Item | Value |
---|---|
geneid | 27043 |
ensemblid | ENSG00000141456.16 |
hgncid | 30134 |
symbol | PELP1 |
name | proline, glutamate and leucine rich protein 1 |
refseq_nuc | NM_014389.3 |
refseq_prot | NP_055204.4 |
ensembl_nuc | ENST00000572293.7 |
ensembl_prot | ENSP00000460300.2 |
mane_status | MANE Select |
chr | chr17 |
start | 4669774 |
end | 4704137 |
strand | - |
ver | v1.2 |
region | chr17:4669774-4704137 |
region5000 | chr17:4664774-4709137 |
regionname0 | PELP1_chr17_4669774_4704137 |
regionname5000 | PELP1_chr17_4664774_4709137 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1130 | 271 | 81 | 50 | 101 | 5 | 32 | 74 | PELP1_chr17_4664774_4709137 | PELP1 | MAAAV others(1125): Show |
chr17 | 4664774 | 4709137 |
a0002 | 0/0 | 1130 | 15 | 1 | 5 | 1 | 3 | 5 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | MAAAV others(1125): Show |
chr17 | 4664774 | 4709137 |
a0003 | 0/0 | 1126 | 9 | 0 | 0 | 9 | 0 | 0 | 7 | PELP1_chr17_4664774_4709137 | PELP1 | MAAAV others(1121): Show |
chr17 | 4664774 | 4709137 |
a0004 | 0/0 | 1129 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | MAAAV others(1124): Show |
chr17 | 4664774 | 4709137 |
a0005 | 0/0 | 1130 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | MAAAV others(1125): Show |
chr17 | 4664774 | 4709137 |
a0006 | 0/0 | 1130 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | PELP1_chr17_4664774_4709137 | PELP1 | MAAAV others(1125): Show |
chr17 | 4664774 | 4709137 |
a0007 | 0/0 | 1130 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | MAAAV others(1125): Show |
chr17 | 4664774 | 4709137 |
a0008 | 0/0 | 1130 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | MAAAV others(1125): Show |
chr17 | 4664774 | 4709137 |
a0009 | 0/0 | 1130 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | MAAAV others(1125): Show |
chr17 | 4664774 | 4709137 |
a0010 | 0/0 | 1130 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | MAAAV others(1125): Show |
chr17 | 4664774 | 4709137 |
a0011 | 0/0 | 1130 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | MAAAV others(1125): Show |
chr17 | 4664774 | 4709137 |
a0012 | 0/0 | 1130 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | MAAAV others(1125): Show |
chr17 | 4664774 | 4709137 |
a0013 | 0/0 | 1130 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | MAAAV others(1125): Show |
chr17 | 4664774 | 4709137 |
a0014 | 0/0 | 1130 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | MAAAV others(1125): Show |
chr17 | 4664774 | 4709137 |
a0015 | 0/0 | 1130 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | MAAAV others(1125): Show |
chr17 | 4664774 | 4709137 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 3390 | 201 | 36 | 39 | 100 | 3 | 22 | PELP1_chr17_4664774_4709137 | PELP1 | ATGGC others(3385): Show |
chr17 | 4664774 | 4709137 | ||
a0001c0002 | 1/0 | 3390 | 33 | 31 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ATGGC others(3385): Show |
chr17 | 4664774 | 4709137 | ||
a0001c0004 | 0/0 | 3390 | 10 | 2 | 6 | 0 | 1 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | ATGGC others(3385): Show |
chr17 | 4664774 | 4709137 | ||
a0001c0006 | 0/0 | 3390 | 5 | 2 | 2 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | ATGGC others(3385): Show |
chr17 | 4664774 | 4709137 | ||
a0001c0007 | 0/0 | 3390 | 5 | 5 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ATGGC others(3385): Show |
chr17 | 4664774 | 4709137 | ||
a0001c0010 | 0/0 | 3390 | 3 | 0 | 0 | 0 | 0 | 3 | PELP1_chr17_4664774_4709137 | PELP1 | ATGGC others(3385): Show |
chr17 | 4664774 | 4709137 | ||
a0001c0013 | 0/0 | 3390 | 2 | 2 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ATGGC others(3385): Show |
chr17 | 4664774 | 4709137 | ||
a0001c0014 | 0/0 | 3390 | 2 | 0 | 0 | 0 | 0 | 2 | PELP1_chr17_4664774_4709137 | PELP1 | ATGGC others(3385): Show |
chr17 | 4664774 | 4709137 | ||
a0001c0015 | 0/0 | 3390 | 2 | 0 | 1 | 0 | 1 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ATGGC others(3385): Show |
chr17 | 4664774 | 4709137 | ||
a0001c0016 | 0/0 | 3390 | 2 | 0 | 0 | 0 | 0 | 2 | PELP1_chr17_4664774_4709137 | PELP1 | ATGGC others(3385): Show |
chr17 | 4664774 | 4709137 | ||
a0001c0023 | 0/0 | 3390 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ATGGC others(3385): Show |
chr17 | 4664774 | 4709137 | ||
a0001c0025 | 0/0 | 3390 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ATGGC others(3385): Show |
chr17 | 4664774 | 4709137 | ||
a0001c0028 | 0/0 | 3390 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | ATGGC others(3385): Show |
chr17 | 4664774 | 4709137 | ||
a0001c0029 | 0/0 | 3390 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ATGGC others(3385): Show |
chr17 | 4664774 | 4709137 | ||
a0001c0030 | 0/0 | 3390 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ATGGC others(3385): Show |
chr17 | 4664774 | 4709137 | ||
a0001c0032 | 0/0 | 3390 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ATGGC others(3385): Show |
chr17 | 4664774 | 4709137 | ||
a0002c0003 | 0/0 | 3390 | 14 | 1 | 4 | 1 | 3 | 5 | PELP1_chr17_4664774_4709137 | PELP1 | ATGGC others(3385): Show |
chr17 | 4664774 | 4709137 | ||
a0002c0022 | 0/0 | 3390 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ATGGC others(3385): Show |
chr17 | 4664774 | 4709137 | ||
a0003c0005 | 0/0 | 3378 | 9 | 0 | 0 | 9 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ATGGC others(3373): Show |
chr17 | 4664774 | 4709137 | ||
a0004c0009 | 0/0 | 3387 | 3 | 3 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ATGGC others(3382): Show |
chr17 | 4664774 | 4709137 | ||
a0004c0017 | 0/0 | 3387 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ATGGC others(3382): Show |
chr17 | 4664774 | 4709137 | ||
a0004c0018 | 0/0 | 3387 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ATGGC others(3382): Show |
chr17 | 4664774 | 4709137 | ||
a0005c0008 | 0/0 | 3390 | 3 | 3 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ATGGC others(3385): Show |
chr17 | 4664774 | 4709137 | ||
a0006c0011 | 0/0 | 3390 | 3 | 0 | 0 | 3 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ATGGC others(3385): Show |
chr17 | 4664774 | 4709137 | ||
a0007c0012 | 0/0 | 3390 | 2 | 0 | 0 | 0 | 0 | 2 | PELP1_chr17_4664774_4709137 | PELP1 | ATGGC others(3385): Show |
chr17 | 4664774 | 4709137 | ||
a0008c0031 | 0/0 | 3390 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ATGGC others(3385): Show |
chr17 | 4664774 | 4709137 | ||
a0009c0021 | 0/0 | 3390 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ATGGC others(3385): Show |
chr17 | 4664774 | 4709137 | ||
a0010c0033 | 0/0 | 3390 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ATGGC others(3385): Show |
chr17 | 4664774 | 4709137 | ||
a0011c0026 | 0/0 | 3390 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ATGGC others(3385): Show |
chr17 | 4664774 | 4709137 | ||
a0012c0020 | 0/0 | 3390 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | ATGGC others(3385): Show |
chr17 | 4664774 | 4709137 | ||
a0013c0027 | 0/0 | 3390 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ATGGC others(3385): Show |
chr17 | 4664774 | 4709137 | ||
a0014c0019 | 0/0 | 3390 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ATGGC others(3385): Show |
chr17 | 4664774 | 4709137 | ||
a0015c0024 | 0/0 | 3390 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ATGGC others(3385): Show |
chr17 | 4664774 | 4709137 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 5084 | 155 | 32 | 36 | 65 | 3 | 18 | PELP1_chr17_4664774_4709137 | PELP1 | ACGCC others(5079): Show |
chr17 | 4664774 | 4709137 |
a0001c0001t0002 | 0/0 | 5084 | 27 | 1 | 1 | 23 | 0 | 2 | PELP1_chr17_4664774_4709137 | PELP1 | ACGCC others(5079): Show |
chr17 | 4664774 | 4709137 |
a0001c0001t0007 | 0/0 | 5080 | 3 | 2 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ACGCC others(5075): Show |
chr17 | 4664774 | 4709137 |
a0001c0001t0009 | 0/0 | 5085 | 7 | 1 | 0 | 6 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ACGCC others(5080): Show |
chr17 | 4664774 | 4709137 |
a0001c0001t0010 | 0/0 | 5085 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ACGCC others(5080): Show |
chr17 | 4664774 | 4709137 |
a0001c0001t0012 | 0/0 | 5084 | 2 | 0 | 0 | 0 | 0 | 2 | PELP1_chr17_4664774_4709137 | PELP1 | ACGCC others(5079): Show |
chr17 | 4664774 | 4709137 |
a0001c0001t0013 | 0/0 | 5084 | 2 | 0 | 0 | 2 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ACGCC others(5079): Show |
chr17 | 4664774 | 4709137 |
a0001c0001t0014 | 0/0 | 5084 | 2 | 0 | 0 | 2 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ACGCC others(5079): Show |
chr17 | 4664774 | 4709137 |
a0001c0001t0020 | 0/0 | 5084 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ACGCC others(5079): Show |
chr17 | 4664774 | 4709137 |
a0001c0001t0021 | 0/0 | 5084 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ACGCC others(5079): Show |
chr17 | 4664774 | 4709137 |
a0001c0002t0005 | 1/0 | 5084 | 11 | 10 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ACGCC others(5079): Show |
chr17 | 4664774 | 4709137 |
a0001c0002t0006 | 0/0 | 5078 | 11 | 11 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ACGCC others(5073): Show |
chr17 | 4664774 | 4709137 |
a0001c0002t0007 | 0/0 | 5080 | 2 | 1 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ACGCC others(5075): Show |
chr17 | 4664774 | 4709137 |
a0001c0002t0008 | 0/0 | 5084 | 8 | 8 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ACGCC others(5079): Show |
chr17 | 4664774 | 4709137 |
a0001c0002t0017 | 0/0 | 5084 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ACGCC others(5079): Show |
chr17 | 4664774 | 4709137 |
a0001c0004t0004 | 0/0 | 5084 | 10 | 2 | 6 | 0 | 1 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | ACGCC others(5079): Show |
chr17 | 4664774 | 4709137 |
a0001c0006t0001 | 0/0 | 5084 | 5 | 2 | 2 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | ACGCC others(5079): Show |
chr17 | 4664774 | 4709137 |
a0001c0007t0011 | 0/0 | 5084 | 2 | 2 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ACGCC others(5079): Show |
chr17 | 4664774 | 4709137 |
a0001c0007t0016 | 0/0 | 5080 | 2 | 2 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ACGCC others(5075): Show |
chr17 | 4664774 | 4709137 |
a0001c0007t0019 | 0/0 | 5085 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ACGCC others(5080): Show |
chr17 | 4664774 | 4709137 |
a0001c0010t0001 | 0/0 | 5084 | 3 | 0 | 0 | 0 | 0 | 3 | PELP1_chr17_4664774_4709137 | PELP1 | ACGCC others(5079): Show |
chr17 | 4664774 | 4709137 |
a0001c0013t0015 | 0/0 | 5084 | 2 | 2 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ACGCC others(5079): Show |
chr17 | 4664774 | 4709137 |
a0001c0014t0001 | 0/0 | 5084 | 2 | 0 | 0 | 0 | 0 | 2 | PELP1_chr17_4664774_4709137 | PELP1 | ACGCC others(5079): Show |
chr17 | 4664774 | 4709137 |
a0001c0015t0001 | 0/0 | 5084 | 1 | 0 | 0 | 0 | 1 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ACGCC others(5079): Show |
chr17 | 4664774 | 4709137 |
a0001c0015t0018 | 0/0 | 5084 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ACGCC others(5079): Show |
chr17 | 4664774 | 4709137 |
a0001c0016t0001 | 0/0 | 5084 | 2 | 0 | 0 | 0 | 0 | 2 | PELP1_chr17_4664774_4709137 | PELP1 | ACGCC others(5079): Show |
chr17 | 4664774 | 4709137 |
a0001c0023t0005 | 0/0 | 5084 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ACGCC others(5079): Show |
chr17 | 4664774 | 4709137 |
a0001c0025t0007 | 0/0 | 5080 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ACGCC others(5075): Show |
chr17 | 4664774 | 4709137 |
a0001c0028t0001 | 0/0 | 5084 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | ACGCC others(5079): Show |
chr17 | 4664774 | 4709137 |
a0001c0029t0001 | 0/0 | 5084 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ACGCC others(5079): Show |
chr17 | 4664774 | 4709137 |
a0001c0030t0004 | 0/0 | 5084 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ACGCC others(5079): Show |
chr17 | 4664774 | 4709137 |
a0001c0032t0002 | 0/0 | 5084 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ACGCC others(5079): Show |
chr17 | 4664774 | 4709137 |
a0002c0003t0003 | 0/0 | 5084 | 14 | 1 | 4 | 1 | 3 | 5 | PELP1_chr17_4664774_4709137 | PELP1 | ACGCC others(5079): Show |
chr17 | 4664774 | 4709137 |
a0002c0022t0003 | 0/0 | 5084 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ACGCC others(5079): Show |
chr17 | 4664774 | 4709137 |
a0003c0005t0001 | 0/0 | 5072 | 9 | 0 | 0 | 9 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ACGCC others(5067): Show |
chr17 | 4664774 | 4709137 |
a0004c0009t0007 | 0/0 | 5077 | 3 | 3 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ACGCC others(5072): Show |
chr17 | 4664774 | 4709137 |
a0004c0017t0007 | 0/0 | 5077 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ACGCC others(5072): Show |
chr17 | 4664774 | 4709137 |
a0004c0018t0007 | 0/0 | 5077 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ACGCC others(5072): Show |
chr17 | 4664774 | 4709137 |
a0005c0008t0004 | 0/0 | 5084 | 3 | 3 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ACGCC others(5079): Show |
chr17 | 4664774 | 4709137 |
a0006c0011t0010 | 0/0 | 5085 | 3 | 0 | 0 | 3 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ACGCC others(5080): Show |
chr17 | 4664774 | 4709137 |
a0007c0012t0001 | 0/0 | 5084 | 2 | 0 | 0 | 0 | 0 | 2 | PELP1_chr17_4664774_4709137 | PELP1 | ACGCC others(5079): Show |
chr17 | 4664774 | 4709137 |
a0008c0031t0004 | 0/0 | 5084 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ACGCC others(5079): Show |
chr17 | 4664774 | 4709137 |
a0009c0021t0010 | 0/0 | 5085 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ACGCC others(5080): Show |
chr17 | 4664774 | 4709137 |
a0010c0033t0003 | 0/0 | 5084 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ACGCC others(5079): Show |
chr17 | 4664774 | 4709137 |
a0011c0026t0001 | 0/0 | 5084 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ACGCC others(5079): Show |
chr17 | 4664774 | 4709137 |
a0012c0020t0001 | 0/0 | 5084 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | ACGCC others(5079): Show |
chr17 | 4664774 | 4709137 |
a0013c0027t0002 | 0/0 | 5084 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ACGCC others(5079): Show |
chr17 | 4664774 | 4709137 |
a0014c0019t0001 | 0/0 | 5084 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ACGCC others(5079): Show |
chr17 | 4664774 | 4709137 |
a0015c0024t0002 | 0/0 | 5084 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | ACGCC others(5079): Show |
chr17 | 4664774 | 4709137 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 5 | 1 | 0 | 2 | 1 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0002 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0006 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0011 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0161 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0007g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0007g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0007g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0009g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0009g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0009g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0009g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0009g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0009g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0009g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0010g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0012g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0012g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0013g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0013g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0014g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0014g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0020g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0001t0021g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0002t0005g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0002t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0002t0005g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0002t0005g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0002t0005g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0002t0005g0038 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0002t0005g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0002t0005g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0002t0005g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0002t0006g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0002t0006g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0002t0006g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0002t0006g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0002t0006g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0002t0006g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0002t0006g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0002t0006g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0002t0006g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0002t0007g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0002t0007g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0002t0008g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0002t0008g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0002t0008g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0002t0008g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0002t0008g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0002t0008g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0002t0008g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0002t0008g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0002t0017g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0004t0004g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0004t0004g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0004t0004g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0004t0004g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0004t0004g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0004t0004g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0004t0004g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0004t0004g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0004t0004g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0004t0004g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0006t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0006t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0006t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0006t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0006t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0007t0011g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0007t0011g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0007t0016g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0007t0016g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0007t0019g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0010t0001g0013 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0010t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0013t0015g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0014t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0014t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0015t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0015t0018g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0016t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0016t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0023t0005g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0025t0007g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0028t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0029t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0030t0004g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0001c0032t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0002c0003t0003g0022 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0002c0003t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0002c0003t0003g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0002c0003t0003g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0002c0003t0003g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0002c0003t0003g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0002c0003t0003g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0002c0003t0003g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0002c0003t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0002c0003t0003g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0002c0003t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0002c0003t0003g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0002c0003t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0002c0022t0003g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0003c0005t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0003c0005t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0003c0005t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0003c0005t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0003c0005t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0003c0005t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0003c0005t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0003c0005t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0004c0009t0007g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0004c0009t0007g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0004c0009t0007g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0004c0017t0007g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0004c0018t0007g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0005c0008t0004g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0005c0008t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0005c0008t0004g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0006c0011t0010g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0006c0011t0010g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0006c0011t0010g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0007c0012t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0007c0012t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0008c0031t0004g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0009c0021t0010g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0010c0033t0003g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0011c0026t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0012c0020t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0013c0027t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0014c0019t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
