Item | Value |
---|---|
geneid | 5351 |
ensemblid | ENSG00000083444.17 |
hgncid | 9081 |
symbol | PLOD1 |
name | procollagen-lysine,2-oxoglutarate 5-dioxygenase 1 |
refseq_nuc | NM_000302.4 |
refseq_prot | NP_000293.2 |
ensembl_nuc | ENST00000196061.5 |
ensembl_prot | ENSP00000196061.4 |
mane_status | MANE Select |
chr | chr1 |
start | 11934717 |
end | 11975537 |
strand | + |
ver | v1.2 |
region | chr1:11934717-11975537 |
region5000 | chr1:11929717-11980537 |
regionname0 | PLOD1_chr1_11934717_11975537 |
regionname5000 | PLOD1_chr1_11929717_11980537 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 727 | 243 | 41 | 50 | 117 | 7 | 26 | 90 | PLOD1_chr1_11929717_11980537 | PLOD1 | MRPLL others(722): Show |
chr1 | 11929717 | 11980537 |
a0002 | 0/0 | 727 | 68 | 18 | 7 | 35 | 3 | 5 | 26 | PLOD1_chr1_11929717_11980537 | PLOD1 | MRPLL others(722): Show |
chr1 | 11929717 | 11980537 |
a0003 | 0/0 | 727 | 50 | 27 | 4 | 14 | 0 | 5 | 9 | PLOD1_chr1_11929717_11980537 | PLOD1 | MRPLL others(722): Show |
chr1 | 11929717 | 11980537 |
a0004 | 0/0 | 727 | 10 | 9 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | MRPLL others(722): Show |
chr1 | 11929717 | 11980537 |
a0005 | 0/0 | 727 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | MRPLL others(722): Show |
chr1 | 11929717 | 11980537 |
a0006 | 0/0 | 727 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | MRPLL others(722): Show |
chr1 | 11929717 | 11980537 |
a0007 | 0/0 | 727 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | MRPLL others(722): Show |
chr1 | 11929717 | 11980537 |
a0008 | 0/0 | 727 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | MRPLL others(722): Show |
chr1 | 11929717 | 11980537 |
a0009 | 0/0 | 727 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | MRPLL others(722): Show |
chr1 | 11929717 | 11980537 |
a0010 | 0/0 | 727 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | MRPLL others(722): Show |
chr1 | 11929717 | 11980537 |
a0011 | 0/0 | 727 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | MRPLL others(722): Show |
chr1 | 11929717 | 11980537 |
a0012 | 0/0 | 727 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PLOD1_chr1_11929717_11980537 | PLOD1 | MRPLL others(722): Show |
chr1 | 11929717 | 11980537 |
a0013 | 0/0 | 727 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | MRPLL others(722): Show |
chr1 | 11929717 | 11980537 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2181 | 131 | 26 | 30 | 58 | 4 | 11 | PLOD1_chr1_11929717_11980537 | PLOD1 | ATGCG others(2176): Show |
chr1 | 11929717 | 11980537 | ||
a0001c0002 | 0/0 | 2181 | 80 | 1 | 18 | 46 | 3 | 12 | PLOD1_chr1_11929717_11980537 | PLOD1 | ATGCG others(2176): Show |
chr1 | 11929717 | 11980537 | ||
a0001c0006 | 0/0 | 2181 | 11 | 6 | 1 | 2 | 0 | 2 | PLOD1_chr1_11929717_11980537 | PLOD1 | ATGCG others(2176): Show |
chr1 | 11929717 | 11980537 | ||
a0001c0008 | 0/0 | 2181 | 9 | 1 | 0 | 7 | 0 | 1 | PLOD1_chr1_11929717_11980537 | PLOD1 | ATGCG others(2176): Show |
chr1 | 11929717 | 11980537 | ||
a0001c0012 | 0/0 | 2181 | 4 | 4 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | ATGCG others(2176): Show |
chr1 | 11929717 | 11980537 | ||
a0001c0013 | 0/0 | 2181 | 4 | 1 | 0 | 3 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | ATGCG others(2176): Show |
chr1 | 11929717 | 11980537 | ||
a0001c0025 | 0/0 | 2181 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | ATGCG others(2176): Show |
chr1 | 11929717 | 11980537 | ||
a0001c0026 | 0/0 | 2181 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | ATGCG others(2176): Show |
chr1 | 11929717 | 11980537 | ||
a0001c0027 | 0/0 | 2181 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | ATGCG others(2176): Show |
chr1 | 11929717 | 11980537 | ||
a0001c0028 | 0/0 | 2181 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | ATGCG others(2176): Show |
chr1 | 11929717 | 11980537 | ||
a0002c0003 | 0/0 | 2181 | 52 | 8 | 6 | 31 | 3 | 4 | PLOD1_chr1_11929717_11980537 | PLOD1 | ATGCG others(2176): Show |
chr1 | 11929717 | 11980537 | ||
a0002c0010 | 0/0 | 2181 | 6 | 3 | 0 | 2 | 0 | 1 | PLOD1_chr1_11929717_11980537 | PLOD1 | ATGCG others(2176): Show |
chr1 | 11929717 | 11980537 | ||
a0002c0014 | 0/0 | 2181 | 3 | 3 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | ATGCG others(2176): Show |
chr1 | 11929717 | 11980537 | ||
a0002c0015 | 0/0 | 2181 | 3 | 2 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | ATGCG others(2176): Show |
chr1 | 11929717 | 11980537 | ||
a0002c0017 | 0/0 | 2181 | 2 | 0 | 0 | 2 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | ATGCG others(2176): Show |
chr1 | 11929717 | 11980537 | ||
a0002c0018 | 0/0 | 2181 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | ATGCG others(2176): Show |
chr1 | 11929717 | 11980537 | ||
a0002c0019 | 0/0 | 2181 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | ATGCG others(2176): Show |
chr1 | 11929717 | 11980537 | ||
a0003c0004 | 0/0 | 2181 | 21 | 0 | 3 | 13 | 0 | 5 | PLOD1_chr1_11929717_11980537 | PLOD1 | ATGCG others(2176): Show |
chr1 | 11929717 | 11980537 | ||
a0003c0005 | 0/0 | 2181 | 15 | 14 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | ATGCG others(2176): Show |
chr1 | 11929717 | 11980537 | ||
a0003c0007 | 0/0 | 2181 | 10 | 9 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | ATGCG others(2176): Show |
chr1 | 11929717 | 11980537 | ||
a0003c0016 | 0/0 | 2181 | 3 | 3 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | ATGCG others(2176): Show |
chr1 | 11929717 | 11980537 | ||
a0003c0033 | 0/0 | 2181 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | ATGCG others(2176): Show |
chr1 | 11929717 | 11980537 | ||
a0004c0009 | 0/0 | 2181 | 6 | 5 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | ATGCG others(2176): Show |
chr1 | 11929717 | 11980537 | ||
a0004c0011 | 0/0 | 2181 | 4 | 4 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | ATGCG others(2176): Show |
chr1 | 11929717 | 11980537 | ||
a0005c0023 | 0/0 | 2181 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | ATGCG others(2176): Show |
chr1 | 11929717 | 11980537 | ||
a0006c0029 | 0/0 | 2181 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | ATGCG others(2176): Show |
chr1 | 11929717 | 11980537 | ||
a0007c0030 | 0/0 | 2181 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | ATGCG others(2176): Show |
chr1 | 11929717 | 11980537 | ||
a0008c0032 | 0/0 | 2181 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | ATGCG others(2176): Show |
chr1 | 11929717 | 11980537 | ||
a0009c0022 | 0/0 | 2181 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | ATGCG others(2176): Show |
chr1 | 11929717 | 11980537 | ||
a0010c0024 | 0/0 | 2181 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD1_chr1_11929717_11980537 | PLOD1 | ATGCG others(2176): Show |
chr1 | 11929717 | 11980537 | ||
a0011c0021 | 0/0 | 2181 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD1_chr1_11929717_11980537 | PLOD1 | ATGCG others(2176): Show |
chr1 | 11929717 | 11980537 | ||
a0012c0031 | 0/0 | 2181 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | ATGCG others(2176): Show |
chr1 | 11929717 | 11980537 | ||
a0013c0020 | 0/0 | 2181 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | ATGCG others(2176): Show |
chr1 | 11929717 | 11980537 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2976 | 128 | 24 | 30 | 57 | 4 | 11 | PLOD1_chr1_11929717_11980537 | PLOD1 | GTCGC others(2971): Show |
chr1 | 11929717 | 11980537 |
a0001c0001t0003 | 0/0 | 2976 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | GTCGC others(2971): Show |
chr1 | 11929717 | 11980537 |
a0001c0001t0005 | 0/0 | 2976 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | GTCGC others(2971): Show |
chr1 | 11929717 | 11980537 |
a0001c0001t0006 | 0/0 | 2976 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | GTCGC others(2971): Show |
chr1 | 11929717 | 11980537 |
a0001c0002t0001 | 0/0 | 2976 | 79 | 1 | 18 | 46 | 3 | 11 | PLOD1_chr1_11929717_11980537 | PLOD1 | GTCGC others(2971): Show |
chr1 | 11929717 | 11980537 |
a0001c0002t0007 | 0/0 | 2976 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD1_chr1_11929717_11980537 | PLOD1 | GTCGC others(2971): Show |
chr1 | 11929717 | 11980537 |
a0001c0006t0001 | 0/0 | 2976 | 11 | 6 | 1 | 2 | 0 | 2 | PLOD1_chr1_11929717_11980537 | PLOD1 | GTCGC others(2971): Show |
chr1 | 11929717 | 11980537 |
a0001c0008t0002 | 0/0 | 2976 | 8 | 0 | 0 | 7 | 0 | 1 | PLOD1_chr1_11929717_11980537 | PLOD1 | GTCGC others(2971): Show |
chr1 | 11929717 | 11980537 |
a0001c0008t0004 | 0/0 | 2976 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | GTCGC others(2971): Show |
chr1 | 11929717 | 11980537 |
a0001c0012t0002 | 0/0 | 2976 | 4 | 4 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | GTCGC others(2971): Show |
chr1 | 11929717 | 11980537 |
a0001c0013t0001 | 0/0 | 2976 | 4 | 1 | 0 | 3 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | GTCGC others(2971): Show |
chr1 | 11929717 | 11980537 |
a0001c0025t0001 | 0/0 | 2976 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | GTCGC others(2971): Show |
chr1 | 11929717 | 11980537 |
a0001c0026t0002 | 0/0 | 2976 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | GTCGC others(2971): Show |
chr1 | 11929717 | 11980537 |
a0001c0027t0001 | 0/0 | 2976 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | GTCGC others(2971): Show |
chr1 | 11929717 | 11980537 |
a0001c0028t0001 | 0/0 | 2976 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | GTCGC others(2971): Show |
chr1 | 11929717 | 11980537 |
a0002c0003t0001 | 0/0 | 2976 | 52 | 8 | 6 | 31 | 3 | 4 | PLOD1_chr1_11929717_11980537 | PLOD1 | GTCGC others(2971): Show |
chr1 | 11929717 | 11980537 |
a0002c0010t0001 | 0/0 | 2976 | 6 | 3 | 0 | 2 | 0 | 1 | PLOD1_chr1_11929717_11980537 | PLOD1 | GTCGC others(2971): Show |
chr1 | 11929717 | 11980537 |
a0002c0014t0001 | 0/0 | 2976 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | GTCGC others(2971): Show |
chr1 | 11929717 | 11980537 |
a0002c0014t0004 | 0/0 | 2976 | 2 | 2 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | GTCGC others(2971): Show |
chr1 | 11929717 | 11980537 |
a0002c0015t0001 | 0/0 | 2976 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | GTCGC others(2971): Show |
chr1 | 11929717 | 11980537 |
a0002c0015t0003 | 0/0 | 2976 | 2 | 1 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | GTCGC others(2971): Show |
chr1 | 11929717 | 11980537 |
a0002c0017t0001 | 0/0 | 2976 | 2 | 0 | 0 | 2 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | GTCGC others(2971): Show |
chr1 | 11929717 | 11980537 |
a0002c0018t0001 | 0/0 | 2976 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | GTCGC others(2971): Show |
chr1 | 11929717 | 11980537 |
a0002c0019t0002 | 0/0 | 2976 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | GTCGC others(2971): Show |
chr1 | 11929717 | 11980537 |
a0003c0004t0001 | 0/0 | 2976 | 21 | 0 | 3 | 13 | 0 | 5 | PLOD1_chr1_11929717_11980537 | PLOD1 | GTCGC others(2971): Show |
chr1 | 11929717 | 11980537 |
a0003c0005t0001 | 0/0 | 2976 | 15 | 14 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | GTCGC others(2971): Show |
chr1 | 11929717 | 11980537 |
a0003c0007t0001 | 0/0 | 2976 | 5 | 4 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | GTCGC others(2971): Show |
chr1 | 11929717 | 11980537 |
a0003c0007t0003 | 0/0 | 2976 | 5 | 5 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | GTCGC others(2971): Show |
chr1 | 11929717 | 11980537 |
a0003c0016t0001 | 0/0 | 2976 | 3 | 3 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | GTCGC others(2971): Show |
chr1 | 11929717 | 11980537 |
a0003c0033t0003 | 0/0 | 2976 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | GTCGC others(2971): Show |
chr1 | 11929717 | 11980537 |
a0004c0009t0002 | 0/0 | 2976 | 6 | 5 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | GTCGC others(2971): Show |
chr1 | 11929717 | 11980537 |
a0004c0011t0001 | 0/0 | 2976 | 4 | 4 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | GTCGC others(2971): Show |
chr1 | 11929717 | 11980537 |
a0005c0023t0002 | 0/0 | 2976 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | GTCGC others(2971): Show |
chr1 | 11929717 | 11980537 |
a0006c0029t0001 | 0/0 | 2976 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | GTCGC others(2971): Show |
chr1 | 11929717 | 11980537 |
a0007c0030t0001 | 0/0 | 2976 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | GTCGC others(2971): Show |
chr1 | 11929717 | 11980537 |
a0008c0032t0002 | 0/0 | 2976 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | GTCGC others(2971): Show |
chr1 | 11929717 | 11980537 |
a0009c0022t0001 | 0/0 | 2976 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | GTCGC others(2971): Show |
chr1 | 11929717 | 11980537 |
a0010c0024t0001 | 0/0 | 2976 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD1_chr1_11929717_11980537 | PLOD1 | GTCGC others(2971): Show |
chr1 | 11929717 | 11980537 |
a0011c0021t0001 | 0/0 | 2976 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD1_chr1_11929717_11980537 | PLOD1 | GTCGC others(2971): Show |
chr1 | 11929717 | 11980537 |
a0012c0031t0001 | 0/0 | 2976 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | GTCGC others(2971): Show |
chr1 | 11929717 | 11980537 |
a0013c0020t0001 | 0/0 | 2976 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | GTCGC others(2971): Show |
chr1 | 11929717 | 11980537 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0002 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0004 | 0/0 | 5 | 2 | 1 | 2 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0005 | 1/0 | 5 | 1 | 2 | 0 | 1 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0006 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0008 | 0/1 | 3 | 1 | 0 | 0 | 0 | 1 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0003g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0005g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0001t0006g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0001 | 0/0 | 9 | 1 | 3 | 4 | 1 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0002t0007g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0006t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0006t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0006t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0006t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0006t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0006t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0006t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0006t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0006t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0006t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0006t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0008t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0008t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0008t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0008t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0008t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0008t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0008t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0008t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0008t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0012t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0012t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0012t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0012t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0013t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0013t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0013t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0013t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0025t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0026t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0027t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0001c0028t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0003t0001g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0003t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0003t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0003t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0003t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0003t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0003t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0003t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0003t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0003t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0003t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0003t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0003t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0003t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0003t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0003t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0003t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0003t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0003t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0003t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0003t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0003t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0003t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0003t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0003t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0003t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0003t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0003t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0003t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0003t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0003t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0003t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0003t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0003t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0003t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0003t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0003t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0003t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0003t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0003t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0003t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0003t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0003t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0003t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0003t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0003t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0003t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0003t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0003t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0003t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0010t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0010t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0010t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0010t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0010t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0010t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0014t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0014t0004g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0014t0004g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0015t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0015t0003g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0015t0003g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0017t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0017t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0018t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0002c0019t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0003c0004t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0003c0004t0001g0018 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0003c0004t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0003c0004t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0003c0004t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0003c0004t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0003c0004t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0003c0004t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0003c0004t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0003c0004t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0003c0004t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0003c0004t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0003c0004t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0003c0004t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0003c0004t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0003c0004t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0003c0004t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0003c0004t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0003c0004t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0003c0005t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0003c0005t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0003c0005t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0003c0005t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0003c0005t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0003c0005t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0003c0005t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0003c0005t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0003c0005t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0003c0005t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0003c0005t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0003c0005t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0003c0005t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0003c0005t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0003c0007t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0003c0007t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0003c0007t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0003c0007t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0003c0007t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0003c0007t0003g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0003c0007t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0003c0007t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0003c0007t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0003c0007t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0003c0016t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0003c0016t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0003c0033t0003g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0004c0009t0002g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0004c0009t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0004c0009t0002g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0004c0009t0002g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0004c0009t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0004c0009t0002g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0004c0011t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0004c0011t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0004c0011t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0004c0011t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0005c0023t0002g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0006c0029t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0007c0030t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0008c0032t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0009c0022t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0010c0024t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0011c0021t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0012c0031t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
a0013c0020t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0002 | c0003 | t0001 | g0259 | EUR | FIN | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG00408 | hp1 | a0002 | c0003 | t0001 | g0201 | EAS | CHS | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG00408 | hp2 | a0003 | c0004 | t0001 | g0018 | EAS | CHS | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG00423 | hp1 | a0002 | c0003 | t0001 | g0202 | EAS | CHS | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG00438 | hp1 | a0002 | c0003 | t0001 | g0275 | EAS | CHS | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | CHS | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG00597 | hp1 | a0002 | c0003 | t0001 | g0199 | EAS | CHS | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG00597 | hp2 | a0001 | c0002 | t0001 | g0173 | EAS | CHS | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG00609 | hp1 | a0002 | c0003 | t0001 | g0270 | EAS | CHS | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG00609 | hp2 | a0001 | c0002 | t0001 | g0204 | EAS | CHS | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | CHS | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG00621 | hp2 | a0001 | c0013 | t0001 | g0119 | EAS | CHS | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG00642 | hp2 | a0002 | c0003 | t0001 | g0258 | AMR | PUR | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG00733 | hp2 | a0003 | c0004 | t0001 | g0249 | AMR | PUR | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG00735 | hp1 | a0002 | c0003 | t0001 | g0262 | AMR | PUR | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG00735 | hp2 | a0001 | c0002 | t0001 | g0183 | AMR | PUR | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG00738 | hp2 | a0001 | c0002 | t0001 | g0142 | AMR | PUR | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01069 | hp1 | a0002 | c0003 | t0001 | g0253 | AMR | PUR | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01069 | hp2 | a0001 | c0002 | t0001 | g0128 | AMR | PUR | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01070 | hp1 | a0004 | c0009 | t0002 | g0091 | AMR | PUR | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01106 | hp1 | a0003 | c0004 | t0001 | g0244 | AMR | PUR | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01109 | hp2 | a0005 | c0023 | t0002 | g0324 | AMR | PUR | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01167 | hp2 | a0001 | c0026 | t0002 | g0298 | AMR | PUR | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01168 | hp2 | a0001 | c0002 | t0001 | g0111 | AMR | PUR | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01192 | hp1 | a0003 | c0004 | t0001 | g0250 | AMR | PUR | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01192 | hp2 | a0002 | c0015 | t0003 | g0297 | AMR | PUR | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01243 | hp1 | a0002 | c0003 | t0001 | g0019 | AMR | PUR | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01243 | hp2 | a0003 | c0005 | t0001 | g0315 | AMR | PUR | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01255 | hp1 | a0002 | c0003 | t0001 | g0264 | AMR | CLM | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01258 | hp1 | a0001 | c0006 | t0001 | g0028 | AMR | CLM | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01346 | hp1 | a0001 | c0002 | t0001 | g0161 | AMR | CLM | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | CLM | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0153 | AMR | CLM | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01515 | hp2 | a0001 | c0002 | t0001 | g0001 | EUR | IBS | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01516 | hp1 | a0002 | c0003 | t0001 | g0260 | EUR | IBS | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01517 | hp1 | a0001 | c0002 | t0001 | g0120 | EUR | IBS | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01517 | hp2 | a0002 | c0003 | t0001 | g0254 | EUR | IBS | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01884 | hp1 | a0001 | c0006 | t0001 | g0109 | AFR | ACB | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01884 | hp2 | a0003 | c0007 | t0003 | g0069 | AFR | ACB | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01891 | hp1 | a0003 | c0005 | t0001 | g0093 | AFR | ACB | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01891 | hp2 | a0002 | c0003 | t0001 | g0310 | AFR | ACB | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01928 | hp1 | a0001 | c0002 | t0001 | g0165 | AMR | PEL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01934 | hp1 | a0001 | c0002 | t0001 | g0186 | AMR | PEL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01934 | hp2 | a0002 | c0003 | t0001 | g0097 | AMR | PEL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01943 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | PEL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01952 | hp1 | a0001 | c0002 | t0001 | g0182 | AMR | PEL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01975 | hp1 | a0001 | c0002 | t0001 | g0151 | AMR | PEL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01978 | hp2 | a0001 | c0002 | t0001 | g0156 | AMR | PEL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG01993 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02004 | hp1 | a0001 | c0002 | t0001 | g0148 | AMR | PEL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02015 | hp1 | a0001 | c0002 | t0001 | g0185 | EAS | KHV | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02015 | hp2 | a0001 | c0002 | t0001 | g0170 | EAS | KHV | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02027 | hp1 | a0002 | c0003 | t0001 | g0200 | EAS | KHV | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02027 | hp2 | a0003 | c0004 | t0001 | g0132 | EAS | KHV | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02040 | hp2 | a0003 | c0004 | t0001 | g0135 | EAS | KHV | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02055 | hp1 | a0002 | c0003 | t0001 | g0237 | AFR | ACB | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02055 | hp2 | a0001 | c0027 | t0001 | g0220 | AFR | ACB | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02056 | hp2 | a0003 | c0004 | t0001 | g0242 | EAS | KHV | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02071 | hp1 | a0003 | c0004 | t0001 | g0176 | EAS | KHV | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02071 | hp2 | a0001 | c0002 | t0001 | g0112 | EAS | KHV | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02074 | hp1 | a0001 | c0006 | t0001 | g0131 | EAS | KHV | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02074 | hp2 | a0001 | c0002 | t0001 | g0154 | EAS | KHV | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02083 | hp1 | a0001 | c0008 | t0002 | g0094 | EAS | KHV | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02129 | hp2 | a0001 | c0013 | t0001 | g0117 | EAS | KHV | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02132 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | KHV | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02135 | hp1 | a0001 | c0002 | t0001 | g0171 | EAS | KHV | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02135 | hp2 | a0001 | c0002 | t0001 | g0177 | EAS | KHV | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02145 | hp1 | a0001 | c0012 | t0002 | g0214 | AFR | ACB | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02145 | hp2 | a0004 | c0009 | t0002 | g0323 | AFR | ACB | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02148 | hp2 | a0001 | c0002 | t0001 | g0149 | AMR | PEL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02165 | hp1 | a0002 | c0003 | t0001 | g0096 | EAS | CDX | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02165 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | CDX | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | ACB | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02257 | hp2 | a0003 | c0005 | t0001 | g0230 | AFR | ACB | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02258 | hp2 | a0003 | c0005 | t0001 | g0074 | AFR | ACB | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02273 | hp1 | a0001 | c0002 | t0001 | g0160 | AMR | PEL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02273 | hp2 | a0006 | c0029 | t0001 | g0166 | AMR | PEL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02280 | hp2 | a0003 | c0005 | t0001 | g0011 | AFR | ACB | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02293 | hp2 | a0001 | c0002 | t0001 | g0159 | AMR | PEL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02451 | hp1 | a0002 | c0003 | t0001 | g0203 | AFR | ACB | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02451 | hp2 | a0003 | c0016 | t0001 | g0309 | AFR | ACB | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02523 | hp1 | a0002 | c0003 | t0001 | g0197 | EAS | KHV | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02523 | hp2 | a0007 | c0030 | t0001 | g0007 | EAS | KHV | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02572 | hp1 | a0003 | c0005 | t0001 | g0228 | AFR | GWD | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | GWD | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02602 | hp1 | a0001 | c0002 | t0001 | g0013 | SAS | PJL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02615 | hp1 | a0003 | c0007 | t0001 | g0194 | AFR | GWD | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | GWD | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02622 | hp1 | a0003 | c0005 | t0001 | g0071 | AFR | GWD | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02622 | hp2 | a0004 | c0009 | t0002 | g0320 | AFR | GWD | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02630 | hp1 | a0004 | c0011 | t0001 | g0291 | AFR | GWD | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | GWD | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02647 | hp2 | a0003 | c0007 | t0001 | g0073 | AFR | GWD | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02683 | hp1 | a0002 | c0003 | t0001 | g0261 | SAS | PJL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02683 | hp2 | a0003 | c0004 | t0001 | g0245 | SAS | PJL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02698 | hp1 | a0001 | c0002 | t0001 | g0138 | SAS | PJL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02717 | hp1 | a0001 | c0001 | t0005 | g0210 | AFR | GWD | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02717 | hp2 | a0001 | c0028 | t0001 | g0196 | AFR | GWD | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02723 | hp1 | a0003 | c0005 | t0001 | g0325 | AFR | GWD | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02723 | hp2 | a0003 | c0005 | t0001 | g0303 | AFR | GWD | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | GWD | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02818 | hp2 | a0004 | c0011 | t0001 | g0321 | AFR | GWD | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | GWD | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02886 | hp2 | a0003 | c0033 | t0003 | g0311 | AFR | GWD | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02895 | hp1 | a0001 | c0006 | t0001 | g0212 | AFR | GWD | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02896 | hp1 | a0003 | c0007 | t0003 | g0066 | AFR | GWD | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02896 | hp2 | a0002 | c0010 | t0001 | g0293 | AFR | GWD | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02897 | hp1 | a0001 | c0006 | t0001 | g0211 | AFR | GWD | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02897 | hp2 | a0003 | c0007 | t0003 | g0067 | AFR | GWD | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02922 | hp1 | a0003 | c0005 | t0001 | g0070 | AFR | ESN | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | ESN | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02965 | hp1 | a0002 | c0003 | t0001 | g0313 | AFR | ESN | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02970 | hp1 | a0003 | c0007 | t0001 | g0072 | AFR | ESN | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02970 | hp2 | a0002 | c0014 | t0004 | g0295 | AFR | ESN | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02976 | hp1 | a0001 | c0012 | t0002 | g0213 | AFR | ESN | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | ESN | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG03041 | hp2 | a0002 | c0015 | t0003 | g0314 | AFR | GWD | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG03098 | hp1 | a0003 | c0005 | t0001 | g0229 | AFR | MSL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG03098 | hp2 | a0004 | c0009 | t0002 | g0317 | AFR | MSL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG03130 | hp1 | a0003 | c0005 | t0001 | g0075 | AFR | ESN | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG03139 | hp1 | a0002 | c0003 | t0001 | g0019 | AFR | ESN | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG03139 | hp2 | a0002 | c0015 | t0001 | g0106 | AFR | ESN | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | ESN | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG03195 | hp2 | a0002 | c0003 | t0001 | g0287 | AFR | ESN | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG03209 | hp1 | a0001 | c0008 | t0004 | g0065 | AFR | MSL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG03225 | hp1 | a0002 | c0003 | t0001 | g0294 | AFR | MSL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG03225 | hp2 | a0001 | c0006 | t0001 | g0108 | AFR | MSL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG03453 | hp2 | a0002 | c0018 | t0001 | g0021 | AFR | MSL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG03486 | hp1 | a0002 | c0010 | t0001 | g0292 | AFR | MSL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG03486 | hp2 | a0008 | c0032 | t0002 | g0312 | AFR | MSL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG03490 | hp2 | a0001 | c0002 | t0001 | g0193 | SAS | PJL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG03491 | hp1 | a0002 | c0010 | t0001 | g0257 | SAS | PJL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG03491 | hp2 | a0001 | c0002 | t0001 | g0121 | SAS | PJL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0125 | SAS | PJL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG03516 | hp1 | a0002 | c0014 | t0004 | g0296 | AFR | ESN | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG03516 | hp2 | a0004 | c0011 | t0001 | g0289 | AFR | ESN | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG03540 | hp1 | a0004 | c0009 | t0002 | g0319 | AFR | GWD | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG03540 | hp2 | a0002 | c0003 | t0001 | g0322 | AFR | GWD | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG03579 | hp1 | a0004 | c0011 | t0001 | g0290 | AFR | MSL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG03579 | hp2 | a0009 | c0022 | t0001 | g0089 | AFR | MSL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG03654 | hp1 | a0003 | c0004 | t0001 | g0248 | SAS | PJL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG03654 | hp2 | a0002 | c0003 | t0001 | g0279 | SAS | PJL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG03669 | hp1 | a0001 | c0006 | t0001 | g0162 | SAS | PJL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG03669 | hp2 | a0003 | c0004 | t0001 | g0018 | SAS | PJL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG03688 | hp1 | a0001 | c0002 | t0001 | g0168 | SAS | STU | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG03688 | hp2 | a0003 | c0004 | t0001 | g0247 | SAS | STU | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0127 | SAS | PJL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG03710 | hp1 | a0001 | c0002 | t0007 | g0167 | SAS | PJL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG03831 | hp1 | a0001 | c0002 | t0001 | g0013 | SAS | BEB | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG03831 | hp2 | a0002 | c0003 | t0001 | g0285 | SAS | BEB | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | BEB | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG03834 | hp2 | a0003 | c0004 | t0001 | g0251 | SAS | BEB | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG03927 | hp1 | a0002 | c0003 | t0001 | g0263 | SAS | BEB | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | BEB | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG03942 | hp1 | a0010 | c0024 | t0001 | g0218 | SAS | BEB | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | BEB | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG04199 | hp1 | a0011 | c0021 | t0001 | g0286 | SAS | STU | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG04199 | hp2 | a0001 | c0002 | t0001 | g0139 | SAS | STU | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0233 | SAS | STU | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0022 | SAS | STU | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG04228 | hp1 | a0001 | c0002 | t0001 | g0164 | SAS | STU | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG04228 | hp2 | a0001 | c0008 | t0002 | g0205 | SAS | STU | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18522 | hp1 | a0003 | c0016 | t0001 | g0020 | AFR | YRI | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18522 | hp2 | a0003 | c0005 | t0001 | g0011 | AFR | YRI | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18612 | hp1 | a0002 | c0003 | t0001 | g0267 | EAS | CHB | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | CHB | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18906 | hp1 | a0002 | c0014 | t0001 | g0105 | AFR | YRI | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18906 | hp2 | a0003 | c0007 | t0003 | g0215 | AFR | YRI | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18940 | hp2 | a0012 | c0031 | t0001 | g0130 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18942 | hp1 | a0001 | c0002 | t0001 | g0144 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18943 | hp2 | a0003 | c0007 | t0001 | g0243 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18946 | hp1 | a0002 | c0003 | t0001 | g0282 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18946 | hp2 | a0001 | c0002 | t0001 | g0189 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18947 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18948 | hp1 | a0001 | c0008 | t0002 | g0095 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18948 | hp2 | a0001 | c0013 | t0001 | g0150 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18951 | hp1 | a0001 | c0025 | t0001 | g0042 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18951 | hp2 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18952 | hp1 | a0001 | c0008 | t0002 | g0206 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18952 | hp2 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18956 | hp1 | a0001 | c0002 | t0001 | g0155 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18957 | hp1 | a0002 | c0003 | t0001 | g0274 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18959 | hp2 | a0001 | c0002 | t0001 | g0179 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18960 | hp1 | a0002 | c0003 | t0001 | g0283 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18960 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18961 | hp1 | a0002 | c0003 | t0001 | g0266 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18962 | hp2 | a0003 | c0004 | t0001 | g0012 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18967 | hp1 | a0001 | c0008 | t0002 | g0163 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18967 | hp2 | a0002 | c0003 | t0001 | g0277 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18973 | hp1 | a0002 | c0003 | t0001 | g0099 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18973 | hp2 | a0003 | c0004 | t0001 | g0246 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18975 | hp2 | a0001 | c0006 | t0001 | g0140 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18977 | hp2 | a0003 | c0004 | t0001 | g0241 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18980 | hp1 | a0001 | c0002 | t0001 | g0184 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18981 | hp2 | a0002 | c0003 | t0001 | g0192 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18982 | hp2 | a0001 | c0001 | t0006 | g0100 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18984 | hp1 | a0002 | c0010 | t0001 | g0273 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18984 | hp2 | a0001 | c0002 | t0001 | g0129 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18985 | hp1 | a0002 | c0003 | t0001 | g0284 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18985 | hp2 | a0003 | c0004 | t0001 | g0134 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18988 | hp2 | a0001 | c0002 | t0001 | g0107 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18989 | hp2 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18990 | hp1 | a0001 | c0008 | t0002 | g0207 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18993 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18994 | hp1 | a0001 | c0008 | t0002 | g0208 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18998 | hp1 | a0001 | c0002 | t0001 | g0143 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18998 | hp2 | a0002 | c0003 | t0001 | g0256 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19000 | hp1 | a0002 | c0003 | t0001 | g0098 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19002 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19005 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19005 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19007 | hp2 | a0001 | c0002 | t0001 | g0015 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19009 | hp2 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19010 | hp2 | a0003 | c0004 | t0001 | g0012 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19011 | hp2 | a0002 | c0003 | t0001 | g0326 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19012 | hp2 | a0002 | c0003 | t0001 | g0265 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19030 | hp1 | a0003 | c0005 | t0001 | g0092 | AFR | LWK | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | LWK | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19043 | hp1 | a0013 | c0020 | t0001 | g0090 | AFR | LWK | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19043 | hp2 | a0003 | c0007 | t0003 | g0068 | AFR | LWK | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19054 | hp1 | a0003 | c0004 | t0001 | g0175 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19056 | hp1 | a0002 | c0003 | t0001 | g0272 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19056 | hp2 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19057 | hp1 | a0003 | c0004 | t0001 | g0122 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19060 | hp2 | a0002 | c0003 | t0001 | g0252 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19062 | hp2 | a0002 | c0003 | t0001 | g0255 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19064 | hp1 | a0001 | c0002 | t0001 | g0141 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19064 | hp2 | a0002 | c0003 | t0001 | g0271 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19065 | hp1 | a0002 | c0010 | t0001 | g0269 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19065 | hp2 | a0002 | c0003 | t0001 | g0281 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19066 | hp2 | a0001 | c0002 | t0001 | g0152 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19067 | hp1 | a0002 | c0003 | t0001 | g0198 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19068 | hp1 | a0002 | c0017 | t0001 | g0278 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19070 | hp2 | a0001 | c0002 | t0001 | g0146 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19074 | hp1 | a0001 | c0002 | t0001 | g0126 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19078 | hp1 | a0002 | c0003 | t0001 | g0268 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19079 | hp1 | a0001 | c0002 | t0001 | g0136 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19079 | hp2 | a0001 | c0002 | t0001 | g0113 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19080 | hp1 | a0001 | c0002 | t0001 | g0114 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19080 | hp2 | a0002 | c0017 | t0001 | g0276 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19083 | hp1 | a0001 | c0002 | t0001 | g0157 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19084 | hp1 | a0001 | c0002 | t0001 | g0180 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19084 | hp2 | a0003 | c0004 | t0001 | g0133 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19085 | hp2 | a0002 | c0003 | t0001 | g0190 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19087 | hp1 | a0002 | c0003 | t0001 | g0280 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19087 | hp2 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19088 | hp1 | a0001 | c0002 | t0001 | g0115 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19088 | hp2 | a0002 | c0003 | t0001 | g0191 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19090 | hp1 | a0001 | c0002 | t0001 | g0169 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19090 | hp2 | a0001 | c0008 | t0002 | g0209 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19091 | hp2 | a0001 | c0002 | t0001 | g0016 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0327 | AFR | YRI | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA19240 | hp2 | a0001 | c0006 | t0001 | g0299 | AFR | YRI | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | ASW | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA20129 | hp2 | a0002 | c0010 | t0001 | g0288 | AFR | ASW | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0181 | EUR | TSI | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0010 | EUR | TSI | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA20905 | hp1 | a0001 | c0006 | t0001 | g0224 | SAS | GIH | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | GIH | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02109 | hp1 | a0001 | c0006 | t0001 | g0300 | AFR | ACB | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02109 | hp2 | a0001 | c0012 | t0002 | g0187 | AFR | ACB | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02486 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | ACB | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02559 | hp1 | a0002 | c0019 | t0002 | g0316 | AFR | ACB | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG02559 | hp2 | a0003 | c0016 | t0001 | g0020 | AFR | ACB | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG03471 | hp1 | a0003 | c0007 | t0001 | g0195 | AFR | MSL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG03471 | hp2 | a0003 | c0005 | t0001 | g0227 | AFR | MSL | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG06807 | hp1 | a0001 | c0012 | t0002 | g0064 | AFR | USA | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
HG06807 | hp2 | a0004 | c0009 | t0002 | g0318 | AFR | USA | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA18955 | hp2 | a0001 | c0002 | t0001 | g0137 | EAS | JPT | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | USA | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA20300 | hp2 | a0001 | c0013 | t0001 | g0147 | AFR | USA | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | LWK | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
NA21309 | hp2 | a0001 | c0001 | t0003 | g0302 | AFR | LWK | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0008 | REF | REF | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0005 | REF | REF | PLOD1_chr1_11929717_11980537 | PLOD1 | chr1 | 11929717 | 11980537 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:11949854 | G | A | 1 | a0004 | 10 | HG01070.hp1 HG02145.hp2 HG02622.hp2 others(7): Show |
missense_variant | MODERATE | c.250G>A | p.Ala84Thr | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 3/19 | 313/2976 | 250/2184 | 84/727 | chr1 | 11949854 | |||
chr1:11949899 | G | A | 7 | a0002 a0003 a0004 others(4): Show |
132 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(129): Show |
missense_variant | MODERATE | c.295G>A | p.Ala99Thr | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 3/19 | 358/2976 | 295/2184 | 99/727 | chr1 | 11949899 | |||
chr1:11950412 | G | T | 3 | a0003 a0008 a0009 |
52 | HG00408.hp2 HG00733.hp2 HG01106.hp1 others(49): Show |
missense_variant | MODERATE | c.358G>T | p.Ala120Ser | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 4/19 | 421/2976 | 358/2184 | 120/727 | chr1 | 11950412 | |||
chr1:11952665 | A | T | 1 | a0011 | 1 | HG04199.hp1 | missense_variant | MODERATE | c.509A>T | p.Glu170Val | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 5/19 | 572/2976 | 509/2184 | 170/727 | chr1 | 11952665 | |||
chr1:11952720 | G | C | 1 | a0006 | 1 | HG02273.hp2 | missense_variant | MODERATE | c.564G>C | p.Leu188Phe | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 5/19 | 627/2976 | 564/2184 | 188/727 | chr1 | 11952720 | |||
chr1:11957902 | A | G | 1 | a0013 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.802A>G | p.Thr268Ala | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 8/19 | 865/2976 | 802/2184 | 268/727 | chr1 | 11957902 | |||
chr1:11960701 | A | G | 1 | a0012 | 1 | NA18940.hp2 | missense_variant | MODERATE | c.1031A>G | p.Tyr344Cys | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 10/19 | 1094/2976 | 1031/2184 | 344/727 | chr1 | 11960701 | |||
chr1:11963575 | G | A | 2 | a0005 a0008 |
2 | HG01109.hp2 HG03486.hp2 |
missense_variant | MODERATE | c.1141G>A | p.Val381Met | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 11/19 | 1204/2976 | 1141/2184 | 381/727 | chr1 | 11963575 | |||
chr1:11965504 | C | T | 1 | a0007 | 1 | HG02523.hp2 | missense_variant | MODERATE | c.1495C>T | p.Arg499Trp | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 14/19 | 1558/2976 | 1495/2184 | 499/727 | chr1 | 11965504 | |||
chr1:11965591 | G | A | 1 | a0009 | 1 | HG03579.hp2 | missense_variant&splice_region_variant | MODERATE | c.1582G>A | p.Glu528Lys | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 14/19 | 1645/2976 | 1582/2184 | 528/727 | chr1 | 11965591 | |||
chr1:11974699 | C | T | 1 | a0010 | 1 | HG03942.hp1 | missense_variant | MODERATE | c.2075C>T | p.Pro692Leu | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 19/19 | 2138/2976 | 2075/2184 | 692/727 | chr1 | 11974699 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:11949781 | C | T | 3 | a0003c0016 a0003c0033 a0008c0032 |
5 | HG02451.hp2 HG02559.hp2 HG02886.hp2 others(2): Show |
synonymous_variant | LOW | c.177C>T | p.Gly59Gly | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 3/19 | 240/2976 | 177/2184 | 59/727 | chr1 | 11949781 | |||
chr1:11949898 | C | T | 5 | a0001c0002 a0001c0013 a0006c0029 others(2): Show |
87 | HG00597.hp2 HG00609.hp2 HG00621.hp2 others(84): Show |
synonymous_variant | LOW | c.294C>T | p.Phe98Phe | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 3/19 | 357/2976 | 294/2184 | 98/727 | chr1 | 11949898 | |||
chr1:11952696 | G | A | 3 | a0002c0014 a0002c0015 a0002c0018 |
7 | HG01192.hp2 HG02970.hp2 HG03041.hp2 others(4): Show |
synonymous_variant | LOW | c.540G>A | p.Gln180Gln | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 5/19 | 603/2976 | 540/2184 | 180/727 | chr1 | 11952696 | |||
chr1:11958525 | C | T | 1 | a0001c0028 | 1 | HG02717.hp2 | synonymous_variant | LOW | c.853C>T | p.Leu285Leu | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 9/19 | 916/2976 | 853/2184 | 285/727 | chr1 | 11958525 | |||
chr1:11963598 | C | T | 2 | a0001c0027 a0001c0028 |
2 | HG02055.hp2 HG02717.hp2 |
synonymous_variant | LOW | c.1164C>T | p.Thr388Thr | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 11/19 | 1227/2976 | 1164/2184 | 388/727 | chr1 | 11963598 | |||
chr1:11964178 | C | T | 10 | a0001c0002 a0001c0006 a0001c0026 others(7): Show |
120 | HG00597.hp2 HG00609.hp2 HG00735.hp2 others(117): Show |
synonymous_variant | LOW | c.1206C>T | p.Asn402Asn | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 12/19 | 1269/2976 | 1206/2184 | 402/727 | chr1 | 11964178 | |||
chr1:11965590 | C | T | 1 | a0001c0025 | 1 | NA18951.hp1 | synonymous_variant | LOW | c.1581C>T | p.Pro527Pro | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 14/19 | 1644/2976 | 1581/2184 | 527/727 | chr1 | 11965590 | |||
chr1:11966274 | C | T | 1 | a0002c0019 | 1 | HG02559.hp1 | synonymous_variant | LOW | c.1608C>T | p.His536His | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 15/19 | 1671/2976 | 1608/2184 | 536/727 | chr1 | 11966274 | |||
chr1:11966298 | A | C | 2 | a0002c0017 a0003c0004 |
23 | HG00408.hp2 HG00733.hp2 HG01106.hp1 others(20): Show |
synonymous_variant | LOW | c.1632A>C | p.Ala544Ala | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 15/19 | 1695/2976 | 1632/2184 | 544/727 | chr1 | 11966298 | |||
