Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 3937 |
| ensemblid | ENSG00000043462.13 |
| hgncid | 6529 |
| symbol | LCP2 |
| name | lymphocyte cytosolic protein 2 |
| refseq_nuc | NM_005565.5 |
| refseq_prot | NP_005556.1 |
| ensembl_nuc | ENST00000046794.10 |
| ensembl_prot | ENSP00000046794.5 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 170246233 |
| end | 170297777 |
| strand | - |
| ver | v1.2 |
| region | chr5:170246233-170297777 |
| region5000 | chr5:170241233-170302777 |
| regionname0 | LCP2_chr5_170246233_170297777 |
| regionname5000 | LCP2_chr5_170241233_170302777 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 533 | 379 | 94 | 78 | 145 | 18 | 42 | 109 | LCP2_chr5_170241233_170302777 | LCP2 | MALRN others(528): Show |
chr5 | 170241233 | 170302777 |
| a0002 | 0/0 | 533 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | MALRN others(528): Show |
chr5 | 170241233 | 170302777 |
| a0003 | 0/0 | 533 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | MALRN others(528): Show |
chr5 | 170241233 | 170302777 |
| a0004 | 0/0 | 533 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LCP2_chr5_170241233_170302777 | LCP2 | MALRN others(528): Show |
chr5 | 170241233 | 170302777 |
| a0005 | 0/0 | 533 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | MALRN others(528): Show |
chr5 | 170241233 | 170302777 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 1599 | 99 | 19 | 17 | 54 | 3 | 6 | LCP2_chr5_170241233_170302777 | LCP2 | ATGGC others(1594): Show |
chr5 | 170241233 | 170302777 | ||
| a0001c0002 | 0/0 | 1599 | 98 | 47 | 17 | 25 | 5 | 4 | LCP2_chr5_170241233_170302777 | LCP2 | ATGGC others(1594): Show |
chr5 | 170241233 | 170302777 | ||
| a0001c0003 | 0/0 | 1599 | 96 | 12 | 19 | 47 | 3 | 15 | LCP2_chr5_170241233_170302777 | LCP2 | ATGGC others(1594): Show |
chr5 | 170241233 | 170302777 | ||
| a0001c0004 | 1/1 | 1599 | 63 | 15 | 20 | 13 | 5 | 8 | LCP2_chr5_170241233_170302777 | LCP2 | ATGGC others(1594): Show |
chr5 | 170241233 | 170302777 | ||
| a0001c0005 | 0/0 | 1599 | 11 | 0 | 3 | 3 | 2 | 3 | LCP2_chr5_170241233_170302777 | LCP2 | ATGGC others(1594): Show |
chr5 | 170241233 | 170302777 | ||
| a0001c0006 | 0/0 | 1599 | 7 | 1 | 2 | 1 | 0 | 3 | LCP2_chr5_170241233_170302777 | LCP2 | ATGGC others(1594): Show |
chr5 | 170241233 | 170302777 | ||
| a0001c0007 | 0/0 | 1599 | 2 | 0 | 0 | 2 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | ATGGC others(1594): Show |
chr5 | 170241233 | 170302777 | ||
| a0001c0008 | 0/0 | 1599 | 2 | 0 | 0 | 0 | 0 | 2 | LCP2_chr5_170241233_170302777 | LCP2 | ATGGC others(1594): Show |
chr5 | 170241233 | 170302777 | ||
| a0001c0010 | 0/0 | 1599 | 1 | 0 | 0 | 0 | 0 | 1 | LCP2_chr5_170241233_170302777 | LCP2 | ATGGC others(1594): Show |
chr5 | 170241233 | 170302777 | ||
| a0002c0011 | 0/0 | 1599 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | ATGGC others(1594): Show |
chr5 | 170241233 | 170302777 | ||
| a0002c0013 | 0/0 | 1599 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | ATGGC others(1594): Show |
chr5 | 170241233 | 170302777 | ||
| a0003c0012 | 0/0 | 1599 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | ATGGC others(1594): Show |
chr5 | 170241233 | 170302777 | ||
| a0004c0009 | 0/0 | 1599 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | ATGGC others(1594): Show |
chr5 | 170241233 | 170302777 | ||
| a0005c0014 | 0/0 | 1599 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | ATGGC others(1594): Show |
chr5 | 170241233 | 170302777 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4232 | 50 | 12 | 6 | 28 | 2 | 2 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4227): Show |
chr5 | 170241233 | 170302777 |
| a0001c0001t0002 | 0/0 | 4231 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4226): Show |
chr5 | 170241233 | 170302777 |
| a0001c0001t0003 | 0/0 | 4232 | 27 | 2 | 9 | 12 | 1 | 3 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4227): Show |
chr5 | 170241233 | 170302777 |
| a0001c0001t0005 | 0/0 | 4231 | 7 | 1 | 0 | 6 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4226): Show |
chr5 | 170241233 | 170302777 |
| a0001c0001t0006 | 0/0 | 4231 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4226): Show |
chr5 | 170241233 | 170302777 |
| a0001c0001t0007 | 0/0 | 4231 | 3 | 3 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4226): Show |
chr5 | 170241233 | 170302777 |
| a0001c0001t0009 | 0/0 | 4232 | 3 | 0 | 0 | 3 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4227): Show |
chr5 | 170241233 | 170302777 |
| a0001c0001t0011 | 0/0 | 4232 | 2 | 0 | 0 | 2 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4227): Show |
chr5 | 170241233 | 170302777 |
| a0001c0001t0012 | 0/0 | 4232 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4227): Show |
chr5 | 170241233 | 170302777 |
| a0001c0001t0014 | 0/0 | 4232 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4227): Show |
chr5 | 170241233 | 170302777 |
| a0001c0001t0015 | 0/0 | 4232 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4227): Show |
chr5 | 170241233 | 170302777 |
| a0001c0001t0018 | 0/0 | 4231 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4226): Show |
chr5 | 170241233 | 170302777 |
| a0001c0001t0022 | 0/0 | 4232 | 1 | 0 | 0 | 0 | 0 | 1 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4227): Show |
chr5 | 170241233 | 170302777 |
| a0001c0002t0001 | 0/0 | 4232 | 46 | 21 | 12 | 7 | 4 | 2 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4227): Show |
chr5 | 170241233 | 170302777 |
| a0001c0002t0002 | 0/0 | 4231 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4226): Show |
chr5 | 170241233 | 170302777 |
| a0001c0002t0003 | 0/0 | 4232 | 21 | 2 | 3 | 13 | 1 | 2 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4227): Show |
chr5 | 170241233 | 170302777 |
| a0001c0002t0004 | 0/0 | 4231 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4226): Show |
chr5 | 170241233 | 170302777 |
| a0001c0002t0005 | 0/0 | 4231 | 5 | 4 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4226): Show |
chr5 | 170241233 | 170302777 |
| a0001c0002t0006 | 0/0 | 4231 | 11 | 11 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4226): Show |
chr5 | 170241233 | 170302777 |
| a0001c0002t0007 | 0/0 | 4231 | 7 | 4 | 0 | 3 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4226): Show |
chr5 | 170241233 | 170302777 |
| a0001c0002t0008 | 0/0 | 4231 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4226): Show |
chr5 | 170241233 | 170302777 |
| a0001c0002t0009 | 0/0 | 4232 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4227): Show |
chr5 | 170241233 | 170302777 |
| a0001c0002t0012 | 0/0 | 4232 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4227): Show |
chr5 | 170241233 | 170302777 |
| a0001c0002t0020 | 0/0 | 4232 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4227): Show |
chr5 | 170241233 | 170302777 |
| a0001c0002t0021 | 0/0 | 4232 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4227): Show |
chr5 | 170241233 | 170302777 |
| a0001c0002t0023 | 0/0 | 4232 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4227): Show |
chr5 | 170241233 | 170302777 |
| a0001c0003t0001 | 0/0 | 4232 | 2 | 0 | 0 | 1 | 0 | 1 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4227): Show |
chr5 | 170241233 | 170302777 |
| a0001c0003t0002 | 0/0 | 4231 | 46 | 4 | 8 | 25 | 2 | 7 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4226): Show |
chr5 | 170241233 | 170302777 |
| a0001c0003t0003 | 0/0 | 4232 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4227): Show |
chr5 | 170241233 | 170302777 |
| a0001c0003t0004 | 0/0 | 4231 | 37 | 1 | 10 | 19 | 1 | 6 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4226): Show |
chr5 | 170241233 | 170302777 |
| a0001c0003t0008 | 0/0 | 4231 | 5 | 5 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4226): Show |
chr5 | 170241233 | 170302777 |
| a0001c0003t0010 | 0/0 | 4232 | 2 | 1 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4227): Show |
chr5 | 170241233 | 170302777 |
| a0001c0003t0013 | 0/0 | 4232 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4227): Show |
chr5 | 170241233 | 170302777 |
| a0001c0003t0019 | 0/0 | 4231 | 1 | 0 | 0 | 0 | 0 | 1 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4226): Show |
chr5 | 170241233 | 170302777 |
| a0001c0003t0027 | 0/0 | 4231 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4226): Show |
chr5 | 170241233 | 170302777 |
| a0001c0004t0001 | 0/0 | 4232 | 6 | 2 | 1 | 2 | 0 | 1 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4227): Show |
chr5 | 170241233 | 170302777 |
| a0001c0004t0002 | 0/1 | 4231 | 41 | 6 | 18 | 6 | 4 | 6 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4226): Show |
chr5 | 170241233 | 170302777 |
| a0001c0004t0003 | 1/0 | 4232 | 1 | 0 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4227): Show |
chr5 | 170241233 | 170302777 |
| a0001c0004t0004 | 0/0 | 4231 | 9 | 1 | 1 | 5 | 1 | 1 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4226): Show |
chr5 | 170241233 | 170302777 |
| a0001c0004t0008 | 0/0 | 4231 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4226): Show |
chr5 | 170241233 | 170302777 |
| a0001c0004t0010 | 0/0 | 4232 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4227): Show |
chr5 | 170241233 | 170302777 |
| a0001c0004t0016 | 0/0 | 4231 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4226): Show |
chr5 | 170241233 | 170302777 |
| a0001c0004t0024 | 0/0 | 4232 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4227): Show |
chr5 | 170241233 | 170302777 |
| a0001c0004t0025 | 0/0 | 4231 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4226): Show |
chr5 | 170241233 | 170302777 |
| a0001c0004t0026 | 0/0 | 4231 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4226): Show |
chr5 | 170241233 | 170302777 |
| a0001c0005t0001 | 0/0 | 4232 | 4 | 0 | 2 | 1 | 0 | 1 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4227): Show |
chr5 | 170241233 | 170302777 |
| a0001c0005t0002 | 0/0 | 4231 | 5 | 0 | 1 | 2 | 1 | 1 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4226): Show |
chr5 | 170241233 | 170302777 |
| a0001c0005t0004 | 0/0 | 4231 | 1 | 0 | 0 | 0 | 0 | 1 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4226): Show |
chr5 | 170241233 | 170302777 |
| a0001c0005t0017 | 0/0 | 4231 | 1 | 0 | 0 | 0 | 1 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4226): Show |
chr5 | 170241233 | 170302777 |
| a0001c0006t0001 | 0/0 | 4232 | 7 | 1 | 2 | 1 | 0 | 3 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4227): Show |
chr5 | 170241233 | 170302777 |
| a0001c0007t0002 | 0/0 | 4231 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4226): Show |
chr5 | 170241233 | 170302777 |
| a0001c0007t0003 | 0/0 | 4232 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4227): Show |
chr5 | 170241233 | 170302777 |
| a0001c0008t0001 | 0/0 | 4232 | 2 | 0 | 0 | 0 | 0 | 2 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4227): Show |
chr5 | 170241233 | 170302777 |
| a0001c0010t0004 | 0/0 | 4231 | 1 | 0 | 0 | 0 | 0 | 1 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4226): Show |
chr5 | 170241233 | 170302777 |
| a0002c0011t0001 | 0/0 | 4232 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4227): Show |
chr5 | 170241233 | 170302777 |
| a0002c0013t0001 | 0/0 | 4232 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4227): Show |
chr5 | 170241233 | 170302777 |
| a0003c0012t0001 | 0/0 | 4232 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4227): Show |
chr5 | 170241233 | 170302777 |
| a0004c0009t0004 | 0/0 | 4231 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4226): Show |
chr5 | 170241233 | 170302777 |
| a0005c0014t0013 | 0/0 | 4232 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | GGGAT others(4227): Show |
chr5 | 170241233 | 170302777 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0001g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0003g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0003g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0005g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0005g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0005g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0005g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0005g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0005g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0005g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0006g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0007g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0007g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0007g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0009g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0009g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0009g0341 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0011g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0011g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0012g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0014g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0015g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0018g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0001t0022g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0001g0006 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0001g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0001g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0001g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0001g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0001g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0001g0368 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0001g0371 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0003g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0003g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0003g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0003g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0003g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0003g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0004g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0005g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0005g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0005g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0005g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0006g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0006g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0006g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0006g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0006g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0006g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0006g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0006g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0006g0366 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0006g0369 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0006g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0007g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0007g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0007g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0007g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0007g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0007g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0007g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0008g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0009g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0012g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0020g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0021g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0002t0023g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0001g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0002g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0002g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0002g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0002g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0002g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0002g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0002g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0002g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0002g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0002g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0002g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0002g0375 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0004g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0004g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0004g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0004g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0004g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0004g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0004g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0004g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0004g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0004g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0004g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0004g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0004g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0004g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0004g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0004g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0004g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0004g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0004g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0004g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0004g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0004g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0004g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0004g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0004g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0004g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0008g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0008g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0008g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0008g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0008g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0010g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0010g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0013g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0019g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0003t0027g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0002g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0002g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0002g0217 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0002g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0002g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0002g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0002g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0002g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0002g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0002g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0002g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0003g0068 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0004g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0004g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0004g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0004g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0004g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0004g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0008g0372 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0010g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0016g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0024g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0025g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0004t0026g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0005t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0005t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0005t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0005t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0005t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0005t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0005t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0005t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0005t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0005t0004g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0005t0017g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0006t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0006t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0006t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0006t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0006t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0006t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0006t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0007t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0007t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0008t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0008t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0001c0010t0004g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0002c0011t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0002c0013t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0003c0012t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0004c0009t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| a0005c0014t0013g0378 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0202 | EUR | GBR | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG00099 | hp2 | a0001 | c0005 | t0017 | g0098 | EUR | GBR | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG00140 | hp1 | a0001 | c0002 | t0003 | g0085 | EUR | GBR | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0214 | EUR | GBR | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG00280 | hp1 | a0001 | c0003 | t0002 | g0261 | EUR | FIN | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0321 | EUR | FIN | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG00323 | hp1 | a0001 | c0004 | t0002 | g0234 | EUR | FIN | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0111 | EUR | FIN | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG00408 | hp1 | a0001 | c0001 | t0009 | g0128 | EAS | CHS | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG00408 | hp2 | a0001 | c0002 | t0003 | g0030 | EAS | CHS | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG00423 | hp1 | a0001 | c0003 | t0004 | g0050 | EAS | CHS | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG00423 | hp2 | a0001 | c0002 | t0003 | g0052 | EAS | CHS | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG00438 | hp1 | a0001 | c0003 | t0002 | g0185 | EAS | CHS | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG00438 | hp2 | a0001 | c0001 | t0015 | g0079 | EAS | CHS | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG00544 | hp1 | a0001 | c0003 | t0002 | g0003 | EAS | CHS | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG00544 | hp2 | a0001 | c0003 | t0002 | g0355 | EAS | CHS | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG00558 | hp1 | a0001 | c0003 | t0004 | g0114 | EAS | CHS | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0345 | EAS | CHS | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG00621 | hp1 | a0001 | c0002 | t0003 | g0078 | EAS | CHS | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0065 | EAS | CHS | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG00639 | hp1 | a0001 | c0005 | t0001 | g0264 | AMR | PUR | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG00642 | hp1 | a0001 | c0004 | t0002 | g0221 | AMR | PUR | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG00642 | hp2 | a0001 | c0003 | t0004 | g0012 | AMR | PUR | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG00673 | hp1 | a0001 | c0002 | t0001 | g0189 | EAS | CHS | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG00673 | hp2 | a0001 | c0003 | t0027 | g0310 | EAS | CHS | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG00735 | hp1 | a0001 | c0004 | t0004 | g0092 | AMR | PUR | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG00735 | hp2 | a0001 | c0001 | t0003 | g0011 | AMR | PUR | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG00738 | hp1 | a0001 | c0001 | t0003 | g0125 | AMR | PUR | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG00738 | hp2 | a0001 | c0002 | t0003 | g0100 | AMR | PUR | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG00741 | hp1 | a0001 | c0002 | t0003 | g0075 | AMR | PUR | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG00741 | hp2 | a0001 | c0004 | t0002 | g0209 | AMR | PUR | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01070 | hp1 | a0001 | c0003 | t0002 | g0374 | AMR | PUR | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01070 | hp2 | a0001 | c0004 | t0002 | g0192 | AMR | PUR | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01071 | hp1 | a0001 | c0004 | t0001 | g0322 | AMR | PUR | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01071 | hp2 | a0001 | c0003 | t0002 | g0373 | AMR | PUR | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01074 | hp2 | a0001 | c0004 | t0002 | g0224 | AMR | PUR | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01081 | hp1 | a0001 | c0002 | t0001 | g0274 | AMR | PUR | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01081 | hp2 | a0001 | c0004 | t0002 | g0220 | AMR | PUR | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01099 | hp1 | a0001 | c0004 | t0002 | g0226 | AMR | PUR | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01099 | hp2 | a0001 | c0003 | t0002 | g0375 | AMR | PUR | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0097 | AMR | PUR | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0099 | AMR | PUR | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01109 | hp1 | a0001 | c0006 | t0001 | g0211 | AMR | PUR | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01109 | hp2 | a0001 | c0004 | t0002 | g0208 | AMR | PUR | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0279 | AMR | PUR | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01167 | hp2 | a0001 | c0003 | t0004 | g0072 | AMR | PUR | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01168 | hp1 | a0001 | c0004 | t0002 | g0233 | AMR | PUR | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01168 | hp2 | a0001 | c0004 | t0002 | g0179 | AMR | PUR | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01169 | hp1 | a0001 | c0004 | t0002 | g0235 | AMR | PUR | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01169 | hp2 | a0001 | c0003 | t0004 | g0063 | AMR | PUR | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01175 | hp1 | a0002 | c0011 | t0001 | g0210 | AMR | PUR | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0181 | AMR | PUR | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01192 | hp1 | a0001 | c0003 | t0004 | g0069 | AMR | PUR | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01243 | hp1 | a0001 | c0001 | t0012 | g0323 | AMR | PUR | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01243 | hp2 | a0001 | c0003 | t0010 | g0145 | AMR | PUR | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0223 | AMR | CLM | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01255 | hp2 | a0001 | c0004 | t0002 | g0316 | AMR | CLM | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01256 | hp1 | a0001 | c0002 | t0004 | g0043 | AMR | CLM | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01256 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | CLM | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01257 | hp1 | a0001 | c0002 | t0002 | g0216 | AMR | CLM | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01257 | hp2 | a0001 | c0003 | t0002 | g0004 | AMR | CLM | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01258 | hp1 | a0001 | c0003 | t0002 | g0004 | AMR | CLM | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01258 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | CLM | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01261 | hp2 | a0001 | c0004 | t0002 | g0331 | AMR | CLM | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01346 | hp1 | a0001 | c0003 | t0004 | g0013 | AMR | CLM | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01346 | hp2 | a0001 | c0003 | t0004 | g0094 | AMR | CLM | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01358 | hp1 | a0001 | c0002 | t0001 | g0155 | AMR | CLM | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01358 | hp2 | a0001 | c0004 | t0002 | g0313 | AMR | CLM | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01361 | hp1 | a0001 | c0003 | t0004 | g0023 | AMR | CLM | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01361 | hp2 | a0001 | c0004 | t0002 | g0149 | AMR | CLM | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01433 | hp1 | a0001 | c0006 | t0001 | g0263 | AMR | CLM | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01433 | hp2 | a0002 | c0013 | t0001 | g0230 | AMR | CLM | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0154 | AMR | CLM | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0015 | AMR | CLM | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0219 | EUR | IBS | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01515 | hp2 | a0001 | c0004 | t0002 | g0273 | EUR | IBS | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01516 | hp1 | a0001 | c0003 | t0004 | g0066 | EUR | IBS | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01516 | hp2 | a0001 | c0002 | t0001 | g0006 | EUR | IBS | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0006 | EUR | IBS | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01517 | hp2 | a0001 | c0004 | t0002 | g0272 | EUR | IBS | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0344 | AFR | ACB | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01884 | hp2 | a0001 | c0002 | t0001 | g0367 | AFR | ACB | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01891 | hp1 | a0001 | c0002 | t0006 | g0284 | AFR | ACB | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01891 | hp2 | a0001 | c0001 | t0007 | g0218 | AFR | ACB | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01928 | hp1 | a0001 | c0001 | t0014 | g0007 | AMR | PEL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01928 | hp2 | a0001 | c0003 | t0002 | g0198 | AMR | PEL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0222 | AMR | PEL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01934 | hp2 | a0001 | c0002 | t0003 | g0059 | AMR | PEL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0022 | AMR | PEL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01943 | hp2 | a0001 | c0005 | t0002 | g0130 | AMR | PEL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0165 | AMR | PEL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0016 | AMR | PEL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PEL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0168 | AMR | PEL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01978 | hp1 | a0001 | c0005 | t0001 | g0265 | AMR | PEL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01978 | hp2 | a0001 | c0004 | t0002 | g0193 | AMR | PEL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01981 | hp1 | a0001 | c0001 | t0003 | g0073 | AMR | PEL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01981 | hp2 | a0001 | c0003 | t0002 | g0142 | AMR | PEL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01993 | hp1 | a0001 | c0003 | t0002 | g0161 | AMR | PEL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01993 | hp2 | a0001 | c0004 | t0002 | g0157 | AMR | PEL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02015 | hp1 | a0001 | c0005 | t0001 | g0270 | EAS | KHV | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02015 | hp2 | a0001 | c0003 | t0002 | g0184 | EAS | KHV | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02027 | hp1 | a0001 | c0006 | t0001 | g0291 | EAS | KHV | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02027 | hp2 | a0001 | c0001 | t0018 | g0026 | EAS | KHV | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0353 | EAS | KHV | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02040 | hp2 | a0001 | c0003 | t0004 | g0055 | EAS | KHV | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | ACB | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02055 | hp2 | a0001 | c0006 | t0001 | g0212 | AFR | ACB | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | KHV | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02056 | hp2 | a0001 | c0002 | t0007 | g0262 | EAS | KHV | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02080 | hp1 | a0001 | c0001 | t0011 | g0019 | EAS | KHV | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0359 | EAS | KHV | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02132 | hp1 | a0001 | c0003 | t0002 | g0162 | EAS | KHV | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02132 | hp2 | a0001 | c0002 | t0009 | g0176 | EAS | KHV | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02135 | hp1 | a0001 | c0002 | t0003 | g0077 | EAS | KHV | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02135 | hp2 | a0001 | c0005 | t0002 | g0290 | EAS | KHV | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02145 | hp1 | a0001 | c0002 | t0006 | g0245 | AFR | ACB | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0143 | AFR | ACB | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02148 | hp2 | a0001 | c0003 | t0004 | g0024 | AMR | PEL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02165 | hp1 | a0001 | c0001 | t0011 | g0053 | EAS | CDX | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02165 | hp2 | a0001 | c0003 | t0002 | g0178 | EAS | CDX | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02258 | hp1 | a0001 | c0004 | t0002 | g0203 | AFR | ACB | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02258 | hp2 | a0001 | c0004 | t0010 | g0360 | AFR | ACB | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02280 | hp1 | a0001 | c0004 | t0024 | g0327 | AFR | ACB | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02280 | hp2 | a0001 | c0003 | t0008 | g0146 | AFR | ACB | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02293 | hp1 | a0001 | c0002 | t0001 | g0259 | AMR | PEL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02293 | hp2 | a0001 | c0003 | t0004 | g0042 | AMR | PEL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02300 | hp1 | a0001 | c0004 | t0002 | g0163 | AMR | PEL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02300 | hp2 | a0001 | c0003 | t0004 | g0106 | AMR | PEL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | KHV | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02523 | hp2 | a0001 | c0004 | t0004 | g0088 | EAS | KHV | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02572 | hp1 | a0003 | c0012 | t0001 | g0282 | AFR | GWD | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02572 | hp2 | a0001 | c0003 | t0013 | g0283 | AFR | GWD | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02602 | hp1 | a0001 | c0003 | t0002 | g0225 | SAS | PJL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02602 | hp2 | a0001 | c0003 | t0019 | g0060 | SAS | PJL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02615 | hp1 | a0001 | c0002 | t0003 | g0090 | AFR | GWD | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02615 | hp2 | a0001 | c0004 | t0004 | g0123 | AFR | GWD | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02622 | hp1 | a0001 | c0002 | t0003 | g0010 | AFR | GWD | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02622 | hp2 | a0001 | c0002 | t0006 | g0325 | AFR | GWD | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02630 | hp1 | a0001 | c0002 | t0001 | g0287 | AFR | GWD | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02630 | hp2 | a0001 | c0002 | t0023 | g0335 | AFR | GWD | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0187 | AFR | GWD | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02647 | hp2 | a0001 | c0004 | t0016 | g0108 | AFR | GWD | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02683 | hp1 | a0001 | c0002 | t0003 | g0054 | SAS | PJL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02683 | hp2 | a0001 | c0001 | t0003 | g0095 | SAS | PJL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02698 | hp1 | a0001 | c0004 | t0002 | g0348 | SAS | PJL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02698 | hp2 | a0001 | c0004 | t0002 | g0180 | SAS | PJL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02717 | hp1 | a0001 | c0002 | t0005 | g0115 | AFR | GWD | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02717 | hp2 | a0001 | c0002 | t0001 | g0362 | AFR | GWD | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02723 | hp1 | a0001 | c0003 | t0002 | g0370 | AFR | GWD | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02723 | hp2 | a0001 | c0002 | t0006 | g0144 | AFR | GWD | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02735 | hp1 | a0001 | c0004 | t0002 | g0148 | SAS | PJL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02735 | hp2 | a0001 | c0003 | t0004 | g0070 | SAS | PJL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02738 | hp1 | a0001 | c0005 | t0001 | g0298 | SAS | PJL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02738 | hp2 | a0001 | c0004 | t0002 | g0294 | SAS | PJL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02809 | hp1 | a0001 | c0003 | t0002 | g0318 | AFR | GWD | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02809 | hp2 | a0001 | c0002 | t0005 | g0109 | AFR | GWD | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0361 | AFR | GWD | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02818 | hp2 | a0001 | c0004 | t0026 | g0213 | AFR | GWD | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02886 | hp1 | a0001 | c0002 | t0021 | g0336 | AFR | GWD | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0315 | AFR | GWD | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02895 | hp1 | a0001 | c0002 | t0006 | g0127 | AFR | GWD | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02895 | hp2 | a0001 | c0002 | t0006 | g0369 | AFR | GWD | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02896 | hp1 | a0001 | c0002 | t0005 | g0028 | AFR | GWD | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02896 | hp2 | a0001 | c0004 | t0002 | g0333 | AFR | GWD | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02897 | hp1 | a0001 | c0002 | t0006 | g0366 | AFR | GWD | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02897 | hp2 | a0001 | c0004 | t0002 | g0334 | AFR | GWD | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0364 | AFR | ESN | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | ESN | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02965 | hp1 | a0001 | c0001 | t0007 | g0343 | AFR | ESN | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02965 | hp2 | a0001 | c0004 | t0002 | g0324 | AFR | ESN | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02970 | hp1 | a0001 | c0001 | t0005 | g0120 | AFR | ESN | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02970 | hp2 | a0001 | c0004 | t0025 | g0338 | AFR | ESN | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02976 | hp1 | a0001 | c0002 | t0006 | g0244 | AFR | ESN | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02976 | hp2 | a0001 | c0002 | t0007 | g0365 | AFR | ESN | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG03017 | hp1 | a0001 | c0005 | t0004 | g0071 | SAS | PJL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG03017 | hp2 | a0001 | c0001 | t0022 | g0237 | SAS | PJL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG03041 | hp1 | a0001 | c0002 | t0006 | g0246 | AFR | GWD | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0002 | AFR | GWD | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG03098 | hp1 | a0001 | c0003 | t0008 | g0252 | AFR | MSL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0330 | AFR | MSL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0371 | AFR | ESN | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG03130 | hp2 | a0001 | c0002 | t0001 | g0248 | AFR | ESN | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0339 | AFR | ESN | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG03139 | hp2 | a0001 | c0004 | t0002 | g0280 | AFR | ESN | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG03195 | hp1 | a0001 | c0002 | t0006 | g0317 | AFR | ESN | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0126 | AFR | ESN | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG03209 | hp1 | a0001 | c0004 | t0001 | g0329 | AFR | MSL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | MSL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0314 | AFR | MSL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG03225 | hp2 | a0001 | c0004 | t0002 | g0376 | AFR | MSL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0288 | AFR | MSL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0286 | AFR | MSL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG03486 | hp1 | a0001 | c0003 | t0010 | g0342 | AFR | MSL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG03486 | hp2 | a0001 | c0002 | t0001 | g0368 | AFR | MSL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG03491 | hp1 | a0001 | c0008 | t0001 | g0306 | SAS | PJL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG03491 | hp2 | a0001 | c0003 | t0004 | g0001 | SAS | PJL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG03492 | hp1 | a0001 | c0008 | t0001 | g0307 | SAS | PJL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG03492 | hp2 | a0001 | c0003 | t0002 | g0305 | SAS | PJL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG03516 | hp1 | a0001 | c0002 | t0012 | g0326 | AFR | ESN | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | ESN | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG03540 | hp1 | a0001 | c0002 | t0006 | g0377 | AFR | GWD | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG03540 | hp2 | a0001 | c0002 | t0005 | g0061 | AFR | GWD | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0340 | AFR | MSL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | MSL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0354 | SAS | PJL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG03654 | hp2 | a0001 | c0003 | t0001 | g0356 | SAS | PJL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG03669 | hp1 | a0001 | c0003 | t0002 | g0227 | SAS | PJL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0089 | SAS | PJL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG03688 | hp1 | a0001 | c0003 | t0002 | g0276 | SAS | STU | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG03688 | hp2 | a0001 | c0006 | t0001 | g0293 | SAS | STU | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG03704 | hp1 | a0001 | c0004 | t0002 | g0268 | SAS | PJL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG03704 | hp2 | a0001 | c0003 | t0004 | g0039 | SAS | PJL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG03710 | hp1 | a0001 | c0002 | t0003 | g0045 | SAS | PJL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG03710 | hp2 | a0001 | c0004 | t0002 | g0308 | SAS | PJL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG03831 | hp1 | a0001 | c0003 | t0004 | g0001 | SAS | BEB | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG03831 | hp2 | a0001 | c0006 | t0001 | g0295 | SAS | BEB | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG03834 | hp1 | a0001 | c0003 | t0002 | g0177 | SAS | BEB | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG03834 | hp2 | a0001 | c0006 | t0001 | g0271 | SAS | BEB | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0297 | SAS | BEB | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG03942 | hp2 | a0001 | c0004 | t0004 | g0107 | SAS | BEB | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG04184 | hp1 | a0001 | c0003 | t0002 | g0332 | SAS | BEB | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG04184 | hp2 | a0001 | c0003 | t0004 | g0027 | SAS | BEB | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0311 | SAS | STU | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG04199 | hp2 | a0001 | c0003 | t0002 | g0349 | SAS | STU | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG04204 | hp1 | a0001 | c0003 | t0004 | g0101 | SAS | STU | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG04204 | hp2 | a0001 | c0010 | t0004 | g0124 | SAS | STU | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0036 | SAS | STU | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0302 | SAS | STU | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18522 | hp1 | a0001 | c0002 | t0008 | g0285 | AFR | YRI | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18522 | hp2 | a0001 | c0002 | t0007 | g0319 | AFR | YRI | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18612 | hp1 | a0001 | c0003 | t0004 | g0029 | EAS | CHB | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18612 | hp2 | a0001 | c0002 | t0007 | g0199 | EAS | CHB | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | CHB | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18747 | hp2 | a0001 | c0004 | t0002 | g0231 | EAS | CHB | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0278 | AFR | YRI | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0118 | AFR | YRI | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18940 | hp1 | a0001 | c0002 | t0003 | g0062 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18940 | hp2 | a0001 | c0003 | t0003 | g0056 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18941 | hp1 | a0001 | c0003 | t0002 | g0200 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18941 | hp2 | a0001 | c0003 | t0001 | g0141 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18942 | hp1 | a0001 | c0003 | t0002 | g0196 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18942 | hp2 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18943 | hp1 | a0001 | c0003 | t0004 | g0051 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0008 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18944 | hp2 | a0004 | c0009 | t0004 | g0038 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18945 | hp1 | a0001 | c0001 | t0009 | g0341 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18946 | hp1 | a0001 | c0003 | t0002 | g0164 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18947 | hp1 | a0001 | c0005 | t0002 | g0292 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0102 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18951 | hp1 | a0001 | c0003 | t0004 | g0082 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18951 | hp2 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0358 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18952 | hp2 | a0001 | c0004 | t0004 | g0047 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18953 | hp1 | a0001 | c0002 | t0003 | g0021 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18953 | hp2 | a0001 | c0002 | t0001 | g0266 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18954 | hp2 | a0001 | c0003 | t0002 | g0239 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18957 | hp1 | a0001 | c0003 | t0004 | g0009 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18957 | hp2 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18960 | hp1 | a0001 | c0003 | t0002 | g0188 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18960 | hp2 | a0001 | c0001 | t0005 | g0104 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18963 | hp1 | a0001 | c0003 | t0002 | g0183 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18963 | hp2 | a0001 | c0001 | t0003 | g0121 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18966 | hp1 | a0001 | c0004 | t0004 | g0117 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18968 | hp2 | a0001 | c0003 | t0002 | g0153 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18970 | hp1 | a0001 | c0002 | t0003 | g0119 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18970 | hp2 | a0001 | c0001 | t0005 | g0091 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18971 | hp1 | a0001 | c0003 | t0004 | g0048 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18971 | hp2 | a0001 | c0003 | t0002 | g0195 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18972 | hp2 | a0001 | c0003 | t0002 | g0134 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18974 | hp1 | a0001 | c0003 | t0002 | g0136 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18974 | hp2 | a0001 | c0003 | t0004 | g0057 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18979 | hp1 | a0001 | c0003 | t0004 | g0110 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0363 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18980 | hp1 | a0001 | c0003 | t0004 | g0080 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18981 | hp1 | a0001 | c0003 | t0004 | g0058 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18982 | hp1 | a0001 | c0004 | t0002 | g0169 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18983 | hp1 | a0001 | c0001 | t0005 | g0018 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18988 | hp1 | a0001 | c0003 | t0004 | g0093 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18988 | hp2 | a0001 | c0002 | t0001 | g0232 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18990 | hp1 | a0001 | c0004 | t0002 | g0299 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18990 | hp2 | a0001 | c0002 | t0003 | g0096 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18994 | hp1 | a0001 | c0003 | t0004 | g0081 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18995 | hp1 | a0001 | c0004 | t0001 | g0300 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18997 | hp1 | a0001 | c0003 | t0002 | g0138 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18997 | hp2 | a0001 | c0001 | t0009 | g0312 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18998 | hp1 | a0001 | c0002 | t0005 | g0086 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA19001 | hp1 | a0001 | c0003 | t0004 | g0041 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA19002 | hp1 | a0001 | c0003 | t0002 | g0166 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA19009 | hp1 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA19009 | hp2 | a0001 | c0003 | t0004 | g0014 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA19010 | hp1 | a0001 | c0003 | t0002 | g0159 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA19010 | hp2 | a0001 | c0002 | t0003 | g0087 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA19011 | hp1 | a0001 | c0002 | t0003 | g0046 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA19011 | hp2 | a0001 | c0004 | t0001 | g0301 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0304 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA19012 | hp2 | a0001 | c0001 | t0003 | g0113 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0243 | AFR | LWK | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA19030 | hp2 | a0005 | c0014 | t0013 | g0378 | AFR | LWK | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA19043 | hp1 | a0001 | c0002 | t0007 | g0337 | AFR | LWK | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA19043 | hp2 | a0001 | c0003 | t0002 | g0250 | AFR | LWK | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA19055 | hp1 | a0001 | c0004 | t0004 | g0020 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA19055 | hp2 | a0001 | c0003 | t0002 | g0206 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA19058 | hp1 | a0001 | c0002 | t0001 | g0357 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA19058 | hp2 | a0001 | c0003 | t0002 | g0240 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA19060 | hp2 | a0001 | c0003 | t0002 | g0197 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA19062 | hp1 | a0001 | c0003 | t0002 | g0170 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA19062 | hp2 | a0001 | c0003 | t0002 | g0350 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA19063 | hp1 | a0001 | c0004 | t0002 | g0194 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA19063 | hp2 | a0001 | c0004 | t0002 | g0309 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA19065 | hp1 | a0001 | c0003 | t0004 | g0084 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0275 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA19068 | hp1 | a0001 | c0002 | t0007 | g0229 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA19070 | hp1 | a0001 | c0003 | t0004 | g0033 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA19070 | hp2 | a0001 | c0002 | t0003 | g0017 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0352 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA19074 | hp2 | a0001 | c0002 | t0003 | g0076 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0347 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA19079 | hp2 | a0001 | c0001 | t0005 | g0049 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA19081 | hp1 | a0001 | c0001 | t0005 | g0074 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA19082 | hp2 | a0001 | c0004 | t0004 | g0040 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA19083 | hp1 | a0001 | c0007 | t0002 | g0204 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA19083 | hp2 | a0001 | c0007 | t0003 | g0031 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA19084 | hp1 | a0001 | c0001 | t0005 | g0044 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA19084 | hp2 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA19086 | hp1 | a0001 | c0004 | t0002 | g0191 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA19091 | hp1 | a0001 | c0002 | t0003 | g0034 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA19091 | hp2 | a0001 | c0003 | t0004 | g0032 | EAS | JPT | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA19240 | hp1 | a0001 | c0003 | t0008 | g0241 | AFR | YRI | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA19240 | hp2 | a0001 | c0001 | t0007 | g0247 | AFR | YRI | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA20129 | hp1 | a0001 | c0002 | t0007 | g0320 | AFR | ASW | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0289 | AFR | ASW | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA20752 | hp1 | a0001 | c0004 | t0004 | g0116 | EUR | TSI | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA20752 | hp2 | a0001 | c0005 | t0002 | g0260 | EUR | TSI | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA20805 | hp1 | a0001 | c0003 | t0002 | g0215 | EUR | TSI | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA20805 | hp2 | a0001 | c0004 | t0002 | g0150 | EUR | TSI | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA20905 | hp1 | a0001 | c0005 | t0002 | g0269 | SAS | GIH | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA20905 | hp2 | a0001 | c0004 | t0001 | g0303 | SAS | GIH | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0064 | AMR | CLM | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG01123 | hp2 | a0001 | c0004 | t0002 | g0156 | AMR | CLM | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0002 | AFR | ACB | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0103 | AFR | ACB | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02486 | hp1 | a0001 | c0004 | t0008 | g0372 | AFR | ACB | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02486 | hp2 | a0001 | c0003 | t0008 | g0251 | AFR | ACB | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0296 | AFR | ACB | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG02559 | hp2 | a0001 | c0003 | t0002 | g0257 | AFR | ACB | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | MSL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | MSL | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG06807 | hp1 | a0001 | c0001 | t0006 | g0228 | AFR | USA | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| HG06807 | hp2 | a0001 | c0003 | t0008 | g0328 | AFR | USA | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA20300 | hp1 | a0001 | c0003 | t0004 | g0035 | AFR | USA | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA20300 | hp2 | a0001 | c0004 | t0001 | g0242 | AFR | USA | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0351 | AFR | LWK | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| NA21309 | hp2 | a0001 | c0002 | t0020 | g0207 | AFR | LWK | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| homoSapiens | chm13v2 | a0001 | c0004 | t0002 | g0217 | REF | REF | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| homoSapiens | grch38p0 | a0001 | c0004 | t0003 | g0068 | REF | REF | LCP2_chr5_170241233_170302777 | LCP2 | chr5 | 170241233 | 170302777 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:170253135 | G | C | 1 | a0002 | 2 | HG01175.hp1 HG01433.hp2 |
missense_variant | MODERATE | c.1229C>G | p.Ser410Cys | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 18/21 | 1395/4232 | 1229/1602 | 410/533 | chr5 | 170253135 | |||
| chr5:170253138 | G | C | 1 | a0004 | 1 | NA18944.hp2 | missense_variant | MODERATE | c.1226C>G | p.Pro409Arg | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 18/21 | 1392/4232 | 1226/1602 | 409/533 | chr5 | 170253138 | |||
| chr5:170266814 | T | C | 1 | a0003 | 1 | HG02572.hp1 | missense_variant | MODERATE | c.766A>G | p.Thr256Ala | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/21 | 932/4232 | 766/1602 | 256/533 | chr5 | 170266814 | |||
| chr5:170297547 | T | A | 1 | a0005 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.65A>T | p.Asp22Val | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/21 | 231/4232 | 65/1602 | 22/533 | chr5 | 170297547 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:170253185 | G | A | 1 | a0001c0010 | 1 | HG04204.hp2 | synonymous_variant | LOW | c.1179C>T | p.Ala393Ala | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 18/21 | 1345/4232 | 1179/1602 | 393/533 | chr5 | 170253185 | |||
| chr5:170258159 | C | T | 6 | a0001c0001 a0001c0002 a0001c0006 others(3): Show |
208 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(205): Show |
synonymous_variant | LOW | c.978G>A | p.Gln326Gln | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 16/21 | 1144/4232 | 978/1602 | 326/533 | chr5 | 170258159 | |||
| chr5:170266854 | G | A | 2 | a0001c0005 a0001c0006 |
18 | HG00099.hp2 HG00639.hp1 HG01109.hp1 others(15): Show |
synonymous_variant | LOW | c.726C>T | p.Pro242Pro | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/21 | 892/4232 | 726/1602 | 242/533 | chr5 | 170266854 | |||
| chr5:170268436 | G | C | 2 | a0001c0008 a0002c0013 |
3 | HG01433.hp2 HG03491.hp1 HG03492.hp1 |
synonymous_variant | LOW | c.570C>G | p.Pro190Pro | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 8/21 | 736/4232 | 570/1602 | 190/533 | chr5 | 170268436 | |||
| chr5:170268442 | C | T | 5 | a0001c0001 a0001c0003 a0001c0007 others(2): Show |
199 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(196): Show |
synonymous_variant | LOW | c.564G>A | p.Val188Val | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 8/21 | 730/4232 | 564/1602 | 188/533 | chr5 | 170268442 | |||
| chr5:170275336 | C | T | 1 | a0001c0007 | 2 | NA19083.hp1 NA19083.hp2 |
synonymous_variant | LOW | c.270G>A | p.Arg90Arg | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 5/21 | 436/4232 | 270/1602 | 90/533 | chr5 | 170275336 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:170246248 | G | A | 1 | a0001c0004t0026 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2449C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 21/21 | 2449 | chr5 | 170246248 | ||||||
| chr5:170246262 | T | G | 1 | a0001c0001t0015 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2435A>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 21/21 | 2435 | chr5 | 170246262 | ||||||
| chr5:170246308 | G | A | 1 | a0001c0001t0022 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2389C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 21/21 | 2389 | chr5 | 170246308 | ||||||
| chr5:170246333 | A | T | 1 | a0001c0004t0025 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2364T>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 21/21 | 2364 | chr5 | 170246333 | ||||||
| chr5:170246398 | A | T | 13 | a0001c0001t0005 a0001c0001t0006 a0001c0001t0007 others(10): Show |
42 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*2299T>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 21/21 | 2299 | chr5 | 170246398 | ||||||
| chr5:170246532 | A | G | 1 | a0001c0002t0021 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2165T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 21/21 | 2165 | chr5 | 170246532 | ||||||
| chr5:170246576 | T | A | 21 | a0001c0001t0002 a0001c0002t0002 a0001c0002t0004 others(18): Show |
157 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*2121A>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 21/21 | 2121 | chr5 | 170246576 | ||||||
| chr5:170246780 | A | C | 2 | a0001c0003t0010 a0001c0004t0010 |
3 | HG01243.hp2 HG02258.hp2 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1917T>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 21/21 | 1917 | chr5 | 170246780 | ||||||
| chr5:170246809 | C | T | 1 | a0001c0005t0017 | 1 | HG00099.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1888G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 21/21 | 1888 | chr5 | 170246809 | ||||||
| chr5:170247002 | C | T | 4 | a0001c0001t0005 a0001c0001t0007 a0001c0002t0005 others(1): Show |
22 | HG01891.hp2 HG02056.hp2 HG02717.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1695G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 21/21 | 1695 | chr5 | 170247002 | ||||||
| chr5:170247485 | G | A | 1 | a0001c0002t0023 | 1 | HG02630.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1212C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 21/21 | 1212 | chr5 | 170247485 | ||||||
| chr5:170247524 | C | A | 2 | a0001c0001t0006 a0001c0002t0006 |
12 | HG01891.hp1 HG02145.hp1 HG02622.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1173G>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 21/21 | 1173 | chr5 | 170247524 | ||||||
| chr5:170247881 | T | C | 1 | a0001c0003t0019 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*816A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 21/21 | 816 | chr5 | 170247881 | ||||||
| chr5:170248007 | G | A | 2 | a0001c0003t0013 a0005c0014t0013 |
2 | HG02572.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*690C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 21/21 | 690 | chr5 | 170248007 | ||||||
| chr5:170248142 | A | T | 5 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0015 others(2): Show |
23 | HG00438.hp2 HG01891.hp2 HG02056.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*555T>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 21/21 | 555 | chr5 | 170248142 | ||||||
| chr5:170248161 | G | C | 28 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(25): Show |
188 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(185): Show |
3_prime_UTR_variant | MODIFIER | c.*536C>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 21/21 | 536 | chr5 | 170248161 | ||||||
| chr5:170248161 | G | T | 1 | a0001c0002t0020 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*536C>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 21/21 | 536 | chr5 | 170248161 | ||||||
| chr5:170248281 | C | T | 1 | a0001c0004t0025 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*416G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 21/21 | 416 | chr5 | 170248281 | ||||||
| chr5:170248314 | A | G | 3 | a0001c0001t0009 a0001c0001t0011 a0001c0002t0009 |
6 | HG00408.hp1 HG02080.hp1 HG02132.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*383T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 21/21 | 383 | chr5 | 170248314 | ||||||
| chr5:170248445 | T | C | 1 | a0001c0003t0027 | 1 | HG00673.hp2 | 3_prime_UTR_variant | MODIFIER | c.*252A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 21/21 | 252 | chr5 | 170248445 | ||||||
| chr5:170248689 | AT | A | 28 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(25): Show |
192 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(189): Show |
3_prime_UTR_variant | MODIFIER | c.*7delA | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 21/21 | 7 | chr5 | 170248689 | ||||||
| chr5:170297763 | G | C | 39 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(36): Show |
262 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
5_prime_UTR_variant | MODIFIER | c.-152C>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/21 | 152 | chr5 | 170297763 | ||||||
| chr5:170297764 | C | T | 1 | a0001c0001t0014 | 1 | HG01928.hp1 | 5_prime_UTR_variant | MODIFIER | c.-153G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/21 | 153 | chr5 | 170297764 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:170248875 | C | G | 1 | a0001c0004t0025g0338 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1480-56G>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 20/20 | chr5 | 170248875 | |||||||
| chr5:170248938 | GA | G | 5 | a0001c0002t0006g0317 a0001c0002t0006g0325 a0001c0002t0006g0366 others(2): Show |
5 | HG01993.hp1 HG02622.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1480-120delT | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 20/20 | chr5 | 170248938 | |||||||
| chr5:170248957 | A | G | 1 | a0001c0003t0004g0057 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1480-138T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 20/20 | chr5 | 170248957 | |||||||
| chr5:170249198 | G | A | 25 | a0001c0001t0001g0147 a0001c0001t0001g0151 a0001c0001t0001g0277 others(22): Show |
26 | HG00140.hp1 HG01074.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.1480-379C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 20/20 | chr5 | 170249198 | |||||||
| chr5:170249291 | G | A | 18 | a0001c0001t0001g0147 a0001c0001t0001g0151 a0001c0001t0001g0277 others(15): Show |
19 | HG00140.hp1 HG01074.hp1 HG01106.hp2 others(16): Show |
intron_variant | MODIFIER | c.1480-472C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 20/20 | chr5 | 170249291 | |||||||
| chr5:170249362 | G | GTA | 17 | a0001c0001t0001g0256 a0001c0001t0001g0315 a0001c0001t0001g0321 others(14): Show |
17 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(14): Show |
intron_variant | MODIFIER | c.1480-545_1480-544d others(4): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 20/20 | chr5 | 170249362 | |||||||
| chr5:170249362 | G | GTATA | 9 | a0001c0001t0001g0351 a0001c0003t0002g0206 a0001c0003t0004g0001 others(6): Show |
10 | HG01243.hp2 HG02258.hp2 HG03486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1480-547_1480-544d others(6): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 20/20 | chr5 | 170249362 | |||||||
| chr5:170249362 | G | GTATATA | 3 | a0001c0001t0012g0323 a0001c0002t0012g0326 a0001c0003t0013g0283 |
3 | HG01243.hp1 HG02572.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1480-549_1480-544d others(8): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 20/20 | chr5 | 170249362 | |||||||
| chr5:170249362 | G | GTATATAT others(1): Show |
10 | a0001c0001t0005g0018 a0001c0001t0005g0049 a0001c0001t0005g0074 others(7): Show |
10 | HG02965.hp1 NA18612.hp2 NA18960.hp2 others(7): Show |
intron_variant | MODIFIER | c.1480-551_1480-544d others(10): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 20/20 | chr5 | 170249362 | |||||||
| chr5:170249362 | G | GTATATAT others(3): Show |
6 | a0001c0001t0005g0044 a0001c0001t0005g0091 a0001c0001t0015g0079 others(3): Show |
6 | HG00438.hp2 HG02056.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1480-553_1480-544d others(12): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 20/20 | chr5 | 170249362 | |||||||
| chr5:170249362 | G | GTATATAT others(5): Show |
5 | a0001c0001t0005g0120 a0001c0001t0007g0218 a0001c0002t0005g0061 others(2): Show |
5 | HG01891.hp2 HG02717.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1480-555_1480-544d others(14): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 20/20 | chr5 | 170249362 | |||||||
