Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 59342 |
| ensemblid | ENSG00000121064.13 |
| hgncid | 29507 |
| symbol | SCPEP1 |
| name | serine carboxypeptidase 1 |
| refseq_nuc | NM_021626.3 |
| refseq_prot | NP_067639.1 |
| ensembl_nuc | ENST00000262288.8 |
| ensembl_prot | ENSP00000262288.3 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 56978131 |
| end | 57006768 |
| strand | + |
| ver | v1.2 |
| region | chr17:56978131-57006768 |
| region5000 | chr17:56973131-57011768 |
| regionname0 | SCPEP1_chr17_56978131_57006768 |
| regionname5000 | SCPEP1_chr17_56973131_57011768 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 452 | 373 | 96 | 70 | 151 | 14 | 40 | 117 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | MELAL others(447): Show |
chr17 | 56973131 | 57011768 |
| a0002 | 0/0 | 452 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | MELAL others(447): Show |
chr17 | 56973131 | 57011768 |
| a0003 | 0/0 | 452 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | MELAL others(447): Show |
chr17 | 56973131 | 57011768 |
| a0004 | 0/0 | 452 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | MEVAL others(447): Show |
chr17 | 56973131 | 57011768 |
| a0005 | 0/0 | 452 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | MELAL others(447): Show |
chr17 | 56973131 | 57011768 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1356 | 345 | 94 | 57 | 146 | 9 | 37 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | ATGGA others(1351): Show |
chr17 | 56973131 | 57011768 | ||
| a0001c0002 | 0/0 | 1356 | 24 | 2 | 13 | 1 | 5 | 3 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | ATGGA others(1351): Show |
chr17 | 56973131 | 57011768 | ||
| a0001c0003 | 0/0 | 1356 | 4 | 0 | 0 | 4 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | ATGGA others(1351): Show |
chr17 | 56973131 | 57011768 | ||
| a0002c0004 | 0/0 | 1356 | 3 | 0 | 0 | 3 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | ATGGA others(1351): Show |
chr17 | 56973131 | 57011768 | ||
| a0003c0005 | 0/0 | 1356 | 2 | 0 | 0 | 2 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | ATGGA others(1351): Show |
chr17 | 56973131 | 57011768 | ||
| a0004c0007 | 0/0 | 1356 | 1 | 1 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | ATGGA others(1351): Show |
chr17 | 56973131 | 57011768 | ||
| a0005c0006 | 0/0 | 1356 | 1 | 1 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | ATGGA others(1351): Show |
chr17 | 56973131 | 57011768 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1921 | 284 | 86 | 51 | 107 | 6 | 32 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | GTTGC others(1916): Show |
chr17 | 56973131 | 57011768 |
| a0001c0001t0002 | 0/0 | 1921 | 58 | 7 | 6 | 38 | 3 | 4 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | GTTGC others(1916): Show |
chr17 | 56973131 | 57011768 |
| a0001c0001t0003 | 0/0 | 1921 | 1 | 0 | 0 | 0 | 0 | 1 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | GTTGC others(1916): Show |
chr17 | 56973131 | 57011768 |
| a0001c0001t0004 | 0/0 | 1921 | 1 | 1 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | GTTGC others(1916): Show |
chr17 | 56973131 | 57011768 |
| a0001c0001t0005 | 0/0 | 1921 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | GTTGC others(1916): Show |
chr17 | 56973131 | 57011768 |
| a0001c0002t0001 | 0/0 | 1921 | 22 | 2 | 11 | 1 | 5 | 3 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | GTTGC others(1916): Show |
chr17 | 56973131 | 57011768 |
| a0001c0002t0002 | 0/0 | 1921 | 2 | 0 | 2 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | GTTGC others(1916): Show |
chr17 | 56973131 | 57011768 |
| a0001c0003t0001 | 0/0 | 1921 | 3 | 0 | 0 | 3 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | GTTGC others(1916): Show |
chr17 | 56973131 | 57011768 |
| a0001c0003t0002 | 0/0 | 1921 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | GTTGC others(1916): Show |
chr17 | 56973131 | 57011768 |
| a0002c0004t0002 | 0/0 | 1921 | 3 | 0 | 0 | 3 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | GTTGC others(1916): Show |
chr17 | 56973131 | 57011768 |
| a0003c0005t0001 | 0/0 | 1921 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | GTTGC others(1916): Show |
chr17 | 56973131 | 57011768 |
| a0003c0005t0002 | 0/0 | 1921 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | GTTGC others(1916): Show |
chr17 | 56973131 | 57011768 |
| a0004c0007t0001 | 0/0 | 1921 | 1 | 1 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | GTTGC others(1916): Show |
chr17 | 56973131 | 57011768 |
| a0005c0006t0001 | 0/0 | 1921 | 1 | 1 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | GTTGC others(1916): Show |
chr17 | 56973131 | 57011768 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 38 | 8 | 5 | 21 | 1 | 3 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0002 | 0/0 | 35 | 2 | 4 | 22 | 3 | 4 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0008 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0009 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0010 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0013 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0199 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0001g0203 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0002g0003 | 0/0 | 11 | 0 | 1 | 9 | 0 | 1 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0002g0004 | 0/0 | 8 | 0 | 2 | 6 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0002g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0002g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0003g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0001t0005g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0002t0001g0005 | 0/0 | 8 | 1 | 5 | 0 | 1 | 1 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0002t0001g0006 | 0/0 | 6 | 0 | 3 | 0 | 3 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0002t0001g0024 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0002t0001g0045 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0002t0001g0048 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0002t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0002t0002g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0003t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0003t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0001c0003t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0002c0004t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0003c0005t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0003c0005t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0004c0007t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| a0005c0006t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0006 | EUR | GBR | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0159 | EUR | GBR | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0024 | EUR | GBR | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0055 | EUR | FIN | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0094 | EUR | FIN | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | CHS | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | CHS | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0045 | AMR | PUR | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG00733 | hp2 | a0001 | c0002 | t0002 | g0206 | AMR | PUR | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | PUR | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0081 | AMR | PUR | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0056 | AMR | PUR | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | PUR | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0045 | AMR | PUR | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | CLM | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01256 | hp2 | a0001 | c0002 | t0002 | g0135 | AMR | CLM | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0006 | AMR | CLM | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0195 | AMR | CLM | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | CLM | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01433 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | CLM | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0024 | AMR | CLM | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0126 | EUR | IBS | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01515 | hp2 | a0001 | c0002 | t0001 | g0006 | EUR | IBS | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01517 | hp1 | a0001 | c0002 | t0001 | g0006 | EUR | IBS | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0127 | EUR | IBS | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0026 | AFR | ACB | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01934 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | PEL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0005 | AMR | PEL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PEL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02015 | hp1 | a0001 | c0002 | t0001 | g0024 | EAS | KHV | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | KHV | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | KHV | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02080 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | KHV | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | KHV | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | KHV | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | CDX | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | CDX | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CDX | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | ACB | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02258 | hp1 | a0001 | c0002 | t0001 | g0005 | AFR | ACB | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | KHV | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02717 | hp1 | a0004 | c0007 | t0001 | g0149 | AFR | GWD | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | GWD | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0204 | SAS | PJL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02896 | hp2 | a0005 | c0006 | t0001 | g0011 | AFR | GWD | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | ESN | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0166 | AFR | ESN | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0080 | AFR | ESN | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | MSL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | MSL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG03139 | hp2 | a0001 | c0001 | t0002 | g0151 | AFR | ESN | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | MSL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | MSL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | MSL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0054 | SAS | STU | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | PJL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0096 | SAS | PJL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | BEB | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0048 | SAS | BEB | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | BEB | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0061 | SAS | BEB | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | STU | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | STU | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | STU | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0205 | SAS | STU | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0005 | SAS | STU | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | YRI | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | CHB | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | CHB | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHB | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18906 | hp2 | a0001 | c0001 | t0002 | g0171 | AFR | YRI | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18945 | hp1 | a0002 | c0004 | t0002 | g0003 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18964 | hp2 | a0001 | c0003 | t0001 | g0043 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18965 | hp2 | a0001 | c0003 | t0001 | g0160 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18983 | hp2 | a0002 | c0004 | t0002 | g0003 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18988 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18990 | hp2 | a0001 | c0003 | t0001 | g0043 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18993 | hp1 | a0003 | c0005 | t0002 | g0108 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18993 | hp2 | a0001 | c0001 | t0005 | g0017 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19002 | hp1 | a0001 | c0003 | t0002 | g0176 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19011 | hp2 | a0002 | c0004 | t0002 | g0003 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | LWK | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | LWK | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0168 | AFR | LWK | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | LWK | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19076 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19077 | hp1 | a0003 | c0005 | t0001 | g0002 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | YRI | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | YRI | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | ASW | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ASW | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA20805 | hp2 | a0001 | c0002 | t0001 | g0005 | EUR | TSI | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | GIH | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | GIH | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ACB | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG06807 | hp1 | a0001 | c0001 | t0002 | g0184 | AFR | USA | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | USA | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | USA | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA20300 | hp2 | a0001 | c0002 | t0001 | g0048 | AFR | USA | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | LWK | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0199 | REF | REF | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0203 | REF | REF | SCPEP1_chr17_56973131_57011768 | SCPEP1 | chr17 | 56973131 | 57011768 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:56978166 | C | G | 1 | a0004 | 1 | HG02717.hp1 | missense_variant | MODERATE | c.7C>G | p.Leu3Val | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 1/13 | 36/1921 | 7/1359 | 3/452 | chr17 | 56978166 | |||
| chr17:56981197 | C | A | 1 | a0002 | 3 | NA18945.hp1 NA18983.hp2 NA19011.hp2 |
missense_variant | MODERATE | c.192C>A | p.Asn64Lys | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 2/13 | 221/1921 | 192/1359 | 64/452 | chr17 | 56981197 | |||
| chr17:56988261 | G | A | 1 | a0003 | 2 | NA18993.hp1 NA19077.hp1 |
missense_variant | MODERATE | c.517G>A | p.Ala173Thr | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 5/13 | 546/1921 | 517/1359 | 173/452 | chr17 | 56988261 | |||
| chr17:57000923 | G | A | 1 | a0005 | 1 | HG02896.hp2 | missense_variant | MODERATE | c.1063G>A | p.Glu355Lys | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 11/13 | 1092/1921 | 1063/1359 | 355/452 | chr17 | 57000923 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:56985461 | C | T | 1 | a0001c0003 | 4 | NA18964.hp2 NA18965.hp2 NA18990.hp2 others(1): Show |
synonymous_variant | LOW | c.309C>T | p.Thr103Thr | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 3/13 | 338/1921 | 309/1359 | 103/452 | chr17 | 56985461 | |||
| chr17:57002110 | T | C | 1 | a0001c0002 | 24 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(21): Show |
synonymous_variant | LOW | c.1225T>C | p.Leu409Leu | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 12/13 | 1254/1921 | 1225/1359 | 409/452 | chr17 | 57002110 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:57006549 | G | A | 1 | a0001c0001t0003 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*314G>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 13/13 | 314 | chr17 | 57006549 | ||||||
| chr17:57006572 | C | A | 6 | a0001c0001t0002 a0001c0001t0004 a0001c0002t0002 others(3): Show |
66 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*337C>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 13/13 | 337 | chr17 | 57006572 | ||||||
| chr17:57006601 | T | C | 1 | a0001c0001t0004 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*366T>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 13/13 | 366 | chr17 | 57006601 | ||||||
| chr17:57006657 | A | T | 1 | a0001c0001t0005 | 1 | NA18993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*422A>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 13/13 | 422 | chr17 | 57006657 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:56978380 | CT | C | 126 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(123): Show |
211 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.76+159delT | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 56978380 | ||||||
| chr17:56978436 | C | G | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG02135.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.76+201C>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 1/12 | chr17 | 56978436 | |||||||
| chr17:56978556 | T | A | 1 | a0001c0001t0001g0147 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.76+321T>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 1/12 | chr17 | 56978556 | |||||||
| chr17:56978993 | T | G | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(176): Show |
325 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.76+758T>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 1/12 | chr17 | 56978993 | |||||||
| chr17:56979010 | T | G | 1 | a0001c0001t0001g0049 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.76+775T>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 1/12 | chr17 | 56979010 | |||||||
| chr17:56979078 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.76+843T>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 1/12 | chr17 | 56979078 | |||||||
| chr17:56979177 | C | T | 1 | a0001c0001t0001g0185 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.76+942C>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 1/12 | chr17 | 56979177 | |||||||
| chr17:56979222 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.76+987C>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 1/12 | chr17 | 56979222 | |||||||
| chr17:56979259 | G | A | 1 | a0001c0002t0001g0045 | 2 | HG00733.hp1 HG01109.hp1 |
intron_variant | MODIFIER | c.76+1024G>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 1/12 | chr17 | 56979259 | |||||||
| chr17:56979372 | C | T | 1 | a0001c0001t0001g0143 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.76+1137C>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 1/12 | chr17 | 56979372 | |||||||
| chr17:56979477 | T | C | 1 | a0001c0001t0001g0046 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.76+1242T>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 1/12 | chr17 | 56979477 | |||||||
| chr17:56979841 | T | C | 1 | a0001c0001t0001g0051 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.77-1241T>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 1/12 | chr17 | 56979841 | |||||||
| chr17:56979879 | C | T | 5 | a0001c0001t0001g0044 a0001c0001t0001g0181 a0001c0001t0001g0182 others(2): Show |
6 | HG02257.hp1 HG02572.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.77-1203C>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 1/12 | chr17 | 56979879 | |||||||
| chr17:56979975 | G | A | 20 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0020 others(17): Show |
31 | HG00639.hp2 HG02055.hp2 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.77-1107G>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 1/12 | chr17 | 56979975 | |||||||
| chr17:56980012 | T | C | 2 | a0001c0001t0001g0186 a0001c0001t0001g0187 |
2 | HG03492.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.77-1070T>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 1/12 | chr17 | 56980012 | |||||||
| chr17:56980141 | A | G | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(176): Show |
325 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.77-941A>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 1/12 | chr17 | 56980141 | |||||||
| chr17:56980283 | T | A | 1 | a0001c0001t0001g0052 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.77-799T>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 1/12 | chr17 | 56980283 | |||||||
| chr17:56980321 | C | A | 6 | a0001c0001t0002g0004 a0001c0001t0002g0007 a0001c0001t0002g0053 others(3): Show |
17 | HG00280.hp1 HG01099.hp2 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.77-761C>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 1/12 | chr17 | 56980321 | |||||||
| chr17:56980517 | T | G | 1 | a0001c0001t0001g0148 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.77-565T>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 1/12 | chr17 | 56980517 | |||||||
| chr17:56980672 | T | C | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(176): Show |
325 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.77-410T>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 1/12 | chr17 | 56980672 | |||||||
| chr17:56980770 | A | G | 13 | a0001c0001t0001g0008 a0001c0001t0001g0019 a0001c0001t0001g0020 others(10): Show |
23 | HG00639.hp2 HG02055.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.77-312A>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 1/12 | chr17 | 56980770 | |||||||
| chr17:56980788 | CA | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(142): Show |
276 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(273): Show |
intron_variant | MODIFIER | c.77-270delA | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 56980788 | ||||||
| chr17:56980788 | CAA | C | 17 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0035 others(14): Show |
