Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 9413 |
| ensemblid | ENSG00000135063.20 |
| hgncid | 24820 |
| symbol | ENTREP1 |
| name | endosomal transmembrane epsin interactor 1 |
| refseq_nuc | NM_001347995.2 |
| refseq_prot | NP_001334924.1 |
| ensembl_nuc | ENST00000303068.14 |
| ensembl_prot | ENSP00000304435.8 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 69325215 |
| end | 69392456 |
| strand | + |
| ver | v1.2 |
| region | chr9:69325215-69392456 |
| region5000 | chr9:69320215-69397456 |
| regionname0 | ENTREP1_chr9_69325215_69392456 |
| regionname5000 | ENTREP1_chr9_69320215_69397456 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 603 | 330 | 77 | 55 | 141 | 14 | 41 | 111 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | MSLPV others(598): Show |
chr9 | 69320215 | 69397456 |
| a0002 | 0/0 | 603 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | MSLPV others(598): Show |
chr9 | 69320215 | 69397456 |
| a0003 | 0/0 | 603 | 2 | 1 | 0 | 0 | 0 | 1 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | MSLPV others(598): Show |
chr9 | 69320215 | 69397456 |
| a0004 | 0/0 | 603 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | MSLPV others(598): Show |
chr9 | 69320215 | 69397456 |
| a0005 | 0/0 | 603 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | MSLPV others(598): Show |
chr9 | 69320215 | 69397456 |
| a0006 | 0/0 | 603 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | MSLPV others(598): Show |
chr9 | 69320215 | 69397456 |
| a0007 | 0/0 | 603 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | MSLPV others(598): Show |
chr9 | 69320215 | 69397456 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1809 | 327 | 75 | 54 | 141 | 14 | 41 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | ATGTC others(1804): Show |
chr9 | 69320215 | 69397456 | ||
| a0001c0003 | 0/0 | 1809 | 3 | 2 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | ATGTC others(1804): Show |
chr9 | 69320215 | 69397456 | ||
| a0002c0002 | 0/0 | 1809 | 6 | 5 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | ATGTC others(1804): Show |
chr9 | 69320215 | 69397456 | ||
| a0003c0006 | 0/0 | 1809 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | ATGTC others(1804): Show |
chr9 | 69320215 | 69397456 | ||
| a0003c0008 | 0/0 | 1809 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | ATGTC others(1804): Show |
chr9 | 69320215 | 69397456 | ||
| a0004c0004 | 0/0 | 1809 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | ATGTC others(1804): Show |
chr9 | 69320215 | 69397456 | ||
| a0005c0005 | 0/0 | 1809 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | ATGTC others(1804): Show |
chr9 | 69320215 | 69397456 | ||
| a0006c0007 | 0/0 | 1809 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | ATGTC others(1804): Show |
chr9 | 69320215 | 69397456 | ||
| a0007c0009 | 0/0 | 1809 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | ATGTC others(1804): Show |
chr9 | 69320215 | 69397456 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2549 | 171 | 66 | 19 | 54 | 8 | 24 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | AGTGC others(2544): Show |
chr9 | 69320215 | 69397456 |
| a0001c0001t0002 | 0/1 | 2550 | 98 | 8 | 25 | 47 | 6 | 11 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | AGTGC others(2545): Show |
chr9 | 69320215 | 69397456 |
| a0001c0001t0003 | 1/0 | 2559 | 44 | 0 | 7 | 32 | 0 | 4 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | AGTGC others(2554): Show |
chr9 | 69320215 | 69397456 |
| a0001c0001t0004 | 0/0 | 2560 | 10 | 0 | 1 | 8 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | AGTGC others(2555): Show |
chr9 | 69320215 | 69397456 |
| a0001c0001t0005 | 0/0 | 2560 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | AGTGC others(2555): Show |
chr9 | 69320215 | 69397456 |
| a0001c0001t0006 | 0/0 | 2549 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | AGTGC others(2544): Show |
chr9 | 69320215 | 69397456 |
| a0001c0001t0007 | 0/0 | 2549 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | AGTGC others(2544): Show |
chr9 | 69320215 | 69397456 |
| a0001c0001t0008 | 0/0 | 2550 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | AGTGC others(2545): Show |
chr9 | 69320215 | 69397456 |
| a0001c0003t0001 | 0/0 | 2549 | 3 | 2 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | AGTGC others(2544): Show |
chr9 | 69320215 | 69397456 |
| a0002c0002t0001 | 0/0 | 2549 | 6 | 5 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | AGTGC others(2544): Show |
chr9 | 69320215 | 69397456 |
| a0003c0006t0001 | 0/0 | 2549 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | AGTGC others(2544): Show |
chr9 | 69320215 | 69397456 |
| a0003c0008t0001 | 0/0 | 2549 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | AGTGC others(2544): Show |
chr9 | 69320215 | 69397456 |
| a0004c0004t0001 | 0/0 | 2549 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | AGTGC others(2544): Show |
chr9 | 69320215 | 69397456 |
| a0005c0005t0001 | 0/0 | 2549 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | AGTGC others(2544): Show |
chr9 | 69320215 | 69397456 |
| a0006c0007t0001 | 0/0 | 2549 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | AGTGC others(2544): Show |
chr9 | 69320215 | 69397456 |
| a0007c0009t0001 | 0/0 | 2549 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | AGTGC others(2544): Show |
chr9 | 69320215 | 69397456 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0011 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0121 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0002g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0001 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0261 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0003g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0004g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0004g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0004g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0005g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0006g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0007g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0001t0008g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0003t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0003t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0001c0003t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0002c0002t0001g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0002c0002t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0002c0002t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0003c0006t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0003c0008t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0004c0004t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0005c0005t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0006c0007t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| a0007c0009t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0165 | EUR | GBR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0067 | EUR | GBR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0198 | EUR | GBR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0194 | EUR | GBR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0139 | EUR | FIN | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0286 | EUR | FIN | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG00423 | hp1 | a0001 | c0001 | t0003 | g0232 | EAS | CHS | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | CHS | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0239 | EAS | CHS | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG00597 | hp1 | a0001 | c0001 | t0003 | g0267 | EAS | CHS | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | CHS | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG00621 | hp1 | a0001 | c0001 | t0003 | g0269 | EAS | CHS | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG00621 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | CHS | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | CHS | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0155 | AMR | PUR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG00735 | hp2 | a0001 | c0001 | t0004 | g0268 | AMR | PUR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0288 | AMR | PUR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01099 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0080 | AMR | PUR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0181 | AMR | PUR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01168 | hp1 | a0001 | c0001 | t0007 | g0180 | AMR | PUR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | PUR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0173 | AMR | PUR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01175 | hp1 | a0002 | c0002 | t0001 | g0214 | AMR | PUR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0279 | AMR | PUR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01243 | hp2 | a0001 | c0003 | t0001 | g0315 | AMR | PUR | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | CLM | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01256 | hp1 | a0001 | c0001 | t0003 | g0270 | AMR | CLM | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0071 | AMR | CLM | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0146 | AMR | CLM | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0197 | AMR | CLM | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | CLM | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01496 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | CLM | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | CLM | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0150 | EUR | IBS | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0117 | EUR | IBS | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0145 | EUR | IBS | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0144 | EUR | IBS | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01891 | hp1 | a0001 | c0003 | t0001 | g0314 | AFR | ACB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | ACB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01943 | hp2 | a0001 | c0001 | t0008 | g0101 | AMR | PEL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PEL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01952 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0068 | AMR | PEL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0179 | AMR | PEL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0069 | AMR | PEL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0178 | AMR | PEL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0203 | AMR | PEL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0240 | AMR | PEL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0277 | EAS | KHV | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02040 | hp2 | a0001 | c0001 | t0004 | g0256 | EAS | KHV | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | ACB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | ACB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | KHV | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | KHV | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | KHV | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | KHV | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0233 | EAS | KHV | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02129 | hp1 | a0001 | c0001 | t0003 | g0253 | EAS | KHV | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | KHV | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02135 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | KHV | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02145 | hp2 | a0001 | c0001 | t0005 | g0265 | AFR | ACB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CDX | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02155 | hp2 | a0001 | c0001 | t0003 | g0250 | EAS | CDX | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | ACB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0280 | AMR | PEL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0060 | AMR | PEL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | ACB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0207 | AMR | PEL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0241 | EAS | KHV | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0052 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0312 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02602 | hp1 | a0001 | c0001 | t0003 | g0257 | SAS | PJL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0130 | SAS | PJL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0309 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0151 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02683 | hp2 | a0001 | c0001 | t0004 | g0237 | SAS | PJL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0124 | SAS | PJL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02723 | hp1 | a0001 | c0003 | t0001 | g0050 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02735 | hp1 | a0001 | c0001 | t0003 | g0262 | SAS | PJL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0222 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0307 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0231 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02886 | hp2 | a0004 | c0004 | t0001 | g0218 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ESN | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02976 | hp1 | a0002 | c0002 | t0001 | g0223 | AFR | ESN | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | ESN | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03098 | hp1 | a0005 | c0005 | t0001 | g0221 | AFR | MSL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | MSL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ESN | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0004 | AFR | ESN | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | MSL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0289 | SAS | PJL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03239 | hp2 | a0001 | c0001 | t0002 | g0058 | SAS | PJL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | MSL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0125 | SAS | PJL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03516 | hp1 | a0003 | c0006 | t0001 | g0209 | AFR | ESN | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0219 | AFR | ESN | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0053 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | MSL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | MSL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03669 | hp2 | a0001 | c0001 | t0002 | g0084 | SAS | PJL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0196 | SAS | STU | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | STU | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0156 | SAS | PJL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03710 | hp1 | a0001 | c0001 | t0003 | g0260 | SAS | PJL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | BEB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0037 | SAS | BEB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | BEB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03927 | hp2 | a0003 | c0008 | t0001 | g0275 | SAS | BEB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0072 | SAS | BEB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | BEB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0287 | SAS | STU | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG04115 | hp2 | a0001 | c0001 | t0006 | g0127 | SAS | STU | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | BEB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG04184 | hp2 | a0001 | c0001 | t0003 | g0264 | SAS | BEB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | STU | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | STU | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0036 | SAS | STU | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | STU | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | STU | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | STU | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | YRI | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | YRI | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | CHB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18747 | hp2 | a0001 | c0001 | t0003 | g0244 | EAS | CHB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | YRI | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18906 | hp2 | a0002 | c0002 | t0001 | g0004 | AFR | YRI | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0272 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0263 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0273 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0276 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0242 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18954 | hp1 | a0001 | c0001 | t0003 | g0248 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18960 | hp2 | a0001 | c0001 | t0004 | g0247 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18964 | hp2 | a0001 | c0001 | t0004 | g0245 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0282 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18966 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18967 | hp2 | a0001 | c0001 | t0004 | g0266 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18969 | hp2 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0234 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18970 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18980 | hp2 | a0001 | c0001 | t0003 | g0255 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18981 | hp1 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18987 | hp1 | a0001 | c0001 | t0003 | g0254 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18990 | hp2 | a0001 | c0001 | t0004 | g0271 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18992 | hp1 | a0006 | c0007 | t0001 | g0030 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18992 | hp2 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19002 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19003 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19007 | hp1 | a0001 | c0001 | t0004 | g0246 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19010 | hp1 | a0001 | c0001 | t0004 | g0258 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | LWK | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | LWK | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19054 | hp1 | a0001 | c0001 | t0003 | g0274 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19062 | hp1 | a0001 | c0001 | t0003 | g0278 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0249 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19065 | hp1 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19067 | hp1 | a0001 | c0001 | t0004 | g0243 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19072 | hp1 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19072 | hp2 | a0001 | c0001 | t0002 | g0283 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19074 | hp2 | a0001 | c0001 | t0003 | g0001 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0259 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19084 | hp2 | a0001 | c0001 | t0003 | g0235 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19090 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | YRI | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | YRI | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ASW | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0004 | AFR | ASW | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0195 | EUR | TSI | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0019 | EUR | TSI | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0015 | EUR | TSI | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0123 | EUR | TSI | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0220 | AMR | CLM | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | USA | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0066 | AFR | USA | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA18955 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0070 | AFR | USA | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | USA | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | LWK | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| NA21309 | hp2 | a0007 | c0009 | t0001 | g0107 | AFR | LWK | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0121 | REF | REF | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0261 | REF | REF | ENTREP1_chr9_69320215_69397456 | ENTREP1 | chr9 | 69320215 | 69397456 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:69325403 | G | A | 1 | a0004 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.94G>A | p.Ala32Thr | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/11 | 189/2559 | 94/1812 | 32/603 | chr9 | 69325403 | |||
| chr9:69325484 | G | A | 2 | a0002 a0005 |
7 | HG01175.hp1 HG02809.hp1 HG02976.hp1 others(4): Show |
missense_variant | MODERATE | c.175G>A | p.Ala59Thr | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/11 | 270/2559 | 175/1812 | 59/603 | chr9 | 69325484 | |||
| chr9:69377647 | C | T | 1 | a0007 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.856C>T | p.His286Tyr | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/11 | 951/2559 | 856/1812 | 286/603 | chr9 | 69377647 | |||
| chr9:69384020 | C | T | 2 | a0003 a0005 |
3 | HG03098.hp1 HG03516.hp1 HG03927.hp2 |
missense_variant | MODERATE | c.1157C>T | p.Thr386Ile | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/11 | 1252/2559 | 1157/1812 | 386/603 | chr9 | 69384020 | |||
| chr9:69391650 | C | T | 1 | a0006 | 1 | NA18992.hp1 | missense_variant | MODERATE | c.1658C>T | p.Ser553Leu | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 11/11 | 1753/2559 | 1658/1812 | 553/603 | chr9 | 69391650 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:69371606 | T | C | 2 | a0003c0006 a0005c0005 |
2 | HG03098.hp1 HG03516.hp1 |
synonymous_variant | LOW | c.579T>C | p.Asp193Asp | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 3/11 | 674/2559 | 579/1812 | 193/603 | chr9 | 69371606 | |||
| chr9:69391687 | C | T | 1 | a0001c0003 | 3 | HG01243.hp2 HG01891.hp1 HG02723.hp1 |
synonymous_variant | LOW | c.1695C>T | p.Cys565Cys | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 11/11 | 1790/2559 | 1695/1812 | 565/603 | chr9 | 69391687 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:69325273 | GCCGGCCG others(3): Show |
G | 13 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(10): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
5_prime_UTR_variant | MODIFIER | c.-24_-15delGGCCGCAC others(2): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/11 | 15 | INFO_REALIGN_3_PRIME | chr9 | 69325273 | |||||
| chr9:69325290 | G | T | 1 | a0001c0001t0008 | 1 | HG01943.hp2 | 5_prime_UTR_variant | MODIFIER | c.-20G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/11 | 20 | chr9 | 69325290 | ||||||
| chr9:69391887 | C | CA | 4 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(1): Show |
109 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*91dupA | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 11/11 | 92 | INFO_REALIGN_3_PRIME | chr9 | 69391887 | |||||
| chr9:69392248 | G | A | 1 | a0001c0001t0005 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*444G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 11/11 | 444 | chr9 | 69392248 | ||||||
| chr9:69392407 | C | T | 1 | a0001c0001t0007 | 1 | HG01168.hp1 | 3_prime_UTR_variant | MODIFIER | c.*603C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 11/11 | 603 | chr9 | 69392407 | ||||||
| chr9:69392416 | C | A | 1 | a0001c0001t0006 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*612C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 11/11 | 612 | chr9 | 69392416 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:69325730 | A | G | 2 | a0001c0003t0001g0314 a0001c0003t0001g0315 |
2 | HG01243.hp2 HG01891.hp1 |
splice_region_variant&intron_variant | LOW | c.414+7A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69325730 | |||||||
| chr9:69325875 | C | T | 35 | a0001c0001t0001g0281 a0001c0001t0001g0289 a0001c0001t0001g0290 others(32): Show |
37 | HG00280.hp2 HG00673.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.414+152C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69325875 | |||||||
| chr9:69325923 | CTGTT | C | 4 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(1): Show |
4 | HG00621.hp2 HG00673.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.414+201_414+204del others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69325923 | |||||||
| chr9:69325974 | T | TAAAC | 264 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(261): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.414+254_414+255ins others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 69325974 | ||||||
| chr9:69326040 | A | C | 1 | a0001c0001t0003g0280 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.414+317A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69326040 | |||||||
| chr9:69326041 | T | A | 1 | a0001c0001t0003g0280 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.414+318T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69326041 | |||||||
| chr9:69326051 | T | C | 1 | a0001c0001t0003g0280 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.414+328T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69326051 | |||||||
| chr9:69326097 | G | A | 1 | a0001c0001t0001g0024 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.414+374G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69326097 | |||||||
| chr9:69326155 | G | T | 22 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0017 others(19): Show |
29 | HG01123.hp1 HG01175.hp1 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.414+432G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69326155 | |||||||
| chr9:69326163 | A | G | 4 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 others(1): Show |
4 | HG02451.hp1 HG02451.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.414+440A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69326163 | |||||||
| chr9:69326226 | G | A | 4 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 others(1): Show |
4 | HG02451.hp1 HG02451.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.414+503G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69326226 | |||||||
| chr9:69326301 | C | A | 1 | a0002c0002t0001g0214 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.414+578C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69326301 | |||||||
| chr9:69326342 | G | T | 19 | a0001c0001t0001g0002 a0001c0001t0001g0016 a0001c0001t0001g0017 others(16): Show |
26 | HG01123.hp1 HG01175.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.414+619G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69326342 | |||||||
| chr9:69326572 | G | C | 34 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(31): Show |
37 | HG00597.hp2 HG01167.hp1 HG01256.hp2 others(34): Show |
intron_variant | MODIFIER | c.414+849G>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69326572 | |||||||
| chr9:69326593 | A | G | 4 | a0001c0001t0003g0276 a0001c0001t0003g0277 a0001c0001t0003g0278 others(1): Show |