| chr5:170249362 | G | GTATATAT others(7): Show |
2 | a0001c0002t0007g0319 a0001c0002t0007g0320 |
2 | NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1480-557_1480-544d others(16): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 20/20 | chr5 | 170249362 | |||||||
| chr5:170249362 | G | GTGTA | 8 | a0001c0003t0002g0142 a0001c0003t0002g0250 a0001c0003t0002g0257 others(5): Show |
8 | HG01981.hp2 HG02559.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1480-544_1480-543i others(6): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 20/20 | chr5 | 170249362 | |||||||
| chr5:170249364 | A | G | 3 | a0001c0001t0001g0339 a0001c0002t0003g0034 a0001c0002t0003g0076 |
3 | HG03139.hp1 NA19074.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1480-545T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 20/20 | chr5 | 170249364 | |||||||
| chr5:170249380 | A | ATATATC | 12 | a0001c0003t0002g0177 a0001c0003t0004g0041 a0001c0003t0004g0063 others(9): Show |
12 | HG00099.hp2 HG01074.hp2 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.1480-562_1480-561i others(8): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 20/20 | chr5 | 170249380 | |||||||
| chr5:170249380 | A | ATATC | 128 | a0001c0001t0002g0152 a0001c0001t0018g0026 a0001c0002t0002g0216 others(125): Show |
129 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.1480-562_1480-561i others(6): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 20/20 | chr5 | 170249380 | |||||||
| chr5:170249380 | A | ATCTC | 2 | a0001c0003t0002g0004 a0001c0004t0004g0047 |
3 | HG01257.hp2 HG01258.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.1480-562_1480-561i others(6): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 20/20 | chr5 | 170249380 | |||||||
| chr5:170249380 | A | C | 8 | a0001c0003t0002g0142 a0001c0003t0002g0250 a0001c0003t0002g0257 others(5): Show |
8 | HG01981.hp2 HG02559.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.1480-561T>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 20/20 | chr5 | 170249380 | |||||||
| chr5:170249390 | CTA | C | 9 | a0001c0001t0012g0323 a0001c0002t0012g0326 a0001c0003t0010g0145 others(6): Show |
9 | HG01243.hp1 HG01243.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1480-573_1480-572d others(4): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 20/20 | chr5 | 170249390 | |||||||
| chr5:170249742 | G | A | 1 | a0001c0001t0001g0256 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1480-923C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 20/20 | chr5 | 170249742 | |||||||
| chr5:170249831 | T | A | 3 | a0001c0001t0001g0339 a0001c0002t0001g0367 a0001c0004t0001g0242 |
3 | HG01884.hp2 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1479+899A>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 20/20 | chr5 | 170249831 | |||||||
| chr5:170249883 | T | A | 3 | a0001c0003t0010g0145 a0001c0003t0010g0342 a0001c0004t0010g0360 |
3 | HG01243.hp2 HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1479+847A>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 20/20 | chr5 | 170249883 | |||||||
| chr5:170249919 | G | T | 1 | a0001c0003t0004g0069 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1479+811C>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 20/20 | chr5 | 170249919 | |||||||
| chr5:170249973 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1479+757C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 20/20 | chr5 | 170249973 | |||||||
| chr5:170249990 | A | G | 1 | a0001c0004t0025g0338 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1479+740T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 20/20 | chr5 | 170249990 | |||||||
| chr5:170250000 | A | AT | 5 | a0001c0001t0001g0344 a0001c0002t0001g0286 a0001c0002t0001g0287 others(2): Show |
5 | HG01884.hp1 HG02615.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1479+729dupA | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 20/20 | chr5 | 170250000 | |||||||
| chr5:170250138 | G | A | 1 | a0003c0012t0001g0282 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1479+592C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 20/20 | chr5 | 170250138 | |||||||
| chr5:170250907 | A | C | 13 | a0001c0001t0006g0228 a0001c0002t0006g0127 a0001c0002t0006g0144 others(10): Show |
13 | HG01891.hp1 HG02145.hp1 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.1324-22T>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 19/20 | chr5 | 170250907 | |||||||
| chr5:170251454 | T | C | 2 | a0001c0002t0001g0154 a0001c0002t0001g0243 |
2 | HG01496.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1324-569A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 19/20 | chr5 | 170251454 | |||||||
| chr5:170251499 | A | G | 1 | a0001c0003t0004g0039 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1324-614T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 19/20 | chr5 | 170251499 | |||||||
| chr5:170251740 | G | A | 4 | a0001c0001t0001g0302 a0001c0002t0003g0045 a0001c0008t0001g0306 others(1): Show |
4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1323+694C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 19/20 | chr5 | 170251740 | |||||||
| chr5:170251810 | G | C | 45 | a0001c0001t0001g0147 a0001c0001t0001g0151 a0001c0001t0001g0277 others(42): Show |
46 | HG00140.hp1 HG00438.hp2 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.1323+624C>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 19/20 | chr5 | 170251810 | |||||||
| chr5:170251956 | G | A | 2 | a0001c0002t0021g0336 a0001c0004t0025g0338 |
2 | HG02886.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1323+478C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 19/20 | chr5 | 170251956 | |||||||
| chr5:170252007 | A | G | 1 | a0001c0003t0004g0001 | 2 | HG03491.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1323+427T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 19/20 | chr5 | 170252007 | |||||||
| chr5:170252033 | A | G | 191 | a0001c0001t0002g0152 a0001c0001t0005g0018 a0001c0001t0005g0044 others(188): Show |
194 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(191): Show |
intron_variant | MODIFIER | c.1323+401T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 19/20 | chr5 | 170252033 | |||||||
| chr5:170252075 | G | A | 1 | a0001c0003t0013g0283 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1323+359C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 19/20 | chr5 | 170252075 | |||||||
| chr5:170252219 | G | A | 1 | a0001c0003t0004g0058 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1323+215C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 19/20 | chr5 | 170252219 | |||||||
| chr5:170252278 | T | C | 1 | a0003c0012t0001g0282 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1323+156A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 19/20 | chr5 | 170252278 | |||||||
| chr5:170252350 | C | T | 157 | a0001c0002t0004g0043 a0001c0002t0008g0285 a0001c0003t0001g0356 others(154): Show |
160 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.1323+84G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 19/20 | chr5 | 170252350 | |||||||
| chr5:170252699 | G | A | 11 | a0001c0001t0001g0249 a0001c0001t0001g0253 a0001c0001t0001g0254 others(8): Show |
12 | HG00639.hp2 HG02055.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1246-188C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 18/20 | chr5 | 170252699 | |||||||
| chr5:170252767 | C | T | 1 | a0001c0004t0024g0327 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1246-256G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 18/20 | chr5 | 170252767 | |||||||
| chr5:170252943 | C | T | 154 | a0001c0002t0004g0043 a0001c0002t0008g0285 a0001c0003t0001g0356 others(151): Show |
157 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.1245+176G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 18/20 | chr5 | 170252943 | |||||||
| chr5:170253016 | C | T | 1 | a0001c0004t0002g0294 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1245+103G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 18/20 | chr5 | 170253016 | |||||||
| chr5:170253092 | A | G | 1 | a0005c0014t0013g0378 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1245+27T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 18/20 | chr5 | 170253092 | |||||||
| chr5:170253297 | T | TC | 5 | a0001c0001t0001g0344 a0001c0002t0001g0286 a0001c0002t0001g0287 others(2): Show |
5 | HG01884.hp1 HG02615.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1151-85dupG | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 17/20 | chr5 | 170253297 | |||||||
| chr5:170253302 | C | CA | 17 | a0001c0001t0001g0147 a0001c0001t0001g0151 a0001c0001t0001g0277 others(14): Show |
18 | HG00140.hp1 HG01074.hp1 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.1151-90dupT | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 17/20 | chr5 | 170253302 | |||||||
| chr5:170253303 | A | C | 1 | a0003c0012t0001g0282 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1151-90T>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 17/20 | chr5 | 170253303 | |||||||
| chr5:170253318 | C | T | 2 | a0001c0002t0021g0336 a0001c0004t0025g0338 |
2 | HG02886.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1151-105G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 17/20 | chr5 | 170253318 | |||||||
| chr5:170253336 | G | A | 1 | a0001c0002t0005g0086 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1151-123C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 17/20 | chr5 | 170253336 | |||||||
| chr5:170253518 | C | T | 1 | a0001c0004t0002g0234 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1151-305G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 17/20 | chr5 | 170253518 | |||||||
| chr5:170253562 | A | C | 3 | a0001c0003t0010g0145 a0001c0003t0010g0342 a0001c0004t0010g0360 |
3 | HG01243.hp2 HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1151-349T>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 17/20 | chr5 | 170253562 | |||||||
| chr5:170253642 | A | G | 3 | a0001c0002t0006g0325 a0001c0002t0006g0366 a0001c0002t0006g0369 |
3 | HG02622.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1151-429T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 17/20 | chr5 | 170253642 | |||||||
| chr5:170253646 | AGAT | A | 21 | a0001c0001t0005g0018 a0001c0001t0005g0044 a0001c0001t0005g0049 others(18): Show |
21 | HG00438.hp2 HG01891.hp2 HG02056.hp2 others(18): Show |
intron_variant | MODIFIER | c.1151-436_1151-434d others(5): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 17/20 | chr5 | 170253646 | |||||||
| chr5:170253650 | A | C | 21 | a0001c0001t0005g0018 a0001c0001t0005g0044 a0001c0001t0005g0049 others(18): Show |
21 | HG00438.hp2 HG01891.hp2 HG02056.hp2 others(18): Show |
intron_variant | MODIFIER | c.1151-437T>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 17/20 | chr5 | 170253650 | |||||||
| chr5:170253822 | T | C | 3 | a0001c0003t0002g0188 a0001c0003t0002g0195 a0001c0003t0004g0014 |
3 | NA18960.hp1 NA18971.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.1151-609A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 17/20 | chr5 | 170253822 | |||||||
| chr5:170253907 | G | T | 3 | a0001c0003t0002g0188 a0001c0003t0002g0195 a0001c0003t0004g0014 |
3 | NA18960.hp1 NA18971.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.1151-694C>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 17/20 | chr5 | 170253907 | |||||||
| chr5:170254147 | G | A | 1 | a0001c0001t0001g0347 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1151-934C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 17/20 | chr5 | 170254147 | |||||||
| chr5:170254279 | C | T | 1 | a0003c0012t0001g0282 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1151-1066G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 17/20 | chr5 | 170254279 | |||||||
| chr5:170254329 | C | G | 5 | a0001c0003t0010g0145 a0001c0003t0010g0342 a0001c0003t0013g0283 others(2): Show |
5 | HG01243.hp2 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1151-1116G>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 17/20 | chr5 | 170254329 | |||||||
| chr5:170254446 | G | C | 1 | a0005c0014t0013g0378 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1151-1233C>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 17/20 | chr5 | 170254446 | |||||||
| chr5:170255163 | A | T | 1 | a0001c0001t0022g0237 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1150+1363T>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 17/20 | chr5 | 170255163 | |||||||
| chr5:170255226 | A | G | 1 | a0001c0007t0002g0204 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1150+1300T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 17/20 | chr5 | 170255226 | |||||||
| chr5:170255622 | C | T | 3 | a0001c0001t0001g0182 a0001c0001t0001g0238 a0001c0002t0007g0337 |
3 | NA18980.hp2 NA19002.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1150+904G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 17/20 | chr5 | 170255622 | |||||||
| chr5:170255623 | G | A | 2 | a0001c0002t0001g0289 a0001c0002t0001g0330 |
2 | HG03098.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1150+903C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 17/20 | chr5 | 170255623 | |||||||
| chr5:170255745 | C | T | 1 | a0001c0003t0027g0310 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1150+781G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 17/20 | chr5 | 170255745 | |||||||
| chr5:170256071 | C | T | 4 | a0001c0003t0002g0164 a0001c0003t0002g0170 a0001c0003t0002g0239 others(1): Show |
4 | NA18946.hp1 NA18954.hp2 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.1150+455G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 17/20 | chr5 | 170256071 | |||||||
| chr5:170256178 | T | C | 3 | a0001c0003t0010g0145 a0001c0003t0010g0342 a0001c0004t0010g0360 |
3 | HG01243.hp2 HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1150+348A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 17/20 | chr5 | 170256178 | |||||||
| chr5:170256188 | T | C | 1 | a0001c0002t0007g0229 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1150+338A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 17/20 | chr5 | 170256188 | |||||||
| chr5:170256260 | A | G | 1 | a0001c0001t0022g0237 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1150+266T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 17/20 | chr5 | 170256260 | |||||||
| chr5:170256295 | T | C | 7 | a0001c0003t0002g0004 a0001c0003t0002g0161 a0001c0003t0002g0198 others(4): Show |
8 | HG00642.hp2 HG01257.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1150+231A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 17/20 | chr5 | 170256295 | |||||||
| chr5:170256362 | G | A | 5 | a0001c0003t0010g0145 a0001c0003t0010g0342 a0001c0003t0013g0283 others(2): Show |
5 | HG01243.hp2 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1150+164C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 17/20 | chr5 | 170256362 | |||||||
| chr5:170256364 | C | T | 21 | a0001c0001t0005g0018 a0001c0001t0005g0044 a0001c0001t0005g0049 others(18): Show |
21 | HG00438.hp2 HG01891.hp2 HG02056.hp2 others(18): Show |
intron_variant | MODIFIER | c.1150+162G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 17/20 | chr5 | 170256364 | |||||||
| chr5:170256365 | A | G | 23 | a0001c0001t0005g0018 a0001c0001t0005g0044 a0001c0001t0005g0049 others(20): Show |
23 | HG00438.hp2 HG01891.hp2 HG02056.hp2 others(20): Show |
intron_variant | MODIFIER | c.1150+161T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 17/20 | chr5 | 170256365 | |||||||
| chr5:170256427 | A | T | 5 | a0001c0003t0010g0145 a0001c0003t0010g0342 a0001c0003t0013g0283 others(2): Show |
5 | HG01243.hp2 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1150+99T>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 17/20 | chr5 | 170256427 | |||||||
| chr5:170256478 | A | G | 5 | a0001c0003t0010g0145 a0001c0003t0010g0342 a0001c0003t0013g0283 others(2): Show |
5 | HG01243.hp2 HG02258.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1150+48T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 17/20 | chr5 | 170256478 | |||||||
| chr5:170256667 | T | G | 3 | a0001c0003t0010g0145 a0001c0003t0010g0342 a0001c0004t0010g0360 |
3 | HG01243.hp2 HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1101-92A>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 16/20 | chr5 | 170256667 | |||||||
| chr5:170257047 | G | A | 1 | a0001c0002t0021g0336 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1101-472C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 16/20 | chr5 | 170257047 | |||||||
| chr5:170257090 | G | A | 1 | a0001c0005t0002g0290 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1101-515C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 16/20 | chr5 | 170257090 | |||||||
| chr5:170257150 | T | C | 7 | a0001c0003t0010g0145 a0001c0003t0010g0342 a0001c0003t0013g0283 others(4): Show |
7 | HG01243.hp2 HG02258.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1101-575A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 16/20 | chr5 | 170257150 | |||||||
| chr5:170257270 | C | T | 1 | a0001c0003t0002g0184 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1101-695G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 16/20 | chr5 | 170257270 | |||||||
| chr5:170257365 | T | A | 1 | a0001c0004t0025g0338 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1100+672A>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 16/20 | chr5 | 170257365 | |||||||
| chr5:170257578 | C | G | 1 | a0001c0004t0024g0327 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1100+459G>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 16/20 | chr5 | 170257578 | |||||||
| chr5:170257697 | A | C | 10 | a0001c0003t0002g0178 a0001c0003t0002g0355 a0001c0003t0004g0009 others(7): Show |
10 | HG00544.hp2 HG01346.hp1 HG01361.hp1 others(7): Show |
intron_variant | MODIFIER | c.1100+340T>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 16/20 | chr5 | 170257697 | |||||||
| chr5:170257707 | A | G | 1 | a0001c0004t0004g0040 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1100+330T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 16/20 | chr5 | 170257707 | |||||||
| chr5:170257709 | T | C | 1 | a0001c0001t0001g0344 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1100+328A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 16/20 | chr5 | 170257709 | |||||||
| chr5:170257767 | G | A | 1 | a0001c0004t0026g0213 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1100+270C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 16/20 | chr5 | 170257767 | |||||||
| chr5:170258183 | A | G | 3 | a0001c0002t0001g0154 a0001c0002t0001g0243 a0001c0002t0004g0043 |
3 | HG01256.hp1 HG01496.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.971-17T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 15/20 | chr5 | 170258183 | |||||||
| chr5:170258236 | C | T | 1 | a0001c0001t0001g0344 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.971-70G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 15/20 | chr5 | 170258236 | |||||||
| chr5:170258294 | G | T | 1 | a0001c0004t0002g0150 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.971-128C>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 15/20 | chr5 | 170258294 | |||||||
| chr5:170258528 | C | T | 1 | a0001c0003t0002g0136 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.970+338G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 15/20 | chr5 | 170258528 | |||||||
| chr5:170258562 | G | A | 181 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(178): Show |
184 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(181): Show |
intron_variant | MODIFIER | c.970+304C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 15/20 | chr5 | 170258562 | |||||||
| chr5:170258643 | T | C | 5 | a0001c0003t0010g0145 a0001c0003t0010g0342 a0001c0004t0001g0242 others(2): Show |
5 | HG01243.hp2 HG02258.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.970+223A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 15/20 | chr5 | 170258643 | |||||||
| chr5:170258667 | G | T | 1 | a0001c0004t0002g0280 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.970+199C>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 15/20 | chr5 | 170258667 | |||||||
| chr5:170258704 | G | T | 238 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(235): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.970+162C>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 15/20 | chr5 | 170258704 | |||||||
| chr5:170258761 | T | G | 3 | a0001c0003t0002g0305 a0001c0004t0004g0107 a0001c0004t0004g0116 |
3 | HG03492.hp2 HG03942.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.970+105A>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 15/20 | chr5 | 170258761 | |||||||
| chr5:170259003 | T | C | 187 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(184): Show |
190 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(187): Show |
intron_variant | MODIFIER | c.958-125A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 14/20 | chr5 | 170259003 | |||||||
| chr5:170259009 | T | C | 7 | a0001c0003t0004g0009 a0001c0003t0004g0013 a0001c0003t0004g0023 others(4): Show |
7 | HG01346.hp1 HG01361.hp1 NA18944.hp2 others(4): Show |
intron_variant | MODIFIER | c.958-131A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 14/20 | chr5 | 170259009 | |||||||
| chr5:170259146 | G | T | 1 | a0001c0003t0001g0356 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.958-268C>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 14/20 | chr5 | 170259146 | |||||||
| chr5:170259319 | A | T | 1 | a0001c0001t0022g0237 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.958-441T>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 14/20 | chr5 | 170259319 | |||||||
| chr5:170259410 | C | T | 2 | a0001c0003t0013g0283 a0001c0004t0025g0338 |
2 | HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.958-532G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 14/20 | chr5 | 170259410 | |||||||
| chr5:170259457 | G | C | 3 | a0001c0004t0001g0242 a0001c0004t0001g0329 a0001c0004t0026g0213 |
3 | HG02818.hp2 HG03209.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.958-579C>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 14/20 | chr5 | 170259457 | |||||||
| chr5:170259587 | G | A | 9 | a0001c0001t0005g0018 a0001c0001t0005g0044 a0001c0001t0005g0049 others(6): Show |
9 | HG00438.hp2 HG02056.hp2 NA18612.hp2 others(6): Show |
intron_variant | MODIFIER | c.958-709C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 14/20 | chr5 | 170259587 | |||||||
| chr5:170259735 | G | A | 2 | a0001c0003t0002g0332 a0001c0004t0002g0316 |
2 | HG01255.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.958-857C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 14/20 | chr5 | 170259735 | |||||||
| chr5:170259821 | C | T | 3 | a0001c0003t0002g0177 a0001c0004t0002g0268 a0001c0004t0002g0308 |
3 | HG03704.hp1 HG03710.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.958-943G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 14/20 | chr5 | 170259821 | |||||||
| chr5:170259827 | C | T | 3 | a0001c0001t0007g0247 a0001c0001t0007g0343 a0001c0003t0002g0318 |
3 | HG02809.hp1 HG02965.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.958-949G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 14/20 | chr5 | 170259827 | |||||||
| chr5:170259832 | C | T | 3 | a0001c0003t0010g0145 a0001c0003t0010g0342 a0001c0004t0010g0360 |
3 | HG01243.hp2 HG02258.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.958-954G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 14/20 | chr5 | 170259832 | |||||||
| chr5:170259835 | A | G | 19 | a0001c0001t0001g0249 a0001c0001t0001g0253 a0001c0001t0001g0254 others(16): Show |
20 | HG00639.hp2 HG01243.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.958-957T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 14/20 | chr5 | 170259835 | |||||||
| chr5:170260038 | C | T | 181 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0135 others(178): Show |
183 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.957+1069G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 14/20 | chr5 | 170260038 | |||||||
| chr5:170260122 | C | T | 1 | a0001c0001t0003g0036 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.957+985G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 14/20 | chr5 | 170260122 | |||||||
| chr5:170260144 | C | G | 1 | a0001c0001t0001g0160 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.957+963G>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 14/20 | chr5 | 170260144 | |||||||
| chr5:170260234 | T | C | 1 | a0001c0003t0002g0240 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.957+873A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 14/20 | chr5 | 170260234 | |||||||
| chr5:170260343 | G | A | 5 | a0001c0002t0001g0154 a0001c0002t0001g0243 a0001c0002t0004g0043 others(2): Show |
5 | HG01256.hp1 HG01496.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.957+764C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 14/20 | chr5 | 170260343 | |||||||
| chr5:170260503 | G | A | 1 | a0005c0014t0013g0378 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.957+604C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 14/20 | chr5 | 170260503 | |||||||
| chr5:170260541 | C | T | 2 | a0001c0004t0002g0333 a0001c0004t0002g0334 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.957+566G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 14/20 | chr5 | 170260541 | |||||||
| chr5:170261151 | G | A | 5 | a0001c0002t0001g0154 a0001c0002t0001g0243 a0001c0002t0004g0043 others(2): Show |
5 | HG01256.hp1 HG01496.hp1 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.927-14C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 13/20 | chr5 | 170261151 | |||||||
| chr5:170261389 | A | ATG | 30 | a0001c0001t0001g0147 a0001c0001t0001g0277 a0001c0001t0001g0296 others(27): Show |
31 | HG00140.hp1 HG00438.hp2 HG01074.hp1 others(28): Show |
intron_variant | MODIFIER | c.927-254_927-253dup others(2): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 13/20 | chr5 | 170261389 | |||||||
| chr5:170261389 | A | ATGTG | 5 | a0001c0001t0001g0151 a0001c0001t0001g0302 a0001c0002t0003g0045 others(2): Show |
5 | HG03209.hp2 HG03491.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.927-256_927-253dup others(4): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 13/20 | chr5 | 170261389 | |||||||
| chr5:170261389 | A | G | 1 | a0001c0003t0002g0138 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.927-252T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 13/20 | chr5 | 170261389 | |||||||
| chr5:170261407 | G | GTA | 24 | a0001c0001t0005g0120 a0001c0001t0007g0218 a0001c0002t0005g0028 others(21): Show |
24 | HG01243.hp2 HG01346.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.927-272_927-271dup others(2): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 13/20 | chr5 | 170261407 | |||||||
| chr5:170261407 | G | GTGTGTA | 15 | a0001c0001t0001g0129 a0001c0001t0001g0321 a0001c0001t0001g0353 others(12): Show |
15 | HG00099.hp1 HG00280.hp2 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.927-271_927-270ins others(6): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 13/20 | chr5 | 170261407 | |||||||
| chr5:170261407 | G | GTGTGTAT others(1): Show |
93 | a0001c0001t0001g0131 a0001c0001t0001g0135 a0001c0001t0001g0137 others(90): Show |
94 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.927-271_927-270ins others(8): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 13/20 | chr5 | 170261407 | |||||||
| chr5:170261407 | G | GTGTGTAT others(3): Show |
22 | a0001c0001t0001g0132 a0001c0001t0001g0172 a0001c0001t0001g0175 others(19): Show |
22 | HG00738.hp2 HG00741.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.927-271_927-270ins others(10): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 13/20 | chr5 | 170261407 | |||||||
| chr5:170261407 | G | GTGTGTGT others(3): Show |
3 | a0001c0001t0003g0083 a0001c0001t0003g0121 a0001c0001t0011g0019 |
3 | HG02080.hp1 NA18951.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.927-271_927-270ins others(10): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 13/20 | chr5 | 170261407 | |||||||
| chr5:170261407 | G | GTGTGTGT others(5): Show |
1 | a0001c0001t0001g0311 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.927-271_927-270ins others(12): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 13/20 | chr5 | 170261407 | |||||||
| chr5:170261409 | A | G | 2 | a0001c0001t0001g0315 a0005c0014t0013g0378 |
2 | HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.927-272T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 13/20 | chr5 | 170261409 | |||||||
| chr5:170261422 | T | C | 8 | a0001c0003t0002g0142 a0001c0003t0002g0250 a0001c0003t0002g0257 others(5): Show |
8 | HG01981.hp2 HG02280.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.927-285A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 13/20 | chr5 | 170261422 | |||||||
| chr5:170261451 | C | T | 12 | a0001c0001t0005g0120 a0001c0001t0007g0218 a0001c0002t0005g0028 others(9): Show |
12 | HG01891.hp2 HG02717.hp1 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.927-314G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 13/20 | chr5 | 170261451 | |||||||
| chr5:170261459 | G | GTATA | 41 | a0001c0001t0001g0249 a0001c0001t0001g0253 a0001c0001t0001g0254 others(38): Show |
42 | HG00639.hp2 HG01243.hp2 HG01981.hp2 others(39): Show |
intron_variant | MODIFIER | c.927-326_927-323dup others(4): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 13/20 | chr5 | 170261459 | |||||||
| chr5:170261464 | T | TATATAC | 166 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0135 others(163): Show |
168 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.927-328_927-327ins others(6): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 13/20 | chr5 | 170261464 | |||||||
| chr5:170261464 | TAC | T | 7 | a0001c0003t0004g0063 a0001c0003t0004g0072 a0001c0003t0004g0106 others(4): Show |
7 | HG00099.hp2 HG01167.hp2 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.927-329_927-328del others(2): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 13/20 | chr5 | 170261464 | |||||||
| chr5:170261466 | C | T | 28 | a0001c0001t0001g0132 a0001c0001t0001g0172 a0001c0001t0001g0175 others(25): Show |
28 | HG01496.hp2 HG01891.hp2 HG02717.hp1 others(25): Show |
intron_variant | MODIFIER | c.927-329G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 13/20 | chr5 | 170261466 | |||||||
| chr5:170261482 | C | T | 207 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0135 others(204): Show |
210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.927-345G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 13/20 | chr5 | 170261482 | |||||||
| chr5:170261484 | C | CACATAT | 15 | a0001c0001t0001g0132 a0001c0001t0001g0172 a0001c0001t0001g0175 others(12): Show |
15 | HG01496.hp2 NA18947.hp2 NA18948.hp2 others(12): Show |
intron_variant | MODIFIER | c.927-348_927-347ins others(6): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 13/20 | chr5 | 170261484 | |||||||
| chr5:170261484 | C | CATAT | 12 | a0001c0001t0005g0120 a0001c0001t0007g0218 a0001c0002t0005g0028 others(9): Show |
12 | HG01891.hp2 HG02717.hp1 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.927-348_927-347ins others(4): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 13/20 | chr5 | 170261484 | |||||||
| chr5:170261484 | C | T | 207 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0135 others(204): Show |
210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.927-347G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 13/20 | chr5 | 170261484 | |||||||
| chr5:170261526 | A | G | 5 | a0001c0003t0010g0145 a0001c0003t0010g0342 a0001c0004t0001g0242 others(2): Show |
5 | HG01243.hp2 HG02258.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.927-389T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 13/20 | chr5 | 170261526 | |||||||
| chr5:170261553 | G | A | 41 | a0001c0001t0001g0249 a0001c0001t0001g0253 a0001c0001t0001g0254 others(38): Show |
42 | HG00639.hp2 HG01256.hp1 HG01496.hp1 others(39): Show |
intron_variant | MODIFIER | c.927-416C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 13/20 | chr5 | 170261553 | |||||||
| chr5:170261574 | A | G | 2 | a0001c0002t0001g0243 a0001c0002t0006g0144 |
2 | HG02723.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.927-437T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 13/20 | chr5 | 170261574 | |||||||
| chr5:170261593 | C | T | 241 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(238): Show |
244 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(241): Show |
intron_variant | MODIFIER | c.927-456G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 13/20 | chr5 | 170261593 | |||||||
| chr5:170261758 | G | T | 1 | a0001c0002t0003g0010 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.927-621C>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 13/20 | chr5 | 170261758 | |||||||
| chr5:170261786 | C | G | 11 | a0001c0001t0001g0339 a0001c0001t0005g0018 a0001c0001t0005g0049 others(8): Show |
11 | HG00438.hp2 HG01243.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.927-649G>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 13/20 | chr5 | 170261786 | |||||||
| chr5:170261970 | G | A | 1 | a0001c0001t0001g0339 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.926+665C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 13/20 | chr5 | 170261970 | |||||||
| chr5:170261991 | G | A | 1 | a0001c0002t0021g0336 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.926+644C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 13/20 | chr5 | 170261991 | |||||||
| chr5:170262119 | C | T | 1 | a0001c0002t0001g0248 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.926+516G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 13/20 | chr5 | 170262119 | |||||||