25 | HG01243.hp2 HG01256.hp2 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.77-271_77-270delAA | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 56980788 | ||||||
| chr17:56980788 | CAAAAAAA others(5): Show |
C | 3 | a0001c0001t0001g0036 a0001c0001t0001g0141 a0001c0001t0001g0142 |
4 | HG01346.hp1 HG01433.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.77-281_77-270delAA others(10): Show |
SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr17 | 56980788 | ||||||
| chr17:56980866 | A | G | 2 | a0001c0001t0001g0019 a0001c0001t0002g0151 |
4 | HG02922.hp1 HG03139.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.77-216A>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 1/12 | chr17 | 56980866 | |||||||
| chr17:56980884 | C | G | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG02135.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.77-198C>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 1/12 | chr17 | 56980884 | |||||||
| chr17:56981023 | T | C | 4 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0001c0001t0001g0190 others(1): Show |
4 | HG02486.hp1 HG02559.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.77-59T>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 1/12 | chr17 | 56981023 | |||||||
| chr17:56981056 | A | G | 32 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0021 others(29): Show |
82 | HG00099.hp2 HG00639.hp1 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.77-26A>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 1/12 | chr17 | 56981056 | |||||||
| chr17:56981265 | G | A | 3 | a0001c0001t0002g0057 a0001c0001t0002g0061 a0001c0001t0002g0062 |
3 | HG02080.hp2 HG02132.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.225+35G>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 2/12 | chr17 | 56981265 | |||||||
| chr17:56981328 | G | C | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(176): Show |
325 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.225+98G>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 2/12 | chr17 | 56981328 | |||||||
| chr17:56981343 | G | C | 2 | a0001c0001t0001g0063 a0001c0001t0001g0064 |
2 | NA18985.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.225+113G>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 2/12 | chr17 | 56981343 | |||||||
| chr17:56981363 | G | C | 1 | a0004c0007t0001g0149 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.225+133G>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 2/12 | chr17 | 56981363 | |||||||
| chr17:56981598 | C | T | 2 | a0001c0001t0001g0150 a0001c0001t0001g0153 |
2 | HG02615.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.225+368C>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 2/12 | chr17 | 56981598 | |||||||
| chr17:56981631 | A | G | 1 | a0001c0001t0001g0133 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.225+401A>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 2/12 | chr17 | 56981631 | |||||||
| chr17:56981747 | G | A | 7 | a0001c0001t0001g0044 a0001c0001t0001g0150 a0001c0001t0001g0153 others(4): Show |
8 | HG02257.hp1 HG02572.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.225+517G>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 2/12 | chr17 | 56981747 | |||||||
| chr17:56981872 | G | A | 32 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0021 others(29): Show |
82 | HG00099.hp2 HG00639.hp1 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.225+642G>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 2/12 | chr17 | 56981872 | |||||||
| chr17:56981942 | C | G | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(176): Show |
325 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.225+712C>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 2/12 | chr17 | 56981942 | |||||||
| chr17:56981996 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.225+766C>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 2/12 | chr17 | 56981996 | |||||||
| chr17:56982160 | A | G | 1 | a0001c0001t0001g0132 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.225+930A>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 2/12 | chr17 | 56982160 | |||||||
| chr17:56982209 | G | A | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG02135.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.225+979G>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 2/12 | chr17 | 56982209 | |||||||
| chr17:56982215 | G | A | 1 | a0001c0001t0001g0065 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.225+985G>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 2/12 | chr17 | 56982215 | |||||||
| chr17:56982255 | C | A | 14 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0001g0046 others(11): Show |
22 | HG00735.hp2 HG01070.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.225+1025C>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 2/12 | chr17 | 56982255 | |||||||
| chr17:56982266 | A | G | 1 | a0001c0001t0002g0034 | 2 | HG02040.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.225+1036A>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 2/12 | chr17 | 56982266 | |||||||
| chr17:56982290 | G | A | 32 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0021 others(29): Show |
82 | HG00099.hp2 HG00639.hp1 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.225+1060G>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 2/12 | chr17 | 56982290 | |||||||
| chr17:56982383 | C | T | 10 | a0001c0001t0001g0008 a0001c0001t0001g0020 a0001c0001t0001g0037 others(7): Show |
18 | HG00639.hp2 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.225+1153C>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 2/12 | chr17 | 56982383 | |||||||
| chr17:56982472 | A | G | 32 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0021 others(29): Show |
82 | HG00099.hp2 HG00639.hp1 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.225+1242A>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 2/12 | chr17 | 56982472 | |||||||
| chr17:56982490 | G | A | 5 | a0001c0001t0001g0044 a0001c0001t0001g0181 a0001c0001t0001g0182 others(2): Show |
6 | HG02257.hp1 HG02572.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.225+1260G>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 2/12 | chr17 | 56982490 | |||||||
| chr17:56982571 | C | T | 1 | a0001c0001t0001g0012 | 4 | NA18961.hp1 NA18986.hp1 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.225+1341C>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 2/12 | chr17 | 56982571 | |||||||
| chr17:56982620 | G | A | 1 | a0001c0001t0001g0019 | 3 | HG02922.hp1 HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.225+1390G>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 2/12 | chr17 | 56982620 | |||||||
| chr17:56982683 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.225+1453C>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 2/12 | chr17 | 56982683 | |||||||
| chr17:56982704 | G | T | 32 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0021 others(29): Show |
82 | HG00099.hp2 HG00639.hp1 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.225+1474G>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 2/12 | chr17 | 56982704 | |||||||
| chr17:56982707 | G | A | 32 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0021 others(29): Show |
82 | HG00099.hp2 HG00639.hp1 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.225+1477G>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 2/12 | chr17 | 56982707 | |||||||
| chr17:56982742 | CT | C | 32 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0021 others(29): Show |
82 | HG00099.hp2 HG00639.hp1 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.225+1524delT | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 56982742 | ||||||
| chr17:56982827 | T | G | 36 | a0001c0001t0001g0013 a0001c0001t0001g0063 a0001c0001t0001g0064 others(33): Show |
63 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(60): Show |
intron_variant | MODIFIER | c.225+1597T>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 2/12 | chr17 | 56982827 | |||||||
| chr17:56982900 | T | A | 1 | a0001c0001t0001g0192 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.225+1670T>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 2/12 | chr17 | 56982900 | |||||||
| chr17:56982967 | T | C | 32 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0021 others(29): Show |
82 | HG00099.hp2 HG00639.hp1 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.225+1737T>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 2/12 | chr17 | 56982967 | |||||||
| chr17:56983236 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.225+2006G>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 2/12 | chr17 | 56983236 | |||||||
| chr17:56983250 | G | C | 1 | a0001c0001t0001g0084 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.225+2020G>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 2/12 | chr17 | 56983250 | |||||||
| chr17:56983313 | A | T | 1 | a0001c0001t0001g0131 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.226-2065A>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 2/12 | chr17 | 56983313 | |||||||
| chr17:56983496 | G | A | 32 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0021 others(29): Show |
82 | HG00099.hp2 HG00639.hp1 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.226-1882G>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 2/12 | chr17 | 56983496 | |||||||
| chr17:56983700 | G | C | 3 | a0001c0001t0002g0057 a0001c0001t0002g0061 a0001c0001t0002g0062 |
3 | HG02080.hp2 HG02132.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.226-1678G>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 2/12 | chr17 | 56983700 | |||||||
| chr17:56983910 | T | C | 1 | a0001c0001t0001g0200 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.226-1468T>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 2/12 | chr17 | 56983910 | |||||||
| chr17:56983979 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.226-1399G>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 2/12 | chr17 | 56983979 | |||||||
| chr17:56983994 | C | T | 74 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0016 others(71): Show |
124 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.226-1384C>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 2/12 | chr17 | 56983994 | |||||||
| chr17:56984094 | G | A | 5 | a0001c0001t0001g0011 a0001c0001t0001g0059 a0001c0001t0001g0085 others(2): Show |
7 | HG02895.hp2 HG02896.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.226-1284G>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 2/12 | chr17 | 56984094 | |||||||
| chr17:56984213 | C | T | 5 | a0001c0001t0001g0044 a0001c0001t0001g0181 a0001c0001t0001g0182 others(2): Show |
6 | HG02257.hp1 HG02572.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.226-1165C>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 2/12 | chr17 | 56984213 | |||||||