4 | HG01243.hp1 HG02040.hp1 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.414+870A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69326593 | |||||||
| chr9:69326726 | A | T | 1 | a0003c0006t0001g0209 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.414+1003A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69326726 | |||||||
| chr9:69326738 | T | C | 1 | a0002c0002t0001g0214 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.414+1015T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69326738 | |||||||
| chr9:69326826 | A | C | 34 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(31): Show |
37 | HG00597.hp2 HG01167.hp1 HG01256.hp2 others(34): Show |
intron_variant | MODIFIER | c.414+1103A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69326826 | |||||||
| chr9:69326826 | AGT | A | 173 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(170): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.414+1107_414+1108d others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 69326826 | ||||||
| chr9:69326841 | G | A | 74 | a0001c0001t0001g0011 a0001c0001t0001g0020 a0001c0001t0001g0022 others(71): Show |
78 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.414+1118G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69326841 | |||||||
| chr9:69326922 | G | T | 263 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(260): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.414+1199G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69326922 | |||||||
| chr9:69326978 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.414+1255G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69326978 | |||||||
| chr9:69327010 | GA | G | 254 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(251): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.414+1301delA | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 69327010 | ||||||
| chr9:69327098 | T | A | 1 | a0001c0001t0002g0058 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.414+1375T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69327098 | |||||||
| chr9:69327099 | C | T | 1 | a0001c0001t0001g0007 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.414+1376C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69327099 | |||||||
| chr9:69327176 | G | A | 27 | a0001c0001t0001g0281 a0001c0001t0001g0289 a0001c0001t0001g0290 others(24): Show |
29 | HG00280.hp2 HG00673.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.414+1453G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69327176 | |||||||
| chr9:69327370 | G | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0002g0219 others(1): Show |
6 | HG02280.hp2 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.414+1647G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69327370 | |||||||
| chr9:69327414 | G | A | 1 | a0001c0001t0003g0232 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.414+1691G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69327414 | |||||||
| chr9:69327619 | C | CAAAAG | 60 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(57): Show |
70 | HG00597.hp2 HG01123.hp1 HG01167.hp1 others(67): Show |
intron_variant | MODIFIER | c.414+1911_414+1915d others(7): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 69327619 | ||||||
| chr9:69327634 | G | GAAAAGA | 48 | a0001c0001t0001g0059 a0001c0001t0001g0061 a0001c0001t0001g0062 others(45): Show |
50 | HG00280.hp2 HG00673.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.414+1915_414+1916i others(8): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 69327634 | ||||||
| chr9:69327634 | G | GAAAAGAA others(4): Show |
156 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(153): Show |
166 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(163): Show |
intron_variant | MODIFIER | c.414+1915_414+1916i others(13): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 69327634 | ||||||
| chr9:69327926 | C | T | 4 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0002g0219 others(1): Show |
6 | HG02280.hp2 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.414+2203C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69327926 | |||||||
| chr9:69327929 | T | TTAAC | 208 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(205): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.414+2209_414+2210i others(6): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 69327929 | ||||||
| chr9:69327988 | A | G | 2 | a0001c0003t0001g0314 a0001c0003t0001g0315 |
2 | HG01243.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.414+2265A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69327988 | |||||||
| chr9:69328044 | A | G | 7 | a0001c0001t0001g0002 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
10 | HG02055.hp2 HG02717.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.414+2321A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69328044 | |||||||
| chr9:69328086 | C | T | 208 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(205): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.414+2363C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69328086 | |||||||
| chr9:69328227 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.414+2504C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69328227 | |||||||
| chr9:69328295 | T | C | 1 | a0001c0001t0006g0127 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.414+2572T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69328295 | |||||||
| chr9:69328455 | C | A | 11 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0002g0219 others(8): Show |
15 | HG01123.hp1 HG01175.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.414+2732C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69328455 | |||||||
| chr9:69328546 | G | A | 1 | a0001c0001t0001g0025 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.414+2823G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69328546 | |||||||
| chr9:69328635 | C | A | 1 | a0003c0006t0001g0209 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.414+2912C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69328635 | |||||||
| chr9:69328661 | T | TA | 160 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(157): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.414+2948dupA | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 69328661 | ||||||
| chr9:69328831 | A | G | 39 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(36): Show |
41 | HG00280.hp2 HG00673.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.414+3108A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69328831 | |||||||
| chr9:69328935 | T | A | 1 | a0001c0001t0003g0233 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.414+3212T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69328935 | |||||||
| chr9:69329214 | C | A | 1 | a0001c0001t0002g0063 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.414+3491C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69329214 | |||||||
| chr9:69329351 | A | G | 6 | a0001c0001t0002g0199 a0001c0001t0002g0200 a0001c0001t0002g0201 others(3): Show |
6 | HG01993.hp1 HG02071.hp1 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.414+3628A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69329351 | |||||||
| chr9:69329378 | C | A | 1 | a0001c0001t0001g0064 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.414+3655C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69329378 | |||||||
| chr9:69329559 | C | T | 4 | a0001c0001t0002g0015 a0001c0001t0002g0196 a0001c0001t0002g0197 others(1): Show |
5 | HG00140.hp1 HG01261.hp2 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.414+3836C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69329559 | |||||||
| chr9:69329763 | G | T | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.414+4040G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69329763 | |||||||
| chr9:69329800 | G | A | 217 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(214): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.414+4077G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69329800 | |||||||
| chr9:69329805 | AGTTAACG others(27): Show |
A | 7 | a0001c0001t0001g0002 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
10 | HG02055.hp2 HG02717.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.414+4089_414+4122d others(36): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 69329805 | ||||||
| chr9:69329812 | G | T | 210 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(207): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.414+4089G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69329812 | |||||||
| chr9:69329828 | A | G | 210 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(207): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.414+4105A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69329828 | |||||||
| chr9:69329832 | GCGTTAA | G | 210 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(207): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.414+4110_414+4115d others(8): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69329832 | |||||||
| chr9:69329839 | T | A | 210 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(207): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.414+4116T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69329839 | |||||||
| chr9:69329846 | T | G | 210 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(207): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.414+4123T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69329846 | |||||||
| chr9:69329862 | A | G | 7 | a0001c0001t0001g0002 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
10 | HG02055.hp2 HG02717.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.414+4139A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69329862 | |||||||
| chr9:69329867 | A | C | 210 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(207): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.414+4144A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69329867 | |||||||
| chr9:69329872 | ACTAGGTT others(4): Show |
A | 210 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(207): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.414+4150_414+4160d others(13): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69329872 | |||||||
| chr9:69329885 | GGGT | G | 210 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(207): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.414+4163_414+4165d others(5): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69329885 | |||||||
| chr9:69329893 | T | C | 210 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(207): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.414+4170T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69329893 | |||||||
| chr9:69329893 | TTAGATTC others(75): Show |
T | 56 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(53): Show |
66 | HG00597.hp2 HG01123.hp1 HG01167.hp1 others(63): Show |
intron_variant | MODIFIER | c.414+4349_414+4430d others(84): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 69329893 | ||||||
| chr9:69329941 | TTAGATTC others(27): Show |
T | 210 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(207): Show |
222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.414+4246_414+4279d others(36): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 69329941 | ||||||
| chr9:69329994 | G | A | 15 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0026 others(12): Show |
16 | HG00597.hp2 HG02132.hp1 HG02683.hp1 others(13): Show |
intron_variant | MODIFIER | c.414+4271G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69329994 | |||||||
| chr9:69330084 | A | G | 1 | a0001c0001t0003g0207 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.414+4361A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69330084 | |||||||
| chr9:69330198 | G | C | 217 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(214): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.414+4475G>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69330198 | |||||||
| chr9:69330200 | G | C | 36 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(33): Show |
39 | HG00597.hp2 HG01167.hp1 HG01256.hp2 others(36): Show |
intron_variant | MODIFIER | c.414+4477G>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69330200 | |||||||
| chr9:69330584 | G | A | 1 | a0001c0001t0002g0008 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.414+4861G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69330584 | |||||||
| chr9:69330960 | A | G | 228 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(225): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): Show |
intron_variant | MODIFIER | c.414+5237A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69330960 | |||||||
| chr9:69331004 | G | A | 5 | a0001c0001t0001g0123 a0001c0001t0001g0126 a0001c0001t0002g0122 others(2): Show |
5 | HG02074.hp2 HG02698.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.415-5209G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69331004 | |||||||
| chr9:69331044 | GT | G | 213 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(210): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.415-5161delT | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 69331044 | ||||||
| chr9:69331048 | T | C | 1 | a0001c0001t0001g0026 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.415-5165T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69331048 | |||||||
| chr9:69331080 | G | A | 213 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(210): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.415-5133G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69331080 | |||||||
| chr9:69331083 | A | G | 1 | a0001c0001t0002g0203 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.415-5130A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69331083 | |||||||
| chr9:69331109 | T | A | 34 | a0001c0001t0001g0281 a0001c0001t0001g0289 a0001c0001t0001g0290 others(31): Show |
36 | HG00280.hp2 HG00673.hp2 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.415-5104T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69331109 | |||||||
| chr9:69331247 | G | A | 160 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(157): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.415-4966G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69331247 | |||||||
| chr9:69331359 | G | A | 1 | a0001c0001t0002g0122 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.415-4854G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69331359 | |||||||
| chr9:69331409 | TC | T | 4 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0002g0219 others(1): Show |
6 | HG02280.hp2 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.415-4801delC | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 69331409 | ||||||
| chr9:69331442 | C | A | 264 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(261): Show |
286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.415-4771C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69331442 | |||||||
| chr9:69331518 | G | A | 2 | a0001c0001t0001g0307 a0001c0001t0001g0308 |
2 | HG02818.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.415-4695G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69331518 | |||||||
| chr9:69331668 | G | A | 2 | a0001c0001t0003g0234 a0001c0001t0003g0235 |
2 | NA18970.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.415-4545G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69331668 | |||||||
| chr9:69331815 | C | T | 2 | a0001c0001t0001g0195 a0001c0001t0002g0194 |
2 | HG00140.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.415-4398C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69331815 | |||||||
| chr9:69332030 | C | A | 1 | a0001c0001t0002g0130 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.415-4183C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69332030 | |||||||
| chr9:69332030 | C | T | 1 | a0001c0001t0002g0193 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.415-4183C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69332030 | |||||||
| chr9:69332048 | A | T | 4 | a0001c0001t0001g0189 a0001c0001t0001g0190 a0001c0001t0001g0191 others(1): Show |
4 | HG01496.hp2 HG01884.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.415-4165A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69332048 | |||||||
| chr9:69332289 | C | T | 16 | a0001c0001t0001g0014 a0001c0001t0001g0120 a0001c0001t0001g0182 others(13): Show |
17 | HG01255.hp2 HG01496.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.415-3924C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69332289 | |||||||
| chr9:69332345 | G | A | 7 | a0001c0001t0002g0220 a0002c0002t0001g0004 a0002c0002t0001g0214 others(4): Show |
9 | HG01123.hp1 HG01175.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.415-3868G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69332345 | |||||||
| chr9:69332418 | G | T | 9 | a0001c0001t0001g0002 a0001c0001t0001g0224 a0001c0001t0001g0225 others(6): Show |
12 | HG02055.hp2 HG02109.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.415-3795G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69332418 | |||||||
| chr9:69332749 | C | T | 1 | a0001c0001t0003g0273 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.415-3464C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69332749 | |||||||
| chr9:69332952 | C | T | 2 | a0001c0001t0001g0210 a0001c0001t0001g0211 |
2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.415-3261C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69332952 | |||||||
| chr9:69333123 | T | C | 1 | a0001c0001t0001g0123 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.415-3090T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69333123 | |||||||
| chr9:69333236 | G | C | 1 | a0001c0001t0003g0236 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.415-2977G>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69333236 | |||||||
| chr9:69333313 | T | A | 9 | a0001c0001t0001g0002 a0001c0001t0001g0224 a0001c0001t0001g0225 others(6): Show |
12 | HG02055.hp2 HG02109.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.415-2900T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69333313 | |||||||
| chr9:69333317 | T | A | 2 | a0001c0001t0002g0220 a0003c0008t0001g0275 |
2 | HG01123.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.415-2896T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69333317 | |||||||
| chr9:69333318 | A | T | 1 | a0001c0001t0001g0119 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.415-2895A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69333318 | |||||||
| chr9:69333321 | T | A | 1 | a0001c0001t0001g0131 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.415-2892T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69333321 | |||||||
| chr9:69333327 | T | G | 2 | a0001c0001t0002g0220 a0003c0008t0001g0275 |
2 | HG01123.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.415-2886T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69333327 | |||||||
| chr9:69333350 | G | A | 1 | a0001c0001t0001g0039 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.415-2863G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69333350 | |||||||
| chr9:69333468 | C | T | 3 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 |
3 | HG02258.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.415-2745C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69333468 | |||||||
| chr9:69333630 | T | C | 4 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0212 others(1): Show |
4 | HG02451.hp1 HG02451.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.415-2583T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69333630 | |||||||
| chr9:69333694 | C | T | 4 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0002g0219 others(1): Show |
6 | HG02280.hp2 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.415-2519C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69333694 | |||||||
| chr9:69333743 | G | A | 1 | a0001c0001t0002g0027 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.415-2470G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69333743 | |||||||
| chr9:69333825 | G | A | 34 | a0001c0001t0001g0281 a0001c0001t0001g0289 a0001c0001t0001g0290 others(31): Show |
36 | HG00280.hp2 HG00673.hp2 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.415-2388G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69333825 | |||||||
| chr9:69333977 | A | G | 2 | a0001c0001t0002g0220 a0003c0008t0001g0275 |
2 | HG01123.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.415-2236A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69333977 | |||||||
| chr9:69334189 | A | G | 37 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(34): Show |
40 | HG00597.hp2 HG01167.hp1 HG01256.hp2 others(37): Show |
intron_variant | MODIFIER | c.415-2024A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69334189 | |||||||
| chr9:69334195 | G | A | 2 | a0001c0001t0002g0220 a0003c0008t0001g0275 |
2 | HG01123.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.415-2018G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69334195 | |||||||
| chr9:69334291 | C | T | 217 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(214): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.415-1922C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69334291 | |||||||
| chr9:69334417 | A | T | 213 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0012 others(210): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.415-1796A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69334417 | |||||||
| chr9:69334440 | G | C | 1 | a0001c0001t0001g0040 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.415-1773G>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69334440 | |||||||
| chr9:69334552 | A | G | 265 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(262): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.415-1661A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69334552 | |||||||
| chr9:69334645 | A | T | 9 | a0001c0001t0001g0002 a0001c0001t0001g0224 a0001c0001t0001g0225 others(6): Show |
12 | HG02055.hp2 HG02109.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.415-1568A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69334645 | |||||||
| chr9:69334659 | T | A | 2 | a0001c0001t0001g0208 a0003c0006t0001g0209 |
2 | HG01884.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.415-1554T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69334659 | |||||||
| chr9:69334774 | T | C | 9 | a0001c0001t0001g0002 a0001c0001t0001g0224 a0001c0001t0001g0225 others(6): Show |
12 | HG02055.hp2 HG02109.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.415-1439T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69334774 | |||||||
| chr9:69334775 | C | CT | 11 | a0001c0001t0001g0123 a0001c0001t0001g0126 a0001c0001t0001g0204 others(8): Show |
11 | HG02074.hp2 HG02258.hp2 HG02698.hp2 others(8): Show |
intron_variant | MODIFIER | c.415-1419dupT | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 69334775 | ||||||
| chr9:69334775 | CT | C | 58 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0025 others(55): Show |
64 | HG00280.hp2 HG00597.hp2 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.415-1419delT | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 69334775 | ||||||
| chr9:69334775 | CTT | C | 8 | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0001g0041 others(5): Show |
9 | HG01167.hp1 HG01256.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.415-1420_415-1419d others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 69334775 | ||||||
| chr9:69334775 | CTTTT | C | 9 | a0001c0001t0001g0002 a0001c0001t0001g0224 a0001c0001t0001g0225 others(6): Show |
12 | HG02055.hp2 HG02109.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.415-1422_415-1419d others(6): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 69334775 | ||||||
| chr9:69334908 | C | T | 1 | a0001c0001t0003g0272 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.415-1305C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69334908 | |||||||
| chr9:69335011 | C | T | 1 | a0001c0001t0004g0271 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.415-1202C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69335011 | |||||||
| chr9:69335090 | G | GT | 4 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0002g0219 others(1): Show |
6 | HG02280.hp2 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.415-1117dupT | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 69335090 | ||||||
| chr9:69335373 | G | T | 69 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0131 others(66): Show |
74 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(71): Show |
intron_variant | MODIFIER | c.415-840G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69335373 | |||||||
| chr9:69335415 | G | A | 16 | a0001c0001t0001g0014 a0001c0001t0001g0059 a0001c0001t0001g0120 others(13): Show |
17 | HG01255.hp2 HG01496.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.415-798G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69335415 | |||||||
| chr9:69335576 | A | G | 177 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0011 others(174): Show |
193 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.415-637A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69335576 | |||||||
| chr9:69335617 | A | G | 1 | a0001c0001t0001g0126 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.415-596A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69335617 | |||||||
| chr9:69335638 | G | A | 1 | a0001c0001t0004g0237 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.415-575G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69335638 | |||||||
| chr9:69335834 | A | ATGCGCCT others(12): Show |
68 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(65): Show |
75 | HG00280.hp2 HG00597.hp2 HG00673.hp2 others(72): Show |
intron_variant | MODIFIER | c.415-363_415-345dup others(19): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 69335834 | ||||||
| chr9:69335834 | A | ATGCGCCT others(31): Show |
115 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(112): Show |
123 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.415-345_415-344ins others(38): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 69335834 | ||||||
| chr9:69335834 | A | ATGCGCCT others(69): Show |
1 | a0002c0002t0001g0214 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.415-345_415-344ins others(76): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 69335834 | ||||||
| chr9:69335852 | C | CGTGCGCC others(69): Show |
3 | a0002c0002t0001g0004 a0002c0002t0001g0222 a0002c0002t0001g0223 |
5 | HG02809.hp1 HG02976.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.415-345_415-344ins others(76): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 69335852 | ||||||
| chr9:69335857 | G | GCCTGTAG others(31): Show |
2 | a0001c0001t0002g0135 a0001c0001t0002g0136 |
2 | NA18971.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.415-345_415-344ins others(38): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr9 | 69335857 | ||||||
| chr9:69335939 | G | A | 2 | a0001c0001t0001g0195 a0001c0001t0002g0194 |
2 | HG00140.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.415-274G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69335939 | |||||||