| chr5:170262123 | C | T | 4 | a0001c0002t0006g0317 a0001c0002t0006g0325 a0001c0002t0006g0366 others(1): Show |
4 | HG02622.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.926+512G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 13/20 | chr5 | 170262123 | |||||||
| chr5:170262237 | C | A | 11 | a0001c0002t0006g0325 a0001c0002t0006g0366 a0001c0002t0006g0369 others(8): Show |
11 | HG02559.hp2 HG02622.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.926+398G>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 13/20 | chr5 | 170262237 | |||||||
| chr5:170262280 | C | G | 1 | a0001c0002t0001g0274 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.926+355G>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 13/20 | chr5 | 170262280 | |||||||
| chr5:170262489 | C | T | 2 | a0001c0001t0001g0363 a0001c0001t0003g0102 |
2 | NA18948.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.926+146G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 13/20 | chr5 | 170262489 | |||||||
| chr5:170262515 | G | A | 80 | a0001c0001t0001g0147 a0001c0001t0001g0160 a0001c0001t0001g0171 others(77): Show |
80 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(77): Show |
intron_variant | MODIFIER | c.926+120C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 13/20 | chr5 | 170262515 | |||||||
| chr5:170262534 | G | A | 2 | a0001c0001t0003g0064 a0001c0004t0004g0107 |
2 | HG01123.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.926+101C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 13/20 | chr5 | 170262534 | |||||||
| chr5:170262539 | C | G | 1 | a0001c0002t0006g0317 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.926+96G>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 13/20 | chr5 | 170262539 | |||||||
| chr5:170262600 | G | C | 353 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(350): Show |
358 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(355): Show |
intron_variant | MODIFIER | c.926+35C>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 13/20 | chr5 | 170262600 | |||||||
| chr5:170262609 | A | C | 1 | a0001c0001t0001g0281 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.926+26T>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 13/20 | chr5 | 170262609 | |||||||
| chr5:170262769 | A | G | 2 | a0001c0003t0004g0048 a0001c0004t0004g0040 |
2 | NA18971.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.819-27T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 12/20 | chr5 | 170262769 | |||||||
| chr5:170262786 | G | A | 1 | a0001c0001t0001g0351 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.819-44C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 12/20 | chr5 | 170262786 | |||||||
| chr5:170262958 | A | G | 2 | a0001c0001t0015g0079 a0001c0002t0007g0262 |
2 | HG00438.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.798+9T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 11/20 | chr5 | 170262958 | |||||||
| chr5:170263013 | A | G | 1 | a0001c0005t0017g0098 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.773-21T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/20 | chr5 | 170263013 | |||||||
| chr5:170263243 | T | C | 300 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(297): Show |
305 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.773-251A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/20 | chr5 | 170263243 | |||||||
| chr5:170263244 | G | A | 2 | a0001c0004t0002g0333 a0001c0004t0002g0334 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.773-252C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/20 | chr5 | 170263244 | |||||||
| chr5:170263263 | T | A | 5 | a0001c0002t0001g0126 a0001c0002t0001g0314 a0001c0002t0001g0364 others(2): Show |
5 | HG02895.hp1 HG02922.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.773-271A>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/20 | chr5 | 170263263 | |||||||
| chr5:170263395 | T | A | 5 | a0001c0002t0001g0243 a0001c0002t0003g0090 a0001c0002t0005g0109 others(2): Show |
5 | HG02615.hp1 HG02809.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.773-403A>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/20 | chr5 | 170263395 | |||||||
| chr5:170263406 | C | T | 6 | a0001c0002t0001g0368 a0001c0002t0003g0010 a0001c0002t0005g0115 others(3): Show |
6 | HG01255.hp2 HG02615.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.773-414G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/20 | chr5 | 170263406 | |||||||
| chr5:170263407 | G | A | 2 | a0001c0004t0002g0316 a0001c0004t0002g0348 |
2 | HG01255.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.773-415C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/20 | chr5 | 170263407 | |||||||
| chr5:170263510 | G | C | 1 | a0003c0012t0001g0282 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.773-518C>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/20 | chr5 | 170263510 | |||||||
| chr5:170263563 | T | G | 1 | a0001c0001t0003g0037 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.773-571A>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/20 | chr5 | 170263563 | |||||||
| chr5:170263647 | A | C | 1 | a0001c0003t0004g0082 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.773-655T>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/20 | chr5 | 170263647 | |||||||
| chr5:170263751 | G | A | 1 | a0001c0002t0001g0364 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.773-759C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/20 | chr5 | 170263751 | |||||||
| chr5:170263771 | A | G | 2 | a0001c0006t0001g0211 a0001c0006t0001g0212 |
2 | HG01109.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.773-779T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/20 | chr5 | 170263771 | |||||||
| chr5:170263825 | A | G | 1 | a0001c0002t0006g0317 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.773-833T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/20 | chr5 | 170263825 | |||||||
| chr5:170263850 | T | C | 66 | a0001c0001t0001g0151 a0001c0001t0001g0344 a0001c0001t0007g0218 others(63): Show |
67 | HG00423.hp2 HG01255.hp2 HG01256.hp1 others(64): Show |
intron_variant | MODIFIER | c.773-858A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/20 | chr5 | 170263850 | |||||||
| chr5:170263859 | C | T | 1 | a0001c0002t0001g0314 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.773-867G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/20 | chr5 | 170263859 | |||||||
| chr5:170264054 | A | C | 6 | a0001c0001t0001g0344 a0001c0002t0001g0002 a0001c0002t0001g0143 others(3): Show |
7 | HG01884.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.773-1062T>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/20 | chr5 | 170264054 | |||||||
| chr5:170264076 | C | A | 17 | a0001c0005t0001g0264 a0001c0005t0001g0265 a0001c0005t0001g0298 others(14): Show |
17 | HG00099.hp2 HG00639.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.773-1084G>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/20 | chr5 | 170264076 | |||||||
| chr5:170264273 | T | C | 2 | a0001c0002t0001g0288 a0001c0002t0001g0314 |
2 | HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.773-1281A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/20 | chr5 | 170264273 | |||||||
| chr5:170264453 | G | A | 1 | a0001c0003t0002g0184 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.773-1461C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/20 | chr5 | 170264453 | |||||||
| chr5:170264623 | T | C | 58 | a0001c0001t0001g0344 a0001c0002t0001g0002 a0001c0002t0001g0126 others(55): Show |
59 | HG00423.hp2 HG01255.hp2 HG01256.hp1 others(56): Show |
intron_variant | MODIFIER | c.773-1631A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/20 | chr5 | 170264623 | |||||||
| chr5:170264742 | C | A | 1 | a0001c0001t0011g0053 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.773-1750G>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/20 | chr5 | 170264742 | |||||||
| chr5:170264768 | C | T | 5 | a0001c0002t0001g0340 a0001c0002t0006g0377 a0001c0002t0012g0326 others(2): Show |
5 | HG02965.hp2 HG03225.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.773-1776G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/20 | chr5 | 170264768 | |||||||
| chr5:170264807 | CTAAAAAT others(7): Show |
C | 242 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(239): Show |
245 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.773-1829_773-1816d others(16): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/20 | chr5 | 170264807 | |||||||
| chr5:170264925 | C | T | 1 | a0001c0004t0001g0300 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.772+1883G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/20 | chr5 | 170264925 | |||||||
| chr5:170264978 | C | CT | 25 | a0001c0001t0001g0254 a0001c0001t0006g0228 a0001c0002t0001g0155 others(22): Show |
25 | HG00642.hp1 HG00735.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.772+1829dupA | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/20 | chr5 | 170264978 | |||||||
| chr5:170264978 | C | CTT | 7 | a0001c0001t0001g0249 a0001c0001t0001g0253 a0001c0001t0001g0255 others(4): Show |
7 | HG00639.hp2 HG02055.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.772+1828_772+1829d others(4): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/20 | chr5 | 170264978 | |||||||
| chr5:170264978 | CT | C | 16 | a0001c0002t0001g0279 a0001c0002t0001g0286 a0001c0002t0001g0287 others(13): Show |
16 | HG00099.hp2 HG00639.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.772+1829delA | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/20 | chr5 | 170264978 | |||||||
| chr5:170264978 | CTTTTT | C | 10 | a0001c0002t0001g0143 a0001c0002t0001g0165 a0001c0002t0001g0340 others(7): Show |
10 | HG01358.hp2 HG01952.hp1 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.772+1825_772+1829d others(7): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/20 | chr5 | 170264978 | |||||||
| chr5:170264978 | CTTTTTT | C | 40 | a0001c0001t0001g0344 a0001c0002t0001g0002 a0001c0002t0001g0126 others(37): Show |
41 | HG00423.hp2 HG01255.hp2 HG01256.hp1 others(38): Show |
intron_variant | MODIFIER | c.772+1824_772+1829d others(8): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/20 | chr5 | 170264978 | |||||||
| chr5:170264978 | CTTTTTTT others(4): Show |
C | 3 | a0001c0001t0001g0281 a0001c0001t0003g0016 a0001c0001t0009g0312 |
3 | HG01952.hp2 HG03516.hp2 NA18997.hp2 |
intron_variant | MODIFIER | c.772+1819_772+1829d others(13): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/20 | chr5 | 170264978 | |||||||
| chr5:170264978 | CTTTTTTT others(5): Show |
C | 210 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(207): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.772+1818_772+1829d others(14): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/20 | chr5 | 170264978 | |||||||
| chr5:170265219 | C | T | 1 | a0001c0003t0004g0106 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.772+1589G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/20 | chr5 | 170265219 | |||||||
| chr5:170265233 | C | T | 2 | a0001c0004t0002g0148 a0001c0004t0002g0294 |
2 | HG02735.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.772+1575G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/20 | chr5 | 170265233 | |||||||
| chr5:170265257 | G | C | 2 | a0001c0002t0003g0017 a0001c0004t0002g0194 |
2 | NA19063.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.772+1551C>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/20 | chr5 | 170265257 | |||||||
| chr5:170265266 | C | G | 5 | a0001c0002t0001g0340 a0001c0002t0006g0377 a0001c0002t0012g0326 others(2): Show |
5 | HG02965.hp2 HG03225.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.772+1542G>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/20 | chr5 | 170265266 | |||||||
| chr5:170265287 | A | G | 55 | a0001c0001t0001g0344 a0001c0002t0001g0002 a0001c0002t0001g0126 others(52): Show |
56 | HG00423.hp2 HG01255.hp2 HG01256.hp1 others(53): Show |
intron_variant | MODIFIER | c.772+1521T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/20 | chr5 | 170265287 | |||||||
| chr5:170265486 | T | C | 2 | a0001c0001t0005g0104 a0001c0002t0007g0337 |
2 | NA18960.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.772+1322A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/20 | chr5 | 170265486 | |||||||
| chr5:170265545 | G | A | 3 | a0001c0002t0003g0010 a0001c0002t0005g0115 a0001c0004t0004g0123 |
3 | HG02615.hp2 HG02622.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.772+1263C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/20 | chr5 | 170265545 | |||||||
| chr5:170265550 | G | A | 295 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(292): Show |
299 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.772+1258C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/20 | chr5 | 170265550 | |||||||
| chr5:170265581 | A | G | 1 | a0001c0005t0002g0260 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.772+1227T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/20 | chr5 | 170265581 | |||||||
| chr5:170265619 | A | G | 2 | a0001c0002t0012g0326 a0001c0004t0002g0324 |
2 | HG02965.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.772+1189T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/20 | chr5 | 170265619 | |||||||
| chr5:170265623 | C | A | 1 | a0001c0001t0001g0351 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.772+1185G>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/20 | chr5 | 170265623 | |||||||
| chr5:170265688 | C | T | 6 | a0001c0002t0001g0248 a0001c0002t0001g0354 a0001c0002t0003g0021 others(3): Show |
6 | HG01255.hp2 HG02698.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.772+1120G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/20 | chr5 | 170265688 | |||||||
| chr5:170266009 | C | G | 1 | a0001c0003t0004g0048 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.772+799G>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/20 | chr5 | 170266009 | |||||||
| chr5:170266037 | T | C | 1 | a0005c0014t0013g0378 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.772+771A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/20 | chr5 | 170266037 | |||||||
| chr5:170266177 | A | C | 1 | a0001c0003t0004g0001 | 2 | HG03491.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.772+631T>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/20 | chr5 | 170266177 | |||||||
| chr5:170266184 | T | C | 1 | a0001c0001t0001g0186 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.772+624A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/20 | chr5 | 170266184 | |||||||
| chr5:170266189 | T | A | 1 | a0001c0004t0002g0316 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.772+619A>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/20 | chr5 | 170266189 | |||||||
| chr5:170266201 | C | T | 1 | a0001c0004t0004g0088 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.772+607G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/20 | chr5 | 170266201 | |||||||
| chr5:170266652 | C | T | 1 | a0001c0003t0002g0370 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.772+156G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/20 | chr5 | 170266652 | |||||||
| chr5:170266742 | G | A | 7 | a0001c0001t0001g0132 a0001c0001t0001g0135 a0001c0001t0001g0139 others(4): Show |
7 | NA18941.hp2 NA18943.hp2 NA18968.hp1 others(4): Show |
intron_variant | MODIFIER | c.772+66C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/20 | chr5 | 170266742 | |||||||
| chr5:170266753 | G | T | 1 | a0001c0002t0001g0367 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.772+55C>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 10/20 | chr5 | 170266753 | |||||||
| chr5:170267152 | C | G | 5 | a0001c0001t0001g0135 a0001c0001t0001g0139 a0001c0002t0003g0034 others(2): Show |
5 | NA18943.hp2 NA18974.hp1 NA18997.hp1 others(2): Show |
intron_variant | MODIFIER | c.622-77G>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 8/20 | chr5 | 170267152 | |||||||
| chr5:170267437 | T | C | 1 | a0001c0003t0002g0134 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.622-362A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 8/20 | chr5 | 170267437 | |||||||
| chr5:170267564 | C | T | 1 | a0001c0003t0002g0332 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.622-489G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 8/20 | chr5 | 170267564 | |||||||
| chr5:170267586 | C | G | 1 | a0001c0001t0005g0049 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.622-511G>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 8/20 | chr5 | 170267586 | |||||||
| chr5:170267596 | T | C | 5 | a0001c0002t0001g0243 a0001c0002t0003g0090 a0001c0002t0005g0109 others(2): Show |
5 | HG02615.hp1 HG02809.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.622-521A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 8/20 | chr5 | 170267596 | |||||||
| chr5:170267899 | C | T | 33 | a0001c0002t0001g0002 a0001c0002t0001g0126 a0001c0002t0001g0143 others(30): Show |
34 | HG01255.hp2 HG01884.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.621+486G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 8/20 | chr5 | 170267899 | |||||||
| chr5:170267936 | T | A | 2 | a0001c0002t0001g0288 a0001c0002t0001g0314 |
2 | HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.621+449A>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 8/20 | chr5 | 170267936 | |||||||
| chr5:170268066 | T | G | 1 | a0001c0004t0002g0163 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.621+319A>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 8/20 | chr5 | 170268066 | |||||||
| chr5:170268231 | T | C | 3 | a0001c0002t0001g0286 a0001c0002t0001g0287 a0001c0004t0001g0242 |
3 | HG02630.hp1 HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.621+154A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 8/20 | chr5 | 170268231 | |||||||
| chr5:170268232 | G | C | 2 | a0001c0002t0001g0288 a0001c0002t0001g0314 |
2 | HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.621+153C>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 8/20 | chr5 | 170268232 | |||||||
| chr5:170268302 | G | A | 1 | a0001c0002t0001g0364 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.621+83C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 8/20 | chr5 | 170268302 | |||||||
| chr5:170268607 | C | A | 238 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(235): Show |
241 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.524-125G>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 7/20 | chr5 | 170268607 | |||||||
| chr5:170268774 | CAGCTCAG others(13): Show |
C | 1 | a0001c0003t0002g0134 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.524-312_524-293del others(20): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 7/20 | chr5 | 170268774 | |||||||
| chr5:170268874 | C | T | 4 | a0001c0002t0001g0286 a0001c0002t0001g0287 a0001c0002t0001g0340 others(1): Show |
4 | HG02630.hp1 HG03453.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.524-392G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 7/20 | chr5 | 170268874 | |||||||
| chr5:170268880 | C | CATGCACA others(13): Show |
33 | a0001c0001t0001g0133 a0001c0001t0001g0140 a0001c0001t0001g0167 others(30): Show |
33 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(30): Show |
intron_variant | MODIFIER | c.524-418_524-399dup others(20): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 7/20 | chr5 | 170268880 | |||||||
| chr5:170268880 | C | CATGCACA others(33): Show |
214 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(211): Show |
217 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(214): Show |
intron_variant | MODIFIER | c.524-399_524-398ins others(40): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 7/20 | chr5 | 170268880 | |||||||
| chr5:170268880 | C | CATGCACA others(13): Show |
1 | a0005c0014t0013g0378 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.524-399_524-398ins others(20): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 7/20 | chr5 | 170268880 | |||||||
| chr5:170268911 | C | A | 226 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(223): Show |
229 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.524-429G>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 7/20 | chr5 | 170268911 | |||||||
| chr5:170269018 | G | A | 20 | a0001c0001t0001g0214 a0001c0001t0007g0218 a0001c0004t0002g0294 others(17): Show |
20 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(17): Show |
intron_variant | MODIFIER | c.524-536C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 7/20 | chr5 | 170269018 | |||||||
| chr5:170269036 | C | T | 6 | a0001c0002t0001g0248 a0001c0002t0001g0354 a0001c0002t0003g0021 others(3): Show |
6 | HG01255.hp2 HG02698.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.524-554G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 7/20 | chr5 | 170269036 | |||||||
| chr5:170269081 | T | C | 1 | a0001c0003t0004g0033 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.524-599A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 7/20 | chr5 | 170269081 | |||||||
| chr5:170269177 | C | T | 243 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(240): Show |
246 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(243): Show |
intron_variant | MODIFIER | c.524-695G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 7/20 | chr5 | 170269177 | |||||||
| chr5:170269229 | C | G | 269 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(266): Show |
272 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(269): Show |
intron_variant | MODIFIER | c.524-747G>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 7/20 | chr5 | 170269229 | |||||||
| chr5:170269318 | G | A | 15 | a0001c0002t0001g0243 a0001c0002t0001g0367 a0001c0002t0003g0010 others(12): Show |
15 | HG01884.hp2 HG02572.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.524-836C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 7/20 | chr5 | 170269318 | |||||||
| chr5:170269369 | C | T | 244 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(241): Show |
247 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.524-887G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 7/20 | chr5 | 170269369 | |||||||
| chr5:170269370 | G | T | 2 | a0001c0004t0002g0224 a0001c0004t0002g0226 |
2 | HG01074.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.524-888C>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 7/20 | chr5 | 170269370 | |||||||
| chr5:170269473 | A | G | 1 | a0005c0014t0013g0378 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.524-991T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 7/20 | chr5 | 170269473 | |||||||
| chr5:170269665 | C | T | 1 | a0001c0004t0025g0338 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.523+1054G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 7/20 | chr5 | 170269665 | |||||||
| chr5:170269731 | G | A | 1 | a0001c0002t0004g0043 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.523+988C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 7/20 | chr5 | 170269731 | |||||||
| chr5:170269739 | C | A | 249 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(246): Show |
252 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.523+980G>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 7/20 | chr5 | 170269739 | |||||||
| chr5:170269752 | C | T | 15 | a0001c0002t0001g0368 a0001c0002t0001g0371 a0001c0002t0003g0052 others(12): Show |
15 | HG00423.hp2 HG01256.hp1 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.523+967G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 7/20 | chr5 | 170269752 | |||||||
| chr5:170269875 | T | A | 1 | a0001c0004t0001g0303 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.523+844A>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 7/20 | chr5 | 170269875 | |||||||
| chr5:170270066 | AT | A | 3 | a0001c0002t0003g0010 a0001c0002t0005g0115 a0001c0004t0004g0123 |
3 | HG02615.hp2 HG02622.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.523+652delA | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 7/20 | chr5 | 170270066 | |||||||
| chr5:170270118 | T | G | 239 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(236): Show |
242 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.523+601A>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 7/20 | chr5 | 170270118 | |||||||
| chr5:170270152 | T | A | 2 | a0001c0004t0001g0300 a0001c0004t0001g0301 |
2 | NA18995.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.523+567A>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 7/20 | chr5 | 170270152 | |||||||
| chr5:170270156 | G | C | 4 | a0001c0002t0001g0286 a0001c0002t0001g0287 a0001c0002t0001g0340 others(1): Show |
4 | HG02630.hp1 HG03453.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.523+563C>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 7/20 | chr5 | 170270156 | |||||||
| chr5:170270181 | T | C | 5 | a0001c0001t0001g0339 a0001c0001t0001g0344 a0001c0001t0003g0118 others(2): Show |
5 | HG01243.hp1 HG01884.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.523+538A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 7/20 | chr5 | 170270181 | |||||||
| chr5:170270358 | G | A | 7 | a0001c0002t0005g0028 a0001c0002t0006g0244 a0001c0002t0006g0245 others(4): Show |
7 | HG02145.hp1 HG02818.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.523+361C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 7/20 | chr5 | 170270358 | |||||||
| chr5:170270509 | A | G | 19 | a0001c0001t0001g0214 a0001c0001t0007g0218 a0001c0004t0002g0294 others(16): Show |
19 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.523+210T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 7/20 | chr5 | 170270509 | |||||||
| chr5:170270605 | C | G | 3 | a0001c0002t0003g0010 a0001c0002t0005g0115 a0001c0004t0004g0123 |
3 | HG02615.hp2 HG02622.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.523+114G>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 7/20 | chr5 | 170270605 | |||||||
| chr5:170270703 | G | A | 255 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(252): Show |
258 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.523+16C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 7/20 | chr5 | 170270703 | |||||||
| chr5:170270711 | G | A | 3 | a0001c0001t0007g0247 a0001c0001t0007g0343 a0001c0003t0010g0342 |
3 | HG02965.hp1 HG03486.hp1 NA19240.hp2 |
splice_region_variant&intron_variant | LOW | c.523+8C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 7/20 | chr5 | 170270711 | |||||||
| chr5:170270712 | C | T | 2 | a0001c0002t0001g0288 a0001c0002t0001g0314 |
2 | HG03225.hp1 HG03453.hp1 |
splice_region_variant&intron_variant | LOW | c.523+7G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 7/20 | chr5 | 170270712 | |||||||
| chr5:170270942 | T | C | 1 | a0001c0001t0014g0007 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.325-25A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170270942 | |||||||
| chr5:170271024 | A | G | 262 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(259): Show |
265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.325-107T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170271024 | |||||||
| chr5:170271324 | C | A | 2 | a0001c0002t0001g0278 a0001c0002t0007g0337 |
2 | NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.325-407G>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170271324 | |||||||
| chr5:170271388 | T | C | 1 | a0001c0003t0008g0328 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.325-471A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170271388 | |||||||
| chr5:170271415 | T | A | 1 | a0003c0012t0001g0282 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.325-498A>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170271415 | |||||||
| chr5:170271876 | G | A | 1 | a0001c0004t0024g0327 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.325-959C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170271876 | |||||||
| chr5:170271987 | G | A | 1 | a0001c0003t0002g0164 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.325-1070C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170271987 | |||||||
| chr5:170272052 | G | C | 1 | a0001c0004t0024g0327 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.325-1135C>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170272052 | |||||||
| chr5:170272052 | G | T | 54 | a0001c0001t0001g0151 a0001c0001t0001g0249 a0001c0001t0001g0253 others(51): Show |
54 | HG00423.hp2 HG00639.hp2 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.325-1135C>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170272052 | |||||||
| chr5:170272287 | T | C | 1 | a0001c0004t0002g0316 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.325-1370A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170272287 | |||||||
| chr5:170272568 | G | A | 3 | a0001c0001t0003g0064 a0001c0003t0004g0063 a0001c0003t0004g0072 |
3 | HG01123.hp1 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.325-1651C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170272568 | |||||||
| chr5:170272573 | T | C | 13 | a0001c0001t0001g0151 a0001c0001t0001g0281 a0001c0001t0001g0296 others(10): Show |
13 | HG01981.hp2 HG02280.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.325-1656A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170272573 | |||||||
| chr5:170272592 | ATTTTCTT others(12): Show |
A | 1 | a0001c0002t0001g0340 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.324+1690_325-1676d others(21): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170272592 | |||||||
| chr5:170272597 | C | CT | 39 | a0001c0001t0001g0140 a0001c0001t0001g0302 a0001c0001t0001g0311 others(36): Show |
39 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.325-1681dupA | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170272597 | |||||||
| chr5:170272597 | C | CTT | 6 | a0001c0003t0004g0001 a0001c0003t0004g0041 a0001c0003t0004g0050 others(3): Show |
6 | HG00423.hp1 HG03831.hp1 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.325-1682_325-1681d others(4): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170272597 | |||||||
| chr5:170272597 | C | CTTT | 32 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0001g0351 others(29): Show |
33 | HG00099.hp1 HG00639.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.325-1683_325-1681d others(5): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170272597 | |||||||
| chr5:170272597 | C | CTTTCTTT others(5): Show |
1 | a0001c0003t0027g0310 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.325-1681_325-1680i others(14): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170272597 | |||||||
| chr5:170272597 | C | CTTTT | 47 | a0001c0001t0001g0236 a0001c0001t0001g0249 a0001c0001t0001g0253 others(44): Show |
47 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.325-1684_325-1681d others(6): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170272597 | |||||||
| chr5:170272597 | C | CTTTTT | 19 | a0001c0001t0003g0118 a0001c0002t0001g0279 a0001c0002t0001g0297 others(16): Show |
19 | HG01099.hp1 HG01123.hp2 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.325-1685_325-1681d others(7): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170272597 | |||||||
| chr5:170272597 | C | CTTTTTT | 7 | a0001c0002t0003g0010 a0001c0002t0005g0115 a0001c0002t0006g0366 others(4): Show |
7 | HG01109.hp2 HG02486.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.325-1686_325-1681d others(8): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170272597 | |||||||
| chr5:170272597 | C | CTTTTTTT others(3): Show |
3 | a0001c0001t0001g0160 a0001c0001t0003g0122 a0001c0003t0002g0196 |
3 | NA18942.hp1 NA18942.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.325-1690_325-1681d others(12): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170272597 | |||||||
| chr5:170272597 | C | CTTTTTTT others(4): Show |
28 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0158 others(25): Show |
29 | HG00438.hp1 HG00544.hp1 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.325-1691_325-1681d others(13): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170272597 | |||||||
| chr5:170272597 | C | CTTTTTTT others(5): Show |
42 | a0001c0001t0001g0129 a0001c0001t0001g0132 a0001c0001t0001g0135 others(39): Show |
43 | HG00408.hp1 HG00642.hp2 HG00673.hp1 others(40): Show |
intron_variant | MODIFIER | c.324+1692_325-1681d others(14): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170272597 | |||||||
| chr5:170272597 | C | CTTTTTTT others(6): Show |
12 | a0001c0001t0001g0167 a0001c0001t0001g0205 a0001c0001t0001g0358 others(9): Show |
12 | HG01361.hp1 HG01928.hp1 HG02165.hp2 others(9): Show |
intron_variant | MODIFIER | c.324+1691_325-1681d others(15): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170272597 | |||||||
| chr5:170272597 | C | CTTTTTTT others(7): Show |
4 | a0001c0002t0001g0165 a0001c0004t0002g0163 a0001c0004t0002g0193 others(1): Show |
4 | HG01952.hp1 HG01978.hp2 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.324+1690_325-1681d others(16): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170272597 | |||||||
| chr5:170272597 | C | CTTTTTTT others(8): Show |
1 | a0001c0001t0001g0277 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.324+1689_325-1681d others(17): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170272597 | |||||||
| chr5:170272597 | C | T | 1 | a0001c0002t0021g0336 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.325-1680G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170272597 | |||||||
| chr5:170272597 | CT | C | 10 | a0001c0001t0001g0238 a0001c0001t0005g0104 a0001c0002t0003g0076 others(7): Show |
10 | HG00558.hp1 HG02015.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.325-1681delA | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170272597 | |||||||
| chr5:170272597 | CTT | C | 8 | a0001c0001t0001g0182 a0001c0002t0005g0028 a0001c0002t0006g0244 others(5): Show |
8 | HG02055.hp2 HG02818.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.325-1682_325-1681d others(4): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170272597 | |||||||