| chr17:56984277 | A | G | 1 | a0001c0001t0002g0151 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.226-1101A>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 2/12 | chr17 | 56984277 | |||||||
| chr17:56984346 | C | G | 1 | a0001c0002t0002g0206 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.226-1032C>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 2/12 | chr17 | 56984346 | |||||||
| chr17:56984390 | A | C | 5 | a0001c0001t0001g0023 a0001c0001t0001g0047 a0001c0001t0001g0147 others(2): Show |
8 | HG01255.hp1 HG01257.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.226-988A>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 2/12 | chr17 | 56984390 | |||||||
| chr17:56984402 | G | T | 1 | a0001c0001t0001g0130 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.226-976G>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 2/12 | chr17 | 56984402 | |||||||
| chr17:56984606 | T | C | 1 | a0001c0001t0002g0066 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.226-772T>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 2/12 | chr17 | 56984606 | |||||||
| chr17:56984748 | C | T | 12 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0027 others(9): Show |
18 | HG01884.hp1 HG01884.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.226-630C>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 2/12 | chr17 | 56984748 | |||||||
| chr17:56984749 | G | T | 32 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0021 others(29): Show |
82 | HG00099.hp2 HG00639.hp1 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.226-629G>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 2/12 | chr17 | 56984749 | |||||||
| chr17:56984780 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.226-598C>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 2/12 | chr17 | 56984780 | |||||||
| chr17:56984952 | A | T | 1 | a0001c0001t0001g0128 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.226-426A>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 2/12 | chr17 | 56984952 | |||||||
| chr17:56985103 | T | TGAAAA | 174 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(171): Show |
320 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.226-254_226-250dup others(5): Show |
SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 56985103 | ||||||
| chr17:56985103 | T | TGAAAAGA others(3): Show |
3 | a0001c0001t0002g0126 a0001c0001t0002g0127 a0001c0001t0002g0184 |
3 | HG01515.hp1 HG01517.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.226-259_226-250dup others(10): Show |
SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 56985103 | ||||||
| chr17:56985237 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.226-141G>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 2/12 | chr17 | 56985237 | |||||||
| chr17:56985660 | A | G | 1 | a0001c0001t0001g0148 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.315+193A>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 3/12 | chr17 | 56985660 | |||||||
| chr17:56985661 | T | C | 5 | a0001c0001t0001g0044 a0001c0001t0001g0181 a0001c0001t0001g0182 others(2): Show |
6 | HG02257.hp1 HG02572.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.315+194T>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 3/12 | chr17 | 56985661 | |||||||
| chr17:56985772 | C | T | 1 | a0001c0001t0002g0151 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.315+305C>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 3/12 | chr17 | 56985772 | |||||||
| chr17:56985774 | C | T | 2 | a0001c0001t0001g0014 a0001c0001t0001g0089 |
4 | HG01891.hp1 HG02109.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.315+307C>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 3/12 | chr17 | 56985774 | |||||||
| chr17:56985841 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.315+374C>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 3/12 | chr17 | 56985841 | |||||||
| chr17:56986125 | A | G | 53 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0009 others(50): Show |
114 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(111): Show |
intron_variant | MODIFIER | c.315+658A>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 3/12 | chr17 | 56986125 | |||||||
| chr17:56986219 | C | G | 33 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0021 others(30): Show |
83 | HG00099.hp2 HG00639.hp1 HG00738.hp2 others(80): Show |
intron_variant | MODIFIER | c.315+752C>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 3/12 | chr17 | 56986219 | |||||||
| chr17:56986221 | C | CTT | 5 | a0001c0001t0001g0044 a0001c0001t0001g0181 a0001c0001t0001g0182 others(2): Show |
6 | HG02257.hp1 HG02572.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.315+768_315+769dup others(2): Show |
SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr17 | 56986221 | ||||||
| chr17:56986381 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.315+914G>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 3/12 | chr17 | 56986381 | |||||||
| chr17:56986396 | T | A | 1 | a0001c0001t0001g0095 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.315+929T>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 3/12 | chr17 | 56986396 | |||||||
| chr17:56986417 | A | T | 4 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0180 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.315+950A>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 3/12 | chr17 | 56986417 | |||||||
| chr17:56986496 | G | A | 2 | a0001c0001t0001g0019 a0001c0001t0002g0151 |
4 | HG02922.hp1 HG03139.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.315+1029G>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 3/12 | chr17 | 56986496 | |||||||
| chr17:56986536 | G | GT | 32 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0021 others(29): Show |
82 | HG00099.hp2 HG00639.hp1 HG00738.hp2 others(79): Show |
intron_variant | MODIFIER | c.315+1080dupT | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr17 | 56986536 | ||||||
| chr17:56986536 | G | T | 1 | a0001c0001t0001g0163 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.315+1069G>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 3/12 | chr17 | 56986536 | |||||||
| chr17:56986569 | A | G | 2 | a0001c0001t0002g0205 a0001c0002t0001g0204 |
2 | HG02735.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.315+1102A>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 3/12 | chr17 | 56986569 | |||||||
| chr17:56986839 | G | C | 179 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(176): Show |
325 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.316-856G>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 3/12 | chr17 | 56986839 | |||||||
| chr17:56986998 | T | G | 33 | a0001c0001t0001g0001 a0001c0001t0001g0009 a0001c0001t0001g0021 others(30): Show |
83 | HG00099.hp2 HG00639.hp1 HG00738.hp2 others(80): Show |
intron_variant | MODIFIER | c.316-697T>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 3/12 | chr17 | 56986998 | |||||||
| chr17:56987077 | C | T | 1 | a0004c0007t0001g0149 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.316-618C>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 3/12 | chr17 | 56987077 | |||||||
| chr17:56987438 | G | C | 155 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0011 others(152): Show |
264 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.316-257G>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 3/12 | chr17 | 56987438 | |||||||
| chr17:56987467 | CT | C | 174 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(171): Show |
293 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.316-215delT | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr17 | 56987467 | ||||||
| chr17:56987494 | C | T | 1 | a0001c0001t0001g0047 | 2 | HG01257.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.316-201C>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 3/12 | chr17 | 56987494 | |||||||
| chr17:56988022 | T | C | 1 | a0001c0001t0001g0188 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.471+172T>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 4/12 | chr17 | 56988022 | |||||||
| chr17:56988132 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.472-84C>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 4/12 | chr17 | 56988132 | |||||||
| chr17:56988169 | A | G | 128 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(125): Show |
213 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(210): Show |
intron_variant | MODIFIER | c.472-47A>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 4/12 | chr17 | 56988169 | |||||||
| chr17:56988197 | T | TA | 178 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(175): Show |
298 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(295): Show |
intron_variant | MODIFIER | c.472-17dupA | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr17 | 56988197 | ||||||
| chr17:56988537 | G | C | 1 | a0001c0001t0001g0039 | 2 | NA18956.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.546+247G>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 5/12 | chr17 | 56988537 | |||||||
| chr17:56988578 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.546+288T>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 5/12 | chr17 | 56988578 | |||||||
| chr17:56988580 | T | A | 39 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0063 others(36): Show |
68 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(65): Show |
intron_variant | MODIFIER | c.546+290T>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 5/12 | chr17 | 56988580 | |||||||
| chr17:56988845 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.546+555G>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 5/12 | chr17 | 56988845 | |||||||
| chr17:56989023 | C | CA | 6 | a0001c0001t0001g0131 a0001c0001t0001g0177 a0001c0001t0001g0180 others(3): Show |
7 | HG01256.hp2 HG02683.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.546+747dupA | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr17 | 56989023 | ||||||
| chr17:56989032 | A | T | 1 | a0001c0001t0001g0123 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.546+742A>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 5/12 | chr17 | 56989032 | |||||||
| chr17:56989035 | A | T | 5 | a0001c0001t0001g0083 a0001c0001t0001g0122 a0001c0001t0001g0165 others(2): Show |
5 | HG02145.hp1 HG02965.hp2 NA18965.hp2 others(2): Show |
intron_variant | MODIFIER | c.546+745A>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 5/12 | chr17 | 56989035 | |||||||
| chr17:56989123 | G | A | 3 | a0001c0001t0002g0126 a0001c0001t0002g0127 a0001c0001t0003g0096 |
3 | HG01515.hp1 HG01517.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.546+833G>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 5/12 | chr17 | 56989123 | |||||||
| chr17:56989170 | A | G | 1 | a0001c0001t0001g0179 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.546+880A>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 5/12 | chr17 | 56989170 | |||||||
| chr17:56989214 | A | G | 6 | a0001c0001t0001g0023 a0001c0001t0001g0047 a0001c0001t0001g0147 others(3): Show |