a0015c0024t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0003 | t0003 | g0022 | EUR | GBR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0206 | EUR | GBR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG00140 | hp2 | a0001 | c0004 | t0004 | g0205 | EUR | GBR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | CHS | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | CHS | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG00423 | hp2 | a0003 | c0005 | t0001 | g0113 | EAS | CHS | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG00438 | hp2 | a0001 | c0001 | t0009 | g0028 | EAS | CHS | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | CHS | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG00597 | hp1 | a0001 | c0001 | t0009 | g0174 | EAS | CHS | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | CHS | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG00642 | hp1 | a0001 | c0004 | t0004 | g0040 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG00673 | hp1 | a0001 | c0001 | t0020 | g0149 | EAS | CHS | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG00735 | hp2 | a0001 | c0004 | t0004 | g0207 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG00741 | hp2 | a0008 | c0031 | t0004 | g0200 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG01070 | hp2 | a0001 | c0015 | t0018 | g0232 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG01099 | hp2 | a0001 | c0004 | t0004 | g0123 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG01106 | hp1 | a0001 | c0004 | t0004 | g0212 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG01109 | hp1 | a0002 | c0003 | t0003 | g0239 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG01109 | hp2 | a0001 | c0001 | t0007 | g0202 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG01167 | hp2 | a0001 | c0002 | t0007 | g0204 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG01168 | hp1 | a0001 | c0030 | t0004 | g0214 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG01175 | hp2 | a0002 | c0022 | t0003 | g0230 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG01243 | hp1 | a0001 | c0004 | t0004 | g0199 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG01256 | hp1 | a0002 | c0003 | t0003 | g0228 | AMR | CLM | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG01258 | hp2 | a0002 | c0003 | t0003 | g0227 | AMR | CLM | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG01261 | hp2 | a0002 | c0003 | t0003 | g0022 | AMR | CLM | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG01346 | hp1 | a0009 | c0021 | t0010 | g0173 | AMR | CLM | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG01361 | hp1 | a0001 | c0006 | t0001 | g0107 | AMR | CLM | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | CLM | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0283 | AMR | CLM | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG01515 | hp1 | a0001 | c0015 | t0001 | g0099 | EUR | IBS | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG01515 | hp2 | a0002 | c0003 | t0003 | g0226 | EUR | IBS | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG01517 | hp1 | a0002 | c0003 | t0003 | g0234 | EUR | IBS | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0182 | EUR | IBS | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG01884 | hp1 | a0001 | c0002 | t0006 | g0223 | AFR | ACB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG01884 | hp2 | a0001 | c0007 | t0016 | g0241 | AFR | ACB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | ACB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0246 | AMR | PEL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG01952 | hp1 | a0001 | c0004 | t0004 | g0211 | AMR | PEL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG01978 | hp2 | a0001 | c0006 | t0001 | g0097 | AMR | PEL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG01981 | hp2 | a0010 | c0033 | t0003 | g0284 | AMR | PEL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | KHV | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02055 | hp1 | a0001 | c0002 | t0008 | g0094 | AFR | ACB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0253 | EAS | KHV | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0262 | EAS | KHV | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02129 | hp2 | a0003 | c0005 | t0001 | g0018 | EAS | KHV | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02145 | hp1 | a0001 | c0002 | t0005 | g0037 | AFR | ACB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02145 | hp2 | a0001 | c0007 | t0011 | g0242 | AFR | ACB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02155 | hp1 | a0001 | c0001 | t0009 | g0160 | EAS | CDX | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0260 | EAS | CDX | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02257 | hp1 | a0001 | c0002 | t0006 | g0222 | AFR | ACB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02257 | hp2 | a0001 | c0002 | t0008 | g0087 | AFR | ACB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02258 | hp1 | a0004 | c0009 | t0007 | g0032 | AFR | ACB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02273 | hp2 | a0001 | c0001 | t0010 | g0058 | AMR | PEL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02280 | hp1 | a0005 | c0008 | t0004 | g0215 | AFR | ACB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02280 | hp2 | a0001 | c0002 | t0008 | g0091 | AFR | ACB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02451 | hp1 | a0001 | c0002 | t0005 | g0003 | AFR | ACB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02451 | hp2 | a0001 | c0002 | t0006 | g0220 | AFR | ACB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02523 | hp1 | a0002 | c0003 | t0003 | g0237 | EAS | KHV | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02572 | hp1 | a0001 | c0001 | t0007 | g0203 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02572 | hp2 | a0005 | c0008 | t0004 | g0209 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02602 | hp1 | a0002 | c0003 | t0003 | g0238 | SAS | PJL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02602 | hp2 | a0001 | c0016 | t0001 | g0169 | SAS | PJL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02615 | hp1 | a0001 | c0013 | t0015 | g0007 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02622 | hp2 | a0001 | c0001 | t0009 | g0082 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02630 | hp2 | a0001 | c0002 | t0006 | g0005 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02647 | hp2 | a0002 | c0003 | t0003 | g0235 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0183 | SAS | PJL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02717 | hp1 | a0001 | c0002 | t0006 | g0221 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0273 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02723 | hp2 | a0001 | c0002 | t0006 | g0081 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02738 | hp1 | a0001 | c0006 | t0001 | g0104 | SAS | PJL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02738 | hp2 | a0002 | c0003 | t0003 | g0229 | SAS | PJL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02809 | hp2 | a0004 | c0017 | t0007 | g0026 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02818 | hp1 | a0001 | c0002 | t0005 | g0036 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02886 | hp1 | a0001 | c0002 | t0008 | g0095 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02886 | hp2 | a0001 | c0002 | t0005 | g0225 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02895 | hp1 | a0001 | c0002 | t0005 | g0034 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02895 | hp2 | a0001 | c0002 | t0005 | g0224 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02896 | hp1 | a0001 | c0002 | t0017 | g0088 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02897 | hp2 | a0001 | c0002 | t0005 | g0035 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02922 | hp1 | a0001 | c0004 | t0004 | g0041 | AFR | ESN | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ESN | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | ESN | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | ESN | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | ESN | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02976 | hp1 | a0001 | c0002 | t0008 | g0093 | AFR | ESN | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02976 | hp2 | a0004 | c0009 | t0007 | g0031 | AFR | ESN | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG03017 | hp1 | a0001 | c0010 | t0001 | g0013 | SAS | PJL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG03041 | hp1 | a0001 | c0006 | t0001 | g0114 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG03041 | hp2 | a0004 | c0009 | t0007 | g0030 | AFR | GWD | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0275 | AFR | MSL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG03098 | hp2 | a0004 | c0018 | t0007 | g0027 | AFR | MSL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG03130 | hp1 | a0001 | c0002 | t0007 | g0042 | AFR | ESN | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG03139 | hp1 | a0005 | c0008 | t0004 | g0208 | AFR | ESN | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG03209 | hp1 | a0001 | c0002 | t0006 | g0005 | AFR | MSL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG03209 | hp2 | a0001 | c0002 | t0005 | g0003 | AFR | MSL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | MSL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG03225 | hp2 | a0001 | c0002 | t0005 | g0039 | AFR | MSL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG03453 | hp1 | a0001 | c0002 | t0005 | g0003 | AFR | MSL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | MSL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG03486 | hp1 | a0001 | c0023 | t0005 | g0089 | AFR | MSL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG03490 | hp1 | a0002 | c0003 | t0003 | g0233 | SAS | PJL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG03490 | hp2 | a0001 | c0001 | t0012 | g0175 | SAS | PJL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG03491 | hp1 | a0007 | c0012 | t0001 | g0024 | SAS | PJL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG03492 | hp1 | a0007 | c0012 | t0001 | g0025 | SAS | PJL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG03492 | hp2 | a0001 | c0001 | t0012 | g0151 | SAS | PJL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG03516 | hp1 | a0001 | c0002 | t0006 | g0216 | AFR | ESN | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | ESN | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG03579 | hp1 | a0001 | c0002 | t0008 | g0092 | AFR | MSL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG03579 | hp2 | a0001 | c0002 | t0006 | g0219 | AFR | MSL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG03654 | hp1 | a0001 | c0014 | t0001 | g0217 | SAS | PJL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG03654 | hp2 | a0001 | c0010 | t0001 | g0013 | SAS | PJL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG03669 | hp1 | a0012 | c0020 | t0001 | g0144 | SAS | PJL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | STU | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | STU | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG03704 | hp2 | a0001 | c0004 | t0004 | g0210 | SAS | PJL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | BEB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG03831 | hp2 | a0002 | c0003 | t0003 | g0236 | SAS | BEB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | BEB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | BEB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | BEB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG03927 | hp2 | a0002 | c0003 | t0003 | g0231 | SAS | BEB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | BEB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG03942 | hp2 | a0001 | c0028 | t0001 | g0186 | SAS | BEB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG04204 | hp1 | a0001 | c0014 | t0001 | g0218 | SAS | STU | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | STU | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0163 | SAS | STU | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG04228 | hp2 | a0001 | c0010 | t0001 | g0070 | SAS | STU | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA18522 | hp1 | a0001 | c0002 | t0008 | g0086 | AFR | YRI | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA18522 | hp2 | a0001 | c0007 | t0019 | g0240 | AFR | YRI | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | CHB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | CHB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA18906 | hp2 | a0001 | c0013 | t0015 | g0007 | AFR | YRI | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA18946 | hp2 | a0006 | c0011 | t0010 | g0059 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA18979 | hp1 | a0003 | c0005 | t0001 | g0179 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA18981 | hp2 | a0003 | c0005 | t0001 | g0155 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA18983 | hp1 | a0001 | c0001 | t0009 | g0180 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA18985 | hp1 | a0006 | c0011 | t0010 | g0057 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA18990 | hp1 | a0003 | c0005 | t0001 | g0018 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA18991 | hp2 | a0003 | c0005 | t0001 | g0166 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA18993 | hp1 | a0001 | c0001 | t0009 | g0029 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA18993 | hp2 | a0006 | c0011 | t0010 | g0056 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA18995 | hp1 | a0001 | c0001 | t0009 | g0157 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA19003 | hp2 | a0001 | c0001 | t0013 | g0134 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA19006 | hp1 | a0013 | c0027 | t0002 | g0254 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA19006 | hp2 | a0014 | c0019 | t0001 | g0067 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA19011 | hp1 | a0001 | c0032 | t0002 | g0266 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA19043 | hp1 | a0015 | c0024 | t0002 | g0258 | AFR | LWK | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA19043 | hp2 | a0001 | c0001 | t0007 | g0213 | AFR | LWK | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA19064 | hp1 | a0001 | c0001 | t0014 | g0044 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA19070 | hp2 | a0001 | c0001 | t0021 | g0118 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA19082 | hp2 | a0001 | c0001 | t0013 | g0103 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA19083 | hp2 | a0003 | c0005 | t0001 | g0188 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA19085 | hp2 | a0001 | c0001 | t0014 | g0047 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA19089 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA19090 | hp1 | a0003 | c0005 | t0001 | g0185 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | YRI | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA19240 | hp2 | a0001 | c0029 | t0001 | g0140 | AFR | YRI | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA20129 | hp2 | a0001 | c0002 | t0006 | g0083 | AFR | ASW | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA20905 | hp1 | a0001 | c0016 | t0001 | g0168 | SAS | GIH | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | GIH | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02486 | hp1 | a0001 | c0002 | t0008 | g0090 | AFR | ACB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | ACB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | ACB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG02559 | hp2 | a0011 | c0026 | t0001 | g0098 | AFR | ACB | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG03471 | hp1 | a0001 | c0002 | t0006 | g0005 | AFR | MSL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG06807 | hp1 | a0001 | c0025 | t0007 | g0146 | AFR | USA | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
HG06807 | hp2 | a0001 | c0007 | t0016 | g0274 | AFR | USA | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA18955 | hp2 | a0003 | c0005 | t0001 | g0172 | EAS | JPT | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA20300 | hp1 | a0001 | c0007 | t0011 | g0243 | AFR | USA | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA20300 | hp2 | a0001 | c0006 | t0001 | g0105 | AFR | USA | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | LWK | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
NA21309 | hp2 | a0001 | c0004 | t0004 | g0201 | AFR | LWK | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0161 | REF | REF | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
homoSapiens | grch38p0 | a0001 | c0002 | t0005 | g0038 | REF | REF | PELP1_chr17_4664774_4709137 | PELP1 | chr17 | 4664774 | 4709137 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:4671456 | T | A | 2 | a0002 a0010 |
16 | HG00099.hp1 HG01109.hp1 HG01175.hp2 others(13): Show |
missense_variant | MODERATE | c.3376A>T | p.Thr1126Ser | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 3402/5084 | 3376/3393 | 1126/1130 | chr17 | 4671456 | |||
chr17:4672027 | GGGAGGCA others(5): Show |
G | 1 | a0003 | 9 | HG00423.hp2 HG02129.hp2 NA18955.hp2 others(6): Show |
disruptive_inframe_deletion | MODERATE | c.2952_2963delAGCTCT others(6): Show |
p.Ala985_Pro988del | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 16/17 | 2989/5084 | 2952/3393 | 984/1130 | chr17 | 4672027 | |||
chr17:4672141 | ATCC | A | 1 | a0004 | 5 | HG02258.hp1 HG02809.hp2 HG02976.hp2 others(2): Show |
disruptive_inframe_deletion | MODERATE | c.2847_2849delGGA | p.Glu949del | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 16/17 | 2875/5084 | 2847/3393 | 949/1130 | chr17 | 4672141 | |||
chr17:4672422 | G | A | 1 | a0015 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.2569C>T | p.Pro857Ser | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 16/17 | 2595/5084 | 2569/3393 | 857/1130 | chr17 | 4672422 | |||
chr17:4672463 | G | T | 1 | a0013 | 1 | NA19006.hp1 | missense_variant | MODERATE | c.2528C>A | p.Pro843Gln | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 16/17 | 2554/5084 | 2528/3393 | 843/1130 | chr17 | 4672463 | |||
chr17:4672487 | G | C | 1 | a0013 | 1 | NA19006.hp1 | missense_variant | MODERATE | c.2504C>G | p.Ala835Gly | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 16/17 | 2530/5084 | 2504/3393 | 835/1130 | chr17 | 4672487 | |||
chr17:4672488 | C | A | 1 | a0013 | 1 | NA19006.hp1 | missense_variant | MODERATE | c.2503G>T | p.Ala835Ser | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 16/17 | 2529/5084 | 2503/3393 | 835/1130 | chr17 | 4672488 | |||