| chr9:69335992 | A | G | 2 | a0001c0001t0001g0210 a0001c0001t0001g0211 |
2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.415-221A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 1/10 | chr9 | 69335992 | |||||||
| chr9:69336537 | T | A | 1 | a0001c0001t0001g0212 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.471+268T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69336537 | |||||||
| chr9:69336662 | C | T | 1 | a0001c0001t0001g0313 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.471+393C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69336662 | |||||||
| chr9:69336889 | G | A | 112 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(109): Show |
120 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.471+620G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69336889 | |||||||
| chr9:69336931 | C | T | 1 | a0001c0001t0008g0101 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.471+662C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69336931 | |||||||
| chr9:69336944 | C | A | 3 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 |
3 | HG02258.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.471+675C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69336944 | |||||||
| chr9:69336981 | A | G | 3 | a0001c0001t0001g0208 a0003c0006t0001g0209 a0005c0005t0001g0221 |
3 | HG01884.hp1 HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.471+712A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69336981 | |||||||
| chr9:69337005 | C | CT | 10 | a0001c0001t0003g0207 a0001c0001t0003g0263 a0001c0001t0003g0264 others(7): Show |
10 | HG00597.hp1 HG00621.hp1 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.471+765dupT | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69337005 | ||||||
| chr9:69337005 | CTT | C | 10 | a0001c0001t0001g0057 a0001c0001t0001g0094 a0001c0001t0002g0063 others(7): Show |
10 | HG01123.hp1 HG02723.hp1 HG03927.hp2 others(7): Show |
intron_variant | MODIFIER | c.471+764_471+765del others(2): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69337005 | ||||||
| chr9:69337005 | CTTT | C | 94 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0020 others(91): Show |
98 | HG00099.hp2 HG00438.hp1 HG00621.hp2 others(95): Show |
intron_variant | MODIFIER | c.471+763_471+765del others(3): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69337005 | ||||||
| chr9:69337005 | CTTTT | C | 149 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(146): Show |
167 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.471+762_471+765del others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69337005 | ||||||
| chr9:69337023 | T | G | 1 | a0001c0001t0003g0276 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.471+754T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69337023 | |||||||
| chr9:69337251 | G | T | 2 | a0001c0003t0001g0314 a0001c0003t0001g0315 |
2 | HG01243.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.471+982G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69337251 | |||||||
| chr9:69337398 | A | G | 1 | a0001c0001t0003g0262 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.471+1129A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69337398 | |||||||
| chr9:69337425 | T | C | 1 | a0001c0001t0002g0284 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.471+1156T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69337425 | |||||||
| chr9:69337528 | A | G | 1 | a0001c0001t0002g0010 | 2 | HG00438.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.471+1259A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69337528 | |||||||
| chr9:69337551 | A | G | 1 | a0001c0001t0001g0132 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.471+1282A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69337551 | |||||||
| chr9:69337775 | T | C | 2 | a0001c0001t0001g0210 a0001c0001t0001g0211 |
2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.471+1506T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69337775 | |||||||
| chr9:69337904 | T | C | 5 | a0001c0001t0001g0123 a0001c0001t0001g0126 a0001c0001t0002g0122 others(2): Show |
5 | HG02074.hp2 HG02698.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.471+1635T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69337904 | |||||||
| chr9:69337931 | A | T | 4 | a0001c0001t0003g0276 a0001c0001t0003g0277 a0001c0001t0003g0278 others(1): Show |
4 | HG01243.hp1 HG02040.hp1 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.471+1662A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69337931 | |||||||
| chr9:69338210 | A | AT | 3 | a0001c0001t0001g0002 a0001c0001t0001g0230 a0001c0001t0002g0231 |
6 | HG02717.hp2 HG02886.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.471+1942dupT | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69338210 | ||||||
| chr9:69338212 | A | T | 3 | a0001c0001t0001g0002 a0001c0001t0001g0230 a0001c0001t0002g0231 |
6 | HG02717.hp2 HG02886.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.471+1943A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69338212 | |||||||
| chr9:69338214 | C | G | 3 | a0001c0001t0001g0002 a0001c0001t0001g0230 a0001c0001t0002g0231 |
6 | HG02717.hp2 HG02886.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.471+1945C>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69338214 | |||||||
| chr9:69338215 | C | A | 3 | a0001c0001t0001g0002 a0001c0001t0001g0230 a0001c0001t0002g0231 |
6 | HG02717.hp2 HG02886.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.471+1946C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69338215 | |||||||
| chr9:69338279 | A | C | 73 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0017 others(70): Show |
78 | HG00099.hp2 HG00438.hp1 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.471+2010A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69338279 | |||||||
| chr9:69338476 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.471+2207T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69338476 | |||||||
| chr9:69338587 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.471+2318C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69338587 | |||||||
| chr9:69338703 | A | G | 113 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(110): Show |
121 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.471+2434A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69338703 | |||||||
| chr9:69338730 | A | G | 14 | a0001c0001t0001g0011 a0001c0001t0001g0024 a0001c0001t0001g0038 others(11): Show |
16 | HG00423.hp2 HG01168.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.471+2461A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69338730 | |||||||
| chr9:69338732 | G | A | 8 | a0001c0001t0002g0009 a0001c0001t0002g0058 a0001c0001t0002g0060 others(5): Show |
9 | HG00099.hp2 HG01106.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.471+2463G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69338732 | |||||||
| chr9:69338776 | T | C | 2 | a0001c0001t0002g0220 a0003c0008t0001g0275 |
2 | HG01123.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.471+2507T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69338776 | |||||||
| chr9:69338803 | A | G | 190 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(187): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.471+2534A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69338803 | |||||||
| chr9:69339060 | C | T | 5 | a0001c0001t0001g0014 a0001c0001t0001g0187 a0001c0001t0001g0189 others(2): Show |
6 | HG01496.hp2 HG01884.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.471+2791C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69339060 | |||||||
| chr9:69339144 | T | C | 4 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0003g0238 others(1): Show |
4 | NA18942.hp1 NA18994.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.471+2875T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69339144 | |||||||
| chr9:69339588 | G | A | 9 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(6): Show |
11 | HG01175.hp1 HG02258.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.471+3319G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69339588 | |||||||
| chr9:69339698 | A | C | 243 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(240): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.471+3429A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69339698 | |||||||
| chr9:69339743 | C | T | 1 | a0001c0001t0002g0198 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.471+3474C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69339743 | |||||||
| chr9:69339769 | C | A | 241 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(238): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.471+3500C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69339769 | |||||||
| chr9:69339942 | A | C | 13 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(10): Show |
13 | HG01167.hp1 HG01243.hp2 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.471+3673A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69339942 | |||||||
| chr9:69339961 | A | C | 1 | a0001c0001t0002g0037 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.471+3692A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69339961 | |||||||
| chr9:69340259 | G | A | 243 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(240): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.471+3990G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340259 | |||||||
| chr9:69340282 | C | G | 1 | a0001c0001t0002g0090 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.471+4013C>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340282 | |||||||
| chr9:69340334 | G | A | 5 | a0001c0001t0001g0123 a0001c0001t0001g0126 a0001c0001t0002g0122 others(2): Show |
5 | HG02074.hp2 HG02698.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.471+4065G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340334 | |||||||
| chr9:69340436 | C | T | 5 | a0001c0001t0001g0014 a0001c0001t0001g0187 a0001c0001t0001g0189 others(2): Show |
6 | HG01496.hp2 HG01884.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.471+4167C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340436 | |||||||
| chr9:69340475 | T | G | 1 | a0001c0001t0001g0126 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.471+4206T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340475 | |||||||
| chr9:69340585 | G | T | 1 | a0001c0001t0002g0197 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.471+4316G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340585 | |||||||
| chr9:69340595 | A | ATGCGTGT others(3): Show |
1 | a0001c0001t0001g0313 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.471+4329_471+4330i others(12): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69340595 | ||||||
| chr9:69340595 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.471+4326A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340595 | |||||||
| chr9:69340595 | ATGCATGT others(35): Show |
A | 2 | a0001c0001t0001g0210 a0001c0001t0001g0211 |
2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.471+4341_471+4382d others(44): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69340595 | ||||||
| chr9:69340598 | CATGT | C | 102 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(99): Show |
109 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(106): Show |
intron_variant | MODIFIER | c.471+4330_471+4333d others(6): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340598 | |||||||
| chr9:69340599 | A | G | 12 | a0001c0001t0001g0002 a0001c0001t0001g0208 a0001c0001t0001g0224 others(9): Show |
15 | HG01884.hp1 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.471+4330A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340599 | |||||||
| chr9:69340613 | A | ATG | 15 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(12): Show |
15 | HG01123.hp1 HG01167.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.471+4353_471+4354d others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69340613 | ||||||
| chr9:69340625 | A | ATGCATG | 7 | a0001c0001t0001g0123 a0001c0001t0001g0126 a0001c0001t0002g0122 others(4): Show |
7 | HG02074.hp2 HG02698.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.471+4358_471+4359i others(8): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69340625 | ||||||
| chr9:69340625 | ATGTGTGT others(17): Show |
A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0054 |
3 | HG02809.hp2 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.471+4359_471+4382d others(26): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69340625 | ||||||
| chr9:69340627 | G | GCA | 229 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(226): Show |
248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.471+4358_471+4359i others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340627 | |||||||
| chr9:69340628 | T | C | 2 | a0001c0001t0001g0111 a0001c0001t0001g0191 |
2 | HG02818.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.471+4359T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340628 | |||||||
| chr9:69340629 | G | A | 2 | a0001c0001t0001g0111 a0001c0001t0001g0191 |
2 | HG02818.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.471+4360G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340629 | |||||||
| chr9:69340636 | C | CATGCATG others(3): Show |
1 | a0001c0001t0001g0017 | 2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.471+4367_471+4368i others(12): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340636 | |||||||
| chr9:69340636 | C | CATGTGTG others(1): Show |
7 | a0001c0001t0001g0123 a0001c0001t0001g0126 a0001c0001t0002g0122 others(4): Show |
7 | HG02074.hp2 HG02698.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.471+4367_471+4368i others(10): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340636 | |||||||
| chr9:69340636 | C | T | 231 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(228): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.471+4367C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340636 | |||||||
| chr9:69340637 | G | A | 18 | a0001c0001t0001g0016 a0001c0001t0001g0039 a0001c0001t0001g0040 others(15): Show |
19 | HG01123.hp1 HG01167.hp1 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.471+4368G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340637 | |||||||
| chr9:69340641 | ATGTGTGT others(19): Show |
A | 2 | a0001c0001t0001g0210 a0001c0001t0001g0211 |
2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.471+4387_471+4412d others(28): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69340641 | ||||||
| chr9:69340652 | C | T | 1 | a0001c0001t0001g0017 | 2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.471+4383C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340652 | |||||||
| chr9:69340653 | A | G | 1 | a0001c0001t0001g0017 | 2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.471+4384A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340653 | |||||||
| chr9:69340653 | ATG | A | 14 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(11): Show |
14 | HG01123.hp1 HG01167.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.471+4395_471+4396d others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69340653 | ||||||
| chr9:69340654 | T | C | 1 | a0001c0001t0001g0017 | 2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.471+4385T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340654 | |||||||
| chr9:69340655 | G | A | 1 | a0001c0001t0001g0017 | 2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.471+4386G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340655 | |||||||
| chr9:69340655 | G | GTGTGTGT others(3): Show |
14 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0056 others(11): Show |
17 | HG01884.hp1 HG02109.hp2 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.471+4394_471+4395i others(12): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69340655 | ||||||
| chr9:69340655 | G | GTGTGTGT others(5): Show |
2 | a0001c0001t0001g0016 a0004c0004t0001g0218 |
3 | HG02886.hp2 HG03130.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.471+4397_471+4398i others(14): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69340655 | ||||||
| chr9:69340664 | T | C | 5 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0111 others(2): Show |
5 | HG02055.hp2 HG03490.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.471+4395T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340664 | |||||||
| chr9:69340665 | G | A | 5 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0111 others(2): Show |
5 | HG02055.hp2 HG03490.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.471+4396G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340665 | |||||||
| chr9:69340666 | C | CAT | 86 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(83): Show |
94 | HG00099.hp2 HG00280.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.471+4397_471+4398i others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340666 | |||||||
| chr9:69340666 | C | CATGTGTG others(7): Show |
101 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(98): Show |
109 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.471+4397_471+4398i others(16): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340666 | |||||||
| chr9:69340666 | C | CATGTGTG others(9): Show |
36 | a0001c0001t0001g0007 a0001c0001t0001g0047 a0001c0001t0001g0048 others(33): Show |
38 | HG01074.hp1 HG01106.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.471+4397_471+4398i others(18): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340666 | |||||||
| chr9:69340666 | C | T | 5 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0111 others(2): Show |
5 | HG02055.hp2 HG03490.hp1 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.471+4397C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340666 | |||||||
| chr9:69340667 | G | A | 13 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(10): Show |
15 | HG00438.hp1 HG00621.hp2 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.471+4398G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340667 | |||||||
| chr9:69340668 | T | C | 3 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0004c0004t0001g0218 |
5 | HG02280.hp2 HG02886.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.471+4399T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340668 | |||||||
| chr9:69340677 | GCA | G | 12 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(9): Show |
13 | HG00438.hp1 HG00621.hp2 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.471+4409_471+4410d others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340677 | |||||||
| chr9:69340679 | A | ATGTGTGT others(3): Show |
3 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0008g0101 |
3 | HG00099.hp2 HG01943.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.471+4412_471+4413i others(12): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69340679 | ||||||
| chr9:69340686 | T | C | 1 | a0001c0001t0008g0101 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.471+4417T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340686 | |||||||
| chr9:69340687 | G | A | 1 | a0001c0001t0008g0101 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.471+4418G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340687 | |||||||
| chr9:69340694 | T | C | 1 | a0001c0001t0002g0072 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.471+4425T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340694 | |||||||
| chr9:69340695 | A | G | 13 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(10): Show |
14 | HG00438.hp1 HG00621.hp2 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.471+4426A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340695 | |||||||
| chr9:69340695 | ATG | A | 13 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(10): Show |
13 | HG01167.hp1 HG01243.hp2 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.471+4436_471+4437d others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69340695 | ||||||
| chr9:69340696 | T | C | 11 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(8): Show |
12 | HG00438.hp1 HG00621.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.471+4427T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340696 | |||||||
| chr9:69340697 | G | A | 11 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(8): Show |
12 | HG00438.hp1 HG00621.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.471+4428G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340697 | |||||||
| chr9:69340697 | G | GTGTGTGT others(29): Show |
2 | a0001c0001t0002g0220 a0003c0008t0001g0275 |
2 | HG01123.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.471+4435_471+4436i others(38): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69340697 | ||||||
| chr9:69340700 | T | C | 11 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(8): Show |
12 | HG00438.hp1 HG00621.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.471+4431T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340700 | |||||||
| chr9:69340701 | G | A | 11 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(8): Show |
12 | HG00438.hp1 HG00621.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.471+4432G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340701 | |||||||
| chr9:69340702 | T | TGTATGTG others(7): Show |
12 | a0001c0001t0001g0002 a0001c0001t0001g0208 a0001c0001t0001g0224 others(9): Show |
15 | HG01884.hp1 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.471+4435_471+4436i others(16): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69340702 | ||||||
| chr9:69340718 | C | T | 1 | a0001c0001t0001g0094 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.471+4449C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340718 | |||||||
| chr9:69340723 | ATG | A | 65 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0022 others(62): Show |
69 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.471+4464_471+4465d others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69340723 | ||||||
| chr9:69340733 | G | A | 174 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(171): Show |
187 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.471+4464G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340733 | |||||||
| chr9:69340733 | GTA | G | 3 | a0001c0001t0001g0002 a0001c0001t0001g0230 a0001c0001t0002g0231 |
4 | HG02717.hp2 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.471+4466_471+4467d others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69340733 | ||||||
| chr9:69340735 | A | G | 174 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(171): Show |
187 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.471+4466A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340735 | |||||||
| chr9:69340737 | G | A | 1 | a0001c0001t0002g0077 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.471+4468G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340737 | |||||||
| chr9:69340747 | T | G | 1 | a0001c0001t0001g0184 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.471+4478T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340747 | |||||||
| chr9:69340747 | TTGTG | T | 6 | a0001c0001t0001g0123 a0001c0001t0001g0126 a0001c0001t0001g0204 others(3): Show |
6 | HG02074.hp2 HG02698.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.471+4485_471+4488d others(6): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69340747 | ||||||
| chr9:69340749 | G | T | 1 | a0001c0001t0001g0184 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.471+4480G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340749 | |||||||
| chr9:69340758 | C | T | 2 | a0001c0001t0001g0210 a0001c0001t0001g0211 |
2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.471+4489C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340758 | |||||||
| chr9:69340763 | ATG | A | 51 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0025 others(48): Show |
55 | HG00280.hp2 HG00597.hp2 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.471+4506_471+4507d others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69340763 | ||||||
| chr9:69340763 | ATGTG | A | 7 | a0001c0001t0001g0002 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
10 | HG02055.hp2 HG02717.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.471+4504_471+4507d others(6): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69340763 | ||||||
| chr9:69340765 | G | GTGTGTA | 19 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0039 others(16): Show |
21 | HG01123.hp1 HG01167.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.471+4501_471+4502i others(8): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69340765 | ||||||
| chr9:69340765 | G | GTGTGTGT others(1): Show |
5 | a0001c0001t0001g0208 a0001c0001t0001g0225 a0001c0001t0002g0058 others(2): Show |
5 | HG01884.hp1 HG02109.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.471+4503_471+4504i others(10): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69340765 | ||||||
| chr9:69340765 | G | GTGTGTGT others(3): Show |
177 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(174): Show |
190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.471+4505_471+4506i others(12): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69340765 | ||||||
| chr9:69340788 | C | T | 58 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(55): Show |
65 | HG00280.hp2 HG00597.hp2 HG00673.hp2 others(62): Show |
intron_variant | MODIFIER | c.471+4519C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340788 | |||||||
| chr9:69340789 | A | ATG | 175 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(172): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.471+4529_471+4530d others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69340789 | ||||||
| chr9:69340797 | GTGCA | G | 4 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0224 others(1): Show |
4 | HG02109.hp2 HG02280.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.471+4531_471+4534d others(6): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69340797 | ||||||
| chr9:69340801 | A | G | 13 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(10): Show |
13 | HG01167.hp1 HG01243.hp2 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.471+4532A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340801 | |||||||
| chr9:69340804 | T | C | 2 | a0003c0006t0001g0209 a0005c0005t0001g0221 |
2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.471+4535T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340804 | |||||||
| chr9:69340805 | G | A | 2 | a0003c0006t0001g0209 a0005c0005t0001g0221 |
2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.471+4536G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340805 | |||||||
| chr9:69340805 | G | GTGTGTGT others(3): Show |
49 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0026 others(46): Show |
53 | HG00280.hp2 HG00597.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.471+4543_471+4544i others(12): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69340805 | ||||||
| chr9:69340806 | T | C | 4 | a0001c0001t0001g0210 a0001c0001t0001g0211 a0001c0001t0001g0224 others(1): Show |
4 | HG02109.hp2 HG02280.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.471+4537T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340806 | |||||||