chr1:11967043 | G | A | 1 | a0002c0018 | 1 | HG03453.hp2 | synonymous_variant | LOW | c.1707G>A | p.Leu569Leu | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/19 | 1770/2976 | 1707/2184 | 569/727 | chr1 | 11967043 | |||
chr1:11970702 | G | T | 4 | a0001c0012 a0001c0026 a0002c0019 others(1): Show |
12 | HG01070.hp1 HG01167.hp2 HG02109.hp2 others(9): Show |
synonymous_variant | LOW | c.1788G>T | p.Val596Val | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 17/19 | 1851/2976 | 1788/2184 | 596/727 | chr1 | 11970702 | |||
chr1:11974748 | T | C | 9 | a0001c0008 a0001c0012 a0001c0026 others(6): Show |
27 | HG01070.hp1 HG01109.hp2 HG01167.hp2 others(24): Show |
synonymous_variant | LOW | c.2124T>C | p.His708His | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 19/19 | 2187/2976 | 2124/2184 | 708/727 | chr1 | 11974748 | |||
chr1:11974757 | C | G | 4 | a0001c0012 a0001c0026 a0002c0019 others(1): Show |
12 | HG01070.hp1 HG01167.hp2 HG02109.hp2 others(9): Show |
synonymous_variant | LOW | c.2133C>G | p.Leu711Leu | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 19/19 | 2196/2976 | 2133/2184 | 711/727 | chr1 | 11974757 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:11934754 | G | A | 1 | a0001c0001t0005 | 1 | HG02717.hp1 | 5_prime_UTR_variant | MODIFIER | c.-26G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/19 | 26 | chr1 | 11934754 | ||||||
chr1:11974879 | C | G | 4 | a0001c0001t0003 a0002c0015t0003 a0003c0007t0003 others(1): Show |
9 | HG01192.hp2 HG01884.hp2 HG02886.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*71C>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 19/19 | 71 | chr1 | 11974879 | ||||||
chr1:11974982 | G | A | 1 | a0001c0001t0006 | 1 | NA18982.hp2 | 3_prime_UTR_variant | MODIFIER | c.*174G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 19/19 | 174 | chr1 | 11974982 | ||||||
chr1:11975210 | C | G | 1 | a0001c0001t0006 | 1 | NA18982.hp2 | 3_prime_UTR_variant | MODIFIER | c.*402C>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 19/19 | 402 | chr1 | 11975210 | ||||||
chr1:11975216 | C | G | 1 | a0001c0002t0007 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*408C>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 19/19 | 408 | chr1 | 11975216 | ||||||
chr1:11975248 | G | C | 7 | a0001c0008t0002 a0001c0012t0002 a0001c0026t0002 others(4): Show |
22 | HG01070.hp1 HG01109.hp2 HG01167.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*440G>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 19/19 | 440 | chr1 | 11975248 | ||||||
chr1:11975422 | G | T | 2 | a0001c0008t0004 a0002c0014t0004 |
3 | HG02970.hp2 HG03209.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*614G>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 19/19 | 614 | chr1 | 11975422 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:11934872 | C | T | 1 | a0001c0001t0001g0327 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.76+17C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11934872 | |||||||
chr1:11934948 | T | C | 1 | a0002c0018t0001g0021 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.76+93T>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11934948 | |||||||
chr1:11934973 | C | T | 1 | a0002c0003t0001g0326 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.76+118C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11934973 | |||||||
chr1:11935119 | A | G | 118 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0216 others(115): Show |
124 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(121): Show |
intron_variant | MODIFIER | c.76+264A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11935119 | |||||||
chr1:11935158 | A | G | 17 | a0001c0001t0005g0210 a0001c0006t0001g0211 a0001c0006t0001g0212 others(14): Show |
17 | HG01109.hp2 HG01243.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.76+303A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11935158 | |||||||
chr1:11935188 | G | GT | 5 | a0001c0008t0002g0205 a0001c0008t0002g0206 a0001c0008t0002g0207 others(2): Show |
5 | HG04228.hp2 NA18952.hp1 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.76+334dupT | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 11935188 | ||||||
chr1:11935302 | A | C | 1 | a0001c0002t0001g0204 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.76+447A>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11935302 | |||||||
chr1:11935352 | A | G | 217 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0014 others(214): Show |
237 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(234): Show |
intron_variant | MODIFIER | c.76+497A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11935352 | |||||||
chr1:11935354 | G | A | 75 | a0001c0001t0001g0010 a0001c0001t0001g0238 a0001c0001t0001g0239 others(72): Show |
79 | HG00280.hp1 HG00408.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.76+499G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11935354 | |||||||
chr1:11935370 | G | A | 2 | a0002c0015t0003g0297 a0002c0018t0001g0021 |
2 | HG01192.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.76+515G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11935370 | |||||||
chr1:11935503 | C | T | 116 | a0001c0001t0001g0010 a0001c0001t0001g0239 a0001c0001t0001g0240 others(113): Show |
121 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.76+648C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11935503 | |||||||
chr1:11935575 | G | A | 1 | a0001c0002t0001g0022 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.76+720G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11935575 | |||||||
chr1:11935584 | G | A | 5 | a0003c0005t0001g0303 a0003c0007t0001g0194 a0003c0007t0001g0195 others(2): Show |
5 | HG02615.hp1 HG02723.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.76+729G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11935584 | |||||||
chr1:11935628 | C | CT | 98 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0088 others(95): Show |
113 | HG00597.hp2 HG00609.hp2 HG00621.hp2 others(110): Show |
intron_variant | MODIFIER | c.76+787dupT | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 11935628 | ||||||
chr1:11935713 | C | T | 7 | a0001c0008t0002g0094 a0001c0008t0002g0095 a0001c0008t0002g0205 others(4): Show |
7 | HG02083.hp1 HG04228.hp2 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.76+858C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11935713 | |||||||
chr1:11935785 | T | C | 1 | a0001c0028t0001g0196 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.76+930T>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11935785 | |||||||
chr1:11935790 | A | G | 7 | a0002c0003t0001g0203 a0002c0003t0001g0313 a0002c0014t0004g0295 others(4): Show |
7 | HG01192.hp2 HG02451.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.76+935A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11935790 | |||||||
chr1:11935856 | C | T | 3 | a0001c0001t0001g0087 a0001c0001t0001g0235 a0001c0001t0001g0236 |
3 | HG02257.hp1 HG02615.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.76+1001C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11935856 | |||||||
chr1:11935866 | G | A | 1 | a0001c0002t0001g0111 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.76+1011G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11935866 | |||||||
chr1:11935894 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.76+1039A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11935894 | |||||||
chr1:11935914 | C | T | 3 | a0002c0014t0004g0295 a0002c0014t0004g0296 a0002c0015t0003g0314 |
3 | HG02970.hp2 HG03041.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.76+1059C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11935914 | |||||||
chr1:11935970 | A | G | 1 | a0001c0002t0001g0193 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.76+1115A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11935970 | |||||||
chr1:11935984 | A | G | 75 | a0001c0001t0001g0327 a0001c0028t0001g0196 a0002c0003t0001g0019 others(72): Show |
77 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(74): Show |
intron_variant | MODIFIER | c.76+1129A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11935984 | |||||||
chr1:11936016 | A | G | 1 | a0002c0003t0001g0237 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.76+1161A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11936016 | |||||||
chr1:11936085 | T | C | 8 | a0001c0002t0001g0112 a0001c0002t0001g0113 a0001c0002t0001g0114 others(5): Show |
8 | HG00621.hp2 HG02071.hp2 HG02129.hp2 others(5): Show |
intron_variant | MODIFIER | c.76+1230T>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11936085 | |||||||
chr1:11936105 | A | G | 1 | a0001c0001t0001g0085 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.76+1250A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11936105 | |||||||
chr1:11936213 | C | T | 21 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(18): Show |
21 | HG02132.hp2 HG02257.hp1 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.76+1358C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11936213 | |||||||
chr1:11936480 | G | T | 3 | a0001c0001t0001g0231 a0001c0001t0001g0232 a0001c0001t0001g0233 |
3 | HG01106.hp2 HG02258.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.76+1625G>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11936480 | |||||||
chr1:11936489 | G | T | 7 | a0001c0008t0002g0094 a0001c0008t0002g0095 a0001c0008t0002g0205 others(4): Show |
7 | HG02083.hp1 HG04228.hp2 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.76+1634G>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11936489 | |||||||
chr1:11936571 | G | A | 8 | a0002c0003t0001g0313 a0002c0014t0004g0295 a0002c0014t0004g0296 others(5): Show |
8 | HG01109.hp2 HG01192.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.76+1716G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11936571 | |||||||
chr1:11936592 | G | A | 8 | a0002c0003t0001g0313 a0002c0014t0004g0295 a0002c0014t0004g0296 others(5): Show |
8 | HG01109.hp2 HG01192.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.76+1737G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11936592 | |||||||
chr1:11936702 | T | C | 1 | a0002c0003t0001g0252 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.76+1847T>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11936702 | |||||||
chr1:11936828 | C | G | 1 | a0001c0001t0001g0076 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.76+1973C>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11936828 | |||||||
chr1:11936851 | C | CT | 35 | a0001c0001t0001g0010 a0001c0001t0001g0063 a0001c0001t0001g0239 others(32): Show |
38 | HG00408.hp2 HG00673.hp1 HG00733.hp2 others(35): Show |
intron_variant | MODIFIER | c.76+2009dupT | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 11936851 | ||||||
chr1:11936851 | C | CTT | 174 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0110 others(171): Show |
191 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(188): Show |
intron_variant | MODIFIER | c.76+2008_76+2009dup others(2): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 11936851 | ||||||
chr1:11936851 | C | CTTT | 18 | a0001c0006t0001g0212 a0003c0005t0001g0011 a0003c0005t0001g0070 others(15): Show |
19 | HG01243.hp2 HG01884.hp2 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.76+2007_76+2009dup others(3): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 11936851 | ||||||
chr1:11936951 | G | T | 4 | a0001c0001t0001g0327 a0003c0016t0001g0020 a0003c0033t0003g0311 others(1): Show |
5 | HG02559.hp2 HG02886.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.76+2096G>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11936951 | |||||||
chr1:11937006 | C | T | 1 | a0001c0013t0001g0119 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.76+2151C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11937006 | |||||||
chr1:11937036 | C | T | 68 | a0002c0003t0001g0019 a0002c0003t0001g0096 a0002c0003t0001g0097 others(65): Show |
69 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.76+2181C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11937036 | |||||||
chr1:11937037 | G | A | 3 | a0001c0001t0001g0216 a0001c0001t0001g0217 a0010c0024t0001g0218 |
3 | HG00741.hp2 HG01081.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.76+2182G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11937037 | |||||||
chr1:11937037 | G | C | 5 | a0001c0001t0001g0327 a0003c0016t0001g0020 a0003c0016t0001g0309 others(2): Show |
6 | HG02451.hp2 HG02559.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.76+2182G>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11937037 | |||||||
chr1:11937091 | G | A | 1 | a0001c0028t0001g0196 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.76+2236G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11937091 | |||||||
chr1:11937115 | C | T | 1 | a0001c0028t0001g0196 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.76+2260C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11937115 | |||||||
chr1:11937143 | C | T | 3 | a0001c0028t0001g0196 a0003c0005t0001g0229 a0003c0005t0001g0230 |
3 | HG02257.hp2 HG02717.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.76+2288C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11937143 | |||||||
chr1:11937210 | C | T | 1 | a0001c0001t0001g0327 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.76+2355C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11937210 | |||||||
chr1:11937239 | T | C | 8 | a0002c0003t0001g0313 a0002c0014t0004g0295 a0002c0014t0004g0296 others(5): Show |
8 | HG01109.hp2 HG01192.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.76+2384T>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11937239 | |||||||
chr1:11937380 | C | T | 1 | a0001c0002t0001g0189 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.76+2525C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11937380 | |||||||
chr1:11937420 | A | G | 2 | a0001c0001t0001g0083 a0001c0001t0001g0084 |
2 | HG02132.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.76+2565A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11937420 | |||||||
chr1:11937461 | G | A | 49 | a0002c0003t0001g0096 a0002c0003t0001g0097 a0002c0003t0001g0098 others(46): Show |
49 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(46): Show |
intron_variant | MODIFIER | c.76+2606G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11937461 | |||||||
chr1:11937584 | C | T | 8 | a0002c0003t0001g0313 a0002c0014t0004g0295 a0002c0014t0004g0296 others(5): Show |
8 | HG01109.hp2 HG01192.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.76+2729C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11937584 | |||||||
chr1:11937922 | A | AT | 7 | a0001c0001t0001g0006 a0001c0001t0001g0058 a0001c0001t0001g0059 others(4): Show |
11 | HG01099.hp2 HG01346.hp2 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.76+3084dupT | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 11937922 | ||||||
chr1:11937922 | AT | A | 93 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0025 others(90): Show |
95 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.76+3084delT | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 11937922 | ||||||
chr1:11937922 | ATT | A | 8 | a0001c0002t0001g0121 a0002c0003t0001g0197 a0002c0003t0001g0253 others(5): Show |
8 | HG01069.hp1 HG01517.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.76+3083_76+3084del others(2): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 11937922 | ||||||
chr1:11937948 | A | G | 1 | a0003c0005t0001g0303 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.76+3093A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11937948 | |||||||
chr1:11937953 | CT | C | 10 | a0001c0001t0001g0027 a0002c0003t0001g0313 a0002c0014t0004g0295 others(7): Show |
10 | HG00741.hp1 HG01109.hp2 HG01192.hp2 others(7): Show |
intron_variant | MODIFIER | c.76+3111delT | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 11937953 | ||||||
chr1:11937992 | G | A | 1 | a0001c0027t0001g0220 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.76+3137G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11937992 | |||||||
chr1:11938025 | G | A | 8 | a0002c0003t0001g0313 a0002c0014t0004g0295 a0002c0014t0004g0296 others(5): Show |
8 | HG01109.hp2 HG01192.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.76+3170G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11938025 | |||||||
chr1:11938026 | C | T | 1 | a0002c0015t0003g0297 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.76+3171C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11938026 | |||||||
chr1:11938121 | T | G | 9 | a0002c0003t0001g0253 a0002c0003t0001g0254 a0002c0003t0001g0258 others(6): Show |
9 | HG00280.hp1 HG00642.hp2 HG00735.hp1 others(6): Show |
intron_variant | MODIFIER | c.76+3266T>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11938121 | |||||||
chr1:11938172 | C | CGA | 232 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0110 others(229): Show |
251 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(248): Show |
intron_variant | MODIFIER | c.76+3317_76+3318ins others(2): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11938172 | |||||||
chr1:11938174 | A | C | 232 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0110 others(229): Show |
251 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(248): Show |
intron_variant | MODIFIER | c.76+3319A>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11938174 | |||||||
chr1:11938269 | A | C | 1 | a0002c0003t0001g0264 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.76+3414A>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11938269 | |||||||
chr1:11938281 | A | G | 5 | a0001c0001t0001g0327 a0003c0016t0001g0020 a0003c0016t0001g0309 others(2): Show |
6 | HG02451.hp2 HG02559.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.76+3426A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11938281 | |||||||
chr1:11938505 | G | A | 1 | a0004c0009t0002g0091 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.76+3650G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11938505 | |||||||
chr1:11938563 | T | G | 1 | a0001c0006t0001g0131 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.76+3708T>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11938563 | |||||||
chr1:11938568 | T | C | 1 | a0001c0002t0001g0112 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.76+3713T>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11938568 | |||||||
chr1:11938585 | G | T | 1 | a0001c0001t0001g0188 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.76+3730G>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11938585 | |||||||
chr1:11938702 | C | T | 1 | a0001c0028t0001g0196 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.76+3847C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11938702 | |||||||
chr1:11938716 | G | C | 2 | a0002c0003t0001g0190 a0002c0003t0001g0191 |
2 | NA19085.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.76+3861G>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11938716 | |||||||
chr1:11938822 | G | A | 8 | a0002c0003t0001g0313 a0002c0014t0004g0295 a0002c0014t0004g0296 others(5): Show |
8 | HG01109.hp2 HG01192.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.76+3967G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11938822 | |||||||
chr1:11939037 | C | T | 1 | a0002c0003t0001g0294 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.76+4182C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11939037 | |||||||
chr1:11939067 | C | T | 18 | a0001c0001t0001g0240 a0003c0004t0001g0018 a0003c0004t0001g0241 others(15): Show |
19 | HG00408.hp2 HG00673.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.76+4212C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11939067 | |||||||
chr1:11939107 | GAGA | G | 4 | a0003c0016t0001g0020 a0003c0016t0001g0309 a0003c0033t0003g0311 others(1): Show |
5 | HG02451.hp2 HG02559.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.76+4255_76+4257del others(3): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 11939107 | ||||||
chr1:11939108 | A | G | 8 | a0002c0003t0001g0313 a0002c0014t0004g0295 a0002c0014t0004g0296 others(5): Show |
8 | HG01109.hp2 HG01192.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.76+4253A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11939108 | |||||||
chr1:11939139 | C | T | 49 | a0002c0003t0001g0096 a0002c0003t0001g0097 a0002c0003t0001g0098 others(46): Show |
49 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(46): Show |
intron_variant | MODIFIER | c.76+4284C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11939139 | |||||||
chr1:11939228 | C | T | 1 | a0001c0028t0001g0196 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.76+4373C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11939228 | |||||||
chr1:11939499 | G | A | 43 | a0001c0001t0001g0240 a0003c0004t0001g0012 a0003c0004t0001g0018 others(40): Show |
46 | HG00408.hp2 HG00673.hp1 HG00733.hp2 others(43): Show |
intron_variant | MODIFIER | c.76+4644G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11939499 | |||||||
chr1:11939598 | C | T | 1 | a0002c0003t0001g0203 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.76+4743C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11939598 | |||||||
chr1:11939686 | C | T | 1 | a0003c0004t0001g0135 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.76+4831C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11939686 | |||||||
chr1:11939769 | A | G | 8 | a0002c0003t0001g0313 a0002c0014t0004g0295 a0002c0014t0004g0296 others(5): Show |
8 | HG01109.hp2 HG01192.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.76+4914A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11939769 | |||||||
chr1:11939885 | G | A | 95 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0110 others(92): Show |
109 | HG00597.hp2 HG00609.hp2 HG00621.hp2 others(106): Show |
intron_variant | MODIFIER | c.76+5030G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11939885 | |||||||
chr1:11939914 | T | C | 48 | a0002c0003t0001g0096 a0002c0003t0001g0097 a0002c0003t0001g0098 others(45): Show |
48 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.76+5059T>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11939914 | |||||||
chr1:11940015 | T | C | 1 | a0001c0002t0001g0193 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.76+5160T>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11940015 | |||||||
chr1:11940282 | C | G | 2 | a0002c0003t0001g0285 a0011c0021t0001g0286 |
2 | HG03831.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.76+5427C>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11940282 | |||||||
chr1:11940308 | C | T | 2 | a0002c0003t0001g0019 a0002c0003t0001g0294 |
3 | HG01243.hp1 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.76+5453C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11940308 | |||||||
chr1:11940311 | C | T | 1 | a0004c0009t0002g0091 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.76+5456C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11940311 | |||||||
chr1:11940313 | C | G | 1 | a0001c0001t0001g0082 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.76+5458C>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11940313 | |||||||
chr1:11940367 | C | A | 4 | a0002c0003t0001g0019 a0002c0003t0001g0287 a0002c0003t0001g0294 others(1): Show |
5 | HG01243.hp1 HG02559.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.76+5512C>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11940367 | |||||||
chr1:11940454 | C | G | 7 | a0001c0008t0002g0094 a0001c0008t0002g0095 a0001c0008t0002g0205 others(4): Show |
7 | HG02083.hp1 HG04228.hp2 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.76+5599C>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11940454 | |||||||
chr1:11940464 | C | T | 1 | a0001c0002t0001g0186 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.76+5609C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11940464 | |||||||
chr1:11940575 | A | G | 125 | a0001c0001t0001g0240 a0001c0001t0001g0327 a0002c0003t0001g0019 others(122): Show |
130 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.76+5720A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11940575 | |||||||
chr1:11940613 | T | C | 68 | a0002c0003t0001g0019 a0002c0003t0001g0096 a0002c0003t0001g0097 others(65): Show |
69 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.76+5758T>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11940613 | |||||||
chr1:11940783 | A | G | 125 | a0001c0001t0001g0240 a0001c0001t0001g0327 a0002c0003t0001g0019 others(122): Show |
130 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.76+5928A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11940783 | |||||||
chr1:11940801 | C | G | 1 | a0004c0009t0002g0091 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.76+5946C>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11940801 | |||||||
chr1:11940962 | T | C | 1 | a0002c0015t0003g0297 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.76+6107T>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11940962 | |||||||
chr1:11941093 | G | A | 44 | a0001c0001t0001g0240 a0003c0004t0001g0012 a0003c0004t0001g0018 others(41): Show |
47 | HG00408.hp2 HG00673.hp1 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.76+6238G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11941093 | |||||||
chr1:11941103 | T | A | 1 | a0002c0010t0001g0288 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.76+6248T>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11941103 | |||||||
chr1:11941133 | T | C | 7 | a0002c0003t0001g0313 a0002c0014t0004g0295 a0002c0014t0004g0296 others(4): Show |
7 | HG01192.hp2 HG02965.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.76+6278T>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11941133 | |||||||
chr1:11941154 | G | T | 1 | a0001c0002t0001g0185 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.76+6299G>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11941154 | |||||||
chr1:11941374 | C | G | 1 | a0001c0001t0006g0100 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.76+6519C>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11941374 | |||||||
chr1:11941374 | C | T | 8 | a0002c0003t0001g0313 a0002c0014t0004g0295 a0002c0014t0004g0296 others(5): Show |
8 | HG01109.hp2 HG01192.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.76+6519C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11941374 | |||||||
chr1:11941442 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.77-6534C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11941442 | |||||||
chr1:11941467 | G | GATT | 25 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0058 others(22): Show |
30 | HG01099.hp2 HG01243.hp2 HG01258.hp1 others(27): Show |
intron_variant | MODIFIER | c.77-6484_77-6482dup others(3): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 11941467 | ||||||
chr1:11941467 | G | GATTATT | 6 | a0001c0008t0002g0094 a0001c0008t0002g0205 a0001c0008t0002g0206 others(3): Show |
6 | HG02083.hp1 HG04228.hp2 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.77-6487_77-6482dup others(6): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 11941467 | ||||||
chr1:11941467 | G | GATTATTA others(12): Show |
1 | a0002c0015t0003g0314 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.77-6500_77-6499ins others(19): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 11941467 | ||||||
chr1:11941467 | G | GATTATTA others(15): Show |
3 | a0002c0015t0003g0297 a0002c0018t0001g0021 a0013c0020t0001g0090 |
3 | HG01192.hp2 HG03453.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.77-6500_77-6499ins others(22): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 11941467 | ||||||
chr1:11941467 | G | GATTATTA others(18): Show |
3 | a0002c0014t0004g0295 a0002c0014t0004g0296 a0005c0023t0002g0324 |
3 | HG01109.hp2 HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.77-6500_77-6499ins others(25): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 11941467 | ||||||
chr1:11941467 | G | GATTATTA others(21): Show |
1 | a0002c0003t0001g0313 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.77-6500_77-6499ins others(28): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 11941467 | ||||||
chr1:11941467 | GATT | G | 72 | a0002c0003t0001g0019 a0002c0003t0001g0096 a0002c0003t0001g0097 others(69): Show |
