| Tag | Content |
|---|
EnhancerAtlas ID | HS091-09824 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chr12:49669550-49671920 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr12:49671810-49671823 | GAACCTTCCAGAA | - | 6.19 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CGAGAGCAAC CATAGTTTTA TGTCCTTCGG GGCAAGGTAA GACCCCAGCA CAAATTCAGC 60
CACTGCTACT TCTCAGATGA GCCAGGTTCT TCCTGCAGCC TGGGCAGGGG AGCGGGGTGG 120
GATGCCTGAA ATGAAGGTGA ACCTTGAAGA CGCTGGCTAG CCTGCCAGAG GGGATTTTGA 180
GACCTTCCCA GGCCAGGAGA TCTGCTGATT GCCATAGTGC AAGCACTGGA GGAAATGGGA 240
ATGGGACACC CGTGTATGAA AAGGAGCAGA TAAATCACAA AGCTTAGGCG AGTGTGACAC 300
CCCATGACAC CAGCATTTCC CAAGCAGGGT GCCCTGAGAA TAGGATTCAG GGTGCCCATA 360
TAGGATCCCT TCGGCTTTTA GAATGACATG GTGGAAACTG GAGAGCCTGA CTCACCCATC 420
CTCCCTGGGG CCAGTCACCC TGGCCAGGAG TAGCCCCCTC CATTTACCTC TGTACACCTT 480
ACAGATGAAT TATTTTCTAC ATGTGCCAAG ATGTGAAAAA GGTTGGAAAG CTTTAAGCAG 540
CCACAGAGGT CTGGGGTGAA AGAAGGTGAG AGAAAAGTTT AGCTGAGAAG AAATATTCCA 600
GTAGAATAAA GCCTGGGGAA TTGGAAGAGC AAAGTGCCAG TGGTTGGGGG GGCATTTGTC 660
CTTGTAAAGA TGATTTCCCC CTCCTGCGTT GGAGGGAGAG TGAATAGAAG TTAGCCTGCA 720
GCAAGAACAA ATATACCCCA AGGTCTAGGT CACTGCTTTG TGGCTGACAA TCATCTGATC 780
TGCCCTTGAG CACGAATGGA AAGTCTGGAC CCAGAGCTGC GACTGATGCT GATGCTGAGG 840
CCGCTGAAGC TTGATGGGAA TAAATGCACA CAGCCTAAGA GGATTCGGGC TCCTGAGGCT 900
GGCGGCAGCC CCAGGTCCGG CTGTGTGGAC AGAGGGCTTA GTCTGCCCTC ACCTAACCTG 960
GCCAGAGGAG CAACCTGCTT CCCCCCACAG AGGCCGCTGA CCACTGAGAG GTTAGCATGT 1020
CTGGGCAGAG GTGTTTTGGG CAGGGATGAG AAGGGGGATA ATGACTTTGA GGGGCTAAGG 1080
GCCTGCCTGT CCACCTGTCA TTCTGTGTTT GGGAAGCAGC TGGCAAGTGA CTCTTCTCCA 1140
GCAGGAATCT GTCAGGCCAG AGGATGGCCA AGTGGGTTAT GCAATTACAA ATCAGTCTTC 1200
AGGCCTCTGC TGGAAGGTGG TGTGGCAGTC CTGGGTGAGG CTGAAGGAGG TCAGGGGAGG 1260
CGCTGTCAGG GTGGGAGGAA AAGGTGCCTT CACAGTTTCC ACAGTACCCT GGGAGGTGAT 1320
GTTATTATAC CCACTTCCAT AGCTCACAGA GATTGAATAT CTAGCCTAAG GCTACAGAAT 1380
GAGTGGCAGA ACTGAAATTT TACCGCAGAG CTCTGGCTCT AAAGCCTAGG CTGACTCCAC 1440
TCTGTCGTCC AGCCATCGAG GAGCTCCAGA GGAAATCGGC TCTGCACCTG GCAGCCTTTC 1500
CAGTCCTGGG GGGATAGTGC CACCTCCCAG GACCCTTGGG GCATGAGGTC AACAAGGGCC 1560
AGCCCTCACA TGAGCACTGG ATGGAGCTGT AGTCACAGAG AGATCTCATT ATGCCAGTGA 1620
TTGTCAGAAA ACCTCCCAAG AGCCCCGTTC CTGGGCCCAG GTGGCAGCCC ATTGACCTTA 1680
AATAGCAAAG CCAGCTGGTC CCCATGTCCA GGCTGTAGCT TCCCTAGTGA GGGGGCATTT 1740
TTGTCCAGGC CTCCCTCTGA ACTCAGTTCT CAGGTCACGG GGAGATACAG TGCCCTTGCA 1800
GGATGGCTGC TGCCACCTGC CTGGTCTCCT GCCAACAGGG ACACCAGCTG AGGCACAGGC 1860
AGGACAGTGT ACACCTGGAG CCTCGCTCCT CTATGCTCCA GGGCCAGAGT GGTCAGTGCC 1920
CGTCAGCTGA GGCGGCAAGG TGAAGCTGGC AGAGATGACC CAGGCAGATG GCTCCAGGAG 1980
CCCAATGCCA GGGCGACTAT CTAGGAGACA CAAGGCAGCA GAAGCTGAAG AGAAAATAGA 2040
CCCTTGGGTG TGGGGGCTGT GGAGCAGGAG TGGGCCCTCG CCCCGTGAAA TAGGTCCCCT 2100
TTGCTGACAT CTCATTAGCC TGTCACTGCC CCTTTCATGC CAAGAACCTA GTGCCCCTGA 2160
ATTTGTCATT GTCAGCCCCA AGCAGGTTTT GGGAAAACAG TTCTTTCCTC CTCTACACTC 2220
CCTCCGAGTC TACAGCAGGA GAGCAATAGT CAGAATCAAT GAACCTTCCA GAACTAGAGA 2280
CATGTCTGCT TTAGTCATAA TACAAAAAAT GCTTTTAAAC AGTCGTCTCC CTACTGGACT 2340
TTTTTTTCTC TCTCTCTCTT ATTTATTTAT 2370
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