chr17:4672491 | C | T | 1 | a0009 | 1 | HG01346.hp1 | missense_variant | MODERATE | c.2500G>A | p.Ala834Thr | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 16/17 | 2526/5084 | 2500/3393 | 834/1130 | chr17 | 4672491 | |||
chr17:4672799 | C | T | 1 | a0012 | 1 | HG03669.hp1 | missense_variant | MODERATE | c.2192G>A | p.Arg731Gln | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 16/17 | 2218/5084 | 2192/3393 | 731/1130 | chr17 | 4672799 | |||
chr17:4673000 | G | A | 1 | a0011 | 1 | HG02559.hp2 | missense_variant | MODERATE | c.1991C>T | p.Pro664Leu | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 16/17 | 2017/5084 | 1991/3393 | 664/1130 | chr17 | 4673000 | |||
chr17:4673250 | C | A | 1 | a0014 | 1 | NA19006.hp2 | missense_variant&splice_region_variant | MODERATE | c.1845G>T | p.Glu615Asp | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 15/17 | 1871/5084 | 1845/3393 | 615/1130 | chr17 | 4673250 | |||
chr17:4674659 | G | A | 1 | a0006 | 3 | NA18946.hp2 NA18985.hp1 NA18993.hp2 |
missense_variant | MODERATE | c.1433C>T | p.Pro478Leu | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 13/17 | 1459/5084 | 1433/3393 | 478/1130 | chr17 | 4674659 | |||
chr17:4675274 | G | A | 1 | a0008 | 1 | HG00741.hp2 | missense_variant&splice_region_variant | MODERATE | c.1157C>T | p.Ala386Val | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 10/17 | 1183/5084 | 1157/3393 | 386/1130 | chr17 | 4675274 | |||
chr17:4676389 | A | C | 1 | a0014 | 1 | NA19006.hp2 | missense_variant | MODERATE | c.821T>G | p.Leu274Arg | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 7/17 | 847/5084 | 821/3393 | 274/1130 | chr17 | 4676389 | |||
chr17:4676405 | C | T | 1 | a0005 | 3 | HG02280.hp1 HG02572.hp2 HG03139.hp1 |
missense_variant | MODERATE | c.805G>A | p.Ala269Thr | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 7/17 | 831/5084 | 805/3393 | 269/1130 | chr17 | 4676405 | |||
chr17:4676462 | A | T | 1 | a0014 | 1 | NA19006.hp2 | missense_variant | MODERATE | c.748T>A | p.Phe250Ile | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 7/17 | 774/5084 | 748/3393 | 250/1130 | chr17 | 4676462 | |||
chr17:4703943 | G | C | 1 | a0010 | 1 | HG01981.hp2 | missense_variant | MODERATE | c.169C>G | p.His57Asp | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/17 | 195/5084 | 169/3393 | 57/1130 | chr17 | 4703943 | |||
chr17:4704077 | C | G | 1 | a0007 | 2 | HG03491.hp1 HG03492.hp1 |
missense_variant | MODERATE | c.35G>C | p.Gly12Ala | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/17 | 61/5084 | 35/3393 | 12/1130 | chr17 | 4704077 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:4671844 | A | T | 1 | a0001c0023 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.3147T>A | p.Pro1049Pro | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 16/17 | 3173/5084 | 3147/3393 | 1049/1130 | chr17 | 4671844 | |||
chr17:4671988 | A | G | 22 | a0001c0001 a0001c0006 a0001c0010 others(19): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
synonymous_variant | LOW | c.3003T>C | p.Pro1001Pro | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 16/17 | 3029/5084 | 3003/3393 | 1001/1130 | chr17 | 4671988 | |||
chr17:4672396 | A | T | 1 | a0013c0027 | 1 | NA19006.hp1 | synonymous_variant | LOW | c.2595T>A | p.Thr865Thr | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 16/17 | 2621/5084 | 2595/3393 | 865/1130 | chr17 | 4672396 | |||
chr17:4672450 | C | T | 1 | a0001c0016 | 2 | HG02602.hp2 NA20905.hp1 |
synonymous_variant | LOW | c.2541G>A | p.Pro847Pro | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 16/17 | 2567/5084 | 2541/3393 | 847/1130 | chr17 | 4672450 | |||
chr17:4672615 | G | A | 1 | a0001c0013 | 2 | HG02615.hp1 NA18906.hp2 |
synonymous_variant | LOW | c.2376C>T | p.Pro792Pro | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 16/17 | 2402/5084 | 2376/3393 | 792/1130 | chr17 | 4672615 | |||
chr17:4672864 | T | A | 1 | a0013c0027 | 1 | NA19006.hp1 | synonymous_variant | LOW | c.2127A>T | p.Leu709Leu | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 16/17 | 2153/5084 | 2127/3393 | 709/1130 | chr17 | 4672864 | |||
chr17:4672894 | G | A | 1 | a0001c0025 | 1 | HG06807.hp1 | synonymous_variant | LOW | c.2097C>T | p.Arg699Arg | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 16/17 | 2123/5084 | 2097/3393 | 699/1130 | chr17 | 4672894 | |||
chr17:4672921 | G | A | 1 | a0001c0010 | 3 | HG03017.hp1 HG03654.hp2 HG04228.hp2 |
synonymous_variant | LOW | c.2070C>T | p.Pro690Pro | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 16/17 | 2096/5084 | 2070/3393 | 690/1130 | chr17 | 4672921 | |||
chr17:4673325 | C | T | 3 | a0001c0013 a0002c0003 a0010c0033 |
17 | HG00099.hp1 HG01109.hp1 HG01256.hp1 others(14): Show |
synonymous_variant | LOW | c.1770G>A | p.Pro590Pro | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 15/17 | 1796/5084 | 1770/3393 | 590/1130 | chr17 | 4673325 | |||
chr17:4673376 | G | C | 1 | a0013c0027 | 1 | NA19006.hp1 | synonymous_variant | LOW | c.1719C>G | p.Ser573Ser | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 15/17 | 1745/5084 | 1719/3393 | 573/1130 | chr17 | 4673376 | |||
chr17:4674532 | G | A | 1 | a0001c0028 | 1 | HG03942.hp2 | synonymous_variant | LOW | c.1560C>T | p.Asp520Asp | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 13/17 | 1586/5084 | 1560/3393 | 520/1130 | chr17 | 4674532 | |||
chr17:4674589 | C | G | 1 | a0001c0015 | 2 | HG01070.hp2 HG01515.hp1 |
synonymous_variant | LOW | c.1503G>C | p.Val501Val | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 13/17 | 1529/5084 | 1503/3393 | 501/1130 | chr17 | 4674589 | |||
chr17:4674655 | C | A | 4 | a0001c0004 a0001c0030 a0005c0008 others(1): Show |
15 | HG00140.hp2 HG00642.hp1 HG00735.hp2 others(12): Show |
synonymous_variant | LOW | c.1437G>T | p.Arg479Arg | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 13/17 | 1463/5084 | 1437/3393 | 479/1130 | chr17 | 4674655 | |||
chr17:4674839 | G | A | 1 | a0001c0029 | 1 | NA19240.hp2 | synonymous_variant | LOW | c.1392C>T | p.Ser464Ser | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 12/17 | 1418/5084 | 1392/3393 | 464/1130 | chr17 | 4674839 | |||
chr17:4682526 | G | A | 1 | a0001c0006 | 5 | HG01361.hp1 HG01978.hp2 HG02738.hp1 others(2): Show |
synonymous_variant | LOW | c.618C>T | p.Phe206Phe | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/17 | 644/5084 | 618/3393 | 206/1130 | chr17 | 4682526 | |||
chr17:4682925 | G | A | 1 | a0001c0007 | 5 | HG01884.hp2 HG02145.hp2 HG06807.hp2 others(2): Show |
synonymous_variant | LOW | c.448C>T | p.Leu150Leu | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 4/17 | 474/5084 | 448/3393 | 150/1130 | chr17 | 4682925 | |||
chr17:4682950 | G | C | 2 | a0001c0030 a0008c0031 |
2 | HG00741.hp2 HG01168.hp1 |
splice_region_variant&synonymous_variant | LOW | c.423C>G | p.Thr141Thr | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 4/17 | 449/5084 | 423/3393 | 141/1130 | chr17 | 4682950 | |||
chr17:4690933 | C | T | 1 | a0001c0014 | 2 | HG03654.hp1 HG04204.hp1 |
synonymous_variant | LOW | c.375G>A | p.Gln125Gln | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/17 | 401/5084 | 375/3393 | 125/1130 | chr17 | 4690933 | |||
chr17:4691422 | T | C | 1 | a0001c0032 | 1 | NA19011.hp1 | synonymous_variant | LOW | c.270A>G | p.Ala90Ala | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 2/17 | 296/5084 | 270/3393 | 90/1130 | chr17 | 4691422 | |||
chr17:4703995 | C | T | 1 | a0004c0018 | 1 | HG03098.hp2 | synonymous_variant | LOW | c.117G>A | p.Glu39Glu | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/17 | 143/5084 | 117/3393 | 39/1130 | chr17 | 4703995 | |||
chr17:4704055 | G | T | 2 | a0001c0013 a0004c0017 |
3 | HG02615.hp1 HG02809.hp2 NA18906.hp2 |
synonymous_variant | LOW | c.57C>A | p.Gly19Gly | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/17 | 83/5084 | 57/3393 | 19/1130 | chr17 | 4704055 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:4669779 | GAATT | G | 8 | a0001c0001t0007 a0001c0002t0006 a0001c0002t0007 others(5): Show |
24 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1656_*1659delAATT | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 1656 | chr17 | 4669779 | ||||||
chr17:4669840 | T | G | 2 | a0001c0002t0008 a0001c0002t0017 |
9 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1599A>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 1599 | chr17 | 4669840 | ||||||
chr17:4669884 | G | A | 27 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0009 others(24): Show |
234 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(231): Show |
3_prime_UTR_variant | MODIFIER | c.*1555C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 1555 | chr17 | 4669884 | ||||||
chr17:4669986 | GTA | G | 1 | a0001c0002t0006 | 11 | HG01884.hp1 HG02257.hp1 HG02451.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1451_*1452delTA | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 1451 | chr17 | 4669986 | ||||||
chr17:4670004 | T | C | 1 | a0001c0001t0014 | 2 | NA19064.hp1 NA19085.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1435A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 1435 | chr17 | 4670004 | ||||||
chr17:4670041 | C | T | 1 | a0001c0001t0013 | 2 | NA19003.hp2 NA19082.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1398G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 1398 | chr17 | 4670041 | ||||||
chr17:4670112 | T | C | 3 | a0002c0003t0003 a0002c0022t0003 a0010c0033t0003 |
16 | HG00099.hp1 HG01109.hp1 HG01175.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1327A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 1327 | chr17 | 4670112 | ||||||
chr17:4670113 | A | G | 1 | a0001c0001t0021 | 1 | NA19070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1326T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 1326 | chr17 | 4670113 | ||||||
chr17:4670119 | C | G | 27 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0009 others(24): Show |
234 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(231): Show |
3_prime_UTR_variant | MODIFIER | c.*1320G>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 1320 | chr17 | 4670119 | ||||||
chr17:4670248 | T | C | 4 | a0001c0001t0002 a0001c0032t0002 a0013c0027t0002 others(1): Show |
30 | HG00544.hp2 HG01943.hp1 HG02027.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1191A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 1191 | chr17 | 4670248 | ||||||
chr17:4670264 | C | T | 1 | a0001c0001t0020 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1175G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 1175 | chr17 | 4670264 | ||||||
chr17:4670281 | C | T | 1 | a0001c0001t0012 | 2 | HG03490.hp2 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1158G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 1158 | chr17 | 4670281 | ||||||
chr17:4670316 | C | T | 27 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0009 others(24): Show |
234 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(231): Show |
3_prime_UTR_variant | MODIFIER | c.*1123G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 1123 | chr17 | 4670316 | ||||||
chr17:4670317 | G | A | 4 | a0001c0013t0015 a0002c0003t0003 a0002c0022t0003 others(1): Show |
18 | HG00099.hp1 HG01109.hp1 HG01175.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1122C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 1122 | chr17 | 4670317 | ||||||
chr17:4670372 | G | A | 4 | a0001c0013t0015 a0002c0003t0003 a0002c0022t0003 others(1): Show |
18 | HG00099.hp1 HG01109.hp1 HG01175.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1067C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 1067 | chr17 | 4670372 | ||||||
chr17:4670377 | A | C | 2 | a0001c0007t0011 a0001c0007t0019 |
3 | HG02145.hp2 NA18522.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1062T>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 1062 | chr17 | 4670377 | ||||||
chr17:4670503 | C | T | 45 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0007 others(42): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
3_prime_UTR_variant | MODIFIER | c.*936G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 936 | chr17 | 4670503 | ||||||
chr17:4670551 | C | G | 3 | a0002c0003t0003 a0002c0022t0003 a0010c0033t0003 |
16 | HG00099.hp1 HG01109.hp1 HG01175.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*888G>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 888 | chr17 | 4670551 | ||||||
chr17:4670560 | T | C | 3 | a0001c0001t0010 a0006c0011t0010 a0009c0021t0010 |
5 | HG01346.hp1 HG02273.hp2 NA18946.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*879A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 879 | chr17 | 4670560 | ||||||
chr17:4670573 | A | G | 8 | a0001c0001t0007 a0001c0002t0006 a0001c0002t0007 others(5): Show |
24 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*866T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 866 | chr17 | 4670573 | ||||||
chr17:4670697 | G | A | 27 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0009 others(24): Show |
234 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(231): Show |
3_prime_UTR_variant | MODIFIER | c.*742C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 742 | chr17 | 4670697 | ||||||
chr17:4670699 | G | A | 10 | a0001c0004t0004 a0001c0007t0011 a0001c0007t0019 others(7): Show |
36 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*740C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 740 | chr17 | 4670699 | ||||||
chr17:4670719 | C | CA | 5 | a0001c0001t0009 a0001c0001t0010 a0001c0007t0019 others(2): Show |
13 | HG00438.hp2 HG00597.hp1 HG01346.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*719dupT | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 719 | chr17 | 4670719 | ||||||
chr17:4670738 | A | C | 2 | a0001c0007t0011 a0001c0007t0019 |
3 | HG02145.hp2 NA18522.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*701T>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 701 | chr17 | 4670738 | ||||||
chr17:4670758 | A | G | 37 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0009 others(34): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
3_prime_UTR_variant | MODIFIER | c.*681T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 681 | chr17 | 4670758 | ||||||
chr17:4670774 | T | C | 1 | a0001c0007t0016 | 2 | HG01884.hp2 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*665A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 665 | chr17 | 4670774 | ||||||
chr17:4670922 | C | T | 1 | a0001c0015t0018 | 1 | HG01070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*517G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 517 | chr17 | 4670922 | ||||||
chr17:4671027 | C | T | 1 | a0001c0002t0017 | 1 | HG02896.hp1 | 3_prime_UTR_variant | MODIFIER | c.*412G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 412 | chr17 | 4671027 | ||||||
chr17:4671171 | G | A | 8 | a0001c0001t0007 a0001c0002t0006 a0001c0002t0007 others(5): Show |
24 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*268C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 17/17 | 268 | chr17 | 4671171 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:4671536 | T | C | 1 | a0011c0026t0001g0098 | 1 | HG02559.hp2 | splice_region_variant&intron_variant | LOW | c.3301-5A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 16/16 | chr17 | 4671536 | |||||||
chr17:4673542 | C | T | 1 | a0001c0001t0002g0163 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1638+77G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 14/16 | chr17 | 4673542 | |||||||
chr17:4673817 | G | A | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(205): Show |
234 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.1583-143C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 13/16 | chr17 | 4673817 | |||||||
chr17:4673844 | G | T | 1 | a0014c0019t0001g0067 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1583-170C>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 13/16 | chr17 | 4673844 | |||||||
chr17:4674049 | T | C | 2 | a0003c0005t0001g0018 a0003c0005t0001g0155 |
3 | HG02129.hp2 NA18981.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1583-375A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 13/16 | chr17 | 4674049 | |||||||
chr17:4674083 | T | G | 1 | a0014c0019t0001g0067 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1583-409A>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 13/16 | chr17 | 4674083 | |||||||
chr17:4674171 | A | C | 1 | a0014c0019t0001g0067 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.1582+339T>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 13/16 | chr17 | 4674171 | |||||||
chr17:4674176 | G | A | 1 | a0001c0001t0007g0203 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1582+334C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 13/16 | chr17 | 4674176 | |||||||
chr17:4674241 | C | T | 1 | a0002c0003t0003g0231 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1582+269G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 13/16 | chr17 | 4674241 | |||||||
chr17:4674312 | G | A | 15 | a0001c0004t0004g0040 a0001c0004t0004g0041 a0001c0004t0004g0123 others(12): Show |
15 | HG00140.hp2 HG00642.hp1 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.1582+198C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 13/16 | chr17 | 4674312 | |||||||
chr17:4674441 | G | C | 1 | a0013c0027t0002g0254 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1582+69C>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 13/16 | chr17 | 4674441 | |||||||
chr17:4674688 | T | G | 1 | a0001c0001t0001g0062 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1423-19A>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 12/16 | chr17 | 4674688 | |||||||
chr17:4674712 | C | G | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(261): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.1423-43G>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 12/16 | chr17 | 4674712 | |||||||
chr17:4674992 | G | T | 1 | a0001c0001t0001g0167 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1275-36C>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 11/16 | chr17 | 4674992 | |||||||
chr17:4675012 | C | T | 3 | a0005c0008t0004g0208 a0005c0008t0004g0209 a0005c0008t0004g0215 |
3 | HG02280.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1275-56G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 11/16 | chr17 | 4675012 | |||||||
chr17:4675446 | A | G | 2 | a0001c0007t0016g0241 a0001c0007t0016g0274 |
2 | HG01884.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1069-84T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 9/16 | chr17 | 4675446 | |||||||
chr17:4675598 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1068+199G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 9/16 | chr17 | 4675598 | |||||||
chr17:4675635 | T | C | 32 | a0001c0001t0002g0247 a0001c0001t0002g0248 a0001c0001t0002g0249 others(29): Show |
34 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.1068+162A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 9/16 | chr17 | 4675635 | |||||||
chr17:4675636 | G | A | 1 | a0001c0001t0007g0213 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1068+161C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 9/16 | chr17 | 4675636 | |||||||
chr17:4675643 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1068+154C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 9/16 | chr17 | 4675643 | |||||||
chr17:4675668 | G | A | 1 | a0001c0001t0009g0174 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1068+129C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 9/16 | chr17 | 4675668 | |||||||
chr17:4675902 | A | G | 1 | a0001c0001t0001g0129 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.981-18T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 8/16 | chr17 | 4675902 | |||||||
chr17:4675921 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.981-37C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 8/16 | chr17 | 4675921 | |||||||
chr17:4676002 | C | G | 1 | a0001c0013t0015g0007 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.980+34G>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 8/16 | chr17 | 4676002 | |||||||
chr17:4676006 | G | A | 14 | a0002c0003t0003g0022 a0002c0003t0003g0226 a0002c0003t0003g0227 others(11): Show |
15 | HG00099.hp1 HG01109.hp1 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.980+30C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 8/16 | chr17 | 4676006 | |||||||
chr17:4676011 | C | T | 5 | a0001c0001t0001g0275 a0001c0001t0001g0277 a0001c0001t0001g0278 others(2): Show |