| chr9:69340807 | G | A | 2 | a0001c0001t0001g0210 a0001c0001t0001g0211 |
2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.471+4538G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340807 | |||||||
| chr9:69340808 | T | TGTGTGC | 7 | a0001c0001t0001g0002 a0001c0001t0001g0226 a0001c0001t0001g0227 others(4): Show |
10 | HG02055.hp2 HG02717.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.471+4543_471+4544i others(8): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69340808 | ||||||
| chr9:69340813 | A | G | 66 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(63): Show |
73 | HG00280.hp2 HG00597.hp2 HG00673.hp2 others(70): Show |
intron_variant | MODIFIER | c.471+4544A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340813 | |||||||
| chr9:69340813 | ATG | A | 176 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(173): Show |
189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.471+4558_471+4559d others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69340813 | ||||||
| chr9:69340815 | G | A | 1 | a0002c0002t0001g0214 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.471+4546G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340815 | |||||||
| chr9:69340963 | G | A | 243 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(240): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.471+4694G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69340963 | |||||||
| chr9:69341450 | T | C | 312 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(309): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.471+5181T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69341450 | |||||||
| chr9:69341484 | AT | A | 259 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(256): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.471+5227delT | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69341484 | ||||||
| chr9:69341793 | A | G | 1 | a0001c0001t0002g0282 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.471+5524A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69341793 | |||||||
| chr9:69341909 | A | C | 241 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(238): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.471+5640A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69341909 | |||||||
| chr9:69341970 | A | C | 4 | a0002c0002t0001g0004 a0002c0002t0001g0214 a0002c0002t0001g0222 others(1): Show |
6 | HG01175.hp1 HG02809.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.471+5701A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69341970 | |||||||
| chr9:69342504 | A | G | 4 | a0001c0001t0003g0276 a0001c0001t0003g0277 a0001c0001t0003g0278 others(1): Show |
4 | HG01243.hp1 HG02040.hp1 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.471+6235A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69342504 | |||||||
| chr9:69342556 | A | C | 241 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(238): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.471+6287A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69342556 | |||||||
| chr9:69342710 | G | A | 260 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(257): Show |
282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.471+6441G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69342710 | |||||||
| chr9:69342735 | T | C | 311 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(308): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.471+6466T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69342735 | |||||||
| chr9:69342887 | T | G | 1 | a0001c0001t0003g0239 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.471+6618T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69342887 | |||||||
| chr9:69343340 | G | A | 2 | a0001c0003t0001g0314 a0001c0003t0001g0315 |
2 | HG01243.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.471+7071G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69343340 | |||||||
| chr9:69343437 | G | T | 1 | a0001c0001t0001g0056 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.471+7168G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69343437 | |||||||
| chr9:69343448 | G | T | 2 | a0001c0001t0002g0220 a0003c0008t0001g0275 |
2 | HG01123.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.471+7179G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69343448 | |||||||
| chr9:69343807 | GTTGGGAG others(4): Show |
G | 1 | a0001c0001t0003g0207 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.471+7539_471+7549d others(13): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69343807 | |||||||
| chr9:69343892 | T | C | 2 | a0001c0001t0001g0210 a0001c0001t0001g0211 |
2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.471+7623T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69343892 | |||||||
| chr9:69344250 | C | T | 243 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(240): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.471+7981C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69344250 | |||||||
| chr9:69344264 | T | C | 18 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0039 others(15): Show |
20 | HG01123.hp1 HG01167.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.471+7995T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69344264 | |||||||
| chr9:69344307 | A | C | 5 | a0001c0001t0001g0123 a0001c0001t0001g0126 a0001c0001t0002g0122 others(2): Show |
5 | HG02074.hp2 HG02698.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.471+8038A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69344307 | |||||||
| chr9:69344311 | A | C | 50 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(47): Show |
52 | HG00099.hp2 HG00438.hp1 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.471+8042A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69344311 | |||||||
| chr9:69344340 | C | A | 18 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0039 others(15): Show |
20 | HG01123.hp1 HG01167.hp1 HG01243.hp2 others(17): Show |
intron_variant | MODIFIER | c.471+8071C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69344340 | |||||||
| chr9:69344478 | GT | G | 3 | a0001c0001t0001g0048 a0001c0001t0002g0052 a0001c0001t0002g0053 |
3 | HG02572.hp1 HG02647.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.471+8212delT | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69344478 | ||||||
| chr9:69344573 | G | A | 1 | a0001c0001t0003g0240 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.471+8304G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69344573 | |||||||
| chr9:69344590 | T | C | 1 | a0001c0001t0001g0307 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.471+8321T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69344590 | |||||||
| chr9:69344666 | C | G | 2 | a0001c0001t0002g0220 a0003c0008t0001g0275 |
2 | HG01123.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.471+8397C>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69344666 | |||||||
| chr9:69344755 | A | C | 1 | a0001c0001t0002g0175 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.471+8486A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69344755 | |||||||
| chr9:69344862 | T | G | 243 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(240): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.471+8593T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69344862 | |||||||
| chr9:69344951 | G | A | 2 | a0001c0001t0001g0210 a0001c0001t0001g0211 |
2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.471+8682G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69344951 | |||||||
| chr9:69345036 | T | C | 3 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0004c0004t0001g0218 |
5 | HG02280.hp2 HG02886.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.471+8767T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69345036 | |||||||
| chr9:69345049 | A | T | 123 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(120): Show |
133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.471+8780A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69345049 | |||||||
| chr9:69345471 | A | T | 1 | a0001c0001t0002g0036 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.471+9202A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69345471 | |||||||
| chr9:69345482 | A | G | 99 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(96): Show |
106 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.471+9213A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69345482 | |||||||
| chr9:69345485 | C | T | 1 | a0001c0001t0001g0184 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.471+9216C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69345485 | |||||||
| chr9:69345539 | C | A | 2 | a0001c0001t0002g0220 a0003c0008t0001g0275 |
2 | HG01123.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.471+9270C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69345539 | |||||||
| chr9:69346107 | C | T | 4 | a0002c0002t0001g0004 a0002c0002t0001g0214 a0002c0002t0001g0222 others(1): Show |
6 | HG01175.hp1 HG02809.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.471+9838C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69346107 | |||||||
| chr9:69346344 | A | G | 2 | a0001c0001t0001g0133 a0001c0001t0002g0219 |
2 | HG03516.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.471+10075A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69346344 | |||||||
| chr9:69346365 | G | A | 1 | a0001c0001t0001g0079 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.471+10096G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69346365 | |||||||
| chr9:69346397 | T | G | 1 | a0001c0001t0001g0020 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.471+10128T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69346397 | |||||||
| chr9:69346452 | T | A | 22 | a0001c0001t0001g0132 a0001c0001t0001g0142 a0001c0001t0001g0147 others(19): Show |
22 | HG00140.hp2 HG01261.hp1 HG01978.hp2 others(19): Show |
intron_variant | MODIFIER | c.471+10183T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69346452 | |||||||
| chr9:69346604 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.471+10335C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69346604 | |||||||
| chr9:69346612 | T | A | 1 | a0001c0001t0002g0080 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.471+10343T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69346612 | |||||||
| chr9:69346679 | C | T | 3 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0004c0004t0001g0218 |
5 | HG02280.hp2 HG02886.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.471+10410C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69346679 | |||||||
| chr9:69346816 | C | A | 5 | a0001c0001t0001g0123 a0001c0001t0001g0126 a0001c0001t0002g0122 others(2): Show |
5 | HG02074.hp2 HG02698.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.471+10547C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69346816 | |||||||
| chr9:69346841 | C | T | 241 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(238): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.471+10572C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69346841 | |||||||
| chr9:69346991 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.471+10722C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69346991 | |||||||
| chr9:69346998 | G | C | 1 | a0001c0001t0001g0215 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.471+10729G>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69346998 | |||||||
| chr9:69347007 | T | C | 243 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(240): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.471+10738T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69347007 | |||||||
| chr9:69347014 | G | A | 243 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(240): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.471+10745G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69347014 | |||||||
| chr9:69347045 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.471+10776G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69347045 | |||||||
| chr9:69347053 | A | T | 2 | a0001c0001t0001g0210 a0001c0001t0001g0211 |
2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.471+10784A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69347053 | |||||||
| chr9:69347107 | T | C | 103 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(100): Show |
110 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.471+10838T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69347107 | |||||||
| chr9:69347392 | G | A | 3 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0004c0004t0001g0218 |
5 | HG02280.hp2 HG02886.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.471+11123G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69347392 | |||||||
| chr9:69347465 | A | G | 1 | a0001c0001t0001g0089 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.471+11196A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69347465 | |||||||
| chr9:69347612 | T | C | 103 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(100): Show |
110 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.471+11343T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69347612 | |||||||
| chr9:69347619 | A | G | 1 | a0001c0001t0003g0260 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.471+11350A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69347619 | |||||||
| chr9:69347637 | G | A | 1 | a0001c0001t0003g0241 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.471+11368G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69347637 | |||||||
| chr9:69347704 | C | A | 243 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(240): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.471+11435C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69347704 | |||||||
| chr9:69347735 | G | A | 12 | a0001c0001t0001g0002 a0001c0001t0001g0208 a0001c0001t0001g0224 others(9): Show |
15 | HG01884.hp1 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.471+11466G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69347735 | |||||||
| chr9:69347799 | C | G | 9 | a0001c0001t0001g0002 a0001c0001t0001g0224 a0001c0001t0001g0225 others(6): Show |
12 | HG02055.hp2 HG02109.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.471+11530C>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69347799 | |||||||
| chr9:69347840 | G | A | 103 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(100): Show |
110 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(107): Show |
intron_variant | MODIFIER | c.471+11571G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69347840 | |||||||
| chr9:69348098 | A | G | 13 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(10): Show |
13 | HG01167.hp1 HG01243.hp2 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.471+11829A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69348098 | |||||||
| chr9:69348448 | G | C | 6 | a0001c0001t0001g0307 a0001c0001t0001g0308 a0001c0001t0001g0310 others(3): Show |
6 | HG02572.hp2 HG02622.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.471+12179G>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69348448 | |||||||
| chr9:69348476 | A | G | 2 | a0001c0001t0002g0220 a0003c0008t0001g0275 |
2 | HG01123.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.471+12207A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69348476 | |||||||
| chr9:69348509 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0002g0036 |
2 | HG04184.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.471+12240C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69348509 | |||||||
| chr9:69348566 | A | G | 1 | a0001c0001t0001g0174 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.471+12297A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69348566 | |||||||
| chr9:69348738 | T | A | 1 | a0001c0001t0002g0081 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.471+12469T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69348738 | |||||||
| chr9:69348761 | A | G | 266 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(263): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.471+12492A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69348761 | |||||||
| chr9:69348953 | G | A | 1 | a0001c0001t0001g0298 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.471+12684G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69348953 | |||||||
| chr9:69348955 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0054 |
3 | HG02809.hp2 HG02965.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.471+12686G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69348955 | |||||||
| chr9:69349085 | G | C | 1 | a0001c0001t0001g0183 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.471+12816G>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69349085 | |||||||
| chr9:69349099 | G | A | 2 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.471+12830G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69349099 | |||||||
| chr9:69349184 | C | CA | 11 | a0001c0001t0001g0098 a0001c0001t0003g0232 a0001c0001t0003g0239 others(8): Show |
11 | HG00423.hp1 HG00438.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.471+12942dupA | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69349184 | ||||||
| chr9:69349184 | CAAAAAA | C | 23 | a0001c0001t0001g0048 a0001c0001t0001g0059 a0001c0001t0001g0142 others(20): Show |
23 | HG00280.hp2 HG01175.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.471+12937_471+1294 others(10): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69349184 | ||||||
| chr9:69349184 | CAAAAAAA | C | 216 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(213): Show |
236 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(233): Show |
intron_variant | MODIFIER | c.471+12936_471+1294 others(11): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69349184 | ||||||
| chr9:69349184 | CAAAAAAA others(12): Show |
C | 12 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(9): Show |
12 | HG01167.hp1 HG01243.hp2 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.471+12924_471+1294 others(23): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69349184 | ||||||
| chr9:69349191 | A | C | 1 | a0001c0001t0001g0225 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.471+12922A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69349191 | |||||||
| chr9:69349511 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.471+13242T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69349511 | |||||||
| chr9:69349536 | T | C | 3 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0004c0004t0001g0218 |
5 | HG02280.hp2 HG02886.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.471+13267T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69349536 | |||||||
| chr9:69349721 | C | T | 3 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0004c0004t0001g0218 |
5 | HG02280.hp2 HG02886.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.471+13452C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69349721 | |||||||
| chr9:69349722 | G | A | 243 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(240): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.471+13453G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69349722 | |||||||
| chr9:69349784 | C | T | 2 | a0001c0001t0002g0220 a0003c0008t0001g0275 |
2 | HG01123.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.471+13515C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69349784 | |||||||
| chr9:69349797 | A | C | 1 | a0001c0001t0001g0119 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.471+13528A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69349797 | |||||||
| chr9:69349856 | T | C | 3 | a0001c0001t0002g0220 a0001c0003t0001g0314 a0003c0008t0001g0275 |
3 | HG01123.hp1 HG01891.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.471+13587T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69349856 | |||||||
| chr9:69350138 | A | G | 49 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0025 others(46): Show |
53 | HG00280.hp2 HG00597.hp2 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.471+13869A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69350138 | |||||||
| chr9:69350167 | C | T | 7 | a0001c0001t0002g0086 a0001c0001t0002g0087 a0001c0001t0002g0088 others(4): Show |
7 | HG02135.hp2 NA18939.hp2 NA18971.hp2 others(4): Show |
intron_variant | MODIFIER | c.471+13898C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69350167 | |||||||
| chr9:69350181 | A | C | 1 | a0001c0001t0002g0282 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.471+13912A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69350181 | |||||||
| chr9:69350307 | C | T | 1 | a0001c0001t0001g0304 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.471+14038C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69350307 | |||||||
| chr9:69350335 | T | TC | 261 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(258): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.471+14066_471+1406 others(5): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69350335 | |||||||
| chr9:69350360 | C | T | 1 | a0001c0001t0004g0256 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.471+14091C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69350360 | |||||||
| chr9:69350556 | CTTAAA | C | 3 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0004c0004t0001g0218 |
5 | HG02280.hp2 HG02886.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.471+14294_471+1429 others(9): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69350556 | ||||||
| chr9:69350697 | A | G | 13 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(10): Show |
13 | HG01167.hp1 HG01243.hp2 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.471+14428A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69350697 | |||||||
| chr9:69350773 | CA | C | 4 | a0001c0001t0001g0120 a0001c0001t0001g0215 a0001c0001t0001g0216 others(1): Show |
4 | HG01891.hp2 HG02055.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.471+14510delA | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69350773 | ||||||
| chr9:69351060 | T | C | 243 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(240): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.471+14791T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69351060 | |||||||
| chr9:69351088 | C | T | 2 | a0001c0001t0002g0173 a0001c0001t0002g0181 |
2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.471+14819C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69351088 | |||||||
| chr9:69351129 | A | G | 5 | a0001c0001t0001g0296 a0001c0001t0002g0018 a0001c0001t0002g0283 others(2): Show |
6 | NA18951.hp2 NA18978.hp1 NA18998.hp2 others(3): Show |
intron_variant | MODIFIER | c.471+14860A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69351129 | |||||||
| chr9:69351388 | T | TTGA | 16 | a0001c0001t0001g0132 a0001c0001t0001g0204 a0001c0001t0001g0205 others(13): Show |
18 | HG01109.hp1 HG01175.hp1 HG02074.hp2 others(15): Show |
intron_variant | MODIFIER | c.471+15148_471+1515 others(7): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69351388 | ||||||
| chr9:69351388 | T | TTGATGA | 3 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0004c0004t0001g0218 |
5 | HG02280.hp2 HG02886.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.471+15145_471+1515 others(10): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69351388 | ||||||
| chr9:69351388 | T | TTGATGAT others(5): Show |
6 | a0001c0001t0001g0040 a0001c0001t0001g0046 a0001c0001t0002g0220 others(3): Show |
6 | HG01123.hp1 HG01243.hp2 HG01891.hp1 others(3): Show |
intron_variant | MODIFIER | c.471+15139_471+1515 others(16): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69351388 | ||||||
| chr9:69351388 | T | TTGATGAT others(8): Show |
9 | a0001c0001t0001g0039 a0001c0001t0001g0041 a0001c0001t0001g0042 others(6): Show |
9 | HG01167.hp1 HG01361.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.471+15136_471+1515 others(19): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69351388 | ||||||
| chr9:69351490 | C | A | 1 | a0001c0001t0001g0138 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.471+15221C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69351490 | |||||||
| chr9:69351502 | C | T | 1 | a0001c0001t0001g0149 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.471+15233C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69351502 | |||||||
| chr9:69351503 | A | G | 261 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(258): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.471+15234A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69351503 | |||||||
| chr9:69351551 | G | T | 13 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0041 others(10): Show |
13 | HG01167.hp1 HG01243.hp2 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.471+15282G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69351551 | |||||||
| chr9:69351554 | C | A | 1 | a0001c0001t0001g0112 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.471+15285C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69351554 | |||||||
| chr9:69351610 | G | T | 243 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(240): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.471+15341G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69351610 | |||||||
| chr9:69351629 | C | T | 1 | a0007c0009t0001g0107 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.471+15360C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69351629 | |||||||
| chr9:69351666 | C | T | 1 | a0001c0001t0001g0026 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.471+15397C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69351666 | |||||||
| chr9:69351679 | T | G | 261 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(258): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.471+15410T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69351679 | |||||||
| chr9:69351981 | T | C | 1 | a0001c0001t0008g0101 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.471+15712T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69351981 | |||||||
| chr9:69352082 | T | C | 261 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(258): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.471+15813T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69352082 | |||||||
| chr9:69352178 | A | G | 261 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(258): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.471+15909A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69352178 | |||||||
| chr9:69352293 | AT | A | 7 | a0001c0001t0001g0057 a0001c0001t0001g0094 a0001c0001t0001g0297 others(4): Show |
7 | HG01943.hp2 NA18966.hp2 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.471+16029delT | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69352293 | ||||||
| chr9:69352421 | G | A | 9 | a0001c0001t0001g0002 a0001c0001t0001g0224 a0001c0001t0001g0225 others(6): Show |
12 | HG02055.hp2 HG02109.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.471+16152G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69352421 | |||||||
| chr9:69352437 | A | G | 2 | a0001c0001t0002g0220 a0003c0008t0001g0275 |