9 | HG01255.hp1 HG01257.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.546+924A>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 5/12 | chr17 | 56989214 | |||||||
| chr17:56989463 | G | C | 1 | a0001c0001t0002g0054 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.546+1173G>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 5/12 | chr17 | 56989463 | |||||||
| chr17:56989531 | T | A | 2 | a0001c0001t0001g0165 a0001c0001t0002g0166 |
2 | HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.546+1241T>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 5/12 | chr17 | 56989531 | |||||||
| chr17:56989668 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.546+1378C>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 5/12 | chr17 | 56989668 | |||||||
| chr17:56989672 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.546+1382C>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 5/12 | chr17 | 56989672 | |||||||
| chr17:56989674 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0120 |
4 | NA18947.hp1 NA18985.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.546+1384C>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 5/12 | chr17 | 56989674 | |||||||
| chr17:56989719 | G | A | 1 | a0001c0002t0001g0024 | 3 | HG00140.hp1 HG01496.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.547-1380G>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 5/12 | chr17 | 56989719 | |||||||
| chr17:56989726 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.547-1373C>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 5/12 | chr17 | 56989726 | |||||||
| chr17:56989848 | G | A | 1 | a0001c0001t0001g0097 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.547-1251G>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 5/12 | chr17 | 56989848 | |||||||
| chr17:56989906 | C | T | 1 | a0001c0001t0002g0056 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.547-1193C>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 5/12 | chr17 | 56989906 | |||||||
| chr17:56990237 | A | G | 1 | a0001c0001t0002g0082 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.547-862A>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 5/12 | chr17 | 56990237 | |||||||
| chr17:56990309 | C | T | 3 | a0001c0001t0001g0017 a0001c0001t0001g0118 a0001c0001t0005g0017 |
4 | HG00621.hp1 HG02129.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.547-790C>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 5/12 | chr17 | 56990309 | |||||||
| chr17:56990327 | G | A | 11 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0015 others(8): Show |
20 | HG01884.hp2 HG02055.hp2 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.547-772G>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 5/12 | chr17 | 56990327 | |||||||
| chr17:56990656 | C | T | 106 | a0001c0001t0001g0002 a0001c0001t0001g0010 a0001c0001t0001g0012 others(103): Show |
181 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.547-443C>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 5/12 | chr17 | 56990656 | |||||||
| chr17:56990679 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.547-420G>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 5/12 | chr17 | 56990679 | |||||||
| chr17:56990737 | T | TG | 181 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(178): Show |
302 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.547-362_547-361ins others(1): Show |
SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 5/12 | chr17 | 56990737 | |||||||
| chr17:56990856 | A | G | 129 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0011 others(126): Show |
218 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(215): Show |
intron_variant | MODIFIER | c.547-243A>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 5/12 | chr17 | 56990856 | |||||||
| chr17:56990903 | G | A | 1 | a0001c0001t0001g0185 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.547-196G>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 5/12 | chr17 | 56990903 | |||||||
| chr17:56991050 | C | A | 1 | a0001c0001t0001g0153 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.547-49C>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 5/12 | chr17 | 56991050 | |||||||
| chr17:56991455 | G | A | 165 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(162): Show |
279 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.619+284G>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 6/12 | chr17 | 56991455 | |||||||
| chr17:56991619 | G | A | 6 | a0001c0001t0001g0044 a0001c0001t0001g0150 a0001c0001t0001g0181 others(3): Show |
7 | HG02257.hp1 HG02572.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.619+448G>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 6/12 | chr17 | 56991619 | |||||||
| chr17:56991671 | G | A | 165 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(162): Show |
279 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.619+500G>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 6/12 | chr17 | 56991671 | |||||||
| chr17:56991885 | C | T | 11 | a0001c0001t0001g0020 a0001c0001t0001g0028 a0001c0001t0001g0037 others(8): Show |
16 | HG00639.hp2 HG01884.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.619+714C>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 6/12 | chr17 | 56991885 | |||||||
| chr17:56991990 | A | G | 1 | a0001c0001t0002g0053 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.619+819A>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 6/12 | chr17 | 56991990 | |||||||
| chr17:56991993 | C | G | 1 | a0001c0001t0001g0129 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.619+822C>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 6/12 | chr17 | 56991993 | |||||||
| chr17:56991997 | C | G | 1 | a0001c0001t0002g0081 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.619+826C>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 6/12 | chr17 | 56991997 | |||||||
| chr17:56992039 | G | T | 3 | a0001c0002t0001g0006 a0001c0002t0001g0024 a0001c0002t0001g0045 |
11 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(8): Show |
intron_variant | MODIFIER | c.619+868G>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 6/12 | chr17 | 56992039 | |||||||
| chr17:56992441 | T | C | 2 | a0001c0001t0001g0165 a0001c0001t0002g0166 |
2 | HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.619+1270T>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 6/12 | chr17 | 56992441 | |||||||
| chr17:56992470 | A | C | 1 | a0001c0001t0001g0090 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.619+1299A>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 6/12 | chr17 | 56992470 | |||||||
| chr17:56992839 | A | T | 1 | a0001c0001t0001g0117 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.619+1668A>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 6/12 | chr17 | 56992839 | |||||||
| chr17:56992848 | C | T | 1 | a0001c0001t0001g0158 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.619+1677C>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 6/12 | chr17 | 56992848 | |||||||
| chr17:56992861 | G | C | 1 | a0001c0001t0004g0168 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.619+1690G>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 6/12 | chr17 | 56992861 | |||||||
| chr17:56993086 | T | C | 2 | a0001c0001t0001g0165 a0001c0001t0002g0166 |
2 | HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.620-1895T>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 6/12 | chr17 | 56993086 | |||||||
| chr17:56993097 | A | C | 13 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0028 others(10): Show |
20 | HG00639.hp2 HG01884.hp1 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.620-1884A>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 6/12 | chr17 | 56993097 | |||||||
| chr17:56993365 | A | G | 1 | a0001c0001t0002g0080 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.620-1616A>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 6/12 | chr17 | 56993365 | |||||||
| chr17:56993431 | GTTGTTTG others(7): Show |
G | 2 | a0001c0001t0001g0009 a0001c0001t0001g0134 |
6 | HG01109.hp2 HG02559.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.620-1534_620-1521d others(16): Show |
SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr17 | 56993431 | ||||||
| chr17:56993522 | C | A | 165 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(162): Show |
279 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.620-1459C>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 6/12 | chr17 | 56993522 | |||||||
| chr17:56993530 | G | A | 2 | a0001c0001t0001g0141 a0001c0001t0001g0142 |
2 | HG03654.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.620-1451G>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 6/12 | chr17 | 56993530 | |||||||
| chr17:56993795 | G | T | 1 | a0001c0001t0001g0185 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.620-1186G>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 6/12 | chr17 | 56993795 | |||||||
| chr17:56993813 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.620-1168G>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 6/12 | chr17 | 56993813 | |||||||
| chr17:56993815 | G | T | 1 | a0001c0001t0001g0197 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.620-1166G>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 6/12 | chr17 | 56993815 | |||||||
| chr17:56993831 | A | G | 181 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(178): Show |
302 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.620-1150A>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 6/12 | chr17 | 56993831 | |||||||
| chr17:56993991 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.620-990T>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 6/12 | chr17 | 56993991 | |||||||
| chr17:56994154 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.620-827T>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 6/12 | chr17 | 56994154 | |||||||
| chr17:56994283 | A | T | 1 | a0001c0001t0001g0060 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.620-698A>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 6/12 | chr17 | 56994283 | |||||||
| chr17:56994296 | G | T | 1 | a0001c0001t0001g0129 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.620-685G>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 6/12 | chr17 | 56994296 | |||||||
| chr17:56994522 | A | T | 6 | a0001c0001t0001g0044 a0001c0001t0001g0150 a0001c0001t0001g0181 others(3): Show |
7 | HG02257.hp1 HG02572.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.620-459A>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 6/12 | chr17 | 56994522 | |||||||
| chr17:56994685 | T | C | 167 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0010 others(164): Show |
281 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.620-296T>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 6/12 | chr17 | 56994685 | |||||||
| chr17:56994703 | G | C | 2 | a0001c0001t0001g0165 a0001c0001t0002g0166 |
