 a0001c0001t0002g0289 others(63): Show |
67 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(64): Show |
intron_variant | MODIFIER | c.-33-11897A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100417800 | |||||||
| chr3:100417844 | C | T | 1 | a0001c0001t0002g0302 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-33-11853C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100417844 | |||||||
| chr3:100418007 | A | G | 1 | a0001c0001t0001g0256 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-33-11690A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100418007 | |||||||
| chr3:100418059 | A | AC | 55 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(52): Show |
68 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.-33-11638_-33-1163 others(5): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100418059 | |||||||
| chr3:100418060 | T | C | 245 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(242): Show |
259 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.-33-11637T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100418060 | |||||||
| chr3:100418220 | C | A | 1 | a0002c0002t0001g0261 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-33-11477C>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100418220 | |||||||
| chr3:100418220 | C | T | 7 | a0001c0001t0005g0072 a0001c0001t0005g0281 a0001c0001t0005g0282 others(4): Show |
7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-33-11477C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100418220 | |||||||
| chr3:100418226 | AT | A | 8 | a0001c0001t0001g0013 a0001c0001t0001g0141 a0001c0001t0001g0142 others(5): Show |
9 | HG02109.hp2 HG02280.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-33-11456delT | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100418226 | ||||||
| chr3:100418355 | G | A | 1 | a0001c0001t0007g0333 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-33-11342G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100418355 | |||||||
| chr3:100418529 | C | G | 1 | a0002c0002t0001g0261 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-33-11168C>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100418529 | |||||||
| chr3:100418848 | A | G | 2 | a0001c0001t0002g0302 a0001c0001t0002g0303 |
2 | HG00741.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.-33-10849A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100418848 | |||||||
| chr3:100418876 | G | T | 3 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0061 |
3 | HG02257.hp1 HG02622.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-33-10821G>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100418876 | |||||||
| chr3:100418941 | A | G | 58 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(55): Show |
71 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.-33-10756A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100418941 | |||||||
| chr3:100419412 | A | T | 2 | a0001c0001t0001g0219 a0001c0001t0001g0221 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-33-10285A>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100419412 | |||||||
| chr3:100419559 | C | T | 2 | a0002c0002t0001g0005 a0002c0002t0001g0054 |
4 | NA18961.hp2 NA18966.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.-33-10138C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100419559 | |||||||
| chr3:100419839 | G | T | 1 | a0001c0001t0001g0145 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-33-9858G>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100419839 | |||||||
| chr3:100419851 | G | C | 7 | a0001c0001t0005g0072 a0001c0001t0005g0281 a0001c0001t0005g0282 others(4): Show |
7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-33-9846G>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100419851 | |||||||
| chr3:100420300 | G | T | 1 | a0001c0001t0002g0311 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-33-9397G>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100420300 | |||||||
| chr3:100420371 | G | T | 7 | a0001c0001t0001g0013 a0001c0001t0001g0141 a0001c0001t0001g0142 others(4): Show |
8 | HG02109.hp2 HG02280.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-33-9326G>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100420371 | |||||||
| chr3:100420860 | C | T | 1 | a0002c0002t0001g0052 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-33-8837C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100420860 | |||||||
| chr3:100420873 | C | G | 1 | a0001c0001t0002g0293 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-33-8824C>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100420873 | |||||||
| chr3:100421035 | G | A | 1 | a0002c0002t0012g0291 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-33-8662G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100421035 | |||||||
| chr3:100421036 | T | G | 7 | a0001c0001t0005g0072 a0001c0001t0005g0281 a0001c0001t0005g0282 others(4): Show |
7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-33-8661T>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100421036 | |||||||
| chr3:100421047 | C | T | 7 | a0001c0001t0001g0013 a0001c0001t0001g0141 a0001c0001t0001g0142 others(4): Show |
8 | HG02109.hp2 HG02280.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-33-8650C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100421047 | |||||||
| chr3:100421148 | A | T | 1 | a0002c0003t0010g0195 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-33-8549A>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100421148 | |||||||
| chr3:100421196 | T | G | 7 | a0001c0001t0001g0013 a0001c0001t0001g0141 a0001c0001t0001g0142 others(4): Show |
8 | HG02109.hp2 HG02280.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-33-8501T>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100421196 | |||||||
| chr3:100421569 | G | A | 7 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0029 others(4): Show |
9 | NA18945.hp1 NA18954.hp1 NA18965.hp2 others(6): Show |
intron_variant | MODIFIER | c.-33-8128G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100421569 | |||||||
| chr3:100421716 | G | T | 1 | a0001c0001t0001g0226 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-33-7981G>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100421716 | |||||||
| chr3:100422182 | CT | C | 275 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(272): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.-33-7496delT | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100422182 | ||||||
| chr3:100422182 | CTT | C | 7 | a0001c0001t0001g0192 a0001c0001t0001g0354 a0001c0001t0001g0355 others(4): Show |
7 | HG02559.hp2 HG02615.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-33-7497_-33-7496d others(4): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100422182 | ||||||
| chr3:100422486 | G | A | 2 | a0001c0001t0001g0192 a0001c0004t0004g0193 |
2 | HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-33-7211G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100422486 | |||||||
| chr3:100422803 | C | CT | 14 | a0001c0001t0002g0290 a0001c0001t0002g0293 a0001c0001t0002g0297 others(11): Show |
14 | HG00741.hp1 HG00741.hp2 HG01069.hp2 others(11): Show |
intron_variant | MODIFIER | c.-33-6867dupT | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100422803 | ||||||
| chr3:100422803 | CT | C | 126 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(123): Show |
138 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(135): Show |
intron_variant | MODIFIER | c.-33-6867delT | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100422803 | ||||||
| chr3:100422803 | CTT | C | 19 | a0001c0001t0001g0036 a0001c0001t0001g0198 a0001c0001t0001g0204 others(16): Show |
19 | HG01069.hp1 HG01167.hp2 HG02015.hp2 others(16): Show |
intron_variant | MODIFIER | c.-33-6868_-33-6867d others(4): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100422803 | ||||||
| chr3:100422803 | CTTT | C | 51 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(48): Show |
64 | HG00423.hp2 HG00558.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.-33-6869_-33-6867d others(5): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100422803 | ||||||
| chr3:100422803 | CTTTTTTT others(3): Show |
C | 8 | a0001c0001t0001g0013 a0001c0001t0001g0141 a0001c0001t0001g0142 others(5): Show |
9 | HG02109.hp2 HG02280.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-33-6876_-33-6867d others(12): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100422803 | ||||||
| chr3:100422803 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0354 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-33-6877_-33-6867d others(13): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100422803 | ||||||
| chr3:100422803 | CTTTTTTT others(5): Show |
C | 6 | a0001c0001t0001g0355 a0001c0001t0001g0356 a0002c0002t0004g0139 others(3): Show |
6 | HG01099.hp1 HG02280.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-33-6878_-33-6867d others(14): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100422803 | ||||||
| chr3:100422827 | T | A | 2 | a0001c0001t0005g0072 a0001c0001t0005g0286 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-33-6870T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100422827 | |||||||
| chr3:100422870 | A | C | 66 | a0001c0001t0002g0021 a0001c0001t0002g0288 a0001c0001t0002g0289 others(63): Show |
67 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(64): Show |
intron_variant | MODIFIER | c.-33-6827A>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100422870 | |||||||
| chr3:100423120 | T | C | 1 | a0001c0001t0002g0317 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-33-6577T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100423120 | |||||||
| chr3:100423241 | T | C | 1 | a0001c0001t0006g0222 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-33-6456T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100423241 | |||||||
| chr3:100423315 | A | G | 1 | a0001c0001t0002g0350 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-33-6382A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100423315 | |||||||
| chr3:100423436 | T | C | 4 | a0002c0002t0001g0017 a0002c0002t0001g0148 a0002c0002t0001g0233 others(1): Show |
5 | HG00735.hp1 HG01975.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-33-6261T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100423436 | |||||||
| chr3:100423455 | C | T | 3 | a0001c0001t0001g0013 a0001c0001t0001g0141 a0001c0001t0001g0143 |
4 | HG02109.hp2 HG02630.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.-33-6242C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100423455 | |||||||
| chr3:100423477 | G | C | 112 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(109): Show |
124 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(121): Show |
intron_variant | MODIFIER | c.-33-6220G>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100423477 | |||||||
| chr3:100423612 | G | A | 1 | a0002c0002t0013g0096 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-33-6085G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100423612 | |||||||
| chr3:100423704 | A | C | 1 | a0002c0002t0001g0159 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-33-5993A>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100423704 | |||||||
| chr3:100423739 | A | G | 14 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0071 others(11): Show |
16 | HG00438.hp1 HG00609.hp2 HG00673.hp1 others(13): Show |
intron_variant | MODIFIER | c.-33-5958A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100423739 | |||||||
| chr3:100423843 | C | T | 1 | a0002c0002t0003g0085 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-33-5854C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100423843 | |||||||
| chr3:100423977 | C | T | 1 | a0001c0001t0002g0308 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-33-5720C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100423977 | |||||||
| chr3:100424153 | C | T | 1 | a0002c0002t0011g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-33-5544C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100424153 | |||||||