5 | HG02559.hp1 HG02647.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.980+25G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 8/16 | chr17 | 4676011 | |||||||
chr17:4676343 | G | A | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(205): Show |
234 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(231): Show |
intron_variant | MODIFIER | c.853+14C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 7/16 | chr17 | 4676343 | |||||||
chr17:4676575 | C | T | 2 | a0007c0012t0001g0024 a0007c0012t0001g0025 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.703-68G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 6/16 | chr17 | 4676575 | |||||||
chr17:4676642 | G | A | 15 | a0001c0004t0004g0040 a0001c0004t0004g0041 a0001c0004t0004g0123 others(12): Show |
15 | HG00140.hp2 HG00642.hp1 HG00735.hp2 others(12): Show |
intron_variant | MODIFIER | c.702+111C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 6/16 | chr17 | 4676642 | |||||||
chr17:4676842 | A | G | 274 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(271): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.643-30T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4676842 | |||||||
chr17:4676929 | C | T | 241 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(238): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.643-117G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4676929 | |||||||
chr17:4677034 | C | T | 5 | a0001c0001t0001g0275 a0001c0001t0001g0277 a0001c0001t0001g0278 others(2): Show |
5 | HG02559.hp1 HG02647.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.643-222G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4677034 | |||||||
chr17:4677124 | AC | A | 11 | a0001c0004t0004g0040 a0001c0004t0004g0041 a0001c0004t0004g0123 others(8): Show |
11 | HG00140.hp2 HG00642.hp1 HG00735.hp2 others(8): Show |
intron_variant | MODIFIER | c.643-313delG | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4677124 | |||||||
chr17:4677244 | C | A | 22 | a0001c0001t0007g0202 a0001c0001t0007g0203 a0001c0001t0007g0213 others(19): Show |
24 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.643-432G>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4677244 | |||||||
chr17:4677275 | G | A | 2 | a0001c0001t0001g0178 a0003c0005t0001g0113 |
2 | HG00423.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.643-463C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4677275 | |||||||
chr17:4677284 | A | G | 19 | a0001c0004t0004g0040 a0001c0004t0004g0041 a0001c0004t0004g0123 others(16): Show |
20 | HG00140.hp2 HG00642.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.643-472T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4677284 | |||||||
chr17:4677295 | G | A | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(261): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.643-483C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4677295 | |||||||
chr17:4677490 | A | C | 6 | a0001c0002t0007g0042 a0004c0009t0007g0030 a0004c0009t0007g0031 others(3): Show |
6 | HG02258.hp1 HG02809.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.643-678T>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4677490 | |||||||
chr17:4677537 | A | C | 211 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(208): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.643-725T>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4677537 | |||||||
chr17:4677787 | G | A | 14 | a0001c0001t0007g0202 a0001c0001t0007g0203 a0001c0001t0007g0213 others(11): Show |
16 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.643-975C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4677787 | |||||||
chr17:4677808 | T | C | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(163): Show |
189 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.643-996A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4677808 | |||||||
chr17:4677817 | C | T | 1 | a0001c0001t0001g0117 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.643-1005G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4677817 | |||||||
chr17:4677836 | G | A | 22 | a0001c0001t0007g0202 a0001c0001t0007g0203 a0001c0001t0007g0213 others(19): Show |
24 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.643-1024C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4677836 | |||||||
chr17:4677866 | C | T | 3 | a0001c0001t0001g0150 a0001c0001t0001g0154 a0001c0001t0001g0165 |
3 | NA18968.hp2 NA18991.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.643-1054G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4677866 | |||||||
chr17:4678042 | C | A | 1 | a0014c0019t0001g0067 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.643-1230G>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4678042 | |||||||
chr17:4678051 | T | C | 3 | a0001c0002t0005g0003 a0001c0002t0005g0034 a0001c0002t0005g0035 |
5 | HG02451.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.643-1239A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4678051 | |||||||
chr17:4678080 | G | A | 1 | a0001c0004t0004g0201 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.643-1268C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4678080 | |||||||
chr17:4678163 | G | A | 4 | a0001c0004t0004g0201 a0005c0008t0004g0208 a0005c0008t0004g0209 others(1): Show |
4 | HG02280.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.643-1351C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4678163 | |||||||
chr17:4678224 | A | G | 1 | a0001c0001t0001g0033 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.643-1412T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4678224 | |||||||
chr17:4678382 | G | C | 6 | a0001c0002t0007g0042 a0004c0009t0007g0030 a0004c0009t0007g0031 others(3): Show |
6 | HG02258.hp1 HG02809.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.643-1570C>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4678382 | |||||||
chr17:4678468 | C | A | 1 | a0001c0001t0002g0272 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.643-1656G>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4678468 | |||||||
chr17:4678494 | C | A | 22 | a0001c0001t0007g0202 a0001c0001t0007g0203 a0001c0001t0007g0213 others(19): Show |
24 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.643-1682G>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4678494 | |||||||
chr17:4678525 | G | A | 2 | a0001c0007t0016g0241 a0001c0007t0016g0274 |
2 | HG01884.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.643-1713C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4678525 | |||||||
chr17:4678549 | C | T | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(261): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.643-1737G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4678549 | |||||||
chr17:4678603 | A | G | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(261): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.643-1791T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4678603 | |||||||
chr17:4678724 | C | G | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(261): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.643-1912G>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4678724 | |||||||
chr17:4678731 | G | C | 3 | a0001c0007t0011g0242 a0001c0007t0011g0243 a0001c0007t0019g0240 |
3 | HG02145.hp2 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.643-1919C>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4678731 | |||||||
chr17:4678738 | C | A | 3 | a0001c0001t0002g0259 a0001c0001t0002g0271 a0001c0001t0002g0272 |
3 | NA18946.hp1 NA18948.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.643-1926G>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4678738 | |||||||
chr17:4678754 | T | C | 1 | a0001c0002t0007g0204 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.643-1942A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4678754 | |||||||
chr17:4678794 | G | A | 1 | a0001c0004t0004g0201 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.643-1982C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4678794 | |||||||
chr17:4678888 | G | A | 15 | a0002c0003t0003g0022 a0002c0003t0003g0226 a0002c0003t0003g0227 others(12): Show |
16 | HG00099.hp1 HG01109.hp1 HG01175.hp2 others(13): Show |
intron_variant | MODIFIER | c.643-2076C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4678888 | |||||||
chr17:4679032 | C | CT | 16 | a0001c0001t0001g0048 a0002c0003t0003g0022 a0002c0003t0003g0226 others(13): Show |
17 | HG00099.hp1 HG01109.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.643-2221dupA | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4679032 | |||||||
chr17:4679131 | A | C | 227 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(224): Show |
254 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(251): Show |
intron_variant | MODIFIER | c.643-2319T>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4679131 | |||||||
chr17:4679272 | T | C | 1 | a0001c0001t0001g0048 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.643-2460A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4679272 | |||||||
chr17:4679274 | C | T | 1 | a0001c0001t0001g0048 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.643-2462G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4679274 | |||||||
chr17:4679289 | G | A | 22 | a0001c0001t0007g0202 a0001c0001t0007g0203 a0001c0001t0007g0213 others(19): Show |
24 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.643-2477C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4679289 | |||||||
chr17:4679352 | G | A | 2 | a0001c0001t0002g0251 a0001c0001t0002g0255 |
2 | NA18968.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.643-2540C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4679352 | |||||||
chr17:4679529 | G | A | 3 | a0001c0007t0011g0242 a0001c0007t0011g0243 a0001c0007t0019g0240 |
3 | HG02145.hp2 NA18522.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.643-2717C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4679529 | |||||||
chr17:4679577 | T | C | 30 | a0001c0001t0002g0163 a0001c0001t0002g0183 a0001c0001t0002g0246 others(27): Show |
30 | HG00544.hp2 HG01943.hp1 HG02027.hp1 others(27): Show |
intron_variant | MODIFIER | c.643-2765A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4679577 | |||||||
chr17:4679616 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.643-2804T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4679616 | |||||||
chr17:4679656 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.643-2844G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4679656 | |||||||
chr17:4679728 | A | G | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(207): Show |
237 | HG00099.hp2 HG00140.hp1 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.642+2774T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4679728 | |||||||
chr17:4679765 | T | A | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(261): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.642+2737A>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4679765 | |||||||
chr17:4679783 | C | A | 1 | a0001c0001t0001g0048 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.642+2719G>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4679783 | |||||||
chr17:4679801 | T | C | 22 | a0001c0001t0007g0202 a0001c0001t0007g0203 a0001c0001t0007g0213 others(19): Show |
24 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.642+2701A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4679801 | |||||||
chr17:4679862 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.642+2640C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4679862 | |||||||
chr17:4680159 | C | T | 1 | a0001c0013t0015g0007 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.642+2343G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4680159 | |||||||
chr17:4680353 | T | C | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(261): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.642+2149A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4680353 | |||||||
chr17:4680524 | C | T | 1 | a0001c0004t0004g0210 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.642+1978G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4680524 | |||||||
chr17:4680569 | C | A | 22 | a0001c0001t0007g0202 a0001c0001t0007g0203 a0001c0001t0007g0213 others(19): Show |
24 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.642+1933G>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4680569 | |||||||
chr17:4680741 | G | A | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(261): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.642+1761C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4680741 | |||||||
chr17:4680750 | TCAAACCA others(21): Show |
T | 1 | a0001c0001t0001g0148 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.642+1724_642+1751d others(30): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4680750 | |||||||
chr17:4680803 | T | C | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(261): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.642+1699A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4680803 | |||||||
chr17:4680920 | T | C | 22 | a0001c0001t0007g0202 a0001c0001t0007g0203 a0001c0001t0007g0213 others(19): Show |
24 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.642+1582A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4680920 | |||||||
chr17:4680936 | C | G | 30 | a0001c0001t0002g0163 a0001c0001t0002g0183 a0001c0001t0002g0246 others(27): Show |
30 | HG00544.hp2 HG01943.hp1 HG02027.hp1 others(27): Show |
intron_variant | MODIFIER | c.642+1566G>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4680936 | |||||||
chr17:4681255 | C | T | 7 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0244 others(4): Show |
10 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.642+1247G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4681255 | |||||||
chr17:4681322 | A | T | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(261): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.642+1180T>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4681322 | |||||||
chr17:4681361 | A | G | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(261): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
intron_variant | MODIFIER | c.642+1141T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4681361 | |||||||
chr17:4681375 | C | CT | 16 | a0001c0015t0018g0232 a0002c0003t0003g0022 a0002c0003t0003g0226 others(13): Show |
17 | HG00099.hp1 HG01070.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.642+1126dupA | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4681375 | |||||||
chr17:4681527 | C | T | 5 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0276 others(2): Show |
8 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.642+975G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4681527 | |||||||
chr17:4681539 | T | C | 1 | a0001c0001t0001g0187 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.642+963A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4681539 | |||||||
chr17:4681605 | T | G | 7 | a0001c0001t0001g0054 a0001c0001t0001g0124 a0001c0001t0001g0278 others(4): Show |
7 | HG01109.hp2 HG01168.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.642+897A>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4681605 | |||||||
chr17:4681611 | C | A | 1 | a0001c0002t0008g0095 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.642+891G>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4681611 | |||||||
chr17:4681629 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.642+873T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4681629 | |||||||
chr17:4681686 | G | T | 1 | a0001c0001t0002g0273 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.642+816C>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4681686 | |||||||
chr17:4681758 | C | T | 1 | a0001c0002t0006g0083 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.642+744G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4681758 | |||||||
chr17:4681764 | C | T | 2 | a0001c0014t0001g0217 a0001c0014t0001g0218 |
2 | HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.642+738G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4681764 | |||||||
chr17:4681782 | G | C | 16 | a0001c0002t0005g0003 a0001c0002t0005g0034 a0001c0002t0005g0035 others(13): Show |
18 | HG02055.hp1 HG02257.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.642+720C>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4681782 | |||||||
chr17:4681851 | T | TA | 4 | a0001c0002t0006g0081 a0001c0002t0006g0083 a0001c0002t0007g0204 others(1): Show |
4 | HG01167.hp2 HG02723.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.642+650_642+651ins others(1): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4681851 | |||||||
chr17:4681852 | T | A | 5 | a0001c0002t0006g0081 a0001c0002t0006g0083 a0001c0002t0007g0204 others(2): Show |
5 | HG01167.hp2 HG02723.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.642+650A>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4681852 | |||||||
chr17:4681853 | A | T | 18 | a0001c0001t0001g0085 a0001c0002t0005g0003 a0001c0002t0005g0034 others(15): Show |
20 | HG02055.hp1 HG02055.hp2 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.642+649T>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4681853 | |||||||
chr17:4682126 | C | A | 1 | a0001c0001t0001g0132 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.642+376G>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4682126 | |||||||
chr17:4682180 | G | T | 2 | a0002c0003t0003g0227 a0002c0003t0003g0228 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.642+322C>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4682180 | |||||||
chr17:4682275 | T | C | 1 | a0001c0001t0001g0178 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.642+227A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4682275 | |||||||
chr17:4682302 | G | A | 1 | a0001c0001t0002g0262 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.642+200C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4682302 | |||||||
chr17:4682476 | G | A | 1 | a0001c0013t0015g0007 | 2 | HG02615.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.642+26C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 5/16 | chr17 | 4682476 | |||||||
chr17:4682735 | CAATT | C | 3 | a0001c0001t0007g0202 a0001c0001t0007g0203 a0001c0001t0007g0213 |
3 | HG01109.hp2 HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.570+64_570+67delAA others(2): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 4/16 | chr17 | 4682735 | |||||||
chr17:4682958 | GA | G | 264 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(261): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): Show |
splice_region_variant&intron_variant | LOW | c.421-7delT | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4682958 | |||||||
chr17:4683221 | CTT | C | 12 | a0001c0001t0001g0181 a0001c0001t0002g0270 a0001c0001t0009g0082 others(9): Show |
12 | HG01167.hp2 HG02258.hp1 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.421-271_421-270del others(2): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683221 | |||||||
chr17:4683221 | CTTT | C | 252 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(249): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.421-272_421-270del others(3): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683221 | |||||||
chr17:4683260 | A | G | 265 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(262): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.421-308T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683260 | |||||||
chr17:4683271 | A | G | 262 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(259): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.421-319T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683271 | |||||||
chr17:4683281 | C | T | 1 | a0001c0006t0001g0114 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.421-329G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683281 | |||||||
chr17:4683307 | G | A | 1 | a0001c0002t0006g0005 | 3 | HG02630.hp2 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.421-355C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683307 | |||||||
chr17:4683339 | G | C | 2 | a0001c0030t0004g0214 a0008c0031t0004g0200 |
2 | HG00741.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.421-387C>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683339 | |||||||
chr17:4683345 | C | T | 2 | a0001c0030t0004g0214 a0008c0031t0004g0200 |
2 | HG00741.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.421-393G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683345 | |||||||
