Tag | Content |
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EnhancerAtlas ID | HS072-00695 |
Organism | Homo sapiens |
Tissue/cell | GM19193 |
Coordinate | chr16:11299450-11301690 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Hnf4a | MA0114.3 | chr16:11299763-11299779 | GGCGCACTTTGACCCC | - | 6.15 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_61758 | chr16:11291618-11352989 | Toledo |
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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 |
GH16I011205 | chr16 | 11299538 | 11300909 |
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Enhancer Sequence | GACTGAGGCC CATGAGGTCC AGGGCTCCAG GGGCACCTGG CTCTGATGAG GCTAAACTCA 60 AGCTTGCCCC TTCTCTGCAC CCCAAACTCC TGGTTTCTGG ACCCAGCTCA GCACGTGGAG 120 CCTTGGGTCA CACCCAGCAC CCAGTGAACG GCATCCGAGA AACACTCTTC CTGCTGAAAG 180 CCTGGCTTTC TGGAAGGGAG CTGGGGGAAA CTGGGAGAGG ATGGAGGGGG GCCAGGTAGC 240 AGATAGCCAC ACTCCTTGCG GCAGGAAGTT CTACACATCA TTTCTGGGAA CCAGGATAGC 300 TTGGCAGTAA CTCGGCGCAC TTTGACCCCA ATAGAGCACC CAGCTGTCAC TGTTGACAGC 360 CCCCCTTCCT TCCCAGGGGA TGCTGCTGAG CTGCTTGGAG CCTTCATGTC GGACATCCAG 420 GTGGGCCTGG GGACAGCCTT GGAGCTCCCG GGCCACCTGT CTGGCCACCA CCGGATGGAG 480 TGCCCAGATG GGGCTTCTGC CAGCTGTCCA GGAGGCAGCC CAGGCTGGGA CATCCAAGCT 540 GAGCCCTGAG CTGGCCTGGC CTGGCCCAGC CCGCACTGAT GAGGCAATGT GAGTCCTGTT 600 TCCTGTTACT GTGGCTATGC AAATGGGGGG AAATCAGGGC CTCTCCTGGG GTAGGCTTCC 660 CGGAATGATG GCATTGATTG TCCCAAGAAA CCTGGCCCCA GTGGGGCTGC TATGGGAGGG 720 CAGTTGTCAA CGGCTAAGAT CCCTTTCCTG GTGCATCTCT CCTGCGTGCT GGGCTACATA 780 CTGCTGGGAA AAGCTTCTTC AGCCCAGACC TAGGTCATCA CTGCATGTCC ACTCCCGGAC 840 CCACTGCCCA TGAGAGCTGG GCTGTGGCTT CCACTTCTTG TCACTGCATC CCCAGCTCCT 900 GGTACATCGT GGGAGTGGGG CGGACAGGAC CAGGAAGTGG GTGGCCTCAA TGGCTCTCAG 960 CCCCTGGCCT GGAGATCACC ACACCCTTCT CTTTACACAT AAGGAAACTG AGGACACCAG 1020 ACTGGGCCAG GGACTTGCCC ACGTCTCTCT GCCTCGCCCA GACATGCCGC AGCAGCAGTG 1080 GCAAACTTCT GCTTGCCCCC AGAAGCCAGC TGAGTCTTCC AGGTCAAGTC CCTCTCCTGC 1140 TCCCCACAGT CCTGTCACAC CCCTGGCTGC TCCCCAGGTC AGCCTCTCCT AGGGGTCGTT 1200 CTCAGCTCAC ATCTGACCAT GCCACTCCCC TGCCCTGGCA CCTAGCCCTC ACTCAAAGCC 1260 AGGCCTCATA AGCCAGCAGT GATTGGGTAC CTTCCACCCT GAGTGGTCTC ATCTCTTGAC 1320 AACTCTGCCT CACACATTAC CCCTGGTGAT GCCAGAACTC CTTGGAATTC CCCCTTGCAC 1380 CTCTGTGGCT TTGCAAAGCT GTTGCCTCAG CCTGAGAGGA TGCCTCCAAC ACCTTTCTTT 1440 CTCTCTTTAT TTTTTTTTTC TGAGACCGAG TCTCACTCTG TCACCCAGGC TGGAGTGCAG 1500 TGGCACGATC TCAGCTCACT GCAGCCTCTG CCTCCTGGGT TCAAGCAATT CTTGTGCCTC 1560 AGCGTCCCAA GTAGCTGGGA TTACAGGCAT GTACACCACG CTCAGCTAAT TTTTGTATTT 1620 TTAGTAGAGA TGGGGTCTCG CCATGTTGGC CAGGTTGGTC TCGAACTCCT GACCTTGTGA 1680 TCCGCCCACC TTGGCCTCCC AGACTGCTAG GATTACAGTT GTGAGCCACT GCACAAGGCC 1740 TAACACCTTT GTTTCTATAA TTCCTATTTT TTCTCCAACA CTCAGCAGTG TCACCTCCAG 1800 GAAGCCTTCC CAGATGCCCG CAGCTGGACC AGGTGCCTCC TCTAGGCTCC CTGCATGTCC 1860 CCATCACAGC ATGTATCACA CTGGGCTGTC CTCATGATTT TAGTGCCTGT CTCCTCCACT 1920 GCATGGGAGA CTCATCACGG AAGCTTGCAC AGAGAAGGAG GCAGAGATGT GGAAATGCCC 1980 ATGGGTGCAA GACACACGCA GGAAGTCGAA CCTGTGGACT TGGGGTGCAG CAGAGGGCTG 2040 TGTCAAGGAC TGAGTGACCA GATATTCGAC TGTGCCTCTC CTGAGATGGG GAATGCTGAG 2100 GTTTGGGGAG GCACAGAGCC TTAGTCTATG AGCCCTAACT CTCTGAACTC CCACCCCAGA 2160 GTTAGGAAAC TCCTCCCACA TAGGACAATG GGCAAGTAGA GCCCGCCTTC CATGGGAGGA 2220 GCCCAAATAG TCCACACCCA 2240
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