Tag | Content |
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EnhancerAtlas ID | HS172-08936 |
Organism | Homo sapiens |
Tissue/cell | SGBS_adipocyte |
Coordinate | chr6:2865880-2867290 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HNF1A | MA0046.2 | chr6:2866596-2866611 | AATTAATCAATAACA | + | 6.08 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_28080 | chr6:2865882-2867415 | Fetal_Intestine | SE_28996 | chr6:2865858-2867021 | Fetal_Intestine_Large | SE_38162 | chr6:2865399-2867166 | HUVEC |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr6 | 2866705 | 2867019 | chr6 | 2866631 | 2866750 |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I002864 | chr6 | 2865041 | 2867315 |
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Enhancer Sequence | CGGGCCAGAA AGGAAACTTT TTATCTGAGG AATATGAACC CCTTTAAGTC ATCAGGTCCA 60 GACAGGCATT GAAATGTGAC AGTAGTCACA TCTCACTCAC TGCTTGAGCT ATGTATGTAT 120 GTAATCTGCC TGCTATGTGG ACTCTTGACC CAATGCCACC ACCAATAGCT ATAAATTAAC 180 CTAACGACGG CATATGCTGG ACAACATAAC TTATACCCTA TAGTTCAACT ATAGCCAATC 240 ACTAATCAAT GTTATTTCTG TAAACCAATG AGAATTCTTA ACCAACAATG TTGGTAATTG 300 CCTCCTCTCC TGATTCATCC TTTGTTCTCT GGGCACTTCC CAAGACAACT TGGAAGTGTT 360 TCCCAAGCAG CTGTTCTCAA CCCTGACCCA AATAAACTCT CATATTAATT TTGCCTCAGC 420 TTCTTCCTGT CAGTCGACAA CTCCTAACTA GCTATTTTCA TCCCTTTTCA AGCTTCCTAA 480 GAGGTTACTT TCATTTAGGT TCGTGATATA ATAAAAAATA TATCTGGTGT TTATCCCCAG 540 TTCCCGGCAC AGAGCTCCTA AAACCCTTGG AATTTCCTGA GTAATGCGAG TGTGTTTTGC 600 TATTCAAAAT GAGCCGCTTT AGCTACACCT GAGCTTATGC TGATGAGGCG GCTCTTGGTG 660 ATCCCCTGGG GAGGGAAGAA GGGCTGGGAA TTGAGTTCAG CCACCAATGG CCAGTGAATT 720 AATCAATAAC ACCTATGTAA TGGAACCTCC ATAAAAATCA AAAAGACCAG GTTGAGGGAG 780 CATGTGGGTT AATGAACAGA CAGGTGCTGA GAGGGTGGAG TGTCTAGAGA GGGAATGGAA 840 GCTCTCTGCA CGCACCCCCG ACCCCCCTTA ACTTGCTCTC TGCATCTCTT CCACTGGTTG 900 TTTCTGCCTT TATAATAAAC TGGTGATAAT AATAAAGTGC TTTCTTGAGT TCTGTGAGTC 960 ATTCTAGTAA ATTATTAAGC CTGAGGGAGG TTATGGGAAT CCCCAAATTT GTACTTGGCC 1020 GGGCAGCAGT GTGAAGAGCC TGGGCACCCC ATTTGTGACA GGTGTCTGAA GAGGGGGTAG 1080 TCTTGGGGGC TGAGCCCTCT AACTGGACGT TAAGTACTGT CAGAATTGAA TTGAATTGTT 1140 GGACACCCAG TTGGTGTCAA AGAACTGATT GGTGTGAGGA AAAAAACCTC TTAAAGGTCT 1200 TTACTCCCAC TTACTGGTAG TGTTGCTAAG TTCATAATGC CTTTTTCTTA TCACTCATGG 1260 CTTCATTAGG CTTGACTTAC TGGTCTTACT TGCCTAGATT GGTCTTGAAC TCCTGGGCTC 1320 AAGCCATCTT CCTGCCTTGG CCTCCCAAAG TGCTGGGATT GCGGGTGTAA GCTACCATGC 1380 CCAGCCTCAG TGTTTTTAAT ACACACAATA 1410
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