| chr3:100424175 | G | A | 1 | a0001c0001t0002g0299 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-33-5522G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100424175 | |||||||
| chr3:100424280 | G | A | 7 | a0001c0001t0005g0072 a0001c0001t0005g0281 a0001c0001t0005g0282 others(4): Show |
7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-33-5417G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100424280 | |||||||
| chr3:100424461 | A | C | 1 | a0001c0001t0001g0273 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-33-5236A>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100424461 | |||||||
| chr3:100424464 | C | A | 7 | a0002c0002t0001g0153 a0002c0002t0001g0168 a0002c0002t0001g0173 others(4): Show |
7 | NA18953.hp1 NA18974.hp1 NA18986.hp2 others(4): Show |
intron_variant | MODIFIER | c.-33-5233C>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100424464 | |||||||
| chr3:100424526 | A | G | 1 | a0002c0002t0012g0291 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-33-5171A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100424526 | |||||||
| chr3:100424617 | G | A | 7 | a0001c0001t0001g0013 a0001c0001t0001g0141 a0001c0001t0001g0142 others(4): Show |
8 | HG02109.hp2 HG02280.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-33-5080G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100424617 | |||||||
| chr3:100424627 | A | G | 1 | a0002c0002t0003g0126 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-33-5070A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100424627 | |||||||
| chr3:100424712 | G | A | 1 | a0002c0003t0010g0195 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-33-4985G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100424712 | |||||||
| chr3:100424743 | C | T | 7 | a0001c0001t0005g0072 a0001c0001t0005g0281 a0001c0001t0005g0282 others(4): Show |
7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-33-4954C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100424743 | |||||||
| chr3:100425143 | A | G | 2 | a0001c0001t0001g0192 a0001c0004t0004g0193 |
2 | HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-33-4554A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100425143 | |||||||
| chr3:100425180 | A | G | 2 | a0001c0001t0002g0302 a0001c0001t0002g0303 |
2 | HG00741.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.-33-4517A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100425180 | |||||||
| chr3:100425215 | C | T | 19 | a0001c0001t0001g0051 a0002c0002t0001g0002 a0002c0002t0001g0005 others(16): Show |
27 | HG00558.hp1 HG00609.hp1 HG01928.hp2 others(24): Show |
intron_variant | MODIFIER | c.-33-4482C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100425215 | |||||||
| chr3:100425240 | C | T | 2 | a0001c0001t0001g0188 a0001c0001t0002g0363 |
2 | HG02572.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.-33-4457C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100425240 | |||||||
| chr3:100425271 | C | A | 2 | a0002c0002t0001g0062 a0002c0002t0009g0045 |
2 | HG02922.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-33-4426C>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100425271 | |||||||
| chr3:100425342 | T | G | 7 | a0001c0001t0001g0013 a0001c0001t0001g0141 a0001c0001t0001g0142 others(4): Show |
8 | HG02109.hp2 HG02280.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.-33-4355T>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100425342 | |||||||
| chr3:100425537 | T | C | 2 | a0001c0001t0001g0192 a0001c0004t0004g0193 |
2 | HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-33-4160T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100425537 | |||||||
| chr3:100425562 | G | A | 1 | a0002c0002t0004g0166 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-33-4135G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100425562 | |||||||
| chr3:100425567 | T | C | 2 | a0001c0001t0001g0192 a0001c0004t0004g0193 |
2 | HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.-33-4130T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100425567 | |||||||
| chr3:100425569 | T | A | 1 | a0002c0002t0001g0272 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-33-4128T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100425569 | |||||||
| chr3:100425578 | C | G | 2 | a0002c0002t0001g0148 a0002c0002t0001g0233 |
2 | HG01975.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-33-4119C>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100425578 | |||||||
| chr3:100425686 | G | A | 4 | a0001c0001t0001g0188 a0001c0001t0001g0192 a0001c0004t0004g0193 others(1): Show |
4 | HG02559.hp2 HG02572.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.-33-4011G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100425686 | |||||||
| chr3:100425846 | A | G | 117 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(114): Show |
129 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.-33-3851A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100425846 | |||||||
| chr3:100425909 | C | G | 1 | a0002c0002t0004g0183 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-33-3788C>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100425909 | |||||||
| chr3:100425982 | C | A | 1 | a0001c0001t0002g0288 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-33-3715C>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100425982 | |||||||
| chr3:100426581 | G | A | 1 | a0002c0002t0001g0287 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-33-3116G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100426581 | |||||||
| chr3:100426667 | G | A | 1 | a0002c0002t0001g0186 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-33-3030G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100426667 | |||||||
| chr3:100426725 | A | C | 10 | a0001c0001t0001g0218 a0002c0002t0001g0196 a0002c0002t0001g0236 others(7): Show |
10 | HG02109.hp1 HG02258.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.-33-2972A>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100426725 | |||||||
| chr3:100426955 | T | G | 2 | a0002c0002t0004g0139 a0002c0002t0004g0140 |
2 | HG01099.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.-33-2742T>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100426955 | |||||||
| chr3:100427025 | T | C | 24 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0022 others(21): Show |
27 | HG01069.hp2 HG01243.hp2 HG01952.hp2 others(24): Show |
intron_variant | MODIFIER | c.-33-2672T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100427025 | |||||||
| chr3:100427081 | T | C | 20 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0024 others(17): Show |
22 | HG01952.hp2 HG02055.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.-33-2616T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100427081 | |||||||
| chr3:100427704 | C | T | 7 | a0001c0001t0005g0072 a0001c0001t0005g0281 a0001c0001t0005g0282 others(4): Show |
7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.-33-1993C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100427704 | |||||||
| chr3:100427726 | A | G | 1 | a0002c0002t0004g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-33-1971A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100427726 | |||||||
| chr3:100427765 | G | A | 4 | a0002c0002t0001g0017 a0002c0002t0001g0148 a0002c0002t0001g0233 others(1): Show |
5 | HG00735.hp1 HG01975.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-33-1932G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100427765 | |||||||
| chr3:100428063 | A | G | 1 | a0001c0001t0001g0211 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-33-1634A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100428063 | |||||||
| chr3:100428132 | G | A | 4 | a0001c0001t0002g0319 a0001c0001t0002g0320 a0001c0001t0002g0326 others(1): Show |
4 | HG00099.hp2 HG00140.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.-33-1565G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100428132 | |||||||
| chr3:100428168 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-33-1529A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100428168 | |||||||
| chr3:100428267 | C | T | 10 | a0002c0002t0004g0027 a0002c0002t0004g0074 a0002c0002t0004g0075 others(7): Show |
10 | HG02145.hp1 HG02615.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.-33-1430C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100428267 | |||||||
| chr3:100428348 | A | G | 1 | a0002c0002t0003g0117 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-33-1349A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100428348 | |||||||
| chr3:100428409 | G | A | 1 | a0001c0001t0002g0312 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-33-1288G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100428409 | |||||||
| chr3:100428459 | G | A | 1 | a0001c0001t0001g0033 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-33-1238G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100428459 | |||||||
| chr3:100428462 | G | C | 1 | a0001c0004t0004g0193 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-33-1235G>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100428462 | |||||||
| chr3:100428467 | G | T | 6 | a0002c0002t0004g0027 a0002c0002t0004g0074 a0002c0002t0004g0075 others(3): Show |
6 | HG02145.hp1 HG03041.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.-33-1230G>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100428467 | |||||||
| chr3:100428531 | C | CAA | 45 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(42): Show |
51 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.-33-1154_-33-1153d others(4): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 100428531 | ||||||
| chr3:100428548 | A | G | 1 | a0001c0001t0005g0284 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-33-1149A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100428548 | |||||||
| chr3:100428795 | C | T | 1 | a0002c0002t0001g0042 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.-33-902C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100428795 | |||||||
| chr3:100428961 | A | C | 8 | a0001c0001t0001g0013 a0001c0001t0001g0073 a0001c0001t0001g0141 others(5): Show |
9 | HG02109.hp2 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-33-736A>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100428961 | |||||||
| chr3:100428986 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-33-711G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100428986 | |||||||
| chr3:100429079 | T | C | 1 | a0001c0001t0002g0322 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-33-618T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100429079 | |||||||
| chr3:100429140 | C | G | 1 | a0001c0001t0002g0345 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-33-557C>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100429140 | |||||||
| chr3:100429283 | G | A | 2 | a0002c0002t0003g0095 a0002c0002t0003g0135 |
2 | HG02257.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-33-414G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100429283 | |||||||
| chr3:100429315 | G | A | 1 | a0002c0002t0001g0280 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-33-382G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100429315 | |||||||
| chr3:100429329 | T | A | 1 | a0001c0001t0001g0216 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-33-368T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100429329 | |||||||
| chr3:100429427 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-33-270G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100429427 | |||||||
| chr3:100429513 | A | G | 1 | a0001c0004t0004g0193 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-33-184A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100429513 | |||||||
| chr3:100429541 | C | G | 1 | a0002c0002t0003g0094 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-33-156C>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 1/3 | chr3 | 100429541 | |||||||
| chr3:100429907 | G | A | 1 | a0002c0002t0003g0117 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.156+22G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100429907 | |||||||