2 | HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.620-278G>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 6/12 | chr17 | 56994703 | |||||||
| chr17:56995074 | G | T | 1 | a0001c0001t0002g0116 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.657+56G>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 7/12 | chr17 | 56995074 | |||||||
| chr17:56995288 | G | A | 1 | a0001c0001t0002g0116 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.658-219G>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 7/12 | chr17 | 56995288 | |||||||
| chr17:56995323 | T | G | 3 | a0001c0001t0001g0016 a0001c0001t0001g0101 a0001c0001t0001g0102 |
5 | HG00738.hp1 HG01943.hp2 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.658-184T>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 7/12 | chr17 | 56995323 | |||||||
| chr17:56995325 | G | C | 1 | a0001c0001t0002g0080 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.658-182G>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 7/12 | chr17 | 56995325 | |||||||
| chr17:56995441 | C | T | 1 | a0001c0001t0001g0185 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.658-66C>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 7/12 | chr17 | 56995441 | |||||||
| chr17:56995876 | TA | T | 78 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0014 others(75): Show |
130 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(127): Show |
intron_variant | MODIFIER | c.786+259delA | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 56995876 | ||||||
| chr17:56995876 | TAA | T | 19 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0023 others(16): Show |
31 | HG00735.hp2 HG01070.hp1 HG01168.hp1 others(28): Show |
intron_variant | MODIFIER | c.786+258_786+259del others(2): Show |
SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 56995876 | ||||||
| chr17:56996016 | G | A | 1 | a0001c0001t0001g0133 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.786+381G>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 8/12 | chr17 | 56996016 | |||||||
| chr17:56996042 | C | A | 1 | a0001c0001t0001g0084 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.786+407C>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 8/12 | chr17 | 56996042 | |||||||
| chr17:56996045 | G | C | 1 | a0001c0001t0001g0084 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.786+410G>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 8/12 | chr17 | 56996045 | |||||||
| chr17:56996046 | T | C | 1 | a0001c0001t0001g0084 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.786+411T>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 8/12 | chr17 | 56996046 | |||||||
| chr17:56996047 | A | C | 1 | a0001c0001t0001g0084 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.786+412A>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 8/12 | chr17 | 56996047 | |||||||
| chr17:56996050 | T | G | 1 | a0001c0001t0001g0084 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.786+415T>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 8/12 | chr17 | 56996050 | |||||||
| chr17:56996052 | A | C | 1 | a0001c0001t0001g0084 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.786+417A>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 8/12 | chr17 | 56996052 | |||||||
| chr17:56996054 | C | A | 1 | a0001c0001t0001g0084 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.786+419C>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 8/12 | chr17 | 56996054 | |||||||
| chr17:56996055 | A | G | 1 | a0001c0001t0001g0084 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.786+420A>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 8/12 | chr17 | 56996055 | |||||||
| chr17:56996060 | G | C | 1 | a0001c0001t0001g0084 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.786+425G>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 8/12 | chr17 | 56996060 | |||||||
| chr17:56996068 | G | T | 1 | a0001c0001t0001g0084 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.786+433G>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 8/12 | chr17 | 56996068 | |||||||
| chr17:56996070 | T | C | 1 | a0001c0001t0001g0084 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.786+435T>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 8/12 | chr17 | 56996070 | |||||||
| chr17:56996079 | G | T | 1 | a0001c0001t0001g0084 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.786+444G>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 8/12 | chr17 | 56996079 | |||||||
| chr17:56996081 | A | T | 1 | a0001c0001t0001g0084 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.786+446A>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 8/12 | chr17 | 56996081 | |||||||
| chr17:56996084 | G | C | 1 | a0001c0001t0001g0084 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.786+449G>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 8/12 | chr17 | 56996084 | |||||||
| chr17:56996089 | A | G | 1 | a0001c0001t0001g0084 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.786+454A>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 8/12 | chr17 | 56996089 | |||||||
| chr17:56996093 | C | A | 1 | a0001c0001t0001g0084 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.786+458C>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 8/12 | chr17 | 56996093 | |||||||
| chr17:56996096 | C | T | 1 | a0001c0001t0001g0084 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.786+461C>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 8/12 | chr17 | 56996096 | |||||||
| chr17:56996098 | C | G | 1 | a0001c0001t0001g0084 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.786+463C>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 8/12 | chr17 | 56996098 | |||||||
| chr17:56996099 | A | C | 1 | a0001c0001t0001g0084 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.786+464A>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 8/12 | chr17 | 56996099 | |||||||
| chr17:56996101 | A | T | 1 | a0001c0001t0001g0084 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.786+466A>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 8/12 | chr17 | 56996101 | |||||||
| chr17:56996102 | T | G | 1 | a0001c0001t0001g0084 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.786+467T>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 8/12 | chr17 | 56996102 | |||||||
| chr17:56996104 | A | C | 1 | a0001c0001t0001g0084 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.786+469A>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 8/12 | chr17 | 56996104 | |||||||
| chr17:56996105 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.786+470G>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 8/12 | chr17 | 56996105 | |||||||
| chr17:56996107 | T | G | 1 | a0001c0001t0001g0084 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.786+472T>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 8/12 | chr17 | 56996107 | |||||||
| chr17:56996109 | C | G | 1 | a0001c0001t0001g0084 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.786+474C>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 8/12 | chr17 | 56996109 | |||||||
| chr17:56996116 | C | A | 1 | a0001c0001t0001g0084 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.786+481C>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 8/12 | chr17 | 56996116 | |||||||
| chr17:56996129 | G | A | 1 | a0001c0001t0001g0084 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.786+494G>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 8/12 | chr17 | 56996129 | |||||||
| chr17:56996130 | G | T | 1 | a0001c0001t0001g0084 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.786+495G>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 8/12 | chr17 | 56996130 | |||||||
| chr17:56996150 | G | C | 1 | a0001c0001t0001g0084 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.786+515G>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 8/12 | chr17 | 56996150 | |||||||
| chr17:56996152 | G | C | 1 | a0001c0001t0001g0084 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.786+517G>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 8/12 | chr17 | 56996152 | |||||||
| chr17:56996159 | G | C | 1 | a0001c0001t0001g0084 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.786+524G>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 8/12 | chr17 | 56996159 | |||||||
| chr17:56996160 | A | C | 1 | a0001c0001t0001g0084 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.786+525A>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 8/12 | chr17 | 56996160 | |||||||
| chr17:56996161 | G | T | 1 | a0001c0001t0001g0084 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.786+526G>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 8/12 | chr17 | 56996161 | |||||||
| chr17:56996167 | T | A | 1 | a0001c0001t0001g0084 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.786+532T>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 8/12 | chr17 | 56996167 | |||||||
| chr17:56996168 | T | G | 1 | a0001c0001t0001g0084 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.786+533T>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 8/12 | chr17 | 56996168 | |||||||
| chr17:56996183 | A | T | 1 | a0001c0001t0001g0084 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.786+548A>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 8/12 | chr17 | 56996183 | |||||||
| chr17:56996207 | C | CTATT | 3 | a0001c0001t0001g0017 a0001c0001t0001g0153 a0001c0001t0005g0017 |
4 | HG00621.hp1 HG02615.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.786+594_786+597dup others(4): Show |
SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 56996207 | ||||||
| chr17:56996207 | CTATTTAT others(1): Show |
C | 2 | a0001c0001t0001g0014 a0001c0001t0001g0089 |
4 | HG01891.hp1 HG02109.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.786+590_786+597del others(8): Show |
SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 56996207 | ||||||
| chr17:56996278 | C | A | 1 | a0001c0001t0001g0103 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.786+643C>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 8/12 | chr17 | 56996278 | |||||||
| chr17:56996351 | C | T | 14 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0028 others(11): Show |
21 | HG00639.hp2 HG01884.hp1 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.787-611C>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 8/12 | chr17 | 56996351 | |||||||
| chr17:56996363 | C | A | 11 | a0001c0001t0001g0020 a0001c0001t0001g0028 a0001c0001t0001g0037 others(8): Show |
16 | HG00639.hp2 HG01884.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.787-599C>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 8/12 | chr17 | 56996363 | |||||||
| chr17:56996401 | C | T | 3 | a0001c0001t0001g0022 a0001c0001t0001g0163 a0001c0001t0001g0175 |
5 | HG02040.hp1 NA18612.hp1 NA18963.hp1 others(2): Show |
intron_variant | MODIFIER | c.787-561C>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 8/12 | chr17 | 56996401 | |||||||