2 | HG01123.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.471+16168A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69352437 | |||||||
| chr9:69352448 | T | A | 1 | a0001c0001t0003g0274 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.471+16179T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69352448 | |||||||
| chr9:69352544 | C | T | 5 | a0001c0001t0001g0013 a0001c0001t0001g0145 a0001c0001t0001g0150 others(2): Show |
6 | HG01123.hp2 HG01255.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.471+16275C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69352544 | |||||||
| chr9:69352554 | C | T | 9 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(6): Show |
11 | HG01175.hp1 HG02258.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.471+16285C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69352554 | |||||||
| chr9:69352571 | A | G | 5 | a0001c0001t0003g0239 a0001c0001t0003g0257 a0001c0001t0003g0259 others(2): Show |
5 | HG00438.hp2 HG00621.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.471+16302A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69352571 | |||||||
| chr9:69352609 | G | A | 243 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(240): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.471+16340G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69352609 | |||||||
| chr9:69352966 | A | G | 1 | a0001c0001t0002g0080 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.471+16697A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69352966 | |||||||
| chr9:69352998 | A | G | 1 | a0001c0001t0003g0279 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.471+16729A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69352998 | |||||||
| chr9:69353008 | A | G | 1 | a0001c0001t0001g0051 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.471+16739A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69353008 | |||||||
| chr9:69353027 | T | C | 261 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(258): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.471+16758T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69353027 | |||||||
| chr9:69353032 | G | C | 5 | a0001c0001t0001g0123 a0001c0001t0001g0126 a0001c0001t0002g0122 others(2): Show |
5 | HG02074.hp2 HG02698.hp2 HG03490.hp2 others(2): Show |
intron_variant | MODIFIER | c.471+16763G>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69353032 | |||||||
| chr9:69353082 | A | G | 1 | a0001c0001t0002g0125 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.471+16813A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69353082 | |||||||
| chr9:69353086 | G | A | 261 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(258): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.471+16817G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69353086 | |||||||
| chr9:69353091 | C | T | 1 | a0001c0001t0001g0170 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.471+16822C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69353091 | |||||||
| chr9:69353135 | T | C | 1 | a0001c0001t0003g0244 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.471+16866T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69353135 | |||||||
| chr9:69353285 | C | T | 1 | a0001c0001t0004g0243 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.471+17016C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69353285 | |||||||
| chr9:69353310 | G | A | 261 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(258): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.471+17041G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69353310 | |||||||
| chr9:69353418 | A | G | 3 | a0001c0001t0001g0048 a0001c0001t0002g0052 a0001c0001t0002g0053 |
3 | HG02572.hp1 HG02647.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.471+17149A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69353418 | |||||||
| chr9:69353595 | C | T | 120 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(117): Show |
130 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.471+17326C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69353595 | |||||||
| chr9:69353688 | G | C | 1 | a0001c0001t0001g0134 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.471+17419G>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69353688 | |||||||
| chr9:69353739 | A | G | 266 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(263): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.471+17470A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69353739 | |||||||
| chr9:69353814 | A | G | 122 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(119): Show |
132 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.471+17545A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69353814 | |||||||
| chr9:69353867 | T | C | 1 | a0001c0001t0001g0182 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.471+17598T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69353867 | |||||||
| chr9:69353909 | C | T | 243 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(240): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.472-17590C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69353909 | |||||||
| chr9:69353968 | A | G | 1 | a0001c0001t0001g0017 | 2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.472-17531A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69353968 | |||||||
| chr9:69354030 | T | G | 1 | a0003c0008t0001g0275 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.472-17469T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69354030 | |||||||
| chr9:69354098 | T | G | 1 | a0001c0001t0003g0280 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.472-17401T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69354098 | |||||||
| chr9:69354137 | C | T | 3 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 |
3 | HG02258.hp2 NA18522.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.472-17362C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69354137 | |||||||
| chr9:69354254 | A | AT | 7 | a0001c0001t0001g0061 a0001c0001t0001g0213 a0001c0001t0001g0292 others(4): Show |
7 | HG02451.hp2 HG03490.hp1 NA18980.hp2 others(4): Show |
intron_variant | MODIFIER | c.472-17225dupT | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69354254 | ||||||
| chr9:69354254 | A | ATT | 98 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(95): Show |
105 | HG00099.hp2 HG00280.hp2 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.472-17226_472-1722 others(6): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69354254 | ||||||
| chr9:69354254 | A | ATTT | 38 | a0001c0001t0001g0002 a0001c0001t0001g0028 a0001c0001t0001g0035 others(35): Show |
46 | HG00140.hp1 HG01109.hp1 HG01167.hp2 others(43): Show |
intron_variant | MODIFIER | c.472-17227_472-1722 others(7): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69354254 | ||||||
| chr9:69354254 | A | ATTTT | 89 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0013 others(86): Show |
94 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.472-17228_472-1722 others(8): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69354254 | ||||||
| chr9:69354254 | A | ATTTTT | 14 | a0001c0001t0001g0056 a0001c0001t0001g0064 a0001c0001t0001g0168 others(11): Show |
14 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.472-17229_472-1722 others(9): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69354254 | ||||||
| chr9:69354254 | AT | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0039 others(1): Show |
6 | HG02280.hp2 HG02886.hp2 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.472-17225delT | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69354254 | ||||||
| chr9:69354254 | ATT | A | 13 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(10): Show |
13 | HG01123.hp1 HG01167.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.472-17226_472-1722 others(6): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69354254 | ||||||
| chr9:69354566 | T | C | 261 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(258): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.472-16933T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69354566 | |||||||
| chr9:69354650 | C | T | 2 | a0001c0001t0001g0296 a0001c0001t0002g0285 |
2 | NA19003.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.472-16849C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69354650 | |||||||
| chr9:69354801 | A | G | 2 | a0001c0001t0002g0220 a0003c0008t0001g0275 |
2 | HG01123.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.472-16698A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69354801 | |||||||
| chr9:69354929 | T | G | 2 | a0001c0001t0001g0091 a0001c0001t0002g0003 |
4 | HG01346.hp2 HG01952.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.472-16570T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69354929 | |||||||
| chr9:69355004 | T | G | 1 | a0001c0001t0002g0077 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.472-16495T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69355004 | |||||||
| chr9:69355066 | T | C | 1 | a0001c0001t0002g0177 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.472-16433T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69355066 | |||||||
| chr9:69355089 | A | G | 3 | a0001c0001t0001g0224 a0001c0003t0001g0314 a0001c0003t0001g0315 |
3 | HG01243.hp2 HG01891.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.472-16410A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69355089 | |||||||
| chr9:69355164 | A | G | 243 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(240): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.472-16335A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69355164 | |||||||
| chr9:69355224 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.472-16275C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69355224 | |||||||
| chr9:69355233 | T | G | 1 | a0001c0001t0001g0120 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.472-16266T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69355233 | |||||||
| chr9:69355526 | G | A | 2 | a0001c0001t0001g0210 a0001c0001t0001g0225 |
2 | HG02109.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.472-15973G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69355526 | |||||||
| chr9:69355546 | G | A | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG02559.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.472-15953G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69355546 | |||||||
| chr9:69355746 | G | A | 2 | a0001c0001t0001g0025 a0001c0001t0001g0031 |
2 | NA18949.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.472-15753G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69355746 | |||||||
| chr9:69355830 | G | A | 8 | a0001c0001t0002g0009 a0001c0001t0002g0058 a0001c0001t0002g0060 others(5): Show |
9 | HG00280.hp2 HG01106.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.472-15669G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69355830 | |||||||
| chr9:69355835 | C | T | 2 | a0003c0006t0001g0209 a0005c0005t0001g0221 |
2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.472-15664C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69355835 | |||||||
| chr9:69355850 | T | C | 2 | a0001c0001t0002g0080 a0001c0001t0002g0084 |
2 | HG01109.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.472-15649T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69355850 | |||||||
| chr9:69355885 | T | C | 1 | a0001c0001t0001g0017 | 2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.472-15614T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69355885 | |||||||
| chr9:69355918 | T | C | 2 | a0003c0006t0001g0209 a0005c0005t0001g0221 |
2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.472-15581T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69355918 | |||||||
| chr9:69356041 | G | A | 2 | a0001c0001t0002g0155 a0001c0001t0002g0156 |
2 | HG00735.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.472-15458G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69356041 | |||||||
| chr9:69356052 | G | A | 186 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(183): Show |
199 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(196): Show |
intron_variant | MODIFIER | c.472-15447G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69356052 | |||||||
| chr9:69356087 | T | A | 29 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0025 others(26): Show |
31 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.472-15412T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69356087 | |||||||
| chr9:69356099 | G | A | 12 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0210 others(9): Show |
14 | HG01175.hp1 HG01243.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.472-15400G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69356099 | |||||||
| chr9:69356290 | C | T | 1 | a0003c0008t0001g0275 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.472-15209C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69356290 | |||||||
| chr9:69356348 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.472-15151A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69356348 | |||||||
| chr9:69356494 | C | CAT | 235 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(232): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.472-15004_472-1500 others(6): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69356494 | ||||||
| chr9:69356734 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.472-14765G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69356734 | |||||||
| chr9:69356885 | T | G | 4 | a0002c0002t0001g0004 a0002c0002t0001g0214 a0002c0002t0001g0222 others(1): Show |
6 | HG01175.hp1 HG02809.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.472-14614T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69356885 | |||||||
| chr9:69357095 | C | CA | 9 | a0001c0001t0001g0094 a0001c0001t0001g0299 a0001c0001t0001g0308 others(6): Show |
9 | HG00621.hp1 HG02300.hp2 HG03098.hp2 others(6): Show |
intron_variant | MODIFIER | c.472-14382dupA | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69357095 | ||||||
| chr9:69357095 | CA | C | 171 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0013 others(168): Show |
183 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(180): Show |
intron_variant | MODIFIER | c.472-14382delA | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69357095 | ||||||
| chr9:69357095 | CAA | C | 15 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0108 others(12): Show |
17 | HG01167.hp2 HG01243.hp2 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.472-14383_472-1438 others(6): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69357095 | ||||||
| chr9:69357095 | CAAA | C | 11 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(8): Show |
13 | HG01175.hp1 HG02109.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.472-14384_472-1438 others(7): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69357095 | ||||||
| chr9:69357473 | A | G | 11 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(8): Show |
11 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(8): Show |
intron_variant | MODIFIER | c.472-14026A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69357473 | |||||||
| chr9:69357586 | T | G | 45 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0034 others(42): Show |
49 | HG01106.hp2 HG01167.hp1 HG01175.hp1 others(46): Show |
intron_variant | MODIFIER | c.472-13913T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69357586 | |||||||
| chr9:69357687 | A | G | 1 | a0001c0001t0001g0142 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.472-13812A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69357687 | |||||||
| chr9:69357911 | C | A | 1 | a0001c0001t0003g0263 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.472-13588C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69357911 | |||||||
| chr9:69358015 | T | G | 1 | a0001c0001t0002g0194 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.472-13484T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69358015 | |||||||
| chr9:69358081 | A | G | 1 | a0001c0001t0001g0110 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.472-13418A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69358081 | |||||||
| chr9:69358149 | C | A | 1 | a0001c0001t0001g0311 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.472-13350C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69358149 | |||||||
| chr9:69358287 | T | C | 32 | a0001c0001t0002g0018 a0001c0001t0002g0019 a0001c0001t0002g0029 others(29): Show |
34 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.472-13212T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69358287 | |||||||
| chr9:69358365 | T | C | 1 | a0001c0001t0002g0199 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.472-13134T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69358365 | |||||||
| chr9:69358510 | C | A | 1 | a0001c0001t0002g0140 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.472-12989C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69358510 | |||||||
| chr9:69358519 | G | T | 130 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(127): Show |
137 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(134): Show |
intron_variant | MODIFIER | c.472-12980G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69358519 | |||||||
| chr9:69358535 | G | A | 4 | a0002c0002t0001g0004 a0002c0002t0001g0214 a0002c0002t0001g0222 others(1): Show |
6 | HG01175.hp1 HG02809.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.472-12964G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69358535 | |||||||
| chr9:69358601 | A | G | 10 | a0001c0001t0001g0014 a0001c0001t0001g0047 a0001c0001t0001g0054 others(7): Show |
11 | HG01255.hp2 HG02055.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.472-12898A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69358601 | |||||||
| chr9:69358621 | G | T | 1 | a0001c0001t0002g0068 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.472-12878G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69358621 | |||||||
| chr9:69358749 | A | G | 6 | a0001c0001t0001g0051 a0001c0001t0001g0059 a0001c0001t0001g0065 others(3): Show |
6 | HG02572.hp2 HG02630.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.472-12750A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69358749 | |||||||
| chr9:69358750 | C | T | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG02559.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.472-12749C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69358750 | |||||||
| chr9:69358828 | G | T | 93 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(90): Show |
101 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.472-12671G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69358828 | |||||||
| chr9:69358884 | T | A | 111 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0108 others(108): Show |
123 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.472-12615T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69358884 | |||||||
| chr9:69358902 | CT | C | 6 | a0001c0001t0001g0116 a0001c0001t0001g0169 a0001c0001t0001g0230 others(3): Show |
6 | HG01256.hp1 HG02738.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.472-12578delT | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69358902 | ||||||
| chr9:69358902 | CTT | C | 237 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(234): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.472-12579_472-1257 others(6): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69358902 | ||||||
| chr9:69358909 | T | C | 1 | a0001c0001t0001g0224 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.472-12590T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69358909 | |||||||
| chr9:69358925 | A | G | 130 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(127): Show |
137 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(134): Show |
intron_variant | MODIFIER | c.472-12574A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69358925 | |||||||
| chr9:69359048 | G | T | 1 | a0001c0001t0001g0064 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.472-12451G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69359048 | |||||||
| chr9:69359051 | G | A | 1 | a0001c0001t0001g0210 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.472-12448G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69359051 | |||||||
| chr9:69359061 | G | A | 111 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0108 others(108): Show |
123 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.472-12438G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69359061 | |||||||
| chr9:69359146 | C | G | 1 | a0001c0001t0003g0207 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.472-12353C>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69359146 | |||||||
| chr9:69359153 | G | A | 1 | a0001c0001t0003g0234 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.472-12346G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69359153 | |||||||
| chr9:69359185 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.472-12314C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69359185 | |||||||
| chr9:69359428 | A | G | 1 | a0001c0001t0001g0024 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.472-12071A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69359428 | |||||||
| chr9:69359525 | A | G | 29 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0025 others(26): Show |
31 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.472-11974A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69359525 | |||||||
| chr9:69359553 | G | T | 1 | a0001c0003t0001g0050 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.472-11946G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69359553 | |||||||
| chr9:69359784 | T | G | 244 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(241): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.472-11715T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69359784 | |||||||
| chr9:69359970 | C | CT | 6 | a0001c0001t0001g0057 a0001c0001t0001g0102 a0001c0001t0001g0103 others(3): Show |
6 | HG00597.hp1 HG02055.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.472-11514dupT | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69359970 | ||||||
| chr9:69360115 | A | C | 94 | a0001c0001t0001g0091 a0001c0001t0002g0003 a0001c0001t0002g0008 others(91): Show |
102 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.472-11384A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69360115 | |||||||
| chr9:69360395 | A | G | 93 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(90): Show |
101 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.472-11104A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69360395 | |||||||
| chr9:69360480 | T | C | 1 | a0001c0001t0001g0185 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.472-11019T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69360480 | |||||||
| chr9:69360557 | G | A | 2 | a0001c0001t0001g0183 a0001c0001t0001g0190 |
2 | HG02559.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.472-10942G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69360557 | |||||||
| chr9:69360640 | A | G | 2 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
2 | HG02970.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.472-10859A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69360640 | |||||||
| chr9:69360682 | T | G | 310 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(307): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.472-10817T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69360682 | |||||||
| chr9:69360819 | T | G | 1 | a0001c0001t0001g0164 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.472-10680T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69360819 | |||||||
| chr9:69360898 | CA | C | 219 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(216): Show |
234 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(231): Show |
intron_variant | MODIFIER | c.472-10590delA | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69360898 | ||||||
| chr9:69360963 | G | A | 130 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(127): Show |
137 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(134): Show |
intron_variant | MODIFIER | c.472-10536G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69360963 | |||||||
| chr9:69360994 | T | A | 93 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(90): Show |
101 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.472-10505T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69360994 | |||||||
| chr9:69361100 | GA | G | 130 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(127): Show |
137 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(134): Show |
intron_variant | MODIFIER | c.472-10397delA | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69361100 | ||||||
| chr9:69361163 | G | A | 261 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(258): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.472-10336G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69361163 | |||||||
| chr9:69361255 | G | A | 111 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0108 others(108): Show |
123 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.472-10244G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69361255 | |||||||
| chr9:69361282 | T | C | 2 | a0001c0001t0001g0157 a0001c0001t0001g0158 |
2 | NA18944.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.472-10217T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69361282 | |||||||
| chr9:69361418 | T | C | 111 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0108 others(108): Show |
123 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.472-10081T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69361418 | |||||||
| chr9:69361600 | T | A | 1 | a0001c0001t0003g0249 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.472-9899T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69361600 | |||||||
| chr9:69361787 | T | A | 3 | a0001c0001t0001g0141 a0001c0001t0001g0176 a0001c0001t0003g0252 |
3 | HG03927.hp1 NA18981.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.472-9712T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69361787 | |||||||
| chr9:69361802 | G | T | 2 | a0001c0001t0002g0128 a0001c0001t0002g0129 |
2 | NA18978.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.472-9697G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69361802 | |||||||
| chr9:69362044 | A | G | 1 | a0001c0001t0001g0166 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.472-9455A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69362044 | |||||||
| chr9:69362143 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.472-9356C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69362143 | |||||||
| chr9:69362269 | A | G | 3 | a0001c0003t0001g0050 a0001c0003t0001g0314 a0001c0003t0001g0315 |
3 | HG01243.hp2 HG01891.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.472-9230A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69362269 | |||||||
| chr9:69362487 | G | T | 9 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0189 others(6): Show |