| chr3:100429960 | A | G | 1 | a0001c0001t0002g0309 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.156+75A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100429960 | |||||||
| chr3:100429991 | A | C | 2 | a0002c0002t0001g0164 a0002c0002t0001g0165 |
2 | HG00741.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.156+106A>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100429991 | |||||||
| chr3:100430170 | C | T | 2 | a0002c0002t0001g0249 a0002c0002t0001g0251 |
2 | HG03704.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.156+285C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100430170 | |||||||
| chr3:100430189 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.156+304A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100430189 | |||||||
| chr3:100430221 | C | A | 3 | a0001c0001t0003g0100 a0001c0001t0003g0133 a0001c0001t0003g0134 |
3 | HG01074.hp1 HG03927.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.156+336C>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100430221 | |||||||
| chr3:100430310 | G | A | 65 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(62): Show |
72 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(69): Show |
intron_variant | MODIFIER | c.156+425G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100430310 | |||||||
| chr3:100430434 | A | G | 6 | a0002c0002t0001g0153 a0002c0002t0001g0168 a0002c0002t0001g0173 others(3): Show |
6 | NA18953.hp1 NA18974.hp1 NA19010.hp1 others(3): Show |
intron_variant | MODIFIER | c.156+549A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100430434 | |||||||
| chr3:100430698 | G | A | 1 | a0002c0002t0002g0352 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.156+813G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100430698 | |||||||
| chr3:100430891 | C | G | 1 | a0001c0004t0004g0193 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.156+1006C>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100430891 | |||||||
| chr3:100431183 | A | G | 57 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(54): Show |
64 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.156+1298A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100431183 | |||||||
| chr3:100431198 | T | G | 2 | a0001c0001t0003g0133 a0001c0001t0003g0134 |
2 | HG03927.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.156+1313T>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100431198 | |||||||
| chr3:100431643 | A | G | 1 | a0001c0001t0005g0285 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.156+1758A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100431643 | |||||||
| chr3:100431694 | C | A | 1 | a0002c0002t0001g0272 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.156+1809C>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100431694 | |||||||
| chr3:100431821 | C | T | 9 | a0001c0001t0001g0013 a0001c0001t0001g0073 a0001c0001t0001g0141 others(6): Show |
10 | HG02109.hp2 HG02280.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.156+1936C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100431821 | |||||||
| chr3:100431828 | C | CA | 30 | a0001c0001t0001g0030 a0001c0001t0001g0188 a0001c0001t0001g0192 others(27): Show |
30 | HG00423.hp1 HG00738.hp2 HG01074.hp1 others(27): Show |
intron_variant | MODIFIER | c.156+1963dupA | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431828 | ||||||
| chr3:100431828 | CA | C | 27 | a0001c0001t0001g0013 a0001c0001t0001g0025 a0001c0001t0001g0035 others(24): Show |
28 | HG01070.hp2 HG01123.hp2 HG01975.hp2 others(25): Show |
intron_variant | MODIFIER | c.156+1963delA | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431828 | ||||||
| chr3:100431828 | CAA | C | 43 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(40): Show |
49 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.156+1962_156+1963d others(4): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431828 | ||||||
| chr3:100431948 | A | T | 57 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(54): Show |
64 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.156+2063A>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100431948 | |||||||
| chr3:100431990 | GTTTATA | G | 3 | a0002c0002t0003g0090 a0002c0002t0003g0114 a0002c0002t0003g0130 |
3 | HG01934.hp1 HG01934.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.156+2107_156+2112d others(8): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431990 | ||||||
| chr3:100431990 | GTTTATAT others(3): Show |
G | 1 | a0002c0002t0003g0131 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.156+2107_156+2116d others(12): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431990 | ||||||
| chr3:100431990 | GTTTATAT others(11): Show |
G | 1 | a0002c0002t0001g0037 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.156+2107_156+2124d others(20): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431990 | ||||||
| chr3:100431990 | GTTTATAT others(15): Show |
G | 1 | a0001c0001t0001g0267 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.156+2107_156+2128d others(24): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431990 | ||||||
| chr3:100431990 | GTTTATAT others(17): Show |
G | 3 | a0001c0001t0001g0258 a0001c0001t0001g0354 a0001c0001t0001g0356 |
3 | HG01346.hp1 HG02896.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.156+2107_156+2130d others(26): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431990 | ||||||
| chr3:100431990 | GTTTATAT others(19): Show |
G | 16 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0020 others(13): Show |
19 | HG00438.hp1 HG00609.hp2 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.156+2107_156+2132d others(28): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431990 | ||||||
| chr3:100431990 | GTTTATAT others(21): Show |
G | 11 | a0001c0001t0001g0010 a0001c0001t0001g0024 a0001c0001t0001g0025 others(8): Show |
12 | HG01074.hp1 HG02055.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.156+2107_156+2134d others(30): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431990 | ||||||
| chr3:100431990 | GTTTATAT others(23): Show |
G | 23 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0029 others(20): Show |
25 | HG00597.hp2 HG00642.hp1 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.156+2107_156+2136d others(32): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431990 | ||||||
| chr3:100431990 | GTTTATAT others(25): Show |
G | 1 | a0001c0001t0001g0056 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.156+2107_156+2138d others(34): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431990 | ||||||
| chr3:100431990 | GTTTATAT others(27): Show |
G | 6 | a0001c0001t0001g0192 a0001c0001t0001g0209 a0001c0001t0002g0303 others(3): Show |
6 | HG00438.hp2 HG00741.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.156+2107_156+2140d others(36): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431990 | ||||||
| chr3:100431990 | GTTTATAT others(29): Show |
G | 62 | a0001c0001t0001g0014 a0001c0001t0001g0035 a0001c0001t0001g0036 others(59): Show |
64 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(61): Show |
intron_variant | MODIFIER | c.156+2107_156+2142d others(38): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431990 | ||||||
| chr3:100431991 | TTTATATA others(6): Show |
T | 1 | a0002c0002t0003g0127 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.156+2108_156+2120d others(15): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431991 | ||||||
| chr3:100431992 | TTA | T | 12 | a0002c0002t0001g0160 a0002c0002t0001g0167 a0002c0002t0001g0251 others(9): Show |
13 | HG00738.hp1 HG01358.hp2 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.156+2167_156+2168d others(4): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431992 | ||||||
| chr3:100431992 | TTATA | T | 9 | a0002c0002t0001g0017 a0002c0002t0001g0270 a0002c0002t0003g0001 others(6): Show |
9 | HG01099.hp1 HG02004.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.156+2165_156+2168d others(6): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431992 | ||||||
| chr3:100431992 | TTATATA | T | 14 | a0002c0002t0001g0184 a0002c0002t0001g0186 a0002c0002t0001g0239 others(11): Show |
14 | HG00735.hp2 HG01258.hp1 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.156+2163_156+2168d others(8): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431992 | ||||||
| chr3:100431992 | TTATATAT others(1): Show |
T | 30 | a0002c0002t0001g0011 a0002c0002t0001g0148 a0002c0002t0001g0158 others(27): Show |
30 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.156+2161_156+2168d others(10): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431992 | ||||||
| chr3:100431992 | TTATATAT others(3): Show |
T | 34 | a0001c0001t0001g0051 a0001c0001t0001g0188 a0002c0002t0001g0002 others(31): Show |
36 | HG00323.hp2 HG00423.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.156+2159_156+2168d others(12): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431992 | ||||||
| chr3:100431992 | TTATATAT others(5): Show |
T | 17 | a0002c0002t0001g0012 a0002c0002t0001g0034 a0002c0002t0001g0042 others(14): Show |
17 | HG00323.hp1 HG00639.hp2 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.156+2157_156+2168d others(14): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431992 | ||||||
| chr3:100431992 | TTATATAT others(7): Show |
T | 10 | a0002c0002t0001g0044 a0002c0002t0001g0048 a0002c0002t0001g0049 others(7): Show |
10 | HG00558.hp1 HG00609.hp1 HG01099.hp2 others(7): Show |
intron_variant | MODIFIER | c.156+2155_156+2168d others(16): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431992 | ||||||
| chr3:100431992 | TTATATAT others(9): Show |
T | 21 | a0002c0002t0001g0002 a0002c0002t0001g0005 a0002c0002t0001g0008 others(18): Show |
24 | HG00741.hp1 HG01169.hp1 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.156+2153_156+2168d others(18): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431992 | ||||||
| chr3:100431992 | TTATATAT others(11): Show |
T | 4 | a0002c0002t0001g0157 a0002c0002t0001g0171 a0002c0002t0001g0175 others(1): Show |
4 | HG01070.hp1 HG01168.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.156+2151_156+2168d others(20): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431992 | ||||||
| chr3:100431992 | TTATATAT others(13): Show |
T | 8 | a0002c0002t0001g0023 a0002c0002t0001g0062 a0002c0002t0001g0155 others(5): Show |
8 | HG01175.hp1 HG01243.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.156+2149_156+2168d others(22): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431992 | ||||||
| chr3:100431992 | TTATATAT others(15): Show |
T | 2 | a0002c0002t0001g0060 a0002c0002t0003g0104 |
2 | NA18945.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.156+2147_156+2168d others(24): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431992 | ||||||
| chr3:100431992 | TTATATAT others(19): Show |
T | 1 | a0002c0002t0004g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.156+2143_156+2168d others(28): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431992 | ||||||
| chr3:100431992 | TTATATAT others(21): Show |
T | 1 | a0002c0002t0003g0129 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.156+2141_156+2168d others(30): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431992 | ||||||
| chr3:100431992 | TTATATAT others(23): Show |
T | 1 | a0002c0002t0001g0008 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.156+2139_156+2168d others(32): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431992 | ||||||
| chr3:100431992 | TTATATAT others(25): Show |
T | 4 | a0002c0002t0001g0241 a0002c0002t0001g0243 a0002c0002t0001g0248 others(1): Show |
4 | HG02647.hp1 HG02818.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.156+2137_156+2168d others(34): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431992 | ||||||
| chr3:100431992 | TTATATAT others(27): Show |
T | 1 | a0002c0003t0010g0195 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.156+2135_156+2168d others(36): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431992 | ||||||
