Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 3991 |
| ensemblid | ENSG00000079435.10 |
| hgncid | 6621 |
| symbol | LIPE |
| name | lipase E, hormone sensitive type |
| refseq_nuc | NM_005357.4 |
| refseq_prot | NP_005348.2 |
| ensembl_nuc | ENST00000244289.9 |
| ensembl_prot | ENSP00000244289.3 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 42401514 |
| end | 42427388 |
| strand | - |
| ver | v1.2 |
| region | chr19:42401514-42427388 |
| region5000 | chr19:42396514-42432388 |
| regionname0 | LIPE_chr19_42401514_42427388 |
| regionname5000 | LIPE_chr19_42396514_42432388 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1076 | 177 | 47 | 50 | 46 | 5 | 27 | 26 | LIPE_chr19_42396514_42432388 | LIPE | MEPGS others(1071): Show |
chr19 | 42396514 | 42432388 |
| a0002 | 0/0 | 1076 | 16 | 15 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | MEPGS others(1071): Show |
chr19 | 42396514 | 42432388 |
| a0003 | 0/0 | 1076 | 11 | 0 | 6 | 5 | 0 | 0 | 4 | LIPE_chr19_42396514_42432388 | LIPE | MEPGS others(1071): Show |
chr19 | 42396514 | 42432388 |
| a0004 | 0/0 | 1076 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | MEPGS others(1071): Show |
chr19 | 42396514 | 42432388 |
| a0005 | 0/0 | 1076 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | MEPGS others(1071): Show |
chr19 | 42396514 | 42432388 |
| a0006 | 0/0 | 1076 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | MEPGS others(1071): Show |
chr19 | 42396514 | 42432388 |
| a0007 | 0/0 | 1076 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | MEPGS others(1071): Show |
chr19 | 42396514 | 42432388 |
| a0008 | 0/0 | 1076 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | MEPGS others(1071): Show |
chr19 | 42396514 | 42432388 |
| a0009 | 0/0 | 1076 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | MEPGS others(1071): Show |
chr19 | 42396514 | 42432388 |
| a0010 | 0/0 | 1076 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | MEPGS others(1071): Show |
chr19 | 42396514 | 42432388 |
| a0011 | 0/0 | 1076 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LIPE_chr19_42396514_42432388 | LIPE | MEPGS others(1071): Show |
chr19 | 42396514 | 42432388 |
| a0012 | 0/0 | 1076 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | MEPGS others(1071): Show |
chr19 | 42396514 | 42432388 |
| a0013 | 0/0 | 1076 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | MEPGS others(1071): Show |
chr19 | 42396514 | 42432388 |
| a0014 | 0/0 | 1076 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | MEPGS others(1071): Show |
chr19 | 42396514 | 42432388 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 3228 | 169 | 46 | 48 | 44 | 4 | 25 | LIPE_chr19_42396514_42432388 | LIPE | ATGGA others(3223): Show |
chr19 | 42396514 | 42432388 | ||
| a0001c0008 | 0/0 | 3228 | 2 | 0 | 2 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | ATGGA others(3223): Show |
chr19 | 42396514 | 42432388 | ||
| a0001c0009 | 0/0 | 3228 | 2 | 0 | 0 | 2 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | ATGGA others(3223): Show |
chr19 | 42396514 | 42432388 | ||
| a0001c0014 | 0/0 | 3228 | 1 | 0 | 0 | 0 | 1 | 0 | LIPE_chr19_42396514_42432388 | LIPE | ATGGA others(3223): Show |
chr19 | 42396514 | 42432388 | ||
| a0001c0019 | 0/0 | 3228 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | ATGGA others(3223): Show |
chr19 | 42396514 | 42432388 | ||
| a0001c0020 | 0/0 | 3228 | 1 | 0 | 0 | 0 | 0 | 1 | LIPE_chr19_42396514_42432388 | LIPE | ATGGA others(3223): Show |
chr19 | 42396514 | 42432388 | ||
| a0001c0021 | 0/0 | 3228 | 1 | 0 | 0 | 0 | 0 | 1 | LIPE_chr19_42396514_42432388 | LIPE | ATGGA others(3223): Show |
chr19 | 42396514 | 42432388 | ||
| a0002c0002 | 0/0 | 3228 | 14 | 13 | 1 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | ATGGA others(3223): Show |
chr19 | 42396514 | 42432388 | ||
| a0002c0007 | 0/0 | 3228 | 2 | 2 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | ATGGA others(3223): Show |
chr19 | 42396514 | 42432388 | ||
| a0003c0003 | 0/0 | 3228 | 11 | 0 | 6 | 5 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | ATGGA others(3223): Show |
chr19 | 42396514 | 42432388 | ||
| a0004c0004 | 0/0 | 3228 | 7 | 6 | 1 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | ATGGA others(3223): Show |
chr19 | 42396514 | 42432388 | ||
| a0005c0005 | 0/0 | 3228 | 6 | 6 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | ATGGA others(3223): Show |
chr19 | 42396514 | 42432388 | ||
| a0006c0006 | 0/0 | 3228 | 3 | 3 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | ATGGA others(3223): Show |
chr19 | 42396514 | 42432388 | ||
| a0007c0017 | 0/0 | 3228 | 1 | 0 | 0 | 0 | 1 | 0 | LIPE_chr19_42396514_42432388 | LIPE | ATGGA others(3223): Show |
chr19 | 42396514 | 42432388 | ||
| a0008c0013 | 0/0 | 3228 | 1 | 0 | 0 | 1 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | ATGGA others(3223): Show |
chr19 | 42396514 | 42432388 | ||
| a0009c0016 | 0/0 | 3228 | 1 | 0 | 0 | 1 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | ATGGA others(3223): Show |
chr19 | 42396514 | 42432388 | ||
| a0010c0015 | 0/0 | 3228 | 1 | 0 | 0 | 1 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | ATGGA others(3223): Show |
chr19 | 42396514 | 42432388 | ||
| a0011c0018 | 0/0 | 3228 | 1 | 0 | 0 | 0 | 0 | 1 | LIPE_chr19_42396514_42432388 | LIPE | ATGGA others(3223): Show |
chr19 | 42396514 | 42432388 | ||
| a0012c0012 | 0/0 | 3228 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | ATGGA others(3223): Show |
chr19 | 42396514 | 42432388 | ||
| a0013c0010 | 0/0 | 3228 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | ATGGA others(3223): Show |
chr19 | 42396514 | 42432388 | ||
| a0014c0011 | 0/0 | 3228 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | ATGGA others(3223): Show |
chr19 | 42396514 | 42432388 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3768 | 166 | 44 | 48 | 44 | 4 | 24 | LIPE_chr19_42396514_42432388 | LIPE | ATTCC others(3763): Show |
chr19 | 42396514 | 42432388 |
| a0001c0001t0002 | 0/0 | 3768 | 2 | 2 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | ATTCC others(3763): Show |
chr19 | 42396514 | 42432388 |
| a0001c0001t0003 | 0/0 | 3768 | 1 | 0 | 0 | 0 | 0 | 1 | LIPE_chr19_42396514_42432388 | LIPE | ATTCC others(3763): Show |
chr19 | 42396514 | 42432388 |
| a0001c0008t0001 | 0/0 | 3768 | 2 | 0 | 2 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | ATTCC others(3763): Show |
chr19 | 42396514 | 42432388 |
| a0001c0009t0001 | 0/0 | 3768 | 2 | 0 | 0 | 2 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | ATTCC others(3763): Show |
chr19 | 42396514 | 42432388 |
| a0001c0014t0001 | 0/0 | 3768 | 1 | 0 | 0 | 0 | 1 | 0 | LIPE_chr19_42396514_42432388 | LIPE | ATTCC others(3763): Show |
chr19 | 42396514 | 42432388 |
| a0001c0019t0001 | 0/0 | 3768 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | ATTCC others(3763): Show |
chr19 | 42396514 | 42432388 |
| a0001c0020t0001 | 0/0 | 3768 | 1 | 0 | 0 | 0 | 0 | 1 | LIPE_chr19_42396514_42432388 | LIPE | ATTCC others(3763): Show |
chr19 | 42396514 | 42432388 |
| a0001c0021t0001 | 0/0 | 3768 | 1 | 0 | 0 | 0 | 0 | 1 | LIPE_chr19_42396514_42432388 | LIPE | ATTCC others(3763): Show |
chr19 | 42396514 | 42432388 |
| a0002c0002t0001 | 0/0 | 3768 | 14 | 13 | 1 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | ATTCC others(3763): Show |
chr19 | 42396514 | 42432388 |
| a0002c0007t0001 | 0/0 | 3768 | 2 | 2 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | ATTCC others(3763): Show |
chr19 | 42396514 | 42432388 |
| a0003c0003t0001 | 0/0 | 3768 | 11 | 0 | 6 | 5 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | ATTCC others(3763): Show |
chr19 | 42396514 | 42432388 |
| a0004c0004t0001 | 0/0 | 3768 | 7 | 6 | 1 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | ATTCC others(3763): Show |
chr19 | 42396514 | 42432388 |
| a0005c0005t0001 | 0/0 | 3768 | 6 | 6 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | ATTCC others(3763): Show |
chr19 | 42396514 | 42432388 |
| a0006c0006t0001 | 0/0 | 3768 | 3 | 3 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | ATTCC others(3763): Show |
chr19 | 42396514 | 42432388 |
| a0007c0017t0001 | 0/0 | 3768 | 1 | 0 | 0 | 0 | 1 | 0 | LIPE_chr19_42396514_42432388 | LIPE | ATTCC others(3763): Show |
chr19 | 42396514 | 42432388 |
| a0008c0013t0001 | 0/0 | 3768 | 1 | 0 | 0 | 1 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | ATTCC others(3763): Show |
chr19 | 42396514 | 42432388 |
| a0009c0016t0001 | 0/0 | 3768 | 1 | 0 | 0 | 1 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | ATTCC others(3763): Show |
chr19 | 42396514 | 42432388 |
| a0010c0015t0001 | 0/0 | 3768 | 1 | 0 | 0 | 1 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | ATTCC others(3763): Show |
chr19 | 42396514 | 42432388 |
| a0011c0018t0001 | 0/0 | 3768 | 1 | 0 | 0 | 0 | 0 | 1 | LIPE_chr19_42396514_42432388 | LIPE | ATTCC others(3763): Show |
chr19 | 42396514 | 42432388 |
| a0012c0012t0001 | 0/0 | 3768 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | ATTCC others(3763): Show |
chr19 | 42396514 | 42432388 |
| a0013c0010t0001 | 0/0 | 3768 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | ATTCC others(3763): Show |
chr19 | 42396514 | 42432388 |
| a0014c0011t0001 | 0/0 | 3768 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | ATTCC others(3763): Show |
chr19 | 42396514 | 42432388 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 6 | 1 | 3 | 2 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0007 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0015 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0017 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0018 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0101 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0113 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0008t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0008t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0009t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0009t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0014t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0019t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0020t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0001c0021t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0002c0002t0001g0002 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0002c0002t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0002c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0002c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0002c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0002c0002t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0002c0002t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0002c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0002c0002t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0002c0007t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0002c0007t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0003c0003t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0003c0003t0001g0005 