| chr17:56996404 | C | T | 2 | a0001c0001t0001g0014 a0001c0001t0001g0089 |
4 | HG01891.hp1 HG02109.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.787-558C>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 8/12 | chr17 | 56996404 | |||||||
| chr17:56996411 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.787-551C>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 8/12 | chr17 | 56996411 | |||||||
| chr17:56996496 | C | G | 1 | a0001c0001t0002g0079 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.787-466C>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 8/12 | chr17 | 56996496 | |||||||
| chr17:56996502 | G | A | 18 | a0001c0001t0001g0017 a0001c0001t0001g0029 a0001c0001t0001g0030 others(15): Show |
22 | HG00621.hp1 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.787-460G>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 8/12 | chr17 | 56996502 | |||||||
| chr17:56996513 | C | G | 1 | a0001c0001t0001g0019 | 3 | HG02922.hp1 HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.787-449C>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 8/12 | chr17 | 56996513 | |||||||
| chr17:56996778 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.787-184C>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 8/12 | chr17 | 56996778 | |||||||
| chr17:56996799 | A | T | 1 | a0001c0001t0001g0078 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.787-163A>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 8/12 | chr17 | 56996799 | |||||||
| chr17:56997121 | T | TA | 5 | a0001c0001t0001g0031 a0001c0001t0001g0093 a0001c0001t0001g0094 others(2): Show |
6 | HG00280.hp2 HG01074.hp2 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.880+80dupA | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 56997121 | ||||||
| chr17:56997121 | TA | T | 6 | a0001c0001t0001g0032 a0001c0001t0001g0044 a0001c0001t0001g0181 others(3): Show |
8 | HG02257.hp1 HG02572.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.880+80delA | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 56997121 | ||||||
| chr17:56997194 | A | G | 1 | a0001c0001t0001g0150 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.880+139A>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 9/12 | chr17 | 56997194 | |||||||
| chr17:56997266 | C | T | 2 | a0001c0001t0001g0115 a0001c0001t0001g0139 |
2 | NA18968.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.880+211C>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 9/12 | chr17 | 56997266 | |||||||
| chr17:56997365 | A | G | 5 | a0001c0001t0001g0023 a0001c0001t0001g0047 a0001c0001t0001g0147 others(2): Show |
8 | HG01255.hp1 HG01257.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.880+310A>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 9/12 | chr17 | 56997365 | |||||||
| chr17:56997377 | G | A | 1 | a0001c0001t0001g0052 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.880+322G>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 9/12 | chr17 | 56997377 | |||||||
| chr17:56997662 | A | G | 2 | a0001c0001t0001g0097 a0001c0001t0002g0087 |
2 | HG02015.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.880+607A>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 9/12 | chr17 | 56997662 | |||||||
| chr17:56997739 | A | G | 12 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0015 others(9): Show |
21 | HG01884.hp2 HG02055.hp2 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.881-646A>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 9/12 | chr17 | 56997739 | |||||||
| chr17:56997843 | T | G | 1 | a0001c0001t0001g0107 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.881-542T>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 9/12 | chr17 | 56997843 | |||||||
| chr17:56997851 | C | CAAAAACC others(321): Show |
2 | a0001c0001t0001g0044 a0001c0001t0002g0184 |
3 | HG03041.hp2 HG06807.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.881-519_881-518ins others(328): Show |
SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 56997851 | ||||||
| chr17:56997851 | C | CAAAAACC others(322): Show |
3 | a0001c0001t0001g0181 a0001c0001t0001g0182 a0001c0001t0001g0183 |
3 | HG02257.hp1 HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.881-519_881-518ins others(329): Show |
SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 56997851 | ||||||
| chr17:56997852 | A | G | 2 | a0001c0001t0001g0014 a0001c0001t0001g0089 |
4 | HG01891.hp1 HG02109.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.881-533A>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 9/12 | chr17 | 56997852 | |||||||
| chr17:56998100 | CAA | C | 10 | a0001c0001t0001g0020 a0001c0001t0001g0028 a0001c0001t0001g0037 others(7): Show |
15 | HG00639.hp2 HG01884.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.881-284_881-283del others(2): Show |
SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 9/12 | chr17 | 56998100 | |||||||
| chr17:56998123 | C | T | 6 | a0001c0001t0001g0017 a0001c0001t0001g0030 a0001c0001t0001g0105 others(3): Show |
8 | HG00621.hp1 HG01070.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.881-262C>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 9/12 | chr17 | 56998123 | |||||||
| chr17:56998180 | G | A | 5 | a0001c0001t0002g0057 a0001c0001t0002g0061 a0001c0001t0002g0062 others(2): Show |
5 | HG00408.hp2 HG02080.hp2 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.881-205G>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 9/12 | chr17 | 56998180 | |||||||
| chr17:56998221 | A | G | 109 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(106): Show |
176 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.881-164A>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 9/12 | chr17 | 56998221 | |||||||
| chr17:56998227 | C | G | 1 | a0001c0001t0001g0129 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.881-158C>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 9/12 | chr17 | 56998227 | |||||||
| chr17:56998252 | A | G | 1 | a0001c0001t0002g0007 | 5 | NA18942.hp2 NA18971.hp2 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.881-133A>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 9/12 | chr17 | 56998252 | |||||||
| chr17:56998269 | C | T | 12 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0028 others(9): Show |
19 | HG00639.hp2 HG01884.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.881-116C>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 9/12 | chr17 | 56998269 | |||||||
| chr17:56998309 | C | CA | 23 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0029 others(20): Show |
29 | HG00621.hp1 HG01070.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.881-60dupA | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 56998309 | ||||||
| chr17:56998365 | A | G | 1 | a0001c0001t0001g0027 | 2 | HG02280.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.881-20A>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 9/12 | chr17 | 56998365 | |||||||
| chr17:56998567 | C | T | 107 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(104): Show |
174 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.994+69C>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 10/12 | chr17 | 56998567 | |||||||
| chr17:56998580 | G | A | 12 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0028 others(9): Show |
19 | HG00639.hp2 HG01884.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.994+82G>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 10/12 | chr17 | 56998580 | |||||||
| chr17:56998909 | A | G | 121 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(118): Show |
195 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.994+411A>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 10/12 | chr17 | 56998909 | |||||||
| chr17:56998960 | A | C | 107 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(104): Show |
174 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.994+462A>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 10/12 | chr17 | 56998960 | |||||||
| chr17:56999012 | CTGAGTGG others(7): Show |
C | 2 | a0001c0001t0001g0165 a0001c0001t0002g0166 |
2 | HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.994+515_994+528del others(14): Show |
SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 10/12 | chr17 | 56999012 | |||||||
| chr17:56999083 | G | A | 4 | a0001c0001t0001g0022 a0001c0001t0001g0040 a0001c0001t0001g0163 others(1): Show |
7 | HG02040.hp1 HG02135.hp2 NA18612.hp1 others(4): Show |
intron_variant | MODIFIER | c.994+585G>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 10/12 | chr17 | 56999083 | |||||||
| chr17:56999090 | T | G | 1 | a0001c0001t0001g0094 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.994+592T>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 10/12 | chr17 | 56999090 | |||||||
| chr17:56999158 | G | C | 107 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(104): Show |
174 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.994+660G>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 10/12 | chr17 | 56999158 | |||||||
| chr17:56999198 | G | A | 5 | a0001c0001t0001g0044 a0001c0001t0001g0181 a0001c0001t0001g0182 others(2): Show |
6 | HG02257.hp1 HG02572.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.994+700G>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 10/12 | chr17 | 56999198 | |||||||
| chr17:56999302 | AC | A | 3 | a0001c0001t0001g0018 a0001c0001t0001g0113 a0001c0001t0001g0120 |
5 | NA18947.hp1 NA18985.hp2 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.994+805delC | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 10/12 | chr17 | 56999302 | |||||||
| chr17:56999304 | T | G | 3 | a0001c0001t0001g0018 a0001c0001t0001g0113 a0001c0001t0001g0120 |
5 | NA18947.hp1 NA18985.hp2 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.994+806T>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 10/12 | chr17 | 56999304 | |||||||
| chr17:56999399 | T | C | 107 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(104): Show |
174 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.994+901T>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 10/12 | chr17 | 56999399 | |||||||
| chr17:56999569 | G | A | 1 | a0001c0001t0002g0151 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.994+1071G>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 10/12 | chr17 | 56999569 | |||||||
| chr17:56999780 | C | T | 39 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0015 others(36): Show |
62 | HG00408.hp2 HG00597.hp2 HG00642.hp1 others(59): Show |
intron_variant | MODIFIER | c.995-1075C>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 10/12 | chr17 | 56999780 | |||||||
| chr17:56999876 | G | C | 1 | a0001c0001t0001g0041 | 2 | NA19000.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.995-979G>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 10/12 | chr17 | 56999876 | |||||||
| chr17:56999906 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.995-949C>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 10/12 | chr17 | 56999906 | |||||||