| chr3:100431992 | TTATATAT others(29): Show |
T | 1 | a0002c0002t0001g0272 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.156+2133_156+2168d others(38): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431992 | ||||||
| chr3:100431992 | TTATATAT others(35): Show |
T | 57 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(54): Show |
64 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.156+2127_156+2168d others(44): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431992 | ||||||
| chr3:100431992 | TTATATAT others(41): Show |
T | 7 | a0001c0001t0005g0072 a0001c0001t0005g0281 a0001c0001t0005g0282 others(4): Show |
7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.156+2121_156+2168d others(50): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100431992 | ||||||
| chr3:100432000 | ATATATAT others(32): Show |
A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0357 a0001c0001t0001g0358 |
4 | HG01243.hp2 HG02055.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.156+2116_156+2154d others(41): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100432000 | |||||||
| chr3:100432140 | C | T | 57 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(54): Show |
64 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.156+2255C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100432140 | |||||||
| chr3:100432141 | CT | C | 57 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(54): Show |
64 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.156+2258delT | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100432141 | ||||||
| chr3:100432255 | T | A | 1 | a0002c0002t0001g0174 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.156+2370T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100432255 | |||||||
| chr3:100432285 | CT | C | 45 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(42): Show |
51 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.156+2407delT | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100432285 | ||||||
| chr3:100432311 | G | T | 2 | a0001c0001t0001g0219 a0001c0001t0001g0221 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.156+2426G>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100432311 | |||||||
| chr3:100432322 | T | C | 57 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(54): Show |
64 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.156+2437T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100432322 | |||||||
| chr3:100432600 | T | G | 1 | a0001c0001t0001g0188 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.156+2715T>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100432600 | |||||||
| chr3:100432643 | A | G | 57 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(54): Show |
64 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.156+2758A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100432643 | |||||||
| chr3:100432666 | A | G | 57 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(54): Show |
64 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.156+2781A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100432666 | |||||||
| chr3:100432669 | A | G | 6 | a0002c0002t0004g0027 a0002c0002t0004g0074 a0002c0002t0004g0075 others(3): Show |
6 | HG02145.hp1 HG03041.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.156+2784A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100432669 | |||||||
| chr3:100433096 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.156+3211C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100433096 | |||||||
| chr3:100433114 | G | A | 57 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(54): Show |
64 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.156+3229G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100433114 | |||||||
| chr3:100433178 | C | A | 57 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(54): Show |
64 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.156+3293C>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100433178 | |||||||
| chr3:100433250 | G | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0357 a0001c0001t0001g0358 |
4 | HG01243.hp2 HG02055.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.156+3365G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100433250 | |||||||
| chr3:100433263 | C | T | 1 | a0002c0002t0003g0126 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.156+3378C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100433263 | |||||||
| chr3:100433353 | G | A | 9 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0024 others(6): Show |
11 | HG01952.hp2 HG02055.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.156+3468G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100433353 | |||||||
| chr3:100433396 | T | A | 1 | a0001c0001t0002g0323 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.156+3511T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100433396 | |||||||
| chr3:100433493 | T | C | 4 | a0001c0001t0002g0319 a0001c0001t0002g0320 a0001c0001t0002g0326 others(1): Show |
4 | HG00099.hp2 HG00140.hp2 HG01192.hp2 others(1): Show |
intron_variant | MODIFIER | c.156+3608T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100433493 | |||||||
| chr3:100433587 | G | A | 19 | a0001c0001t0001g0051 a0002c0002t0001g0002 a0002c0002t0001g0005 others(16): Show |
27 | HG00558.hp1 HG00609.hp1 HG01928.hp2 others(24): Show |
intron_variant | MODIFIER | c.156+3702G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100433587 | |||||||
| chr3:100433641 | A | G | 45 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(42): Show |
51 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.156+3756A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100433641 | |||||||
| chr3:100433730 | G | A | 8 | a0001c0001t0001g0013 a0001c0001t0001g0073 a0001c0001t0001g0141 others(5): Show |
9 | HG02109.hp2 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.156+3845G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100433730 | |||||||
| chr3:100433767 | G | A | 1 | a0001c0004t0004g0193 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.156+3882G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100433767 | |||||||
| chr3:100433778 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.156+3893T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100433778 | |||||||
| chr3:100433827 | C | T | 1 | a0002c0002t0001g0155 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.156+3942C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100433827 | |||||||
| chr3:100433933 | T | C | 1 | a0002c0002t0001g0048 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.156+4048T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100433933 | |||||||
| chr3:100433962 | T | C | 60 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(57): Show |
68 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.156+4077T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100433962 | |||||||
| chr3:100433986 | T | C | 1 | a0001c0001t0002g0302 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.156+4101T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100433986 | |||||||
| chr3:100434014 | T | C | 2 | a0002c0002t0001g0232 a0002c0002t0002g0352 |
2 | HG00735.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.156+4129T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100434014 | |||||||
| chr3:100434022 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.156+4137T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100434022 | |||||||
| chr3:100434142 | C | T | 1 | a0002c0002t0003g0123 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.156+4257C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100434142 | |||||||
| chr3:100434226 | C | T | 61 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(58): Show |
69 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.156+4341C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100434226 | |||||||
| chr3:100434428 | T | C | 1 | a0001c0001t0002g0323 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.156+4543T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100434428 | |||||||
| chr3:100434477 | C | A | 45 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(42): Show |
51 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.156+4592C>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100434477 | |||||||
| chr3:100434673 | C | T | 4 | a0002c0002t0001g0017 a0002c0002t0001g0148 a0002c0002t0001g0233 others(1): Show |
5 | HG00735.hp1 HG01975.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.156+4788C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100434673 | |||||||
| chr3:100434780 | C | T | 2 | a0002c0002t0001g0260 a0002c0002t0001g0263 |
2 | HG02976.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.156+4895C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100434780 | |||||||
| chr3:100434785 | T | C | 2 | a0001c0001t0001g0013 a0001c0001t0001g0143 |
3 | HG02109.hp2 HG02630.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.156+4900T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100434785 | |||||||
| chr3:100434825 | G | A | 1 | a0001c0004t0004g0193 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.156+4940G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100434825 | |||||||
| chr3:100434831 | CT | C | 159 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(156): Show |
174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.156+4963delT | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100434831 | ||||||
| chr3:100434848 | T | A | 55 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(52): Show |
62 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.156+4963T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100434848 | |||||||
| chr3:100434912 | A | G | 2 | a0002c0002t0004g0139 a0002c0002t0004g0140 |
2 | HG01099.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.156+5027A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100434912 | |||||||
| chr3:100435022 | C | T | 2 | a0002c0002t0003g0095 a0002c0002t0003g0135 |
2 | HG02257.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.156+5137C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100435022 | |||||||
| chr3:100435024 | C | G | 1 | a0002c0002t0012g0291 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.156+5139C>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100435024 | |||||||
| chr3:100435078 | TTGTATTT others(4): Show |
T | 1 | a0001c0001t0002g0341 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.156+5207_156+5217d others(13): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100435078 | ||||||
| chr3:100435231 | C | G | 61 | a0002c0002t0001g0011 a0002c0002t0001g0034 a0002c0002t0001g0043 others(58): Show |
70 | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.156+5346C>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100435231 | |||||||
| chr3:100435273 | T | C | 329 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(326): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.156+5388T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100435273 | |||||||
| chr3:100435317 | G | T | 55 | a0001c0001t0001g0051 a0002c0002t0001g0002 a0002c0002t0001g0005 others(52): Show |
63 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.156+5432G>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100435317 | |||||||
| chr3:100435336 | A | C | 1 | a0001c0004t0004g0193 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.156+5451A>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100435336 | |||||||
| chr3:100435555 | A | G | 57 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(54): Show |
64 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.156+5670A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100435555 | |||||||
| chr3:100435640 | G | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0032 |
2 | NA18965.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.156+5755G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100435640 | |||||||