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0003c0003t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0003c0003t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0003c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0003c0003t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0003c0003t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0004c0004t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0004c0004t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0004c0004t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0004c0004t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0004c0004t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0004c0004t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0004c0004t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0005c0005t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0005c0005t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0005c0005t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0005c0005t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0006c0006t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0006c0006t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0006c0006t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0007c0017t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0008c0013t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0009c0016t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0010c0015t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0011c0018t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0012c0012t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0013c0010t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| a0014c0011t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00323 | hp1 | a0007 | c0017 | t0001 | g0150 | EUR | FIN | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0089 | EUR | FIN | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG00642 | hp2 | a0003 | c0003 | t0001 | g0060 | AMR | PUR | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG00673 | hp1 | a0008 | c0013 | t0001 | g0054 | EAS | CHS | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG00738 | hp2 | a0001 | c0008 | t0001 | g0125 | AMR | PUR | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG01069 | hp1 | a0003 | c0003 | t0001 | g0005 | AMR | PUR | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG01074 | hp2 | a0001 | c0008 | t0001 | g0118 | AMR | PUR | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG01109 | hp2 | a0002 | c0002 | t0001 | g0035 | AMR | PUR | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG01243 | hp2 | a0004 | c0004 | t0001 | g0037 | AMR | PUR | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0141 | EUR | IBS | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0142 | EUR | IBS | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG01884 | hp2 | a0006 | c0006 | t0001 | g0046 | AFR | ACB | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG01934 | hp2 | a0003 | c0003 | t0001 | g0134 | AMR | PEL | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG01952 | hp1 | a0003 | c0003 | t0001 | g0151 | AMR | PEL | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PEL | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02015 | hp1 | a0009 | c0016 | t0001 | g0124 | EAS | KHV | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | KHV | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02135 | hp2 | a0003 | c0003 | t0001 | g0005 | EAS | KHV | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02145 | hp2 | a0002 | c0002 | t0001 | g0031 | AFR | ACB | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02148 | hp2 | a0003 | c0003 | t0001 | g0110 | AMR | PEL | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CDX | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CDX | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CDX | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CDX | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02258 | hp2 | a0005 | c0005 | t0001 | g0016 | AFR | ACB | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PEL | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02280 | hp1 | a0006 | c0006 | t0001 | g0045 | AFR | ACB | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02293 | hp1 | a0003 | c0003 | t0001 | g0005 | AMR | PEL | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02451 | hp2 | a0002 | c0002 | t0001 | g0033 | AFR | ACB | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02523 | hp2 | a0010 | c0015 | t0001 | g0146 | EAS | KHV | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0008 | AFR | GWD | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02615 | hp1 | a0004 | c0004 | t0001 | g0042 | AFR | GWD | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0029 | AFR | GWD | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02630 | hp1 | a0004 | c0004 | t0001 | g0040 | AFR | GWD | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0106 | AFR | GWD | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02647 | hp1 | a0005 | c0005 | t0001 | g0011 | AFR | GWD | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02698 | hp2 | a0011 | c0018 | t0001 | g0076 | SAS | PJL | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02717 | hp1 | a0005 | c0005 | t0001 | g0016 | AFR | GWD | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02717 | hp2 | a0002 | c0002 | t0001 | g0002 | AFR | GWD | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | GWD | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02723 | hp2 | a0004 | c0004 | t0001 | g0038 | AFR | GWD | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02818 | hp2 | a0012 | c0012 | t0001 | g0043 | AFR | GWD | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0074 | AFR | GWD | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02897 | hp1 | a0005 | c0005 | t0001 | g0011 | AFR | GWD | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0027 | AFR | GWD | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02922 | hp2 | a0002 | c0007 | t0001 | g0028 | AFR | ESN | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02970 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | ESN | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ESN | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02976 | hp2 | a0013 | c0010 | t0001 | g0025 | AFR | ESN | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0032 | AFR | GWD | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | MSL | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG03098 | hp2 | a0002 | c0002 | t0001 | g0008 | AFR | MSL | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG03130 | hp2 | a0002 | c0007 | t0001 | g0034 | AFR | ESN | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG03139 | hp2 | a0004 | c0004 | t0001 | g0039 | AFR | ESN | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG03209 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | MSL | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG03225 | hp2 | a0002 | c0002 | t0001 | g0030 | AFR | MSL | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG03239 | hp1 | a0001 | c0020 | t0001 | g0132 | SAS | PJL | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | MSL | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG03516 | hp1 | a0014 | c0011 | t0001 | g0026 | AFR | ESN | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG03516 | hp2 | a0006 | c0006 | t0001 | g0044 | AFR | ESN | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0191 | SAS | PJL | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG03654 | hp2 | a0001 | c0021 | t0001 | g0133 | SAS | PJL | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | BEB | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | BEB | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | STU | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | STU | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0024 | SAS | STU | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | STU | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | STU | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | STU | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | STU | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | STU | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CHB | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | CHB | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| NA18906 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | YRI | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | YRI | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| NA18940 | hp2 | a0001 | c0009 | t0001 | g0051 | EAS | JPT | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| NA18977 | hp1 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| NA18982 | hp2 | a0001 | c0009 | t0001 | g0088 | EAS | JPT | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| NA19011 | hp1 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| NA19043 | hp1 | a0005 | c0005 | t0001 | g0153 | AFR | LWK | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| NA19043 | hp2 | a0001 | c0019 | t0001 | g0152 | AFR | LWK | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| NA19081 | hp1 | a0003 | c0003 | t0001 | g0004 | EAS | JPT | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| NA19088 | hp2 | a0003 | c0003 | t0001 | g0111 | EAS | JPT | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | YRI | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| NA19240 | hp2 | a0004 | c0004 | t0001 | g0036 | AFR | YRI | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ASW | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ASW | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| NA20805 | hp1 | a0001 | c0014 | t0001 | g0114 | EUR | TSI | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0176 | EUR | TSI | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02109 | hp1 | a0004 | c0004 | t0001 | g0041 | AFR | ACB | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | MSL | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG03471 | hp2 | a0005 | c0005 | t0001 | g0192 | AFR | MSL | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0002 | AFR | USA | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | USA | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | USA | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | USA | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0101 | REF | REF | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0113 | REF | REF | LIPE_chr19_42396514_42432388 | LIPE | chr19 | 42396514 | 42432388 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:42401822 | C | G | 1 | a0007 | 1 | HG00323.hp1 | missense_variant | MODERATE | c.3221G>C | p.Gly1074Ala | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 10/10 | 3460/3768 | 3221/3231 | 1074/1076 | chr19 | 42401822 | |||
| chr19:42402762 | G | T | 1 | a0004 | 7 | HG01243.hp2 HG02109.hp1 HG02615.hp1 others(4): Show |
missense_variant | MODERATE | c.2812C>A | p.Arg938Ser | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 9/10 | 3051/3768 | 2812/3231 | 938/1076 | chr19 | 42402762 | |||