| chr5:170272597 | CTTTTTTT others(2): Show |
C | 21 | a0001c0001t0001g0151 a0001c0001t0001g0315 a0001c0001t0001g0339 others(18): Show |
21 | HG01243.hp1 HG01243.hp2 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.325-1689_325-1681d others(11): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170272597 | |||||||
| chr5:170272597 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0296 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.325-1690_325-1681d others(12): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170272597 | |||||||
| chr5:170272597 | CTTTTTTT others(7): Show |
C | 1 | a0001c0002t0001g0367 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.324+1690_325-1681d others(16): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170272597 | |||||||
| chr5:170272669 | A | G | 138 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(135): Show |
141 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.324+1632T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170272669 | |||||||
| chr5:170272762 | A | G | 1 | a0001c0003t0002g0162 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.324+1539T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170272762 | |||||||
| chr5:170272793 | T | C | 3 | a0001c0001t0001g0256 a0001c0003t0002g0257 a0001c0004t0025g0338 |
3 | HG02559.hp2 HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.324+1508A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170272793 | |||||||
| chr5:170272796 | T | C | 34 | a0001c0001t0001g0249 a0001c0001t0001g0253 a0001c0001t0001g0254 others(31): Show |
34 | HG00639.hp2 HG01891.hp1 HG02055.hp1 others(31): Show |
intron_variant | MODIFIER | c.324+1505A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170272796 | |||||||
| chr5:170272803 | G | C | 1 | a0001c0004t0024g0327 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.324+1498C>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170272803 | |||||||
| chr5:170272815 | T | C | 139 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(136): Show |
142 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.324+1486A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170272815 | |||||||
| chr5:170272974 | C | T | 1 | a0001c0002t0001g0364 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.324+1327G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170272974 | |||||||
| chr5:170273012 | T | C | 133 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(130): Show |
136 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.324+1289A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170273012 | |||||||
| chr5:170273018 | A | C | 123 | a0001c0001t0001g0236 a0001c0001t0001g0249 a0001c0001t0001g0253 others(120): Show |
125 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.324+1283T>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170273018 | |||||||
| chr5:170273041 | T | TA | 105 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(102): Show |
108 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.324+1259dupT | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170273041 | |||||||
| chr5:170273041 | T | TAA | 97 | a0001c0001t0001g0172 a0001c0001t0001g0174 a0001c0001t0001g0175 others(94): Show |
99 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.324+1258_324+1259d others(4): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170273041 | |||||||
| chr5:170273041 | T | TAAA | 18 | a0001c0001t0001g0315 a0001c0001t0001g0352 a0001c0002t0001g0243 others(15): Show |
18 | HG00741.hp1 HG01175.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.324+1257_324+1259d others(5): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170273041 | |||||||
| chr5:170273041 | T | TAAAAAA | 6 | a0001c0001t0001g0277 a0001c0002t0001g0286 a0001c0002t0003g0010 others(3): Show |
6 | HG01109.hp1 HG02615.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.324+1254_324+1259d others(8): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170273041 | |||||||
| chr5:170273041 | T | TAAAAAAA | 12 | a0001c0001t0007g0218 a0001c0002t0001g0248 a0001c0002t0001g0287 others(9): Show |
12 | HG01891.hp2 HG02055.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.324+1253_324+1259d others(9): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170273041 | |||||||
| chr5:170273041 | TA | T | 20 | a0001c0001t0001g0151 a0001c0001t0001g0296 a0001c0001t0001g0339 others(17): Show |
20 | HG00621.hp2 HG01981.hp2 HG02080.hp1 others(17): Show |
intron_variant | MODIFIER | c.324+1259delT | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170273041 | |||||||
| chr5:170273177 | C | T | 1 | a0001c0003t0004g0094 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.324+1124G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170273177 | |||||||
| chr5:170273215 | C | T | 16 | a0001c0001t0001g0214 a0001c0001t0003g0065 a0001c0002t0001g0266 others(13): Show |
16 | HG00099.hp2 HG00140.hp2 HG00621.hp2 others(13): Show |
intron_variant | MODIFIER | c.324+1086G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170273215 | |||||||
| chr5:170273236 | C | T | 1 | a0001c0002t0001g0288 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.324+1065G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170273236 | |||||||
| chr5:170273249 | C | G | 5 | a0001c0001t0007g0218 a0001c0002t0006g0317 a0001c0003t0002g0318 others(2): Show |
5 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.324+1052G>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170273249 | |||||||
| chr5:170273348 | G | A | 258 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(255): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(260): Show |
intron_variant | MODIFIER | c.324+953C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170273348 | |||||||
| chr5:170273422 | C | A | 153 | a0001c0001t0001g0151 a0001c0001t0001g0214 a0001c0001t0001g0236 others(150): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(152): Show |
intron_variant | MODIFIER | c.324+879G>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170273422 | |||||||
| chr5:170273469 | T | C | 19 | a0001c0002t0001g0248 a0001c0002t0001g0286 a0001c0002t0001g0287 others(16): Show |
19 | HG01891.hp1 HG02145.hp1 HG02486.hp2 others(16): Show |
intron_variant | MODIFIER | c.324+832A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170273469 | |||||||
| chr5:170273581 | C | T | 1 | a0001c0002t0001g0364 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.324+720G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170273581 | |||||||
| chr5:170273585 | C | A | 15 | a0001c0002t0001g0248 a0001c0002t0001g0278 a0001c0002t0001g0286 others(12): Show |
15 | HG01891.hp1 HG02486.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.324+716G>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170273585 | |||||||
| chr5:170273590 | C | T | 7 | a0001c0002t0005g0028 a0001c0002t0006g0244 a0001c0002t0006g0245 others(4): Show |
7 | HG02145.hp1 HG02818.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.324+711G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170273590 | |||||||
| chr5:170273648 | G | A | 8 | a0001c0001t0001g0249 a0001c0001t0001g0253 a0001c0001t0001g0254 others(5): Show |
8 | HG00639.hp2 HG02055.hp1 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.324+653C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170273648 | |||||||
| chr5:170273654 | T | C | 1 | a0005c0014t0013g0378 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.324+647A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170273654 | |||||||
| chr5:170273664 | C | T | 1 | a0001c0003t0004g0027 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.324+637G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170273664 | |||||||
| chr5:170273667 | A | C | 9 | a0001c0001t0001g0296 a0001c0001t0001g0315 a0001c0001t0007g0218 others(6): Show |
9 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.324+634T>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170273667 | |||||||
| chr5:170273782 | G | T | 1 | a0001c0001t0003g0016 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.324+519C>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170273782 | |||||||
| chr5:170273852 | G | A | 4 | a0001c0001t0001g0256 a0001c0003t0002g0257 a0001c0004t0002g0280 others(1): Show |
4 | HG02559.hp2 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.324+449C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170273852 | |||||||
| chr5:170273919 | AC | A | 99 | a0001c0001t0001g0236 a0001c0001t0001g0256 a0001c0001t0001g0277 others(96): Show |
101 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.324+381delG | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170273919 | |||||||
| chr5:170273920 | CG | C | 130 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(127): Show |
133 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.324+380delC | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170273920 | |||||||
| chr5:170273921 | G | T | 99 | a0001c0001t0001g0236 a0001c0001t0001g0256 a0001c0001t0001g0277 others(96): Show |
101 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.324+380C>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170273921 | |||||||
| chr5:170273924 | G | T | 2 | a0001c0002t0007g0337 a0001c0002t0021g0336 |
2 | HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.324+377C>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170273924 | |||||||
| chr5:170273954 | G | A | 1 | a0001c0004t0002g0191 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.324+347C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170273954 | |||||||
| chr5:170273994 | A | G | 16 | a0001c0001t0001g0315 a0001c0002t0001g0248 a0001c0002t0001g0286 others(13): Show |
16 | HG01891.hp1 HG02486.hp2 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.324+307T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170273994 | |||||||
| chr5:170274013 | C | T | 67 | a0001c0001t0001g0296 a0001c0001t0001g0344 a0001c0002t0001g0005 others(64): Show |
69 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(66): Show |
intron_variant | MODIFIER | c.324+288G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 6/20 | chr5 | 170274013 | |||||||
| chr5:170274471 | C | T | 52 | a0001c0001t0001g0151 a0001c0001t0001g0256 a0001c0001t0001g0281 others(49): Show |
52 | HG01109.hp1 HG01243.hp1 HG01243.hp2 others(49): Show |
intron_variant | MODIFIER | c.287-133G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 5/20 | chr5 | 170274471 | |||||||
| chr5:170274505 | G | A | 3 | a0001c0003t0002g0373 a0001c0003t0002g0374 a0001c0003t0002g0375 |
3 | HG01070.hp1 HG01071.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.287-167C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 5/20 | chr5 | 170274505 | |||||||
| chr5:170274542 | G | C | 94 | a0001c0001t0001g0236 a0001c0001t0001g0277 a0001c0001t0001g0296 others(91): Show |
96 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.287-204C>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 5/20 | chr5 | 170274542 | |||||||
| chr5:170274685 | A | C | 7 | a0001c0001t0012g0323 a0001c0002t0006g0325 a0001c0002t0006g0377 others(4): Show |
7 | HG01243.hp1 HG01243.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.287-347T>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 5/20 | chr5 | 170274685 | |||||||
| chr5:170274743 | A | G | 1 | a0001c0003t0004g0050 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.287-405T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 5/20 | chr5 | 170274743 | |||||||
| chr5:170274747 | C | T | 7 | a0001c0001t0001g0256 a0001c0002t0007g0337 a0001c0002t0021g0336 others(4): Show |
7 | HG02559.hp2 HG02886.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.287-409G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 5/20 | chr5 | 170274747 | |||||||
| chr5:170274771 | T | A | 1 | a0001c0002t0023g0335 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.287-433A>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 5/20 | chr5 | 170274771 | |||||||
| chr5:170274790 | C | T | 1 | a0001c0004t0002g0280 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.287-452G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 5/20 | chr5 | 170274790 | |||||||
| chr5:170274838 | A | G | 3 | a0001c0001t0003g0118 a0001c0002t0005g0109 a0001c0004t0016g0108 |
3 | HG02647.hp2 HG02809.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.286+482T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 5/20 | chr5 | 170274838 | |||||||
| chr5:170274849 | T | C | 4 | a0001c0002t0003g0059 a0001c0004t0002g0149 a0001c0004t0002g0150 others(1): Show |
4 | HG01261.hp2 HG01361.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.286+471A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 5/20 | chr5 | 170274849 | |||||||
| chr5:170274888 | A | G | 115 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(112): Show |
118 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.286+432T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 5/20 | chr5 | 170274888 | |||||||
| chr5:170274915 | T | C | 220 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(217): Show |
224 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(221): Show |
intron_variant | MODIFIER | c.286+405A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 5/20 | chr5 | 170274915 | |||||||
| chr5:170274933 | T | C | 2 | a0001c0001t0001g0277 a0001c0002t0001g0288 |
2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.286+387A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 5/20 | chr5 | 170274933 | |||||||
| chr5:170274976 | C | CA | 33 | a0001c0001t0001g0132 a0001c0001t0001g0347 a0001c0001t0003g0016 others(30): Show |
33 | HG00423.hp2 HG00741.hp2 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.286+343dupT | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 5/20 | chr5 | 170274976 | |||||||
| chr5:170274976 | CA | C | 39 | a0001c0001t0001g0256 a0001c0001t0001g0281 a0001c0001t0001g0315 others(36): Show |
39 | HG00099.hp1 HG01109.hp1 HG01891.hp2 others(36): Show |
intron_variant | MODIFIER | c.286+343delT | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 5/20 | chr5 | 170274976 | |||||||
| chr5:170274996 | C | T | 1 | a0005c0014t0013g0378 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.286+324G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 5/20 | chr5 | 170274996 | |||||||
| chr5:170275069 | C | T | 2 | a0001c0001t0001g0277 a0001c0002t0001g0288 |
2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.286+251G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 5/20 | chr5 | 170275069 | |||||||
| chr5:170275165 | T | C | 9 | a0001c0001t0001g0345 a0001c0001t0001g0347 a0001c0001t0005g0104 others(6): Show |
9 | HG00544.hp2 HG00558.hp2 HG04184.hp2 others(6): Show |
intron_variant | MODIFIER | c.286+155A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 5/20 | chr5 | 170275165 | |||||||
| chr5:170275386 | C | A | 92 | a0001c0001t0001g0236 a0001c0001t0001g0277 a0001c0001t0001g0296 others(89): Show |
94 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.255-35G>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 4/20 | chr5 | 170275386 | |||||||
| chr5:170275399 | G | A | 4 | a0001c0002t0001g0354 a0001c0002t0003g0021 a0001c0004t0002g0316 others(1): Show |
4 | HG01255.hp2 HG02698.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.255-48C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 4/20 | chr5 | 170275399 | |||||||
| chr5:170275441 | C | A | 2 | a0001c0003t0002g0332 a0001c0003t0004g0070 |
2 | HG02735.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.255-90G>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 4/20 | chr5 | 170275441 | |||||||
| chr5:170275443 | A | T | 2 | a0001c0003t0002g0332 a0001c0003t0004g0070 |
2 | HG02735.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.255-92T>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 4/20 | chr5 | 170275443 | |||||||
| chr5:170275445 | T | G | 2 | a0001c0003t0002g0332 a0001c0003t0004g0070 |
2 | HG02735.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.255-94A>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 4/20 | chr5 | 170275445 | |||||||
| chr5:170275617 | C | T | 7 | a0001c0001t0001g0256 a0001c0001t0001g0315 a0001c0002t0001g0314 others(4): Show |
7 | HG02559.hp2 HG02886.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.254+178G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 4/20 | chr5 | 170275617 | |||||||
| chr5:170275644 | C | T | 25 | a0001c0001t0001g0214 a0001c0001t0001g0344 a0001c0001t0003g0065 others(22): Show |
25 | HG00099.hp2 HG00140.hp2 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.254+151G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 4/20 | chr5 | 170275644 | |||||||
| chr5:170275662 | C | T | 1 | a0001c0002t0001g0367 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.254+133G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 4/20 | chr5 | 170275662 | |||||||
| chr5:170275727 | GT | G | 3 | a0001c0002t0003g0046 a0001c0002t0003g0062 a0001c0002t0003g0096 |
3 | NA18940.hp1 NA18990.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.254+67delA | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 4/20 | chr5 | 170275727 | |||||||
| chr5:170276011 | G | T | 1 | a0001c0001t0012g0323 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.189-151C>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170276011 | |||||||
| chr5:170276027 | C | T | 11 | a0001c0001t0001g0151 a0001c0001t0001g0339 a0001c0001t0007g0247 others(8): Show |
11 | HG01981.hp2 HG02280.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.189-167G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170276027 | |||||||
| chr5:170276141 | C | G | 12 | a0001c0002t0001g0248 a0001c0002t0001g0286 a0001c0002t0001g0287 others(9): Show |
12 | HG01891.hp1 HG02486.hp2 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.189-281G>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170276141 | |||||||
| chr5:170276147 | GACTTGTC others(5): Show |
G | 1 | a0001c0002t0006g0284 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.189-299_189-288del others(12): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170276147 | |||||||
| chr5:170276415 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.189-555G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170276415 | |||||||
| chr5:170276534 | A | G | 118 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(115): Show |
121 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.189-674T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170276534 | |||||||
| chr5:170276620 | C | A | 1 | a0001c0002t0006g0127 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.189-760G>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170276620 | |||||||
| chr5:170276644 | A | G | 3 | a0001c0003t0002g0250 a0001c0003t0008g0251 a0001c0003t0008g0252 |
3 | HG02486.hp2 HG03098.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.189-784T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170276644 | |||||||
| chr5:170276780 | G | A | 12 | a0001c0001t0001g0256 a0001c0001t0001g0315 a0001c0001t0007g0218 others(9): Show |
12 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.189-920C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170276780 | |||||||
| chr5:170276998 | C | T | 253 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(250): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.189-1138G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170276998 | |||||||
| chr5:170277024 | C | T | 1 | a0001c0002t0003g0076 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.189-1164G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170277024 | |||||||
| chr5:170277074 | T | TA | 30 | a0001c0001t0001g0129 a0001c0001t0001g0140 a0001c0001t0001g0190 others(27): Show |
30 | HG00280.hp2 HG01192.hp2 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.189-1215dupT | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170277074 | |||||||
| chr5:170277074 | T | TAAA | 11 | a0001c0001t0001g0351 a0001c0001t0003g0118 a0001c0002t0001g0371 others(8): Show |
11 | HG01256.hp1 HG02486.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.189-1217_189-1215d others(5): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170277074 | |||||||
| chr5:170277074 | TA | T | 85 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0296 others(82): Show |
87 | HG00099.hp1 HG00323.hp1 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.189-1215delT | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170277074 | |||||||
| chr5:170277097 | A | G | 1 | a0003c0012t0001g0282 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.189-1237T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170277097 | |||||||
| chr5:170277125 | T | C | 1 | a0003c0012t0001g0282 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.189-1265A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170277125 | |||||||
| chr5:170277161 | C | T | 1 | a0001c0003t0002g0370 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.189-1301G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170277161 | |||||||
| chr5:170277188 | T | C | 2 | a0001c0002t0007g0337 a0001c0002t0021g0336 |
2 | HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.189-1328A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170277188 | |||||||
| chr5:170277210 | C | T | 1 | a0001c0003t0019g0060 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.189-1350G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170277210 | |||||||
| chr5:170277243 | G | A | 3 | a0001c0001t0001g0256 a0001c0003t0002g0257 a0001c0004t0025g0338 |
3 | HG02559.hp2 HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.189-1383C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170277243 | |||||||
| chr5:170277263 | T | C | 1 | a0001c0001t0001g0175 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.189-1403A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170277263 | |||||||
| chr5:170277294 | C | T | 7 | a0001c0002t0001g0368 a0001c0002t0001g0371 a0001c0002t0004g0043 others(4): Show |
7 | HG01256.hp1 HG02486.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.189-1434G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170277294 | |||||||
| chr5:170277302 | G | A | 3 | a0001c0002t0003g0046 a0001c0002t0003g0062 a0001c0002t0003g0096 |
3 | NA18940.hp1 NA18990.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.189-1442C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170277302 | |||||||
| chr5:170277458 | G | T | 85 | a0001c0001t0001g0296 a0001c0001t0003g0111 a0001c0001t0012g0323 others(82): Show |
87 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.189-1598C>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170277458 | |||||||
| chr5:170277545 | G | A | 7 | a0001c0002t0005g0028 a0001c0002t0006g0244 a0001c0002t0006g0245 others(4): Show |
7 | HG02145.hp1 HG02818.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.189-1685C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170277545 | |||||||
| chr5:170277680 | G | A | 1 | a0001c0003t0002g0161 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.189-1820C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170277680 | |||||||
| chr5:170277697 | T | A | 1 | a0001c0004t0024g0327 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.189-1837A>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170277697 | |||||||
| chr5:170277700 | C | T | 1 | a0001c0002t0001g0278 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.189-1840G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170277700 | |||||||
| chr5:170277743 | C | CA | 29 | a0001c0001t0001g0133 a0001c0001t0001g0140 a0001c0001t0001g0249 others(26): Show |
29 | HG00639.hp2 HG01071.hp2 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.189-1884dupT | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170277743 | |||||||
| chr5:170277743 | C | CAA | 85 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(82): Show |
88 | HG00408.hp1 HG00544.hp1 HG00642.hp2 others(85): Show |
intron_variant | MODIFIER | c.189-1885_189-1884d others(4): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170277743 | |||||||
| chr5:170277743 | C | CAAA | 6 | a0001c0001t0001g0190 a0001c0001t0001g0346 a0001c0001t0001g0363 others(3): Show |
6 | HG00438.hp1 NA18960.hp1 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.189-1886_189-1884d others(5): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170277743 | |||||||
| chr5:170277743 | CA | C | 6 | a0001c0001t0001g0214 a0001c0001t0001g0345 a0001c0002t0003g0076 others(3): Show |
6 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(3): Show |
intron_variant | MODIFIER | c.189-1884delT | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170277743 | |||||||
| chr5:170277743 | CAAAAA | C | 51 | a0001c0001t0001g0151 a0001c0001t0001g0236 a0001c0001t0001g0256 others(48): Show |
51 | HG00280.hp2 HG01109.hp1 HG01192.hp2 others(48): Show |
intron_variant | MODIFIER | c.189-1888_189-1884d others(7): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170277743 | |||||||
| chr5:170277760 | A | AAG | 80 | a0001c0001t0001g0296 a0001c0001t0012g0323 a0001c0002t0001g0005 others(77): Show |
82 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(79): Show |
intron_variant | MODIFIER | c.189-1901_189-1900i others(4): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170277760 | |||||||
| chr5:170277760 | A | AG | 4 | a0001c0001t0003g0111 a0001c0002t0007g0229 a0001c0002t0007g0365 others(1): Show |
4 | HG00323.hp2 HG02976.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-1901_189-1900i others(3): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170277760 | |||||||
| chr5:170277760 | A | G | 1 | a0001c0003t0002g0355 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.189-1900T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170277760 | |||||||
| chr5:170278094 | G | A | 1 | a0001c0004t0002g0280 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.189-2234C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170278094 | |||||||
| chr5:170278260 | G | A | 3 | a0001c0004t0002g0294 a0001c0006t0001g0293 a0001c0006t0001g0295 |
3 | HG02738.hp2 HG03688.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.189-2400C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170278260 | |||||||
| chr5:170278287 | C | T | 142 | a0001c0001t0001g0151 a0001c0001t0001g0236 a0001c0001t0001g0249 others(139): Show |
144 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(141): Show |
intron_variant | MODIFIER | c.189-2427G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170278287 | |||||||
| chr5:170278312 | A | AGTGGGGG others(118): Show |
1 | a0001c0003t0002g0350 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.189-2577_189-2453d others(127): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170278312 | |||||||
| chr5:170278314 | T | TG | 26 | a0001c0001t0001g0140 a0001c0001t0001g0190 a0001c0001t0001g0236 others(23): Show |
26 | HG00280.hp2 HG01192.hp2 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.189-2455dupC | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170278314 | |||||||
| chr5:170278343 | AG | A | 24 | a0001c0001t0001g0151 a0001c0001t0001g0339 a0001c0001t0007g0247 others(21): Show |
25 | HG01257.hp1 HG01358.hp2 HG01516.hp2 others(22): Show |
intron_variant | MODIFIER | c.189-2484delC | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170278343 | |||||||
| chr5:170278347 | G | A | 21 | a0001c0001t0001g0151 a0001c0001t0001g0339 a0001c0001t0007g0247 others(18): Show |
22 | HG01257.hp1 HG01358.hp2 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.189-2487C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170278347 | |||||||
| chr5:170278352 | C | G | 1 | a0001c0007t0002g0204 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.189-2492G>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170278352 | |||||||
| chr5:170278353 | T | C | 1 | a0001c0007t0002g0204 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.189-2493A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170278353 | |||||||
| chr5:170278354 | G | T | 3 | a0001c0002t0001g0286 a0001c0002t0001g0287 a0001c0007t0002g0204 |
3 | HG02630.hp1 HG03453.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.189-2494C>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170278354 | |||||||
| chr5:170278377 | G | T | 3 | a0001c0002t0001g0243 a0001c0003t0008g0241 a0001c0004t0001g0242 |
3 | NA19030.hp1 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.189-2517C>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170278377 | |||||||
| chr5:170278386 | C | CGAGGGGG others(88): Show |
1 | a0001c0001t0001g0249 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.189-2527_189-2526i others(97): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170278386 | |||||||
| chr5:170278388 | AGGGGGAT others(23): Show |
A | 1 | a0001c0002t0001g0340 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.189-2558_189-2529d others(32): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170278388 | |||||||
| chr5:170278410 | T | G | 151 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(148): Show |
155 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(152): Show |
intron_variant | MODIFIER | c.189-2550A>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170278410 | |||||||
| chr5:170278411 | G | A | 91 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(88): Show |
94 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.189-2551C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170278411 | |||||||
| chr5:170278416 | CG | C | 24 | a0001c0001t0001g0236 a0001c0001t0001g0321 a0001c0001t0001g0344 others(21): Show |
24 | HG00280.hp2 HG01192.hp2 HG01256.hp1 others(21): Show |
intron_variant | MODIFIER | c.189-2557delC | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170278416 | |||||||
| chr5:170278417 | G | GGGGGGGA others(52): Show |
4 | a0001c0001t0001g0147 a0001c0001t0003g0073 a0001c0001t0003g0095 others(1): Show |
4 | HG01074.hp1 HG01106.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-2558_189-2557i others(61): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170278417 | |||||||
| chr5:170278418 | G | GGGGGGAT others(57): Show |
7 | a0001c0002t0005g0028 a0001c0002t0006g0244 a0001c0002t0006g0245 others(4): Show |
7 | HG02145.hp1 HG02818.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.189-2622_189-2559d others(66): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170278418 | |||||||
| chr5:170278447 | T | G | 1 | a0001c0001t0001g0281 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.189-2587A>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170278447 | |||||||
| chr5:170278448 | G | GGGGGGAT others(27): Show |
2 | a0001c0002t0001g0243 a0001c0004t0001g0242 |
2 | NA19030.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.189-2622_189-2589d others(36): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170278448 | |||||||
| chr5:170278448 | G | GGGGGGAT others(97): Show |
1 | a0001c0003t0008g0241 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.189-2589_189-2588i others(106): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170278448 | |||||||
| chr5:170278453 | G | T | 1 | a0001c0004t0002g0313 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.189-2593C>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170278453 | |||||||
| chr5:170278463 | C | T | 2 | a0001c0001t0001g0311 a0001c0003t0004g0101 |
2 | HG04199.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.189-2603G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170278463 | |||||||
| chr5:170278469 | T | G | 2 | a0001c0003t0002g0188 a0001c0007t0002g0204 |
2 | NA18960.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.189-2609A>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170278469 | |||||||
| chr5:170278469 | T | TG | 32 | a0001c0001t0001g0236 a0001c0001t0001g0249 a0001c0001t0001g0277 others(29): Show |
32 | HG00280.hp2 HG01192.hp2 HG01256.hp1 others(29): Show |
intron_variant | MODIFIER | c.189-2610dupC | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170278469 | |||||||
| chr5:170278469 | T | TGGGGGGC others(88): Show |
4 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0001c0001t0001g0255 others(1): Show |
4 | HG00639.hp2 HG02922.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.189-2610_189-2609i others(97): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170278469 | |||||||
| chr5:170278470 | G | T | 1 | a0001c0003t0002g0188 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.189-2610C>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170278470 | |||||||
| chr5:170278628 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.189-2768G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170278628 | |||||||
| chr5:170278673 | G | A | 1 | a0001c0004t0024g0327 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.189-2813C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170278673 | |||||||
| chr5:170278677 | G | C | 1 | a0001c0001t0014g0007 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.189-2817C>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170278677 | |||||||
| chr5:170278701 | T | C | 1 | a0001c0002t0001g0364 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.189-2841A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170278701 | |||||||
| chr5:170278882 | G | T | 7 | a0001c0001t0012g0323 a0001c0002t0006g0325 a0001c0002t0006g0377 others(4): Show |
7 | HG01243.hp1 HG01243.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.189-3022C>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170278882 | |||||||
| chr5:170278929 | GA | G | 132 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(129): Show |
136 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(133): Show |
intron_variant | MODIFIER | c.189-3070delT | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170278929 | |||||||
| chr5:170278930 | A | G | 26 | a0001c0001t0001g0249 a0001c0001t0001g0253 a0001c0001t0001g0254 others(23): Show |