| chr3:100435677 | G | A | 12 | a0002c0002t0004g0027 a0002c0002t0004g0074 a0002c0002t0004g0075 others(9): Show |
12 | HG01099.hp1 HG02145.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.156+5792G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100435677 | |||||||
| chr3:100435861 | A | G | 1 | a0002c0002t0001g0176 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.156+5976A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100435861 | |||||||
| chr3:100435960 | G | T | 1 | a0002c0002t0001g0279 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.156+6075G>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100435960 | |||||||
| chr3:100436072 | T | C | 1 | a0002c0003t0010g0195 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.156+6187T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100436072 | |||||||
| chr3:100436194 | G | A | 3 | a0001c0001t0001g0022 a0001c0001t0001g0357 a0001c0001t0001g0358 |
4 | HG01243.hp2 HG02055.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.156+6309G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100436194 | |||||||
| chr3:100436329 | T | C | 3 | a0001c0001t0001g0022 a0001c0001t0001g0357 a0001c0001t0001g0358 |
4 | HG01243.hp2 HG02055.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.156+6444T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100436329 | |||||||
| chr3:100436338 | C | A | 1 | a0002c0002t0003g0124 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.156+6453C>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100436338 | |||||||
| chr3:100436396 | G | A | 1 | a0001c0001t0002g0322 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.156+6511G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100436396 | |||||||
| chr3:100436445 | C | T | 3 | a0001c0001t0001g0225 a0001c0001t0002g0346 a0001c0001t0002g0348 |
3 | NA18950.hp2 NA18983.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.156+6560C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100436445 | |||||||
| chr3:100436446 | G | A | 2 | a0001c0001t0001g0061 a0001c0001t0001g0220 |
2 | HG02257.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.156+6561G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100436446 | |||||||
| chr3:100436569 | T | A | 7 | a0001c0001t0005g0072 a0001c0001t0005g0281 a0001c0001t0005g0282 others(4): Show |
7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.156+6684T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100436569 | |||||||
| chr3:100436682 | T | C | 2 | a0002c0002t0003g0095 a0002c0002t0003g0135 |
2 | HG02257.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.156+6797T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100436682 | |||||||
| chr3:100436703 | A | G | 8 | a0001c0001t0001g0013 a0001c0001t0001g0073 a0001c0001t0001g0141 others(5): Show |
9 | HG02109.hp2 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.156+6818A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100436703 | |||||||
| chr3:100436810 | T | C | 8 | a0001c0001t0001g0013 a0001c0001t0001g0073 a0001c0001t0001g0141 others(5): Show |
9 | HG02109.hp2 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.156+6925T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100436810 | |||||||
| chr3:100436853 | G | A | 8 | a0001c0001t0001g0013 a0001c0001t0001g0073 a0001c0001t0001g0141 others(5): Show |
9 | HG02109.hp2 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.156+6968G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100436853 | |||||||
| chr3:100436904 | C | G | 1 | a0001c0001t0001g0144 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.156+7019C>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100436904 | |||||||
| chr3:100436923 | T | A | 8 | a0001c0001t0001g0013 a0001c0001t0001g0073 a0001c0001t0001g0141 others(5): Show |
9 | HG02109.hp2 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.156+7038T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100436923 | |||||||
| chr3:100436924 | A | T | 1 | a0001c0001t0001g0215 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.156+7039A>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100436924 | |||||||
| chr3:100436943 | G | A | 2 | a0002c0002t0002g0292 a0002c0002t0002g0330 |
2 | HG01361.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.156+7058G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100436943 | |||||||
| chr3:100437225 | T | C | 1 | a0002c0002t0003g0362 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.156+7340T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100437225 | |||||||
| chr3:100437693 | T | C | 8 | a0001c0001t0001g0013 a0001c0001t0001g0073 a0001c0001t0001g0141 others(5): Show |
9 | HG02109.hp2 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.156+7808T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100437693 | |||||||
| chr3:100437860 | A | G | 80 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(77): Show |
88 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.156+7975A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100437860 | |||||||
| chr3:100437879 | C | A | 7 | a0002c0002t0003g0097 a0002c0002t0003g0115 a0002c0002t0003g0116 others(4): Show |
7 | HG01123.hp1 HG01175.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.156+7994C>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100437879 | |||||||
| chr3:100437956 | G | A | 7 | a0001c0001t0005g0072 a0001c0001t0005g0281 a0001c0001t0005g0282 others(4): Show |
7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.156+8071G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100437956 | |||||||
| chr3:100438172 | A | G | 10 | a0002c0002t0004g0027 a0002c0002t0004g0074 a0002c0002t0004g0075 others(7): Show |
10 | HG02145.hp1 HG02615.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.156+8287A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100438172 | |||||||
| chr3:100438214 | A | T | 1 | a0001c0001t0001g0071 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.156+8329A>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100438214 | |||||||
| chr3:100438288 | T | G | 329 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(326): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.156+8403T>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100438288 | |||||||
| chr3:100438684 | A | G | 8 | a0001c0001t0001g0013 a0001c0001t0001g0073 a0001c0001t0001g0141 others(5): Show |
9 | HG02109.hp2 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.156+8799A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100438684 | |||||||
| chr3:100438744 | A | C | 2 | a0001c0001t0001g0219 a0001c0001t0001g0221 |
2 | HG02818.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.156+8859A>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100438744 | |||||||
| chr3:100438869 | G | C | 2 | a0001c0001t0003g0133 a0001c0001t0003g0134 |
2 | HG03927.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.156+8984G>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100438869 | |||||||
| chr3:100438874 | G | A | 1 | a0001c0001t0001g0070 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.156+8989G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100438874 | |||||||
| chr3:100438917 | T | C | 1 | a0002c0002t0001g0043 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.156+9032T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100438917 | |||||||
| chr3:100438938 | G | A | 2 | a0001c0001t0001g0064 a0001c0001t0001g0065 |
2 | HG01346.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.156+9053G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100438938 | |||||||
| chr3:100438940 | G | T | 5 | a0002c0002t0001g0017 a0002c0002t0001g0148 a0002c0002t0001g0233 others(2): Show |
6 | HG00735.hp1 HG01975.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.156+9055G>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100438940 | |||||||
| chr3:100438982 | A | AT | 45 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(42): Show |
51 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.156+9103dupT | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100438982 | ||||||
| chr3:100438991 | G | A | 7 | a0001c0001t0005g0072 a0001c0001t0005g0281 a0001c0001t0005g0282 others(4): Show |
7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.156+9106G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100438991 | |||||||
| chr3:100439000 | C | T | 8 | a0001c0001t0001g0013 a0001c0001t0001g0073 a0001c0001t0001g0141 others(5): Show |
9 | HG02109.hp2 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.156+9115C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100439000 | |||||||
| chr3:100439063 | C | T | 1 | a0001c0001t0002g0359 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.156+9178C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100439063 | |||||||
| chr3:100439129 | A | G | 8 | a0001c0001t0001g0013 a0001c0001t0001g0073 a0001c0001t0001g0141 others(5): Show |
9 | HG02109.hp2 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.156+9244A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100439129 | |||||||
| chr3:100439160 | T | C | 4 | a0001c0001t0001g0013 a0001c0001t0001g0141 a0001c0001t0001g0143 others(1): Show |
5 | HG02109.hp2 HG02630.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.156+9275T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100439160 | |||||||
| chr3:100439238 | A | G | 4 | a0002c0002t0004g0074 a0002c0002t0004g0075 a0002c0002t0004g0076 others(1): Show |
4 | HG02145.hp1 HG03041.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.156+9353A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100439238 | |||||||
| chr3:100439251 | T | A | 1 | a0002c0002t0003g0120 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.156+9366T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100439251 | |||||||
| chr3:100439267 | C | T | 8 | a0001c0001t0001g0013 a0001c0001t0001g0073 a0001c0001t0001g0141 others(5): Show |
9 | HG02109.hp2 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.156+9382C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100439267 | |||||||
| chr3:100439268 | G | A | 1 | a0001c0001t0002g0342 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.156+9383G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100439268 | |||||||
| chr3:100439277 | TAA | T | 8 | a0001c0001t0001g0013 a0001c0001t0001g0073 a0001c0001t0001g0141 others(5): Show |
9 | HG02109.hp2 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.156+9402_156+9403d others(4): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100439277 | ||||||
| chr3:100439340 | C | T | 8 | a0001c0001t0001g0013 a0001c0001t0001g0073 a0001c0001t0001g0141 others(5): Show |
9 | HG02109.hp2 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.156+9455C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100439340 | |||||||
| chr3:100439346 | T | C | 3 | a0001c0001t0001g0022 a0001c0001t0001g0357 a0001c0001t0001g0358 |
4 | HG01243.hp2 HG02055.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.156+9461T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100439346 | |||||||
| chr3:100439490 | T | G | 1 | a0002c0002t0013g0096 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.156+9605T>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100439490 | |||||||
| chr3:100439556 | C | T | 1 | a0002c0002t0012g0291 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.156+9671C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100439556 | |||||||
| chr3:100439558 | T | C | 73 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(70): Show |
81 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.156+9673T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100439558 | |||||||
| chr3:100439562 | G | A | 8 | a0001c0001t0001g0013 a0001c0001t0001g0073 a0001c0001t0001g0141 others(5): Show |
9 | HG02109.hp2 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.156+9677G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100439562 | |||||||
| chr3:100439610 | C | T | 8 | a0001c0001t0001g0013 a0001c0001t0001g0073 a0001c0001t0001g0141 others(5): Show |
9 | HG02109.hp2 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.156+9725C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100439610 | |||||||