| chr19:42402912 | A | G | 1 | a0009 | 1 | HG02015.hp1 | missense_variant | MODERATE | c.2662T>C | p.Ser888Pro | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 9/10 | 2901/3768 | 2662/3231 | 888/1076 | chr19 | 42402912 | |||
| chr19:42405418 | G | A | 1 | a0011 | 1 | HG02698.hp2 | missense_variant | MODERATE | c.2509C>T | p.Arg837Cys | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 8/10 | 2748/3768 | 2509/3231 | 837/1076 | chr19 | 42405418 | |||
| chr19:42406170 | C | T | 1 | a0014 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.2356G>A | p.Ala786Thr | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 7/10 | 2595/3768 | 2356/3231 | 786/1076 | chr19 | 42406170 | |||
| chr19:42406326 | C | T | 1 | a0010 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.2200G>A | p.Val734Met | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 7/10 | 2439/3768 | 2200/3231 | 734/1076 | chr19 | 42406326 | |||
| chr19:42407617 | G | A | 1 | a0003 | 11 | HG00642.hp2 HG01069.hp1 HG01934.hp2 others(8): Show |
missense_variant | MODERATE | c.1831C>T | p.Arg611Cys | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 5/10 | 2070/3768 | 1831/3231 | 611/1076 | chr19 | 42407617 | |||
| chr19:42408244 | C | T | 1 | a0008 | 1 | HG00673.hp1 | missense_variant | MODERATE | c.1498G>A | p.Glu500Lys | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 3/10 | 1737/3768 | 1498/3231 | 500/1076 | chr19 | 42408244 | |||
| chr19:42408247 | T | G | 1 | a0005 | 6 | HG02258.hp2 HG02647.hp1 HG02717.hp1 others(3): Show |
missense_variant | MODERATE | c.1495A>C | p.Asn499His | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 3/10 | 1734/3768 | 1495/3231 | 499/1076 | chr19 | 42408247 | |||
| chr19:42408251 | T | A | 1 | a0012 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.1491A>T | p.Lys497Asn | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 3/10 | 1730/3768 | 1491/3231 | 497/1076 | chr19 | 42408251 | |||
| chr19:42426500 | C | T | 2 | a0002 a0014 |
17 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(14): Show |
missense_variant | MODERATE | c.650G>A | p.Arg217Gln | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/10 | 889/3768 | 650/3231 | 217/1076 | chr19 | 42426500 | |||
| chr19:42426582 | G | T | 1 | a0006 | 3 | HG01884.hp2 HG02280.hp1 HG03516.hp2 |
missense_variant | MODERATE | c.568C>A | p.Pro190Thr | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/10 | 807/3768 | 568/3231 | 190/1076 | chr19 | 42426582 | |||
| chr19:42426621 | A | T | 2 | a0002 a0014 |
17 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(14): Show |
missense_variant | MODERATE | c.529T>A | p.Ser177Thr | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/10 | 768/3768 | 529/3231 | 177/1076 | chr19 | 42426621 | |||
| chr19:42426714 | G | A | 1 | a0012 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.436C>T | p.Pro146Ser | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/10 | 675/3768 | 436/3231 | 146/1076 | chr19 | 42426714 | |||
| chr19:42426852 | A | G | 5 | a0002 a0004 a0012 others(2): Show |
26 | HG01109.hp2 HG01243.hp2 HG02109.hp1 others(23): Show |
missense_variant | MODERATE | c.298T>C | p.Tyr100His | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/10 | 537/3768 | 298/3231 | 100/1076 | chr19 | 42426852 | |||
| chr19:42426983 | C | T | 1 | a0013 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.167G>A | p.Arg56Lys | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/10 | 406/3768 | 167/3231 | 56/1076 | chr19 | 42426983 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:42401872 | G | A | 1 | a0001c0008 | 2 | HG00738.hp2 HG01074.hp2 |
synonymous_variant | LOW | c.3171C>T | p.Ala1057Ala | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 10/10 | 3410/3768 | 3171/3231 | 1057/1076 | chr19 | 42401872 | |||
| chr19:42401923 | T | C | 1 | a0001c0009 | 2 | NA18940.hp2 NA18982.hp2 |
synonymous_variant | LOW | c.3120A>G | p.Ala1040Ala | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 10/10 | 3359/3768 | 3120/3231 | 1040/1076 | chr19 | 42401923 | |||
| chr19:42406264 | C | T | 1 | a0004c0004 | 7 | HG01243.hp2 HG02109.hp1 HG02615.hp1 others(4): Show |
synonymous_variant | LOW | c.2262G>A | p.Pro754Pro | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 7/10 | 2501/3768 | 2262/3231 | 754/1076 | chr19 | 42406264 | |||
| chr19:42407382 | C | T | 1 | a0001c0014 | 1 | NA20805.hp1 | synonymous_variant | LOW | c.1929G>A | p.Ser643Ser | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 6/10 | 2168/3768 | 1929/3231 | 643/1076 | chr19 | 42407382 | |||
| chr19:42407406 | C | T | 2 | a0004c0004 a0013c0010 |
8 | HG01243.hp2 HG02109.hp1 HG02615.hp1 others(5): Show |
synonymous_variant | LOW | c.1905G>A | p.Pro635Pro | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 6/10 | 2144/3768 | 1905/3231 | 635/1076 | chr19 | 42407406 | |||
| chr19:42407979 | T | C | 1 | a0001c0019 | 1 | NA19043.hp2 | synonymous_variant | LOW | c.1653A>G | p.Leu551Leu | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 4/10 | 1892/3768 | 1653/3231 | 551/1076 | chr19 | 42407979 | |||
| chr19:42410457 | G | A | 2 | a0002c0002 a0014c0011 |
15 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(12): Show |
synonymous_variant | LOW | c.1269C>T | p.Arg423Arg | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 2/10 | 1508/3768 | 1269/3231 | 423/1076 | chr19 | 42410457 | |||
| chr19:42410613 | G | A | 1 | a0001c0020 | 1 | HG03239.hp1 | synonymous_variant | LOW | c.1113C>T | p.Asn371Asn | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 2/10 | 1352/3768 | 1113/3231 | 371/1076 | chr19 | 42410613 | |||
| chr19:42410772 | G | A | 1 | a0001c0021 | 1 | HG03654.hp2 | synonymous_variant | LOW | c.954C>T | p.Asn318Asn | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 2/10 | 1193/3768 | 954/3231 | 318/1076 | chr19 | 42410772 | |||
| chr19:42426628 | T | C | 1 | a0013c0010 | 1 | HG02976.hp2 | synonymous_variant | LOW | c.522A>G | p.Glu174Glu | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/10 | 761/3768 | 522/3231 | 174/1076 | chr19 | 42426628 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:42401678 | A | G | 1 | a0001c0001t0002 | 2 | HG02630.hp2 HG02886.hp2 |
3_prime_UTR_variant | MODIFIER | c.*134T>C | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 10/10 | 134 | chr19 | 42401678 | ||||||
| chr19:42427181 | C | G | 1 | a0001c0001t0003 | 1 | HG04199.hp1 | 5_prime_UTR_variant | MODIFIER | c.-32G>C | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/10 | 32 | chr19 | 42427181 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:42402088 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2968-13C>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 9/9 | chr19 | 42402088 | |||||||
| chr19:42402115 | G | T | 4 | a0004c0004t0001g0036 a0004c0004t0001g0037 a0004c0004t0001g0038 others(1): Show |
4 | HG01243.hp2 HG02723.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2968-40C>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 9/9 | chr19 | 42402115 | |||||||
| chr19:42402119 | G | C | 22 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0071 others(19): Show |
24 | HG00639.hp1 HG01069.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.2968-44C>G | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 9/9 | chr19 | 42402119 | |||||||
| chr19:42402121 | C | G | 22 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0071 others(19): Show |
24 | HG00639.hp1 HG01069.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.2968-46G>C | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 9/9 | chr19 | 42402121 | |||||||
| chr19:42402231 | G | A | 5 | a0004c0004t0001g0036 a0004c0004t0001g0039 a0004c0004t0001g0040 others(2): Show |
5 | HG02109.hp1 HG02615.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2968-156C>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 9/9 | chr19 | 42402231 | |||||||
| chr19:42402239 | G | T | 1 | a0010c0015t0001g0146 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2968-164C>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 9/9 | chr19 | 42402239 | |||||||
| chr19:42402573 | A | G | 1 | a0001c0001t0001g0082 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2967+34T>C | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 9/9 | chr19 | 42402573 | |||||||
| chr19:42402590 | C | A | 1 | a0012c0012t0001g0043 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2967+17G>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 9/9 | chr19 | 42402590 | |||||||
| chr19:42403241 | A | ATG | 2 | a0001c0001t0001g0012 a0001c0001t0001g0186 |
3 | HG00438.hp2 HG00558.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.2543-212_2543-211d others(4): Show |
LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 8/9 | chr19 | 42403241 | |||||||
| chr19:42403241 | A | ATGTG | 3 | a0001c0001t0001g0168 a0001c0001t0001g0185 a0001c0001t0001g0189 |
3 | HG01257.hp1 HG01258.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.2543-214_2543-211d others(6): Show |
LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 8/9 | chr19 | 42403241 | |||||||
| chr19:42403241 | ATG | A | 37 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(34): Show |
47 | HG00438.hp1 HG00741.hp1 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.2543-212_2543-211d others(4): Show |
LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 8/9 | chr19 | 42403241 | |||||||
| chr19:42403241 | ATGTG | A | 8 | a0001c0001t0001g0058 a0001c0001t0001g0070 a0001c0001t0001g0082 others(5): Show |
8 | HG00738.hp1 HG02055.hp1 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.2543-214_2543-211d others(6): Show |
LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 8/9 | chr19 | 42403241 | |||||||
| chr19:42403241 | ATGTGTG | A | 8 | a0001c0001t0001g0097 a0001c0001t0001g0102 a0001c0001t0001g0144 others(5): Show |
8 | HG00642.hp1 HG02145.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.2543-216_2543-211d others(8): Show |
LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 8/9 | chr19 | 42403241 | |||||||
| chr19:42403241 | ATGTGTGT others(1): Show |
A | 17 | a0001c0001t0001g0075 a0001c0001t0001g0131 a0001c0001t0001g0155 others(14): Show |
22 | HG01109.hp2 HG01975.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.2543-218_2543-211d others(10): Show |
LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 8/9 | chr19 | 42403241 | |||||||
| chr19:42403241 | ATGTGTGT others(3): Show |
A | 5 | a0001c0001t0001g0015 a0001c0001t0001g0120 a0001c0001t0001g0139 others(2): Show |
6 | HG01517.hp1 HG02155.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.2543-220_2543-211d others(12): Show |
LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 8/9 | chr19 | 42403241 | |||||||
| chr19:42403241 | ATGTGTGT others(5): Show |
A | 2 | a0001c0001t0001g0098 a0001c0001t0001g0107 |
2 | HG01258.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.2543-222_2543-211d others(14): Show |
LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 8/9 | chr19 | 42403241 | |||||||
| chr19:42403241 | ATGTGTGT others(7): Show |
A | 2 | a0001c0001t0001g0081 a0001c0001t0001g0127 |
2 | HG02683.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2543-224_2543-211d others(16): Show |
LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 8/9 | chr19 | 42403241 | |||||||
| chr19:42403241 | ATGTGTGT others(9): Show |
A | 2 | a0001c0001t0001g0066 a0001c0001t0001g0137 |
2 | HG02647.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2543-226_2543-211d others(18): Show |
LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 8/9 | chr19 | 42403241 | |||||||
| chr19:42403290 | T | A | 1 | a0001c0001t0001g0072 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2543-259A>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 8/9 | chr19 | 42403290 | |||||||
| chr19:42403292 | T | A | 110 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(107): Show |
135 | HG00323.hp2 HG00438.hp1 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.2543-261A>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 8/9 | chr19 | 42403292 | |||||||
| chr19:42403292 | T | TGA | 43 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0013 others(40): Show |
52 | HG00738.hp2 HG00741.hp2 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.2543-263_2543-262d others(4): Show |
LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 8/9 | chr19 | 42403292 | |||||||
| chr19:42403292 | T | TGTGA | 7 | a0001c0001t0001g0079 a0001c0001t0001g0086 a0001c0001t0001g0105 others(4): Show |
7 | HG00323.hp1 HG01257.hp2 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.2543-262_2543-261i others(6): Show |
LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 8/9 | chr19 | 42403292 | |||||||
| chr19:42403292 | T | TGTGTGA | 3 | a0001c0001t0001g0061 a0001c0001t0001g0123 a0001c0001t0001g0147 |
3 | HG01099.hp1 HG01993.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.2543-262_2543-261i others(8): Show |
LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 8/9 | chr19 | 42403292 | |||||||
| chr19:42403292 | T | TGTGTGTG others(1): Show |
5 | a0001c0001t0001g0093 a0001c0001t0001g0099 a0001c0001t0001g0104 others(2): Show |
5 | HG02698.hp1 HG03017.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.2543-262_2543-261i others(10): Show |
LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 8/9 | chr19 | 42403292 | |||||||
| chr19:42403292 | T | TGTGTGTG others(3): Show |
1 | a0001c0001t0001g0064 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2543-262_2543-261i others(12): Show |
LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 8/9 | chr19 | 42403292 | |||||||
| chr19:42403345 | A | G | 1 | a0001c0001t0001g0161 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2543-314T>C | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 8/9 | chr19 | 42403345 | |||||||
| chr19:42403360 | A | G | 1 | a0012c0012t0001g0043 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2543-329T>C | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 8/9 | chr19 | 42403360 | |||||||
| chr19:42403452 | G | GT | 26 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0022 others(23): Show |
29 | HG00639.hp1 HG01069.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.2543-422dupA | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 8/9 | chr19 | 42403452 | |||||||
| chr19:42403452 | G | T | 2 | a0001c0001t0001g0083 a0012c0012t0001g0043 |
2 | HG00738.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.2543-421C>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 8/9 | chr19 | 42403452 | |||||||
| chr19:42403452 | GT | G | 10 | a0001c0001t0001g0181 a0001c0001t0001g0183 a0004c0004t0001g0036 others(7): Show |
10 | HG01243.hp2 HG01884.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.2543-422delA | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 8/9 | chr19 | 42403452 | |||||||
| chr19:42403590 | GGCATGTG others(4): Show |
G | 1 | a0013c0010t0001g0025 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2543-570_2543-560d others(13): Show |
LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 8/9 | chr19 | 42403590 | |||||||
| chr19:42403667 | G | A | 10 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0027 others(7): Show |
15 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.2543-636C>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 8/9 | chr19 | 42403667 | |||||||
| chr19:42403695 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2543-664G>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 8/9 | chr19 | 42403695 | |||||||
| chr19:42403699 | C | T | 28 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(25): Show |
34 | HG00438.hp1 HG00642.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.2543-668G>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 8/9 | chr19 | 42403699 | |||||||
| chr19:42403920 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2543-889C>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 8/9 | chr19 | 42403920 | |||||||
| chr19:42403922 | G | A | 10 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0027 others(7): Show |
15 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.2543-891C>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 8/9 | chr19 | 42403922 | |||||||
| chr19:42403977 | C | T | 6 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0049 others(3): Show |
9 | HG01123.hp2 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.2543-946G>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 8/9 | chr19 | 42403977 | |||||||
| chr19:42404131 | C | G | 1 | a0012c0012t0001g0043 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2543-1100G>C | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 8/9 | chr19 | 42404131 | |||||||
| chr19:42404177 | G | A | 1 | a0012c0012t0001g0043 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2543-1146C>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 8/9 | chr19 | 42404177 | |||||||
| chr19:42404232 | T | G | 3 | a0004c0004t0001g0040 a0004c0004t0001g0041 a0004c0004t0001g0042 |
3 | HG02109.hp1 HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.2542+1153A>C | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 8/9 | chr19 | 42404232 | |||||||
| chr19:42404392 | G | A | 4 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0066 others(1): Show |
4 | HG01884.hp1 HG02647.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.2542+993C>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 8/9 | chr19 | 42404392 | |||||||
| chr19:42404606 | C | T | 11 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0027 others(8): Show |
16 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.2542+779G>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 8/9 | chr19 | 42404606 | |||||||
| chr19:42404678 | A | T | 4 | a0005c0005t0001g0011 a0005c0005t0001g0016 a0005c0005t0001g0153 others(1): Show |
6 | HG02258.hp2 HG02647.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2542+707T>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 8/9 | chr19 | 42404678 | |||||||
| chr19:42404861 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2542+524G>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 8/9 | chr19 | 42404861 | |||||||
| chr19:42404902 | G | A | 1 | a0001c0001t0001g0108 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2542+483C>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 8/9 | chr19 | 42404902 | |||||||
| chr19:42404961 | C | T | 8 | a0004c0004t0001g0036 a0004c0004t0001g0037 a0004c0004t0001g0038 others(5): Show |
8 | HG01243.hp2 HG02109.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.2542+424G>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 8/9 | chr19 | 42404961 | |||||||
| chr19:42405011 | C | T | 11 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0027 others(8): Show |
16 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.2542+374G>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 8/9 | chr19 | 42405011 | |||||||
| chr19:42405202 | G | A | 8 | a0004c0004t0001g0036 a0004c0004t0001g0037 a0004c0004t0001g0038 others(5): Show |
8 | HG01243.hp2 HG02109.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.2542+183C>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 8/9 | chr19 | 42405202 | |||||||
| chr19:42405326 | T | C | 1 | a0001c0001t0001g0158 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2542+59A>G | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 8/9 | chr19 | 42405326 | |||||||
| chr19:42405879 | C | T | 1 | a0001c0001t0001g0079 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2365+282G>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 7/9 | chr19 | 42405879 | |||||||
| chr19:42405951 | G | GTGTC | 6 | a0004c0004t0001g0036 a0004c0004t0001g0037 a0004c0004t0001g0038 others(3): Show |
6 | HG01243.hp2 HG02109.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.2365+206_2365+209d others(6): Show |
LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 7/9 | chr19 | 42405951 | |||||||
| chr19:42405961 | G | GTC | 8 | a0001c0001t0001g0059 a0001c0001t0001g0080 a0001c0001t0001g0109 others(5): Show |
8 | HG00323.hp1 HG01934.hp1 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.2365+198_2365+199d others(4): Show |
LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 7/9 | chr19 | 42405961 | |||||||
| chr19:42405972 | TCTCTCAC others(1): Show |
T | 2 | a0001c0001t0001g0021 a0001c0001t0001g0173 |
3 | HG01069.hp2 HG01071.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.2365+181_2365+188d others(10): Show |
LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 7/9 | chr19 | 42405972 | |||||||
| chr19:42405972 | TCTCTCAC others(3): Show |
T | 2 | a0001c0001t0001g0166 a0001c0001t0001g0167 |
2 | HG00639.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.2365+179_2365+188d others(12): Show |
LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 7/9 | chr19 | 42405972 | |||||||
| chr19:42405975 | C | G | 1 | a0001c0001t0001g0162 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.2365+186G>C | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 7/9 | chr19 | 42405975 | |||||||
| chr19:42405976 | T | A | 1 | a0001c0001t0001g0183 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2365+185A>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 7/9 | chr19 | 42405976 | |||||||
| chr19:42405976 | T | TCA | 10 | a0001c0001t0001g0015 a0001c0001t0001g0056 a0001c0001t0001g0094 others(7): Show |
10 | HG00642.hp2 HG00673.hp2 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.2365+183_2365+184d others(4): Show |
LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 7/9 | chr19 | 42405976 | |||||||
| chr19:42405976 | T | TCACA | 15 | a0001c0001t0001g0014 a0001c0001t0001g0078 a0001c0001t0001g0086 others(12): Show |
15 | HG02273.hp1 HG02717.hp1 HG02886.hp2 others(12): Show |
intron_variant | MODIFIER | c.2365+181_2365+184d others(6): Show |
LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 7/9 | chr19 | 42405976 | |||||||
| chr19:42405976 | T | TCACACAC others(3): Show |
1 | a0005c0005t0001g0011 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2365+175_2365+184d others(12): Show |
LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 7/9 | chr19 | 42405976 | |||||||
| chr19:42405976 | T | TCTCACA | 4 | a0001c0001t0001g0003 a0001c0001t0001g0055 a0001c0001t0001g0069 others(1): Show |