| chr17:56999968 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.995-887G>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 10/12 | chr17 | 56999968 | |||||||
| chr17:56999981 | T | TA | 5 | a0001c0001t0001g0046 a0001c0001t0001g0165 a0001c0001t0001g0202 others(2): Show |
6 | HG01256.hp1 HG01258.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.995-854dupA | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 56999981 | ||||||
| chr17:56999981 | TA | T | 8 | a0001c0001t0001g0070 a0001c0001t0001g0092 a0001c0001t0001g0105 others(5): Show |
8 | HG00639.hp1 HG01070.hp2 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.995-854delA | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 56999981 | ||||||
| chr17:57000011 | G | A | 5 | a0001c0001t0001g0044 a0001c0001t0001g0181 a0001c0001t0001g0182 others(2): Show |
6 | HG02257.hp1 HG02572.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.995-844G>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 10/12 | chr17 | 57000011 | |||||||
| chr17:57000212 | G | A | 1 | a0001c0001t0004g0168 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.995-643G>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 10/12 | chr17 | 57000212 | |||||||
| chr17:57000360 | G | C | 1 | a0001c0001t0001g0169 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.995-495G>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 10/12 | chr17 | 57000360 | |||||||
| chr17:57000644 | G | C | 1 | a0001c0001t0001g0170 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.995-211G>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 10/12 | chr17 | 57000644 | |||||||
| chr17:57000696 | C | T | 1 | a0001c0001t0004g0168 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.995-159C>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 10/12 | chr17 | 57000696 | |||||||
| chr17:57001134 | C | T | 3 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0002g0195 |
3 | HG01358.hp2 HG01361.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1132+142C>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 11/12 | chr17 | 57001134 | |||||||
| chr17:57001165 | C | T | 30 | a0001c0001t0001g0010 a0001c0001t0001g0023 a0001c0001t0001g0046 others(27): Show |
54 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.1132+173C>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 11/12 | chr17 | 57001165 | |||||||
| chr17:57001332 | T | C | 12 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0015 others(9): Show |
21 | HG01884.hp2 HG02055.hp2 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.1132+340T>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 11/12 | chr17 | 57001332 | |||||||
| chr17:57001336 | A | G | 2 | a0001c0001t0002g0057 a0001c0001t0002g0062 |
2 | HG02080.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.1132+344A>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 11/12 | chr17 | 57001336 | |||||||
| chr17:57001339 | C | T | 4 | a0001c0001t0001g0028 a0001c0001t0001g0038 a0001c0001t0001g0090 others(1): Show |
6 | HG01884.hp1 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1132+347C>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 11/12 | chr17 | 57001339 | |||||||
| chr17:57001580 | G | T | 10 | a0001c0001t0001g0020 a0001c0001t0001g0028 a0001c0001t0001g0037 others(7): Show |
15 | HG00639.hp2 HG01884.hp1 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.1133-438G>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 11/12 | chr17 | 57001580 | |||||||
| chr17:57001643 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1133-375C>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 11/12 | chr17 | 57001643 | |||||||
| chr17:57001655 | CA | C | 57 | a0001c0001t0001g0013 a0001c0001t0001g0014 a0001c0001t0001g0017 others(54): Show |
90 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.1133-362delA | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 11/12 | chr17 | 57001655 | |||||||
| chr17:57001707 | G | C | 1 | a0001c0001t0001g0042 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1133-311G>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 11/12 | chr17 | 57001707 | |||||||
| chr17:57001931 | G | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0137 |
3 | HG02723.hp2 HG02809.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1133-87G>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 11/12 | chr17 | 57001931 | |||||||
| chr17:57002322 | G | A | 14 | a0001c0001t0001g0017 a0001c0001t0001g0029 a0001c0001t0001g0030 others(11): Show |
17 | HG00621.hp1 HG01070.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.1296+141G>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 12/12 | chr17 | 57002322 | |||||||
| chr17:57002337 | T | C | 1 | a0001c0001t0002g0068 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1296+156T>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 12/12 | chr17 | 57002337 | |||||||
| chr17:57002440 | G | T | 3 | a0001c0001t0001g0017 a0001c0001t0001g0118 a0001c0001t0005g0017 |
4 | HG00621.hp1 HG02129.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.1296+259G>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 12/12 | chr17 | 57002440 | |||||||
| chr17:57002526 | C | T | 1 | a0001c0001t0002g0077 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1296+345C>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 12/12 | chr17 | 57002526 | |||||||
| chr17:57002605 | G | T | 1 | a0001c0001t0001g0142 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1296+424G>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 12/12 | chr17 | 57002605 | |||||||
| chr17:57002663 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1296+482C>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 12/12 | chr17 | 57002663 | |||||||
| chr17:57002706 | C | CA | 27 | a0001c0001t0001g0013 a0001c0001t0001g0070 a0001c0001t0001g0071 others(24): Show |
43 | HG00408.hp2 HG00597.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.1296+531dupA | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr17 | 57002706 | ||||||
| chr17:57002874 | C | CA | 101 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0017 others(98): Show |
162 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(159): Show |
intron_variant | MODIFIER | c.1296+710dupA | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr17 | 57002874 | ||||||
| chr17:57002968 | G | C | 56 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0020 others(53): Show |
92 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(89): Show |
intron_variant | MODIFIER | c.1296+787G>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 12/12 | chr17 | 57002968 | |||||||
| chr17:57003408 | G | T | 1 | a0001c0001t0002g0055 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1296+1227G>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 12/12 | chr17 | 57003408 | |||||||
| chr17:57003445 | A | C | 1 | a0001c0001t0001g0128 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1296+1264A>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 12/12 | chr17 | 57003445 | |||||||
| chr17:57003461 | A | T | 37 | a0001c0001t0001g0078 a0001c0001t0001g0150 a0001c0001t0001g0156 others(34): Show |
62 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.1296+1280A>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 12/12 | chr17 | 57003461 | |||||||
| chr17:57003507 | G | A | 1 | a0001c0001t0002g0026 | 2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1296+1326G>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 12/12 | chr17 | 57003507 | |||||||
| chr17:57003654 | G | C | 1 | a0001c0001t0001g0078 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1296+1473G>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 12/12 | chr17 | 57003654 | |||||||
| chr17:57003768 | C | G | 3 | a0001c0001t0001g0052 a0001c0001t0001g0121 a0001c0001t0001g0122 |
3 | HG01981.hp2 NA18982.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1296+1587C>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 12/12 | chr17 | 57003768 | |||||||
| chr17:57004113 | C | T | 1 | a0001c0001t0001g0039 | 2 | NA18956.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.1296+1932C>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 12/12 | chr17 | 57004113 | |||||||
| chr17:57004269 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1297-1904G>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 12/12 | chr17 | 57004269 | |||||||
| chr17:57004363 | C | A | 52 | a0001c0001t0001g0019 a0001c0001t0001g0020 a0001c0001t0001g0028 others(49): Show |
84 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(81): Show |
intron_variant | MODIFIER | c.1297-1810C>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 12/12 | chr17 | 57004363 | |||||||
| chr17:57004565 | G | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0156 |
2 | HG03225.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1297-1608G>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 12/12 | chr17 | 57004565 | |||||||
| chr17:57005020 | G | A | 1 | a0001c0001t0001g0120 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1297-1153G>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 12/12 | chr17 | 57005020 | |||||||
| chr17:57005273 | G | C | 1 | a0001c0001t0001g0159 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1297-900G>C | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 12/12 | chr17 | 57005273 | |||||||
| chr17:57005274 | G | T | 9 | a0001c0001t0001g0020 a0001c0001t0001g0028 a0001c0001t0001g0037 others(6): Show |
14 | HG00639.hp2 HG01884.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.1297-899G>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 12/12 | chr17 | 57005274 | |||||||
| chr17:57005387 | A | G | 2 | a0001c0001t0001g0153 a0004c0007t0001g0149 |
2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1297-786A>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 12/12 | chr17 | 57005387 | |||||||
| chr17:57005471 | T | G | 114 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0014 others(111): Show |
179 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.1297-702T>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 12/12 | chr17 | 57005471 | |||||||
| chr17:57005766 | C | T | 41 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0007 others(38): Show |
66 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.1297-407C>T | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 12/12 | chr17 | 57005766 | |||||||
| chr17:57005769 | T | A | 41 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0007 others(38): Show |
66 | HG00280.hp1 HG00408.hp2 HG00597.hp2 others(63): Show |
intron_variant | MODIFIER | c.1297-404T>A | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 12/12 | chr17 | 57005769 | |||||||
| chr17:57005865 | A | G | 1 | a0001c0001t0001g0112 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1297-308A>G | SCPEP1 | ENSG00000121064.13 | transcript | ENST00000262288.8 | protein_coding | 12/12 | chr17 | 57005865 |