Tag | Content |
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EnhancerAtlas ID | HS076-01364 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr1:27658590-27660440 |
Target genes | Number: 19 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SREBF2 | MA0596.1 | chr1:27660117-27660127 | ATCACCCCAT | - | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_34417 | chr1:27658614-27659484 | HCT-116 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I027332 | chr1 | 27659061 | 27659922 |
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Enhancer Sequence | AAGTAAGTGA TGAACACCCA TGTGACTGGC TCTAGAGGCA GGTCGCTCCT GCCGGGGCGG 60 GCCAGGCCTT CTGGGGCACA GGAGGGGCCA GCACCCTGAG AATAGAGTAT TTGGGGTCGG 120 GGGAGAGGTC AGCCAGGGTC CACCAGAGCA TGGCAACCCC ATACAGAGTG TGTACCGCAC 180 CAGCCCCTGG CTAGGGCCTT TACCTGTAGA CCATCTGGGC CTTGCCACAG CTCTTCAGGT 240 TTGTATTTTC AACTCCATGG CAAGGGTGAG GAAAGGGAAG GGACTTGGTC AAGGTCACAC 300 AGGAAGTGGC AGAGCTGGGA CCCACACCCA GATCTGTCTC CCTCTAGACT CACTCTCCTG 360 CCCTTTGGGA ACAAATGAGG CATGGAAGGT AGAAGAGAGG CATTGTTTGG AGCTCTGCTG 420 GAAAGTTCTG GTTGGAGAGA ATAAAAACCG TTCAACCTTC TGGGAGCTAT TGCTGGTTTG 480 GTTTGGGACA TTTGGTCTTC ATCTTTGCAG TCTCGGGTGC CCACCTCAGC TGTGGGCCTG 540 GTGAGAGTGC CTCAGTCATC AGTGTCCTCA GGTGACCTGT TGCCCAAGGC TGCACTGGGA 600 GGAGAGACTG GGCCGAGGAG GAGTTGGTGT CCCACACAGC TGAGATGGCC TGGAGCAGGG 660 CTTCCTGCTG CCCTCTCTGG CTTCCTCCGG CAGGCAGCAG TGTAGTCCAG GAGTCTCTGG 720 GCCACCAGGT GTTCGCTGCC AGACTGCTCT TCAAGGACAG TTTTAAGGGC ATCATTTTCC 780 AAGCAGTAGC CCCTAAGCGG CCCCAGTCCA GGCCATGGTC TCTAGACTCC TCCACCAAGC 840 CATTCCCCTA CACAACAGCC AGGGGGCGCC CTGACCTCCC AGCTCTCCTT GGCCTGAGAC 900 CCACCGGGCA CTCTGGTGCT TGGAACAGCA ATTCTCACCC ACCTTGAGGT TTATGGGCTT 960 TAGCACCATC AGCTTCCCTG CCACTCACCC TGGCAAGCTG CCTGGGAGAC TAGGGGAGAG 1020 TGCTTGCTGC TGGGTAAACT CCCCGCGTGA TGTGGCCTCA CCTGCATCTC CAGCCTTAGC 1080 TGCCAGCATT CCATCACCGT GTTTCTCTTT CTGCATCCTC CAGGAGGGCT CAGTCACTTC 1140 AGTTATGGGA CATGCTGCAC AGTTTTATGC CTGTCACTTA GCTTAAGCTG TTCCCTCAGC 1200 CTGGAATGCC CACCTCTTCT TTCTATGCCT GCCTAACCCT CTTCCTTCAT ACTGGACCCA 1260 GGTGTCACCT CCAGGAAGCC TTCTCACACC CCATCTTAGT CCGTTCTGGC TGCCATAACA 1320 AAATCTCATC AATTGGGTAT CTTAGAAACA ACAGAAATGT ATTTCTCACA GTTCCGAAGA 1380 CTGGACAGTC CTGGGTGCGG GTGCTGGTAG AGTCAGTGTC TGGTGAGGGC CTGAGGTGCC 1440 TTTCCACTGT GTCCCCACGT GGTGGAGGGG TGAGGGGTCT CCCTCAGGGC TCTTTTATAA 1500 GGACACGGAT CCCATTCATG AGAGCTAATC ACCCCATGGC CTAATCACCT CCCAAAGGCC 1560 CCACCTCCTC ATACCATCAC CTTGAGGGTT AAGATTTCAA CATATGAACT TGGGGACACA 1620 GACTTTCAGA GCATAGCACC CCCAATTTCA TTCCATATCC CCCCAGGATC CCCCATGGCA 1680 CCAGCCACCT CACCCTGTGT CACAGTTGAC TGCCACATAA CACTTGCCCC AGATCTGGCT 1740 TACTGTACAT CTCAGCACCC AGCTCAGGCC CGGGCACAGG GCAGGCCTCA GAGGACGTGC 1800 GTAGAGCTGA GGGCACAAAG GAGCCAAGCA AGTGTCCAGA GCCCTTCTCT 1850
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