11 | HG01496.hp2 HG01884.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.472-9012G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69362487 | |||||||
| chr9:69362564 | A | G | 29 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0025 others(26): Show |
31 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.472-8935A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69362564 | |||||||
| chr9:69362575 | A | G | 310 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(307): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.472-8924A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69362575 | |||||||
| chr9:69362618 | G | A | 1 | a0003c0008t0001g0275 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.472-8881G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69362618 | |||||||
| chr9:69362681 | G | T | 93 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(90): Show |
101 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.472-8818G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69362681 | |||||||
| chr9:69362713 | G | A | 111 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0108 others(108): Show |
123 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.472-8786G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69362713 | |||||||
| chr9:69362873 | C | T | 85 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(82): Show |
90 | HG00423.hp2 HG00642.hp2 HG01123.hp2 others(87): Show |
intron_variant | MODIFIER | c.472-8626C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69362873 | |||||||
| chr9:69363042 | A | G | 1 | a0003c0008t0001g0275 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.472-8457A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69363042 | |||||||
| chr9:69363062 | A | T | 242 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(239): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.472-8437A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69363062 | |||||||
| chr9:69363088 | T | G | 94 | a0001c0001t0001g0091 a0001c0001t0002g0003 a0001c0001t0002g0008 others(91): Show |
102 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.472-8411T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69363088 | |||||||
| chr9:69363146 | A | T | 1 | a0001c0001t0001g0079 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.472-8353A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69363146 | |||||||
| chr9:69363395 | A | G | 12 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0028 others(9): Show |
13 | NA18944.hp2 NA18960.hp1 NA18964.hp1 others(10): Show |
intron_variant | MODIFIER | c.472-8104A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69363395 | |||||||
| chr9:69363439 | A | T | 1 | a0001c0001t0003g0207 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.472-8060A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69363439 | |||||||
| chr9:69363550 | C | T | 2 | a0001c0001t0001g0211 a0001c0001t0001g0225 |
2 | HG02109.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.472-7949C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69363550 | |||||||
| chr9:69363680 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.472-7819G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69363680 | |||||||
| chr9:69363921 | T | C | 242 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(239): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.472-7578T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69363921 | |||||||
| chr9:69363932 | A | G | 130 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(127): Show |
137 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(134): Show |
intron_variant | MODIFIER | c.472-7567A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69363932 | |||||||
| chr9:69364124 | A | G | 1 | a0001c0001t0002g0072 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.472-7375A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69364124 | |||||||
| chr9:69364379 | C | A | 243 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(240): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.472-7120C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69364379 | |||||||
| chr9:69364389 | A | AT | 109 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0091 others(106): Show |
121 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(118): Show |
intron_variant | MODIFIER | c.472-7097dupT | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69364389 | ||||||
| chr9:69364389 | AT | A | 131 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(128): Show |
138 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(135): Show |
intron_variant | MODIFIER | c.472-7097delT | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69364389 | ||||||
| chr9:69364512 | C | T | 1 | a0001c0001t0002g0058 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.472-6987C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69364512 | |||||||
| chr9:69364583 | T | C | 1 | a0001c0001t0001g0182 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.472-6916T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69364583 | |||||||
| chr9:69364788 | A | G | 1 | a0001c0001t0001g0224 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.472-6711A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69364788 | |||||||
| chr9:69364795 | G | A | 1 | a0001c0001t0002g0285 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.472-6704G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69364795 | |||||||
| chr9:69364854 | A | T | 94 | a0001c0001t0001g0091 a0001c0001t0002g0003 a0001c0001t0002g0008 others(91): Show |
102 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(99): Show |
intron_variant | MODIFIER | c.472-6645A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69364854 | |||||||
| chr9:69364876 | T | G | 1 | a0001c0001t0002g0071 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.472-6623T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69364876 | |||||||
| chr9:69364915 | G | A | 2 | a0001c0001t0001g0141 a0001c0001t0003g0252 |
2 | NA18981.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.472-6584G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69364915 | |||||||
| chr9:69364991 | T | C | 1 | a0001c0001t0004g0268 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.472-6508T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69364991 | |||||||
| chr9:69364994 | CTG | C | 3 | a0001c0001t0001g0099 a0001c0001t0001g0306 a0001c0001t0003g0238 |
3 | NA18985.hp2 NA18994.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.472-6503_472-6502d others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69364994 | ||||||
| chr9:69365035 | G | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0032 |
2 | NA18987.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.472-6464G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69365035 | |||||||
| chr9:69365051 | C | T | 2 | a0001c0001t0003g0234 a0001c0001t0003g0235 |
2 | NA18970.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.472-6448C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69365051 | |||||||
| chr9:69365271 | C | T | 4 | a0001c0001t0001g0054 a0001c0001t0001g0215 a0001c0001t0001g0216 others(1): Show |
4 | HG01891.hp2 HG02055.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.472-6228C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69365271 | |||||||
| chr9:69365305 | C | T | 243 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(240): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.472-6194C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69365305 | |||||||
| chr9:69365437 | G | A | 2 | a0001c0001t0001g0022 a0001c0001t0002g0021 |
2 | HG00621.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.472-6062G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69365437 | |||||||
| chr9:69365461 | G | T | 1 | a0001c0001t0001g0144 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.472-6038G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69365461 | |||||||
| chr9:69365561 | A | C | 130 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(127): Show |
137 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(134): Show |
intron_variant | MODIFIER | c.472-5938A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69365561 | |||||||
| chr9:69365724 | C | CTA | 131 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(128): Show |
138 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(135): Show |
intron_variant | MODIFIER | c.472-5774_472-5773i others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69365724 | ||||||
| chr9:69365831 | C | T | 243 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(240): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.472-5668C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69365831 | |||||||
| chr9:69365952 | C | T | 27 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0031 others(24): Show |
28 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.472-5547C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69365952 | |||||||
| chr9:69366107 | G | T | 1 | a0001c0001t0001g0210 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.472-5392G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69366107 | |||||||
| chr9:69366347 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.472-5152A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69366347 | |||||||
| chr9:69366349 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.472-5150C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69366349 | |||||||
| chr9:69366384 | G | GT | 4 | a0001c0001t0001g0210 a0001c0001t0002g0194 a0001c0001t0002g0197 others(1): Show |
4 | HG00140.hp2 HG01261.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.472-5115_472-5114i others(3): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69366384 | |||||||
| chr9:69366384 | G | GTT | 3 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0005c0005t0001g0221 |
3 | HG02559.hp2 HG03098.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.472-5115_472-5114i others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69366384 | |||||||
| chr9:69366384 | G | GTTT | 19 | a0001c0001t0001g0034 a0001c0001t0001g0041 a0001c0001t0001g0042 others(16): Show |
19 | HG01106.hp2 HG01167.hp1 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.472-5115_472-5114i others(5): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69366384 | |||||||
| chr9:69366384 | G | GTTTT | 75 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(72): Show |
79 | HG00423.hp2 HG00642.hp2 HG01168.hp1 others(76): Show |
intron_variant | MODIFIER | c.472-5115_472-5114i others(6): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69366384 | |||||||
| chr9:69366384 | G | GTTTTT | 7 | a0001c0001t0001g0047 a0001c0001t0001g0056 a0001c0001t0001g0057 others(4): Show |
7 | HG02055.hp1 HG02135.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.472-5115_472-5114i others(7): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69366384 | |||||||
| chr9:69366384 | G | GTTTTTT | 24 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0025 others(21): Show |
26 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(23): Show |
intron_variant | MODIFIER | c.472-5115_472-5114i others(8): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69366384 | |||||||
| chr9:69366384 | G | GTTTTTTT | 5 | a0001c0001t0001g0061 a0001c0001t0001g0212 a0001c0001t0001g0308 others(2): Show |
5 | HG02622.hp1 HG03098.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.472-5115_472-5114i others(9): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69366384 | |||||||
| chr9:69366385 | G | GT | 93 | a0001c0001t0001g0049 a0001c0001t0001g0091 a0001c0001t0001g0176 others(90): Show |
101 | HG00099.hp2 HG00280.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.472-5099dupT | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69366385 | ||||||
| chr9:69366385 | G | GTT | 9 | a0001c0001t0002g0029 a0001c0001t0002g0052 a0001c0001t0002g0063 others(6): Show |
9 | HG00140.hp1 HG00597.hp2 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.472-5100_472-5099d others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69366385 | ||||||
| chr9:69366385 | G | T | 139 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(136): Show |
146 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.472-5114G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69366385 | |||||||
| chr9:69366574 | G | C | 1 | a0001c0001t0002g0155 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.472-4925G>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69366574 | |||||||
| chr9:69366638 | C | G | 1 | a0001c0001t0001g0106 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.472-4861C>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69366638 | |||||||
| chr9:69366755 | T | C | 18 | a0001c0001t0001g0034 a0001c0001t0001g0041 a0001c0001t0001g0042 others(15): Show |
18 | HG01106.hp2 HG01167.hp1 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.472-4744T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69366755 | |||||||
| chr9:69366817 | T | C | 1 | a0001c0001t0003g0257 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.472-4682T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69366817 | |||||||
| chr9:69366870 | G | A | 2 | a0001c0001t0001g0065 a0001c0001t0001g0104 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.472-4629G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69366870 | |||||||
| chr9:69367005 | T | A | 1 | a0001c0001t0001g0210 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.472-4494T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367005 | |||||||
| chr9:69367016 | A | C | 1 | a0001c0001t0001g0210 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.472-4483A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367016 | |||||||
| chr9:69367091 | A | AT | 6 | a0001c0001t0001g0141 a0001c0001t0001g0301 a0001c0001t0003g0242 others(3): Show |
6 | HG02071.hp2 NA18943.hp1 NA18949.hp2 others(3): Show |
intron_variant | MODIFIER | c.472-4386dupT | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69367091 | ||||||
| chr9:69367091 | ATTT | A | 12 | a0001c0001t0001g0114 a0001c0001t0001g0116 a0001c0001t0001g0144 others(9): Show |
12 | HG01516.hp2 HG02055.hp1 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.472-4388_472-4386d others(5): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69367091 | ||||||
| chr9:69367091 | ATTTT | A | 224 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(221): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.472-4389_472-4386d others(6): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69367091 | ||||||
| chr9:69367183 | G | C | 242 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(239): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.472-4316G>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367183 | |||||||
| chr9:69367422 | G | A | 130 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(127): Show |
137 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(134): Show |
intron_variant | MODIFIER | c.472-4077G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367422 | |||||||
| chr9:69367455 | A | G | 1 | a0001c0001t0003g0238 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.472-4044A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367455 | |||||||
| chr9:69367467 | T | C | 130 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(127): Show |
137 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(134): Show |
intron_variant | MODIFIER | c.472-4032T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367467 | |||||||
| chr9:69367484 | T | C | 13 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0189 others(10): Show |
17 | HG01175.hp1 HG01496.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.472-4015T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367484 | |||||||
| chr9:69367601 | A | T | 1 | a0001c0001t0003g0236 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.472-3898A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367601 | |||||||
| chr9:69367614 | T | C | 1 | a0001c0001t0003g0264 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.472-3885T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367614 | |||||||
| chr9:69367668 | CACACATA others(15): Show |
C | 5 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0086 others(2): Show |
5 | HG00099.hp2 HG02135.hp2 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.472-3819_472-3798d others(24): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69367668 | ||||||
| chr9:69367672 | C | CAT | 224 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(221): Show |
241 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.472-3821_472-3820d others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69367672 | ||||||
| chr9:69367672 | C | CATATATA others(21): Show |
8 | a0001c0001t0001g0033 a0001c0001t0001g0204 a0001c0001t0001g0205 others(5): Show |
10 | HG01175.hp1 HG02132.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.472-3820_472-3819i others(30): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69367672 | ||||||
| chr9:69367672 | C | CATATATA others(47): Show |
1 | a0003c0008t0001g0275 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.472-3820_472-3819i others(56): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69367672 | ||||||
| chr9:69367672 | C | CATATATA others(19): Show |
3 | a0001c0003t0001g0050 a0001c0003t0001g0314 a0001c0003t0001g0315 |
3 | HG01243.hp2 HG01891.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.472-3820_472-3819i others(28): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69367672 | ||||||
| chr9:69367696 | T | C | 1 | a0001c0001t0002g0063 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.472-3803T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367696 | |||||||
| chr9:69367704 | A | C | 12 | a0001c0001t0001g0016 a0001c0001t0001g0189 a0001c0001t0001g0191 others(9): Show |
15 | HG01175.hp1 HG01496.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.472-3795A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367704 | |||||||
| chr9:69367706 | T | C | 1 | a0001c0001t0001g0017 | 2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.472-3793T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367706 | |||||||
| chr9:69367708 | TATATATA others(15): Show |
T | 85 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(82): Show |
93 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.472-3783_472-3762d others(24): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69367708 | ||||||
| chr9:69367716 | C | T | 1 | a0001c0001t0002g0179 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.472-3783C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367716 | |||||||
| chr9:69367720 | T | C | 1 | a0001c0001t0002g0179 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.472-3779T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367720 | |||||||
| chr9:69367728 | A | T | 2 | a0001c0001t0001g0061 a0001c0001t0001g0062 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.472-3771A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367728 | |||||||
| chr9:69367730 | A | T | 10 | a0001c0001t0002g0066 a0001c0001t0002g0067 a0001c0001t0002g0086 others(7): Show |
10 | HG00099.hp2 HG01975.hp2 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.472-3769A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367730 | |||||||
| chr9:69367740 | T | C | 3 | a0001c0001t0002g0179 a0003c0006t0001g0209 a0005c0005t0001g0221 |
3 | HG01975.hp2 HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.472-3759T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367740 | |||||||
| chr9:69367740 | TAC | T | 107 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(104): Show |
112 | HG00423.hp1 HG00423.hp2 HG00621.hp2 others(109): Show |
intron_variant | MODIFIER | c.472-3755_472-3754d others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69367740 | ||||||
| chr9:69367744 | C | T | 3 | a0001c0001t0002g0179 a0003c0006t0001g0209 a0005c0005t0001g0221 |
3 | HG01975.hp2 HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.472-3755C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367744 | |||||||
| chr9:69367750 | T | TAAATATA others(17): Show |
13 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0189 others(10): Show |
17 | HG01175.hp1 HG01496.hp2 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.472-3726_472-3725i others(26): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69367750 | ||||||
| chr9:69367752 | A | T | 3 | a0001c0001t0001g0045 a0001c0001t0001g0055 a0001c0001t0001g0089 |
3 | HG01361.hp1 HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.472-3747A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367752 | |||||||
| chr9:69367754 | T | A | 3 | a0001c0001t0001g0045 a0001c0001t0001g0055 a0001c0001t0001g0089 |
3 | HG01361.hp1 HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.472-3745T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367754 | |||||||
| chr9:69367762 | T | C | 12 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(9): Show |
12 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(9): Show |
intron_variant | MODIFIER | c.472-3737T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367762 | |||||||
| chr9:69367764 | C | T | 3 | a0001c0001t0001g0045 a0001c0001t0001g0055 a0001c0001t0001g0089 |
3 | HG01361.hp1 HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.472-3735C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367764 | |||||||
| chr9:69367768 | T | C | 3 | a0001c0001t0001g0045 a0001c0001t0001g0055 a0001c0001t0001g0089 |
3 | HG01361.hp1 HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.472-3731T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367768 | |||||||
| chr9:69367786 | C | T | 237 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(234): Show |
256 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(253): Show |
intron_variant | MODIFIER | c.472-3713C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367786 | |||||||
| chr9:69367790 | CAT | C | 126 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(123): Show |
133 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(130): Show |
intron_variant | MODIFIER | c.472-3701_472-3700d others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69367790 | ||||||
| chr9:69367798 | T | A | 3 | a0001c0001t0001g0045 a0001c0001t0001g0055 a0001c0001t0001g0089 |
3 | HG01361.hp1 HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.472-3701T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367798 | |||||||
| chr9:69367800 | A | T | 3 | a0001c0001t0001g0045 a0001c0001t0001g0055 a0001c0001t0001g0089 |
3 | HG01361.hp1 HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.472-3699A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367800 | |||||||
| chr9:69367810 | C | T | 14 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(11): Show |
14 | HG00423.hp1 HG00621.hp2 HG00673.hp1 others(11): Show |
intron_variant | MODIFIER | c.472-3689C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367810 | |||||||
| chr9:69367814 | C | T | 3 | a0001c0001t0001g0045 a0001c0001t0001g0055 a0001c0001t0001g0089 |
3 | HG01361.hp1 HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.472-3685C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367814 | |||||||
| chr9:69367814 | CAT | C | 126 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(123): Show |
133 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(130): Show |
intron_variant | MODIFIER | c.472-3677_472-3676d others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69367814 | ||||||
| chr9:69367816 | T | TATATAAA others(13): Show |
1 | a0001c0001t0001g0133 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.472-3678_472-3677i others(22): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69367816 | ||||||
| chr9:69367816 | T | TATATATA others(179): Show |
1 | a0001c0001t0001g0134 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.472-3666_472-3665i others(188): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69367816 | ||||||
| chr9:69367816 | T | TATATATA others(179): Show |
1 | a0001c0001t0003g0249 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.472-3652_472-3651i others(188): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69367816 | ||||||
| chr9:69367816 | T | TATATATA others(203): Show |
5 | a0001c0001t0003g0232 a0001c0001t0003g0248 a0001c0001t0003g0250 others(2): Show |
5 | HG00423.hp1 HG02155.hp2 HG02273.hp1 others(2): Show |
intron_variant | MODIFIER | c.472-3652_472-3651i others(212): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69367816 | ||||||
| chr9:69367824 | AATAT | A | 3 | a0001c0001t0001g0045 a0001c0001t0001g0055 a0001c0001t0001g0089 |
3 | HG01361.hp1 HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.472-3667_472-3664d others(6): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69367824 | ||||||
| chr9:69367834 | T | C | 1 | a0001c0001t0002g0179 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.472-3665T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367834 | |||||||
| chr9:69367838 | CAT | C | 97 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0210 others(94): Show |
105 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.472-3651_472-3650d others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69367838 | ||||||
| chr9:69367840 | T | C | 3 | a0001c0001t0001g0045 a0001c0001t0001g0055 a0001c0001t0001g0089 |
3 | HG01361.hp1 HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.472-3659T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367840 | |||||||
| chr9:69367848 | T | A | 6 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(3): Show |
6 | HG00621.hp2 HG00673.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.472-3651T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367848 | |||||||
| chr9:69367850 | A | T | 6 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(3): Show |
6 | HG00621.hp2 HG00673.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.472-3649A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367850 | |||||||
| chr9:69367852 | TATATACA others(3): Show |
T | 3 | a0001c0001t0001g0045 a0001c0001t0001g0055 a0001c0001t0001g0089 |
3 | HG01361.hp1 HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.472-3641_472-3632d others(12): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69367852 | ||||||
| chr9:69367858 | C | T | 1 | a0001c0001t0002g0179 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.472-3641C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367858 | |||||||
| chr9:69367864 | T | C | 1 | a0001c0001t0001g0210 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.472-3635T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367864 | |||||||
| chr9:69367872 | A | C | 4 | a0001c0001t0001g0045 a0001c0001t0001g0055 a0001c0001t0001g0089 others(1): Show |
4 | HG01361.hp1 HG01975.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.472-3627A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367872 | |||||||
| chr9:69367874 | T | C | 4 | a0001c0001t0001g0045 a0001c0001t0001g0055 a0001c0001t0001g0089 others(1): Show |
4 | HG01361.hp1 HG01975.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.472-3625T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367874 | |||||||
| chr9:69367874 | T | TATATATA others(215): Show |
