Tag | Content |
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EnhancerAtlas ID | HS092-00347 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr1:11760840-11762270 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EBF1 | MA0154.3 | chr1:11760841-11760855 | ATTCCCATGGGACC | + | 6.73 | ZNF263 | MA0528.1 | chr1:11762037-11762058 | TCTTCCCCCAGCCCCTCCTCC | - | 7.46 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_68783 | chr1:11760506-11762602 | H9 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 11761755 | 11762049 | chr1 | 11761835 | 11762000 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I011700 | chr1 | 11760585 | 11762161 |
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Enhancer Sequence | GATTCCCATG GGACCCGCCT TGGCCAGCCA TGACTTGCTC CCCCCAACCC ACTATGCAAC 60 AGGAAGGCCG ATCAGCGCCG CAGGAATGCT GGTCCGACAG CTGTCCCGAG AAGCCTGGTG 120 GCCGAGCTCC ACAGTTGTCC CTCAGGCAGG CGGGGCAGGA TCCCCCGAGT CTCCTGGCCC 180 CCAAATGCAA GGCTGTTGTG GGGGGAGGGG CTCAGGAATC AAAGCTGACT CCAGGCTCGA 240 TTCATCGCCT TCGTTTGCAT ACGGCGATGC TGACAGCTCT CCAACTCTCC CCTAGGATGG 300 GGGACAAGAT GGGGGCTTGA GATAAGCCCC TTCCCCTCCC TGGTTAGTGT CTGTTTCCCA 360 GCTGCTGGTG GCTCCTGGGC CCTGACTGCA CTCAAGGAGG AAGATGCCTC TCACCGCGAG 420 GATGAGCGGC TGCGTGAGGG AGGCAGGTGG CCCCACGGGC AATGGGGACA AGAACCATGT 480 CCTGTGTGCA CCGGGTGCCA GGAGAACCCC GGCCTTGAGA TGGGCTTTGC CACTTGCCAG 540 TTGTGCCATC TTGGATTTGT GGCTTACAAC CCCCTCGCCC CCAGAGCCTC GGTTTCGTCA 600 TTTTAAAACC ATGGAAAAGT CTCCCTGATG TACAGCGCAG TTGAGAGGAA AAATGAGATG 660 TGAATGAAAG AAAGAAACGC GGAAAGGCCT GGGCTTCACA GCTGCTCGGG GACAGCAGCT 720 CCTACAATTA CGATTGCTTT TGTTTTAATT TGTTTTGTTT TTAATGATTC GCTATCAGAC 780 CTCAGTTGTG AAAGGGGCCG GCTGTGGGTT GTGGATGTTC CTGCCATCCC TCAGCAACTC 840 TGGTCCAGGG CTACTCCGGG CTGCTGACTG TGCTCGGCTG GGAGGAGCAG ACCCTGGGCC 900 AGAAGCGCAG GCTTTGTGAG CAACCCGGGC CGGGCAGAAC CGCCCCGGGC TGCGGGGAGG 960 CGGAGGGGGC TGCCTCCTCC TTCTGCCTGG TTGCCTGGTG CTTTGTGACA CAGCCTCCAA 1020 CTGGCTTTCA GAGTGACAGA AATGGATTGG AGCCCTTGGT CGCTGTGGAT CCTTGGCACG 1080 ACTTCTGTAG CAGCCCACGT TTCCTCGGGG GCTCCCTGCC AGGCTGGCAT CTCAGTTGCT 1140 GGGCTGTGCC AAGAGCTGTG TACAAATCCT TGGGCTTGGA GAGAGGGGCC CGTGTAGTCT 1200 TCCCCCAGCC CCTCCTCCAG CTGACACACA CTGTTGCACA CAGTCCACAC CCATGCTCAC 1260 AAACATGCTT GTGCACACAC ATACGCTCAC ACATGCTCAC AACACACATG CTCTCACACA 1320 CGCGAGTTCA CACACACATG CTCACACTCA TACGTACACG CCCACACACA TTCACGCTCA 1380 CACATGCTGA CAACACACAT GCTCACACAT ACACACATGC TCACACACAC 1430
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