26 | HG00639.hp2 HG01243.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.189-3070T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170278930 | |||||||
| chr5:170279126 | A | G | 1 | a0001c0002t0001g0364 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.189-3266T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170279126 | |||||||
| chr5:170279142 | C | A | 6 | a0001c0001t0007g0218 a0001c0002t0007g0319 a0001c0002t0007g0320 others(3): Show |
6 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.189-3282G>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170279142 | |||||||
| chr5:170279172 | C | T | 1 | a0001c0001t0001g0296 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.189-3312G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170279172 | |||||||
| chr5:170279203 | T | A | 1 | a0001c0003t0002g0188 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.189-3343A>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170279203 | |||||||
| chr5:170279204 | G | T | 1 | a0001c0003t0002g0188 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.189-3344C>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170279204 | |||||||
| chr5:170279286 | C | A | 9 | a0001c0002t0001g0006 a0001c0002t0001g0297 a0001c0002t0002g0216 others(6): Show |
10 | HG01257.hp1 HG01358.hp2 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.189-3426G>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170279286 | |||||||
| chr5:170279335 | T | C | 13 | a0001c0001t0001g0339 a0001c0001t0007g0218 a0001c0001t0007g0247 others(10): Show |
13 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.189-3475A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170279335 | |||||||
| chr5:170279373 | A | G | 13 | a0001c0001t0001g0339 a0001c0001t0007g0218 a0001c0001t0007g0247 others(10): Show |
13 | HG01109.hp1 HG01891.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.189-3513T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170279373 | |||||||
| chr5:170279430 | G | A | 1 | a0001c0004t0002g0193 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.189-3570C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170279430 | |||||||
| chr5:170279565 | G | A | 2 | a0001c0004t0002g0280 a0005c0014t0013g0378 |
2 | HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.189-3705C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170279565 | |||||||
| chr5:170279570 | G | A | 2 | a0001c0004t0002g0280 a0005c0014t0013g0378 |
2 | HG03139.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.189-3710C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170279570 | |||||||
| chr5:170279654 | T | C | 1 | a0001c0004t0024g0327 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.189-3794A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170279654 | |||||||
| chr5:170279759 | CT | C | 4 | a0001c0001t0001g0277 a0001c0002t0001g0288 a0001c0002t0001g0340 others(1): Show |
4 | HG01884.hp2 HG03453.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.189-3900delA | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170279759 | |||||||
| chr5:170279777 | A | T | 4 | a0001c0001t0001g0277 a0001c0002t0001g0288 a0001c0002t0001g0340 others(1): Show |
4 | HG01884.hp2 HG03453.hp1 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.189-3917T>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170279777 | |||||||
| chr5:170279797 | G | A | 1 | a0001c0007t0003g0031 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.189-3937C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170279797 | |||||||
| chr5:170279801 | G | C | 1 | a0001c0002t0021g0336 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.189-3941C>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170279801 | |||||||
| chr5:170279802 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.189-3942G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170279802 | |||||||
| chr5:170279973 | A | G | 1 | a0001c0002t0007g0337 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.189-4113T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170279973 | |||||||
| chr5:170279975 | G | T | 146 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(143): Show |
150 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.189-4115C>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170279975 | |||||||
| chr5:170279985 | A | T | 1 | a0001c0007t0002g0204 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.189-4125T>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170279985 | |||||||
| chr5:170279993 | G | A | 1 | a0001c0003t0002g0261 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.189-4133C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170279993 | |||||||
| chr5:170280049 | A | G | 3 | a0001c0001t0001g0256 a0001c0003t0002g0257 a0001c0004t0025g0338 |
3 | HG02559.hp2 HG02970.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.189-4189T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170280049 | |||||||
| chr5:170280222 | C | A | 2 | a0001c0001t0001g0344 a0001c0002t0005g0061 |
2 | HG01884.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.189-4362G>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170280222 | |||||||
| chr5:170280257 | C | T | 5 | a0001c0001t0001g0277 a0001c0002t0001g0288 a0001c0002t0001g0340 others(2): Show |
5 | HG01884.hp2 HG03453.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.189-4397G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170280257 | |||||||
| chr5:170280285 | C | G | 14 | a0001c0001t0001g0151 a0001c0002t0001g0006 a0001c0002t0001g0126 others(11): Show |
15 | HG01257.hp1 HG01358.hp2 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.189-4425G>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170280285 | |||||||
| chr5:170280357 | A | T | 1 | a0001c0003t0002g0188 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.189-4497T>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170280357 | |||||||
| chr5:170280374 | C | T | 2 | a0001c0001t0007g0218 a0001c0006t0001g0211 |
2 | HG01109.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.189-4514G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170280374 | |||||||
| chr5:170280553 | C | T | 1 | a0001c0004t0025g0338 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.189-4693G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170280553 | |||||||
| chr5:170280557 | A | G | 1 | a0002c0013t0001g0230 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.189-4697T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170280557 | |||||||
| chr5:170280573 | A | G | 1 | a0001c0001t0001g0281 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.189-4713T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170280573 | |||||||
| chr5:170280639 | A | G | 21 | a0001c0001t0001g0214 a0001c0001t0003g0065 a0001c0002t0001g0168 others(18): Show |
21 | HG00099.hp2 HG00140.hp2 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.189-4779T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170280639 | |||||||
| chr5:170280764 | T | A | 1 | a0001c0005t0001g0298 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.189-4904A>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170280764 | |||||||
| chr5:170280779 | A | G | 159 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(156): Show |
163 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.189-4919T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170280779 | |||||||
| chr5:170280807 | A | G | 3 | a0001c0002t0003g0010 a0001c0002t0005g0115 a0001c0004t0004g0123 |
3 | HG02615.hp2 HG02622.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.189-4947T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170280807 | |||||||
| chr5:170280839 | C | T | 14 | a0001c0001t0007g0218 a0001c0002t0001g0243 a0001c0002t0001g0279 others(11): Show |
14 | HG01109.hp1 HG01167.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.189-4979G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170280839 | |||||||
| chr5:170280847 | A | G | 1 | a0001c0002t0001g0340 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.189-4987T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170280847 | |||||||
| chr5:170280985 | C | T | 2 | a0001c0001t0001g0302 a0001c0003t0002g0177 |
2 | HG03834.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.189-5125G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170280985 | |||||||
| chr5:170281070 | C | CAGCATTT others(11): Show |
1 | a0001c0007t0002g0204 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.189-5211_189-5210i others(20): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170281070 | |||||||
| chr5:170281082 | G | A | 11 | a0001c0001t0001g0249 a0001c0001t0001g0253 a0001c0001t0001g0254 others(8): Show |
11 | HG00639.hp2 HG02055.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.189-5222C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170281082 | |||||||
| chr5:170281183 | A | G | 1 | a0001c0002t0001g0279 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.189-5323T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170281183 | |||||||
| chr5:170281287 | C | CT | 77 | a0001c0001t0001g0296 a0001c0001t0001g0339 a0001c0001t0001g0351 others(74): Show |
78 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.189-5428dupA | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170281287 | |||||||
| chr5:170281319 | C | G | 12 | a0001c0001t0001g0151 a0001c0002t0001g0006 a0001c0002t0001g0297 others(9): Show |
13 | HG01257.hp1 HG01515.hp2 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.189-5459G>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170281319 | |||||||
| chr5:170281362 | T | C | 6 | a0001c0002t0001g0367 a0001c0002t0001g0368 a0001c0002t0001g0371 others(3): Show |
6 | HG01884.hp2 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.189-5502A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170281362 | |||||||
| chr5:170281365 | T | C | 9 | a0001c0002t0001g0367 a0001c0002t0001g0368 a0001c0002t0001g0371 others(6): Show |
9 | HG01070.hp1 HG01071.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.189-5505A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170281365 | |||||||
| chr5:170281366 | G | A | 6 | a0001c0002t0001g0367 a0001c0002t0001g0368 a0001c0002t0001g0371 others(3): Show |
6 | HG01884.hp2 HG02486.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.189-5506C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170281366 | |||||||
| chr5:170281380 | C | A | 1 | a0001c0003t0004g0001 | 2 | HG03491.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.189-5520G>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170281380 | |||||||
| chr5:170281405 | G | A | 1 | a0001c0001t0009g0128 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.189-5545C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170281405 | |||||||
| chr5:170281410 | G | A | 1 | a0001c0001t0009g0128 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.189-5550C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170281410 | |||||||
| chr5:170281428 | T | C | 13 | a0001c0001t0001g0256 a0001c0001t0001g0315 a0001c0001t0022g0237 others(10): Show |
13 | HG01167.hp1 HG02559.hp2 HG02886.hp2 others(10): Show |
intron_variant | MODIFIER | c.189-5568A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170281428 | |||||||
| chr5:170281429 | G | A | 2 | a0001c0001t0001g0256 a0001c0003t0002g0257 |
2 | HG02559.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.189-5569C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170281429 | |||||||
| chr5:170281434 | C | T | 1 | a0001c0002t0001g0340 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.189-5574G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170281434 | |||||||
| chr5:170281437 | A | G | 1 | a0001c0002t0001g0340 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.189-5577T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170281437 | |||||||
| chr5:170281439 | T | C | 1 | a0001c0002t0001g0340 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.189-5579A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170281439 | |||||||
| chr5:170281468 | A | G | 31 | a0001c0001t0001g0186 a0001c0001t0001g0358 a0001c0001t0003g0111 others(28): Show |
32 | HG00323.hp1 HG00323.hp2 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.189-5608T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170281468 | |||||||
| chr5:170281471 | A | G | 1 | a0001c0001t0001g0358 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.189-5611T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170281471 | |||||||
| chr5:170281473 | C | G | 1 | a0001c0001t0001g0358 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.189-5613G>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170281473 | |||||||
| chr5:170281481 | T | C | 222 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(219): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.189-5621A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170281481 | |||||||
| chr5:170281491 | A | G | 1 | a0001c0004t0002g0268 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.189-5631T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170281491 | |||||||
| chr5:170281494 | A | C | 1 | a0001c0001t0001g0182 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.189-5634T>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170281494 | |||||||
| chr5:170281496 | G | A | 1 | a0001c0004t0002g0150 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.189-5636C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170281496 | |||||||
| chr5:170281503 | A | C | 1 | a0001c0004t0002g0348 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.189-5643T>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170281503 | |||||||
| chr5:170281523 | G | A | 2 | a0001c0001t0003g0111 a0002c0013t0001g0230 |
2 | HG00323.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.189-5663C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170281523 | |||||||
| chr5:170281526 | C | T | 20 | a0001c0001t0001g0236 a0001c0001t0001g0321 a0001c0001t0018g0026 others(17): Show |
20 | HG00280.hp2 HG00741.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.189-5666G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170281526 | |||||||
| chr5:170281531 | T | C | 8 | a0001c0001t0012g0323 a0001c0002t0006g0325 a0001c0002t0006g0377 others(5): Show |
8 | HG01243.hp1 HG01243.hp2 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.189-5671A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170281531 | |||||||
| chr5:170281532 | G | T | 1 | a0002c0013t0001g0230 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.189-5672C>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170281532 | |||||||
| chr5:170281538 | C | T | 1 | a0001c0004t0002g0280 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.189-5678G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170281538 | |||||||
| chr5:170281662 | A | G | 4 | a0001c0001t0001g0351 a0001c0002t0023g0335 a0001c0004t0002g0333 others(1): Show |
4 | HG02630.hp2 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.189-5802T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170281662 | |||||||
| chr5:170281687 | G | A | 17 | a0001c0001t0001g0151 a0001c0001t0001g0236 a0001c0001t0001g0321 others(14): Show |
17 | HG00280.hp2 HG01192.hp2 HG01981.hp2 others(14): Show |
intron_variant | MODIFIER | c.189-5827C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170281687 | |||||||
| chr5:170281812 | C | T | 1 | a0001c0001t0003g0121 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.189-5952G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170281812 | |||||||
| chr5:170281834 | T | C | 2 | a0001c0002t0001g0222 a0001c0004t0002g0221 |
2 | HG00642.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.189-5974A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170281834 | |||||||
| chr5:170281949 | C | A | 1 | a0001c0004t0002g0180 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.188+6021G>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170281949 | |||||||
| chr5:170281984 | G | A | 4 | a0001c0002t0001g0126 a0001c0002t0006g0127 a0001c0002t0007g0365 others(1): Show |
4 | HG02818.hp2 HG02895.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.188+5986C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170281984 | |||||||
| chr5:170281997 | C | T | 1 | a0001c0002t0001g0288 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.188+5973G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170281997 | |||||||
| chr5:170282081 | A | C | 3 | a0001c0002t0001g0232 a0001c0002t0007g0229 a0001c0004t0002g0231 |
3 | NA18747.hp2 NA18988.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.188+5889T>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170282081 | |||||||
| chr5:170282106 | C | G | 1 | a0001c0002t0001g0279 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.188+5864G>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170282106 | |||||||
| chr5:170282291 | G | T | 1 | a0001c0004t0004g0040 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.188+5679C>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170282291 | |||||||
| chr5:170282618 | G | C | 1 | a0001c0003t0002g0178 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.188+5352C>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170282618 | |||||||
| chr5:170282740 | G | A | 3 | a0001c0002t0001g0361 a0001c0002t0001g0362 a0001c0004t0010g0360 |
3 | HG02258.hp2 HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.188+5230C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170282740 | |||||||
| chr5:170282788 | C | T | 1 | a0001c0004t0002g0316 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.188+5182G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170282788 | |||||||
| chr5:170282789 | C | T | 1 | a0001c0004t0002g0316 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.188+5181G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170282789 | |||||||
| chr5:170282791 | T | A | 1 | a0001c0004t0002g0316 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.188+5179A>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170282791 | |||||||
| chr5:170283090 | G | A | 1 | a0001c0001t0005g0120 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.188+4880C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170283090 | |||||||
| chr5:170283296 | G | A | 2 | a0001c0001t0001g0315 a0001c0002t0001g0314 |
2 | HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.188+4674C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170283296 | |||||||
| chr5:170283302 | A | G | 1 | a0001c0001t0003g0036 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.188+4668T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170283302 | |||||||
| chr5:170283416 | C | A | 1 | a0001c0002t0001g0278 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.188+4554G>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170283416 | |||||||
| chr5:170283508 | C | A | 1 | a0001c0006t0001g0291 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.188+4462G>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170283508 | |||||||
| chr5:170283617 | T | C | 2 | a0001c0001t0005g0074 a0001c0003t0003g0056 |
2 | NA18940.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.188+4353A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170283617 | |||||||
| chr5:170283778 | G | A | 2 | a0001c0004t0004g0123 a0001c0004t0024g0327 |
2 | HG02280.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.188+4192C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170283778 | |||||||
| chr5:170283899 | G | A | 2 | a0001c0001t0003g0122 a0001c0003t0002g0200 |
2 | NA18941.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.188+4071C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170283899 | |||||||
| chr5:170283958 | C | T | 16 | a0001c0002t0001g0286 a0001c0002t0001g0287 a0001c0002t0001g0288 others(13): Show |
16 | HG01891.hp1 HG02572.hp1 HG02572.hp2 others(13): Show |
intron_variant | MODIFIER | c.188+4012G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170283958 | |||||||
| chr5:170283981 | C | T | 1 | a0001c0002t0001g0278 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.188+3989G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170283981 | |||||||
| chr5:170284329 | C | T | 1 | a0001c0001t0001g0281 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.188+3641G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170284329 | |||||||
| chr5:170284446 | T | G | 1 | a0001c0001t0001g0281 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.188+3524A>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170284446 | |||||||
| chr5:170284456 | CT | C | 230 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0133 others(227): Show |
235 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.188+3513delA | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170284456 | |||||||
| chr5:170284456 | CTT | C | 11 | a0001c0001t0001g0201 a0001c0001t0001g0281 a0001c0001t0001g0352 others(8): Show |
11 | HG01167.hp1 HG02040.hp1 HG03516.hp2 others(8): Show |
intron_variant | MODIFIER | c.188+3512_188+3513d others(4): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170284456 | |||||||
| chr5:170284548 | C | T | 2 | a0001c0004t0002g0208 a0001c0004t0002g0209 |
2 | HG00741.hp2 HG01109.hp2 |
intron_variant | MODIFIER | c.188+3422G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170284548 | |||||||
| chr5:170284585 | A | T | 6 | a0001c0002t0003g0017 a0001c0003t0004g0048 a0001c0003t0004g0050 others(3): Show |
6 | HG00423.hp1 HG02040.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.188+3385T>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170284585 | |||||||
| chr5:170284628 | C | T | 1 | a0001c0004t0002g0280 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.188+3342G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170284628 | |||||||
| chr5:170284670 | G | A | 1 | a0001c0004t0025g0338 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.188+3300C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170284670 | |||||||
| chr5:170284745 | C | G | 1 | a0001c0001t0001g0351 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.188+3225G>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170284745 | |||||||
| chr5:170284753 | C | CT | 106 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(103): Show |
109 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.188+3216dupA | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170284753 | |||||||
| chr5:170284753 | CT | C | 45 | a0001c0001t0001g0267 a0001c0001t0001g0277 a0001c0001t0001g0296 others(42): Show |
45 | HG00621.hp2 HG00639.hp1 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.188+3216delA | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170284753 | |||||||
| chr5:170284809 | G | A | 1 | a0001c0002t0021g0336 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.188+3161C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170284809 | |||||||
| chr5:170284896 | G | A | 7 | a0001c0001t0001g0277 a0001c0001t0001g0296 a0001c0002t0001g0364 others(4): Show |
7 | HG02559.hp1 HG02809.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.188+3074C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170284896 | |||||||
| chr5:170284898 | C | T | 3 | a0001c0002t0001g0361 a0001c0002t0001g0362 a0001c0004t0010g0360 |
3 | HG02258.hp2 HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.188+3072G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170284898 | |||||||
| chr5:170284986 | G | A | 1 | a0001c0001t0009g0341 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.188+2984C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170284986 | |||||||
| chr5:170284992 | C | A | 94 | a0001c0001t0001g0147 a0001c0001t0001g0151 a0001c0001t0001g0214 others(91): Show |
96 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.188+2978G>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170284992 | |||||||
| chr5:170285044 | C | T | 1 | a0001c0002t0001g0364 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.188+2926G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170285044 | |||||||
| chr5:170285046 | C | T | 5 | a0001c0001t0009g0341 a0001c0001t0011g0053 a0001c0003t0002g0153 others(2): Show |
5 | HG02165.hp1 NA18945.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.188+2924G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170285046 | |||||||
| chr5:170285047 | G | A | 1 | a0001c0004t0025g0338 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.188+2923C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170285047 | |||||||
| chr5:170285379 | G | A | 1 | a0001c0002t0001g0364 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.188+2591C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170285379 | |||||||
| chr5:170285405 | C | A | 3 | a0001c0002t0001g0243 a0001c0003t0008g0241 a0001c0004t0001g0242 |
3 | NA19030.hp1 NA19240.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.188+2565G>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170285405 | |||||||
| chr5:170285491 | A | G | 2 | a0001c0002t0003g0059 a0001c0004t0002g0331 |
2 | HG01261.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.188+2479T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170285491 | |||||||
| chr5:170285667 | C | T | 3 | a0001c0002t0001g0361 a0001c0002t0001g0362 a0001c0004t0010g0360 |
3 | HG02258.hp2 HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.188+2303G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170285667 | |||||||
| chr5:170285679 | A | G | 114 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(111): Show |
117 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.188+2291T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170285679 | |||||||
| chr5:170285710 | C | T | 9 | a0001c0002t0001g0286 a0001c0002t0001g0287 a0001c0002t0001g0330 others(6): Show |
9 | HG01891.hp1 HG02572.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.188+2260G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170285710 | |||||||
| chr5:170285746 | C | T | 1 | a0001c0003t0004g0033 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.188+2224G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170285746 | |||||||
| chr5:170285798 | G | C | 1 | a0001c0001t0003g0037 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.188+2172C>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170285798 | |||||||
| chr5:170285801 | G | A | 4 | a0001c0002t0006g0317 a0001c0002t0007g0319 a0001c0002t0007g0320 others(1): Show |
4 | HG02809.hp1 HG03195.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.188+2169C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170285801 | |||||||
| chr5:170285987 | G | A | 2 | a0001c0001t0001g0315 a0001c0002t0001g0314 |
2 | HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.188+1983C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170285987 | |||||||
| chr5:170285995 | C | T | 2 | a0001c0002t0001g0354 a0001c0003t0002g0349 |
2 | HG03654.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.188+1975G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170285995 | |||||||
| chr5:170286015 | C | T | 3 | a0001c0005t0002g0290 a0001c0005t0002g0292 a0001c0006t0001g0291 |
3 | HG02027.hp1 HG02135.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.188+1955G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170286015 | |||||||
| chr5:170286016 | G | A | 2 | a0001c0001t0001g0315 a0001c0002t0001g0314 |
2 | HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.188+1954C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170286016 | |||||||
| chr5:170286057 | A | G | 4 | a0001c0002t0005g0028 a0001c0002t0006g0244 a0001c0002t0006g0245 others(1): Show |
4 | HG02145.hp1 HG02896.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.188+1913T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170286057 | |||||||
| chr5:170286148 | A | G | 244 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(241): Show |
249 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.188+1822T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170286148 | |||||||
| chr5:170286291 | T | C | 1 | a0001c0001t0001g0302 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.188+1679A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170286291 | |||||||
| chr5:170286609 | A | G | 3 | a0001c0002t0001g0361 a0001c0002t0001g0362 a0001c0004t0010g0360 |
3 | HG02258.hp2 HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.188+1361T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170286609 | |||||||
| chr5:170286718 | C | G | 1 | a0001c0004t0002g0191 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.188+1252G>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170286718 | |||||||
| chr5:170286724 | G | A | 15 | a0001c0001t0003g0073 a0001c0001t0003g0095 a0001c0001t0003g0099 others(12): Show |
15 | HG01106.hp2 HG01123.hp2 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.188+1246C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170286724 | |||||||
| chr5:170286741 | T | C | 1 | a0001c0002t0001g0278 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.188+1229A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170286741 | |||||||
| chr5:170286783 | T | G | 1 | a0001c0004t0002g0191 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.188+1187A>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170286783 | |||||||
| chr5:170286784 | C | T | 1 | a0001c0004t0025g0338 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.188+1186G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170286784 | |||||||
| chr5:170286824 | G | C | 5 | a0001c0002t0001g0181 a0001c0002t0001g0202 a0001c0004t0002g0179 others(2): Show |
5 | HG00099.hp1 HG01070.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.188+1146C>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170286824 | |||||||
| chr5:170287005 | A | T | 1 | a0001c0001t0006g0228 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.188+965T>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170287005 | |||||||
| chr5:170287054 | A | G | 6 | a0001c0001t0012g0323 a0001c0002t0006g0325 a0001c0002t0006g0377 others(3): Show |
6 | HG01243.hp1 HG02622.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.188+916T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170287054 | |||||||
| chr5:170287155 | T | C | 1 | a0001c0004t0004g0107 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.188+815A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170287155 | |||||||
| chr5:170287180 | G | A | 1 | a0001c0004t0002g0226 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.188+790C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170287180 | |||||||
| chr5:170287233 | G | C | 3 | a0001c0002t0001g0361 a0001c0002t0001g0362 a0001c0004t0010g0360 |
3 | HG02258.hp2 HG02717.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.188+737C>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170287233 | |||||||
| chr5:170287248 | A | G | 1 | a0001c0001t0006g0228 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.188+722T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170287248 | |||||||
| chr5:170287319 | T | C | 6 | a0001c0001t0012g0323 a0001c0002t0006g0325 a0001c0002t0006g0377 others(3): Show |
6 | HG01243.hp1 HG02622.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.188+651A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170287319 | |||||||
| chr5:170287355 | G | A | 15 | a0001c0001t0001g0281 a0001c0001t0001g0339 a0001c0001t0006g0228 others(12): Show |
15 | HG02280.hp1 HG02615.hp2 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.188+615C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170287355 | |||||||
| chr5:170287432 | G | A | 1 | a0001c0002t0001g0223 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.188+538C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170287432 | |||||||
| chr5:170287470 | A | G | 4 | a0001c0002t0006g0317 a0001c0002t0007g0319 a0001c0002t0007g0320 others(1): Show |
4 | HG02809.hp1 HG03195.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.188+500T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170287470 | |||||||
| chr5:170287493 | G | A | 1 | a0001c0003t0004g0029 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.188+477C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170287493 | |||||||
| chr5:170287706 | A | C | 1 | a0001c0002t0021g0336 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.188+264T>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170287706 | |||||||
| chr5:170287727 | G | A | 1 | a0001c0002t0005g0061 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.188+243C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 3/20 | chr5 | 170287727 | |||||||
| chr5:170288034 | A | G | 136 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(133): Show |
140 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.142-18T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170288034 | |||||||
| chr5:170288086 | T | C | 2 | a0001c0002t0006g0377 a0001c0004t0002g0376 |
2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.142-70A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170288086 | |||||||
| chr5:170288091 | C | T | 9 | a0001c0002t0001g0286 a0001c0002t0001g0287 a0001c0002t0001g0330 others(6): Show |
9 | HG01891.hp1 HG02572.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.142-75G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170288091 | |||||||
| chr5:170288117 | G | A | 4 | a0001c0002t0001g0154 a0001c0002t0001g0155 a0001c0004t0002g0156 others(1): Show |
4 | HG01123.hp2 HG01358.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-101C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170288117 | |||||||
| chr5:170288169 | G | C | 1 | a0001c0002t0001g0364 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.142-153C>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170288169 | |||||||
| chr5:170288198 | C | T | 2 | a0001c0002t0001g0243 a0001c0004t0001g0242 |
2 | NA19030.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.142-182G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170288198 | |||||||