chr17:4683355 | A | G | 2 | a0001c0030t0004g0214 a0008c0031t0004g0200 |
2 | HG00741.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.421-403T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683355 | |||||||
chr17:4683363 | A | G | 6 | a0001c0001t0001g0177 a0001c0001t0002g0259 a0001c0001t0002g0271 others(3): Show |
6 | HG00558.hp2 HG00741.hp2 HG01168.hp1 others(3): Show |
intron_variant | MODIFIER | c.421-411T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683363 | |||||||
chr17:4683365 | C | T | 5 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0276 others(2): Show |
8 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.421-413G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683365 | |||||||
chr17:4683366 | G | A | 2 | a0001c0030t0004g0214 a0008c0031t0004g0200 |
2 | HG00741.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.421-414C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683366 | |||||||
chr17:4683369 | C | T | 5 | a0004c0009t0007g0030 a0004c0009t0007g0031 a0004c0009t0007g0032 others(2): Show |
5 | HG02258.hp1 HG02809.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.421-417G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683369 | |||||||
chr17:4683376 | A | C | 2 | a0001c0001t0001g0278 a0001c0001t0001g0280 |
2 | HG02647.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.421-424T>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683376 | |||||||
chr17:4683376 | A | T | 1 | a0012c0020t0001g0144 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.421-424T>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683376 | |||||||
chr17:4683381 | T | C | 2 | a0001c0001t0001g0277 a0002c0003t0003g0231 |
2 | HG03927.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.421-429A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683381 | |||||||
chr17:4683383 | A | G | 267 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(264): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.421-431T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683383 | |||||||
chr17:4683387 | A | T | 1 | a0002c0003t0003g0231 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.421-435T>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683387 | |||||||
chr17:4683388 | T | G | 1 | a0001c0002t0005g0039 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.421-436A>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683388 | |||||||
chr17:4683410 | C | T | 7 | a0001c0001t0001g0178 a0001c0001t0001g0275 a0001c0001t0001g0277 others(4): Show |
7 | HG00423.hp2 HG02559.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.421-458G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683410 | |||||||
chr17:4683411 | G | A | 7 | a0001c0001t0001g0126 a0001c0001t0007g0203 a0001c0004t0004g0201 others(4): Show |
7 | HG02148.hp2 HG02280.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.421-459C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683411 | |||||||
chr17:4683421 | T | C | 12 | a0001c0001t0001g0206 a0001c0001t0001g0283 a0001c0001t0009g0082 others(9): Show |
12 | HG00140.hp1 HG00140.hp2 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.421-469A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683421 | |||||||
chr17:4683422 | A | G | 39 | a0001c0001t0001g0159 a0001c0001t0001g0162 a0001c0001t0001g0177 others(36): Show |
39 | HG00558.hp2 HG00642.hp1 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.421-470T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683422 | |||||||
chr17:4683422 | A | T | 3 | a0001c0001t0009g0082 a0001c0002t0006g0081 a0001c0002t0006g0083 |
3 | HG02622.hp2 HG02723.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.421-470T>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683422 | |||||||
chr17:4683427 | A | G | 16 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0276 others(13): Show |
20 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.421-475T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683427 | |||||||
chr17:4683431 | A | G | 1 | a0001c0001t0010g0058 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.421-479T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683431 | |||||||
chr17:4683433 | G | T | 4 | a0002c0003t0003g0226 a0002c0003t0003g0229 a0002c0003t0003g0234 others(1): Show |
4 | HG01515.hp2 HG01517.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.421-481C>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683433 | |||||||
chr17:4683436 | G | T | 2 | a0001c0001t0002g0269 a0013c0027t0002g0254 |
2 | NA18954.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.421-484C>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683436 | |||||||
chr17:4683442 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.421-490C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683442 | |||||||
chr17:4683448 | C | CT | 11 | a0001c0001t0001g0182 a0001c0001t0001g0187 a0001c0001t0002g0247 others(8): Show |
11 | HG01106.hp2 HG01517.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.421-497_421-496ins others(1): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683448 | |||||||
chr17:4683455 | G | A | 9 | a0001c0001t0002g0247 a0001c0001t0002g0248 a0001c0001t0002g0249 others(6): Show |
9 | HG02717.hp2 NA18941.hp2 NA18956.hp2 others(6): Show |
intron_variant | MODIFIER | c.421-503C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683455 | |||||||
chr17:4683466 | G | A | 1 | a0001c0002t0008g0095 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.421-514C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683466 | |||||||
chr17:4683498 | T | C | 10 | a0001c0001t0001g0071 a0001c0001t0001g0100 a0001c0001t0001g0101 others(7): Show |
10 | HG00741.hp1 HG01074.hp2 HG01081.hp1 others(7): Show |
intron_variant | MODIFIER | c.421-546A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683498 | |||||||
chr17:4683507 | T | C | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.421-555A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683507 | |||||||
chr17:4683509 | A | ACGCCTGG others(126): Show |
1 | a0001c0001t0009g0029 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.421-558_421-557ins others(133): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683509 | |||||||
chr17:4683509 | A | G | 253 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(250): Show |
283 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(280): Show |
intron_variant | MODIFIER | c.421-557T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683509 | |||||||
chr17:4683510 | C | G | 12 | a0001c0001t0001g0015 a0001c0001t0001g0080 a0001c0001t0001g0085 others(9): Show |
13 | HG01891.hp2 HG02055.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.421-558G>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683510 | |||||||
chr17:4683510 | C | T | 90 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0046 others(87): Show |
97 | HG00099.hp1 HG00544.hp2 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.421-558G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683510 | |||||||
chr17:4683515 | A | G | 14 | a0001c0001t0001g0015 a0001c0001t0001g0080 a0001c0001t0001g0085 others(11): Show |
15 | HG01891.hp2 HG02055.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.421-563T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683515 | |||||||
chr17:4683518 | T | C | 265 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(262): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.421-566A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683518 | |||||||
chr17:4683531 | C | CTT | 8 | a0001c0001t0002g0247 a0001c0001t0002g0248 a0001c0001t0002g0249 others(5): Show |
8 | NA18941.hp2 NA18956.hp2 NA18960.hp2 others(5): Show |
intron_variant | MODIFIER | c.421-581_421-580dup others(2): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683531 | |||||||
chr17:4683531 | C | CTTT | 26 | a0001c0001t0002g0246 a0001c0001t0002g0250 a0001c0001t0002g0251 others(23): Show |
28 | HG00544.hp2 HG01943.hp1 HG02027.hp1 others(25): Show |
intron_variant | MODIFIER | c.421-582_421-580dup others(3): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683531 | |||||||
chr17:4683531 | C | CTTTT | 20 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0043 others(17): Show |
23 | HG01167.hp1 HG01243.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.421-583_421-580dup others(4): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683531 | |||||||
chr17:4683531 | C | CTTTTT | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(164): Show |
186 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.421-584_421-580dup others(5): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683531 | |||||||
chr17:4683531 | C | CTTTTTT | 19 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0019 others(16): Show |
19 | HG00423.hp1 HG00642.hp2 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.421-585_421-580dup others(6): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683531 | |||||||
chr17:4683531 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0015 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.421-590_421-580dup others(11): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683531 | |||||||
chr17:4683531 | CTTT | C | 19 | a0001c0001t0001g0206 a0001c0001t0007g0202 a0001c0001t0007g0203 others(16): Show |
20 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.421-582_421-580del others(3): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683531 | |||||||
chr17:4683787 | T | TC | 265 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(262): Show |
295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.421-836dupG | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683787 | |||||||
chr17:4683800 | G | A | 2 | a0005c0008t0004g0208 a0005c0008t0004g0215 |
2 | HG02280.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.421-848C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683800 | |||||||
chr17:4683829 | C | CT | 100 | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0017 others(97): Show |
107 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.421-878dupA | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683829 | |||||||
chr17:4683829 | C | CTT | 10 | a0001c0001t0001g0196 a0001c0001t0002g0248 a0001c0001t0002g0249 others(7): Show |
10 | HG01884.hp1 HG02717.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.421-879_421-878dup others(2): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683829 | |||||||
chr17:4683829 | CT | C | 12 | a0001c0001t0001g0006 a0001c0001t0001g0276 a0001c0001t0001g0280 others(9): Show |
14 | HG00735.hp2 HG01106.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.421-878delA | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683829 | |||||||
chr17:4683829 | CTT | C | 21 | a0001c0001t0001g0206 a0001c0001t0001g0278 a0001c0001t0007g0203 others(18): Show |
21 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(18): Show |
intron_variant | MODIFIER | c.421-879_421-878del others(2): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683829 | |||||||
chr17:4683943 | A | C | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.421-991T>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4683943 | |||||||
chr17:4684047 | A | G | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.421-1095T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4684047 | |||||||
chr17:4684060 | C | T | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(182): Show |
208 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(205): Show |
intron_variant | MODIFIER | c.421-1108G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4684060 | |||||||
chr17:4684114 | A | C | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.421-1162T>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4684114 | |||||||
chr17:4684165 | G | A | 1 | a0001c0001t0001g0154 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.421-1213C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4684165 | |||||||
chr17:4684228 | C | T | 9 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0053 others(6): Show |
12 | HG00408.hp1 HG00673.hp2 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.421-1276G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4684228 | |||||||
chr17:4684282 | C | T | 5 | a0001c0001t0009g0082 a0001c0002t0006g0081 a0001c0002t0006g0083 others(2): Show |
5 | HG01167.hp2 HG02622.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.421-1330G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4684282 | |||||||
chr17:4684349 | A | C | 1 | a0001c0001t0001g0148 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.421-1397T>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4684349 | |||||||
chr17:4684353 | T | G | 1 | a0001c0001t0001g0148 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.421-1401A>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4684353 | |||||||
chr17:4684375 | A | C | 1 | a0001c0001t0001g0148 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.421-1423T>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4684375 | |||||||
chr17:4684382 | C | G | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.421-1430G>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4684382 | |||||||
chr17:4684431 | A | G | 28 | a0001c0001t0002g0246 a0001c0001t0002g0247 a0001c0001t0002g0248 others(25): Show |
28 | HG00544.hp2 HG01943.hp1 HG02027.hp1 others(25): Show |
intron_variant | MODIFIER | c.421-1479T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4684431 | |||||||
chr17:4684437 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.421-1485T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4684437 | |||||||
chr17:4684576 | T | G | 1 | a0001c0001t0001g0148 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.421-1624A>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4684576 | |||||||
chr17:4684629 | T | TG | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.421-1678dupC | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4684629 | |||||||
chr17:4684731 | G | A | 1 | a0001c0001t0001g0275 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.421-1779C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4684731 | |||||||
chr17:4684783 | C | G | 54 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0244 others(51): Show |
59 | HG00544.hp2 HG01243.hp2 HG01884.hp1 others(56): Show |
intron_variant | MODIFIER | c.421-1831G>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4684783 | |||||||
chr17:4684881 | A | G | 1 | a0001c0001t0001g0275 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.421-1929T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4684881 | |||||||
chr17:4684893 | G | T | 1 | a0001c0001t0001g0148 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.421-1941C>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4684893 | |||||||
chr17:4685205 | G | C | 16 | a0001c0015t0018g0232 a0002c0003t0003g0022 a0002c0003t0003g0226 others(13): Show |
17 | HG00099.hp1 HG01070.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.421-2253C>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4685205 | |||||||
chr17:4685305 | C | A | 1 | a0002c0003t0003g0233 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.421-2353G>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4685305 | |||||||
chr17:4685403 | G | A | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.421-2451C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4685403 | |||||||
chr17:4685561 | G | A | 92 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(89): Show |
103 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.421-2609C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4685561 | |||||||
chr17:4685626 | CA | C | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.421-2675delT | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4685626 | |||||||
chr17:4685641 | T | C | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.421-2689A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4685641 | |||||||
chr17:4685663 | C | T | 9 | a0001c0002t0005g0224 a0001c0002t0005g0225 a0001c0002t0006g0005 others(6): Show |
11 | HG01884.hp1 HG02257.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.421-2711G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4685663 | |||||||
chr17:4685678 | A | T | 1 | a0001c0001t0001g0148 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.421-2726T>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4685678 | |||||||
chr17:4685792 | T | TAAAAAAA others(1): Show |
6 | a0001c0002t0005g0224 a0001c0004t0004g0041 a0001c0015t0018g0232 others(3): Show |
6 | HG01070.hp2 HG01258.hp2 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.421-2848_421-2841d others(10): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4685792 | |||||||
chr17:4685792 | T | TAAAAAAA others(2): Show |
46 | a0001c0001t0001g0206 a0001c0001t0001g0244 a0001c0001t0001g0245 others(43): Show |
49 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(46): Show |
intron_variant | MODIFIER | c.421-2849_421-2841d others(11): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4685792 | |||||||
chr17:4685792 | T | TAAAAAAA others(3): Show |
30 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0276 others(27): Show |
33 | HG00544.hp2 HG01243.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.421-2850_421-2841d others(12): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4685792 | |||||||
chr17:4685792 | T | TAAAAAAA others(4): Show |
1 | a0015c0024t0002g0258 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.421-2841_421-2840i others(13): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4685792 | |||||||
chr17:4685792 | T | TAAAAAAA others(6): Show |
2 | a0001c0001t0001g0277 a0001c0001t0001g0281 |
2 | HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.421-2841_421-2840i others(15): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4685792 | |||||||
chr17:4685799 | A | AAAAAAAA others(1): Show |
189 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(186): Show |
213 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(210): Show |
intron_variant | MODIFIER | c.421-2848_421-2847i others(10): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4685799 | |||||||
chr17:4685828 | A | G | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.421-2876T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4685828 | |||||||
chr17:4685849 | C | T | 2 | a0001c0001t0001g0102 a0001c0001t0001g0106 |
2 | NA18973.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.421-2897G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4685849 | |||||||
chr17:4685861 | C | T | 16 | a0001c0015t0018g0232 a0002c0003t0003g0022 a0002c0003t0003g0226 others(13): Show |
17 | HG00099.hp1 HG01070.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.421-2909G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4685861 | |||||||
chr17:4685899 | C | T | 1 | a0001c0025t0007g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.421-2947G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4685899 | |||||||
chr17:4685914 | T | C | 25 | a0001c0002t0005g0224 a0001c0002t0005g0225 a0001c0002t0006g0005 others(22): Show |
28 | HG00099.hp1 HG01070.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.421-2962A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4685914 | |||||||
chr17:4685952 | C | A | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.421-3000G>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4685952 | |||||||
chr17:4685954 | G | A | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.421-3002C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4685954 | |||||||
chr17:4686155 | C | T | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.421-3203G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4686155 | |||||||
chr17:4686251 | T | C | 1 | a0001c0001t0001g0148 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.421-3299A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4686251 | |||||||
chr17:4686252 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.421-3300G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4686252 | |||||||
chr17:4686254 | A | C | 1 | a0001c0001t0001g0148 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.421-3302T>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4686254 | |||||||
chr17:4686366 | G | A | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.421-3414C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4686366 | |||||||
chr17:4686396 | C | T | 1 | a0001c0002t0017g0088 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.421-3444G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4686396 | |||||||
chr17:4686513 | T | TTTTC | 3 | a0001c0001t0002g0259 a0001c0001t0002g0271 a0001c0001t0002g0272 |
