Tag | Content |
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EnhancerAtlas ID | HS091-33156 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr22:39263210-39265520 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr22:39265030-39265049 | CCGCCACTAGGTGGCAGCA | + | 7.6 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_65848 | chr22:39259435-39265211 | Pancreatic_islets |
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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 |
GH22I038868 | chr22 | 39264616 | 39265570 |
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Enhancer Sequence | GGGCAGAGGG AGGGGTGGGT GGGACCTCAG GACTGCCCGC TGACCTCCCC TGGATGTCCC 60 TACGCCAGCC AGCCCTAAGT AGAGCCTCTC AGCCAGCGAT CCCGAGATCA TTTAAGATAA 120 TCACTGGTCT TCATGACCTC GACTTAGAAA AGGAAACAGA GGTTCAGAGA TGAAGCAATT 180 TGCCTCTGAC TCCAAGGTCA GAGTCAGGAC ACCCTTGTCC AGGCCCAATT CCAAAACTGT 240 GTTTTTTCTA TCACCCACCA CCTCTGTTAG CTCCACAGAG GGCCCTGGGC CACTCCATGG 300 CTGCCCTTGC TGACACGGAG GAGTGTCGAC AATTGGGACA CAGTGTCGGG AGGGCAGCCG 360 TTTGCTCAGA AGCCCCTGCT AAACCCCTGC TCTGTGGCAG ATCCAGCCCA AGTGGGGACT 420 CCTCCACGGA CTCATTCGTG GTGACAGAAA GGAGGAGGTG GGTCCTCCCT GCTCCCCCGC 480 ACCAAGTCCT GCTGAGCCAC CATGTCCCCA ATGCCCCGTA CTCTCTCGCC TTTGAGCAGG 540 CTGACCTCCG GCTCCAGCCT GTCTCCTCAG CTGGCCAGCA CCTCAGCCAC CATACTTCCC 600 TGGATGGGTC TCATTTACTT GTCTGCCCAG TGCCTGGCTC AGAGTGAACT GGTACCAATG 660 CATCCCAAAG CCTGGGCTGG AACCCAACCC GGTCAGACGT GAGTTTGGTG GGGACAGGCC 720 TAGAAGTGGG CCCGACCACT GCCTATTCTC TGTGCCAAGA TGGTCTGGGG CAGGATGATG 780 GTGCAGAGGT CGTGGGCAGC CAGGAATACT GCCCCAGGCT CCCAGGCCTG TCCTTCCAGC 840 TGTCCTTCCA GGCATGAAAT CTCTTTAAAG CCACAGGGCT CTCAAGAGAC CCCAGGTTCC 900 GGTCCAACCC ACCCGTTGTC AGATGCCACT AAATGGAGAG AGGCTAAGGG ACTCCTAAGG 960 CGATGTAAGC TGTCTGCATG GCCAGTCCTT TCTTTACTAA GGAAGGTACT GAGGCACCAG 1020 GCACCAGTTG CTTGGGGTTA CAGCTGCACA CGCACAGACT CTCCCCTGGA GAGCTGCCCT 1080 ATCACAGGGA GGACGGTGGG CAGTGGGAAT ATGAAGTGAT TTCGTGCAGC GAAAGAACCA 1140 CAGAGCCCAG AGAAGCACAG ACCCCAGGCT TGGAGAATGA AACATCAAAG CCCGGCCCTG 1200 ACACCTAAGT AGGAAAAAGT CCTGGTCCTT ACTGAGCCCT GACTGCACCC CAGACAGTTC 1260 CAGAGGCTGC GGTGGCCTGC TAAGACAGAC AGATGGTAGA GGCAGAGAGT CCTCTGGGCA 1320 AGATCCCAGT GGTGTGAGAA GATGGCGAGG AGTCACAGGA CTGAAAGCAA GGGCTGGGGA 1380 CAGAGGCTGG GGTGTGTGTG GGGTGCCACA AGGGGCGTGG GTTTTAGAGA TCCTACTGGG 1440 GCAGGGAGGC TTGTTAGGTG ATGGCTGCCC TCAATCTAGG TGGGAGATGG TTGGGACCGA 1500 GAAGAAGGCC ATGTCCCCAC GGTTGGTCTG TGAGGTCCAT GAGGGTGGGA TCTGTTGTGA 1560 GGTCTCTCTA CCTCCCACTC CCCACAGCAT TGGATGCTTA ACTAGTACCT GGAGGTAGCC 1620 CATATGCCTC TCAGACAAGA CTAGATTACC ATTTGATCAC AACTCTCAGG AGAGATGTTT 1680 GCTGGCTTAT TTGTTGGCTA AGCAAGGATG TCTTCATTTA GAACGTGGCG TTCACCCCCA 1740 TGGGAGAAGG GACTGTGACT CCACGTGGTC CTCCCAGCCC AGGCTGGGGC CTCCTGGGGC 1800 TGCTTGGTTA ACAGTCCCTT CCGCCACTAG GTGGCAGCAC ATGAAGCCGG GCCTGCCCAT 1860 GCCAATGCTG CCAGCCCAGC TCCCAGGGAT TGGGCCCCTC AGACCCCTTC CCACACAAAG 1920 GCAGGGAAAA GCCCAGGCTT TTTTGGCGTG GTAAGCAGAC ATTCTGCAGG TGCATCCCCA 1980 CACTTTCTGA CTCTCAGAAA GTGTTTACTC CCTCTGCAAA CTGCCTGAGC TTCCTGACTT 2040 CTGAAATTAT GCTTCCAAGA GTCCAGTGGT GACGGACTGT TCCTGGGGGA GGGGCAGAGT 2100 GTGGGCAAAT GGCAGGCCCG GAAAGAAACC CTGGCTCAGT GAGTCTCCTT TCCTTATCTG 2160 CTGAACCATC ACAGGGCCTA CTACGGGCAC TCCTATGATG ATCAGAGAGT ACATGGCACC 2220 TGCTCAGCAC AGTGCCTGGC ACGCAGCAAA TAACTGAACA GACCTACCCA TGGGTGGTGG 2280 ACTTATAAGC AGTGATCTTT TTCCAATGTA 2310
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