| chr5:170288275 | T | C | 1 | a0001c0003t0002g0318 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.142-259A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170288275 | |||||||
| chr5:170288387 | C | T | 1 | a0001c0003t0002g0276 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.142-371G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170288387 | |||||||
| chr5:170288567 | G | C | 7 | a0001c0001t0001g0249 a0001c0001t0001g0253 a0001c0001t0001g0254 others(4): Show |
7 | HG00639.hp2 HG02055.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.142-551C>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170288567 | |||||||
| chr5:170288624 | C | A | 2 | a0001c0002t0003g0046 a0001c0002t0003g0062 |
2 | NA18940.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.142-608G>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170288624 | |||||||
| chr5:170288713 | A | G | 24 | a0001c0001t0001g0147 a0001c0001t0001g0151 a0001c0001t0001g0256 others(21): Show |
25 | HG01074.hp1 HG01243.hp2 HG01361.hp2 others(22): Show |
intron_variant | MODIFIER | c.142-697T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170288713 | |||||||
| chr5:170288730 | G | C | 19 | a0001c0001t0001g0147 a0001c0001t0001g0151 a0001c0001t0001g0256 others(16): Show |
20 | HG01074.hp1 HG01243.hp2 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.142-714C>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170288730 | |||||||
| chr5:170288741 | T | C | 10 | a0001c0001t0001g0339 a0001c0001t0007g0343 a0001c0002t0001g0289 others(7): Show |
10 | HG02630.hp2 HG02886.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.142-725A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170288741 | |||||||
| chr5:170288764 | A | G | 1 | a0001c0004t0010g0360 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.142-748T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170288764 | |||||||
| chr5:170288856 | G | C | 1 | a0001c0003t0004g0055 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.142-840C>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170288856 | |||||||
| chr5:170288955 | A | G | 2 | a0001c0001t0001g0315 a0001c0002t0001g0314 |
2 | HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.142-939T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170288955 | |||||||
| chr5:170289010 | TAGTTAGG others(10): Show |
T | 1 | a0001c0002t0003g0034 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.142-1011_142-995de others(18): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289010 | |||||||
| chr5:170289311 | A | G | 1 | a0001c0001t0005g0091 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.142-1295T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289311 | |||||||
| chr5:170289511 | C | T | 19 | a0001c0001t0001g0258 a0001c0001t0001g0267 a0001c0001t0003g0065 others(16): Show |
19 | HG00280.hp1 HG00621.hp2 HG00639.hp1 others(16): Show |
intron_variant | MODIFIER | c.142-1495G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289511 | |||||||
| chr5:170289523 | G | T | 1 | a0001c0002t0001g0288 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.142-1507C>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289523 | |||||||
| chr5:170289590 | CTTTTCTT others(19): Show |
C | 4 | a0001c0001t0001g0147 a0001c0004t0002g0148 a0001c0004t0002g0149 others(1): Show |
4 | HG01074.hp1 HG01361.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-1600_142-1575d others(28): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289590 | |||||||
| chr5:170289591 | TTTTCTTT others(9): Show |
T | 2 | a0001c0002t0007g0319 a0001c0002t0007g0320 |
2 | NA18522.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.142-1591_142-1576d others(18): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289591 | |||||||
| chr5:170289595 | CTTTCTTT others(15): Show |
C | 1 | a0001c0005t0002g0130 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.142-1601_142-1580d others(24): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289595 | |||||||
| chr5:170289603 | CTTTCTTT others(7): Show |
C | 4 | a0001c0002t0001g0278 a0001c0002t0005g0028 a0001c0002t0006g0245 others(1): Show |
4 | HG02145.hp1 HG02896.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-1601_142-1588d others(16): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289603 | |||||||
| chr5:170289607 | CTTTCTTT others(3): Show |
C | 7 | a0001c0001t0001g0256 a0001c0002t0001g0002 a0001c0002t0001g0143 others(4): Show |
7 | HG01981.hp2 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.142-1601_142-1592d others(12): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289607 | |||||||
| chr5:170289611 | CTTTCTT | C | 6 | a0001c0002t0001g0002 a0001c0002t0001g0330 a0001c0002t0006g0284 others(3): Show |
6 | HG01891.hp1 HG02109.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.142-1601_142-1596d others(8): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289611 | |||||||
| chr5:170289613 | TTCTTTTT others(9): Show |
T | 1 | a0002c0013t0001g0230 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.142-1613_142-1598d others(18): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289613 | |||||||
| chr5:170289615 | CTT | C | 8 | a0001c0002t0003g0010 a0001c0002t0006g0144 a0001c0002t0006g0317 others(5): Show |
8 | HG01167.hp2 HG01243.hp2 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.142-1601_142-1600d others(4): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289615 | |||||||
| chr5:170289615 | CTTTTTCT others(4): Show |
C | 1 | a0001c0002t0003g0046 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.142-1610_142-1600d others(13): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289615 | |||||||
| chr5:170289617 | T | C | 10 | a0001c0001t0001g0339 a0001c0001t0007g0343 a0001c0002t0001g0289 others(7): Show |
10 | HG02630.hp2 HG02886.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.142-1601A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289617 | |||||||
| chr5:170289617 | T | TTC | 9 | a0001c0001t0001g0151 a0001c0001t0001g0277 a0001c0001t0001g0296 others(6): Show |
9 | HG02559.hp1 HG02615.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.142-1602_142-1601i others(4): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289617 | |||||||
| chr5:170289617 | T | TTCTTTCT others(7): Show |
1 | a0001c0003t0003g0056 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.142-1602_142-1601i others(16): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289617 | |||||||
| chr5:170289617 | T | TTCTTTTT others(1): Show |
6 | a0001c0001t0003g0083 a0001c0001t0003g0112 a0001c0003t0004g0033 others(3): Show |
6 | HG02027.hp1 NA18951.hp1 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.142-1602_142-1601i others(10): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289617 | |||||||
| chr5:170289617 | T | TTCTTTTT others(9): Show |
1 | a0001c0005t0002g0292 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.142-1602_142-1601i others(18): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289617 | |||||||
| chr5:170289617 | T | TTTTC | 39 | a0001c0001t0001g0255 a0001c0001t0001g0347 a0001c0001t0001g0358 others(36): Show |
39 | HG00323.hp2 HG00438.hp2 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.142-1605_142-1602d others(6): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289617 | |||||||
| chr5:170289617 | T | TTTTCTTT others(1): Show |
16 | a0001c0001t0003g0015 a0001c0001t0003g0025 a0001c0001t0003g0037 others(13): Show |
16 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(13): Show |
intron_variant | MODIFIER | c.142-1609_142-1602d others(10): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289617 | |||||||
| chr5:170289617 | T | TTTTCTTT others(5): Show |
10 | a0001c0001t0001g0249 a0001c0001t0003g0016 a0001c0001t0003g0089 others(7): Show |
10 | HG01952.hp2 HG01993.hp2 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.142-1613_142-1602d others(14): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289617 | |||||||
| chr5:170289617 | TTTTC | T | 28 | a0001c0001t0001g0131 a0001c0001t0001g0346 a0001c0001t0003g0064 others(25): Show |
29 | HG00099.hp2 HG01071.hp1 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.142-1605_142-1602d others(6): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289617 | |||||||
| chr5:170289617 | TTTTCTTT others(1): Show |
T | 12 | a0001c0001t0001g0214 a0001c0001t0003g0095 a0001c0002t0001g0222 others(9): Show |
12 | HG00140.hp2 HG00642.hp1 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.142-1609_142-1602d others(10): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289617 | |||||||
| chr5:170289617 | TTTTCTTT others(5): Show |
T | 3 | a0001c0002t0005g0061 a0001c0003t0019g0060 a0001c0004t0002g0348 |
3 | HG02602.hp2 HG02698.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.142-1613_142-1602d others(14): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289617 | |||||||
| chr5:170289617 | TTTTCTTT others(13): Show |
T | 1 | a0001c0002t0020g0207 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.142-1621_142-1602d others(22): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289617 | |||||||
| chr5:170289619 | T | C | 2 | a0001c0001t0001g0315 a0001c0002t0001g0314 |
2 | HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.142-1603A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289619 | |||||||
| chr5:170289619 | TTCTTTCT others(57): Show |
T | 1 | a0001c0001t0007g0218 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.142-1667_142-1604d others(66): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289619 | |||||||
| chr5:170289621 | C | T | 2 | a0001c0001t0001g0315 a0001c0002t0001g0314 |
2 | HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.142-1605G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289621 | |||||||
| chr5:170289643 | T | TTCTCTCT others(9): Show |
1 | a0001c0002t0001g0288 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.142-1628_142-1627i others(18): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289643 | |||||||
| chr5:170289643 | T | TTCTTTCT others(21): Show |
1 | a0001c0002t0008g0285 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.142-1628_142-1627i others(30): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289643 | |||||||
| chr5:170289643 | T | TTCTTTCT others(24): Show |
1 | a0001c0002t0001g0286 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.142-1628_142-1627i others(33): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289643 | |||||||
| chr5:170289646 | T | TTTCTTTC others(24): Show |
1 | a0001c0002t0001g0287 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.142-1631_142-1630i others(33): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289646 | |||||||
| chr5:170289647 | T | TTCTTTCT others(15): Show |
1 | a0001c0001t0001g0296 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.142-1632_142-1631i others(24): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289647 | |||||||
| chr5:170289653 | CTTTCTTT others(7): Show |
C | 1 | a0001c0004t0002g0180 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.142-1651_142-1638d others(16): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289653 | |||||||
| chr5:170289657 | CTTTCTTT others(3): Show |
C | 3 | a0001c0003t0002g0178 a0001c0004t0004g0123 a0001c0004t0010g0360 |
3 | HG02165.hp2 HG02258.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.142-1651_142-1642d others(12): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289657 | |||||||
| chr5:170289659 | TTCTTTCT others(7): Show |
T | 1 | a0001c0003t0002g0370 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.142-1657_142-1644d others(16): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289659 | |||||||
| chr5:170289661 | CTTTCTT | C | 12 | a0001c0001t0001g0175 a0001c0001t0022g0237 a0001c0002t0001g0165 others(9): Show |
12 | HG01168.hp2 HG01952.hp1 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.142-1651_142-1646d others(8): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289661 | |||||||
| chr5:170289662 | T | C | 5 | a0001c0001t0001g0296 a0001c0002t0001g0286 a0001c0002t0001g0287 others(2): Show |
5 | HG02559.hp1 HG02630.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.142-1646A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289662 | |||||||
| chr5:170289662 | T | TCTCTCTC others(21): Show |
1 | a0001c0001t0001g0277 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.142-1647_142-1646i others(30): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289662 | |||||||
| chr5:170289663 | TTCTTTCT others(3): Show |
T | 2 | a0001c0004t0002g0209 a0001c0004t0008g0372 |
2 | HG00741.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.142-1657_142-1648d others(12): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289663 | |||||||
| chr5:170289665 | CTT | C | 26 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0137 others(23): Show |
27 | HG00408.hp1 HG00544.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.142-1651_142-1650d others(4): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289665 | |||||||
| chr5:170289665 | CTTTCTT | C | 5 | a0001c0001t0001g0171 a0001c0002t0001g0279 a0001c0003t0002g0239 others(2): Show |
5 | HG00280.hp1 HG01167.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.142-1655_142-1650d others(8): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289665 | |||||||
| chr5:170289667 | T | C | 12 | a0001c0001t0001g0135 a0001c0001t0001g0315 a0001c0002t0001g0278 others(9): Show |
12 | HG00639.hp1 HG02132.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.142-1651A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289667 | |||||||
| chr5:170289667 | TTCTTTC | T | 7 | a0001c0001t0001g0236 a0001c0001t0001g0351 a0001c0002t0001g0367 others(4): Show |
7 | HG01192.hp2 HG01884.hp2 HG02056.hp2 others(4): Show |
intron_variant | MODIFIER | c.142-1657_142-1652d others(8): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289667 | |||||||
| chr5:170289669 | CTT | C | 28 | a0001c0001t0001g0140 a0001c0001t0001g0158 a0001c0001t0001g0160 others(25): Show |
28 | HG00099.hp1 HG00280.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.142-1655_142-1654d others(4): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289669 | |||||||
| chr5:170289671 | T | C | 86 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(83): Show |
89 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(86): Show |
intron_variant | MODIFIER | c.142-1655A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289671 | |||||||
| chr5:170289671 | T | TC | 4 | a0001c0002t0001g0155 a0001c0004t0002g0156 a0001c0004t0002g0191 others(1): Show |
4 | HG01123.hp2 HG01358.hp1 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-1656_142-1655i others(3): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289671 | |||||||
| chr5:170289671 | T | TTC | 20 | a0001c0001t0001g0182 a0001c0001t0001g0190 a0001c0001t0001g0258 others(17): Show |
20 | HG00438.hp1 HG00735.hp1 HG01433.hp1 others(17): Show |
intron_variant | MODIFIER | c.142-1657_142-1656d others(4): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289671 | |||||||
| chr5:170289671 | T | TTCTC | 3 | a0001c0001t0001g0281 a0001c0001t0007g0247 a0001c0002t0007g0337 |
3 | HG03516.hp2 NA19043.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.142-1659_142-1656d others(6): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289671 | |||||||
| chr5:170289671 | T | TTCTTTC | 9 | a0001c0001t0001g0238 a0001c0001t0003g0065 a0001c0002t0001g0187 others(6): Show |
9 | HG00621.hp2 HG00673.hp1 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.142-1656_142-1655i others(8): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289671 | |||||||
| chr5:170289671 | T | TTCTTTCT others(3): Show |
3 | a0001c0001t0001g0186 a0001c0001t0001g0267 a0001c0004t0002g0192 |
3 | HG01070.hp2 HG02523.hp1 NA18948.hp2 |
intron_variant | MODIFIER | c.142-1656_142-1655i others(12): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289671 | |||||||
| chr5:170289671 | T | TTCTTTCT others(5): Show |
2 | a0001c0001t0001g0129 a0001c0003t0004g0094 |
2 | HG01346.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.142-1656_142-1655i others(14): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289671 | |||||||
| chr5:170289672 | T | C | 1 | a0001c0003t0002g0374 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.142-1656A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289672 | |||||||
| chr5:170289673 | C | CTT | 3 | a0001c0001t0012g0323 a0001c0002t0006g0325 a0001c0003t0002g0276 |
3 | HG01243.hp1 HG02622.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.142-1658_142-1657i others(4): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289673 | |||||||
| chr5:170289673 | C | T | 1 | a0001c0003t0002g0374 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.142-1657G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289673 | |||||||
| chr5:170289675 | C | T | 12 | a0001c0001t0001g0311 a0001c0001t0001g0344 a0001c0001t0009g0312 others(9): Show |
13 | HG00673.hp2 HG01358.hp2 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.142-1659G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289675 | |||||||
| chr5:170289677 | C | T | 2 | a0001c0001t0012g0323 a0001c0002t0006g0325 |
2 | HG01243.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.142-1661G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289677 | |||||||
| chr5:170289679 | C | T | 4 | a0001c0001t0001g0344 a0001c0003t0002g0305 a0001c0008t0001g0306 others(1): Show |
4 | HG01884.hp1 HG03491.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-1663G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289679 | |||||||
| chr5:170289681 | CTCTCTTT others(3): Show |
C | 1 | a0001c0002t0006g0377 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.142-1675_142-1666d others(12): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289681 | |||||||
| chr5:170289683 | C | T | 1 | a0001c0002t0001g0278 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.142-1667G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289683 | |||||||
| chr5:170289683 | CTCT | C | 3 | a0001c0003t0004g0069 a0001c0004t0004g0107 a0001c0006t0001g0293 |
3 | HG01192.hp1 HG03688.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.142-1670_142-1668d others(5): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289683 | |||||||
| chr5:170289685 | CTT | C | 4 | a0001c0002t0006g0366 a0001c0002t0012g0326 a0001c0003t0002g0373 others(1): Show |
4 | HG01071.hp2 HG01433.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-1671_142-1670d others(4): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289685 | |||||||
| chr5:170289685 | CTTTCTT | C | 3 | a0001c0002t0001g0279 a0001c0004t0002g0324 a0001c0004t0002g0376 |
3 | HG01167.hp1 HG02965.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.142-1675_142-1670d others(8): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289685 | |||||||
| chr5:170289686 | TTTCTTTC others(9): Show |
T | 6 | a0001c0001t0001g0302 a0001c0002t0001g0297 a0001c0004t0001g0300 others(3): Show |
6 | HG02738.hp1 HG03942.hp1 HG04228.hp2 others(3): Show |
intron_variant | MODIFIER | c.142-1686_142-1671d others(18): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289686 | |||||||
| chr5:170289687 | T | C | 137 | a0001c0001t0001g0129 a0001c0001t0001g0139 a0001c0001t0001g0140 others(134): Show |
139 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.142-1671A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289687 | |||||||
| chr5:170289689 | CT | C | 3 | a0001c0001t0001g0205 a0001c0003t0002g0375 a0001c0007t0002g0204 |
3 | HG01099.hp2 NA18972.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.142-1674delA | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289689 | |||||||
| chr5:170289690 | T | C | 1 | a0001c0002t0001g0219 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.142-1674A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289690 | |||||||
| chr5:170289690 | TTTCTTTC others(5): Show |
T | 2 | a0001c0002t0001g0304 a0001c0004t0001g0303 |
2 | NA19012.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.142-1686_142-1675d others(14): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289690 | |||||||
| chr5:170289691 | T | C | 16 | a0001c0001t0001g0311 a0001c0001t0001g0344 a0001c0001t0009g0312 others(13): Show |
17 | HG00673.hp2 HG01243.hp1 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.142-1675A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289691 | |||||||
| chr5:170289694 | TTTCTTTC others(1): Show |
T | 6 | a0001c0001t0001g0311 a0001c0001t0009g0312 a0001c0002t0001g0006 others(3): Show |
7 | HG00673.hp2 HG01358.hp2 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.142-1686_142-1679d others(10): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289694 | |||||||
| chr5:170289695 | T | C | 4 | a0001c0001t0001g0344 a0001c0003t0002g0305 a0001c0008t0001g0306 others(1): Show |
4 | HG01884.hp1 HG03491.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-1679A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289695 | |||||||
| chr5:170289698 | TTTCC | T | 4 | a0001c0001t0001g0344 a0001c0003t0002g0305 a0001c0008t0001g0306 others(1): Show |
4 | HG01884.hp1 HG03491.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.142-1686_142-1683d others(6): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289698 | |||||||
| chr5:170289702 | C | T | 39 | a0001c0001t0001g0129 a0001c0001t0001g0139 a0001c0001t0001g0140 others(36): Show |
39 | HG00099.hp1 HG00438.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.142-1686G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289702 | |||||||
| chr5:170289706 | T | C | 38 | a0001c0001t0001g0129 a0001c0001t0001g0139 a0001c0001t0001g0140 others(35): Show |
38 | HG00099.hp1 HG00438.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.142-1690A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289706 | |||||||
| chr5:170289710 | T | C | 1 | a0001c0003t0002g0159 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.142-1694A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289710 | |||||||
| chr5:170289712 | TCTTTC | T | 37 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(34): Show |
39 | HG00408.hp1 HG00544.hp1 HG01168.hp2 others(36): Show |
intron_variant | MODIFIER | c.142-1701_142-1697d others(7): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289712 | |||||||
| chr5:170289714 | T | TCTCTCTC others(34): Show |
5 | a0001c0002t0001g0330 a0001c0002t0003g0010 a0001c0003t0013g0283 others(2): Show |
5 | HG02572.hp1 HG02572.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.142-1699_142-1698i others(43): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289714 | |||||||
| chr5:170289714 | T | TCTCTCTC others(32): Show |
1 | a0001c0003t0008g0328 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.142-1699_142-1698i others(41): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289714 | |||||||
| chr5:170289714 | T | TCTCTCTC others(30): Show |
1 | a0001c0002t0006g0284 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.142-1699_142-1698i others(39): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289714 | |||||||
| chr5:170289716 | TC | T | 39 | a0001c0001t0001g0129 a0001c0001t0001g0139 a0001c0001t0001g0140 others(36): Show |
39 | HG00099.hp1 HG00438.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.142-1701delG | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289716 | |||||||
| chr5:170289717 | C | T | 7 | a0001c0002t0001g0330 a0001c0002t0003g0010 a0001c0002t0006g0284 others(4): Show |
7 | HG01891.hp1 HG02572.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.142-1701G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289717 | |||||||
| chr5:170289749 | TTTC | T | 5 | a0001c0002t0006g0317 a0001c0002t0007g0319 a0001c0002t0007g0320 others(2): Show |
5 | HG02809.hp1 HG02970.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.142-1736_142-1734d others(5): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289749 | |||||||
| chr5:170289754 | T | C | 5 | a0001c0002t0006g0317 a0001c0002t0007g0319 a0001c0002t0007g0320 others(2): Show |
5 | HG02809.hp1 HG02970.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.142-1738A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289754 | |||||||
| chr5:170289757 | TC | T | 5 | a0001c0002t0006g0317 a0001c0002t0007g0319 a0001c0002t0007g0320 others(2): Show |
5 | HG02809.hp1 HG02970.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.142-1742delG | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289757 | |||||||
| chr5:170289758 | C | CT | 231 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(228): Show |
236 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.142-1743dupA | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289758 | |||||||
| chr5:170289758 | C | CTTT | 19 | a0001c0001t0001g0321 a0001c0001t0006g0228 a0001c0002t0001g0243 others(16): Show |
19 | HG00280.hp2 HG02027.hp1 HG02135.hp2 others(16): Show |
intron_variant | MODIFIER | c.142-1745_142-1743d others(5): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289758 | |||||||
| chr5:170289889 | G | A | 19 | a0001c0001t0001g0321 a0001c0001t0006g0228 a0001c0002t0001g0243 others(16): Show |
19 | HG00280.hp2 HG02027.hp1 HG02135.hp2 others(16): Show |
intron_variant | MODIFIER | c.142-1873C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289889 | |||||||
| chr5:170289897 | A | G | 1 | a0001c0001t0006g0228 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.142-1881T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289897 | |||||||
| chr5:170289934 | C | G | 28 | a0001c0001t0001g0277 a0001c0001t0001g0296 a0001c0001t0001g0321 others(25): Show |
29 | HG00280.hp2 HG01891.hp1 HG02027.hp1 others(26): Show |
intron_variant | MODIFIER | c.142-1918G>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289934 | |||||||
| chr5:170289941 | G | A | 1 | a0001c0003t0004g0093 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.142-1925C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289941 | |||||||
| chr5:170289956 | T | A | 2 | a0001c0001t0001g0315 a0001c0002t0001g0314 |
2 | HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.142-1940A>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289956 | |||||||
| chr5:170289964 | G | T | 3 | a0001c0001t0001g0321 a0001c0002t0003g0059 a0001c0004t0002g0331 |
3 | HG00280.hp2 HG01261.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.142-1948C>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289964 | |||||||
| chr5:170289966 | T | C | 3 | a0001c0003t0004g0057 a0001c0003t0004g0058 a0004c0009t0004g0038 |
3 | NA18944.hp2 NA18974.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.142-1950A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289966 | |||||||
| chr5:170289977 | G | A | 2 | a0001c0001t0001g0315 a0001c0002t0001g0314 |
2 | HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.142-1961C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170289977 | |||||||
| chr5:170290504 | C | T | 174 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(171): Show |
178 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(175): Show |
intron_variant | MODIFIER | c.142-2488G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170290504 | |||||||
| chr5:170290566 | C | T | 1 | a0001c0006t0001g0293 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.142-2550G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170290566 | |||||||
| chr5:170290595 | G | T | 8 | a0001c0002t0001g0286 a0001c0002t0001g0287 a0001c0002t0003g0010 others(5): Show |
8 | HG01891.hp1 HG02572.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.142-2579C>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170290595 | |||||||
| chr5:170290602 | A | G | 3 | a0001c0003t0004g0057 a0001c0003t0004g0058 a0004c0009t0004g0038 |
3 | NA18944.hp2 NA18974.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.142-2586T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170290602 | |||||||
| chr5:170290658 | C | G | 1 | a0001c0003t0002g0161 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.142-2642G>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170290658 | |||||||
| chr5:170290658 | C | T | 1 | a0001c0003t0004g0094 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.142-2642G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170290658 | |||||||
| chr5:170290735 | C | T | 27 | a0001c0001t0001g0277 a0001c0001t0001g0296 a0001c0001t0001g0321 others(24): Show |
27 | HG00280.hp2 HG01891.hp1 HG02027.hp1 others(24): Show |
intron_variant | MODIFIER | c.141+2575G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170290735 | |||||||
| chr5:170290750 | T | C | 1 | a0001c0001t0001g0281 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.141+2560A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170290750 | |||||||
| chr5:170290770 | A | G | 10 | a0001c0001t0001g0339 a0001c0001t0007g0343 a0001c0002t0001g0289 others(7): Show |
10 | HG02630.hp2 HG02886.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.141+2540T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170290770 | |||||||
| chr5:170290825 | C | T | 4 | a0001c0001t0001g0214 a0001c0001t0001g0236 a0001c0002t0002g0216 others(1): Show |
4 | HG00140.hp2 HG01192.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.141+2485G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170290825 | |||||||
| chr5:170290840 | T | TATAACTT others(8): Show |
4 | a0001c0001t0001g0249 a0001c0001t0001g0253 a0001c0001t0001g0254 others(1): Show |
4 | HG00639.hp2 HG02055.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.141+2455_141+2469d others(17): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170290840 | |||||||
| chr5:170290849 | T | C | 1 | a0001c0003t0004g0023 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.141+2461A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170290849 | |||||||
| chr5:170290882 | C | A | 20 | a0001c0001t0001g0147 a0001c0001t0001g0151 a0001c0001t0001g0256 others(17): Show |
21 | HG01074.hp1 HG01243.hp2 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.141+2428G>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170290882 | |||||||
| chr5:170290892 | G | A | 20 | a0001c0001t0001g0147 a0001c0001t0001g0151 a0001c0001t0001g0256 others(17): Show |
21 | HG01074.hp1 HG01243.hp2 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.141+2418C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170290892 | |||||||
| chr5:170290923 | G | C | 20 | a0001c0001t0001g0147 a0001c0001t0001g0151 a0001c0001t0001g0256 others(17): Show |
21 | HG01074.hp1 HG01243.hp2 HG01361.hp2 others(18): Show |
intron_variant | MODIFIER | c.141+2387C>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170290923 | |||||||
| chr5:170290932 | GAA | G | 18 | a0001c0001t0001g0258 a0001c0001t0001g0267 a0001c0002t0001g0259 others(15): Show |
18 | HG00280.hp1 HG00639.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.141+2376_141+2377d others(4): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170290932 | |||||||
| chr5:170290951 | G | A | 5 | a0001c0002t0006g0317 a0001c0002t0007g0319 a0001c0002t0007g0320 others(2): Show |
5 | HG02809.hp1 HG03195.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.141+2359C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170290951 | |||||||
| chr5:170290952 | A | AAAAG | 27 | a0001c0001t0001g0158 a0001c0001t0003g0008 a0001c0001t0003g0011 others(24): Show |
27 | HG00423.hp1 HG00423.hp2 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.141+2354_141+2357d others(6): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170290952 | |||||||
| chr5:170290952 | A | AAAAGAAA others(1): Show |
3 | a0001c0001t0003g0036 a0001c0001t0003g0037 a0001c0001t0005g0018 |
3 | HG04228.hp1 NA18983.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.141+2350_141+2357d others(10): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170290952 | |||||||
| chr5:170290952 | A | AAAAGAAA others(5): Show |
1 | a0001c0003t0004g0035 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.141+2346_141+2357d others(14): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170290952 | |||||||
| chr5:170290952 | A | AAAAGAAA others(10): Show |
1 | a0001c0001t0001g0160 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.141+2357_141+2358i others(19): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170290952 | |||||||
| chr5:170290952 | A | AAAAGAAA others(6): Show |
1 | a0001c0002t0001g0278 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.141+2357_141+2358i others(15): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170290952 | |||||||
| chr5:170290952 | A | AAAG | 4 | a0001c0002t0003g0034 a0001c0003t0004g0032 a0001c0003t0004g0033 others(1): Show |
4 | NA19070.hp1 NA19083.hp2 NA19091.hp1 others(1): Show |
intron_variant | MODIFIER | c.141+2357_141+2358i others(5): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170290952 | |||||||
| chr5:170290952 | A | G | 1 | a0001c0003t0002g0206 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.141+2358T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170290952 | |||||||
| chr5:170290952 | AAAAG | A | 31 | a0001c0001t0001g0347 a0001c0001t0003g0015 a0001c0001t0003g0016 others(28): Show |
32 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(29): Show |
intron_variant | MODIFIER | c.141+2354_141+2357d others(6): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170290952 | |||||||
| chr5:170290952 | AAAAGAAA others(1): Show |
A | 12 | a0001c0001t0003g0118 a0001c0001t0005g0120 a0001c0002t0001g0154 others(9): Show |
12 | HG01361.hp1 HG01496.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.141+2350_141+2357d others(10): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170290952 | |||||||
| chr5:170290952 | AAAAGAAA others(5): Show |
A | 7 | a0001c0001t0001g0281 a0001c0001t0003g0121 a0001c0002t0001g0155 others(4): Show |
7 | HG01123.hp2 HG01358.hp1 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.141+2346_141+2357d others(14): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170290952 | |||||||
| chr5:170290952 | AAAAGAAA others(9): Show |
A | 5 | a0001c0002t0001g0367 a0001c0002t0001g0368 a0001c0002t0006g0366 others(2): Show |