7 | HG01255.hp1 HG01952.hp2 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.2365+184_2365+185i others(8): Show |
LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 7/9 | chr19 | 42405976 | |||||||
| chr19:42405976 | T | TCTCACAC others(1): Show |
3 | a0001c0001t0001g0053 a0001c0001t0001g0084 a0001c0001t0001g0097 |
3 | HG00438.hp1 HG00642.hp1 HG01928.hp1 |
intron_variant | MODIFIER | c.2365+184_2365+185i others(10): Show |
LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 7/9 | chr19 | 42405976 | |||||||
| chr19:42405976 | TCA | T | 20 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0017 others(17): Show |
20 | HG00558.hp1 HG00738.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.2365+183_2365+184d others(4): Show |
LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 7/9 | chr19 | 42405976 | |||||||
| chr19:42405976 | TCACA | T | 30 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0017 others(27): Show |
37 | HG01071.hp1 HG01109.hp2 HG01517.hp2 others(34): Show |
intron_variant | MODIFIER | c.2365+181_2365+184d others(6): Show |
LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 7/9 | chr19 | 42405976 | |||||||
| chr19:42405976 | TCACACAC others(1): Show |
T | 3 | a0001c0001t0001g0073 a0001c0001t0001g0160 a0001c0001t0001g0179 |
3 | HG01261.hp2 HG02135.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.2365+177_2365+184d others(10): Show |
LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 7/9 | chr19 | 42405976 | |||||||
| chr19:42405976 | TCACACAC others(3): Show |
T | 8 | a0001c0001t0001g0006 a0001c0001t0001g0064 a0001c0001t0001g0065 others(5): Show |
10 | HG01884.hp1 HG02055.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.2365+175_2365+184d others(12): Show |
LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 7/9 | chr19 | 42405976 | |||||||
| chr19:42405976 | TCACACAC others(5): Show |
T | 2 | a0001c0008t0001g0118 a0013c0010t0001g0025 |
2 | HG01074.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2365+173_2365+184d others(14): Show |
LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 7/9 | chr19 | 42405976 | |||||||
| chr19:42405976 | TCACACAC others(13): Show |
T | 1 | a0001c0001t0001g0068 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2365+165_2365+184d others(22): Show |
LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 7/9 | chr19 | 42405976 | |||||||
| chr19:42405978 | A | T | 29 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0015 others(26): Show |
31 | HG00438.hp2 HG00558.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.2365+183T>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 7/9 | chr19 | 42405978 | |||||||
| chr19:42405980 | A | T | 15 | a0001c0001t0001g0017 a0001c0001t0001g0081 a0001c0001t0001g0112 others(12): Show |
15 | HG00738.hp2 HG01081.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.2365+181T>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 7/9 | chr19 | 42405980 | |||||||
| chr19:42405982 | A | T | 20 | a0001c0001t0001g0050 a0001c0001t0001g0081 a0001c0001t0001g0099 others(17): Show |
25 | HG01071.hp1 HG01109.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.2365+179T>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 7/9 | chr19 | 42405982 | |||||||
| chr19:42405984 | A | T | 8 | a0001c0001t0001g0081 a0002c0002t0001g0002 a0002c0002t0001g0008 others(5): Show |
13 | HG01109.hp2 HG02572.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.2365+177T>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 7/9 | chr19 | 42405984 | |||||||
| chr19:42405990 | A | T | 2 | a0001c0008t0001g0118 a0013c0010t0001g0025 |
2 | HG01074.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.2365+171T>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 7/9 | chr19 | 42405990 | |||||||
| chr19:42405992 | A | T | 1 | a0013c0010t0001g0025 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2365+169T>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 7/9 | chr19 | 42405992 | |||||||
| chr19:42405994 | A | T | 1 | a0013c0010t0001g0025 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2365+167T>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 7/9 | chr19 | 42405994 | |||||||
| chr19:42405998 | A | T | 1 | a0001c0001t0001g0068 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2365+163T>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 7/9 | chr19 | 42405998 | |||||||
| chr19:42406018 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2365+143T>C | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 7/9 | chr19 | 42406018 | |||||||
| chr19:42406019 | C | CACA | 3 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0049 |
6 | HG01123.hp2 HG02109.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.2365+141_2365+142i others(5): Show |
LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 7/9 | chr19 | 42406019 | |||||||
| chr19:42406019 | C | CACACA | 2 | a0001c0001t0001g0181 a0001c0001t0001g0183 |
2 | HG02145.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.2365+141_2365+142i others(7): Show |
LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 7/9 | chr19 | 42406019 | |||||||
| chr19:42406020 | G | C | 5 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0049 others(2): Show |
8 | HG01123.hp2 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.2365+141C>G | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 7/9 | chr19 | 42406020 | |||||||
| chr19:42406020 | G | GA | 21 | a0001c0001t0001g0081 a0002c0002t0001g0002 a0002c0002t0001g0008 others(18): Show |
26 | HG01109.hp2 HG01243.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.2365+140dupT | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 7/9 | chr19 | 42406020 | |||||||
| chr19:42406021 | A | G | 5 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0049 others(2): Show |
8 | HG01123.hp2 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.2365+140T>C | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 7/9 | chr19 | 42406021 | |||||||
| chr19:42406040 | T | C | 1 | a0012c0012t0001g0043 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2365+121A>G | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 7/9 | chr19 | 42406040 | |||||||
| chr19:42406155 | C | A | 2 | a0006c0006t0001g0044 a0006c0006t0001g0045 |
2 | HG02280.hp1 HG03516.hp2 |
splice_region_variant&intron_variant | LOW | c.2365+6G>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 7/9 | chr19 | 42406155 | |||||||
| chr19:42406521 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2138-133G>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 6/9 | chr19 | 42406521 | |||||||
| chr19:42406588 | T | A | 1 | a0001c0001t0001g0079 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2138-200A>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 6/9 | chr19 | 42406588 | |||||||
| chr19:42406661 | G | C | 1 | a0001c0001t0001g0079 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2138-273C>G | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 6/9 | chr19 | 42406661 | |||||||
| chr19:42406662 | C | A | 1 | a0001c0001t0001g0079 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2138-274G>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 6/9 | chr19 | 42406662 | |||||||
| chr19:42406663 | A | G | 1 | a0001c0001t0001g0079 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2138-275T>C | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 6/9 | chr19 | 42406663 | |||||||
| chr19:42406771 | A | G | 21 | a0001c0001t0001g0081 a0002c0002t0001g0002 a0002c0002t0001g0008 others(18): Show |
26 | HG01109.hp2 HG01243.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.2138-383T>C | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 6/9 | chr19 | 42406771 | |||||||
| chr19:42406813 | C | T | 1 | a0011c0018t0001g0076 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2137+361G>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 6/9 | chr19 | 42406813 | |||||||
| chr19:42406936 | G | A | 19 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0027 others(16): Show |
24 | HG01109.hp2 HG01243.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.2137+238C>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 6/9 | chr19 | 42406936 | |||||||
| chr19:42406947 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2137+227G>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 6/9 | chr19 | 42406947 | |||||||
| chr19:42407073 | GGA | G | 7 | a0004c0004t0001g0036 a0004c0004t0001g0037 a0004c0004t0001g0038 others(4): Show |
7 | HG01243.hp2 HG02109.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.2137+99_2137+100de others(3): Show |
LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 6/9 | chr19 | 42407073 | |||||||
| chr19:42407579 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1842+27A>G | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 5/9 | chr19 | 42407579 | |||||||
| chr19:42407935 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1656+41C>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 4/9 | chr19 | 42407935 | |||||||
| chr19:42408137 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1511-16C>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 3/9 | chr19 | 42408137 | |||||||
| chr19:42408530 | G | A | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | NA18998.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1420-208C>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 2/9 | chr19 | 42408530 | |||||||
| chr19:42408565 | G | GA | 13 | a0001c0001t0001g0081 a0002c0002t0001g0002 a0002c0002t0001g0008 others(10): Show |
18 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.1420-244dupT | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 2/9 | chr19 | 42408565 | |||||||
| chr19:42408759 | G | A | 1 | a0003c0003t0001g0111 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1420-437C>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 2/9 | chr19 | 42408759 | |||||||
| chr19:42408824 | T | TA | 9 | a0001c0001t0001g0078 a0001c0001t0001g0115 a0001c0001t0001g0116 others(6): Show |
9 | HG01243.hp1 HG01257.hp1 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1420-503dupT | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 2/9 | chr19 | 42408824 | |||||||
| chr19:42408853 | G | C | 1 | a0001c0001t0001g0112 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1420-531C>G | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 2/9 | chr19 | 42408853 | |||||||
| chr19:42408994 | C | T | 7 | a0004c0004t0001g0036 a0004c0004t0001g0037 a0004c0004t0001g0038 others(4): Show |
7 | HG01243.hp2 HG02109.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1420-672G>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 2/9 | chr19 | 42408994 | |||||||
| chr19:42409000 | G | T | 7 | a0004c0004t0001g0036 a0004c0004t0001g0037 a0004c0004t0001g0038 others(4): Show |
7 | HG01243.hp2 HG02109.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1420-678C>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 2/9 | chr19 | 42409000 | |||||||
| chr19:42409141 | A | G | 8 | a0004c0004t0001g0036 a0004c0004t0001g0037 a0004c0004t0001g0038 others(5): Show |
