Tag | Content |
---|
EnhancerAtlas ID | HS147-12813 |
Organism | Homo sapiens |
Tissue/cell | NHEK |
Coordinate | chr13:50379840-50381250 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EN2 | MA0642.1 | chr13:50380729-50380739 | GCTAATTGGG | - | 6.02 | IRF1 | MA0050.2 | chr13:50380844-50380865 | AAAAAAAAAAAGAAAGAAAAA | - | 6.59 | Nr2f6(var.2) | MA0728.1 | chr13:50380624-50380639 | GAGGTCAGGAGTTCA | + | 6.22 | ZNF263 | MA0528.1 | chr13:50380481-50380502 | TCCCCCTGCTCCCCCTGCCCC | - | 7.13 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH13I049806 | chr13 | 50380321 | 50380470 |
|
Enhancer Sequence | TTTTGTTCCT TCTCTAGGAG AAAAACAACT TGAATTGCCG TGGAGAAACC TTAGACTCTG 60 GTAGCTGTTT AAACTCATAA ATTGTCCCAG AAGATTTCTA ATTCCCAAAC CATCAAACCG 120 TCCCTCACAT TTAATTCAGG AACACGTTCG GCAAATGTTT GTGTTTGTAC ACGAAGTCTC 180 TCAGCGATCT AAGTTTGACT TGGAGAGCAA TGAGGCAAAA TTCCCATCTT CCTACCCCAC 240 TTTAACTTGG AGATAAAACC TACTCAAGTT ATACATACCA GTACTTTCAA AAGCCCTTCA 300 ACTTATCTAA GCATCTCTCT AGCCCCACAC TCTTCCCCTT TTCATCTCAA TATGGAACTT 360 TGTGTAAAAG CATCCAAAGC TGAAAGACAG AGCTGTGGAT TATGTGCCTG CAGAGCTTAA 420 TCCCTGCCAA TCTCACAGAG GGGCACCTTA CAGTTAGGAA TGTGTGCAAC CAGAGCCAGG 480 ATAAGTTCAG ACTCATCAAA CGATTGTTTT ATCAACCACA ATTACACAAT ACAACTAAAA 540 CAAAAATAAC CTTGAGAAGC AATGAGTAAC CTACAACTCA TCATGATATG AAGTTCAAAT 600 AATTGCTAAT GCCACACTTG GACAGTCAAG TTTTTCAAGC TTCCCCCTGC TCCCCCTGCC 660 CCCAAAAATA GACAAGATTA TGCAATGAGA AGATAAAGGA GATAGAAGAC AATGCTCCAG 720 GGCCAGGCGT GGTGGCTCAC ACCTGTAATC CCAGCACTTA GGGAGGCAGA GGCAGTTGGA 780 TCACGAGGTC AGGAGTTCAA GACCAGCCTG GCCAAGATGG TGAAAGCCTG TCTCTACTAA 840 AAATAAAAAA AAAATTAGCC AGGCATGGTG GTGGGCGCCT GTAATCCCAG CTAATTGGGA 900 GGCTGAGACA GAGAATTGCT TGAACCCGGG AGGTAGAGGT TGCAGTGAGC TGAGATCGCA 960 CTACTGCACT CCAGCGTGGG CGGCAGAGTA AGACTCCATC TCAAAAAAAA AAAAAGAAAG 1020 AAAAAAAGAA ATCAATGCTT CATCCTTATT ATTCAAAGCT AGATTGCAAA ATATACTAAT 1080 CTAAGAAATC TTTAGTTTTT CTCCTCCCTA TAGCTTTAGT TGAGCTTTAT GTAGGGTTTC 1140 TTTCTTTTAT ACAAAGAAGC ACAAATATCT CTCTTGGAAG ACTACAGCTC AGTAACTGAT 1200 GGGAACATGC AAGGGCAGGT GAAAACACAC AGGACAACAA TATAAGAATG TTTTCTGATG 1260 CACAATATGA GCAAATACGG TTCTAGTCAC TCTCTTTCTG CTAAGCAAAA AATCTGACCC 1320 AAGCCAACCC CTGCTATCTA AAATGGTCAT TTTTGAAAAA TGTCTTTATT AGTAATCATT 1380 TGTTTTCTGT AGAAATGGGA ATAATAATAG 1410
|