3 | NA18946.hp1 NA18948.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.421-3565_421-3562d others(6): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4686513 | |||||||
chr17:4686580 | C | T | 17 | a0001c0015t0018g0232 a0001c0023t0005g0089 a0002c0003t0003g0022 others(14): Show |
18 | HG00099.hp1 HG01070.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.421-3628G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4686580 | |||||||
chr17:4686581 | G | A | 1 | a0001c0001t0001g0167 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.421-3629C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4686581 | |||||||
chr17:4686587 | G | A | 12 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0244 others(9): Show |
15 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.421-3635C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4686587 | |||||||
chr17:4686660 | G | A | 1 | a0001c0025t0007g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.421-3708C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4686660 | |||||||
chr17:4686746 | G | A | 16 | a0001c0015t0018g0232 a0002c0003t0003g0022 a0002c0003t0003g0226 others(13): Show |
17 | HG00099.hp1 HG01070.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.421-3794C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4686746 | |||||||
chr17:4686793 | C | T | 16 | a0001c0015t0018g0232 a0002c0003t0003g0022 a0002c0003t0003g0226 others(13): Show |
17 | HG00099.hp1 HG01070.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.421-3841G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4686793 | |||||||
chr17:4686797 | C | T | 2 | a0001c0001t0009g0028 a0001c0001t0009g0029 |
2 | HG00438.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.421-3845G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4686797 | |||||||
chr17:4686805 | A | C | 1 | a0001c0001t0001g0148 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.421-3853T>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4686805 | |||||||
chr17:4686857 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.421-3905G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4686857 | |||||||
chr17:4686879 | G | A | 5 | a0001c0002t0007g0042 a0004c0009t0007g0030 a0004c0009t0007g0031 others(2): Show |
5 | HG02258.hp1 HG02976.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.421-3927C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4686879 | |||||||
chr17:4686954 | C | G | 1 | a0001c0001t0001g0148 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.420+3934G>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4686954 | |||||||
chr17:4686955 | T | C | 1 | a0001c0001t0001g0148 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.420+3933A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4686955 | |||||||
chr17:4686957 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.420+3931G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4686957 | |||||||
chr17:4686982 | A | C | 1 | a0001c0001t0001g0148 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.420+3906T>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4686982 | |||||||
chr17:4686984 | T | A | 1 | a0001c0001t0001g0148 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.420+3904A>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4686984 | |||||||
chr17:4686991 | C | T | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.420+3897G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4686991 | |||||||
chr17:4687201 | C | T | 16 | a0001c0015t0018g0232 a0002c0003t0003g0022 a0002c0003t0003g0226 others(13): Show |
17 | HG00099.hp1 HG01070.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.420+3687G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4687201 | |||||||
chr17:4687301 | C | T | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.420+3587G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4687301 | |||||||
chr17:4687320 | A | G | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.420+3568T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4687320 | |||||||
chr17:4687323 | T | A | 1 | a0001c0001t0001g0148 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.420+3565A>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4687323 | |||||||
chr17:4687340 | C | G | 2 | a0002c0003t0003g0022 a0010c0033t0003g0284 |
3 | HG00099.hp1 HG01261.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.420+3548G>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4687340 | |||||||
chr17:4687341 | G | A | 4 | a0001c0001t0001g0071 a0001c0001t0001g0101 a0001c0001t0001g0117 others(1): Show |
4 | HG00741.hp1 HG01074.hp2 HG01081.hp1 others(1): Show |
intron_variant | MODIFIER | c.420+3547C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4687341 | |||||||
chr17:4687374 | C | G | 13 | a0001c0001t0001g0206 a0001c0001t0007g0202 a0001c0001t0007g0203 others(10): Show |
13 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.420+3514G>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4687374 | |||||||
chr17:4687380 | G | T | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.420+3508C>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4687380 | |||||||
chr17:4687428 | C | T | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.420+3460G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4687428 | |||||||
chr17:4687455 | C | A | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.420+3433G>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4687455 | |||||||
chr17:4687498 | CAAA | C | 45 | a0001c0001t0001g0052 a0001c0001t0001g0148 a0001c0001t0001g0244 others(42): Show |
47 | HG00544.hp2 HG01167.hp2 HG01884.hp1 others(44): Show |
intron_variant | MODIFIER | c.420+3387_420+3389d others(5): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4687498 | |||||||
chr17:4687498 | CAAAA | C | 101 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(98): Show |
117 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.420+3386_420+3389d others(6): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4687498 | |||||||
chr17:4687498 | CAAAAA | C | 121 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0009 others(118): Show |
133 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.420+3385_420+3389d others(7): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4687498 | |||||||
chr17:4687511 | A | C | 1 | a0001c0001t0001g0148 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.420+3377T>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4687511 | |||||||
chr17:4687701 | A | C | 1 | a0001c0001t0001g0148 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.420+3187T>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4687701 | |||||||
chr17:4687761 | T | C | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.420+3127A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4687761 | |||||||
chr17:4687812 | A | C | 1 | a0001c0001t0001g0148 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.420+3076T>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4687812 | |||||||
chr17:4687828 | G | A | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.420+3060C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4687828 | |||||||
chr17:4687891 | A | C | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.420+2997T>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4687891 | |||||||
chr17:4688044 | G | C | 40 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0244 others(37): Show |
43 | HG00544.hp2 HG01243.hp2 HG01891.hp1 others(40): Show |
intron_variant | MODIFIER | c.420+2844C>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4688044 | |||||||
chr17:4688080 | G | A | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.420+2808C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4688080 | |||||||
chr17:4688152 | T | C | 5 | a0001c0007t0011g0242 a0001c0007t0011g0243 a0001c0007t0016g0241 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.420+2736A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4688152 | |||||||
chr17:4688184 | C | A | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.420+2704G>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4688184 | |||||||
chr17:4688191 | C | T | 1 | a0001c0002t0007g0204 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.420+2697G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4688191 | |||||||
chr17:4688195 | C | T | 16 | a0001c0015t0018g0232 a0002c0003t0003g0022 a0002c0003t0003g0226 others(13): Show |
17 | HG00099.hp1 HG01070.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.420+2693G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4688195 | |||||||
chr17:4688272 | G | T | 1 | a0001c0001t0009g0180 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.420+2616C>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4688272 | |||||||
chr17:4688288 | C | T | 1 | a0001c0001t0007g0202 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.420+2600G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4688288 | |||||||
chr17:4688291 | T | C | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.420+2597A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4688291 | |||||||
chr17:4688352 | G | A | 3 | a0001c0001t0001g0071 a0001c0001t0001g0101 a0001c0001t0001g0119 |
3 | HG00741.hp1 HG01074.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.420+2536C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4688352 | |||||||
chr17:4688358 | A | C | 1 | a0001c0001t0001g0245 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.420+2530T>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4688358 | |||||||
chr17:4688489 | G | A | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.420+2399C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4688489 | |||||||
chr17:4688501 | G | A | 2 | a0001c0001t0001g0277 a0001c0001t0001g0281 |
2 | HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.420+2387C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4688501 | |||||||
chr17:4688558 | G | A | 18 | a0001c0001t0001g0206 a0001c0001t0007g0202 a0001c0001t0007g0203 others(15): Show |
18 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.420+2330C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4688558 | |||||||
chr17:4688857 | T | C | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.420+2031A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4688857 | |||||||
chr17:4689220 | C | T | 2 | a0001c0002t0005g0224 a0001c0002t0005g0225 |
2 | HG02886.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.420+1668G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4689220 | |||||||
chr17:4689321 | A | G | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.420+1567T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4689321 | |||||||
chr17:4689396 | G | A | 2 | a0001c0014t0001g0217 a0001c0014t0001g0218 |
2 | HG03654.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.420+1492C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4689396 | |||||||
chr17:4689436 | A | G | 3 | a0001c0001t0001g0085 a0001c0001t0001g0109 a0001c0029t0001g0140 |
3 | HG01891.hp2 HG02055.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.420+1452T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4689436 | |||||||
chr17:4689604 | C | T | 1 | a0002c0003t0003g0231 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.420+1284G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4689604 | |||||||
chr17:4689690 | G | A | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.420+1198C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4689690 | |||||||
chr17:4689820 | G | A | 16 | a0001c0015t0018g0232 a0002c0003t0003g0022 a0002c0003t0003g0226 others(13): Show |
17 | HG00099.hp1 HG01070.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.420+1068C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4689820 | |||||||
chr17:4689823 | T | C | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.420+1065A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4689823 | |||||||
chr17:4689843 | T | A | 5 | a0001c0007t0011g0242 a0001c0007t0011g0243 a0001c0007t0016g0241 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.420+1045A>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4689843 | |||||||
chr17:4689894 | C | T | 2 | a0001c0001t0001g0053 a0001c0010t0001g0070 |
2 | HG04228.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.420+994G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4689894 | |||||||
chr17:4690073 | A | C | 2 | a0001c0013t0015g0007 a0004c0017t0007g0026 |
3 | HG02615.hp1 HG02809.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.420+815T>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4690073 | |||||||
chr17:4690231 | G | A | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.420+657C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4690231 | |||||||
chr17:4690268 | T | C | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.420+620A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4690268 | |||||||
chr17:4690271 | G | A | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(187): Show |
214 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.420+617C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4690271 | |||||||
chr17:4690289 | G | C | 1 | a0001c0001t0009g0029 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.420+599C>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4690289 | |||||||
chr17:4690307 | T | C | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(182): Show |
209 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(206): Show |
intron_variant | MODIFIER | c.420+581A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4690307 | |||||||
chr17:4690375 | G | A | 9 | a0001c0002t0005g0224 a0001c0002t0005g0225 a0001c0002t0006g0005 others(6): Show |
11 | HG01884.hp1 HG02257.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.420+513C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4690375 | |||||||
chr17:4690454 | C | G | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.420+434G>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4690454 | |||||||
chr17:4690460 | A | G | 3 | a0005c0008t0004g0208 a0005c0008t0004g0209 a0005c0008t0004g0215 |
3 | HG02280.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.420+428T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4690460 | |||||||
chr17:4690461 | C | T | 12 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0244 others(9): Show |
15 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.420+427G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4690461 | |||||||
chr17:4690557 | A | G | 5 | a0001c0002t0007g0042 a0004c0009t0007g0030 a0004c0009t0007g0031 others(2): Show |
5 | HG02258.hp1 HG02976.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.420+331T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4690557 | |||||||
chr17:4690572 | A | C | 16 | a0001c0015t0018g0232 a0002c0003t0003g0022 a0002c0003t0003g0226 others(13): Show |
17 | HG00099.hp1 HG01070.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.420+316T>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4690572 | |||||||
chr17:4690583 | G | A | 1 | a0001c0001t0001g0051 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.420+305C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4690583 | |||||||
chr17:4690620 | G | A | 1 | a0003c0005t0001g0155 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.420+268C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4690620 | |||||||
chr17:4690621 | C | T | 271 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(268): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.420+267G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4690621 | |||||||
chr17:4690632 | G | C | 1 | a0001c0001t0001g0033 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.420+256C>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4690632 | |||||||
chr17:4690708 | T | C | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.420+180A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 3/16 | chr17 | 4690708 | |||||||
chr17:4691026 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.315-33C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 2/16 | chr17 | 4691026 | |||||||
chr17:4691028 | G | A | 2 | a0001c0001t0001g0178 a0003c0005t0001g0113 |
2 | HG00423.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.315-35C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 2/16 | chr17 | 4691028 | |||||||
chr17:4691038 | C | T | 3 | a0003c0005t0001g0166 a0003c0005t0001g0179 a0003c0005t0001g0185 |
3 | NA18979.hp1 NA18991.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.315-45G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 2/16 | chr17 | 4691038 | |||||||
chr17:4691552 | T | C | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.250-110A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4691552 | |||||||
chr17:4691642 | A | G | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.250-200T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4691642 | |||||||
chr17:4691670 | C | T | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(171): Show |
197 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.250-228G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4691670 | |||||||
chr17:4691673 | G | A | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.250-231C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4691673 | |||||||
chr17:4691881 | T | A | 2 | a0001c0013t0015g0007 a0004c0017t0007g0026 |
3 | HG02615.hp1 HG02809.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.250-439A>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4691881 | |||||||
chr17:4691907 | C | T | 2 | a0001c0001t0001g0074 a0001c0001t0001g0129 |
2 | NA18963.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.250-465G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4691907 | |||||||
chr17:4692006 | A | C | 1 | a0001c0001t0001g0052 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.250-564T>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4692006 | |||||||
chr17:4692007 | A | C | 275 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(272): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.250-565T>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4692007 | |||||||
chr17:4692008 | A | T | 1 | a0001c0001t0001g0052 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.250-566T>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4692008 | |||||||
chr17:4692054 | A | G | 1 | a0001c0006t0001g0104 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.250-612T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4692054 | |||||||
chr17:4692193 | C | A | 16 | a0001c0015t0018g0232 a0002c0003t0003g0022 a0002c0003t0003g0226 others(13): Show |
17 | HG00099.hp1 HG01070.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.250-751G>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4692193 | |||||||
chr17:4692222 | C | T | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.250-780G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4692222 | |||||||
chr17:4692243 | G | A | 5 | a0001c0007t0011g0242 a0001c0007t0011g0243 a0001c0007t0016g0241 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.250-801C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4692243 | |||||||
chr17:4692264 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.250-822C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4692264 | |||||||
chr17:4692384 | G | A | 1 | a0001c0004t0004g0201 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.250-942C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4692384 | |||||||
chr17:4692404 | T | C | 18 | a0001c0001t0001g0206 a0001c0001t0007g0202 a0001c0001t0007g0203 others(15): Show |
18 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.250-962A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4692404 | |||||||
chr17:4692423 | T | C | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.250-981A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4692423 | |||||||
chr17:4692446 | A | G | 1 | a0001c0015t0018g0232 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.250-1004T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4692446 | |||||||
chr17:4692454 | G | A | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.250-1012C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4692454 | |||||||
chr17:4692466 | CA | C | 274 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(271): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.250-1025delT | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4692466 | |||||||