8 | HG01243.hp2 HG02109.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1420-819T>C | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 2/9 | chr19 | 42409141 | |||||||
| chr19:42409202 | A | G | 175 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(172): Show |
211 | HG00323.hp1 HG00323.hp2 HG00438.hp1 others(208): Show |
intron_variant | MODIFIER | c.1420-880T>C | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 2/9 | chr19 | 42409202 | |||||||
| chr19:42409210 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1420-888G>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 2/9 | chr19 | 42409210 | |||||||
| chr19:42409214 | G | A | 8 | a0004c0004t0001g0036 a0004c0004t0001g0037 a0004c0004t0001g0038 others(5): Show |
8 | HG01243.hp2 HG02109.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1420-892C>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 2/9 | chr19 | 42409214 | |||||||
| chr19:42409400 | C | CA | 50 | a0001c0001t0001g0009 a0001c0001t0001g0017 a0001c0001t0001g0021 others(47): Show |
55 | HG00639.hp1 HG00738.hp2 HG01069.hp2 others(52): Show |
intron_variant | MODIFIER | c.1419+906dupT | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 2/9 | chr19 | 42409400 | |||||||
| chr19:42409400 | C | CAA | 10 | a0001c0001t0001g0073 a0001c0001t0001g0129 a0001c0001t0001g0130 others(7): Show |
10 | HG01081.hp1 HG01175.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.1419+905_1419+906d others(4): Show |
LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 2/9 | chr19 | 42409400 | |||||||
| chr19:42409400 | CA | C | 10 | a0001c0001t0001g0003 a0001c0001t0001g0053 a0001c0001t0001g0069 others(7): Show |
14 | HG00438.hp1 HG00642.hp1 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.1419+906delT | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 2/9 | chr19 | 42409400 | |||||||
| chr19:42409427 | T | C | 13 | a0001c0001t0001g0081 a0002c0002t0001g0002 a0002c0002t0001g0008 others(10): Show |
18 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.1419+880A>G | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 2/9 | chr19 | 42409427 | |||||||
| chr19:42409729 | T | C | 1 | a0001c0001t0001g0131 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1419+578A>G | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 2/9 | chr19 | 42409729 | |||||||
| chr19:42409767 | G | A | 10 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0027 others(7): Show |
15 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1419+540C>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 2/9 | chr19 | 42409767 | |||||||
| chr19:42410082 | G | C | 1 | a0001c0001t0001g0063 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1419+225C>G | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 2/9 | chr19 | 42410082 | |||||||
| chr19:42411218 | T | C | 1 | a0003c0003t0001g0134 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.884-376A>G | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42411218 | |||||||
| chr19:42411458 | T | C | 11 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0027 others(8): Show |
16 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.884-616A>G | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42411458 | |||||||
| chr19:42411620 | A | G | 20 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0027 others(17): Show |
25 | HG01109.hp2 HG01243.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.884-778T>C | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42411620 | |||||||
| chr19:42411876 | T | C | 2 | a0001c0001t0001g0052 a0001c0001t0001g0135 |
2 | HG00741.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.884-1034A>G | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42411876 | |||||||
| chr19:42411931 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.884-1089G>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42411931 | |||||||
| chr19:42412329 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.884-1487G>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42412329 | |||||||
| chr19:42412348 | G | A | 1 | a0012c0012t0001g0043 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.884-1506C>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42412348 | |||||||
| chr19:42412478 | G | C | 21 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0022 others(18): Show |
24 | HG00639.hp1 HG01069.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.884-1636C>G | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42412478 | |||||||
| chr19:42412511 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.884-1669C>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42412511 | |||||||
| chr19:42412564 | C | A | 1 | a0001c0001t0001g0094 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.884-1722G>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42412564 | |||||||
| chr19:42412601 | G | T | 1 | a0001c0001t0001g0094 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.884-1759C>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42412601 | |||||||
| chr19:42412689 | C | T | 11 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0027 others(8): Show |
16 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.884-1847G>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42412689 | |||||||
| chr19:42412950 | C | T | 11 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0027 others(8): Show |
16 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.884-2108G>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42412950 | |||||||
| chr19:42413393 | T | C | 42 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0022 others(39): Show |
50 | HG00639.hp1 HG01069.hp2 HG01071.hp2 others(47): Show |
intron_variant | MODIFIER | c.884-2551A>G | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42413393 | |||||||
| chr19:42413394 | G | A | 12 | a0001c0001t0001g0072 a0002c0002t0001g0002 a0002c0002t0001g0008 others(9): Show |
17 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.884-2552C>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42413394 | |||||||
| chr19:42413595 | C | T | 1 | a0012c0012t0001g0043 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.884-2753G>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42413595 | |||||||
| chr19:42413621 | G | A | 12 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0027 others(9): Show |
17 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.884-2779C>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42413621 | |||||||
| chr19:42413721 | C | G | 8 | a0004c0004t0001g0036 a0004c0004t0001g0037 a0004c0004t0001g0038 others(5): Show |
8 | HG01243.hp2 HG02109.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.884-2879G>C | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42413721 | |||||||
| chr19:42413757 | A | G | 1 | a0012c0012t0001g0043 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.884-2915T>C | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42413757 | |||||||
| chr19:42413993 | T | A | 1 | a0001c0001t0001g0155 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.884-3151A>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42413993 | |||||||
| chr19:42414096 | C | G | 20 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0027 others(17): Show |
25 | HG01109.hp2 HG01243.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.884-3254G>C | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42414096 | |||||||
| chr19:42414291 | A | AAAGGAAA others(6): Show |
20 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0027 others(17): Show |
25 | HG01109.hp2 HG01243.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.884-3462_884-3450d others(15): Show |
LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42414291 | |||||||
| chr19:42414746 | T | C | 11 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0027 others(8): Show |
16 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.884-3904A>G | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42414746 | |||||||
| chr19:42415241 | A | G | 11 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0027 others(8): Show |
16 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.884-4399T>C | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42415241 | |||||||
| chr19:42415461 | A | T | 1 | a0001c0001t0001g0093 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.884-4619T>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42415461 | |||||||
| chr19:42415582 | G | A | 12 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0027 others(9): Show |
17 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.884-4740C>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42415582 | |||||||
| chr19:42415670 | C | T | 1 | a0012c0012t0001g0043 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.884-4828G>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42415670 | |||||||
| chr19:42415741 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.884-4899G>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42415741 | |||||||
| chr19:42415743 | G | A | 11 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0027 others(8): Show |
16 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.884-4901C>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42415743 | |||||||
| chr19:42415804 | C | G | 12 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0027 others(9): Show |
17 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.884-4962G>C | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42415804 | |||||||
| chr19:42415810 | GA | G | 9 | a0001c0001t0001g0050 a0001c0001t0001g0068 a0004c0004t0001g0036 others(6): Show |
9 | HG01243.hp2 HG02109.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.884-4969delT | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42415810 | |||||||
| chr19:42415866 | G | A | 1 | a0013c0010t0001g0025 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.884-5024C>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42415866 | |||||||
| chr19:42415957 | A | G | 1 | a0006c0006t0001g0046 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.884-5115T>C | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42415957 | |||||||
| chr19:42416072 | G | A | 8 | a0004c0004t0001g0036 a0004c0004t0001g0037 a0004c0004t0001g0038 others(5): Show |
8 | HG01243.hp2 HG02109.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.884-5230C>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42416072 | |||||||
| chr19:42416265 | A | C | 3 | a0006c0006t0001g0044 a0006c0006t0001g0045 a0006c0006t0001g0046 |
3 | HG01884.hp2 HG02280.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.884-5423T>G | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42416265 | |||||||
| chr19:42416344 | C | CA | 12 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0027 others(9): Show |
17 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.884-5503dupT | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42416344 | |||||||
| chr19:42416403 | G | A | 2 | a0001c0001t0001g0136 a0001c0001t0001g0143 |
2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.884-5561C>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42416403 | |||||||