74 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.77-6484_77-6482del others(3): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 11941467 | ||||||
chr1:11941495 | T | A | 17 | a0003c0005t0001g0011 a0003c0005t0001g0070 a0003c0005t0001g0071 others(14): Show |
18 | HG01243.hp2 HG01884.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.77-6481T>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11941495 | |||||||
chr1:11941542 | A | G | 8 | a0002c0003t0001g0313 a0002c0014t0004g0295 a0002c0014t0004g0296 others(5): Show |
8 | HG01109.hp2 HG01192.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.77-6434A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11941542 | |||||||
chr1:11941573 | T | C | 8 | a0002c0003t0001g0313 a0002c0014t0004g0295 a0002c0014t0004g0296 others(5): Show |
8 | HG01109.hp2 HG01192.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.77-6403T>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11941573 | |||||||
chr1:11941625 | G | A | 72 | a0002c0003t0001g0019 a0002c0003t0001g0096 a0002c0003t0001g0097 others(69): Show |
74 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.77-6351G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11941625 | |||||||
chr1:11941625 | G | C | 8 | a0002c0003t0001g0313 a0002c0014t0004g0295 a0002c0014t0004g0296 others(5): Show |
8 | HG01109.hp2 HG01192.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.77-6351G>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11941625 | |||||||
chr1:11941631 | C | G | 17 | a0003c0005t0001g0011 a0003c0005t0001g0070 a0003c0005t0001g0071 others(14): Show |
18 | HG01243.hp2 HG01884.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.77-6345C>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11941631 | |||||||
chr1:11941726 | C | T | 1 | a0001c0002t0001g0184 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.77-6250C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11941726 | |||||||
chr1:11941742 | T | C | 8 | a0002c0003t0001g0313 a0002c0014t0004g0295 a0002c0014t0004g0296 others(5): Show |
8 | HG01109.hp2 HG01192.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.77-6234T>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11941742 | |||||||
chr1:11941752 | A | G | 8 | a0002c0003t0001g0313 a0002c0014t0004g0295 a0002c0014t0004g0296 others(5): Show |
8 | HG01109.hp2 HG01192.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.77-6224A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11941752 | |||||||
chr1:11941822 | G | C | 8 | a0002c0003t0001g0313 a0002c0014t0004g0295 a0002c0014t0004g0296 others(5): Show |
8 | HG01109.hp2 HG01192.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.77-6154G>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11941822 | |||||||
chr1:11941823 | T | C | 8 | a0002c0003t0001g0313 a0002c0014t0004g0295 a0002c0014t0004g0296 others(5): Show |
8 | HG01109.hp2 HG01192.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.77-6153T>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11941823 | |||||||
chr1:11941985 | C | CT | 14 | a0001c0001t0001g0056 a0001c0001t0001g0081 a0001c0002t0001g0118 others(11): Show |
14 | HG00735.hp2 HG01109.hp2 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.77-5976dupT | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 11941985 | ||||||
chr1:11941985 | CT | C | 114 | a0001c0001t0001g0240 a0001c0028t0001g0196 a0002c0003t0001g0019 others(111): Show |
119 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.77-5976delT | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 11941985 | ||||||
chr1:11942087 | A | ATTCTCG | 3 | a0001c0002t0001g0181 a0001c0002t0001g0182 a0001c0002t0001g0193 |
3 | HG01952.hp1 HG03490.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.77-5887_77-5882dup others(6): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 11942087 | ||||||
chr1:11942107 | T | C | 133 | a0001c0001t0001g0240 a0001c0001t0001g0327 a0001c0008t0002g0094 others(130): Show |
138 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.77-5869T>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11942107 | |||||||
chr1:11942433 | C | T | 1 | a0010c0024t0001g0218 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.77-5543C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11942433 | |||||||
chr1:11942446 | G | C | 1 | a0002c0003t0001g0198 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.77-5530G>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11942446 | |||||||
chr1:11942657 | A | G | 1 | a0002c0003t0001g0237 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.77-5319A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11942657 | |||||||
chr1:11942671 | G | A | 1 | a0001c0028t0001g0196 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.77-5305G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11942671 | |||||||
chr1:11942711 | C | T | 2 | a0003c0033t0003g0311 a0008c0032t0002g0312 |
2 | HG02886.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.77-5265C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11942711 | |||||||
chr1:11942751 | G | A | 1 | a0001c0002t0001g0136 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.77-5225G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11942751 | |||||||
chr1:11942857 | T | C | 1 | a0003c0016t0001g0309 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.77-5119T>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11942857 | |||||||
chr1:11942946 | C | A | 1 | a0001c0001t0001g0240 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.77-5030C>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11942946 | |||||||
chr1:11942979 | G | GT | 68 | a0002c0003t0001g0019 a0002c0003t0001g0096 a0002c0003t0001g0097 others(65): Show |
69 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.77-4991dupT | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 11942979 | ||||||
chr1:11943055 | C | T | 5 | a0001c0002t0001g0016 a0001c0002t0001g0177 a0001c0002t0001g0178 others(2): Show |
6 | HG02135.hp2 NA18959.hp2 NA19005.hp2 others(3): Show |
intron_variant | MODIFIER | c.77-4921C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11943055 | |||||||
chr1:11943137 | C | A | 9 | a0004c0009t0002g0317 a0004c0009t0002g0318 a0004c0009t0002g0319 others(6): Show |
9 | HG02145.hp2 HG02622.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.77-4839C>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11943137 | |||||||
chr1:11943146 | T | C | 48 | a0001c0001t0001g0240 a0003c0004t0001g0012 a0003c0004t0001g0018 others(45): Show |
52 | HG00408.hp2 HG00673.hp1 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.77-4830T>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11943146 | |||||||
chr1:11943174 | A | G | 48 | a0001c0001t0001g0240 a0003c0004t0001g0012 a0003c0004t0001g0018 others(45): Show |
52 | HG00408.hp2 HG00673.hp1 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.77-4802A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11943174 | |||||||
chr1:11943220 | T | C | 318 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(315): Show |
360 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(357): Show |
intron_variant | MODIFIER | c.77-4756T>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11943220 | |||||||
chr1:11943284 | G | A | 48 | a0001c0001t0001g0240 a0003c0004t0001g0012 a0003c0004t0001g0018 others(45): Show |
52 | HG00408.hp2 HG00673.hp1 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.77-4692G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11943284 | |||||||
chr1:11943292 | T | TTTTC | 73 | a0001c0028t0001g0196 a0002c0003t0001g0019 a0002c0003t0001g0096 others(70): Show |
74 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.77-4676_77-4673dup others(4): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 11943292 | ||||||
chr1:11943300 | C | CT | 31 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0023 others(28): Show |
44 | HG00423.hp2 HG00438.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.77-4663dupT | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 11943300 | ||||||
chr1:11943300 | C | CTTTCT | 28 | a0001c0001t0001g0240 a0002c0003t0001g0284 a0003c0004t0001g0012 others(25): Show |
30 | HG00408.hp2 HG00673.hp1 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.77-4673_77-4672ins others(5): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 11943300 | ||||||
chr1:11943300 | C | CTTTCTT | 21 | a0003c0005t0001g0011 a0003c0005t0001g0070 a0003c0005t0001g0071 others(18): Show |
23 | HG01243.hp2 HG01884.hp2 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.77-4673_77-4672ins others(6): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 11943300 | ||||||
chr1:11943411 | C | T | 2 | a0003c0033t0003g0311 a0008c0032t0002g0312 |
2 | HG02886.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.77-4565C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11943411 | |||||||
chr1:11943454 | G | A | 48 | a0001c0001t0001g0240 a0003c0004t0001g0012 a0003c0004t0001g0018 others(45): Show |
52 | HG00408.hp2 HG00673.hp1 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.77-4522G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11943454 | |||||||
chr1:11943598 | C | T | 48 | a0001c0001t0001g0240 a0003c0004t0001g0012 a0003c0004t0001g0018 others(45): Show |
52 | HG00408.hp2 HG00673.hp1 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.77-4378C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11943598 | |||||||
chr1:11943770 | G | A | 2 | a0003c0005t0001g0092 a0003c0005t0001g0093 |
2 | HG01891.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.77-4206G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11943770 | |||||||
chr1:11943908 | G | A | 17 | a0003c0005t0001g0011 a0003c0005t0001g0070 a0003c0005t0001g0071 others(14): Show |
18 | HG01243.hp2 HG01884.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.77-4068G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11943908 | |||||||
chr1:11944048 | A | G | 1 | a0002c0003t0001g0099 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.77-3928A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11944048 | |||||||
chr1:11944094 | G | A | 48 | a0001c0001t0001g0240 a0003c0004t0001g0012 a0003c0004t0001g0018 others(45): Show |
52 | HG00408.hp2 HG00673.hp1 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.77-3882G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11944094 | |||||||
chr1:11944270 | C | T | 6 | a0001c0008t0002g0094 a0001c0008t0002g0205 a0001c0008t0002g0206 others(3): Show |
6 | HG02083.hp1 HG04228.hp2 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.77-3706C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11944270 | |||||||
chr1:11944344 | C | T | 6 | a0002c0003t0001g0253 a0002c0003t0001g0254 a0002c0003t0001g0260 others(3): Show |
6 | HG00735.hp1 HG01069.hp1 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.77-3632C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11944344 | |||||||
chr1:11944359 | C | A | 1 | a0004c0009t0002g0091 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.77-3617C>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11944359 | |||||||
chr1:11944385 | C | G | 4 | a0003c0016t0001g0020 a0003c0016t0001g0309 a0003c0033t0003g0311 others(1): Show |
5 | HG02451.hp2 HG02559.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.77-3591C>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11944385 | |||||||
chr1:11944422 | T | TAC | 17 | a0001c0001t0001g0003 a0001c0001t0001g0023 a0001c0001t0001g0029 others(14): Show |
22 | HG00423.hp2 HG02129.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.77-3523_77-3522dup others(2): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 11944422 | ||||||
chr1:11944422 | T | TACAC | 8 | a0001c0001t0001g0034 a0001c0001t0001g0058 a0001c0002t0001g0015 others(5): Show |
9 | HG00597.hp2 HG01346.hp2 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.77-3525_77-3522dup others(4): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 11944422 | ||||||
chr1:11944422 | T | TACACAC | 7 | a0001c0002t0001g0169 a0001c0002t0001g0170 a0001c0006t0001g0211 others(4): Show |
7 | HG02015.hp2 HG02895.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.77-3527_77-3522dup others(6): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 11944422 | ||||||
chr1:11944422 | T | TACACACA others(1): Show |
18 | a0001c0001t0001g0014 a0001c0001t0001g0110 a0001c0002t0001g0111 others(15): Show |
19 | HG01168.hp2 HG01928.hp1 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.77-3529_77-3522dup others(8): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 11944422 | ||||||
chr1:11944422 | T | TACACACA others(3): Show |
52 | a0001c0001t0001g0001 a0001c0001t0001g0188 a0001c0002t0001g0001 others(49): Show |
64 | HG00609.hp2 HG00621.hp2 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.77-3531_77-3522dup others(10): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 11944422 | ||||||
chr1:11944422 | T | TACACACA others(5): Show |
13 | a0001c0001t0001g0124 a0001c0002t0001g0112 a0001c0002t0001g0120 others(10): Show |
13 | HG00738.hp2 HG01517.hp1 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.77-3533_77-3522dup others(12): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 11944422 | ||||||
chr1:11944422 | T | TACACACA others(7): Show |
3 | a0001c0002t0001g0137 a0001c0002t0001g0177 a0001c0026t0002g0298 |
3 | HG01167.hp2 HG02135.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.77-3535_77-3522dup others(14): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 11944422 | ||||||
chr1:11944422 | T | TACACACA others(9): Show |
1 | a0001c0002t0001g0123 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.77-3537_77-3522dup others(16): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 11944422 | ||||||
chr1:11944422 | TAC | T | 21 | a0001c0001t0001g0061 a0001c0001t0001g0079 a0001c0001t0001g0307 others(18): Show |
22 | HG01243.hp2 HG01884.hp2 HG01993.hp1 others(19): Show |
intron_variant | MODIFIER | c.77-3523_77-3522del others(2): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 11944422 | ||||||
chr1:11944422 | TACAC | T | 16 | a0002c0003t0001g0237 a0002c0003t0001g0313 a0002c0014t0001g0105 others(13): Show |
17 | HG01070.hp1 HG01109.hp2 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.77-3525_77-3522del others(4): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 11944422 | ||||||
chr1:11944422 | TACACAC | T | 28 | a0001c0001t0001g0080 a0001c0001t0001g0240 a0003c0004t0001g0012 others(25): Show |
30 | HG00408.hp2 HG00673.hp1 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.77-3527_77-3522del others(6): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 11944422 | ||||||
chr1:11944436 | C | CAA | 48 | a0002c0003t0001g0096 a0002c0003t0001g0097 a0002c0003t0001g0098 others(45): Show |
48 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.77-3539_77-3538ins others(2): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 11944436 | ||||||
chr1:11944451 | A | T | 2 | a0003c0033t0003g0311 a0008c0032t0002g0312 |
2 | HG02886.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.77-3525A>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11944451 | |||||||
chr1:11944455 | T | A | 7 | a0001c0008t0002g0094 a0001c0008t0002g0095 a0001c0008t0002g0205 others(4): Show |
7 | HG02083.hp1 HG04228.hp2 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.77-3521T>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11944455 | |||||||
chr1:11944569 | C | T | 8 | a0002c0003t0001g0313 a0002c0014t0001g0105 a0002c0014t0004g0295 others(5): Show |
8 | HG01192.hp2 HG02965.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.77-3407C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11944569 | |||||||
chr1:11944589 | C | T | 1 | a0001c0001t0001g0188 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.77-3387C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11944589 | |||||||
chr1:11944606 | G | A | 16 | a0002c0003t0001g0096 a0002c0003t0001g0255 a0002c0003t0001g0256 others(13): Show |
16 | HG00609.hp1 HG02165.hp1 NA18612.hp1 others(13): Show |
intron_variant | MODIFIER | c.77-3370G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11944606 | |||||||
chr1:11944637 | C | T | 7 | a0001c0008t0002g0094 a0001c0008t0002g0095 a0001c0008t0002g0205 others(4): Show |
7 | HG02083.hp1 HG04228.hp2 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.77-3339C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11944637 | |||||||
chr1:11944694 | G | C | 1 | a0001c0001t0001g0221 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.77-3282G>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11944694 | |||||||
chr1:11944762 | G | A | 1 | a0002c0003t0001g0253 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.77-3214G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11944762 | |||||||
chr1:11944796 | C | T | 2 | a0001c0002t0001g0168 a0001c0002t0007g0167 |
2 | HG03688.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.77-3180C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11944796 | |||||||
chr1:11944942 | G | A | 230 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0110 others(227): Show |
249 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(246): Show |
intron_variant | MODIFIER | c.77-3034G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11944942 | |||||||
chr1:11944947 | G | A | 2 | a0002c0003t0001g0254 a0002c0003t0001g0260 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.77-3029G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11944947 | |||||||
chr1:11945065 | C | T | 2 | a0005c0023t0002g0324 a0013c0020t0001g0090 |
2 | HG01109.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.77-2911C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11945065 | |||||||
chr1:11945189 | G | T | 2 | a0003c0004t0001g0249 a0003c0004t0001g0250 |
2 | HG00733.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.77-2787G>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11945189 | |||||||
chr1:11945193 | G | A | 68 | a0001c0006t0001g0162 a0002c0003t0001g0019 a0002c0003t0001g0096 others(65): Show |
69 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.77-2783G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11945193 | |||||||
chr1:11945425 | C | CA | 230 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0110 others(227): Show |
249 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(246): Show |
intron_variant | MODIFIER | c.77-2540dupA | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 11945425 | ||||||
chr1:11945439 | C | T | 1 | a0002c0003t0001g0203 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.77-2537C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11945439 | |||||||
chr1:11945611 | G | A | 1 | a0002c0003t0001g0203 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.77-2365G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11945611 | |||||||
chr1:11945624 | G | A | 49 | a0001c0001t0001g0240 a0003c0004t0001g0012 a0003c0004t0001g0018 others(46): Show |
53 | HG00408.hp2 HG00673.hp1 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.77-2352G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11945624 | |||||||
chr1:11945695 | C | CTTTA | 8 | a0002c0003t0001g0313 a0002c0014t0001g0105 a0002c0014t0004g0295 others(5): Show |
8 | HG01192.hp2 HG02965.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.77-2277_77-2274dup others(4): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 11945695 | ||||||
chr1:11945770 | G | A | 1 | a0002c0003t0001g0203 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.77-2206G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11945770 | |||||||
chr1:11945853 | C | G | 1 | a0002c0003t0001g0203 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.77-2123C>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11945853 | |||||||
chr1:11946081 | C | T | 1 | a0001c0001t0001g0039 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.77-1895C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11946081 | |||||||
chr1:11946195 | A | G | 1 | a0004c0009t0002g0091 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.77-1781A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11946195 | |||||||
chr1:11946230 | C | T | 1 | a0002c0003t0001g0203 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.77-1746C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11946230 | |||||||
chr1:11946507 | T | C | 1 | a0002c0003t0001g0237 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.77-1469T>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11946507 | |||||||
chr1:11946518 | A | G | 2 | a0005c0023t0002g0324 a0013c0020t0001g0090 |
2 | HG01109.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.77-1458A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11946518 | |||||||
chr1:11946649 | A | G | 1 | a0002c0003t0001g0237 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.77-1327A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11946649 | |||||||
chr1:11946745 | T | G | 28 | a0001c0001t0001g0240 a0003c0004t0001g0012 a0003c0004t0001g0018 others(25): Show |
30 | HG00408.hp2 HG00673.hp1 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.77-1231T>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11946745 | |||||||
chr1:11946757 | CA | C | 28 | a0001c0001t0001g0240 a0003c0004t0001g0012 a0003c0004t0001g0018 others(25): Show |
30 | HG00408.hp2 HG00673.hp1 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.77-1218delA | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11946757 | |||||||
chr1:11946758 | A | G | 5 | a0001c0002t0001g0016 a0001c0002t0001g0177 a0001c0002t0001g0178 others(2): Show |
6 | HG02135.hp2 NA18959.hp2 NA19005.hp2 others(3): Show |
intron_variant | MODIFIER | c.77-1218A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11946758 | |||||||
chr1:11946795 | C | T | 11 | a0002c0003t0001g0313 a0002c0014t0001g0105 a0002c0014t0004g0295 others(8): Show |
11 | HG01070.hp1 HG01109.hp2 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.77-1181C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11946795 | |||||||
chr1:11946862 | A | G | 1 | a0002c0003t0001g0099 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.77-1114A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11946862 | |||||||
chr1:11946912 | G | A | 8 | a0002c0003t0001g0313 a0002c0014t0001g0105 a0002c0014t0004g0295 others(5): Show |
8 | HG01192.hp2 HG02965.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.77-1064G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11946912 | |||||||
chr1:11946914 | A | C | 3 | a0002c0003t0001g0252 a0002c0003t0001g0280 a0002c0003t0001g0281 |
3 | NA19060.hp2 NA19065.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.77-1062A>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11946914 | |||||||
chr1:11946916 | G | T | 2 | a0005c0023t0002g0324 a0013c0020t0001g0090 |
2 | HG01109.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.77-1060G>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11946916 | |||||||
chr1:11947213 | G | A | 7 | a0001c0008t0002g0094 a0001c0008t0002g0095 a0001c0008t0002g0205 others(4): Show |
7 | HG02083.hp1 HG04228.hp2 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.77-763G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11947213 | |||||||
chr1:11947223 | T | G | 17 | a0003c0005t0001g0011 a0003c0005t0001g0070 a0003c0005t0001g0071 others(14): Show |
18 | HG01243.hp2 HG01884.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.77-753T>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11947223 | |||||||
chr1:11947236 | C | CA | 33 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0002t0001g0169 others(30): Show |
34 | HG00597.hp1 HG01070.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.77-727dupA | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 11947236 | ||||||
chr1:11947250 | C | A | 6 | a0003c0007t0001g0194 a0004c0009t0002g0317 a0004c0009t0002g0318 others(3): Show |
6 | HG02145.hp2 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.77-726C>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11947250 | |||||||
chr1:11947252 | A | AAAAC | 10 | a0002c0003t0001g0313 a0002c0014t0001g0105 a0002c0014t0004g0295 others(7): Show |
10 | HG01109.hp2 HG01192.hp2 HG02965.hp1 others(7): Show |
intron_variant | MODIFIER | c.77-708_77-705dupCA others(2): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 11947252 | ||||||
chr1:11947268 | C | A | 7 | a0003c0005t0001g0070 a0003c0005t0001g0229 a0003c0005t0001g0230 others(4): Show |
7 | HG01884.hp2 HG02257.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.77-708C>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11947268 | |||||||
chr1:11947272 | A | C | 1 | a0002c0003t0001g0237 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.77-704A>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11947272 | |||||||
chr1:11947281 | C | T | 17 | a0003c0005t0001g0011 a0003c0005t0001g0070 a0003c0005t0001g0071 others(14): Show |
18 | HG01243.hp2 HG01884.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.77-695C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11947281 | |||||||
chr1:11947381 | C | G | 1 | a0003c0004t0001g0248 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.77-595C>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11947381 | |||||||
chr1:11947443 | G | A | 49 | a0001c0001t0001g0240 a0003c0004t0001g0012 a0003c0004t0001g0018 others(46): Show |
53 | HG00408.hp2 HG00673.hp1 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.77-533G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11947443 | |||||||
chr1:11947760 | C | T | 1 | a0002c0003t0001g0203 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.77-216C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 1/18 | chr1 | 11947760 | |||||||
chr1:11948146 | C | T | 4 | a0003c0016t0001g0020 a0003c0016t0001g0309 a0003c0033t0003g0311 others(1): Show |
5 | HG02451.hp2 HG02559.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+79C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 2/18 | chr1 | 11948146 | |||||||
chr1:11948322 | A | C | 1 | a0001c0001t0001g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.168+255A>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 2/18 | chr1 | 11948322 | |||||||
chr1:11948353 | C | T | 1 | a0002c0003t0001g0237 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.168+286C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 2/18 | chr1 | 11948353 | |||||||
chr1:11948458 | C | G | 128 | a0001c0001t0001g0240 a0002c0003t0001g0019 a0002c0003t0001g0096 others(125): Show |
133 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.168+391C>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 2/18 | chr1 | 11948458 | |||||||
chr1:11948459 | G | A | 2 | a0001c0002t0001g0168 a0001c0002t0007g0167 |
2 | HG03688.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.168+392G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 2/18 | chr1 | 11948459 | |||||||
chr1:11948599 | A | G | 68 | a0002c0003t0001g0019 a0002c0003t0001g0096 a0002c0003t0001g0097 others(65): Show |
69 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.168+532A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 2/18 | chr1 | 11948599 | |||||||
chr1:11948601 | G | A | 68 | a0002c0003t0001g0019 a0002c0003t0001g0096 a0002c0003t0001g0097 others(65): Show |
69 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.168+534G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 2/18 | chr1 | 11948601 | |||||||
chr1:11948636 | G | A | 1 | a0001c0001t0001g0188 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.168+569G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 2/18 | chr1 | 11948636 | |||||||
chr1:11948679 | G | A | 49 | a0002c0003t0001g0096 a0002c0003t0001g0097 a0002c0003t0001g0098 others(46): Show |
49 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(46): Show |
intron_variant | MODIFIER | c.168+612G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 2/18 | chr1 | 11948679 | |||||||
chr1:11948729 | CA | C | 125 | a0001c0001t0001g0088 a0001c0001t0001g0240 a0002c0003t0001g0019 others(122): Show |
129 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.168+674delA | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11948729 | ||||||
chr1:11948736 | A | G | 4 | a0003c0016t0001g0020 a0003c0016t0001g0309 a0003c0033t0003g0311 others(1): Show |