5 | HG01884.hp2 HG02615.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.141+2342_141+2357d others(18): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170290952 | |||||||
| chr5:170290952 | AAAAGAAA others(13): Show |
A | 45 | a0001c0001t0001g0214 a0001c0001t0001g0236 a0001c0001t0001g0345 others(42): Show |
46 | HG00140.hp2 HG00323.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.141+2338_141+2357d others(22): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170290952 | |||||||
| chr5:170290952 | AAAAGAAA others(17): Show |
A | 1 | a0001c0002t0001g0359 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.141+2334_141+2357d others(26): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170290952 | |||||||
| chr5:170290955 | A | G | 1 | a0001c0002t0003g0085 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.141+2355T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170290955 | |||||||
| chr5:170290956 | G | A | 1 | a0001c0002t0003g0085 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.141+2354C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170290956 | |||||||
| chr5:170290956 | G | GAAAGAAA others(2): Show |
6 | a0001c0001t0001g0339 a0001c0002t0001g0143 a0001c0002t0021g0336 others(3): Show |
6 | HG02145.hp2 HG02735.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.141+2345_141+2353d others(11): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170290956 | |||||||
| chr5:170290960 | G | GAAAGA | 24 | a0001c0001t0001g0133 a0001c0001t0001g0171 a0001c0001t0001g0172 others(21): Show |
25 | HG00438.hp1 HG00673.hp1 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.141+2345_141+2349d others(7): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170290960 | |||||||
| chr5:170290964 | G | GA | 28 | a0001c0001t0001g0135 a0001c0001t0001g0139 a0001c0001t0001g0140 others(25): Show |
29 | HG00099.hp1 HG00544.hp1 HG01257.hp2 others(26): Show |
intron_variant | MODIFIER | c.141+2345dupT | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170290964 | |||||||
| chr5:170290965 | AAAG | A | 23 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0175 others(20): Show |
23 | HG01074.hp1 HG01361.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.141+2342_141+2344d others(5): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170290965 | |||||||
| chr5:170290965 | AAAGAAAG | A | 19 | a0001c0001t0001g0129 a0001c0001t0001g0132 a0001c0001t0001g0137 others(16): Show |
19 | HG00408.hp1 HG00673.hp2 HG01070.hp2 others(16): Show |
intron_variant | MODIFIER | c.141+2338_141+2344d others(9): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170290965 | |||||||
| chr5:170290965 | AAAGAAAG others(4): Show |
A | 11 | a0001c0001t0001g0182 a0001c0001t0001g0238 a0001c0001t0001g0302 others(8): Show |
12 | HG01168.hp2 HG01516.hp2 HG01517.hp1 others(9): Show |
intron_variant | MODIFIER | c.141+2334_141+2344d others(13): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170290965 | |||||||
| chr5:170290965 | AAAGAAAG others(8): Show |
A | 7 | a0001c0001t0001g0315 a0001c0002t0001g0314 a0001c0002t0001g0361 others(4): Show |
7 | HG02258.hp2 HG02717.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.141+2330_141+2344d others(17): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170290965 | |||||||
| chr5:170290965 | AAAGAAAG others(12): Show |
A | 5 | a0001c0002t0001g0279 a0001c0002t0006g0317 a0001c0002t0007g0319 others(2): Show |
5 | HG01167.hp1 HG02809.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.141+2326_141+2344d others(21): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170290965 | |||||||
| chr5:170290966 | AAGAAAGA others(19): Show |
A | 27 | a0001c0001t0001g0277 a0001c0001t0001g0296 a0001c0001t0001g0321 others(24): Show |
27 | HG00280.hp2 HG01891.hp1 HG02027.hp1 others(24): Show |
intron_variant | MODIFIER | c.141+2318_141+2343d others(28): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170290966 | |||||||
| chr5:170290966 | AAGAAAGA others(29): Show |
A | 10 | a0001c0001t0001g0249 a0001c0001t0001g0253 a0001c0001t0001g0254 others(7): Show |
10 | HG00639.hp2 HG02055.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.141+2308_141+2343d others(38): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170290966 | |||||||
| chr5:170290970 | AAGAAAGA others(25): Show |
A | 19 | a0001c0001t0001g0258 a0001c0001t0001g0267 a0001c0002t0001g0259 others(16): Show |
19 | HG00280.hp1 HG00639.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.141+2308_141+2339d others(34): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170290970 | |||||||
| chr5:170290970 | AAGAAAGA others(37): Show |
A | 2 | a0001c0002t0001g0126 a0001c0002t0006g0127 |
2 | HG02895.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.141+2296_141+2339d others(46): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170290970 | |||||||
| chr5:170290982 | A | G | 7 | a0001c0001t0001g0346 a0001c0001t0012g0323 a0001c0002t0007g0229 others(4): Show |
7 | HG01109.hp1 HG01109.hp2 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.141+2328T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170290982 | |||||||
| chr5:170290986 | AAGAAAGA others(9): Show |
A | 2 | a0001c0003t0004g0024 a0001c0004t0002g0331 |
2 | HG01261.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.141+2308_141+2323d others(18): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170290986 | |||||||
| chr5:170290989 | AAAGAAAG others(12): Show |
A | 2 | a0001c0006t0001g0212 a0002c0011t0001g0210 |
2 | HG01175.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.141+2302_141+2320d others(21): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170290989 | |||||||
| chr5:170290990 | A | G | 5 | a0001c0001t0001g0347 a0001c0002t0006g0325 a0001c0002t0006g0377 others(2): Show |
5 | HG02622.hp2 HG02965.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.141+2320T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170290990 | |||||||
| chr5:170290990 | AAGAAAGA others(5): Show |
A | 2 | a0001c0002t0003g0059 a0001c0002t0005g0086 |
2 | HG01934.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.141+2308_141+2319d others(14): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170290990 | |||||||
| chr5:170290992 | GAAAGAAA others(11): Show |
G | 4 | a0001c0001t0001g0346 a0001c0002t0007g0229 a0001c0004t0002g0208 others(1): Show |
4 | HG01109.hp1 HG01109.hp2 NA18966.hp2 others(1): Show |
intron_variant | MODIFIER | c.141+2300_141+2317d others(20): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170290992 | |||||||
| chr5:170290994 | A | G | 1 | a0001c0001t0012g0323 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.141+2316T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170290994 | |||||||
| chr5:170291002 | G | A | 157 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(154): Show |
161 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.141+2308C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170291002 | |||||||
| chr5:170291010 | A | AG | 3 | a0001c0002t0003g0034 a0001c0003t0004g0013 a0001c0003t0004g0063 |
3 | HG01169.hp2 HG01346.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.141+2299_141+2300i others(3): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170291010 | |||||||
| chr5:170291010 | A | G | 2 | a0001c0006t0001g0212 a0002c0011t0001g0210 |
2 | HG01175.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.141+2300T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170291010 | |||||||
| chr5:170291016 | G | T | 176 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(173): Show |
180 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.141+2294C>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170291016 | |||||||
| chr5:170291089 | A | G | 2 | a0001c0001t0001g0315 a0001c0002t0001g0314 |
2 | HG02886.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.141+2221T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170291089 | |||||||
| chr5:170291116 | GAGGGAAG others(16): Show |
G | 1 | a0001c0001t0001g0277 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.141+2171_141+2193d others(25): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170291116 | |||||||
| chr5:170291145 | AGGGGAGA others(1): Show |
A | 10 | a0001c0002t0001g0286 a0001c0002t0001g0287 a0001c0002t0001g0330 others(7): Show |
10 | HG01891.hp1 HG02572.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.141+2157_141+2164d others(10): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170291145 | |||||||
| chr5:170291148 | GGAGAGGG others(8): Show |
G | 15 | a0001c0001t0001g0296 a0001c0001t0001g0321 a0001c0002t0001g0243 others(12): Show |
15 | HG00280.hp2 HG02027.hp1 HG02135.hp2 others(12): Show |
intron_variant | MODIFIER | c.141+2147_141+2161d others(17): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170291148 | |||||||
| chr5:170291149 | G | A | 1 | a0001c0002t0001g0288 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.141+2161C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170291149 | |||||||
| chr5:170291150 | A | G | 1 | a0001c0002t0001g0288 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.141+2160T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170291150 | |||||||
| chr5:170291153 | G | A | 1 | a0001c0002t0001g0288 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.141+2157C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170291153 | |||||||
| chr5:170291156 | G | A | 1 | a0001c0002t0001g0288 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.141+2154C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170291156 | |||||||
| chr5:170291159 | G | A | 1 | a0001c0002t0001g0288 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.141+2151C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170291159 | |||||||
| chr5:170291159 | GACA | G | 10 | a0001c0002t0001g0286 a0001c0002t0001g0287 a0001c0002t0001g0330 others(7): Show |
10 | HG01891.hp1 HG02572.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.141+2148_141+2150d others(5): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170291159 | |||||||
| chr5:170291161 | C | G | 1 | a0001c0002t0001g0288 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.141+2149G>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170291161 | |||||||
| chr5:170291162 | A | G | 1 | a0001c0002t0001g0288 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.141+2148T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170291162 | |||||||
| chr5:170291164 | G | A | 26 | a0001c0001t0001g0296 a0001c0001t0001g0321 a0001c0002t0001g0243 others(23): Show |
26 | HG00280.hp2 HG01891.hp1 HG02027.hp1 others(23): Show |
intron_variant | MODIFIER | c.141+2146C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170291164 | |||||||
| chr5:170291169 | G | A | 1 | a0001c0002t0001g0288 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.141+2141C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170291169 | |||||||
| chr5:170291170 | G | A | 10 | a0001c0002t0001g0286 a0001c0002t0001g0287 a0001c0002t0001g0330 others(7): Show |
10 | HG01891.hp1 HG02572.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.141+2140C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170291170 | |||||||
| chr5:170291171 | G | A | 26 | a0001c0001t0001g0296 a0001c0001t0001g0321 a0001c0002t0001g0243 others(23): Show |
26 | HG00280.hp2 HG01891.hp1 HG02027.hp1 others(23): Show |
intron_variant | MODIFIER | c.141+2139C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170291171 | |||||||
| chr5:170291174 | G | A | 15 | a0001c0001t0001g0296 a0001c0001t0001g0321 a0001c0002t0001g0243 others(12): Show |
15 | HG00280.hp2 HG02027.hp1 HG02135.hp2 others(12): Show |
intron_variant | MODIFIER | c.141+2136C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170291174 | |||||||
| chr5:170291175 | A | C | 1 | a0001c0002t0001g0288 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.141+2135T>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170291175 | |||||||
| chr5:170291175 | A | G | 1 | a0001c0001t0006g0228 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.141+2135T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170291175 | |||||||
| chr5:170291181 | G | A | 10 | a0001c0002t0001g0286 a0001c0002t0001g0287 a0001c0002t0001g0330 others(7): Show |
10 | HG01891.hp1 HG02572.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.141+2129C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170291181 | |||||||
| chr5:170291182 | A | G | 26 | a0001c0001t0001g0296 a0001c0001t0001g0321 a0001c0002t0001g0243 others(23): Show |
26 | HG00280.hp2 HG01891.hp1 HG02027.hp1 others(23): Show |
intron_variant | MODIFIER | c.141+2128T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170291182 | |||||||
| chr5:170291185 | G | A | 15 | a0001c0001t0001g0296 a0001c0001t0001g0321 a0001c0002t0001g0243 others(12): Show |
15 | HG00280.hp2 HG02027.hp1 HG02135.hp2 others(12): Show |
intron_variant | MODIFIER | c.141+2125C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170291185 | |||||||
| chr5:170291187 | A | C | 10 | a0001c0002t0001g0286 a0001c0002t0001g0287 a0001c0002t0001g0330 others(7): Show |
10 | HG01891.hp1 HG02572.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.141+2123T>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170291187 | |||||||
| chr5:170291191 | A | C | 15 | a0001c0001t0001g0296 a0001c0001t0001g0321 a0001c0002t0001g0243 others(12): Show |
15 | HG00280.hp2 HG02027.hp1 HG02135.hp2 others(12): Show |
intron_variant | MODIFIER | c.141+2119T>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170291191 | |||||||
| chr5:170291193 | A | G | 26 | a0001c0001t0001g0296 a0001c0001t0001g0321 a0001c0002t0001g0243 others(23): Show |
26 | HG00280.hp2 HG01891.hp1 HG02027.hp1 others(23): Show |
intron_variant | MODIFIER | c.141+2117T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170291193 | |||||||
| chr5:170291199 | C | A | 26 | a0001c0001t0001g0296 a0001c0001t0001g0321 a0001c0002t0001g0243 others(23): Show |
26 | HG00280.hp2 HG01891.hp1 HG02027.hp1 others(23): Show |
intron_variant | MODIFIER | c.141+2111G>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170291199 | |||||||
| chr5:170291199 | C | CAGGA | 82 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(79): Show |
84 | HG00099.hp1 HG00408.hp1 HG00438.hp1 others(81): Show |
intron_variant | MODIFIER | c.141+2107_141+2110d others(6): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170291199 | |||||||
| chr5:170291199 | C | CAGGAAGG others(1): Show |
40 | a0001c0001t0001g0249 a0001c0001t0001g0267 a0001c0001t0001g0277 others(37): Show |
41 | HG00280.hp1 HG00558.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.141+2103_141+2110d others(10): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170291199 | |||||||
| chr5:170291199 | C | CAGGAAGG others(5): Show |
54 | a0001c0001t0001g0214 a0001c0001t0001g0253 a0001c0001t0001g0254 others(51): Show |
55 | HG00140.hp2 HG00544.hp2 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.141+2099_141+2110d others(14): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170291199 | |||||||
| chr5:170291199 | C | CAGGAAGG others(9): Show |
11 | a0001c0001t0006g0228 a0001c0002t0001g0232 a0001c0002t0001g0361 others(8): Show |
11 | HG00323.hp1 HG01168.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.141+2095_141+2110d others(18): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170291199 | |||||||
| chr5:170291199 | C | CAGGAAGG others(13): Show |
6 | a0001c0001t0001g0236 a0001c0002t0001g0364 a0001c0002t0006g0317 others(3): Show |
6 | HG01070.hp1 HG01071.hp2 HG01099.hp2 others(3): Show |
intron_variant | MODIFIER | c.141+2091_141+2110d others(22): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170291199 | |||||||
| chr5:170291199 | C | CAGGAAGG others(17): Show |
9 | a0001c0001t0012g0323 a0001c0002t0006g0325 a0001c0002t0006g0377 others(6): Show |
9 | HG01243.hp1 HG02622.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.141+2087_141+2110d others(26): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170291199 | |||||||
| chr5:170291199 | C | CAGGAAGG others(21): Show |
2 | a0001c0004t0004g0123 a0001c0004t0024g0327 |
2 | HG02280.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.141+2110_141+2111i others(30): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170291199 | |||||||
| chr5:170291222 | G | GAAGGAAG others(5): Show |
6 | a0001c0001t0001g0256 a0001c0002t0005g0028 a0001c0002t0006g0244 others(3): Show |
6 | HG01243.hp2 HG02145.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.141+2087_141+2088i others(14): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170291222 | |||||||
| chr5:170291222 | G | GAAGGAAG others(9): Show |
11 | a0001c0001t0001g0147 a0001c0001t0001g0151 a0001c0002t0001g0002 others(8): Show |
12 | HG01074.hp1 HG01361.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.141+2087_141+2088i others(18): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170291222 | |||||||
| chr5:170291222 | G | GAAGGAAG others(13): Show |
2 | a0001c0003t0002g0142 a0001c0005t0002g0130 |
2 | HG01943.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.141+2087_141+2088i others(22): Show |
LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170291222 | |||||||
| chr5:170291226 | A | G | 21 | a0001c0001t0001g0147 a0001c0001t0001g0151 a0001c0001t0001g0256 others(18): Show |
22 | HG01074.hp1 HG01243.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.141+2084T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170291226 | |||||||
| chr5:170291230 | G | A | 1 | a0001c0004t0001g0329 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.141+2080C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170291230 | |||||||
| chr5:170291351 | G | A | 3 | a0001c0004t0002g0294 a0001c0006t0001g0293 a0001c0006t0001g0295 |
3 | HG02738.hp2 HG03688.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.141+1959C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170291351 | |||||||
| chr5:170291393 | T | G | 1 | a0001c0002t0007g0337 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.141+1917A>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170291393 | |||||||
| chr5:170291425 | C | T | 11 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0133 others(8): Show |
11 | NA18941.hp2 NA18943.hp2 NA18968.hp1 others(8): Show |
intron_variant | MODIFIER | c.141+1885G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170291425 | |||||||
| chr5:170291963 | A | G | 11 | a0001c0002t0001g0286 a0001c0002t0001g0287 a0001c0002t0001g0288 others(8): Show |
11 | HG01891.hp1 HG02572.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.141+1347T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170291963 | |||||||
| chr5:170292155 | C | G | 2 | a0001c0001t0001g0256 a0001c0003t0002g0257 |
2 | HG02559.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.141+1155G>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170292155 | |||||||
| chr5:170292210 | G | A | 1 | a0001c0004t0025g0338 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.141+1100C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170292210 | |||||||
| chr5:170292283 | T | G | 1 | a0001c0001t0018g0026 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.141+1027A>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170292283 | |||||||
| chr5:170292593 | G | A | 1 | a0001c0001t0022g0237 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.141+717C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170292593 | |||||||
| chr5:170292668 | T | C | 33 | a0001c0001t0001g0238 a0001c0001t0001g0277 a0001c0001t0001g0296 others(30): Show |
33 | HG00280.hp2 HG01261.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.141+642A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170292668 | |||||||
| chr5:170292787 | T | A | 7 | a0001c0001t0001g0249 a0001c0001t0001g0253 a0001c0001t0001g0254 others(4): Show |
7 | HG00639.hp2 HG02055.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.141+523A>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170292787 | |||||||
| chr5:170293020 | C | T | 2 | a0001c0002t0001g0279 a0001c0004t0025g0338 |
2 | HG01167.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.141+290G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170293020 | |||||||
| chr5:170293054 | G | A | 3 | a0001c0002t0001g0274 a0001c0004t0002g0272 a0001c0004t0002g0273 |
3 | HG01081.hp1 HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.141+256C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170293054 | |||||||
| chr5:170293132 | G | A | 2 | a0001c0001t0001g0277 a0001c0001t0001g0296 |
2 | HG02559.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.141+178C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170293132 | |||||||
| chr5:170293208 | C | T | 1 | a0001c0005t0002g0130 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.141+102G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170293208 | |||||||
| chr5:170293267 | C | T | 1 | a0001c0002t0001g0279 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.141+43G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 2/20 | chr5 | 170293267 | |||||||
| chr5:170293538 | G | A | 3 | a0001c0002t0006g0244 a0001c0002t0006g0245 a0001c0002t0006g0246 |
3 | HG02145.hp1 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.79-166C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170293538 | |||||||
| chr5:170293581 | C | T | 1 | a0001c0001t0001g0129 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.79-209G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170293581 | |||||||
| chr5:170293720 | T | G | 1 | a0001c0004t0001g0322 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.79-348A>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170293720 | |||||||
| chr5:170293722 | G | A | 21 | a0001c0001t0001g0277 a0001c0001t0001g0281 a0001c0001t0001g0296 others(18): Show |
21 | HG01891.hp1 HG02027.hp1 HG02135.hp2 others(18): Show |
intron_variant | MODIFIER | c.79-350C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170293722 | |||||||
| chr5:170293968 | C | T | 1 | a0001c0002t0001g0279 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.79-596G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170293968 | |||||||
| chr5:170293972 | G | A | 6 | a0001c0001t0012g0323 a0001c0002t0006g0325 a0001c0002t0006g0377 others(3): Show |
6 | HG01243.hp1 HG02622.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.79-600C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170293972 | |||||||
| chr5:170293995 | T | A | 1 | a0001c0004t0024g0327 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.79-623A>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170293995 | |||||||
| chr5:170294063 | G | A | 6 | a0001c0004t0002g0294 a0001c0005t0002g0290 a0001c0005t0002g0292 others(3): Show |
6 | HG02027.hp1 HG02135.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.79-691C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170294063 | |||||||
| chr5:170294106 | T | C | 1 | a0001c0002t0001g0006 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.79-734A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170294106 | |||||||
| chr5:170294160 | T | C | 2 | a0001c0001t0001g0277 a0001c0001t0001g0296 |
2 | HG02559.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.79-788A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170294160 | |||||||
| chr5:170294287 | T | C | 9 | a0001c0001t0001g0249 a0001c0001t0001g0253 a0001c0001t0001g0254 others(6): Show |
9 | HG00639.hp2 HG02055.hp1 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.79-915A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170294287 | |||||||
| chr5:170294326 | C | T | 21 | a0001c0001t0001g0277 a0001c0001t0001g0281 a0001c0001t0001g0296 others(18): Show |
21 | HG01891.hp1 HG02027.hp1 HG02135.hp2 others(18): Show |
intron_variant | MODIFIER | c.79-954G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170294326 | |||||||
| chr5:170294359 | C | T | 1 | a0001c0001t0018g0026 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.79-987G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170294359 | |||||||
| chr5:170294407 | T | C | 1 | a0001c0002t0001g0278 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.79-1035A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170294407 | |||||||
| chr5:170294431 | C | T | 1 | a0001c0001t0003g0025 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.79-1059G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170294431 | |||||||
| chr5:170294580 | C | T | 1 | a0001c0002t0001g0278 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.79-1208G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170294580 | |||||||
| chr5:170294592 | T | C | 1 | a0001c0002t0001g0275 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.79-1220A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170294592 | |||||||
| chr5:170294593 | A | G | 1 | a0005c0014t0013g0378 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.79-1221T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170294593 | |||||||
| chr5:170294618 | C | T | 5 | a0001c0001t0003g0022 a0001c0001t0014g0007 a0001c0002t0003g0021 others(2): Show |
5 | HG01361.hp1 HG01928.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.79-1246G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170294618 | |||||||
| chr5:170294714 | A | G | 23 | a0001c0001t0001g0256 a0001c0001t0001g0277 a0001c0001t0001g0281 others(20): Show |
23 | HG01891.hp1 HG02027.hp1 HG02135.hp2 others(20): Show |
intron_variant | MODIFIER | c.79-1342T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170294714 | |||||||
| chr5:170294760 | G | T | 1 | a0001c0002t0001g0278 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.79-1388C>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170294760 | |||||||
| chr5:170294835 | A | T | 3 | a0001c0001t0005g0018 a0001c0001t0011g0019 a0001c0004t0004g0020 |
3 | HG02080.hp1 NA18983.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.79-1463T>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170294835 | |||||||
| chr5:170295126 | A | C | 1 | a0001c0001t0009g0128 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.79-1754T>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170295126 | |||||||
| chr5:170295127 | C | G | 2 | a0001c0002t0007g0337 a0001c0002t0021g0336 |
2 | HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.79-1755G>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170295127 | |||||||
| chr5:170295156 | C | T | 3 | a0001c0002t0023g0335 a0001c0004t0002g0333 a0001c0004t0002g0334 |
3 | HG02630.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.79-1784G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170295156 | |||||||
| chr5:170295171 | C | G | 2 | a0001c0002t0001g0278 a0005c0014t0013g0378 |
2 | NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.79-1799G>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170295171 | |||||||
| chr5:170295307 | T | G | 21 | a0001c0001t0001g0277 a0001c0001t0001g0281 a0001c0001t0001g0296 others(18): Show |
21 | HG01891.hp1 HG02027.hp1 HG02135.hp2 others(18): Show |
intron_variant | MODIFIER | c.79-1935A>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170295307 | |||||||
| chr5:170295344 | T | A | 23 | a0001c0001t0001g0256 a0001c0001t0001g0277 a0001c0001t0001g0281 others(20): Show |
23 | HG01891.hp1 HG02027.hp1 HG02135.hp2 others(20): Show |
intron_variant | MODIFIER | c.79-1972A>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170295344 | |||||||
| chr5:170295388 | A | T | 1 | a0001c0002t0003g0017 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.79-2016T>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170295388 | |||||||
| chr5:170295468 | A | G | 18 | a0001c0001t0001g0302 a0001c0001t0001g0311 a0001c0001t0009g0312 others(15): Show |
19 | HG00673.hp2 HG01358.hp2 HG01516.hp2 others(16): Show |
intron_variant | MODIFIER | c.78+2066T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170295468 | |||||||
| chr5:170295542 | T | C | 23 | a0001c0001t0001g0256 a0001c0001t0001g0277 a0001c0001t0001g0281 others(20): Show |
23 | HG01891.hp1 HG02027.hp1 HG02135.hp2 others(20): Show |
intron_variant | MODIFIER | c.78+1992A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170295542 | |||||||
| chr5:170295567 | A | G | 1 | a0001c0002t0001g0364 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.78+1967T>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170295567 | |||||||
| chr5:170295859 | A | T | 2 | a0001c0002t0001g0126 a0001c0002t0006g0127 |
2 | HG02895.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.78+1675T>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170295859 | |||||||
| chr5:170295893 | A | C | 36 | a0001c0001t0001g0258 a0001c0001t0001g0267 a0001c0001t0001g0302 others(33): Show |
37 | HG00280.hp1 HG00639.hp1 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.78+1641T>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170295893 | |||||||
| chr5:170295914 | G | A | 18 | a0001c0001t0001g0302 a0001c0001t0001g0311 a0001c0001t0009g0312 others(15): Show |
19 | HG00673.hp2 HG01358.hp2 HG01516.hp2 others(16): Show |
intron_variant | MODIFIER | c.78+1620C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170295914 | |||||||
| chr5:170295918 | G | A | 18 | a0001c0001t0001g0258 a0001c0001t0001g0267 a0001c0002t0001g0259 others(15): Show |
18 | HG00280.hp1 HG00639.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.78+1616C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170295918 | |||||||
| chr5:170295924 | TC | T | 6 | a0001c0001t0003g0011 a0001c0001t0003g0015 a0001c0001t0003g0016 others(3): Show |
6 | HG00642.hp2 HG00735.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.78+1609delG | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170295924 | |||||||
| chr5:170295928 | C | T | 6 | a0001c0001t0003g0011 a0001c0001t0003g0015 a0001c0001t0003g0016 others(3): Show |
6 | HG00642.hp2 HG00735.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.78+1606G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170295928 | |||||||
| chr5:170295953 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.78+1581G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170295953 | |||||||
| chr5:170296023 | G | C | 1 | a0001c0002t0001g0330 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.78+1511C>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170296023 | |||||||
| chr5:170296109 | C | T | 257 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(254): Show |
262 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(259): Show |
intron_variant | MODIFIER | c.78+1425G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170296109 | |||||||
| chr5:170296225 | C | T | 100 | a0001c0001t0001g0258 a0001c0001t0001g0267 a0001c0001t0001g0277 others(97): Show |
101 | HG00280.hp1 HG00544.hp2 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.78+1309G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170296225 | |||||||
| chr5:170296262 | C | T | 1 | a0001c0003t0002g0332 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.78+1272G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170296262 | |||||||
| chr5:170296264 | T | A | 1 | a0001c0003t0002g0332 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.78+1270A>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170296264 | |||||||
| chr5:170296272 | G | A | 1 | a0001c0001t0001g0363 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.78+1262C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170296272 | |||||||
| chr5:170296301 | T | C | 43 | a0001c0001t0001g0339 a0001c0001t0001g0344 a0001c0001t0001g0345 others(40): Show |
43 | HG00544.hp2 HG00558.hp2 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.78+1233A>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170296301 | |||||||
| chr5:170296345 | C | A | 1 | a0001c0002t0001g0364 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.78+1189G>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170296345 | |||||||
| chr5:170296497 | G | A | 1 | a0001c0010t0004g0124 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.78+1037C>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170296497 | |||||||
| chr5:170296650 | A | T | 1 | a0001c0003t0004g0009 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.78+884T>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170296650 | |||||||
| chr5:170296735 | C | A | 11 | a0001c0002t0001g0367 a0001c0002t0001g0368 a0001c0002t0001g0371 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.78+799G>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170296735 | |||||||
| chr5:170296762 | G | T | 1 | a0001c0003t0002g0276 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.78+772C>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170296762 | |||||||
| chr5:170296775 | C | G | 18 | a0001c0001t0001g0258 a0001c0001t0001g0267 a0001c0002t0001g0259 others(15): Show |
18 | HG00280.hp1 HG00639.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.78+759G>C | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170296775 | |||||||
| chr5:170296797 | C | A | 1 | a0001c0001t0003g0125 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.78+737G>T | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170296797 | |||||||
| chr5:170296927 | C | T | 18 | a0001c0001t0001g0258 a0001c0001t0001g0267 a0001c0002t0001g0259 others(15): Show |
18 | HG00280.hp1 HG00639.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.78+607G>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170296927 | |||||||
| chr5:170297037 | A | T | 1 | a0001c0001t0003g0008 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.78+497T>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170297037 | |||||||
| chr5:170297176 | G | C | 2 | a0001c0002t0006g0377 a0001c0004t0002g0376 |
2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.78+358C>G | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170297176 | |||||||
| chr5:170297320 | A | T | 135 | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(132): Show |
139 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.78+214T>A | LCP2 | ENSG00000043462.13 | transcript | ENST00000046794.10 | protein_coding | 1/20 | chr5 | 170297320 |