Tag | Content |
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EnhancerAtlas ID | HS076-02037 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr1:41313620-41315010 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SREBF2 | MA0596.1 | chr1:41314761-41314771 | ATGGGGTGAT | + | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_34647 | chr1:41314331-41316770 | HeLa |
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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 |
GH01I040848 | chr1 | 41314321 | 41314510 |
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Enhancer Sequence | TTTCTTCATG GCATTATCAC GGCAAGACCT GGTTAAGACA GCTAGTAAGG TGGATTTTAC 60 TGGAAGCAAT GTCATAGAAG ACTTACATTA TACATCACAG AGGATTTTAA AAATCCTCCT 120 TCAACATCTT TGTTTTTGTC CCAAATGGCT TCTCTGGGCA TGAGGCATAT CCTCTTCTCT 180 TTCTTTTTTT CCCAAACAGG CTCTAAAATG AGTGGGAGAT GTGAAGGATT TCCTGGAAGA 240 GGTGGGAAGA CTGCTGTCAA ACAGATACCC TGGCAGAAGG ATCTGAGGCC TGAGACCCAA 300 GCTGCCCCGC CTGCCCAGAA CTCGGATGGG GTCTGCCCTT ACTTCCCACT CGCCCCTGCC 360 AGACTTCCCC TAAATCCTCT CCTGGACCCC ACAATCTTGC TCCTTCCCCT GGTGTGACTT 420 CAGCTCCTGG AGGACAAGAA ACACATCTGT GGCCAGTTCA CGGTGGCCCA CACCTTTAAA 480 CCTCAACACT TTGGGAGGCC AAGGAGGGTG AATCACTTGA TACCAGGAGT TCAAGGTTGT 540 AGTGAGCTAT GATCGCGCCA CTGCACTCCA GCCTAGGTGA CAGAGTGAGA CCCTGTCTCT 600 AAAAAAGAAA AGATATGCAT CTGCTGGGGT CATCACTCTC CCCAAAGCAA GGCTGGGCAC 660 ACAGGTGATT CGTATATGCT GGCTGGAAGG GAGGGAAGCA GAGCCACCTG GGATTGATCA 720 TCTCCCAGTG AGAATACACC CAGTCCCTGT TGTGTGTCCC CACGGCCACA AGGCGTCAGT 780 AAAGACCTTG GCTTGGAGTT GTCTGGAGCC AGGAAAACAG ACTGGACTTT GAGGGCAGGA 840 CACCTCACCT GAAGGTGCTT TAGTTAGGTT CAGCACATCT GAAAGAGAGA GAGAGAAATA 900 GGGGTGGTAG AACTGAGCAG TTGACAGAAG GGGACTCCAG GACTTGTCTC AGAGAGTAAG 960 GGGCTGTGTT CTCTGCCCTT CATTCACTTA TTCTACAATT GTTTGTTCAT TTCTAGTACA 1020 TGCCAAGCAC TATTTTAGGT GCCAAGGTCC TAGCAGCTCA CTCACAAAGT CCCTGCTCAC 1080 ATAGAGTAGA TAGTAGATTA CTGTCTAGAC AGAAAACAAA CAAAAAAAAC ACGATAATTT 1140 CATGGGGTGA TAAGTGCCGT GAAGAAAATA AAATGGAAAT GGAATAGTGA CTGTGTTGCA 1200 GGGGGCGTCT TTCAGAGAGA TGGTCAGGGA AGCTCAAGGG GAATCCAAAG CCTTCATAAA 1260 AAGTCAGAGC TGCCAAGGCT CCCAAGGGAC CACTGGTCCC ATAGCCTCAT TTTGCAGCTG 1320 GGAAAACTGA GGCCTAGTAA GCCAAGGCAG AGCCCAGAGC TGAGCCCGAG TCTCTCGACC 1380 TCCAGATGGC 1390
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