5 | HG02451.hp2 HG02559.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+669A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 2/18 | chr1 | 11948736 | |||||||
chr1:11948781 | C | T | 1 | a0001c0006t0001g0299 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.168+714C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 2/18 | chr1 | 11948781 | |||||||
chr1:11948806 | A | G | 137 | a0001c0001t0001g0240 a0001c0008t0002g0094 a0001c0008t0002g0095 others(134): Show |
142 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.168+739A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 2/18 | chr1 | 11948806 | |||||||
chr1:11948832 | CCCTGCAG others(12): Show |
C | 1 | a0001c0002t0001g0144 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.168+770_168+788del others(19): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11948832 | ||||||
chr1:11948840 | G | C | 68 | a0002c0003t0001g0019 a0002c0003t0001g0096 a0002c0003t0001g0097 others(65): Show |
69 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.168+773G>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 2/18 | chr1 | 11948840 | |||||||
chr1:11948885 | G | A | 4 | a0003c0016t0001g0020 a0003c0016t0001g0309 a0003c0033t0003g0311 others(1): Show |
5 | HG02451.hp2 HG02559.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.168+818G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 2/18 | chr1 | 11948885 | |||||||
chr1:11948967 | A | G | 68 | a0002c0003t0001g0019 a0002c0003t0001g0096 a0002c0003t0001g0097 others(65): Show |
69 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.169-806A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 2/18 | chr1 | 11948967 | |||||||
chr1:11949159 | GAGACAGG others(5): Show |
G | 2 | a0002c0003t0001g0256 a0002c0003t0001g0284 |
2 | NA18985.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.169-613_169-602del others(12): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 2/18 | chr1 | 11949159 | |||||||
chr1:11949166 | G | C | 134 | a0001c0001t0001g0240 a0001c0008t0002g0094 a0001c0008t0002g0095 others(131): Show |
139 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.169-607G>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 2/18 | chr1 | 11949166 | |||||||
chr1:11949173 | T | C | 2 | a0002c0003t0001g0256 a0002c0003t0001g0284 |
2 | NA18985.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.169-600T>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 2/18 | chr1 | 11949173 | |||||||
chr1:11949372 | T | A | 1 | a0001c0001t0001g0239 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.169-401T>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 2/18 | chr1 | 11949372 | |||||||
chr1:11949401 | A | C | 49 | a0001c0001t0001g0240 a0003c0004t0001g0012 a0003c0004t0001g0018 others(46): Show |
53 | HG00408.hp2 HG00673.hp1 HG00733.hp2 others(50): Show |
intron_variant | MODIFIER | c.169-372A>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 2/18 | chr1 | 11949401 | |||||||
chr1:11949405 | G | A | 229 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0110 others(226): Show |
248 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(245): Show |
intron_variant | MODIFIER | c.169-368G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 2/18 | chr1 | 11949405 | |||||||
chr1:11949482 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.169-291C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 2/18 | chr1 | 11949482 | |||||||
chr1:11949677 | C | T | 45 | a0001c0001t0001g0240 a0003c0004t0001g0012 a0003c0004t0001g0018 others(42): Show |
48 | HG00408.hp2 HG00673.hp1 HG00733.hp2 others(45): Show |
intron_variant | MODIFIER | c.169-96C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 2/18 | chr1 | 11949677 | |||||||
chr1:11949720 | C | G | 10 | a0004c0009t0002g0091 a0004c0009t0002g0317 a0004c0009t0002g0318 others(7): Show |
10 | HG01070.hp1 HG02145.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.169-53C>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 2/18 | chr1 | 11949720 | |||||||
chr1:11949921 | G | A | 1 | a0002c0003t0001g0203 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.302+15G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 3/18 | chr1 | 11949921 | |||||||
chr1:11949989 | G | A | 27 | a0003c0004t0001g0012 a0003c0004t0001g0018 a0003c0004t0001g0122 others(24): Show |
29 | HG00408.hp2 HG00733.hp2 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.302+83G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 3/18 | chr1 | 11949989 | |||||||
chr1:11950035 | T | G | 1 | a0003c0007t0001g0195 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.302+129T>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 3/18 | chr1 | 11950035 | |||||||
chr1:11950161 | T | C | 1 | a0001c0025t0001g0042 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.303-196T>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 3/18 | chr1 | 11950161 | |||||||
chr1:11950242 | G | A | 1 | a0002c0003t0001g0237 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.303-115G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 3/18 | chr1 | 11950242 | |||||||
chr1:11950284 | C | T | 1 | a0001c0028t0001g0196 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.303-73C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 3/18 | chr1 | 11950284 | |||||||
chr1:11950593 | G | A | 2 | a0002c0003t0001g0310 a0002c0003t0001g0322 |
2 | HG01891.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.466+73G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 4/18 | chr1 | 11950593 | |||||||
chr1:11950646 | T | C | 1 | a0001c0002t0001g0138 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.466+126T>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 4/18 | chr1 | 11950646 | |||||||
chr1:11950721 | A | G | 229 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0110 others(226): Show |
248 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(245): Show |
intron_variant | MODIFIER | c.466+201A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 4/18 | chr1 | 11950721 | |||||||
chr1:11950880 | G | A | 7 | a0001c0008t0002g0094 a0001c0008t0002g0095 a0001c0008t0002g0205 others(4): Show |
7 | HG02083.hp1 HG04228.hp2 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.466+360G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 4/18 | chr1 | 11950880 | |||||||
chr1:11950954 | C | T | 49 | a0002c0003t0001g0203 a0003c0004t0001g0012 a0003c0004t0001g0018 others(46): Show |
53 | HG00408.hp2 HG00733.hp2 HG01106.hp1 others(50): Show |
intron_variant | MODIFIER | c.466+434C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 4/18 | chr1 | 11950954 | |||||||
chr1:11950990 | C | T | 1 | a0001c0002t0001g0161 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.466+470C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 4/18 | chr1 | 11950990 | |||||||
chr1:11951064 | G | GA | 4 | a0003c0016t0001g0020 a0003c0016t0001g0309 a0003c0033t0003g0311 others(1): Show |
5 | HG02451.hp2 HG02559.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.466+545dupA | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr1 | 11951064 | ||||||
chr1:11951179 | C | T | 2 | a0001c0002t0001g0159 a0001c0002t0001g0160 |
2 | HG02273.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.466+659C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 4/18 | chr1 | 11951179 | |||||||
chr1:11951293 | C | G | 1 | a0002c0003t0001g0203 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.466+773C>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 4/18 | chr1 | 11951293 | |||||||
chr1:11951294 | G | A | 22 | a0001c0012t0002g0187 a0001c0012t0002g0213 a0001c0012t0002g0214 others(19): Show |
22 | HG01070.hp1 HG01192.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.466+774G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 4/18 | chr1 | 11951294 | |||||||
chr1:11951295 | G | T | 1 | a0002c0003t0001g0203 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.466+775G>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 4/18 | chr1 | 11951295 | |||||||
chr1:11951369 | C | G | 1 | a0001c0002t0001g0170 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.466+849C>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 4/18 | chr1 | 11951369 | |||||||
chr1:11951422 | C | T | 1 | a0002c0003t0001g0263 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.466+902C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 4/18 | chr1 | 11951422 | |||||||
chr1:11951426 | C | T | 1 | a0002c0003t0001g0237 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.466+906C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 4/18 | chr1 | 11951426 | |||||||
chr1:11951555 | T | A | 5 | a0001c0001t0001g0084 a0003c0016t0001g0020 a0003c0016t0001g0309 others(2): Show |
6 | HG02132.hp2 HG02451.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.466+1035T>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 4/18 | chr1 | 11951555 | |||||||
chr1:11951565 | AT | A | 17 | a0003c0005t0001g0011 a0003c0005t0001g0070 a0003c0005t0001g0071 others(14): Show |
18 | HG01243.hp2 HG01884.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.466+1046delT | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 4/18 | chr1 | 11951565 | |||||||
chr1:11951594 | T | C | 1 | a0002c0003t0001g0198 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.467-1029T>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 4/18 | chr1 | 11951594 | |||||||
chr1:11951701 | C | T | 1 | a0001c0028t0001g0196 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.467-922C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 4/18 | chr1 | 11951701 | |||||||
chr1:11951735 | C | A | 21 | a0001c0012t0002g0187 a0001c0012t0002g0213 a0001c0012t0002g0214 others(18): Show |
21 | HG01070.hp1 HG01192.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.467-888C>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 4/18 | chr1 | 11951735 | |||||||
chr1:11951746 | C | T | 1 | a0002c0010t0001g0288 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.467-877C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 4/18 | chr1 | 11951746 | |||||||
chr1:11951774 | C | A | 1 | a0001c0028t0001g0196 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.467-849C>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 4/18 | chr1 | 11951774 | |||||||
chr1:11951811 | C | T | 13 | a0001c0012t0002g0187 a0001c0012t0002g0213 a0001c0012t0002g0214 others(10): Show |
13 | HG01070.hp1 HG02109.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.467-812C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 4/18 | chr1 | 11951811 | |||||||
chr1:11951891 | C | A | 21 | a0001c0012t0002g0187 a0001c0012t0002g0213 a0001c0012t0002g0214 others(18): Show |
21 | HG01070.hp1 HG01192.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.467-732C>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 4/18 | chr1 | 11951891 | |||||||
chr1:11951903 | A | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0055 |
4 | HG00733.hp1 HG01099.hp1 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.467-720A>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 4/18 | chr1 | 11951903 | |||||||
chr1:11951920 | AAAAT | A | 60 | a0001c0008t0002g0163 a0002c0003t0001g0019 a0002c0003t0001g0096 others(57): Show |
61 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.467-687_467-684del others(4): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr1 | 11951920 | ||||||
chr1:11952122 | C | T | 1 | a0006c0029t0001g0166 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.467-501C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 4/18 | chr1 | 11952122 | |||||||
chr1:11952271 | G | A | 48 | a0003c0004t0001g0012 a0003c0004t0001g0018 a0003c0004t0001g0122 others(45): Show |
52 | HG00408.hp2 HG00733.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.467-352G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 4/18 | chr1 | 11952271 | |||||||
chr1:11952352 | A | G | 59 | a0001c0008t0002g0163 a0002c0003t0001g0019 a0002c0003t0001g0096 others(56): Show |
60 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.467-271A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 4/18 | chr1 | 11952352 | |||||||
chr1:11952910 | G | C | 1 | a0001c0002t0007g0167 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.579+175G>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 5/18 | chr1 | 11952910 | |||||||
chr1:11952923 | G | A | 89 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0110 others(86): Show |
103 | HG00597.hp2 HG00609.hp2 HG00621.hp2 others(100): Show |
intron_variant | MODIFIER | c.579+188G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 5/18 | chr1 | 11952923 | |||||||
chr1:11952924 | G | C | 7 | a0001c0008t0002g0094 a0001c0008t0002g0095 a0001c0008t0002g0205 others(4): Show |
7 | HG02083.hp1 HG04228.hp2 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.579+189G>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 5/18 | chr1 | 11952924 | |||||||
chr1:11952976 | C | G | 139 | a0001c0008t0002g0094 a0001c0008t0002g0095 a0001c0008t0002g0163 others(136): Show |
144 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.579+241C>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 5/18 | chr1 | 11952976 | |||||||
chr1:11953009 | G | A | 60 | a0001c0008t0002g0163 a0002c0003t0001g0019 a0002c0003t0001g0096 others(57): Show |
61 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.579+274G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 5/18 | chr1 | 11953009 | |||||||
chr1:11953092 | A | G | 48 | a0003c0004t0001g0012 a0003c0004t0001g0018 a0003c0004t0001g0122 others(45): Show |
52 | HG00408.hp2 HG00733.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.579+357A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 5/18 | chr1 | 11953092 | |||||||
chr1:11953135 | A | G | 32 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0023 others(29): Show |
45 | HG00423.hp2 HG00438.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.579+400A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 5/18 | chr1 | 11953135 | |||||||
chr1:11953139 | T | A | 32 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0023 others(29): Show |
45 | HG00423.hp2 HG00438.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.579+404T>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 5/18 | chr1 | 11953139 | |||||||
chr1:11953140 | C | A | 32 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0023 others(29): Show |
45 | HG00423.hp2 HG00438.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.579+405C>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 5/18 | chr1 | 11953140 | |||||||
chr1:11953141 | T | C | 32 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0023 others(29): Show |
45 | HG00423.hp2 HG00438.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.579+406T>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 5/18 | chr1 | 11953141 | |||||||
chr1:11953143 | C | T | 60 | a0001c0008t0002g0163 a0002c0003t0001g0019 a0002c0003t0001g0096 others(57): Show |
61 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.579+408C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 5/18 | chr1 | 11953143 | |||||||
chr1:11953151 | G | A | 32 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0023 others(29): Show |
45 | HG00423.hp2 HG00438.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.579+416G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 5/18 | chr1 | 11953151 | |||||||
chr1:11953158 | C | T | 60 | a0001c0008t0002g0163 a0002c0003t0001g0019 a0002c0003t0001g0096 others(57): Show |
61 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.579+423C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 5/18 | chr1 | 11953158 | |||||||
chr1:11953166 | G | A | 27 | a0003c0004t0001g0012 a0003c0004t0001g0018 a0003c0004t0001g0122 others(24): Show |
29 | HG00408.hp2 HG00733.hp2 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.579+431G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 5/18 | chr1 | 11953166 | |||||||
chr1:11953187 | C | T | 1 | a0002c0003t0001g0203 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.579+452C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 5/18 | chr1 | 11953187 | |||||||
chr1:11953261 | C | T | 7 | a0002c0014t0001g0105 a0002c0014t0004g0295 a0002c0014t0004g0296 others(4): Show |
7 | HG01192.hp2 HG02970.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.579+526C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 5/18 | chr1 | 11953261 | |||||||
chr1:11953345 | C | T | 1 | a0013c0020t0001g0090 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.579+610C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 5/18 | chr1 | 11953345 | |||||||
chr1:11953394 | A | C | 5 | a0002c0003t0001g0019 a0002c0003t0001g0287 a0002c0003t0001g0294 others(2): Show |
6 | HG01243.hp1 HG02559.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.579+659A>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 5/18 | chr1 | 11953394 | |||||||
chr1:11953496 | T | C | 5 | a0002c0003t0001g0255 a0002c0003t0001g0265 a0002c0003t0001g0266 others(2): Show |
5 | NA18612.hp1 NA18961.hp1 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.579+761T>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 5/18 | chr1 | 11953496 | |||||||
chr1:11953516 | G | A | 60 | a0001c0008t0002g0163 a0002c0003t0001g0019 a0002c0003t0001g0096 others(57): Show |
61 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.579+781G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 5/18 | chr1 | 11953516 | |||||||
chr1:11953588 | T | C | 3 | a0001c0002t0001g0126 a0001c0002t0001g0145 a0001c0002t0001g0146 |
3 | NA19056.hp2 NA19070.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.579+853T>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 5/18 | chr1 | 11953588 | |||||||
chr1:11953655 | G | A | 1 | a0001c0001t0001g0234 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.579+920G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 5/18 | chr1 | 11953655 | |||||||
chr1:11953749 | G | A | 1 | a0002c0003t0001g0263 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.579+1014G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 5/18 | chr1 | 11953749 | |||||||
chr1:11953770 | T | C | 132 | a0001c0008t0002g0163 a0001c0012t0002g0187 a0001c0012t0002g0213 others(129): Show |
137 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.579+1035T>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 5/18 | chr1 | 11953770 | |||||||
chr1:11953812 | A | G | 27 | a0003c0004t0001g0012 a0003c0004t0001g0018 a0003c0004t0001g0122 others(24): Show |
29 | HG00408.hp2 HG00733.hp2 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.580-1018A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 5/18 | chr1 | 11953812 | |||||||
chr1:11954039 | A | AT | 5 | a0001c0001t0001g0056 a0001c0012t0002g0187 a0001c0012t0002g0213 others(2): Show |
5 | HG01070.hp1 HG02109.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.580-784dupT | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr1 | 11954039 | ||||||
chr1:11954154 | C | T | 3 | a0003c0016t0001g0020 a0003c0033t0003g0311 a0008c0032t0002g0312 |
4 | HG02559.hp2 HG02886.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.580-676C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 5/18 | chr1 | 11954154 | |||||||
chr1:11954310 | C | CA | 79 | a0001c0001t0001g0027 a0001c0001t0001g0030 a0001c0001t0001g0031 others(76): Show |
80 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.580-494dupA | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr1 | 11954310 | ||||||
chr1:11954310 | C | CAA | 10 | a0002c0003t0001g0190 a0002c0003t0001g0198 a0002c0003t0001g0199 others(7): Show |
10 | HG00438.hp1 HG00597.hp1 HG00642.hp2 others(7): Show |
intron_variant | MODIFIER | c.580-495_580-494dup others(2): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr1 | 11954310 | ||||||
chr1:11954310 | C | CAAA | 7 | a0001c0008t0002g0094 a0001c0008t0002g0095 a0001c0008t0002g0205 others(4): Show |
7 | HG02083.hp1 HG04228.hp2 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.580-496_580-494dup others(3): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr1 | 11954310 | ||||||
chr1:11954310 | CA | C | 25 | a0001c0001t0001g0052 a0003c0004t0001g0132 a0003c0004t0001g0241 others(22): Show |
27 | HG01070.hp1 HG01243.hp2 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.580-494delA | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr1 | 11954310 | ||||||
chr1:11954310 | CAA | C | 23 | a0002c0015t0003g0297 a0003c0004t0001g0012 a0003c0004t0001g0018 others(20): Show |
25 | HG00408.hp2 HG00733.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.580-495_580-494del others(2): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr1 | 11954310 | ||||||
chr1:11954310 | CAAA | C | 6 | a0002c0014t0001g0105 a0002c0014t0004g0295 a0002c0014t0004g0296 others(3): Show |
6 | HG02970.hp2 HG03041.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.580-496_580-494del others(3): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr1 | 11954310 | ||||||
chr1:11954400 | C | T | 1 | a0001c0028t0001g0196 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.580-430C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 5/18 | chr1 | 11954400 | |||||||
chr1:11954401 | G | A | 7 | a0001c0008t0002g0094 a0001c0008t0002g0095 a0001c0008t0002g0205 others(4): Show |
7 | HG02083.hp1 HG04228.hp2 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.580-429G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 5/18 | chr1 | 11954401 | |||||||
chr1:11954661 | T | C | 1 | a0001c0001t0001g0222 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.580-169T>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 5/18 | chr1 | 11954661 | |||||||
chr1:11954937 | T | TAGGAGAA others(11): Show |
1 | a0002c0003t0001g0268 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.643+48_643+49insGA others(16): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr1 | 11954937 | ||||||
chr1:11954969 | G | A | 1 | a0003c0004t0001g0241 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.643+76G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 6/18 | chr1 | 11954969 | |||||||
chr1:11955096 | T | C | 5 | a0002c0003t0001g0255 a0002c0003t0001g0265 a0002c0003t0001g0266 others(2): Show |
5 | NA18612.hp1 NA18961.hp1 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.643+203T>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 6/18 | chr1 | 11955096 | |||||||
chr1:11955097 | G | A | 90 | a0001c0001t0001g0001 a0001c0001t0001g0014 a0001c0001t0001g0110 others(87): Show |
104 | HG00597.hp2 HG00609.hp2 HG00621.hp2 others(101): Show |
intron_variant | MODIFIER | c.643+204G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 6/18 | chr1 | 11955097 | |||||||
chr1:11955223 | A | T | 1 | a0005c0023t0002g0324 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.643+330A>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 6/18 | chr1 | 11955223 | |||||||
chr1:11955435 | TTTACAAA others(3): Show |
T | 60 | a0001c0008t0002g0163 a0002c0003t0001g0019 a0002c0003t0001g0096 others(57): Show |
61 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.643+543_643+552del others(10): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 6/18 | chr1 | 11955435 | |||||||
chr1:11955538 | G | A | 1 | a0002c0003t0001g0096 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.643+645G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 6/18 | chr1 | 11955538 | |||||||
chr1:11955759 | G | T | 9 | a0002c0003t0001g0019 a0002c0003t0001g0287 a0002c0003t0001g0294 others(6): Show |
10 | HG01243.hp1 HG01891.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.643+866G>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 6/18 | chr1 | 11955759 | |||||||
chr1:11955768 | C | T | 1 | a0001c0008t0002g0207 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.643+875C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 6/18 | chr1 | 11955768 | |||||||
chr1:11955901 | C | T | 1 | a0001c0001t0001g0014 | 2 | NA18983.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.643+1008C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 6/18 | chr1 | 11955901 | |||||||
chr1:11955954 | G | T | 1 | a0001c0001t0001g0051 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.644-963G>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 6/18 | chr1 | 11955954 | |||||||
chr1:11956151 | A | G | 1 | a0001c0001t0001g0225 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.644-766A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 6/18 | chr1 | 11956151 | |||||||
chr1:11956365 | T | C | 60 | a0001c0008t0002g0163 a0002c0003t0001g0019 a0002c0003t0001g0096 others(57): Show |
61 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.644-552T>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 6/18 | chr1 | 11956365 | |||||||
chr1:11956369 | A | G | 1 | a0002c0003t0001g0272 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.644-548A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 6/18 | chr1 | 11956369 | |||||||
chr1:11956441 | G | T | 7 | a0001c0002t0001g0007 a0001c0002t0001g0136 a0001c0002t0001g0137 others(4): Show |
9 | HG02015.hp1 HG02132.hp1 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.644-476G>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 6/18 | chr1 | 11956441 | |||||||
chr1:11956609 | C | G | 6 | a0002c0003t0001g0197 a0002c0003t0001g0198 a0002c0003t0001g0199 others(3): Show |
6 | HG00408.hp1 HG00423.hp1 HG00597.hp1 others(3): Show |
intron_variant | MODIFIER | c.644-308C>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 6/18 | chr1 | 11956609 | |||||||
chr1:11956715 | T | C | 131 | a0001c0008t0002g0163 a0001c0012t0002g0187 a0001c0012t0002g0213 others(128): Show |
136 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.644-202T>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 6/18 | chr1 | 11956715 | |||||||
chr1:11956723 | A | C | 1 | a0001c0028t0001g0196 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.644-194A>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 6/18 | chr1 | 11956723 | |||||||
chr1:11956762 | AT | A | 7 | a0001c0008t0002g0094 a0001c0008t0002g0095 a0001c0008t0002g0205 others(4): Show |
7 | HG02083.hp1 HG04228.hp2 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.644-151delT | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr1 | 11956762 | ||||||
chr1:11956809 | A | T | 1 | a0002c0003t0001g0203 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.644-108A>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 6/18 | chr1 | 11956809 | |||||||
chr1:11956900 | T | G | 50 | a0001c0008t0002g0163 a0002c0003t0001g0096 a0002c0003t0001g0097 others(47): Show |
50 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(47): Show |
intron_variant | MODIFIER | c.644-17T>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 6/18 | chr1 | 11956900 | |||||||
chr1:11957091 | G | A | 5 | a0003c0005t0001g0303 a0003c0007t0001g0194 a0003c0007t0001g0195 others(2): Show |
5 | HG02615.hp1 HG02723.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.741+77G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 7/18 | chr1 | 11957091 | |||||||
chr1:11957276 | A | G | 1 | a0003c0016t0001g0309 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.741+262A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 7/18 | chr1 | 11957276 | |||||||
chr1:11957389 | A | T | 1 | a0002c0010t0001g0257 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.741+375A>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 7/18 | chr1 | 11957389 | |||||||
chr1:11957422 | C | T | 48 | a0003c0004t0001g0012 a0003c0004t0001g0018 a0003c0004t0001g0122 others(45): Show |
52 | HG00408.hp2 HG00733.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.741+408C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 7/18 | chr1 | 11957422 | |||||||
chr1:11957655 | C | G | 1 | a0001c0001t0001g0041 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.742-187C>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 7/18 | chr1 | 11957655 | |||||||
chr1:11957659 | C | A | 1 | a0003c0004t0001g0132 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.742-183C>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 7/18 | chr1 | 11957659 | |||||||
chr1:11957674 | A | G | 7 | a0001c0008t0002g0094 a0001c0008t0002g0095 a0001c0008t0002g0205 others(4): Show |
7 | HG02083.hp1 HG04228.hp2 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.742-168A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 7/18 | chr1 | 11957674 | |||||||