5 | a0001c0001t0001g0020 a0001c0001t0001g0022 a0001c0001t0001g0023 others(2): Show |
5 | HG00621.hp2 HG00673.hp1 HG01346.hp2 others(2): Show |
intron_variant | MODIFIER | c.472-3618_472-3617i others(224): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69367874 | ||||||
| chr9:69367874 | T | TATATATA others(5): Show |
208 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(205): Show |
223 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(220): Show |
intron_variant | MODIFIER | c.472-3615_472-3604d others(14): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69367874 | ||||||
| chr9:69367888 | T | TATATATA others(3): Show |
31 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0025 others(28): Show |
32 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.472-3604_472-3603i others(12): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69367888 | ||||||
| chr9:69367888 | TATATATA others(3): Show |
T | 2 | a0001c0001t0002g0074 a0001c0001t0002g0075 |
2 | NA19002.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.472-3603_472-3594d others(12): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69367888 | ||||||
| chr9:69367933 | G | T | 2 | a0001c0001t0001g0042 a0001c0001t0001g0043 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.472-3566G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69367933 | |||||||
| chr9:69368037 | C | T | 4 | a0001c0001t0001g0048 a0001c0001t0001g0307 a0001c0001t0001g0308 others(1): Show |
4 | HG02647.hp1 HG02647.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.472-3462C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69368037 | |||||||
| chr9:69368058 | C | CTT | 254 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(251): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.472-3440_472-3439i others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69368058 | ||||||
| chr9:69368468 | A | C | 1 | a0001c0001t0001g0210 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.472-3031A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69368468 | |||||||
| chr9:69368475 | T | A | 254 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(251): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.472-3024T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69368475 | |||||||
| chr9:69368581 | A | G | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG02559.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.472-2918A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69368581 | |||||||
| chr9:69368739 | A | C | 93 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(90): Show |
101 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.472-2760A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69368739 | |||||||
| chr9:69368846 | A | T | 110 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(107): Show |
115 | HG00423.hp1 HG00423.hp2 HG00621.hp2 others(112): Show |
intron_variant | MODIFIER | c.472-2653A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69368846 | |||||||
| chr9:69369033 | A | G | 1 | a0003c0008t0001g0275 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.472-2466A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69369033 | |||||||
| chr9:69369062 | T | C | 93 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(90): Show |
101 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.472-2437T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69369062 | |||||||
| chr9:69369292 | C | T | 1 | a0001c0001t0003g0236 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.472-2207C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69369292 | |||||||
| chr9:69369422 | T | C | 142 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(139): Show |
149 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.472-2077T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69369422 | |||||||
| chr9:69369456 | A | C | 1 | a0001c0001t0001g0092 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.472-2043A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69369456 | |||||||
| chr9:69369594 | C | CTT | 35 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0108 others(32): Show |
40 | HG00597.hp2 HG01175.hp1 HG01261.hp1 others(37): Show |
intron_variant | MODIFIER | c.472-1893_472-1892d others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69369594 | ||||||
| chr9:69369594 | C | CTTT | 74 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(71): Show |
81 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.472-1894_472-1892d others(5): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69369594 | ||||||
| chr9:69369747 | G | A | 5 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0210 others(2): Show |
5 | HG02451.hp1 HG02559.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.472-1752G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69369747 | |||||||
| chr9:69369824 | G | T | 1 | a0001c0001t0001g0182 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.472-1675G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69369824 | |||||||
| chr9:69369863 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.472-1636A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69369863 | |||||||
| chr9:69369971 | A | C | 255 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(252): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.472-1528A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69369971 | |||||||
| chr9:69370056 | AGTGAAGA others(7): Show |
A | 4 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0003c0006t0001g0209 others(1): Show |
4 | HG02559.hp2 HG03098.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.472-1441_472-1428d others(16): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69370056 | ||||||
| chr9:69370112 | T | G | 1 | a0001c0001t0002g0291 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.472-1387T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69370112 | |||||||
| chr9:69370157 | A | G | 140 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(137): Show |
147 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(144): Show |
intron_variant | MODIFIER | c.472-1342A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69370157 | |||||||
| chr9:69370181 | T | C | 143 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(140): Show |
150 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.472-1318T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69370181 | |||||||
| chr9:69370188 | G | A | 93 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(90): Show |
101 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.472-1311G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69370188 | |||||||
| chr9:69370235 | A | G | 23 | a0001c0001t0001g0013 a0001c0001t0001g0020 a0001c0001t0001g0022 others(20): Show |
24 | HG00423.hp1 HG00621.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.472-1264A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69370235 | |||||||
| chr9:69370253 | T | C | 93 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(90): Show |
101 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.472-1246T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69370253 | |||||||
| chr9:69370424 | C | T | 3 | a0001c0001t0002g0063 a0001c0001t0002g0093 a0001c0001t0002g0193 |
3 | NA18985.hp1 NA19000.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.472-1075C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69370424 | |||||||
| chr9:69370720 | G | A | 141 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(138): Show |
148 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.472-779G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69370720 | |||||||
| chr9:69370795 | TCTTTTAT others(5): Show |
T | 30 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0025 others(27): Show |
32 | HG00099.hp1 HG00642.hp1 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.472-690_472-679del others(12): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr9 | 69370795 | ||||||
| chr9:69370967 | T | C | 1 | a0001c0001t0002g0036 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.472-532T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69370967 | |||||||
| chr9:69371100 | C | G | 255 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(252): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.472-399C>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69371100 | |||||||
| chr9:69371360 | G | C | 27 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0025 others(24): Show |
29 | HG00099.hp1 HG00642.hp1 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.472-139G>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69371360 | |||||||
| chr9:69371399 | T | C | 254 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(251): Show |
273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.472-100T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69371399 | |||||||
| chr9:69371400 | G | A | 113 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0108 others(110): Show |
125 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.472-99G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69371400 | |||||||
| chr9:69371480 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.472-19C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 2/10 | chr9 | 69371480 | |||||||
| chr9:69371672 | C | T | 3 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0210 |
3 | HG02451.hp1 HG02559.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.582+63C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 3/10 | chr9 | 69371672 | |||||||
| chr9:69371689 | A | G | 1 | a0001c0001t0001g0165 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.582+80A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 3/10 | chr9 | 69371689 | |||||||
| chr9:69371872 | A | T | 3 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0210 |
3 | HG02451.hp1 HG02559.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.582+263A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 3/10 | chr9 | 69371872 | |||||||
| chr9:69371889 | A | C | 138 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(135): Show |
145 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.582+280A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 3/10 | chr9 | 69371889 | |||||||
| chr9:69372090 | C | T | 1 | a0001c0001t0003g0207 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.582+481C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 3/10 | chr9 | 69372090 | |||||||
| chr9:69372189 | G | A | 97 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(94): Show |
105 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.582+580G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 3/10 | chr9 | 69372189 | |||||||
| chr9:69372674 | T | G | 6 | a0001c0001t0001g0079 a0001c0001t0001g0137 a0001c0001t0001g0138 others(3): Show |
6 | HG02738.hp2 HG04199.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.582+1065T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 3/10 | chr9 | 69372674 | |||||||
| chr9:69372798 | G | A | 1 | a0001c0001t0002g0122 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.582+1189G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 3/10 | chr9 | 69372798 | |||||||
| chr9:69372849 | CT | C | 117 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0108 others(114): Show |
129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.582+1251delT | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 69372849 | ||||||
| chr9:69373028 | TTA | T | 111 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0188 others(108): Show |
123 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(120): Show |
intron_variant | MODIFIER | c.582+1421_582+1422d others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 69373028 | ||||||
| chr9:69373030 | ATT | A | 136 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(133): Show |
143 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(140): Show |
intron_variant | MODIFIER | c.582+1431_582+1432d others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr9 | 69373030 | ||||||
| chr9:69373332 | G | A | 117 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0108 others(114): Show |
129 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.582+1723G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 3/10 | chr9 | 69373332 | |||||||
| chr9:69373441 | C | T | 1 | a0001c0001t0003g0260 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.582+1832C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 3/10 | chr9 | 69373441 | |||||||
| chr9:69374019 | C | T | 2 | a0001c0001t0001g0102 a0001c0001t0001g0103 |
2 | HG02970.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.583-1717C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 3/10 | chr9 | 69374019 | |||||||
| chr9:69374130 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.583-1606T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 3/10 | chr9 | 69374130 | |||||||
| chr9:69374185 | A | G | 1 | a0003c0008t0001g0275 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.583-1551A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 3/10 | chr9 | 69374185 | |||||||
| chr9:69374250 | T | C | 143 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(140): Show |
150 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.583-1486T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 3/10 | chr9 | 69374250 | |||||||
| chr9:69374274 | A | C | 143 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(140): Show |
150 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.583-1462A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 3/10 | chr9 | 69374274 | |||||||
| chr9:69374521 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.583-1215C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 3/10 | chr9 | 69374521 | |||||||
| chr9:69374684 | A | G | 257 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(254): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.583-1052A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 3/10 | chr9 | 69374684 | |||||||
| chr9:69374947 | C | T | 8 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0188 others(5): Show |
10 | HG01496.hp2 HG01884.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.583-789C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 3/10 | chr9 | 69374947 | |||||||
| chr9:69375376 | G | T | 1 | a0001c0001t0001g0105 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.583-360G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 3/10 | chr9 | 69375376 | |||||||
| chr9:69375729 | C | T | 97 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(94): Show |
105 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(102): Show |
splice_region_variant&intron_variant | LOW | c.583-7C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 3/10 | chr9 | 69375729 | |||||||
| chr9:69375895 | A | G | 2 | a0001c0001t0001g0098 a0001c0001t0001g0118 |
2 | HG02083.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.711+31A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 4/10 | chr9 | 69375895 | |||||||
| chr9:69375906 | G | A | 3 | a0001c0003t0001g0050 a0001c0003t0001g0314 a0001c0003t0001g0315 |
3 | HG01243.hp2 HG01891.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.711+42G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 4/10 | chr9 | 69375906 | |||||||
| chr9:69376018 | A | C | 1 | a0001c0001t0001g0306 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.711+154A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 4/10 | chr9 | 69376018 | |||||||
| chr9:69376112 | C | T | 138 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(135): Show |
145 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(142): Show |
intron_variant | MODIFIER | c.711+248C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 4/10 | chr9 | 69376112 | |||||||
| chr9:69376223 | A | G | 3 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0210 |
3 | HG02451.hp1 HG02559.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.711+359A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 4/10 | chr9 | 69376223 | |||||||
| chr9:69376234 | C | T | 2 | a0001c0001t0001g0022 a0001c0001t0002g0177 |
2 | HG00673.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.711+370C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 4/10 | chr9 | 69376234 | |||||||
| chr9:69376402 | A | G | 4 | a0001c0001t0001g0048 a0001c0001t0001g0307 a0001c0001t0001g0308 others(1): Show |
4 | HG02647.hp1 HG02647.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.711+538A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 4/10 | chr9 | 69376402 | |||||||
| chr9:69376574 | G | A | 2 | a0003c0006t0001g0209 a0005c0005t0001g0221 |
2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.711+710G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 4/10 | chr9 | 69376574 | |||||||
| chr9:69376883 | T | G | 238 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(235): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.712-487T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 4/10 | chr9 | 69376883 | |||||||
| chr9:69376972 | G | A | 112 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0188 others(109): Show |
124 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.712-398G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 4/10 | chr9 | 69376972 | |||||||
| chr9:69377026 | C | T | 2 | a0001c0001t0002g0159 a0001c0001t0002g0162 |
2 | NA18965.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.712-344C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 4/10 | chr9 | 69377026 | |||||||
| chr9:69377049 | C | T | 1 | a0001c0001t0003g0241 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.712-321C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 4/10 | chr9 | 69377049 | |||||||
| chr9:69377283 | C | T | 4 | a0001c0003t0001g0050 a0001c0003t0001g0314 a0001c0003t0001g0315 others(1): Show |
4 | HG01243.hp2 HG01891.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.712-87C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 4/10 | chr9 | 69377283 | |||||||
| chr9:69377487 | T | C | 15 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0188 others(12): Show |
19 | HG01175.hp1 HG01496.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.819+10T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 5/10 | chr9 | 69377487 | |||||||
| chr9:69377527 | T | C | 1 | a0001c0001t0008g0101 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.819+50T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 5/10 | chr9 | 69377527 | |||||||
| chr9:69377772 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.953+28T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69377772 | |||||||
| chr9:69377789 | G | A | 1 | a0001c0001t0001g0157 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.953+45G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69377789 | |||||||
| chr9:69377829 | A | G | 2 | a0003c0006t0001g0209 a0005c0005t0001g0221 |
2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.953+85A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69377829 | |||||||
| chr9:69378008 | CTCTG | C | 11 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0028 others(8): Show |
12 | NA18944.hp2 NA18960.hp1 NA18964.hp1 others(9): Show |
intron_variant | MODIFIER | c.953+268_953+271del others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 69378008 | ||||||
| chr9:69378012 | G | GTC | 99 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(96): Show |
107 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(104): Show |
intron_variant | MODIFIER | c.953+280_953+281dup others(2): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 69378012 | ||||||
| chr9:69378123 | G | C | 139 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(136): Show |
146 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(143): Show |
intron_variant | MODIFIER | c.953+379G>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69378123 | |||||||
| chr9:69378159 | G | C | 1 | a0001c0001t0001g0031 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.953+415G>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69378159 | |||||||
| chr9:69378171 | C | A | 1 | a0001c0001t0001g0208 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.953+427C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69378171 | |||||||
| chr9:69378177 | T | TGA | 9 | a0001c0001t0002g0073 a0001c0001t0002g0135 a0001c0001t0002g0143 others(6): Show |
9 | HG01261.hp1 HG01261.hp2 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.953+437_953+438dup others(2): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 69378177 | ||||||
| chr9:69378222 | G | A | 15 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0188 others(12): Show |
19 | HG01175.hp1 HG01496.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.953+478G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69378222 | |||||||
| chr9:69378489 | G | A | 1 | a0001c0001t0002g0088 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.953+745G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69378489 | |||||||
| chr9:69378510 | G | T | 17 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0188 others(14): Show |
21 | HG01175.hp1 HG01496.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.953+766G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69378510 | |||||||
| chr9:69378756 | C | CA | 25 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0188 others(22): Show |
30 | HG00140.hp1 HG01167.hp2 HG01175.hp1 others(27): Show |
intron_variant | MODIFIER | c.953+1026dupA | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 69378756 | ||||||
| chr9:69378756 | CA | C | 152 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(149): Show |
162 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.953+1026delA | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 69378756 | ||||||
| chr9:69378840 | T | G | 1 | a0005c0005t0001g0221 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.953+1096T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69378840 | |||||||
| chr9:69378941 | G | T | 1 | a0001c0001t0001g0117 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.953+1197G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69378941 | |||||||
| chr9:69379025 | T | TAAAGGAT others(318): Show |
1 | a0001c0001t0001g0313 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.953+1294_953+1295i others(327): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 69379025 | ||||||
| chr9:69379086 | A | G | 141 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(138): Show |
149 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(146): Show |
intron_variant | MODIFIER | c.953+1342A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69379086 | |||||||
| chr9:69379116 | C | T | 1 | a0001c0001t0001g0133 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.953+1372C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69379116 | |||||||
| chr9:69379127 | T | C | 1 | a0001c0001t0004g0237 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.953+1383T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69379127 | |||||||
| chr9:69379424 | G | A | 1 | a0001c0001t0002g0194 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.953+1680G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69379424 | |||||||
| chr9:69379606 | A | G | 258 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(255): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.953+1862A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69379606 | |||||||
| chr9:69379618 | G | A | 1 | a0001c0001t0003g0269 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.953+1874G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69379618 | |||||||
| chr9:69379621 | G | A | 1 | a0001c0001t0001g0108 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.953+1877G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69379621 | |||||||
| chr9:69379707 | T | C | 98 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(95): Show |
106 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.953+1963T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69379707 | |||||||
| chr9:69379776 | A | G | 1 | a0001c0001t0001g0024 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.953+2032A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69379776 | |||||||
| chr9:69379906 | A | G | 1 | a0001c0001t0005g0265 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.953+2162A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69379906 | |||||||
| chr9:69379948 | C | G | 4 | a0001c0001t0001g0313 a0001c0003t0001g0050 a0001c0003t0001g0314 others(1): Show |
4 | HG01243.hp2 HG01891.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.953+2204C>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69379948 | |||||||
| chr9:69379966 | T | C | 98 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(95): Show |
106 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(103): Show |
intron_variant | MODIFIER | c.953+2222T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69379966 | |||||||
| chr9:69380109 | A | T | 1 | a0003c0008t0001g0275 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.953+2365A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69380109 | |||||||
| chr9:69380135 | C | T | 1 | a0001c0001t0001g0017 | 2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.953+2391C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69380135 | |||||||
| chr9:69380448 | C | A | 1 | a0003c0008t0001g0275 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.953+2704C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69380448 | |||||||
| chr9:69380550 | C | T | 1 | a0001c0001t0001g0013 | 2 | HG01123.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.953+2806C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69380550 | |||||||
| chr9:69380571 | A | G | 135 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(132): Show |
142 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.953+2827A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69380571 | |||||||
| chr9:69380699 | T | C | 1 | a0001c0001t0001g0044 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.954-2931T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69380699 | |||||||
| chr9:69380828 | A | G | 2 | a0003c0006t0001g0209 a0005c0005t0001g0221 |
2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.954-2802A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69380828 | |||||||
| chr9:69380918 | T | C | 2 | a0001c0001t0001g0133 a0001c0001t0001g0208 |
2 | HG01884.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.954-2712T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69380918 | |||||||
| chr9:69380958 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.954-2672G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69380958 | |||||||
| chr9:69381154 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.954-2476T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69381154 | |||||||
| chr9:69381454 | A | G | 7 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0206 others(4): Show |
9 | HG01175.hp1 HG02258.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.954-2176A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69381454 | |||||||
| chr9:69381520 | G | A | 1 | a0001c0001t0002g0071 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.954-2110G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69381520 | |||||||