chr17:4692631 | C | G | 1 | a0001c0002t0017g0088 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.250-1189G>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4692631 | |||||||
chr17:4692732 | G | A | 18 | a0001c0001t0001g0206 a0001c0001t0007g0202 a0001c0001t0007g0203 others(15): Show |
18 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.250-1290C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4692732 | |||||||
chr17:4692853 | T | C | 10 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0275 others(7): Show |
13 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.250-1411A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4692853 | |||||||
chr17:4692860 | A | G | 2 | a0001c0001t0001g0277 a0001c0001t0001g0281 |
2 | HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.250-1418T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4692860 | |||||||
chr17:4692874 | G | A | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(183): Show |
210 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.250-1432C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4692874 | |||||||
chr17:4692982 | C | G | 1 | a0001c0004t0004g0210 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.250-1540G>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4692982 | |||||||
chr17:4693067 | T | A | 4 | a0001c0001t0001g0206 a0001c0004t0004g0205 a0001c0004t0004g0207 others(1): Show |
4 | HG00140.hp1 HG00140.hp2 HG00735.hp2 others(1): Show |
intron_variant | MODIFIER | c.250-1625A>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4693067 | |||||||
chr17:4693161 | A | C | 11 | a0001c0002t0005g0224 a0001c0002t0005g0225 a0001c0002t0006g0005 others(8): Show |
13 | HG01884.hp1 HG02257.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.250-1719T>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4693161 | |||||||
chr17:4693246 | C | G | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(182): Show |
209 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(206): Show |
intron_variant | MODIFIER | c.250-1804G>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4693246 | |||||||
chr17:4693384 | T | C | 16 | a0001c0015t0018g0232 a0002c0003t0003g0022 a0002c0003t0003g0226 others(13): Show |
17 | HG00099.hp1 HG01070.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.250-1942A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4693384 | |||||||
chr17:4693619 | C | T | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.250-2177G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4693619 | |||||||
chr17:4693648 | G | A | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.250-2206C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4693648 | |||||||
chr17:4693719 | A | G | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.250-2277T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4693719 | |||||||
chr17:4693805 | C | T | 5 | a0003c0005t0001g0166 a0003c0005t0001g0172 a0003c0005t0001g0179 others(2): Show |
5 | NA18955.hp2 NA18979.hp1 NA18991.hp2 others(2): Show |
intron_variant | MODIFIER | c.250-2363G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4693805 | |||||||
chr17:4693876 | G | T | 1 | a0001c0001t0002g0273 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.250-2434C>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4693876 | |||||||
chr17:4694208 | G | A | 2 | a0001c0013t0015g0007 a0004c0017t0007g0026 |
3 | HG02615.hp1 HG02809.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.250-2766C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4694208 | |||||||
chr17:4694368 | G | A | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.250-2926C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4694368 | |||||||
chr17:4694370 | G | A | 1 | a0001c0001t0009g0082 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.250-2928C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4694370 | |||||||
chr17:4694390 | G | A | 4 | a0001c0004t0004g0201 a0005c0008t0004g0208 a0005c0008t0004g0209 others(1): Show |
4 | HG02280.hp1 HG02572.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.250-2948C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4694390 | |||||||
chr17:4694424 | G | A | 2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.250-2982C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4694424 | |||||||
chr17:4694477 | C | T | 2 | a0001c0001t0002g0251 a0001c0001t0002g0255 |
2 | NA18968.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.250-3035G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4694477 | |||||||
chr17:4694497 | C | CAAAAA | 56 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0071 others(53): Show |
61 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(58): Show |
intron_variant | MODIFIER | c.250-3060_250-3056d others(7): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4694497 | |||||||
chr17:4694497 | C | CAAAAAA | 8 | a0001c0001t0001g0101 a0001c0001t0001g0120 a0001c0001t0001g0121 others(5): Show |
8 | HG00741.hp1 HG02129.hp1 HG03688.hp1 others(5): Show |
intron_variant | MODIFIER | c.250-3061_250-3056d others(8): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4694497 | |||||||
chr17:4694497 | C | CAAAAAAA others(7): Show |
1 | a0001c0001t0001g0076 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.250-3056_250-3055i others(16): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4694497 | |||||||
chr17:4694497 | C | CAAAAAAA others(8): Show |
3 | a0001c0001t0001g0016 a0001c0001t0001g0063 a0001c0001t0001g0170 |
4 | HG02735.hp1 HG03688.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.250-3056_250-3055i others(17): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4694497 | |||||||
chr17:4694497 | C | CAAAAAAA others(9): Show |
43 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0014 others(40): Show |
48 | HG01074.hp1 HG01099.hp1 HG01099.hp2 others(45): Show |
intron_variant | MODIFIER | c.250-3056_250-3055i others(18): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4694497 | |||||||
chr17:4694497 | C | CAAAAAAA others(10): Show |
103 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0009 others(100): Show |
117 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(114): Show |
intron_variant | MODIFIER | c.250-3056_250-3055i others(19): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4694497 | |||||||
chr17:4694497 | C | CAAAAAAA others(11): Show |
43 | a0001c0001t0001g0008 a0001c0001t0001g0050 a0001c0001t0001g0053 others(40): Show |
44 | HG00408.hp1 HG00408.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.250-3056_250-3055i others(20): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4694497 | |||||||
chr17:4694497 | C | CAAAAAAA others(12): Show |
5 | a0001c0001t0001g0020 a0001c0001t0001g0165 a0001c0002t0006g0081 others(2): Show |
6 | HG02080.hp1 HG02723.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.250-3056_250-3055i others(21): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4694497 | |||||||
chr17:4694497 | C | CAAAAAAA others(13): Show |
4 | a0001c0002t0005g0224 a0001c0002t0006g0223 a0001c0013t0015g0007 others(1): Show |
5 | HG01884.hp1 HG02615.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.250-3056_250-3055i others(22): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4694497 | |||||||
chr17:4694497 | C | CAAAAAAA others(14): Show |
6 | a0001c0002t0005g0225 a0001c0002t0006g0005 a0001c0002t0006g0219 others(3): Show |
8 | HG02257.hp1 HG02630.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.250-3056_250-3055i others(23): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4694497 | |||||||
chr17:4694497 | C | CAAAAAAA others(15): Show |
2 | a0001c0002t0006g0216 a0001c0002t0006g0220 |
2 | HG02451.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.250-3056_250-3055i others(24): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4694497 | |||||||
chr17:4694521 | G | T | 1 | a0001c0001t0001g0115 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.250-3079C>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4694521 | |||||||
chr17:4694592 | G | A | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(183): Show |
210 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.250-3150C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4694592 | |||||||
chr17:4694628 | C | A | 28 | a0001c0001t0002g0246 a0001c0001t0002g0247 a0001c0001t0002g0248 others(25): Show |
28 | HG00544.hp2 HG01943.hp1 HG02027.hp1 others(25): Show |
intron_variant | MODIFIER | c.250-3186G>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4694628 | |||||||
chr17:4694659 | CA | C | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.250-3218delT | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4694659 | |||||||
chr17:4694700 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.250-3258G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4694700 | |||||||
chr17:4694808 | T | C | 2 | a0001c0004t0004g0040 a0001c0004t0004g0041 |
2 | HG00642.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.250-3366A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4694808 | |||||||
chr17:4694894 | C | T | 51 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0244 others(48): Show |
56 | HG00544.hp2 HG01243.hp2 HG01884.hp1 others(53): Show |
intron_variant | MODIFIER | c.250-3452G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4694894 | |||||||
chr17:4695062 | C | T | 2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.250-3620G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4695062 | |||||||
chr17:4695089 | G | A | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.250-3647C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4695089 | |||||||
chr17:4695105 | G | A | 6 | a0001c0002t0006g0005 a0001c0002t0006g0216 a0001c0002t0006g0219 others(3): Show |
8 | HG01884.hp1 HG02257.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.250-3663C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4695105 | |||||||
chr17:4695158 | T | C | 5 | a0001c0002t0007g0042 a0004c0009t0007g0030 a0004c0009t0007g0031 others(2): Show |
5 | HG02258.hp1 HG02976.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.250-3716A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4695158 | |||||||
chr17:4695174 | T | C | 3 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 |
3 | NA19077.hp1 NA19085.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.250-3732A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4695174 | |||||||
chr17:4695179 | G | A | 1 | a0002c0003t0003g0231 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.250-3737C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4695179 | |||||||
chr17:4695225 | G | A | 1 | a0001c0001t0002g0268 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.250-3783C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4695225 | |||||||
chr17:4695298 | G | A | 16 | a0001c0015t0018g0232 a0002c0003t0003g0022 a0002c0003t0003g0226 others(13): Show |
17 | HG00099.hp1 HG01070.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.250-3856C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4695298 | |||||||
chr17:4695325 | A | AAAATAAA others(1): Show |
274 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(271): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.250-3891_250-3884d others(10): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4695325 | |||||||
chr17:4695325 | A | T | 1 | a0004c0018t0007g0027 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.250-3883T>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4695325 | |||||||
chr17:4695398 | C | T | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.250-3956G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4695398 | |||||||
chr17:4695595 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.250-4153C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4695595 | |||||||
chr17:4695665 | CT | C | 3 | a0001c0001t0007g0202 a0001c0001t0007g0203 a0001c0001t0007g0213 |
3 | HG01109.hp2 HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.250-4224delA | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4695665 | |||||||
chr17:4695666 | TTA | T | 14 | a0001c0001t0001g0206 a0001c0004t0004g0040 a0001c0004t0004g0041 others(11): Show |
14 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(11): Show |
intron_variant | MODIFIER | c.250-4226_250-4225d others(4): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4695666 | |||||||
chr17:4695667 | TA | T | 192 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(189): Show |
215 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(212): Show |
intron_variant | MODIFIER | c.250-4226delT | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4695667 | |||||||
chr17:4695667 | TAA | T | 9 | a0001c0001t0001g0074 a0001c0001t0001g0110 a0001c0001t0002g0248 others(6): Show |
9 | HG01515.hp2 HG02257.hp2 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.250-4227_250-4226d others(4): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4695667 | |||||||
chr17:4695667 | TAAA | T | 12 | a0001c0001t0001g0276 a0001c0002t0005g0224 a0001c0002t0005g0225 others(9): Show |
14 | HG01884.hp1 HG02257.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.250-4228_250-4226d others(5): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4695667 | |||||||
chr17:4695667 | TAAAA | T | 10 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0244 others(7): Show |
13 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.250-4229_250-4226d others(6): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4695667 | |||||||
chr17:4695676 | A | G | 1 | a0001c0001t0001g0167 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.250-4234T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4695676 | |||||||
chr17:4695717 | G | A | 5 | a0001c0002t0007g0042 a0004c0009t0007g0030 a0004c0009t0007g0031 others(2): Show |
5 | HG02258.hp1 HG02976.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.250-4275C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4695717 | |||||||
chr17:4695811 | T | A | 2 | a0001c0001t0009g0028 a0001c0001t0009g0029 |
2 | HG00438.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.250-4369A>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4695811 | |||||||
chr17:4695848 | G | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0137 a0001c0001t0001g0138 others(1): Show |
5 | NA18982.hp1 NA18985.hp2 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.250-4406C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4695848 | |||||||
chr17:4695956 | C | T | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.250-4514G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4695956 | |||||||
chr17:4695957 | A | G | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.250-4515T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4695957 | |||||||
chr17:4695969 | A | G | 2 | a0001c0030t0004g0214 a0008c0031t0004g0200 |
2 | HG00741.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.250-4527T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4695969 | |||||||
chr17:4696007 | T | TA | 74 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0206 others(71): Show |
79 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.250-4566dupT | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4696007 | |||||||
chr17:4696032 | GA | G | 72 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0206 others(69): Show |
77 | HG00140.hp1 HG00140.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.250-4591delT | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4696032 | |||||||
chr17:4696032 | GAA | G | 200 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(197): Show |
225 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(222): Show |
intron_variant | MODIFIER | c.250-4592_250-4591d others(4): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4696032 | |||||||
chr17:4696227 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.250-4785C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4696227 | |||||||
chr17:4696276 | G | A | 5 | a0001c0001t0009g0082 a0001c0002t0006g0081 a0001c0002t0006g0083 others(2): Show |
5 | HG01167.hp2 HG02622.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.250-4834C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4696276 | |||||||
chr17:4696280 | C | A | 1 | a0001c0004t0004g0205 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.250-4838G>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4696280 | |||||||
chr17:4696362 | A | G | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.250-4920T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4696362 | |||||||
chr17:4696586 | T | C | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.250-5144A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4696586 | |||||||
chr17:4696605 | C | T | 275 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(272): Show |
305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.250-5163G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4696605 | |||||||
chr17:4696795 | C | T | 281 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(278): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.250-5353G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4696795 | |||||||
chr17:4696934 | C | T | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.250-5492G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4696934 | |||||||
chr17:4696985 | G | C | 16 | a0001c0015t0018g0232 a0002c0003t0003g0022 a0002c0003t0003g0226 others(13): Show |
17 | HG00099.hp1 HG01070.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.250-5543C>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4696985 | |||||||
chr17:4697215 | C | CGAGAG | 15 | a0001c0015t0018g0232 a0002c0003t0003g0022 a0002c0003t0003g0226 others(12): Show |
16 | HG00099.hp1 HG01070.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.250-5778_250-5774d others(7): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4697215 | |||||||
chr17:4697360 | A | G | 16 | a0001c0015t0018g0232 a0002c0003t0003g0022 a0002c0003t0003g0226 others(13): Show |
17 | HG00099.hp1 HG01070.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.250-5918T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4697360 | |||||||
chr17:4697469 | G | A | 16 | a0001c0015t0018g0232 a0002c0003t0003g0022 a0002c0003t0003g0226 others(13): Show |
17 | HG00099.hp1 HG01070.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.250-6027C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4697469 | |||||||
chr17:4697622 | G | A | 3 | a0001c0001t0007g0202 a0001c0001t0007g0203 a0001c0001t0007g0213 |
3 | HG01109.hp2 HG02572.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.250-6180C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4697622 | |||||||
chr17:4697725 | G | A | 249 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(246): Show |
276 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.249+6138C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4697725 | |||||||
chr17:4697751 | T | C | 1 | a0001c0002t0005g0003 | 3 | HG02451.hp1 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.249+6112A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4697751 | |||||||
chr17:4697813 | G | C | 58 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0244 others(55): Show |
63 | HG00544.hp2 HG00642.hp1 HG01243.hp2 others(60): Show |
intron_variant | MODIFIER | c.249+6050C>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4697813 | |||||||
chr17:4697921 | C | G | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.249+5942G>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4697921 | |||||||
chr17:4697935 | G | T | 3 | a0005c0008t0004g0208 a0005c0008t0004g0209 a0005c0008t0004g0215 |
3 | HG02280.hp1 HG02572.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.249+5928C>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4697935 | |||||||
chr17:4697991 | C | T | 1 | a0001c0006t0001g0114 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.249+5872G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4697991 | |||||||
chr17:4698008 | G | GCT | 5 | a0001c0007t0011g0242 a0001c0007t0011g0243 a0001c0007t0016g0241 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.249+5854_249+5855i others(4): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4698008 | |||||||
chr17:4698008 | G | GT | 27 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0073 others(24): Show |
27 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.249+5854dupA | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4698008 | |||||||
chr17:4698008 | GT | G | 10 | a0001c0001t0001g0015 a0001c0001t0001g0080 a0001c0001t0001g0108 others(7): Show |
11 | HG01891.hp2 HG02723.hp1 HG02738.hp2 others(8): Show |