chr1:11957953 | C | T | 1 | a0001c0001t0001g0238 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.843+10C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 8/18 | chr1 | 11957953 | |||||||
chr1:11958161 | T | C | 1 | a0001c0006t0001g0162 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.843+218T>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 8/18 | chr1 | 11958161 | |||||||
chr1:11958163 | G | A | 1 | a0002c0003t0001g0203 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.843+220G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 8/18 | chr1 | 11958163 | |||||||
chr1:11958233 | T | C | 124 | a0001c0008t0002g0163 a0001c0012t0002g0187 a0001c0012t0002g0213 others(121): Show |
129 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.844-283T>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 8/18 | chr1 | 11958233 | |||||||
chr1:11958273 | A | C | 1 | a0001c0006t0001g0299 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.844-243A>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 8/18 | chr1 | 11958273 | |||||||
chr1:11958321 | C | G | 87 | a0001c0001t0001g0001 a0001c0001t0001g0110 a0001c0001t0001g0188 others(84): Show |
100 | HG00597.hp2 HG00609.hp2 HG00621.hp2 others(97): Show |
intron_variant | MODIFIER | c.844-195C>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 8/18 | chr1 | 11958321 | |||||||
chr1:11958457 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.844-59G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 8/18 | chr1 | 11958457 | |||||||
chr1:11958660 | C | T | 1 | a0002c0003t0001g0203 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.975+13C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 9/18 | chr1 | 11958660 | |||||||
chr1:11958830 | A | T | 7 | a0002c0014t0001g0105 a0002c0014t0004g0295 a0002c0014t0004g0296 others(4): Show |
7 | HG01192.hp2 HG02970.hp2 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.975+183A>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 9/18 | chr1 | 11958830 | |||||||
chr1:11958870 | A | C | 2 | a0001c0002t0001g0165 a0006c0029t0001g0166 |
2 | HG01928.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.975+223A>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 9/18 | chr1 | 11958870 | |||||||
chr1:11958891 | C | T | 7 | a0001c0008t0002g0094 a0001c0008t0002g0095 a0001c0008t0002g0205 others(4): Show |
7 | HG02083.hp1 HG04228.hp2 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.975+244C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 9/18 | chr1 | 11958891 | |||||||
chr1:11958994 | C | T | 3 | a0001c0012t0002g0187 a0001c0012t0002g0213 a0001c0012t0002g0214 |
3 | HG02109.hp2 HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.975+347C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 9/18 | chr1 | 11958994 | |||||||
chr1:11959035 | C | T | 2 | a0002c0010t0001g0292 a0002c0010t0001g0293 |
2 | HG02896.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.975+388C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 9/18 | chr1 | 11959035 | |||||||
chr1:11959078 | G | A | 20 | a0003c0004t0001g0012 a0003c0004t0001g0018 a0003c0004t0001g0122 others(17): Show |
22 | HG00408.hp2 HG00733.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.975+431G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 9/18 | chr1 | 11959078 | |||||||
chr1:11959193 | A | G | 24 | a0002c0014t0001g0105 a0002c0014t0004g0295 a0002c0014t0004g0296 others(21): Show |
25 | HG01192.hp2 HG01243.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.975+546A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 9/18 | chr1 | 11959193 | |||||||
chr1:11959231 | A | G | 1 | a0003c0016t0001g0309 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.975+584A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 9/18 | chr1 | 11959231 | |||||||
chr1:11959312 | C | T | 90 | a0001c0001t0001g0001 a0001c0001t0001g0110 a0001c0001t0001g0188 others(87): Show |
104 | HG00597.hp2 HG00609.hp2 HG00621.hp2 others(101): Show |
intron_variant | MODIFIER | c.975+665C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 9/18 | chr1 | 11959312 | |||||||
chr1:11959445 | C | CT | 87 | a0001c0001t0001g0001 a0001c0001t0001g0110 a0001c0001t0001g0188 others(84): Show |
100 | HG00597.hp2 HG00609.hp2 HG00621.hp2 others(97): Show |
intron_variant | MODIFIER | c.975+813dupT | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 11959445 | ||||||
chr1:11959491 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.975+844G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 9/18 | chr1 | 11959491 | |||||||
chr1:11959546 | GATTCTCC others(168): Show |
G | 5 | a0002c0003t0001g0019 a0002c0003t0001g0287 a0002c0003t0001g0294 others(2): Show |
6 | HG01243.hp1 HG02559.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.975+921_976-904del | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 11959546 | ||||||
chr1:11959618 | A | AT | 16 | a0001c0001t0001g0038 a0001c0001t0001g0047 a0001c0001t0001g0057 others(13): Show |
17 | HG00642.hp1 HG02055.hp1 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.975+988dupT | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 11959618 | ||||||
chr1:11959618 | AT | A | 17 | a0001c0001t0001g0046 a0001c0002t0001g0118 a0001c0012t0002g0187 others(14): Show |
17 | HG01070.hp1 HG02109.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.975+988delT | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 11959618 | ||||||
chr1:11959856 | T | C | 1 | a0013c0020t0001g0090 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.976-790T>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 9/18 | chr1 | 11959856 | |||||||
chr1:11959931 | CT | C | 21 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0034 others(18): Show |
25 | HG01243.hp1 HG01891.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.976-699delT | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 11959931 | ||||||
chr1:11959991 | G | A | 1 | a0013c0020t0001g0090 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.976-655G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 9/18 | chr1 | 11959991 | |||||||
chr1:11960004 | ACTGCAAC others(33): Show |
A | 9 | a0002c0003t0001g0019 a0002c0003t0001g0287 a0002c0003t0001g0294 others(6): Show |
10 | HG01243.hp1 HG01891.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.976-623_976-584del others(40): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 11960004 | ||||||
chr1:11960097 | G | A | 13 | a0001c0012t0002g0187 a0001c0012t0002g0213 a0001c0012t0002g0214 others(10): Show |
13 | HG01070.hp1 HG02109.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.976-549G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 9/18 | chr1 | 11960097 | |||||||
chr1:11960102 | C | G | 131 | a0001c0008t0002g0163 a0001c0012t0002g0187 a0001c0012t0002g0213 others(128): Show |
136 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.976-544C>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 9/18 | chr1 | 11960102 | |||||||
chr1:11960133 | G | A | 1 | a0002c0003t0001g0310 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.976-513G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 9/18 | chr1 | 11960133 | |||||||
chr1:11960228 | C | T | 1 | a0001c0028t0001g0196 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.976-418C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 9/18 | chr1 | 11960228 | |||||||
chr1:11960300 | G | T | 77 | a0001c0008t0002g0163 a0002c0003t0001g0096 a0002c0003t0001g0097 others(74): Show |
79 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.976-346G>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 9/18 | chr1 | 11960300 | |||||||
chr1:11960316 | T | C | 1 | a0001c0001t0001g0221 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.976-330T>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 9/18 | chr1 | 11960316 | |||||||
chr1:11960355 | A | G | 138 | a0001c0008t0002g0094 a0001c0008t0002g0095 a0001c0008t0002g0163 others(135): Show |
143 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.976-291A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 9/18 | chr1 | 11960355 | |||||||
chr1:11960384 | G | A | 25 | a0002c0014t0001g0105 a0002c0014t0004g0295 a0002c0014t0004g0296 others(22): Show |
26 | HG01192.hp2 HG01243.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.976-262G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 9/18 | chr1 | 11960384 | |||||||
chr1:11960391 | C | T | 1 | a0002c0003t0001g0237 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.976-255C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 9/18 | chr1 | 11960391 | |||||||
chr1:11960420 | TAGG | T | 3 | a0001c0002t0001g0136 a0001c0002t0001g0157 a0001c0002t0001g0158 |
3 | NA18952.hp2 NA19079.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.976-222_976-220del others(3): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr1 | 11960420 | ||||||
chr1:11960504 | G | T | 9 | a0002c0003t0001g0019 a0002c0003t0001g0287 a0002c0003t0001g0294 others(6): Show |
10 | HG01243.hp1 HG01891.hp2 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.976-142G>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 9/18 | chr1 | 11960504 | |||||||
chr1:11960605 | C | T | 1 | a0001c0001t0001g0025 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.976-41C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 9/18 | chr1 | 11960605 | |||||||
chr1:11960630 | C | T | 6 | a0001c0008t0002g0094 a0001c0008t0002g0205 a0001c0008t0002g0206 others(3): Show |
6 | HG02083.hp1 HG04228.hp2 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.976-16C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 9/18 | chr1 | 11960630 | |||||||
chr1:11960922 | A | G | 1 | a0001c0028t0001g0196 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1097+155A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 10/18 | chr1 | 11960922 | |||||||
chr1:11960951 | C | T | 2 | a0001c0001t0001g0045 a0001c0001t0001g0050 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1097+184C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 10/18 | chr1 | 11960951 | |||||||
chr1:11960986 | T | C | 5 | a0001c0028t0001g0196 a0002c0003t0001g0019 a0002c0003t0001g0287 others(2): Show |
6 | HG01243.hp1 HG02559.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1097+219T>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 10/18 | chr1 | 11960986 | |||||||
chr1:11960987 | T | C | 70 | a0001c0001t0001g0084 a0001c0001t0003g0302 a0001c0002t0001g0138 others(67): Show |
73 | HG00408.hp2 HG00733.hp2 HG01070.hp1 others(70): Show |
intron_variant | MODIFIER | c.1097+220T>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 10/18 | chr1 | 11960987 | |||||||
chr1:11961012 | AAG | A | 5 | a0001c0002t0001g0016 a0001c0002t0001g0177 a0001c0002t0001g0178 others(2): Show |
6 | HG02135.hp2 NA18959.hp2 NA19005.hp2 others(3): Show |
intron_variant | MODIFIER | c.1097+248_1097+249d others(4): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr1 | 11961012 | ||||||
chr1:11961091 | TAA | T | 11 | a0002c0003t0001g0019 a0002c0003t0001g0287 a0002c0003t0001g0294 others(8): Show |
13 | HG01243.hp1 HG01891.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.1097+333_1097+334d others(4): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr1 | 11961091 | ||||||
chr1:11961093 | A | T | 3 | a0002c0003t0001g0203 a0002c0015t0003g0297 a0003c0033t0003g0311 |
3 | HG01192.hp2 HG02451.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.1097+326A>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 10/18 | chr1 | 11961093 | |||||||
chr1:11961227 | TA | T | 227 | a0001c0001t0001g0001 a0001c0001t0001g0084 a0001c0001t0001g0085 others(224): Show |
245 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(242): Show |
intron_variant | MODIFIER | c.1097+469delA | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr1 | 11961227 | ||||||
chr1:11961428 | G | C | 23 | a0001c0012t0002g0064 a0001c0012t0002g0187 a0001c0012t0002g0213 others(20): Show |
24 | HG01070.hp1 HG01243.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.1097+661G>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 10/18 | chr1 | 11961428 | |||||||
chr1:11961437 | TCAGA | T | 3 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 |
3 | NA18962.hp1 NA18990.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.1097+674_1097+677d others(6): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr1 | 11961437 | ||||||
chr1:11961643 | C | T | 1 | a0002c0003t0001g0277 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1097+876C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 10/18 | chr1 | 11961643 | |||||||
chr1:11961649 | A | C | 6 | a0004c0009t0002g0317 a0004c0009t0002g0318 a0004c0009t0002g0319 others(3): Show |
6 | HG02145.hp2 HG02622.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1097+882A>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 10/18 | chr1 | 11961649 | |||||||
chr1:11961733 | C | A | 1 | a0013c0020t0001g0090 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1097+966C>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 10/18 | chr1 | 11961733 | |||||||
chr1:11961850 | G | A | 2 | a0001c0001t0001g0216 a0001c0001t0001g0225 |
2 | HG00738.hp1 HG00741.hp2 |
intron_variant | MODIFIER | c.1097+1083G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 10/18 | chr1 | 11961850 | |||||||
chr1:11961851 | C | T | 1 | a0002c0003t0001g0279 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1097+1084C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 10/18 | chr1 | 11961851 | |||||||
chr1:11961911 | C | G | 2 | a0004c0009t0002g0317 a0004c0009t0002g0320 |
2 | HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1097+1144C>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 10/18 | chr1 | 11961911 | |||||||
chr1:11962032 | G | A | 3 | a0001c0001t0001g0223 a0003c0007t0003g0066 a0003c0007t0003g0067 |
3 | HG02896.hp1 HG02897.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1097+1265G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 10/18 | chr1 | 11962032 | |||||||
chr1:11962067 | G | A | 2 | a0004c0009t0002g0317 a0004c0009t0002g0320 |
2 | HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1097+1300G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 10/18 | chr1 | 11962067 | |||||||
chr1:11962263 | A | AT | 11 | a0001c0008t0004g0065 a0002c0003t0001g0019 a0002c0003t0001g0294 others(8): Show |
12 | HG01243.hp1 HG02615.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.1098-1264dupT | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr1 | 11962263 | ||||||
chr1:11962263 | ATTTTTGT others(7): Show |
A | 1 | a0013c0020t0001g0090 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1098-1263_1098-125 others(18): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr1 | 11962263 | ||||||
chr1:11962269 | G | T | 135 | a0001c0001t0001g0110 a0001c0001t0003g0302 a0001c0008t0002g0094 others(132): Show |
140 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.1098-1263G>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 10/18 | chr1 | 11962269 | |||||||
chr1:11962273 | T | C | 7 | a0003c0004t0001g0244 a0003c0004t0001g0245 a0003c0004t0001g0249 others(4): Show |
8 | HG00733.hp2 HG01106.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.1098-1259T>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 10/18 | chr1 | 11962273 | |||||||
chr1:11962274 | C | CT | 195 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0023 others(192): Show |
216 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(213): Show |
intron_variant | MODIFIER | c.1098-1238dupT | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr1 | 11962274 | ||||||
chr1:11962274 | C | CTT | 7 | a0001c0002t0001g0120 a0001c0013t0001g0117 a0002c0003t0001g0263 others(4): Show |
7 | HG01517.hp1 HG02129.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1098-1239_1098-123 others(6): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr1 | 11962274 | ||||||
chr1:11962274 | C | T | 7 | a0003c0004t0001g0244 a0003c0004t0001g0245 a0003c0004t0001g0249 others(4): Show |
8 | HG00733.hp2 HG01106.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.1098-1258C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 10/18 | chr1 | 11962274 | |||||||
chr1:11962277 | T | TC | 8 | a0001c0006t0001g0131 a0001c0008t0002g0094 a0001c0008t0002g0095 others(5): Show |
8 | HG02074.hp1 HG02083.hp1 HG04228.hp2 others(5): Show |
intron_variant | MODIFIER | c.1098-1255_1098-125 others(5): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 10/18 | chr1 | 11962277 | |||||||
chr1:11962278 | T | C | 2 | a0005c0023t0002g0324 a0008c0032t0002g0312 |
2 | HG01109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1098-1254T>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 10/18 | chr1 | 11962278 | |||||||
chr1:11962279 | T | TC | 15 | a0001c0001t0001g0110 a0001c0008t0004g0065 a0002c0003t0001g0019 others(12): Show |
16 | HG01243.hp1 HG02055.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.1098-1253_1098-125 others(5): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 10/18 | chr1 | 11962279 | |||||||
chr1:11962372 | G | A | 2 | a0002c0003t0001g0203 a0002c0003t0001g0237 |
2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1098-1160G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 10/18 | chr1 | 11962372 | |||||||
chr1:11962373 | T | A | 1 | a0004c0011t0001g0321 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1098-1159T>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 10/18 | chr1 | 11962373 | |||||||
chr1:11962378 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1098-1154G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 10/18 | chr1 | 11962378 | |||||||
chr1:11962386 | C | T | 1 | a0002c0003t0001g0287 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1098-1146C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 10/18 | chr1 | 11962386 | |||||||
chr1:11962397 | C | T | 1 | a0001c0008t0002g0208 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1098-1135C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 10/18 | chr1 | 11962397 | |||||||
chr1:11962436 | C | T | 90 | a0001c0001t0001g0001 a0001c0001t0001g0188 a0001c0002t0001g0001 others(87): Show |
103 | HG00597.hp2 HG00609.hp2 HG00735.hp2 others(100): Show |
intron_variant | MODIFIER | c.1098-1096C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 10/18 | chr1 | 11962436 | |||||||
chr1:11962437 | C | T | 96 | a0001c0001t0003g0302 a0001c0008t0002g0163 a0001c0013t0001g0117 others(93): Show |
100 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1098-1095C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 10/18 | chr1 | 11962437 | |||||||
chr1:11962703 | T | C | 1 | a0002c0010t0001g0293 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1098-829T>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 10/18 | chr1 | 11962703 | |||||||
chr1:11962734 | C | A | 96 | a0001c0001t0003g0302 a0001c0008t0002g0163 a0001c0013t0001g0117 others(93): Show |
100 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.1098-798C>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 10/18 | chr1 | 11962734 | |||||||
chr1:11962812 | G | A | 2 | a0005c0023t0002g0324 a0008c0032t0002g0312 |
2 | HG01109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1098-720G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 10/18 | chr1 | 11962812 | |||||||
chr1:11963043 | AAAAAT | A | 20 | a0002c0017t0001g0276 a0002c0017t0001g0278 a0003c0004t0001g0012 others(17): Show |
22 | HG00408.hp2 HG00733.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.1098-474_1098-470d others(7): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr1 | 11963043 | ||||||
chr1:11963064 | T | G | 20 | a0001c0008t0002g0094 a0001c0008t0002g0095 a0001c0008t0002g0205 others(17): Show |
20 | HG01070.hp1 HG01891.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.1098-468T>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 10/18 | chr1 | 11963064 | |||||||
chr1:11963161 | T | C | 10 | a0001c0002t0001g0015 a0001c0002t0001g0113 a0001c0002t0001g0118 others(7): Show |
11 | HG00597.hp2 HG02015.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.1098-371T>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 10/18 | chr1 | 11963161 | |||||||
chr1:11963302 | G | A | 2 | a0002c0015t0003g0297 a0003c0033t0003g0311 |
2 | HG01192.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1098-230G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 10/18 | chr1 | 11963302 | |||||||
chr1:11963771 | C | CTCCTCCT others(5): Show |
20 | a0001c0008t0002g0094 a0001c0008t0002g0095 a0001c0008t0002g0205 others(17): Show |
20 | HG01070.hp1 HG01891.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.1202+143_1202+154d others(14): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr1 | 11963771 | ||||||
chr1:11963871 | C | T | 2 | a0001c0027t0001g0220 a0001c0028t0001g0196 |
2 | HG02055.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1202+235C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 11/18 | chr1 | 11963871 | |||||||
chr1:11963886 | C | T | 1 | a0001c0028t0001g0196 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1202+250C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 11/18 | chr1 | 11963886 | |||||||
chr1:11963910 | G | A | 1 | a0001c0002t0001g0165 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1203-265G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 11/18 | chr1 | 11963910 | |||||||
chr1:11963981 | G | T | 20 | a0001c0008t0002g0094 a0001c0008t0002g0095 a0001c0008t0002g0205 others(17): Show |
20 | HG01070.hp1 HG01891.hp2 HG02083.hp1 others(17): Show |
intron_variant | MODIFIER | c.1203-194G>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 11/18 | chr1 | 11963981 | |||||||
chr1:11964001 | T | C | 16 | a0001c0001t0001g0110 a0001c0027t0001g0220 a0001c0028t0001g0196 others(13): Show |
17 | HG01243.hp1 HG02055.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1203-174T>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 11/18 | chr1 | 11964001 | |||||||
chr1:11964020 | C | A | 5 | a0002c0018t0001g0021 a0003c0005t0001g0229 a0003c0005t0001g0230 others(2): Show |
6 | HG02257.hp2 HG02559.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1203-155C>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 11/18 | chr1 | 11964020 | |||||||
chr1:11964021 | C | T | 1 | a0001c0013t0001g0150 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1203-154C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 11/18 | chr1 | 11964021 | |||||||
chr1:11964027 | C | T | 1 | a0003c0005t0001g0303 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1203-148C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 11/18 | chr1 | 11964027 | |||||||
chr1:11964378 | A | T | 2 | a0001c0001t0001g0045 a0001c0001t0001g0050 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1328+78A>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 12/18 | chr1 | 11964378 | |||||||
chr1:11964512 | G | A | 1 | a0001c0002t0001g0146 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1329-132G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 12/18 | chr1 | 11964512 | |||||||
chr1:11964550 | T | A | 50 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0080 others(47): Show |
53 | HG00408.hp2 HG00733.hp2 HG01106.hp1 others(50): Show |
intron_variant | MODIFIER | c.1329-94T>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 12/18 | chr1 | 11964550 | |||||||
chr1:11964624 | G | A | 10 | a0001c0001t0003g0302 a0002c0015t0003g0297 a0002c0015t0003g0314 others(7): Show |
10 | HG01192.hp2 HG01884.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.1329-20G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 12/18 | chr1 | 11964624 | |||||||
chr1:11964812 | C | T | 7 | a0001c0008t0002g0094 a0001c0008t0002g0095 a0001c0008t0002g0205 others(4): Show |
7 | HG02083.hp1 HG04228.hp2 NA18948.hp1 others(4): Show |
intron_variant | MODIFIER | c.1470+27C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 13/18 | chr1 | 11964812 | |||||||
chr1:11964866 | T | C | 73 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0080 others(70): Show |
75 | HG00408.hp2 HG00733.hp2 HG01070.hp1 others(72): Show |
intron_variant | MODIFIER | c.1470+81T>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 13/18 | chr1 | 11964866 | |||||||
chr1:11964981 | G | A | 1 | a0003c0033t0003g0311 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1470+196G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 13/18 | chr1 | 11964981 | |||||||
chr1:11965003 | G | C | 1 | a0001c0002t0001g0114 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1470+218G>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 13/18 | chr1 | 11965003 | |||||||
chr1:11965044 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1470+259G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 13/18 | chr1 | 11965044 | |||||||
chr1:11965046 | A | C | 15 | a0001c0012t0002g0064 a0001c0012t0002g0187 a0001c0012t0002g0213 others(12): Show |
15 | HG01070.hp1 HG01167.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.1470+261A>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 13/18 | chr1 | 11965046 | |||||||
chr1:11965053 | C | T | 1 | a0001c0013t0001g0147 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1470+268C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 13/18 | chr1 | 11965053 | |||||||
chr1:11965125 | C | T | 2 | a0002c0003t0001g0203 a0002c0003t0001g0237 |
2 | HG02055.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.1470+340C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 13/18 | chr1 | 11965125 | |||||||
chr1:11965150 | C | CT | 20 | a0001c0001t0001g0056 a0001c0002t0001g0189 a0001c0012t0002g0064 others(17): Show |
20 | HG01070.hp1 HG01167.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1471-315dupT | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr1 | 11965150 | ||||||
chr1:11965150 | CT | C | 6 | a0001c0001t0001g0025 a0001c0001t0001g0037 a0001c0002t0001g0107 others(3): Show |
6 | HG02896.hp2 NA18951.hp1 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.1471-315delT | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr1 | 11965150 | ||||||
chr1:11965220 | A | G | 8 | a0001c0008t0002g0094 a0001c0008t0002g0095 a0001c0008t0002g0163 others(5): Show |
8 | HG02083.hp1 HG04228.hp2 NA18948.hp1 others(5): Show |
intron_variant | MODIFIER | c.1471-260A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 13/18 | chr1 | 11965220 | |||||||
chr1:11965288 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1471-192C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 13/18 | chr1 | 11965288 | |||||||
chr1:11965296 | T | C | 240 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0077 others(237): Show |
258 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(255): Show |
intron_variant | MODIFIER | c.1471-184T>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 13/18 | chr1 | 11965296 | |||||||
chr1:11965344 | T | C | 8 | a0001c0008t0002g0094 a0001c0008t0002g0095 a0001c0008t0002g0163 others(5): Show |
8 | HG02083.hp1 HG04228.hp2 NA18948.hp1 others(5): Show |
intron_variant | MODIFIER | c.1471-136T>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 13/18 | chr1 | 11965344 | |||||||
chr1:11965359 | G | A | 7 | a0001c0026t0002g0298 a0004c0009t0002g0317 a0004c0009t0002g0318 others(4): Show |
7 | HG01167.hp2 HG02145.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1471-121G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 13/18 | chr1 | 11965359 | |||||||
chr1:11965400 | C | G | 1 | a0013c0020t0001g0090 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1471-80C>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 13/18 | chr1 | 11965400 | |||||||
chr1:11965423 | G | C | 1 | a0001c0006t0001g0300 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1471-57G>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 13/18 | chr1 | 11965423 | |||||||
chr1:11965633 | G | A | 1 | a0002c0003t0001g0310 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1584+40G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 14/18 | chr1 | 11965633 | |||||||
chr1:11965731 | G | C | 3 | a0001c0027t0001g0220 a0002c0014t0001g0105 a0002c0015t0001g0106 |
3 | HG02055.hp2 HG03139.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1584+138G>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 14/18 | chr1 | 11965731 | |||||||