| chr9:69381645 | T | TAAAAAC | 3 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0210 |
3 | HG02451.hp1 HG02559.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.954-1961_954-1956d others(8): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr9 | 69381645 | ||||||
| chr9:69381907 | G | A | 2 | a0001c0001t0002g0155 a0001c0001t0002g0156 |
2 | HG00735.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.954-1723G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69381907 | |||||||
| chr9:69381929 | T | A | 1 | a0001c0001t0002g0203 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.954-1701T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69381929 | |||||||
| chr9:69381999 | G | A | 247 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(244): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.954-1631G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69381999 | |||||||
| chr9:69382051 | G | A | 127 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(124): Show |
134 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(131): Show |
intron_variant | MODIFIER | c.954-1579G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69382051 | |||||||
| chr9:69382187 | T | A | 1 | a0001c0001t0001g0109 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.954-1443T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69382187 | |||||||
| chr9:69382423 | G | T | 15 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0188 others(12): Show |
19 | HG01175.hp1 HG01496.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.954-1207G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69382423 | |||||||
| chr9:69382567 | C | T | 3 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0210 |
3 | HG02451.hp1 HG02559.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.954-1063C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69382567 | |||||||
| chr9:69382902 | A | G | 21 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0108 others(18): Show |
25 | HG01175.hp1 HG01496.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.954-728A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69382902 | |||||||
| chr9:69383165 | A | T | 103 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0210 others(100): Show |
111 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.954-465A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69383165 | |||||||
| chr9:69383411 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.954-219T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69383411 | |||||||
| chr9:69383475 | T | G | 81 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(78): Show |
86 | HG00423.hp2 HG00642.hp2 HG01123.hp2 others(83): Show |
intron_variant | MODIFIER | c.954-155T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69383475 | |||||||
| chr9:69383573 | G | A | 1 | a0001c0001t0001g0007 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.954-57G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 6/10 | chr9 | 69383573 | |||||||
| chr9:69383855 | G | A | 2 | a0003c0006t0001g0209 a0005c0005t0001g0221 |
2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1084-92G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 7/10 | chr9 | 69383855 | |||||||
| chr9:69384048 | A | G | 2 | a0001c0001t0001g0016 a0001c0001t0001g0188 |
3 | HG03130.hp1 NA18906.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1162+23A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | chr9 | 69384048 | |||||||
| chr9:69384049 | T | G | 1 | a0001c0001t0001g0033 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1162+24T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | chr9 | 69384049 | |||||||
| chr9:69384202 | GA | G | 131 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0034 others(128): Show |
143 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.1162+187delA | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 69384202 | ||||||
| chr9:69384299 | T | C | 3 | a0001c0001t0001g0026 a0001c0001t0001g0163 a0006c0007t0001g0030 |
3 | NA18964.hp1 NA18992.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.1162+274T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | chr9 | 69384299 | |||||||
| chr9:69384352 | T | G | 3 | a0001c0003t0001g0050 a0001c0003t0001g0314 a0001c0003t0001g0315 |
3 | HG01243.hp2 HG01891.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1162+327T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | chr9 | 69384352 | |||||||
| chr9:69384598 | A | G | 1 | a0001c0001t0001g0190 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1162+573A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | chr9 | 69384598 | |||||||
| chr9:69384785 | A | C | 2 | a0003c0006t0001g0209 a0005c0005t0001g0221 |
2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1162+760A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | chr9 | 69384785 | |||||||
| chr9:69384848 | GAATT | G | 243 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(240): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.1162+829_1162+832d others(6): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 69384848 | ||||||
| chr9:69384900 | A | AT | 7 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0049 others(4): Show |
10 | HG02109.hp1 HG02717.hp2 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.1163-882dupT | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 69384900 | ||||||
| chr9:69384907 | T | A | 246 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(243): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1162+882T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | chr9 | 69384907 | |||||||
| chr9:69384924 | T | C | 18 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0108 others(15): Show |
22 | HG01175.hp1 HG01496.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.1163-871T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | chr9 | 69384924 | |||||||
| chr9:69384971 | G | A | 100 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(97): Show |
108 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.1163-824G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | chr9 | 69384971 | |||||||
| chr9:69385153 | T | C | 1 | a0001c0001t0001g0079 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1163-642T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | chr9 | 69385153 | |||||||
| chr9:69385248 | T | C | 125 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(122): Show |
132 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(129): Show |
intron_variant | MODIFIER | c.1163-547T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | chr9 | 69385248 | |||||||
| chr9:69385256 | C | G | 2 | a0001c0001t0003g0239 a0001c0001t0003g0269 |
2 | HG00438.hp2 HG00621.hp1 |
intron_variant | MODIFIER | c.1163-539C>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | chr9 | 69385256 | |||||||
| chr9:69385271 | G | A | 243 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(240): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.1163-524G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | chr9 | 69385271 | |||||||
| chr9:69385300 | A | T | 125 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(122): Show |
132 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(129): Show |
intron_variant | MODIFIER | c.1163-495A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | chr9 | 69385300 | |||||||
| chr9:69385429 | T | C | 243 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(240): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.1163-366T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | chr9 | 69385429 | |||||||
| chr9:69385512 | AC | A | 241 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(238): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.1163-279delC | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 69385512 | ||||||
| chr9:69385513 | C | A | 5 | a0001c0001t0001g0164 a0001c0001t0001g0208 a0003c0006t0001g0209 others(2): Show |
5 | HG01884.hp1 HG03098.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1163-282C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | chr9 | 69385513 | |||||||
| chr9:69385541 | T | G | 1 | a0001c0001t0001g0306 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1163-254T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | chr9 | 69385541 | |||||||
| chr9:69385690 | G | T | 1 | a0005c0005t0001g0221 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1163-105G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | chr9 | 69385690 | |||||||
| chr9:69385702 | T | C | 1 | a0001c0001t0003g0274 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1163-93T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | chr9 | 69385702 | |||||||
| chr9:69385758 | C | T | 125 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(122): Show |
132 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(129): Show |
intron_variant | MODIFIER | c.1163-37C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | chr9 | 69385758 | |||||||
| chr9:69385763 | CT | C | 10 | a0001c0001t0001g0228 a0001c0001t0001g0306 a0001c0001t0003g0244 others(7): Show |
10 | HG02040.hp1 HG02155.hp2 HG02897.hp1 others(7): Show |
splice_region_variant&intron_variant | LOW | c.1163-8delT | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 69385763 | ||||||
| chr9:69385763 | CTT | C | 28 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0108 others(25): Show |
33 | HG00280.hp2 HG00735.hp2 HG01106.hp1 others(30): Show |
splice_region_variant&intron_variant | LOW | c.1163-9_1163-8delTT | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 69385763 | ||||||
| chr9:69385763 | CTTT | C | 82 | a0001c0001t0001g0192 a0001c0001t0001g0204 a0001c0001t0002g0003 others(79): Show |
89 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(86): Show |
splice_region_variant&intron_variant | LOW | c.1163-10_1163-8delT others(2): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 69385763 | ||||||
| chr9:69385763 | CTTTT | C | 8 | a0001c0001t0002g0097 a0001c0001t0002g0173 a0001c0001t0002g0179 others(5): Show |
8 | HG01074.hp2 HG01169.hp2 HG01943.hp2 others(5): Show |
splice_region_variant&intron_variant | LOW | c.1163-11_1163-8delT others(3): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 69385763 | ||||||
| chr9:69385764 | T | A | 1 | a0001c0001t0001g0007 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.1163-31T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | chr9 | 69385764 | |||||||
| chr9:69385785 | TTTA | T | 11 | a0001c0001t0001g0028 a0001c0001t0001g0041 a0001c0001t0001g0079 others(8): Show |
11 | HG01167.hp1 HG01943.hp1 HG02451.hp2 others(8): Show |
splice_region_variant&intron_variant | LOW | c.1163-9_1163-7delTT others(1): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | chr9 | 69385785 | |||||||
| chr9:69385786 | TTA | T | 99 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(96): Show |
106 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(103): Show |
splice_region_variant&intron_variant | LOW | c.1163-8_1163-7delTA | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | chr9 | 69385786 | |||||||
| chr9:69385787 | TA | T | 14 | a0001c0001t0001g0031 a0001c0001t0001g0033 a0001c0001t0001g0048 others(11): Show |
14 | HG01515.hp1 HG01516.hp1 HG01891.hp1 others(11): Show |
splice_region_variant&intron_variant | LOW | c.1163-5delA | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr9 | 69385787 | ||||||
| chr9:69385788 | A | T | 1 | a0001c0003t0001g0050 | 1 | HG02723.hp1 | splice_region_variant&intron_variant | LOW | c.1163-7A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 8/10 | chr9 | 69385788 | |||||||
| chr9:69386100 | C | T | 3 | a0001c0001t0001g0154 a0001c0001t0001g0289 a0001c0001t0004g0245 |
3 | HG02698.hp1 HG03239.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.1315+153C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 9/10 | chr9 | 69386100 | |||||||
| chr9:69386148 | G | GT | 4 | a0001c0001t0002g0036 a0001c0003t0001g0050 a0001c0003t0001g0314 others(1): Show |
4 | HG01243.hp2 HG01891.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1315+208dupT | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 69386148 | ||||||
| chr9:69386238 | C | A | 118 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0108 others(115): Show |
130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.1315+291C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 9/10 | chr9 | 69386238 | |||||||
| chr9:69386317 | A | T | 126 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(123): Show |
133 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(130): Show |
intron_variant | MODIFIER | c.1315+370A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 9/10 | chr9 | 69386317 | |||||||
| chr9:69386318 | C | A | 100 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(97): Show |
108 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.1315+371C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 9/10 | chr9 | 69386318 | |||||||
| chr9:69386359 | T | TATCTACT others(1): Show |
3 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0231 |
3 | HG02572.hp1 HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1315+413_1315+414i others(10): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 69386359 | ||||||
| chr9:69386361 | G | T | 3 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0231 |
3 | HG02572.hp1 HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1315+414G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 9/10 | chr9 | 69386361 | |||||||
| chr9:69386362 | A | C | 3 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0231 |
3 | HG02572.hp1 HG02886.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1315+415A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 9/10 | chr9 | 69386362 | |||||||
| chr9:69386420 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1315+473C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 9/10 | chr9 | 69386420 | |||||||
| chr9:69386452 | T | TGA | 247 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(244): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.1315+506_1315+507i others(4): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 69386452 | ||||||
| chr9:69386457 | G | C | 1 | a0001c0001t0001g0298 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1315+510G>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 9/10 | chr9 | 69386457 | |||||||
| chr9:69386507 | T | A | 1 | a0001c0001t0001g0167 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1315+560T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 9/10 | chr9 | 69386507 | |||||||
| chr9:69386601 | T | C | 247 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(244): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.1315+654T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 9/10 | chr9 | 69386601 | |||||||
| chr9:69386750 | A | G | 245 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(242): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1315+803A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 9/10 | chr9 | 69386750 | |||||||
| chr9:69386882 | C | T | 18 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0108 others(15): Show |
22 | HG01175.hp1 HG01496.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.1315+935C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 9/10 | chr9 | 69386882 | |||||||
| chr9:69386905 | A | G | 247 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(244): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.1315+958A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 9/10 | chr9 | 69386905 | |||||||
| chr9:69387076 | C | T | 1 | a0001c0001t0002g0021 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1316-1082C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 9/10 | chr9 | 69387076 | |||||||
| chr9:69387271 | A | G | 245 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(242): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.1316-887A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 9/10 | chr9 | 69387271 | |||||||
| chr9:69387307 | C | T | 3 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0230 |
6 | HG02717.hp2 HG02896.hp1 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1316-851C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 9/10 | chr9 | 69387307 | |||||||
| chr9:69387358 | C | A | 2 | a0001c0001t0003g0257 a0001c0001t0006g0127 |
2 | HG02602.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1316-800C>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 9/10 | chr9 | 69387358 | |||||||
| chr9:69387638 | G | A | 100 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(97): Show |
108 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.1316-520G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 9/10 | chr9 | 69387638 | |||||||
| chr9:69387773 | C | T | 2 | a0001c0001t0002g0080 a0001c0001t0002g0084 |
2 | HG01109.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1316-385C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 9/10 | chr9 | 69387773 | |||||||
| chr9:69387995 | T | TGTTATA | 126 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(123): Show |
133 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(130): Show |
intron_variant | MODIFIER | c.1316-160_1316-159i others(8): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr9 | 69387995 | ||||||
| chr9:69388039 | G | A | 2 | a0001c0001t0001g0154 a0001c0001t0001g0289 |
2 | HG02698.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1316-119G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 9/10 | chr9 | 69388039 | |||||||
| chr9:69388043 | A | C | 18 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0108 others(15): Show |
22 | HG01175.hp1 HG01496.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.1316-115A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 9/10 | chr9 | 69388043 | |||||||
| chr9:69388120 | T | C | 118 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0108 others(115): Show |
130 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.1316-38T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 9/10 | chr9 | 69388120 | |||||||
| chr9:69388512 | G | C | 1 | a0001c0001t0001g0024 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1608+62G>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69388512 | |||||||
| chr9:69388613 | G | A | 126 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(123): Show |
133 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(130): Show |
intron_variant | MODIFIER | c.1608+163G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69388613 | |||||||
| chr9:69388669 | C | T | 8 | a0001c0001t0001g0002 a0001c0001t0001g0040 a0001c0001t0001g0049 others(5): Show |
11 | HG01109.hp2 HG02109.hp1 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.1608+219C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69388669 | |||||||
| chr9:69388807 | G | T | 126 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(123): Show |
133 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(130): Show |
intron_variant | MODIFIER | c.1608+357G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69388807 | |||||||
| chr9:69388873 | GTTCACAT others(2): Show |
G | 4 | a0001c0001t0001g0054 a0001c0001t0001g0215 a0001c0001t0001g0216 others(1): Show |
4 | HG01891.hp2 HG02055.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1608+424_1608+432d others(11): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69388873 | |||||||
| chr9:69388878 | C | T | 23 | a0001c0001t0002g0021 a0001c0001t0002g0073 a0001c0001t0002g0095 others(20): Show |
23 | HG00140.hp2 HG00621.hp2 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.1608+428C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69388878 | |||||||
| chr9:69388886 | T | C | 12 | a0001c0001t0001g0014 a0001c0001t0001g0047 a0001c0001t0001g0054 others(9): Show |
13 | HG01255.hp2 HG01891.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1608+436T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69388886 | |||||||
| chr9:69388975 | C | T | 1 | a0001c0001t0001g0310 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1608+525C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69388975 | |||||||
| chr9:69389001 | A | G | 1 | a0007c0009t0001g0107 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1608+551A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69389001 | |||||||
| chr9:69389077 | C | G | 3 | a0001c0001t0004g0245 a0001c0001t0004g0247 a0001c0001t0004g0256 |
3 | HG02040.hp2 NA18960.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.1608+627C>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69389077 | |||||||
| chr9:69389105 | A | T | 126 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(123): Show |
133 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(130): Show |
intron_variant | MODIFIER | c.1608+655A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69389105 | |||||||
| chr9:69389113 | T | C | 2 | a0003c0006t0001g0209 a0005c0005t0001g0221 |
2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1608+663T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69389113 | |||||||
| chr9:69389130 | C | T | 51 | a0001c0001t0002g0003 a0001c0001t0002g0008 a0001c0001t0002g0009 others(48): Show |
56 | HG00280.hp2 HG00438.hp1 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.1608+680C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69389130 | |||||||
| chr9:69389201 | T | C | 246 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(243): Show |
265 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(262): Show |
intron_variant | MODIFIER | c.1608+751T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69389201 | |||||||
| chr9:69389233 | T | A | 249 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(246): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.1608+783T>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69389233 | |||||||
| chr9:69389359 | C | T | 126 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(123): Show |
133 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(130): Show |
intron_variant | MODIFIER | c.1608+909C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69389359 | |||||||
| chr9:69389466 | T | C | 1 | a0001c0001t0001g0313 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1608+1016T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69389466 | |||||||
| chr9:69389551 | G | C | 18 | a0001c0001t0001g0012 a0001c0001t0001g0025 a0001c0001t0001g0031 others(15): Show |
19 | HG00099.hp1 HG00642.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.1608+1101G>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69389551 | |||||||
| chr9:69389573 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1608+1123C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69389573 | |||||||
| chr9:69389889 | G | GT | 14 | a0001c0001t0001g0034 a0001c0001t0001g0041 a0001c0001t0001g0042 others(11): Show |
14 | HG01106.hp2 HG01167.hp1 HG01361.hp1 others(11): Show |
intron_variant | MODIFIER | c.1608+1440dupT | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 69389889 | ||||||
| chr9:69390142 | T | TGAACTTT others(9): Show |
1 | a0001c0001t0002g0146 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1609-1458_1609-144 others(20): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 69390142 | ||||||
| chr9:69390160 | C | T | 8 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0188 others(5): Show |
10 | HG01496.hp2 HG01884.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1609-1441C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69390160 | |||||||
| chr9:69390199 | T | C | 1 | a0003c0008t0001g0275 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1609-1402T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69390199 | |||||||
| chr9:69390672 | G | A | 2 | a0001c0001t0002g0219 a0001c0001t0002g0309 |
2 | HG02622.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1609-929G>A | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69390672 | |||||||
| chr9:69390683 | A | G | 126 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(123): Show |
133 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(130): Show |
intron_variant | MODIFIER | c.1609-918A>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69390683 | |||||||
| chr9:69390797 | G | T | 18 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0108 others(15): Show |
22 | HG01175.hp1 HG01496.hp2 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.1609-804G>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69390797 | |||||||
| chr9:69390854 | T | C | 7 | a0001c0001t0001g0048 a0001c0001t0001g0212 a0001c0001t0001g0213 others(4): Show |
7 | HG02451.hp2 HG02647.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1609-747T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69390854 | |||||||
| chr9:69390946 | ATTT | A | 238 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(235): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.1609-639_1609-637d others(5): Show |
ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 69390946 | ||||||
| chr9:69391032 | A | C | 243 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(240): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.1609-569A>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69391032 | |||||||
| chr9:69391131 | G | C | 1 | a0001c0001t0002g0003 | 3 | HG01952.hp2 HG02004.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.1609-470G>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69391131 | |||||||
| chr9:69391224 | T | C | 247 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(244): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.1609-377T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69391224 | |||||||
| chr9:69391260 | C | T | 46 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0016 others(43): Show |
52 | HG00099.hp1 HG00642.hp1 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.1609-341C>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69391260 | |||||||
| chr9:69391357 | A | T | 12 | a0001c0001t0001g0034 a0001c0001t0001g0041 a0001c0001t0001g0042 others(9): Show |
12 | HG01106.hp2 HG01167.hp1 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.1609-244A>T | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69391357 | |||||||
| chr9:69391360 | T | C | 2 | a0001c0001t0001g0126 a0001c0001t0001g0147 |
2 | NA19065.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1609-241T>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69391360 | |||||||
| chr9:69391466 | T | G | 4 | a0001c0001t0001g0313 a0001c0003t0001g0050 a0001c0003t0001g0314 others(1): Show |
4 | HG01243.hp2 HG01891.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1609-135T>G | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69391466 | |||||||
| chr9:69391477 | C | CT | 125 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(122): Show |
136 | HG00099.hp1 HG00423.hp2 HG00642.hp1 others(133): Show |
intron_variant | MODIFIER | c.1609-114dupT | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr9 | 69391477 | ||||||
| chr9:69391539 | G | C | 2 | a0003c0006t0001g0209 a0005c0005t0001g0221 |
2 | HG03098.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1609-62G>C | ENTREP1 | ENSG00000135063.20 | transcript | ENST00000303068.14 | protein_coding | 10/10 | chr9 | 69391539 |