| chr3:100439849 | G | A | 20 | a0001c0001t0001g0013 a0001c0001t0001g0073 a0001c0001t0001g0141 others(17): Show |
21 | HG01099.hp1 HG02109.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.156+9964G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100439849 | |||||||
| chr3:100439868 | T | C | 20 | a0001c0001t0001g0013 a0001c0001t0001g0073 a0001c0001t0001g0141 others(17): Show |
21 | HG01099.hp1 HG02109.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.156+9983T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100439868 | |||||||
| chr3:100440257 | A | T | 9 | a0002c0002t0001g0017 a0002c0002t0001g0037 a0002c0002t0001g0148 others(6): Show |
10 | HG00735.hp1 HG01106.hp1 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.156+10372A>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100440257 | |||||||
| chr3:100440390 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.156+10505T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100440390 | |||||||
| chr3:100440489 | C | T | 1 | a0001c0001t0002g0328 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.156+10604C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100440489 | |||||||
| chr3:100440842 | A | C | 61 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(58): Show |
68 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.157-10877A>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100440842 | |||||||
| chr3:100440916 | C | G | 1 | a0001c0001t0001g0188 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.157-10803C>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100440916 | |||||||
| chr3:100440924 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.157-10795T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100440924 | |||||||
| chr3:100440973 | G | A | 45 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(42): Show |
51 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.157-10746G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100440973 | |||||||
| chr3:100441052 | G | C | 1 | a0002c0002t0003g0113 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.157-10667G>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100441052 | |||||||
| chr3:100441064 | A | C | 45 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(42): Show |
51 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.157-10655A>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100441064 | |||||||
| chr3:100441123 | G | C | 13 | a0001c0004t0004g0193 a0002c0002t0004g0027 a0002c0002t0004g0074 others(10): Show |
13 | HG01099.hp1 HG02145.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.157-10596G>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100441123 | |||||||
| chr3:100441337 | G | A | 12 | a0002c0002t0004g0027 a0002c0002t0004g0074 a0002c0002t0004g0075 others(9): Show |
12 | HG01099.hp1 HG02145.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.157-10382G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100441337 | |||||||
| chr3:100441356 | G | C | 1 | a0002c0002t0011g0138 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.157-10363G>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100441356 | |||||||
| chr3:100441450 | A | G | 3 | a0001c0004t0004g0193 a0002c0002t0003g0095 a0002c0002t0003g0135 |
3 | HG02257.hp2 HG02615.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.157-10269A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100441450 | |||||||
| chr3:100441461 | T | C | 1 | a0001c0001t0002g0345 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.157-10258T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100441461 | |||||||
| chr3:100441631 | A | AAT | 3 | a0002c0002t0001g0196 a0002c0002t0001g0236 a0002c0002t0003g0136 |
3 | HG01175.hp2 HG02258.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.157-10069_157-1006 others(6): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100441631 | ||||||
| chr3:100441631 | AAT | A | 129 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0020 others(126): Show |
142 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(139): Show |
intron_variant | MODIFIER | c.157-10069_157-1006 others(6): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100441631 | ||||||
| chr3:100441631 | AATAT | A | 158 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(155): Show |
171 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(168): Show |
intron_variant | MODIFIER | c.157-10071_157-1006 others(8): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100441631 | ||||||
| chr3:100441697 | C | G | 3 | a0001c0001t0001g0022 a0001c0001t0001g0357 a0001c0001t0001g0358 |
4 | HG01243.hp2 HG02055.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.157-10022C>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100441697 | |||||||
| chr3:100441722 | G | A | 1 | a0002c0003t0010g0195 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.157-9997G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100441722 | |||||||
| chr3:100442291 | A | ATGTGAAC others(1): Show |
6 | a0001c0001t0001g0197 a0001c0001t0001g0198 a0001c0001t0001g0201 others(3): Show |
6 | NA18946.hp2 NA18947.hp2 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.157-9427_157-9420d others(10): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100442291 | ||||||
| chr3:100442362 | G | A | 1 | a0001c0001t0001g0355 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.157-9357G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100442362 | |||||||
| chr3:100442401 | G | C | 1 | a0002c0002t0003g0125 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.157-9318G>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100442401 | |||||||
| chr3:100442557 | T | C | 1 | a0001c0001t0001g0229 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.157-9162T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100442557 | |||||||
| chr3:100442775 | T | A | 3 | a0002c0002t0001g0259 a0002c0002t0003g0095 a0002c0002t0003g0135 |
3 | HG02257.hp2 HG02717.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.157-8944T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100442775 | |||||||
| chr3:100442927 | C | T | 10 | a0002c0002t0004g0027 a0002c0002t0004g0074 a0002c0002t0004g0075 others(7): Show |
10 | HG02145.hp1 HG02615.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.157-8792C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100442927 | |||||||
| chr3:100442935 | A | G | 4 | a0001c0001t0001g0056 a0001c0001t0001g0225 a0001c0001t0002g0346 others(1): Show |
4 | HG03688.hp1 NA18950.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.157-8784A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100442935 | |||||||
| chr3:100443014 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.157-8705A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100443014 | |||||||
| chr3:100443027 | C | T | 4 | a0002c0002t0001g0240 a0002c0002t0001g0246 a0002c0002t0001g0278 others(1): Show |
4 | HG02040.hp2 HG02083.hp2 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.157-8692C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100443027 | |||||||
| chr3:100443038 | T | C | 2 | a0002c0002t0003g0095 a0002c0002t0003g0135 |
2 | HG02257.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.157-8681T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100443038 | |||||||
| chr3:100443123 | G | A | 2 | a0002c0002t0004g0139 a0002c0002t0004g0140 |
2 | HG01099.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.157-8596G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100443123 | |||||||
| chr3:100443173 | T | C | 45 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(42): Show |
51 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.157-8546T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100443173 | |||||||
| chr3:100443402 | G | A | 1 | a0001c0004t0004g0193 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.157-8317G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100443402 | |||||||
| chr3:100443511 | TTAA | T | 8 | a0001c0001t0001g0013 a0001c0001t0001g0073 a0001c0001t0001g0141 others(5): Show |
9 | HG02109.hp2 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.157-8207_157-8205d others(5): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100443511 | |||||||
| chr3:100443533 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.157-8186C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100443533 | |||||||
| chr3:100443534 | G | A | 1 | a0002c0002t0004g0027 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.157-8185G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100443534 | |||||||
| chr3:100443547 | T | G | 3 | a0002c0002t0001g0048 a0002c0002t0001g0049 a0002c0002t0001g0057 |
3 | HG00558.hp1 HG00609.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.157-8172T>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100443547 | |||||||
| chr3:100443652 | C | T | 1 | a0002c0002t0001g0187 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.157-8067C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100443652 | |||||||
| chr3:100443912 | T | C | 8 | a0001c0001t0001g0013 a0001c0001t0001g0073 a0001c0001t0001g0141 others(5): Show |
9 | HG02109.hp2 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.157-7807T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100443912 | |||||||
| chr3:100444037 | A | T | 175 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(172): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(186): Show |
intron_variant | MODIFIER | c.157-7682A>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100444037 | |||||||
| chr3:100444176 | T | A | 2 | a0002c0002t0003g0095 a0002c0002t0003g0135 |
2 | HG02257.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.157-7543T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100444176 | |||||||
| chr3:100444203 | C | A | 1 | a0001c0001t0002g0021 | 2 | NA18960.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.157-7516C>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100444203 | |||||||
| chr3:100444273 | C | A | 1 | a0001c0001t0001g0188 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.157-7446C>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100444273 | |||||||
| chr3:100444563 | T | A | 8 | a0001c0001t0001g0013 a0001c0001t0001g0073 a0001c0001t0001g0141 others(5): Show |
9 | HG02109.hp2 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.157-7156T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100444563 | |||||||
| chr3:100444593 | A | T | 1 | a0001c0001t0001g0069 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.157-7126A>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100444593 | |||||||
| chr3:100444672 | A | G | 1 | a0001c0001t0002g0363 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.157-7047A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100444672 | |||||||
| chr3:100444755 | C | A | 7 | a0001c0001t0005g0072 a0001c0001t0005g0281 a0001c0001t0005g0282 others(4): Show |
7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.157-6964C>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100444755 | |||||||
| chr3:100444860 | A | G | 2 | a0002c0002t0003g0095 a0002c0002t0003g0135 |
2 | HG02257.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.157-6859A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100444860 | |||||||
| chr3:100445194 | C | A | 42 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(39): Show |
48 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.157-6525C>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100445194 | |||||||
| chr3:100445417 | A | G | 102 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(99): Show |
109 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.157-6302A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100445417 | |||||||
| chr3:100445572 | G | A | 12 | a0002c0002t0004g0027 a0002c0002t0004g0074 a0002c0002t0004g0075 others(9): Show |
12 | HG01099.hp1 HG02145.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.157-6147G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100445572 | |||||||