chr1:11965788 | A | G | 1 | a0002c0003t0001g0313 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1584+195A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 14/18 | chr1 | 11965788 | |||||||
chr1:11965841 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1584+248A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 14/18 | chr1 | 11965841 | |||||||
chr1:11965982 | C | T | 2 | a0005c0023t0002g0324 a0008c0032t0002g0312 |
2 | HG01109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1585-269C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 14/18 | chr1 | 11965982 | |||||||
chr1:11966033 | A | G | 240 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0077 others(237): Show |
258 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(255): Show |
intron_variant | MODIFIER | c.1585-218A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 14/18 | chr1 | 11966033 | |||||||
chr1:11966137 | A | G | 1 | a0003c0005t0001g0093 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1585-114A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 14/18 | chr1 | 11966137 | |||||||
chr1:11966190 | T | A | 1 | a0009c0022t0001g0089 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1585-61T>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 14/18 | chr1 | 11966190 | |||||||
chr1:11966347 | C | A | 1 | a0003c0016t0001g0020 | 2 | HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1650+31C>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 15/18 | chr1 | 11966347 | |||||||
chr1:11966395 | G | A | 5 | a0001c0001t0001g0110 a0002c0003t0001g0287 a0004c0011t0001g0289 others(2): Show |
5 | HG02630.hp1 HG02895.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1650+79G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 15/18 | chr1 | 11966395 | |||||||
chr1:11966461 | G | A | 1 | a0001c0002t0001g0114 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1650+145G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 15/18 | chr1 | 11966461 | |||||||
chr1:11966486 | T | TG | 29 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(26): Show |
29 | HG00741.hp2 HG01109.hp2 HG01192.hp1 others(26): Show |
intron_variant | MODIFIER | c.1650+177dupG | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 11966486 | ||||||
chr1:11966508 | T | TG | 8 | a0001c0001t0001g0027 a0001c0001t0001g0038 a0001c0001t0001g0049 others(5): Show |
8 | HG00597.hp2 HG00741.hp1 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.1650+198dupG | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 11966508 | ||||||
chr1:11966529 | T | G | 1 | a0001c0001t0001g0038 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1650+213T>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 15/18 | chr1 | 11966529 | |||||||
chr1:11966887 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1651-100A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 15/18 | chr1 | 11966887 | |||||||
chr1:11967131 | G | A | 8 | a0001c0008t0002g0094 a0001c0008t0002g0095 a0001c0008t0002g0163 others(5): Show |
8 | HG02083.hp1 HG04228.hp2 NA18948.hp1 others(5): Show |
intron_variant | MODIFIER | c.1755+40G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11967131 | |||||||
chr1:11967147 | C | T | 203 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0077 others(200): Show |
221 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.1755+56C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11967147 | |||||||
chr1:11967148 | G | A | 3 | a0001c0001t0001g0044 a0005c0023t0002g0324 a0008c0032t0002g0312 |
3 | HG01109.hp2 HG02056.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1755+57G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11967148 | |||||||
chr1:11967154 | T | A | 8 | a0001c0008t0002g0094 a0001c0008t0002g0095 a0001c0008t0002g0163 others(5): Show |
8 | HG02083.hp1 HG04228.hp2 NA18948.hp1 others(5): Show |
intron_variant | MODIFIER | c.1755+63T>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11967154 | |||||||
chr1:11967197 | G | A | 2 | a0005c0023t0002g0324 a0008c0032t0002g0312 |
2 | HG01109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1755+106G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11967197 | |||||||
chr1:11967251 | G | A | 205 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0077 others(202): Show |
223 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.1755+160G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11967251 | |||||||
chr1:11967273 | G | A | 10 | a0002c0010t0001g0288 a0003c0005t0001g0070 a0003c0005t0001g0074 others(7): Show |
10 | HG01243.hp2 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1755+182G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11967273 | |||||||
chr1:11967311 | G | T | 1 | a0001c0002t0001g0193 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1755+220G>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11967311 | |||||||
chr1:11967402 | G | T | 3 | a0001c0008t0004g0065 a0002c0014t0004g0295 a0002c0014t0004g0296 |
3 | HG02970.hp2 HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1755+311G>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11967402 | |||||||
chr1:11967504 | G | A | 3 | a0004c0011t0001g0289 a0004c0011t0001g0290 a0004c0011t0001g0291 |
3 | HG02630.hp1 HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1755+413G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11967504 | |||||||
chr1:11967565 | A | AT | 7 | a0001c0002t0001g0016 a0001c0002t0001g0177 a0001c0002t0001g0178 others(4): Show |
8 | HG01109.hp2 HG02135.hp2 HG03486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1755+485dupT | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967565 | ||||||
chr1:11967565 | AT | A | 9 | a0001c0001t0001g0110 a0002c0003t0001g0192 a0002c0003t0001g0287 others(6): Show |
9 | HG02622.hp2 HG02630.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.1755+485delT | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967565 | ||||||
chr1:11967569 | T | G | 3 | a0001c0008t0004g0065 a0002c0014t0004g0295 a0002c0014t0004g0296 |
3 | HG02970.hp2 HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1755+478T>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11967569 | |||||||
chr1:11967577 | C | T | 3 | a0003c0005t0001g0011 a0003c0005t0001g0071 a0003c0005t0001g0228 |
4 | HG02280.hp2 HG02572.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1755+486C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11967577 | |||||||
chr1:11967583 | ATG | A | 4 | a0001c0008t0004g0065 a0002c0003t0001g0192 a0002c0014t0004g0295 others(1): Show |
4 | HG02970.hp2 HG03209.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1755+506_1755+507d others(4): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967583 | ||||||
chr1:11967593 | G | GTATATAT others(11): Show |
2 | a0004c0011t0001g0289 a0004c0011t0001g0290 |
2 | HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1755+503_1755+504i others(20): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967593 | ||||||
chr1:11967593 | G | GTATATAT others(13): Show |
1 | a0001c0001t0001g0110 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1755+503_1755+504i others(22): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967593 | ||||||
chr1:11967593 | G | GTATATAT others(75): Show |
1 | a0001c0026t0002g0298 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1755+503_1755+504i others(84): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967593 | ||||||
chr1:11967593 | GTGTGTA | G | 8 | a0001c0008t0002g0094 a0001c0008t0002g0095 a0001c0008t0002g0163 others(5): Show |
8 | HG02083.hp1 HG04228.hp2 NA18948.hp1 others(5): Show |
intron_variant | MODIFIER | c.1755+504_1755+509d others(8): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967593 | ||||||
chr1:11967595 | G | A | 14 | a0001c0001t0001g0110 a0001c0026t0002g0298 a0001c0027t0001g0220 others(11): Show |
14 | HG01109.hp2 HG01167.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.1755+504G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11967595 | |||||||
chr1:11967595 | G | GTA | 5 | a0003c0005t0001g0011 a0003c0005t0001g0071 a0003c0005t0001g0228 others(2): Show |
6 | HG02280.hp2 HG02572.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1755+505_1755+506i others(4): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967595 | ||||||
chr1:11967595 | G | GTATATA | 4 | a0002c0003t0001g0019 a0002c0003t0001g0294 a0002c0015t0001g0106 others(1): Show |
5 | HG01243.hp1 HG02615.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1755+505_1755+506i others(8): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967595 | ||||||
chr1:11967595 | G | GTATATAT others(1): Show |
13 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0080 others(10): Show |
13 | HG02572.hp2 HG02630.hp2 HG02647.hp1 others(10): Show |
intron_variant | MODIFIER | c.1755+505_1755+506i others(10): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967595 | ||||||
chr1:11967595 | G | GTATATAT others(3): Show |
5 | a0001c0006t0001g0108 a0001c0006t0001g0109 a0001c0006t0001g0211 others(2): Show |
5 | HG01884.hp1 HG02523.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1755+505_1755+506i others(12): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967595 | ||||||
chr1:11967595 | G | GTATATAT others(7): Show |
3 | a0001c0006t0001g0300 a0002c0003t0001g0264 a0013c0020t0001g0090 |
3 | HG01255.hp1 HG02109.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1755+505_1755+506i others(16): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967595 | ||||||
chr1:11967595 | G | GTATATAT others(9): Show |
1 | a0001c0002t0001g0155 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1755+505_1755+506i others(18): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967595 | ||||||
chr1:11967595 | G | GTATATAT others(13): Show |
1 | a0002c0003t0001g0279 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1755+505_1755+506i others(22): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967595 | ||||||
chr1:11967595 | G | GTATATAT others(15): Show |
7 | a0001c0006t0001g0162 a0002c0003t0001g0198 a0002c0003t0001g0199 others(4): Show |
7 | HG00408.hp1 HG00597.hp1 HG03669.hp1 others(4): Show |
intron_variant | MODIFIER | c.1755+505_1755+506i others(24): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967595 | ||||||
chr1:11967595 | G | GTATATAT others(17): Show |
10 | a0001c0013t0001g0117 a0002c0003t0001g0197 a0002c0003t0001g0202 others(7): Show |
10 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(7): Show |
intron_variant | MODIFIER | c.1755+505_1755+506i others(26): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967595 | ||||||
chr1:11967595 | G | GTATATAT others(19): Show |
10 | a0001c0001t0001g0001 a0001c0001t0001g0188 a0001c0006t0001g0140 others(7): Show |
10 | HG01069.hp1 HG01516.hp1 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.1755+505_1755+506i others(28): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967595 | ||||||
chr1:11967595 | G | GTATATAT others(21): Show |
11 | a0001c0002t0001g0001 a0001c0002t0001g0185 a0002c0003t0001g0096 others(8): Show |
12 | HG02015.hp1 HG02027.hp1 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.1755+505_1755+506i others(30): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967595 | ||||||
chr1:11967595 | G | GTATATAT others(23): Show |
6 | a0001c0002t0001g0007 a0002c0003t0001g0190 a0002c0003t0001g0259 others(3): Show |
6 | HG00280.hp1 HG00735.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.1755+505_1755+506i others(32): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967595 | ||||||
chr1:11967595 | G | GTATATAT others(25): Show |
4 | a0001c0002t0001g0001 a0002c0003t0001g0252 a0002c0003t0001g0255 others(1): Show |
4 | NA18960.hp2 NA19012.hp2 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.1755+505_1755+506i others(34): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967595 | ||||||
chr1:11967595 | G | GTATATAT others(27): Show |
3 | a0002c0003t0001g0266 a0002c0003t0001g0267 a0002c0010t0001g0292 |
3 | HG03486.hp1 NA18612.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.1755+505_1755+506i others(36): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967595 | ||||||
chr1:11967595 | G | GTATATAT others(31): Show |
2 | a0002c0003t0001g0268 a0002c0003t0001g0285 |
2 | HG03831.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.1755+505_1755+506i others(40): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967595 | ||||||
chr1:11967595 | G | GTATATAT others(33): Show |
1 | a0002c0003t0001g0258 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1755+505_1755+506i others(42): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967595 | ||||||
chr1:11967597 | G | A | 113 | a0001c0001t0001g0001 a0001c0001t0001g0077 a0001c0001t0001g0078 others(110): Show |
117 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.1755+506G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11967597 | |||||||
chr1:11967597 | G | GTATATAT others(3): Show |
1 | a0003c0005t0001g0325 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1755+515_1755+524d others(12): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967597 | ||||||
chr1:11967597 | G | GTATATAT others(28): Show |
1 | a0001c0002t0001g0179 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1755+520_1755+521i others(37): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967597 | ||||||
chr1:11967597 | G | GTATATAT others(17): Show |
1 | a0001c0002t0001g0161 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1755+524_1755+525i others(26): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967597 | ||||||
chr1:11967597 | G | GTATATAT others(13): Show |
2 | a0001c0002t0001g0151 a0001c0002t0001g0154 |
2 | HG01975.hp1 HG02074.hp2 |
intron_variant | MODIFIER | c.1755+524_1755+525i others(22): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967597 | ||||||
chr1:11967597 | G | GTATATAT others(15): Show |
12 | a0001c0002t0001g0001 a0001c0002t0001g0123 a0001c0002t0001g0128 others(9): Show |
14 | HG01069.hp2 HG01071.hp1 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.1755+524_1755+525i others(24): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967597 | ||||||
chr1:11967597 | G | GTATATAT others(17): Show |
15 | a0001c0002t0001g0007 a0001c0002t0001g0015 a0001c0002t0001g0016 others(12): Show |
15 | HG01934.hp1 HG02071.hp2 HG02273.hp1 others(12): Show |
intron_variant | MODIFIER | c.1755+524_1755+525i others(26): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967597 | ||||||
chr1:11967597 | G | GTATATAT others(19): Show |
20 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0022 others(17): Show |
20 | HG01496.hp1 HG01515.hp2 HG01517.hp1 others(17): Show |
intron_variant | MODIFIER | c.1755+524_1755+525i others(28): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967597 | ||||||
chr1:11967597 | G | GTATATAT others(21): Show |
18 | a0001c0001t0001g0054 a0001c0002t0001g0001 a0001c0002t0001g0013 others(15): Show |
19 | HG00735.hp2 HG01168.hp1 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.1755+524_1755+525i others(30): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967597 | ||||||
chr1:11967597 | G | GTATATAT others(23): Show |
8 | a0001c0002t0001g0001 a0001c0002t0001g0138 a0001c0002t0001g0204 others(5): Show |
8 | HG00609.hp2 HG01243.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.1755+524_1755+525i others(32): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967597 | ||||||
chr1:11967597 | G | GTATATAT others(25): Show |
3 | a0001c0002t0001g0016 a0001c0002t0001g0139 a0001c0002t0001g0165 |
3 | HG01928.hp1 HG04199.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1755+524_1755+525i others(34): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967597 | ||||||
chr1:11967597 | G | GTATATAT others(27): Show |
3 | a0001c0002t0001g0178 a0001c0006t0001g0224 a0002c0010t0001g0269 |
3 | NA19009.hp2 NA19065.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1755+524_1755+525i others(36): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967597 | ||||||
chr1:11967597 | G | GTATATAT others(29): Show |
2 | a0001c0002t0001g0180 a0003c0005t0001g0074 |
2 | HG02258.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1755+524_1755+525i others(38): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967597 | ||||||
chr1:11967597 | G | GTATATAT others(31): Show |
1 | a0001c0002t0001g0001 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1755+524_1755+525i others(40): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967597 | ||||||
chr1:11967597 | G | GTATGTAT others(17): Show |
1 | a0001c0002t0001g0143 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1755+509_1755+510i others(26): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967597 | ||||||
chr1:11967597 | G | GTGTATAT others(13): Show |
8 | a0002c0017t0001g0276 a0002c0017t0001g0278 a0003c0004t0001g0018 others(5): Show |
9 | HG00408.hp2 HG01106.hp1 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.1755+507_1755+508i others(22): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967597 | ||||||
chr1:11967597 | G | GTGTATAT others(15): Show |
4 | a0003c0004t0001g0135 a0003c0004t0001g0175 a0003c0004t0001g0176 others(1): Show |
4 | HG02040.hp2 HG02071.hp1 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.1755+507_1755+508i others(24): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967597 | ||||||
chr1:11967597 | G | GTGTATAT others(17): Show |
2 | a0003c0004t0001g0012 a0003c0004t0001g0134 |
2 | NA18985.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.1755+507_1755+508i others(26): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967597 | ||||||
chr1:11967597 | G | GTGTATAT others(19): Show |
1 | a0003c0004t0001g0248 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1755+507_1755+508i others(28): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967597 | ||||||
chr1:11967597 | G | GTGTATAT others(21): Show |
5 | a0001c0002t0001g0015 a0001c0002t0001g0152 a0003c0004t0001g0012 others(2): Show |
5 | NA18947.hp2 NA18962.hp2 NA19057.hp1 others(2): Show |
intron_variant | MODIFIER | c.1755+507_1755+508i others(30): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967597 | ||||||
chr1:11967597 | G | GTGTATAT others(23): Show |
3 | a0001c0002t0001g0173 a0003c0004t0001g0132 a0003c0016t0001g0309 |
3 | HG00597.hp2 HG02027.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.1755+507_1755+508i others(32): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967597 | ||||||
chr1:11967597 | G | GTGTGTAT others(13): Show |
2 | a0003c0004t0001g0242 a0003c0004t0001g0251 |
2 | HG02056.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1755+507_1755+508i others(22): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967597 | ||||||
chr1:11967597 | G | GTGTGTAT others(21): Show |
1 | a0001c0001t0003g0302 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1755+507_1755+508i others(30): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967597 | ||||||
chr1:11967597 | G | T | 1 | a0001c0026t0002g0298 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1755+506G>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11967597 | |||||||
chr1:11967599 | A | ATATATAT others(73): Show |
3 | a0004c0009t0002g0318 a0004c0009t0002g0319 a0004c0009t0002g0323 |
3 | HG02145.hp2 HG03540.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1755+522_1755+523i others(82): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967599 | ||||||
chr1:11967599 | A | ATATATAT others(75): Show |
2 | a0004c0009t0002g0317 a0004c0009t0002g0320 |
2 | HG02622.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1755+522_1755+523i others(84): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967599 | ||||||
chr1:11967599 | A | G | 2 | a0002c0010t0001g0288 a0003c0004t0001g0249 |
2 | HG00733.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1755+508A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11967599 | |||||||
chr1:11967601 | A | ATATATAT others(75): Show |
1 | a0002c0003t0001g0313 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1755+524_1755+525i others(84): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967601 | ||||||
chr1:11967610 | TATATAAA others(1): Show |
T | 3 | a0002c0003t0001g0097 a0002c0003t0001g0098 a0002c0003t0001g0099 |
3 | HG01934.hp2 NA18973.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1755+521_1755+528d others(10): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967610 | ||||||
chr1:11967615 | A | ATATATAT others(12): Show |
1 | a0003c0004t0001g0249 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1755+524_1755+525i others(21): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11967615 | |||||||
chr1:11967615 | A | ATATATAT others(18): Show |
1 | a0001c0002t0001g0129 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1755+524_1755+525i others(27): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11967615 | |||||||
chr1:11967615 | A | ATATATAT others(20): Show |
1 | a0001c0006t0001g0299 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1755+524_1755+525i others(29): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11967615 | |||||||
chr1:11967615 | A | ATATATAT others(22): Show |
2 | a0002c0010t0001g0288 a0011c0021t0001g0286 |
2 | HG04199.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1755+524_1755+525i others(31): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11967615 | |||||||
chr1:11967616 | A | AAGAAATA others(73): Show |
6 | a0001c0012t0002g0064 a0001c0012t0002g0187 a0001c0012t0002g0213 others(3): Show |
6 | HG01070.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1755+526_1755+527i others(82): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967616 | ||||||
chr1:11967616 | A | T | 220 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0077 others(217): Show |
238 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(235): Show |
intron_variant | MODIFIER | c.1755+525A>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11967616 | |||||||
chr1:11967617 | A | T | 5 | a0001c0002t0001g0129 a0001c0006t0001g0299 a0002c0010t0001g0288 others(2): Show |
5 | HG00733.hp2 HG04199.hp1 NA18984.hp2 others(2): Show |
intron_variant | MODIFIER | c.1755+526A>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11967617 | |||||||
chr1:11967640 | TTA | T | 16 | a0001c0001t0001g0110 a0002c0003t0001g0287 a0002c0010t0001g0288 others(13): Show |
16 | HG01109.hp2 HG01243.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.1755+567_1755+568d others(4): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967640 | ||||||
chr1:11967642 | A | ATATATAT others(34): Show |
1 | a0004c0011t0001g0291 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1755+568_1755+569i others(43): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967642 | ||||||
chr1:11967642 | A | T | 1 | a0001c0028t0001g0196 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1755+551A>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11967642 | |||||||
chr1:11967650 | A | G | 21 | a0002c0017t0001g0276 a0002c0017t0001g0278 a0003c0004t0001g0012 others(18): Show |
23 | HG00408.hp2 HG00733.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.1755+559A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11967650 | |||||||
chr1:11967656 | A | ATT | 3 | a0001c0012t0002g0187 a0001c0012t0002g0213 a0001c0012t0002g0214 |
3 | HG02109.hp2 HG02145.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1755+566_1755+567i others(4): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967656 | ||||||
chr1:11967656 | A | T | 15 | a0001c0001t0003g0302 a0001c0006t0001g0109 a0001c0006t0001g0299 others(12): Show |
15 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.1755+565A>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11967656 | |||||||
chr1:11967656 | ATATTT | A | 8 | a0001c0008t0002g0094 a0001c0008t0002g0095 a0001c0008t0002g0163 others(5): Show |
8 | HG02083.hp1 HG04228.hp2 NA18948.hp1 others(5): Show |
intron_variant | MODIFIER | c.1755+567_1755+571d others(7): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967656 | ||||||
chr1:11967658 | A | ATAT | 65 | a0001c0001t0001g0001 a0001c0002t0001g0001 a0001c0002t0001g0007 others(62): Show |
75 | HG00597.hp2 HG00609.hp2 HG00735.hp2 others(72): Show |
intron_variant | MODIFIER | c.1755+568_1755+569i others(5): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967658 | ||||||
chr1:11967658 | A | ATT | 8 | a0001c0012t0002g0064 a0001c0026t0002g0298 a0004c0009t0002g0091 others(5): Show |
8 | HG01070.hp1 HG01167.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1755+574_1755+575d others(4): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967658 | ||||||
chr1:11967658 | A | T | 187 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(184): Show |
214 | HG00280.hp1 HG00280.hp2 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.1755+567A>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11967658 | |||||||
chr1:11967659 | T | TATA | 6 | a0001c0001t0001g0188 a0001c0002t0001g0136 a0001c0002t0001g0141 others(3): Show |
6 | HG01496.hp1 HG02074.hp2 NA19063.hp1 others(3): Show |
intron_variant | MODIFIER | c.1755+568_1755+569i others(5): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11967659 | |||||||
chr1:11967739 | TTTAATTA others(1): Show |
T | 15 | a0001c0012t0002g0064 a0001c0012t0002g0187 a0001c0012t0002g0213 others(12): Show |
15 | HG01070.hp1 HG01109.hp2 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.1755+667_1755+674d others(10): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967739 | ||||||
chr1:11967774 | G | A | 2 | a0002c0015t0003g0297 a0003c0033t0003g0311 |
2 | HG01192.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.1755+683G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11967774 | |||||||
chr1:11967908 | C | A | 8 | a0001c0008t0002g0094 a0001c0008t0002g0095 a0001c0008t0002g0163 others(5): Show |
8 | HG02083.hp1 HG04228.hp2 NA18948.hp1 others(5): Show |
intron_variant | MODIFIER | c.1755+817C>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11967908 | |||||||
chr1:11967955 | A | AT | 21 | a0001c0001t0001g0049 a0001c0001t0001g0103 a0001c0002t0001g0161 others(18): Show |
21 | HG00735.hp1 HG01070.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.1755+880dupT | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967955 | ||||||
chr1:11967955 | AT | A | 31 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0080 others(28): Show |
31 | HG02083.hp1 HG02280.hp1 HG02572.hp2 others(28): Show |
intron_variant | MODIFIER | c.1755+880delT | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11967955 | ||||||
chr1:11968098 | C | T | 88 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0188 others(85): Show |
101 | HG00597.hp2 HG00609.hp2 HG00735.hp2 others(98): Show |
intron_variant | MODIFIER | c.1755+1007C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11968098 | |||||||
chr1:11968195 | C | T | 1 | a0002c0003t0001g0310 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1755+1104C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11968195 | |||||||
chr1:11968243 | C | T | 8 | a0001c0008t0002g0094 a0001c0008t0002g0095 a0001c0008t0002g0163 others(5): Show |
8 | HG02083.hp1 HG04228.hp2 NA18948.hp1 others(5): Show |
intron_variant | MODIFIER | c.1755+1152C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11968243 | |||||||
chr1:11968277 | A | AT | 6 | a0001c0001t0001g0083 a0001c0002t0001g0016 a0001c0002t0001g0177 others(3): Show |
7 | HG02135.hp2 HG02602.hp2 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.1755+1194dupT | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11968277 | ||||||
chr1:11968341 | CTTGAATA others(4): Show |
C | 1 | a0001c0001t0001g0038 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1755+1252_1755+126 others(15): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11968341 | ||||||
chr1:11968385 | C | G | 8 | a0001c0008t0002g0094 a0001c0008t0002g0095 a0001c0008t0002g0163 others(5): Show |
8 | HG02083.hp1 HG04228.hp2 NA18948.hp1 others(5): Show |
intron_variant | MODIFIER | c.1755+1294C>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11968385 | |||||||
chr1:11968479 | T | G | 8 | a0001c0008t0002g0094 a0001c0008t0002g0095 a0001c0008t0002g0163 others(5): Show |
8 | HG02083.hp1 HG04228.hp2 NA18948.hp1 others(5): Show |
intron_variant | MODIFIER | c.1755+1388T>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11968479 | |||||||