intron_variant | MODIFIER | c.249+5854delA | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4698008 | |||||||
chr17:4698008 | GTT | G | 15 | a0001c0015t0018g0232 a0002c0003t0003g0022 a0002c0003t0003g0226 others(12): Show |
16 | HG00099.hp1 HG01070.hp2 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.249+5853_249+5854d others(4): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4698008 | |||||||
chr17:4698351 | C | T | 1 | a0001c0025t0007g0146 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.249+5512G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4698351 | |||||||
chr17:4698359 | AAGCTGGG others(11): Show |
A | 1 | a0001c0001t0001g0052 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.249+5486_249+5503d others(20): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4698359 | |||||||
chr17:4698438 | G | A | 16 | a0001c0015t0018g0232 a0002c0003t0003g0022 a0002c0003t0003g0226 others(13): Show |
17 | HG00099.hp1 HG01070.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.249+5425C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4698438 | |||||||
chr17:4698470 | T | TA | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(177): Show |
203 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(200): Show |
intron_variant | MODIFIER | c.249+5392dupT | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4698470 | |||||||
chr17:4698484 | G | A | 1 | a0001c0001t0001g0052 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.249+5379C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4698484 | |||||||
chr17:4698639 | C | CAA | 5 | a0001c0001t0001g0145 a0001c0013t0015g0007 a0001c0014t0001g0217 others(2): Show |
6 | HG02615.hp1 HG02809.hp2 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.249+5222_249+5223d others(4): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4698639 | |||||||
chr17:4698639 | C | CAAA | 257 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(254): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.249+5221_249+5223d others(5): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4698639 | |||||||
chr17:4698639 | C | CAAAA | 14 | a0001c0001t0001g0109 a0001c0001t0001g0194 a0001c0001t0002g0251 others(11): Show |
14 | HG01167.hp2 HG01884.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.249+5220_249+5223d others(6): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4698639 | |||||||
chr17:4698653 | C | A | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.249+5210G>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4698653 | |||||||
chr17:4698727 | A | ATGT | 26 | a0001c0001t0001g0206 a0001c0001t0007g0202 a0001c0001t0007g0203 others(23): Show |
28 | HG00140.hp1 HG00140.hp2 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.249+5133_249+5135d others(5): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4698727 | |||||||
chr17:4698727 | ATGT | A | 15 | a0001c0002t0008g0086 a0001c0002t0008g0087 a0001c0002t0008g0090 others(12): Show |
15 | HG01884.hp2 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.249+5133_249+5135d others(5): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4698727 | |||||||
chr17:4698863 | A | T | 1 | a0001c0001t0001g0052 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.249+5000T>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4698863 | |||||||
chr17:4699045 | G | A | 1 | a0001c0007t0011g0242 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.249+4818C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4699045 | |||||||
chr17:4699151 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.249+4712C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4699151 | |||||||
chr17:4699220 | A | T | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(183): Show |
210 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.249+4643T>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4699220 | |||||||
chr17:4699260 | T | C | 5 | a0001c0007t0011g0242 a0001c0007t0011g0243 a0001c0007t0016g0241 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.249+4603A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4699260 | |||||||
chr17:4699286 | A | G | 1 | a0001c0001t0009g0160 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.249+4577T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4699286 | |||||||
chr17:4699396 | T | A | 2 | a0001c0030t0004g0214 a0008c0031t0004g0200 |
2 | HG00741.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.249+4467A>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4699396 | |||||||
chr17:4699499 | G | T | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.249+4364C>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4699499 | |||||||
chr17:4699642 | G | A | 186 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(183): Show |
210 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(207): Show |
intron_variant | MODIFIER | c.249+4221C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4699642 | |||||||
chr17:4699647 | C | T | 6 | a0001c0001t0001g0159 a0001c0002t0007g0042 a0004c0009t0007g0030 others(3): Show |
6 | HG02258.hp1 HG02615.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.249+4216G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4699647 | |||||||
chr17:4699790 | T | C | 1 | a0001c0002t0006g0221 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.249+4073A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4699790 | |||||||
chr17:4699803 | T | C | 1 | a0001c0001t0009g0157 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.249+4060A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4699803 | |||||||
chr17:4699811 | T | G | 1 | a0001c0001t0001g0158 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.249+4052A>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4699811 | |||||||
chr17:4699897 | A | AT | 48 | a0001c0001t0001g0206 a0001c0001t0001g0275 a0001c0001t0001g0276 others(45): Show |
51 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(48): Show |
intron_variant | MODIFIER | c.249+3965dupA | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4699897 | |||||||
chr17:4699897 | A | ATT | 23 | a0001c0001t0001g0191 a0001c0001t0002g0248 a0001c0001t0002g0249 others(20): Show |
25 | HG01175.hp2 HG01884.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.249+3964_249+3965d others(4): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4699897 | |||||||
chr17:4699897 | A | ATTT | 127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(124): Show |
149 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.249+3963_249+3965d others(5): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4699897 | |||||||
chr17:4699897 | A | ATTTT | 45 | a0001c0001t0001g0011 a0001c0001t0001g0043 a0001c0001t0001g0051 others(42): Show |
46 | HG00438.hp1 HG00673.hp1 HG00735.hp1 others(43): Show |
intron_variant | MODIFIER | c.249+3962_249+3965d others(6): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4699897 | |||||||
chr17:4699897 | A | ATTTTT | 12 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0002t0008g0086 others(9): Show |
12 | HG02055.hp1 HG02055.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.249+3961_249+3965d others(7): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4699897 | |||||||
chr17:4699922 | A | G | 1 | a0001c0004t0004g0205 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.249+3941T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4699922 | |||||||
chr17:4700149 | C | T | 2 | a0002c0003t0003g0227 a0002c0003t0003g0228 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.249+3714G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4700149 | |||||||
chr17:4700352 | C | A | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(171): Show |
197 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(194): Show |
intron_variant | MODIFIER | c.249+3511G>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4700352 | |||||||
chr17:4700353 | G | A | 5 | a0001c0007t0011g0242 a0001c0007t0011g0243 a0001c0007t0016g0241 others(2): Show |
5 | HG01884.hp2 HG02145.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.249+3510C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4700353 | |||||||
chr17:4700410 | C | T | 2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.249+3453G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4700410 | |||||||
chr17:4700442 | C | T | 2 | a0001c0001t0001g0244 a0001c0001t0001g0245 |
2 | HG02965.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.249+3421G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4700442 | |||||||
chr17:4700516 | T | C | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.249+3347A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4700516 | |||||||
chr17:4700735 | G | T | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(182): Show |
209 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(206): Show |
intron_variant | MODIFIER | c.249+3128C>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4700735 | |||||||
chr17:4700755 | T | C | 2 | a0001c0002t0006g0222 a0001c0002t0006g0223 |
2 | HG01884.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.249+3108A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4700755 | |||||||
chr17:4700849 | T | C | 2 | a0001c0001t0001g0143 a0012c0020t0001g0144 |
2 | HG03669.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.249+3014A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4700849 | |||||||
chr17:4700928 | C | CA | 24 | a0001c0001t0007g0202 a0001c0001t0007g0203 a0001c0001t0007g0213 others(21): Show |
25 | HG00099.hp1 HG00642.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.249+2934dupT | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4700928 | |||||||
chr17:4700928 | C | CAA | 9 | a0001c0001t0001g0206 a0001c0004t0004g0205 a0001c0004t0004g0207 others(6): Show |
9 | HG00140.hp1 HG00140.hp2 HG00735.hp2 others(6): Show |
intron_variant | MODIFIER | c.249+2933_249+2934d others(4): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4700928 | |||||||
chr17:4700928 | CA | C | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(176): Show |
203 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(200): Show |
intron_variant | MODIFIER | c.249+2934delT | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4700928 | |||||||
chr17:4700975 | A | G | 27 | a0001c0002t0005g0224 a0001c0002t0005g0225 a0001c0002t0006g0005 others(24): Show |
30 | HG00099.hp1 HG01070.hp2 HG01109.hp1 others(27): Show |
intron_variant | MODIFIER | c.249+2888T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4700975 | |||||||
chr17:4700992 | T | TA | 65 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0016 others(62): Show |
74 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.249+2870dupT | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4700992 | |||||||
chr17:4700992 | T | TAA | 10 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0187 others(7): Show |
10 | HG01106.hp2 HG02258.hp1 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.249+2869_249+2870d others(4): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4700992 | |||||||
chr17:4700992 | TA | T | 69 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(66): Show |
75 | HG00099.hp1 HG00544.hp2 HG01070.hp1 others(72): Show |
intron_variant | MODIFIER | c.249+2870delT | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4700992 | |||||||
chr17:4700992 | TAA | T | 28 | a0001c0001t0001g0206 a0001c0001t0001g0244 a0001c0001t0002g0246 others(25): Show |
30 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(27): Show |
intron_variant | MODIFIER | c.249+2869_249+2870d others(4): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4700992 | |||||||
chr17:4700993 | A | T | 2 | a0002c0003t0003g0237 a0002c0003t0003g0238 |
2 | HG02523.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.249+2870T>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4700993 | |||||||
chr17:4701202 | T | C | 79 | a0001c0001t0001g0206 a0001c0001t0002g0246 a0001c0001t0002g0247 others(76): Show |
82 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(79): Show |
intron_variant | MODIFIER | c.249+2661A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4701202 | |||||||
chr17:4701307 | G | A | 9 | a0001c0001t0001g0021 a0001c0001t0001g0191 a0001c0001t0001g0192 others(6): Show |
10 | HG00597.hp2 HG01192.hp1 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.249+2556C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4701307 | |||||||
chr17:4701324 | T | TG | 50 | a0001c0001t0001g0206 a0001c0001t0007g0202 a0001c0001t0007g0203 others(47): Show |
53 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(50): Show |
intron_variant | MODIFIER | c.249+2538dupC | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4701324 | |||||||
chr17:4701324 | T | TGG | 41 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0244 others(38): Show |
44 | HG00544.hp2 HG01243.hp2 HG01891.hp1 others(41): Show |
intron_variant | MODIFIER | c.249+2537_249+2538d others(4): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4701324 | |||||||
chr17:4701339 | A | G | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(182): Show |
209 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(206): Show |
intron_variant | MODIFIER | c.249+2524T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4701339 | |||||||
chr17:4701490 | G | A | 11 | a0001c0002t0005g0224 a0001c0002t0005g0225 a0001c0002t0006g0005 others(8): Show |
13 | HG01884.hp1 HG02257.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.249+2373C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4701490 | |||||||
chr17:4701495 | C | T | 10 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0275 others(7): Show |
13 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.249+2368G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4701495 | |||||||
chr17:4701498 | G | A | 1 | a0001c0002t0005g0039 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.249+2365C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4701498 | |||||||
chr17:4701527 | T | C | 1 | a0001c0001t0001g0190 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.249+2336A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4701527 | |||||||
chr17:4701535 | A | G | 1 | a0001c0010t0001g0070 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.249+2328T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4701535 | |||||||
chr17:4701541 | T | C | 91 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0206 others(88): Show |
97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.249+2322A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4701541 | |||||||
chr17:4701543 | C | T | 91 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0206 others(88): Show |
97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.249+2320G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4701543 | |||||||
chr17:4701642 | A | T | 10 | a0001c0001t0001g0004 a0001c0001t0001g0008 a0001c0001t0001g0053 others(7): Show |
13 | HG00408.hp1 HG00673.hp2 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.249+2221T>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4701642 | |||||||
chr17:4701701 | C | G | 1 | a0001c0001t0001g0063 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.249+2162G>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4701701 | |||||||
chr17:4701737 | A | G | 3 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 |
3 | HG02630.hp1 HG03453.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.249+2126T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4701737 | |||||||
chr17:4701761 | C | T | 1 | a0004c0017t0007g0026 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.249+2102G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4701761 | |||||||
chr17:4701773 | C | T | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(182): Show |
209 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(206): Show |
intron_variant | MODIFIER | c.249+2090G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4701773 | |||||||
chr17:4701905 | A | C | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(182): Show |
209 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(206): Show |
intron_variant | MODIFIER | c.249+1958T>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4701905 | |||||||
chr17:4702068 | A | G | 11 | a0001c0002t0005g0224 a0001c0002t0005g0225 a0001c0002t0006g0005 others(8): Show |
13 | HG01884.hp1 HG02257.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.249+1795T>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4702068 | |||||||
chr17:4702162 | T | G | 2 | a0001c0013t0015g0007 a0004c0017t0007g0026 |
3 | HG02615.hp1 HG02809.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.249+1701A>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4702162 | |||||||
chr17:4702209 | G | A | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.249+1654C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4702209 | |||||||
chr17:4702230 | G | A | 9 | a0001c0001t0001g0021 a0001c0001t0001g0191 a0001c0001t0001g0192 others(6): Show |
10 | HG00597.hp2 HG01192.hp1 HG01978.hp1 others(7): Show |
intron_variant | MODIFIER | c.249+1633C>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4702230 | |||||||
chr17:4702421 | AAAT | A | 10 | a0001c0001t0001g0006 a0001c0001t0001g0023 a0001c0001t0001g0275 others(7): Show |
13 | HG01243.hp2 HG01891.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.249+1439_249+1441d others(5): Show |
PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4702421 | |||||||
chr17:4702551 | C | T | 5 | a0001c0001t0001g0055 a0001c0001t0010g0058 a0006c0011t0010g0056 others(2): Show |
5 | HG01346.hp2 HG02273.hp2 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.249+1312G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4702551 | |||||||
chr17:4702592 | T | C | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(182): Show |
209 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(206): Show |
intron_variant | MODIFIER | c.249+1271A>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4702592 | |||||||
chr17:4702675 | C | A | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.249+1188G>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4702675 | |||||||
chr17:4702964 | C | G | 19 | a0001c0001t0001g0206 a0001c0001t0007g0202 a0001c0001t0007g0203 others(16): Show |
19 | HG00140.hp1 HG00140.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.249+899G>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4702964 | |||||||
chr17:4703100 | C | G | 184 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(181): Show |
208 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(205): Show |
intron_variant | MODIFIER | c.249+763G>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4703100 | |||||||
chr17:4703125 | C | G | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG02040.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.249+738G>C | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4703125 | |||||||
chr17:4703142 | C | T | 10 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0046 others(7): Show |
10 | HG00408.hp2 NA18956.hp1 NA18973.hp1 others(7): Show |
intron_variant | MODIFIER | c.249+721G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4703142 | |||||||
chr17:4703303 | C | T | 5 | a0001c0002t0007g0042 a0004c0009t0007g0030 a0004c0009t0007g0031 others(2): Show |
5 | HG02258.hp1 HG02976.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.249+560G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4703303 | |||||||
chr17:4703467 | A | C | 2 | a0001c0004t0004g0040 a0001c0004t0004g0041 |
2 | HG00642.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.249+396T>G | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4703467 | |||||||
chr17:4703521 | C | A | 276 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(273): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): Show |
intron_variant | MODIFIER | c.249+342G>T | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4703521 | |||||||
chr17:4703571 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.249+292G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4703571 | |||||||
chr17:4703602 | GC | G | 4 | a0004c0009t0007g0030 a0004c0009t0007g0031 a0004c0009t0007g0032 others(1): Show |
4 | HG02258.hp1 HG02976.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.249+260delG | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4703602 | |||||||
chr17:4703814 | C | T | 2 | a0001c0001t0009g0028 a0001c0001t0009g0029 |
2 | HG00438.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.249+49G>A | PELP1 | ENSG00000141456.16 | transcript | ENST00000572293.7 | protein_coding | 1/16 | chr17 | 4703814 |