| chr3:100445678 | A | T | 1 | a0001c0001t0001g0068 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.157-6041A>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100445678 | |||||||
| chr3:100445793 | C | T | 351 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(348): Show |
386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.157-5926C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100445793 | |||||||
| chr3:100445906 | C | T | 99 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(96): Show |
105 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.157-5813C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100445906 | |||||||
| chr3:100446005 | G | A | 9 | a0001c0001t0001g0013 a0001c0001t0001g0073 a0001c0001t0001g0141 others(6): Show |
10 | HG00140.hp1 HG02109.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.157-5714G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100446005 | |||||||
| chr3:100446155 | A | C | 7 | a0001c0001t0005g0072 a0001c0001t0005g0281 a0001c0001t0005g0282 others(4): Show |
7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.157-5564A>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100446155 | |||||||
| chr3:100446278 | G | A | 9 | a0002c0002t0001g0017 a0002c0002t0001g0037 a0002c0002t0001g0148 others(6): Show |
10 | HG00735.hp1 HG01106.hp1 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.157-5441G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100446278 | |||||||
| chr3:100446316 | C | A | 99 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(96): Show |
105 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.157-5403C>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100446316 | |||||||
| chr3:100446341 | A | C | 1 | a0001c0001t0001g0252 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.157-5378A>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100446341 | |||||||
| chr3:100446347 | A | G | 1 | a0001c0001t0001g0252 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.157-5372A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100446347 | |||||||
| chr3:100446365 | A | C | 2 | a0002c0002t0001g0150 a0002c0002t0001g0151 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.157-5354A>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100446365 | |||||||
| chr3:100446406 | G | A | 2 | a0002c0002t0003g0095 a0002c0002t0003g0135 |
2 | HG02257.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.157-5313G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100446406 | |||||||
| chr3:100446546 | A | G | 1 | a0001c0001t0001g0205 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.157-5173A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100446546 | |||||||
| chr3:100446578 | AC | A | 8 | a0001c0001t0001g0013 a0001c0001t0001g0073 a0001c0001t0001g0141 others(5): Show |
9 | HG02109.hp2 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.157-5140delC | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100446578 | |||||||
| chr3:100446694 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.157-5025C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100446694 | |||||||
| chr3:100446715 | A | C | 1 | a0001c0001t0002g0359 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.157-5004A>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100446715 | |||||||
| chr3:100446781 | G | C | 1 | a0001c0001t0001g0188 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.157-4938G>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100446781 | |||||||
| chr3:100446861 | C | A | 1 | a0001c0001t0001g0035 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.157-4858C>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100446861 | |||||||
| chr3:100446995 | TTGG | T | 13 | a0001c0004t0004g0193 a0002c0002t0004g0027 a0002c0002t0004g0074 others(10): Show |
13 | HG01099.hp1 HG02145.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.157-4720_157-4718d others(5): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100446995 | ||||||
| chr3:100447031 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.157-4688G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100447031 | |||||||
| chr3:100447061 | A | G | 45 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(42): Show |
51 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.157-4658A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100447061 | |||||||
| chr3:100447262 | T | C | 1 | a0002c0002t0003g0087 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.157-4457T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100447262 | |||||||
| chr3:100447368 | A | G | 7 | a0002c0002t0003g0097 a0002c0002t0003g0115 a0002c0002t0003g0116 others(4): Show |
7 | HG01123.hp1 HG01175.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.157-4351A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100447368 | |||||||
| chr3:100447391 | T | A | 1 | a0001c0001t0001g0188 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.157-4328T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100447391 | |||||||
| chr3:100447391 | T | C | 27 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(24): Show |
31 | HG00642.hp1 HG01074.hp1 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.157-4328T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100447391 | |||||||
| chr3:100447432 | C | T | 1 | a0002c0002t0001g0241 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.157-4287C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100447432 | |||||||
| chr3:100447503 | G | A | 302 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(299): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.157-4216G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100447503 | |||||||
| chr3:100447614 | TA | T | 117 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(114): Show |
125 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.157-4095delA | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100447614 | ||||||
| chr3:100448098 | A | AGATT | 205 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(202): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.157-3621_157-3620i others(6): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100448098 | |||||||
| chr3:100448130 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.157-3589C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100448130 | |||||||
| chr3:100448131 | G | A | 9 | a0002c0002t0001g0017 a0002c0002t0001g0037 a0002c0002t0001g0148 others(6): Show |
10 | HG00735.hp1 HG01106.hp1 HG01975.hp1 others(7): Show |
intron_variant | MODIFIER | c.157-3588G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100448131 | |||||||
| chr3:100448158 | AACTGAGA others(21): Show |
A | 1 | a0001c0001t0001g0188 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.157-3555_157-3528d others(30): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100448158 | ||||||
| chr3:100448802 | C | T | 1 | a0001c0001t0002g0311 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.157-2917C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100448802 | |||||||
| chr3:100448865 | G | GT | 6 | a0001c0001t0001g0208 a0001c0001t0001g0217 a0001c0001t0001g0226 others(3): Show |
6 | HG03927.hp2 HG04184.hp1 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.157-2846dupT | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100448865 | ||||||
| chr3:100448952 | A | G | 189 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(186): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.157-2767A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100448952 | |||||||
| chr3:100448999 | A | G | 1 | a0001c0001t0001g0358 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.157-2720A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100448999 | |||||||
| chr3:100449007 | A | G | 359 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(356): Show |
394 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(391): Show |
intron_variant | MODIFIER | c.157-2712A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100449007 | |||||||
| chr3:100449144 | C | T | 27 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(24): Show |
31 | HG00642.hp1 HG01074.hp1 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.157-2575C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100449144 | |||||||
| chr3:100449241 | A | G | 3 | a0001c0001t0002g0293 a0001c0001t0002g0302 a0001c0001t0002g0303 |
3 | HG00741.hp2 HG02738.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.157-2478A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100449241 | |||||||
| chr3:100449248 | CT | C | 103 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(100): Show |
109 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.157-2458delT | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100449248 | ||||||
| chr3:100449386 | G | A | 1 | a0001c0001t0001g0019 | 2 | HG00673.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.157-2333G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100449386 | |||||||
| chr3:100449468 | C | T | 1 | a0001c0001t0002g0293 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.157-2251C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100449468 | |||||||
| chr3:100449469 | G | A | 1 | a0002c0002t0003g0091 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.157-2250G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100449469 | |||||||
| chr3:100449729 | C | T | 3 | a0001c0001t0001g0022 a0001c0001t0001g0357 a0001c0001t0001g0358 |
4 | HG01243.hp2 HG02055.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.157-1990C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100449729 | |||||||
| chr3:100449832 | T | C | 1 | a0002c0002t0001g0240 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.157-1887T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100449832 | |||||||
| chr3:100449921 | C | T | 1 | a0002c0002t0001g0272 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.157-1798C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100449921 | |||||||
| chr3:100450089 | C | CT | 14 | a0002c0002t0001g0196 a0002c0002t0001g0243 a0002c0002t0001g0260 others(11): Show |
14 | HG01123.hp1 HG01175.hp2 HG01516.hp1 others(11): Show |
intron_variant | MODIFIER | c.157-1612dupT | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100450089 | ||||||
| chr3:100450089 | CTT | C | 11 | a0001c0004t0004g0193 a0002c0002t0004g0027 a0002c0002t0004g0074 others(8): Show |
11 | HG02145.hp1 HG02615.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.157-1613_157-1612d others(4): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100450089 | ||||||
| chr3:100450089 | CTTTT | C | 158 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(155): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.157-1615_157-1612d others(6): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100450089 | ||||||
| chr3:100450117 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.157-1602G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100450117 | |||||||
| chr3:100450247 | T | TA | 3 | a0001c0001t0001g0022 a0001c0001t0001g0357 a0001c0001t0001g0358 |
4 | HG01243.hp2 HG02055.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.157-1465dupA | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100450247 | ||||||
| chr3:100450249 | A | AAAAAACA others(13): Show |
7 | a0001c0001t0005g0072 a0001c0001t0005g0281 a0001c0001t0005g0282 others(4): Show |
7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.157-1468_157-1449d others(22): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100450249 | ||||||
| chr3:100450332 | AT | A | 12 | a0001c0001t0001g0056 a0001c0001t0001g0213 a0001c0001t0001g0215 others(9): Show |
12 | HG01106.hp1 HG01934.hp2 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.157-1369delT | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100450332 | ||||||
| chr3:100450426 | T | C | 178 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(175): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.157-1293T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100450426 | |||||||