chr1:11968484 | T | C | 2 | a0001c0027t0001g0220 a0002c0014t0001g0105 |
2 | HG02055.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1755+1393T>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11968484 | |||||||
chr1:11968492 | C | G | 2 | a0001c0027t0001g0220 a0002c0014t0001g0105 |
2 | HG02055.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1755+1401C>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11968492 | |||||||
chr1:11968494 | A | C | 20 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0080 others(17): Show |
21 | HG02280.hp1 HG02280.hp2 HG02572.hp1 others(18): Show |
intron_variant | MODIFIER | c.1755+1403A>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11968494 | |||||||
chr1:11968598 | C | T | 203 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0077 others(200): Show |
221 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(218): Show |
intron_variant | MODIFIER | c.1755+1507C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11968598 | |||||||
chr1:11968639 | G | A | 2 | a0005c0023t0002g0324 a0008c0032t0002g0312 |
2 | HG01109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1755+1548G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11968639 | |||||||
chr1:11968839 | C | CT | 29 | a0001c0001t0001g0024 a0001c0001t0001g0031 a0001c0001t0001g0038 others(26): Show |
31 | HG00597.hp2 HG01175.hp1 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.1755+1765dupT | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11968839 | ||||||
chr1:11968839 | CT | C | 22 | a0001c0008t0002g0094 a0001c0008t0002g0095 a0001c0008t0002g0163 others(19): Show |
23 | HG01070.hp1 HG01167.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.1755+1765delT | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11968839 | ||||||
chr1:11968899 | T | G | 5 | a0001c0001t0001g0110 a0002c0003t0001g0287 a0004c0011t0001g0289 others(2): Show |
5 | HG02630.hp1 HG02895.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1756-1771T>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11968899 | |||||||
chr1:11969010 | A | C | 8 | a0001c0008t0002g0094 a0001c0008t0002g0095 a0001c0008t0002g0163 others(5): Show |
8 | HG02083.hp1 HG04228.hp2 NA18948.hp1 others(5): Show |
intron_variant | MODIFIER | c.1756-1660A>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11969010 | |||||||
chr1:11969020 | A | AT | 36 | a0001c0001t0001g0036 a0001c0001t0001g0049 a0001c0001t0001g0057 others(33): Show |
36 | HG00438.hp1 HG00597.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.1756-1628dupT | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11969020 | ||||||
chr1:11969020 | AT | A | 20 | a0001c0002t0001g0107 a0001c0002t0001g0137 a0001c0002t0001g0157 others(17): Show |
21 | HG01070.hp1 HG01167.hp2 HG02040.hp2 others(18): Show |
intron_variant | MODIFIER | c.1756-1628delT | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11969020 | ||||||
chr1:11969109 | G | GCCTCCTG others(28): Show |
8 | a0001c0008t0002g0094 a0001c0008t0002g0095 a0001c0008t0002g0163 others(5): Show |
8 | HG02083.hp1 HG04228.hp2 NA18948.hp1 others(5): Show |
intron_variant | MODIFIER | c.1756-1558_1756-155 others(39): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11969109 | ||||||
chr1:11969176 | CAG | C | 8 | a0001c0008t0002g0094 a0001c0008t0002g0095 a0001c0008t0002g0163 others(5): Show |
8 | HG02083.hp1 HG04228.hp2 NA18948.hp1 others(5): Show |
intron_variant | MODIFIER | c.1756-1493_1756-149 others(6): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11969176 | |||||||
chr1:11969185 | C | T | 5 | a0001c0002t0001g0016 a0001c0002t0001g0177 a0001c0002t0001g0178 others(2): Show |
6 | HG02135.hp2 NA18959.hp2 NA19005.hp2 others(3): Show |
intron_variant | MODIFIER | c.1756-1485C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11969185 | |||||||
chr1:11969188 | C | T | 8 | a0003c0004t0001g0012 a0003c0004t0001g0122 a0003c0004t0001g0132 others(5): Show |
9 | HG02027.hp2 HG02040.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.1756-1482C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11969188 | |||||||
chr1:11969195 | G | A | 5 | a0003c0005t0001g0011 a0003c0005t0001g0071 a0003c0005t0001g0228 others(2): Show |
6 | HG02280.hp2 HG02572.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1756-1475G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11969195 | |||||||
chr1:11969241 | G | A | 1 | a0003c0007t0001g0195 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1756-1429G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11969241 | |||||||
chr1:11969340 | G | A | 8 | a0001c0008t0002g0094 a0001c0008t0002g0095 a0001c0008t0002g0163 others(5): Show |
8 | HG02083.hp1 HG04228.hp2 NA18948.hp1 others(5): Show |
intron_variant | MODIFIER | c.1756-1330G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11969340 | |||||||
chr1:11969482 | C | T | 3 | a0001c0008t0004g0065 a0002c0014t0004g0295 a0002c0014t0004g0296 |
3 | HG02970.hp2 HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1756-1188C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11969482 | |||||||
chr1:11969610 | C | T | 13 | a0001c0012t0002g0064 a0001c0012t0002g0187 a0001c0012t0002g0213 others(10): Show |
13 | HG01070.hp1 HG01167.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1756-1060C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11969610 | |||||||
chr1:11969632 | T | C | 15 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0080 others(12): Show |
15 | HG02280.hp1 HG02572.hp2 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.1756-1038T>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11969632 | |||||||
chr1:11970052 | C | T | 12 | a0001c0012t0002g0064 a0001c0012t0002g0187 a0001c0012t0002g0213 others(9): Show |
12 | HG01070.hp1 HG01167.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1756-618C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11970052 | |||||||
chr1:11970058 | T | G | 1 | a0011c0021t0001g0286 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1756-612T>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11970058 | |||||||
chr1:11970066 | C | A | 2 | a0005c0023t0002g0324 a0008c0032t0002g0312 |
2 | HG01109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1756-604C>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11970066 | |||||||
chr1:11970086 | C | CA | 31 | a0001c0001t0001g0046 a0001c0001t0001g0049 a0001c0001t0001g0077 others(28): Show |
31 | HG01106.hp1 HG02083.hp1 HG02145.hp2 others(28): Show |
intron_variant | MODIFIER | c.1756-569dupA | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr1 | 11970086 | ||||||
chr1:11970119 | C | T | 3 | a0001c0008t0004g0065 a0002c0014t0004g0295 a0002c0014t0004g0296 |
3 | HG02970.hp2 HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1756-551C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11970119 | |||||||
chr1:11970207 | C | T | 1 | a0002c0003t0001g0281 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1756-463C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11970207 | |||||||
chr1:11970375 | G | C | 2 | a0003c0007t0003g0066 a0003c0007t0003g0067 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1756-295G>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11970375 | |||||||
chr1:11970390 | G | A | 205 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0077 others(202): Show |
223 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.1756-280G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11970390 | |||||||
chr1:11970595 | G | A | 3 | a0001c0008t0004g0065 a0002c0014t0004g0295 a0002c0014t0004g0296 |
3 | HG02970.hp2 HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1756-75G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 16/18 | chr1 | 11970595 | |||||||
chr1:11970829 | G | A | 1 | a0003c0016t0001g0020 | 2 | HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1902+13G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 17/18 | chr1 | 11970829 | |||||||
chr1:11970938 | A | G | 232 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0077 others(229): Show |
250 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(247): Show |
intron_variant | MODIFIER | c.1902+122A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 17/18 | chr1 | 11970938 | |||||||
chr1:11971117 | C | CG | 13 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0043 others(10): Show |
13 | HG00423.hp2 HG00438.hp2 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.1902+308dupG | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 11971117 | ||||||
chr1:11971123 | G | T | 10 | a0001c0001t0001g0047 a0001c0001t0001g0051 a0001c0008t0002g0094 others(7): Show |
10 | HG00621.hp1 HG02083.hp1 HG04228.hp2 others(7): Show |
intron_variant | MODIFIER | c.1902+307G>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 17/18 | chr1 | 11971123 | |||||||
chr1:11971154 | G | C | 2 | a0005c0023t0002g0324 a0008c0032t0002g0312 |
2 | HG01109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1902+338G>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 17/18 | chr1 | 11971154 | |||||||
chr1:11971176 | C | G | 8 | a0001c0008t0002g0094 a0001c0008t0002g0095 a0001c0008t0002g0163 others(5): Show |
8 | HG02083.hp1 HG04228.hp2 NA18948.hp1 others(5): Show |
intron_variant | MODIFIER | c.1902+360C>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 17/18 | chr1 | 11971176 | |||||||
chr1:11971228 | G | A | 1 | a0002c0014t0001g0105 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1902+412G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 17/18 | chr1 | 11971228 | |||||||
chr1:11971332 | C | A | 5 | a0003c0005t0001g0011 a0003c0005t0001g0071 a0003c0005t0001g0228 others(2): Show |
6 | HG02280.hp2 HG02572.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1902+516C>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 17/18 | chr1 | 11971332 | |||||||
chr1:11971371 | G | A | 15 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0080 others(12): Show |
15 | HG02280.hp1 HG02572.hp2 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.1902+555G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 17/18 | chr1 | 11971371 | |||||||
chr1:11971524 | T | C | 243 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0077 others(240): Show |
261 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(258): Show |
intron_variant | MODIFIER | c.1902+708T>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 17/18 | chr1 | 11971524 | |||||||
chr1:11971603 | A | G | 1 | a0001c0002t0001g0146 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1902+787A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 17/18 | chr1 | 11971603 | |||||||
chr1:11971610 | C | T | 3 | a0002c0018t0001g0021 a0003c0005t0001g0303 a0003c0016t0001g0020 |
4 | HG02559.hp2 HG02723.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1902+794C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 17/18 | chr1 | 11971610 | |||||||
chr1:11971611 | G | T | 2 | a0005c0023t0002g0324 a0008c0032t0002g0312 |
2 | HG01109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1902+795G>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 17/18 | chr1 | 11971611 | |||||||
chr1:11971616 | C | T | 1 | a0001c0002t0001g0114 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1902+800C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 17/18 | chr1 | 11971616 | |||||||
chr1:11971637 | G | C | 3 | a0001c0008t0004g0065 a0002c0014t0004g0295 a0002c0014t0004g0296 |
3 | HG02970.hp2 HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1902+821G>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 17/18 | chr1 | 11971637 | |||||||
chr1:11971667 | C | T | 1 | a0001c0028t0001g0196 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1902+851C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 17/18 | chr1 | 11971667 | |||||||
chr1:11971748 | C | T | 21 | a0002c0017t0001g0276 a0002c0017t0001g0278 a0003c0004t0001g0012 others(18): Show |
23 | HG00408.hp2 HG00733.hp2 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.1902+932C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 17/18 | chr1 | 11971748 | |||||||
chr1:11971771 | C | T | 1 | a0003c0016t0001g0020 | 2 | HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1902+955C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 17/18 | chr1 | 11971771 | |||||||
chr1:11971772 | G | A | 1 | a0002c0019t0002g0316 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1902+956G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 17/18 | chr1 | 11971772 | |||||||
chr1:11971809 | C | T | 205 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0077 others(202): Show |
223 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(220): Show |
intron_variant | MODIFIER | c.1902+993C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 17/18 | chr1 | 11971809 | |||||||
chr1:11971829 | C | T | 2 | a0005c0023t0002g0324 a0008c0032t0002g0312 |
2 | HG01109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1902+1013C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 17/18 | chr1 | 11971829 | |||||||
chr1:11971936 | C | T | 2 | a0005c0023t0002g0324 a0008c0032t0002g0312 |
2 | HG01109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1903-936C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 17/18 | chr1 | 11971936 | |||||||
chr1:11971973 | A | G | 206 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0077 others(203): Show |
224 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(221): Show |
intron_variant | MODIFIER | c.1903-899A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 17/18 | chr1 | 11971973 | |||||||
chr1:11972013 | AAGGTACT | A | 207 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0077 others(204): Show |
225 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(222): Show |
intron_variant | MODIFIER | c.1903-858_1903-852d others(9): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 17/18 | chr1 | 11972013 | |||||||
chr1:11972021 | T | G | 207 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0077 others(204): Show |
225 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(222): Show |
intron_variant | MODIFIER | c.1903-851T>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 17/18 | chr1 | 11972021 | |||||||
chr1:11972024 | T | C | 207 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0077 others(204): Show |
225 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(222): Show |
intron_variant | MODIFIER | c.1903-848T>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 17/18 | chr1 | 11972024 | |||||||
chr1:11972026 | CAAG | C | 207 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0077 others(204): Show |
225 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(222): Show |
intron_variant | MODIFIER | c.1903-844_1903-842d others(5): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 11972026 | ||||||
chr1:11972031 | C | G | 1 | a0001c0001t0001g0014 | 2 | NA18983.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.1903-841C>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 17/18 | chr1 | 11972031 | |||||||
chr1:11972205 | CCTTCCT | C | 9 | a0001c0001t0003g0302 a0002c0015t0003g0297 a0002c0015t0003g0314 others(6): Show |
9 | HG01192.hp2 HG01884.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.1903-664_1903-659d others(8): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 11972205 | ||||||
chr1:11972209 | C | CCT | 15 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0080 others(12): Show |
15 | HG02280.hp1 HG02572.hp2 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.1903-644_1903-643d others(4): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 11972209 | ||||||
chr1:11972209 | CCT | C | 182 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0054 others(179): Show |
200 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.1903-644_1903-643d others(4): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 11972209 | ||||||
chr1:11972209 | CCTCT | C | 8 | a0001c0008t0002g0094 a0001c0008t0002g0095 a0001c0008t0002g0163 others(5): Show |
8 | HG02083.hp1 HG04228.hp2 NA18948.hp1 others(5): Show |
intron_variant | MODIFIER | c.1903-646_1903-643d others(6): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 11972209 | ||||||
chr1:11972209 | CCTCTCT | C | 14 | a0001c0012t0002g0064 a0001c0012t0002g0187 a0001c0012t0002g0213 others(11): Show |
14 | HG01070.hp1 HG01109.hp2 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.1903-648_1903-643d others(8): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 11972209 | ||||||
chr1:11972216 | CTCTCTCT others(11): Show |
C | 1 | a0002c0003t0001g0313 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1903-644_1903-627d others(20): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 11972216 | ||||||
chr1:11972246 | T | G | 3 | a0001c0008t0004g0065 a0002c0014t0004g0295 a0002c0014t0004g0296 |
3 | HG02970.hp2 HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1903-626T>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 17/18 | chr1 | 11972246 | |||||||
chr1:11972258 | GTC | G | 3 | a0003c0005t0001g0011 a0003c0005t0001g0071 a0003c0005t0001g0228 |
4 | HG02280.hp2 HG02572.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1903-610_1903-609d others(4): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 11972258 | ||||||
chr1:11972305 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1903-567G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 17/18 | chr1 | 11972305 | |||||||
chr1:11972337 | C | T | 8 | a0001c0008t0002g0094 a0001c0008t0002g0095 a0001c0008t0002g0163 others(5): Show |
8 | HG02083.hp1 HG04228.hp2 NA18948.hp1 others(5): Show |
intron_variant | MODIFIER | c.1903-535C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 17/18 | chr1 | 11972337 | |||||||
chr1:11972338 | G | A | 48 | a0001c0002t0001g0155 a0001c0013t0001g0117 a0002c0003t0001g0096 others(45): Show |
48 | HG00280.hp1 HG00408.hp1 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.1903-534G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 17/18 | chr1 | 11972338 | |||||||
chr1:11972434 | G | A | 1 | a0002c0014t0001g0105 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1903-438G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 17/18 | chr1 | 11972434 | |||||||
chr1:11972537 | G | A | 2 | a0005c0023t0002g0324 a0008c0032t0002g0312 |
2 | HG01109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1903-335G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 17/18 | chr1 | 11972537 | |||||||
chr1:11972548 | G | A | 1 | a0001c0002t0001g0111 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1903-324G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 17/18 | chr1 | 11972548 | |||||||
chr1:11972597 | C | G | 12 | a0001c0012t0002g0064 a0001c0012t0002g0187 a0001c0012t0002g0213 others(9): Show |
12 | HG01070.hp1 HG01167.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1903-275C>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 17/18 | chr1 | 11972597 | |||||||
chr1:11972744 | T | C | 1 | a0001c0028t0001g0196 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1903-128T>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 17/18 | chr1 | 11972744 | |||||||
chr1:11972744 | T | G | 2 | a0001c0027t0001g0220 a0002c0014t0001g0105 |
2 | HG02055.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1903-128T>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 17/18 | chr1 | 11972744 | |||||||
chr1:11973056 | A | G | 237 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0077 others(234): Show |
255 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(252): Show |
intron_variant | MODIFIER | c.2028+59A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 18/18 | chr1 | 11973056 | |||||||
chr1:11973063 | G | C | 240 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0077 others(237): Show |
258 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(255): Show |
intron_variant | MODIFIER | c.2028+66G>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 18/18 | chr1 | 11973063 | |||||||
chr1:11973199 | C | T | 2 | a0002c0015t0003g0314 a0003c0007t0003g0215 |
2 | HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2028+202C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 18/18 | chr1 | 11973199 | |||||||
chr1:11973209 | A | C | 1 | a0001c0008t0002g0208 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2028+212A>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 18/18 | chr1 | 11973209 | |||||||
chr1:11973210 | G | T | 1 | a0001c0008t0002g0208 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2028+213G>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 18/18 | chr1 | 11973210 | |||||||
chr1:11973221 | T | A | 1 | a0001c0008t0002g0208 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2028+224T>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 18/18 | chr1 | 11973221 | |||||||
chr1:11973222 | C | A | 1 | a0001c0008t0002g0208 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2028+225C>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 18/18 | chr1 | 11973222 | |||||||
chr1:11973224 | G | A | 1 | a0001c0008t0002g0208 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2028+227G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 18/18 | chr1 | 11973224 | |||||||
chr1:11973225 | C | G | 1 | a0001c0008t0002g0208 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2028+228C>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 18/18 | chr1 | 11973225 | |||||||
chr1:11973247 | C | T | 1 | a0001c0008t0002g0208 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2028+250C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 18/18 | chr1 | 11973247 | |||||||
chr1:11973294 | G | GGAATCTT others(9): Show |
1 | a0001c0008t0002g0208 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2028+297_2028+298i others(18): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 18/18 | chr1 | 11973294 | |||||||
chr1:11973295 | T | G | 1 | a0001c0008t0002g0208 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2028+298T>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 18/18 | chr1 | 11973295 | |||||||
chr1:11973315 | C | T | 15 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0080 others(12): Show |
15 | HG02280.hp1 HG02572.hp2 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.2028+318C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 18/18 | chr1 | 11973315 | |||||||
chr1:11973355 | C | T | 1 | a0001c0008t0002g0208 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2028+358C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 18/18 | chr1 | 11973355 | |||||||
chr1:11973356 | T | C | 1 | a0001c0008t0002g0208 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2028+359T>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 18/18 | chr1 | 11973356 | |||||||
chr1:11973357 | G | T | 1 | a0001c0008t0002g0208 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2028+360G>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 18/18 | chr1 | 11973357 | |||||||
chr1:11973373 | A | G | 238 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0077 others(235): Show |
256 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(253): Show |
intron_variant | MODIFIER | c.2028+376A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 18/18 | chr1 | 11973373 | |||||||
chr1:11973454 | C | T | 1 | a0002c0003t0001g0202 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2028+457C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 18/18 | chr1 | 11973454 | |||||||
chr1:11973455 | A | G | 238 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0077 others(235): Show |
256 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(253): Show |
intron_variant | MODIFIER | c.2028+458A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 18/18 | chr1 | 11973455 | |||||||
chr1:11973487 | G | A | 2 | a0005c0023t0002g0324 a0008c0032t0002g0312 |
2 | HG01109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2028+490G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 18/18 | chr1 | 11973487 | |||||||
chr1:11973501 | A | G | 1 | a0001c0001t0001g0056 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2028+504A>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 18/18 | chr1 | 11973501 | |||||||
chr1:11973546 | G | A | 3 | a0001c0008t0004g0065 a0002c0014t0004g0295 a0002c0014t0004g0296 |
3 | HG02970.hp2 HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2028+549G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 18/18 | chr1 | 11973546 | |||||||
chr1:11973580 | C | CTTT | 11 | a0001c0012t0002g0064 a0001c0012t0002g0187 a0001c0012t0002g0213 others(8): Show |
11 | HG01070.hp1 HG01167.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.2028+591_2028+593d others(5): Show |
PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr1 | 11973580 | ||||||
chr1:11973591 | C | T | 27 | a0001c0008t0002g0094 a0001c0008t0002g0095 a0001c0008t0002g0163 others(24): Show |
27 | HG01070.hp1 HG01109.hp2 HG01167.hp2 others(24): Show |
intron_variant | MODIFIER | c.2028+594C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 18/18 | chr1 | 11973591 | |||||||
chr1:11973700 | C | T | 8 | a0001c0008t0002g0094 a0001c0008t0002g0095 a0001c0008t0002g0163 others(5): Show |
8 | HG02083.hp1 HG04228.hp2 NA18948.hp1 others(5): Show |
intron_variant | MODIFIER | c.2028+703C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 18/18 | chr1 | 11973700 | |||||||
chr1:11973851 | G | A | 232 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0077 others(229): Show |
250 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(247): Show |
intron_variant | MODIFIER | c.2029-802G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 18/18 | chr1 | 11973851 | |||||||
chr1:11973905 | G | A | 2 | a0005c0023t0002g0324 a0008c0032t0002g0312 |
2 | HG01109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2029-748G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 18/18 | chr1 | 11973905 | |||||||
chr1:11973927 | A | C | 12 | a0001c0012t0002g0064 a0001c0012t0002g0187 a0001c0012t0002g0213 others(9): Show |
12 | HG01070.hp1 HG01167.hp2 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.2029-726A>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 18/18 | chr1 | 11973927 | |||||||
chr1:11973977 | G | A | 1 | a0001c0006t0001g0224 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2029-676G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 18/18 | chr1 | 11973977 | |||||||
chr1:11974001 | G | C | 2 | a0001c0027t0001g0220 a0002c0014t0001g0105 |
2 | HG02055.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2029-652G>C | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 18/18 | chr1 | 11974001 | |||||||
chr1:11974034 | C | G | 1 | a0002c0010t0001g0257 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2029-619C>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 18/18 | chr1 | 11974034 | |||||||
chr1:11974167 | C | G | 2 | a0005c0023t0002g0324 a0008c0032t0002g0312 |
2 | HG01109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2029-486C>G | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 18/18 | chr1 | 11974167 | |||||||
chr1:11974201 | G | GT | 17 | a0001c0001t0001g0033 a0001c0001t0001g0056 a0001c0001t0001g0110 others(14): Show |
17 | HG01109.hp2 HG01192.hp2 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.2029-439dupT | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr1 | 11974201 | ||||||
chr1:11974201 | GT | G | 9 | a0001c0008t0002g0094 a0001c0008t0002g0095 a0001c0008t0002g0163 others(6): Show |
9 | HG02083.hp1 HG04228.hp2 NA18948.hp1 others(6): Show |
intron_variant | MODIFIER | c.2029-439delT | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr1 | 11974201 | ||||||
chr1:11974236 | C | T | 3 | a0001c0008t0004g0065 a0002c0014t0004g0295 a0002c0014t0004g0296 |
3 | HG02970.hp2 HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2029-417C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 18/18 | chr1 | 11974236 | |||||||
chr1:11974463 | G | A | 1 | a0001c0001t0001g0235 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2029-190G>A | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 18/18 | chr1 | 11974463 | |||||||
chr1:11974474 | C | T | 2 | a0001c0027t0001g0220 a0002c0014t0001g0105 |
2 | HG02055.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2029-179C>T | PLOD1 | ENSG00000083444.17 | transcript | ENST00000196061.5 | protein_coding | 18/18 | chr1 | 11974474 |