| chr19:42416492 | G | T | 1 | a0001c0001t0001g0092 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.884-5650C>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42416492 | |||||||
| chr19:42416607 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.884-5765G>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42416607 | |||||||
| chr19:42416608 | G | A | 1 | a0001c0001t0001g0022 | 2 | NA19066.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.884-5766C>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42416608 | |||||||
| chr19:42416788 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.884-5946T>C | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42416788 | |||||||
| chr19:42416819 | G | C | 1 | a0001c0001t0001g0157 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.884-5977C>G | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42416819 | |||||||
| chr19:42416821 | T | C | 11 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0027 others(8): Show |
16 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.884-5979A>G | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42416821 | |||||||
| chr19:42417022 | G | A | 1 | a0012c0012t0001g0043 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.884-6180C>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42417022 | |||||||
| chr19:42417183 | A | G | 20 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0027 others(17): Show |
25 | HG01109.hp2 HG01243.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.884-6341T>C | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42417183 | |||||||
| chr19:42417215 | C | A | 1 | a0004c0004t0001g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.884-6373G>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42417215 | |||||||
| chr19:42417215 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.884-6373G>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42417215 | |||||||
| chr19:42417223 | T | A | 11 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0027 others(8): Show |
16 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.884-6381A>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42417223 | |||||||
| chr19:42417283 | G | A | 11 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0027 others(8): Show |
16 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.884-6441C>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42417283 | |||||||
| chr19:42417413 | C | A | 2 | a0001c0001t0001g0136 a0001c0001t0001g0143 |
2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.884-6571G>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42417413 | |||||||
| chr19:42417426 | AT | A | 12 | a0001c0001t0001g0161 a0002c0002t0001g0002 a0002c0002t0001g0008 others(9): Show |
17 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.884-6585delA | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42417426 | |||||||
| chr19:42417569 | T | C | 10 | a0001c0001t0001g0006 a0001c0001t0001g0064 a0001c0001t0001g0065 others(7): Show |
12 | HG01261.hp2 HG01884.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.884-6727A>G | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42417569 | |||||||
| chr19:42417611 | T | C | 11 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0027 others(8): Show |
16 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.884-6769A>G | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42417611 | |||||||
| chr19:42417776 | T | G | 1 | a0012c0012t0001g0043 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.884-6934A>C | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42417776 | |||||||
| chr19:42417843 | C | A | 3 | a0001c0001t0001g0019 a0001c0001t0001g0156 a0001c0001t0001g0157 |
4 | NA18612.hp2 NA18942.hp2 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.884-7001G>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42417843 | |||||||
| chr19:42417846 | T | A | 1 | a0001c0001t0001g0141 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.884-7004A>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42417846 | |||||||
| chr19:42417915 | A | G | 1 | a0012c0012t0001g0043 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.884-7073T>C | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42417915 | |||||||
| chr19:42417985 | AT | A | 11 | a0001c0001t0001g0142 a0002c0002t0001g0002 a0002c0002t0001g0008 others(8): Show |
16 | HG01109.hp2 HG01517.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.884-7144delA | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42417985 | |||||||
| chr19:42418060 | G | A | 3 | a0001c0001t0001g0020 a0001c0001t0001g0158 a0001c0001t0001g0159 |
4 | HG02280.hp2 HG02886.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.884-7218C>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42418060 | |||||||
| chr19:42418139 | C | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0090 a0001c0001t0001g0091 others(1): Show |
5 | HG02055.hp2 HG02970.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.884-7297G>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42418139 | |||||||
| chr19:42418273 | G | A | 1 | a0012c0012t0001g0043 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.884-7431C>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42418273 | |||||||
| chr19:42418385 | T | C | 13 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0027 others(10): Show |
18 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.884-7543A>G | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42418385 | |||||||
| chr19:42418539 | C | T | 12 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0027 others(9): Show |
17 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.884-7697G>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42418539 | |||||||
| chr19:42418706 | A | G | 1 | a0001c0001t0001g0144 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.883+7561T>C | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42418706 | |||||||
| chr19:42418779 | A | G | 21 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0027 others(18): Show |
26 | HG01109.hp2 HG01243.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.883+7488T>C | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42418779 | |||||||
| chr19:42418780 | C | T | 12 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0027 others(9): Show |
17 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.883+7487G>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42418780 | |||||||
| chr19:42418800 | T | C | 21 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0027 others(18): Show |
26 | HG01109.hp2 HG01243.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.883+7467A>G | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42418800 | |||||||
| chr19:42419007 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.883+7260G>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42419007 | |||||||
| chr19:42419134 | C | T | 1 | a0002c0007t0001g0034 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.883+7133G>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42419134 | |||||||
| chr19:42419218 | C | T | 12 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0027 others(9): Show |
17 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.883+7049G>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42419218 | |||||||
| chr19:42419235 | A | G | 21 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0027 others(18): Show |
26 | HG01109.hp2 HG01243.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.883+7032T>C | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42419235 | |||||||
| chr19:42419581 | G | C | 1 | a0001c0001t0001g0067 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.883+6686C>G | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42419581 | |||||||
| chr19:42419634 | T | C | 12 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0027 others(9): Show |
17 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.883+6633A>G | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42419634 | |||||||
| chr19:42419702 | G | C | 1 | a0001c0001t0001g0143 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.883+6565C>G | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42419702 | |||||||
| chr19:42420009 | CT | C | 33 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0019 others(30): Show |
39 | HG00323.hp1 HG00438.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.883+6257delA | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42420009 | |||||||
| chr19:42420014 | T | C | 1 | a0001c0001t0001g0048 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.883+6253A>G | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42420014 | |||||||
| chr19:42420271 | C | G | 1 | a0001c0009t0001g0088 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.883+5996G>C | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42420271 | |||||||
| chr19:42420319 | C | T | 2 | a0002c0002t0001g0027 a0014c0011t0001g0026 |
2 | HG02897.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.883+5948G>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42420319 | |||||||
| chr19:42420345 | C | T | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | NA18998.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.883+5922G>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42420345 | |||||||
| chr19:42420646 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.883+5621C>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42420646 | |||||||
| chr19:42420694 | C | CG | 4 | a0001c0001t0001g0052 a0001c0001t0001g0085 a0002c0002t0001g0035 others(1): Show |
4 | HG00741.hp1 HG01109.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.883+5572dupC | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42420694 | |||||||
| chr19:42420804 | C | G | 1 | a0001c0001t0001g0084 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.883+5463G>C | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42420804 | |||||||
| chr19:42420924 | A | C | 1 | a0001c0001t0001g0083 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.883+5343T>G | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42420924 | |||||||
| chr19:42420962 | G | A | 1 | a0001c0001t0001g0161 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.883+5305C>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42420962 | |||||||
| chr19:42421186 | G | A | 21 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0027 others(18): Show |
26 | HG01109.hp2 HG01243.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.883+5081C>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42421186 | |||||||
| chr19:42421335 | T | C | 1 | a0004c0004t0001g0042 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.883+4932A>G | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42421335 | |||||||
| chr19:42421425 | G | A | 21 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0027 others(18): Show |
26 | HG01109.hp2 HG01243.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.883+4842C>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42421425 | |||||||