| chr3:100450584 | G | A | 1 | a0002c0002t0003g0118 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.157-1135G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100450584 | |||||||
| chr3:100450678 | A | C | 18 | a0001c0001t0001g0013 a0001c0001t0001g0022 a0001c0001t0001g0073 others(15): Show |
20 | HG01243.hp2 HG02055.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.157-1041A>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100450678 | |||||||
| chr3:100450828 | T | A | 1 | a0001c0001t0001g0214 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.157-891T>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100450828 | |||||||
| chr3:100450882 | A | AAAAT | 8 | a0001c0001t0001g0013 a0001c0001t0001g0073 a0001c0001t0001g0141 others(5): Show |
9 | HG02109.hp2 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.157-819_157-816dup others(4): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100450882 | ||||||
| chr3:100450902 | TAGAG | T | 4 | a0002c0002t0001g0037 a0002c0002t0001g0185 a0002c0002t0001g0186 others(1): Show |
4 | HG01106.hp1 HG02809.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.157-808_157-805del others(4): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 100450902 | ||||||
| chr3:100451187 | A | C | 1 | a0001c0001t0001g0225 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.157-532A>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100451187 | |||||||
| chr3:100451280 | C | T | 1 | a0002c0002t0012g0291 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.157-439C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100451280 | |||||||
| chr3:100451313 | C | T | 1 | a0001c0001t0001g0209 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.157-406C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100451313 | |||||||
| chr3:100451389 | A | G | 7 | a0001c0001t0005g0072 a0001c0001t0005g0281 a0001c0001t0005g0282 others(4): Show |
7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.157-330A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100451389 | |||||||
| chr3:100451423 | T | G | 1 | a0001c0001t0002g0318 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.157-296T>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100451423 | |||||||
| chr3:100451614 | A | G | 1 | a0002c0002t0001g0244 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.157-105A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100451614 | |||||||
| chr3:100451709 | G | A | 54 | a0002c0002t0001g0002 a0002c0002t0001g0005 a0002c0002t0001g0008 others(51): Show |
62 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.157-10G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 2/3 | chr3 | 100451709 | |||||||
| chr3:100451981 | G | A | 200 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(197): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.387+32G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100451981 | |||||||
| chr3:100452147 | G | A | 10 | a0002c0002t0004g0027 a0002c0002t0004g0074 a0002c0002t0004g0075 others(7): Show |
10 | HG02145.hp1 HG02615.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.387+198G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100452147 | |||||||
| chr3:100452202 | C | CT | 81 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(78): Show |
87 | HG00438.hp1 HG00544.hp1 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.387+271dupT | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 100452202 | ||||||
| chr3:100452202 | C | CTT | 19 | a0001c0001t0006g0223 a0002c0002t0001g0018 a0002c0002t0001g0047 others(16): Show |
20 | HG00423.hp1 HG00642.hp2 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.387+270_387+271dup others(2): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 100452202 | ||||||
| chr3:100452202 | CT | C | 6 | a0001c0001t0001g0051 a0001c0001t0001g0234 a0001c0004t0004g0193 others(3): Show |
6 | HG01169.hp1 HG02015.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.387+271delT | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 100452202 | ||||||
| chr3:100452206 | T | C | 2 | a0002c0002t0001g0005 a0002c0002t0001g0054 |
4 | NA18961.hp2 NA18966.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.387+257T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100452206 | |||||||
| chr3:100452333 | G | T | 8 | a0001c0001t0001g0013 a0001c0001t0001g0073 a0001c0001t0001g0141 others(5): Show |
9 | HG02109.hp2 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.387+384G>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100452333 | |||||||
| chr3:100452397 | G | A | 8 | a0001c0001t0001g0013 a0001c0001t0001g0073 a0001c0001t0001g0141 others(5): Show |
9 | HG02109.hp2 HG02280.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.387+448G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100452397 | |||||||
| chr3:100452629 | C | CTAG | 3 | a0002c0002t0004g0154 a0002c0002t0004g0182 a0002c0002t0008g0156 |
3 | HG02615.hp2 HG02717.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.387+681_387+682ins others(3): Show |
LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 100452629 | ||||||
| chr3:100452741 | G | A | 1 | a0002c0002t0003g0092 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.387+792G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100452741 | |||||||
| chr3:100452823 | C | G | 1 | a0001c0001t0001g0004 | 3 | NA18988.hp1 NA19060.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.387+874C>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100452823 | |||||||
| chr3:100452922 | CT | C | 200 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(197): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.387+980delT | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 100452922 | ||||||
| chr3:100453081 | G | A | 31 | a0002c0002t0001g0018 a0002c0002t0001g0047 a0002c0002t0001g0196 others(28): Show |
32 | HG00423.hp1 HG00642.hp2 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.387+1132G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100453081 | |||||||
| chr3:100453086 | G | A | 6 | a0002c0002t0004g0027 a0002c0002t0004g0074 a0002c0002t0004g0075 others(3): Show |
6 | HG02145.hp1 HG03041.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.387+1137G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100453086 | |||||||
| chr3:100453271 | T | C | 1 | a0002c0002t0003g0090 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.387+1322T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100453271 | |||||||
| chr3:100453354 | C | G | 202 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(199): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.387+1405C>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100453354 | |||||||
| chr3:100453398 | T | C | 1 | a0002c0002t0001g0175 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.387+1449T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100453398 | |||||||
| chr3:100453424 | TA | T | 12 | a0001c0001t0001g0039 a0001c0001t0001g0080 a0001c0001t0001g0206 others(9): Show |
12 | HG01167.hp2 HG01496.hp1 HG02004.hp1 others(9): Show |
intron_variant | MODIFIER | c.387+1492delA | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 100453424 | ||||||
| chr3:100453425 | A | T | 1 | a0002c0002t0001g0057 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.387+1476A>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100453425 | |||||||
| chr3:100453515 | G | A | 2 | a0002c0002t0001g0153 a0002c0002t0001g0168 |
2 | NA19072.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.387+1566G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100453515 | |||||||
| chr3:100453523 | G | A | 7 | a0001c0001t0005g0072 a0001c0001t0005g0281 a0001c0001t0005g0282 others(4): Show |
7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.387+1574G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100453523 | |||||||
| chr3:100453578 | G | A | 2 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.387+1629G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100453578 | |||||||
| chr3:100453584 | C | CA | 56 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0013 others(53): Show |
63 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.387+1650dupA | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 100453584 | ||||||
| chr3:100453584 | CA | C | 7 | a0001c0001t0001g0234 a0001c0001t0002g0335 a0002c0002t0001g0050 others(4): Show |
7 | HG00323.hp2 HG01070.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.387+1650delA | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 100453584 | ||||||
| chr3:100453627 | A | T | 1 | a0001c0001t0001g0271 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.387+1678A>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100453627 | |||||||
| chr3:100453888 | C | G | 1 | a0001c0001t0001g0355 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.388-1889C>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100453888 | |||||||
| chr3:100454463 | C | T | 3 | a0001c0001t0002g0298 a0001c0001t0002g0306 a0001c0001t0002g0329 |
3 | NA18964.hp2 NA18965.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.388-1314C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100454463 | |||||||
| chr3:100454631 | A | T | 2 | a0001c0001t0002g0302 a0001c0001t0002g0303 |
2 | HG00741.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.388-1146A>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100454631 | |||||||
| chr3:100454681 | C | T | 190 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(187): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(203): Show |
intron_variant | MODIFIER | c.388-1096C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100454681 | |||||||
| chr3:100454769 | T | C | 7 | a0001c0001t0005g0072 a0001c0001t0005g0281 a0001c0001t0005g0282 others(4): Show |
7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.388-1008T>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100454769 | |||||||
| chr3:100454827 | C | T | 2 | a0002c0002t0003g0095 a0002c0002t0003g0135 |
2 | HG02257.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.388-950C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100454827 | |||||||
| chr3:100454903 | T | G | 3 | a0001c0001t0001g0022 a0001c0001t0001g0357 a0001c0001t0001g0358 |
4 | HG01243.hp2 HG02055.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.388-874T>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100454903 | |||||||
| chr3:100455006 | C | G | 69 | a0001c0001t0001g0014 a0001c0001t0001g0035 a0001c0001t0001g0036 others(66): Show |
71 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(68): Show |
intron_variant | MODIFIER | c.388-771C>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100455006 | |||||||
| chr3:100455293 | C | T | 1 | a0002c0002t0001g0279 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.388-484C>T | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100455293 | |||||||
| chr3:100455317 | G | A | 1 | a0002c0002t0004g0166 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.388-460G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100455317 | |||||||
| chr3:100455377 | A | G | 55 | a0002c0002t0001g0002 a0002c0002t0001g0005 a0002c0002t0001g0008 others(52): Show |
63 | HG00323.hp2 HG00544.hp2 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.388-400A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100455377 | |||||||
| chr3:100455610 | G | A | 4 | a0002c0002t0001g0017 a0002c0002t0001g0148 a0002c0002t0001g0233 others(1): Show |
5 | HG00735.hp1 HG01975.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.388-167G>A | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100455610 | |||||||
| chr3:100455683 | A | G | 1 | a0001c0001t0005g0284 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.388-94A>G | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100455683 | |||||||
| chr3:100455751 | A | C | 7 | a0001c0001t0005g0072 a0001c0001t0005g0281 a0001c0001t0005g0282 others(4): Show |
7 | HG02559.hp1 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.388-26A>C | LNP1 | ENSG00000206535.8 | transcript | ENST00000383693.8 | protein_coding | 3/3 | chr3 | 100455751 |