Tag | Content |
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EnhancerAtlas ID | HS076-01666 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr1:33152670-33154030 |
Target genes | Number: 13 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr1:33153654-33153669 | TGAACTCCTGACCTC | - | 6.22 | Nr2f6(var.2) | MA0728.1 | chr1:33153055-33153070 | GAGGTCAAGAGATCA | + | 7.23 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 33153217 | 33153408 | chr1 | 33153789 | 33153839 |
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Enhancer Sequence | ATAAAACTGG CCAGGCACAG TGGCTCATGC CTGTAATCTC AGCATTTTGG GAGGTTGAGG 60 CGGGTGGATC ATCTGAGGTC AGGAGTTCGA GACCAGCCTG GCCAACATGG TGAAACCCAG 120 CCTCTACTAA AAATACAAAA AATTAGCCGG GCGTGGTGGC AGGTGCCTGT AATCTCAGCT 180 ACTCGGGAGG CTGAGGCAGG AGAATTGCTT GAACCTGGGA GGCGGAGGTT GCAATGAGCT 240 GAGATCGTGC CATTGCACTC CAGCCTGGGG GACAAGAGCG AGACTTCATC TCAAAAAAAA 300 AAAAAAACCA TAAAAGTGTT TAGTAGGCCA GGCACGGTGG TTCACGCCTG TAATCCCAAC 360 ACATTGGGAG GCCAAGGTGG ATCACGAGGT CAAGAGATCA AAACCATCCC GGCCAACGTG 420 GTGAAACCCC ATCTCTACTA AAAATACAAA AATTAGTTGG GCATGGTGGC ACACGCCTGT 480 AGTCCCAACT GCTCAGGAGG CTGAGGCAGG AGAATTGACT TGAACCCGGG AGGCAAAGGT 540 TACAGTGAGC CAAGATTGCG CCACTGCACT CCAGCCTGGA GACAGAGCGA GGCTCCGTCT 600 CAAAAAAAAA AAGAAAAAAA TGTTTAGTCC CAGCTGGATC TAGTTAACAT TCCTTGTGAT 660 TCCACCACTA AGCTCACTTC CCAAAACATG TCTTTTTGTG TTTCCATGCT TTTGTATGAG 720 CTGTTCCCTC TGTCTGGAAG ACCTCTCCCT TACCTGCCCA GTGAATTATT ATTATTATTA 780 TTATTATTAT TATTTTTTGA GATGGAGTCT TGCTCTGTCG CTCAGGCTGG AGTGCGCTGG 840 CACCATCTTG GCTCACTGCA ACCTCCAGCT CCTGGGTTCA AGTGATTCTC CTGTCTCAGC 900 CTCCCAAGTA GCTGGGACTA CAGGCGGCCT AATTTTTGTA TTTTTAGTAG AGACGGGGTT 960 TCACCATATT GGTCAGGTTG GTCTTGAACT CCTGACCTCA GGTGATCCAC CTGCCTCGGC 1020 CTCCCAAAGT GCTGGGATTA CAGGTGTGAG CCACTGCTCC TGGCATGAAT TCATTCTTAA 1080 GGTTCAGCTC CAGCATCTTG AAGAGCCTGA GTATGGACTC AAGCTAGATT GTTCAGGAGT 1140 TACATCCTCG CTCCATCACT CTCAAGCTGC CTAACCCTGG GCAAATCACT GCTCTGCCTT 1200 ACCTCTGTCT TCTTATTTTT CAAATGCCTT ATACCTAACT CATAGAGATG TAAGGACTAA 1260 AGGAATTATT TTGTGTAAAG AACTTCAAGT ACATACTAGC TATTGTTGAT CTATGAAATG 1320 TCCCCTCTTT TGCCCAGGCT GGGGTAGTCA TGCCTGTTTT 1360
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