| chr19:42421570 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.883+4697A>G | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42421570 | |||||||
| chr19:42421637 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.883+4630G>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42421637 | |||||||
| chr19:42421867 | C | T | 1 | a0001c0001t0001g0081 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.883+4400G>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42421867 | |||||||
| chr19:42421873 | C | T | 1 | a0013c0010t0001g0025 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.883+4394G>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42421873 | |||||||
| chr19:42422344 | G | A | 13 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0027 others(10): Show |
18 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.883+3923C>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42422344 | |||||||
| chr19:42422488 | G | T | 1 | a0001c0001t0001g0080 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.883+3779C>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42422488 | |||||||
| chr19:42422782 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.883+3485C>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42422782 | |||||||
| chr19:42422922 | C | T | 1 | a0001c0001t0001g0079 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.883+3345G>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42422922 | |||||||
| chr19:42422974 | C | T | 1 | a0001c0009t0001g0051 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.883+3293G>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42422974 | |||||||
| chr19:42423117 | T | G | 1 | a0002c0007t0001g0034 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.883+3150A>C | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42423117 | |||||||
| chr19:42423210 | T | A | 7 | a0004c0004t0001g0036 a0004c0004t0001g0037 a0004c0004t0001g0038 others(4): Show |
7 | HG01243.hp2 HG02109.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.883+3057A>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42423210 | |||||||
| chr19:42423364 | C | G | 1 | a0012c0012t0001g0043 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.883+2903G>C | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42423364 | |||||||
| chr19:42423369 | T | C | 42 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0022 others(39): Show |
50 | HG00639.hp1 HG01069.hp2 HG01071.hp2 others(47): Show |
intron_variant | MODIFIER | c.883+2898A>G | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42423369 | |||||||
| chr19:42423413 | G | A | 1 | a0001c0001t0001g0178 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.883+2854C>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42423413 | |||||||
| chr19:42423560 | G | A | 13 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0027 others(10): Show |
18 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.883+2707C>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42423560 | |||||||
| chr19:42423564 | C | G | 12 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0027 others(9): Show |
17 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.883+2703G>C | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42423564 | |||||||
| chr19:42423579 | AG | A | 13 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0027 others(10): Show |
18 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.883+2687delC | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42423579 | |||||||
| chr19:42423587 | C | A | 1 | a0001c0001t0001g0179 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.883+2680G>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42423587 | |||||||
| chr19:42423624 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.883+2643G>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42423624 | |||||||
| chr19:42423786 | C | T | 1 | a0012c0012t0001g0043 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.883+2481G>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42423786 | |||||||
| chr19:42423791 | G | C | 1 | a0013c0010t0001g0025 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.883+2476C>G | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42423791 | |||||||
| chr19:42423822 | T | G | 1 | a0001c0001t0001g0180 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.883+2445A>C | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42423822 | |||||||
| chr19:42423948 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.883+2319T>C | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42423948 | |||||||
| chr19:42424115 | C | T | 1 | a0001c0001t0001g0010 | 2 | HG03225.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.883+2152G>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42424115 | |||||||
| chr19:42424211 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.883+2056C>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42424211 | |||||||
| chr19:42424245 | T | C | 2 | a0004c0004t0001g0036 a0004c0004t0001g0039 |
2 | HG03139.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.883+2022A>G | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42424245 | |||||||
| chr19:42424255 | C | A | 1 | a0012c0012t0001g0043 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.883+2012G>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42424255 | |||||||
| chr19:42424401 | T | A | 1 | a0001c0001t0001g0190 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.883+1866A>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42424401 | |||||||
| chr19:42424439 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.883+1828C>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42424439 | |||||||
| chr19:42424453 | C | G | 1 | a0001c0001t0001g0050 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.883+1814G>C | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42424453 | |||||||
| chr19:42424461 | CTG | C | 6 | a0001c0001t0001g0007 a0001c0001t0001g0023 a0001c0001t0001g0049 others(3): Show |
9 | HG01123.hp2 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.883+1804_883+1805d others(4): Show |
LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42424461 | |||||||
| chr19:42424831 | TC | T | 12 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0027 others(9): Show |
17 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.883+1435delG | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42424831 | |||||||
| chr19:42425102 | G | A | 12 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0027 others(9): Show |
17 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.883+1165C>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42425102 | |||||||
| chr19:42425183 | C | G | 1 | a0011c0018t0001g0076 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.883+1084G>C | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42425183 | |||||||
| chr19:42425226 | G | T | 1 | a0012c0012t0001g0043 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.883+1041C>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42425226 | |||||||
| chr19:42425350 | C | G | 1 | a0012c0012t0001g0043 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.883+917G>C | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42425350 | |||||||
| chr19:42425440 | T | A | 8 | a0001c0001t0001g0047 a0001c0001t0001g0184 a0001c0001t0001g0185 others(5): Show |
8 | HG00639.hp2 HG01074.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.883+827A>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42425440 | |||||||
| chr19:42425609 | C | T | 1 | a0001c0001t0001g0009 | 2 | HG02155.hp1 HG02165.hp2 |
intron_variant | MODIFIER | c.883+658G>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42425609 | |||||||
| chr19:42425696 | C | T | 1 | a0004c0004t0001g0036 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.883+571G>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42425696 | |||||||
| chr19:42425731 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.883+536C>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42425731 | |||||||
| chr19:42425789 | G | A | 1 | a0012c0012t0001g0043 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.883+478C>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42425789 | |||||||
| chr19:42425834 | A | T | 1 | a0001c0001t0001g0075 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.883+433T>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42425834 | |||||||
| chr19:42425927 | G | C | 12 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0027 others(9): Show |
17 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.883+340C>G | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42425927 | |||||||
| chr19:42425953 | C | T | 1 | a0012c0012t0001g0043 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.883+314G>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42425953 | |||||||
| chr19:42426002 | A | G | 1 | a0001c0001t0002g0074 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.883+265T>C | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42426002 | |||||||
| chr19:42426012 | G | C | 1 | a0005c0005t0001g0192 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.883+255C>G | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42426012 | |||||||
| chr19:42426065 | G | A | 1 | a0012c0012t0001g0043 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.883+202C>T | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42426065 | |||||||
| chr19:42426101 | C | CT | 33 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0053 others(30): Show |
33 | HG00642.hp2 HG00673.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.883+165dupA | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42426101 | |||||||
| chr19:42426101 | C | CTTT | 10 | a0002c0002t0001g0002 a0002c0002t0001g0027 a0002c0002t0001g0029 others(7): Show |
14 | HG02145.hp2 HG02451.hp2 HG02615.hp2 others(11): Show |
intron_variant | MODIFIER | c.883+163_883+165dup others(3): Show |
LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42426101 | |||||||
| chr19:42426136 | A | T | 12 | a0002c0002t0001g0002 a0002c0002t0001g0008 a0002c0002t0001g0027 others(9): Show |
17 | HG01109.hp2 HG02145.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.883+131T>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42426136 | |||||||
| chr19:42426205 | A | G | 1 | a0001c0001t0001g0049 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.883+62T>C | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42426205 | |||||||
| chr19:42426236 | G | T | 1 | a0001c0001t0001g0048 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.883+31C>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42426236 | |||||||
| chr19:42426250 | T | C | 3 | a0004c0004t0001g0040 a0004c0004t0001g0041 a0004c0004t0001g0042 |
3 | HG02109.hp1 HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.883+17A>G | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42426250 | |||||||
| chr19:42426266 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG01496.hp2 | splice_donor_variant&intron_variant | HIGH | c.883+1G>A | LIPE | ENSG00000079435.10 | transcript | ENST00000244289.9 | protein_coding | 1/9 | chr19 | 42426266 |