Tag | Content |
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EnhancerAtlas ID | HS091-11121 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr12:121664150-121666330 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CEBPA | MA0102.3 | chr12:121664393-121664404 | ATTGCACAACA | + | 6.14 | Nr2f6(var.2) | MA0728.1 | chr12:121665672-121665687 | GAGGTCAGGAGTTCA | + | 6.22 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_28089 | chr12:121664209-121668971 | Fetal_Intestine | SE_28761 | chr12:121664047-121669000 | Fetal_Intestine_Large |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr12 | 121664724 | 121665671 | chr12 | 121664970 | 121665566 |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I121226 | chr12 | 121664242 | 121668712 |
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Enhancer Sequence | AGCCTGGCCA ACATGGTGAA ACCCCCTCTC TACTAAAAAT ATAAAAATTA GCCAGGCGTG 60 GTGGTGCGCA CCTGTAATCC CACTACTCAG GAGGCTGAGG CACGAGAATT GCTTGAACCC 120 GGGAGATAGA AGTTGCAGTG AGCCAAGATC ATGCCACTGC GCTCCAGCCC GGGTGACAGA 180 ATAAGACCCT GTCTCAAAAA CAGAACAAAG ACTAAAACGT TTTGGAACTA GACAGAGGTG 240 ATGATTGCAC AACATTATGA ATGTACTAAA TGCCACAGAA TTGTCCAGTT TAAAATGGTT 300 AATTTTATGT TATGTGAATT TCATCTCAAT TTCTCTAAAA AGGTGAGTTG ATCTTAAAGT 360 ATTACATGTG AGGTACACAG GTGTGTGTGT GGGTGTTACG GTACAGGAAA TGACAAAAAC 420 TTGAACACCC CTGTTGTAAG CCATCCCTCT TGAGGGAGTG GGGACTTTGA AGACCTGAGA 480 GAAGTCCAGG CACAGTGGCC CATGCCTGTA ATCCCAGCAC TTTGGGAGAC CGAGGTGGGT 540 GGATCATCTG AGGTCAGGAG TTTGAGACCA GCCTGACCAA CATGGTGAAA CCCCATCTCT 600 ACTAAAAATA TGAAAAAATT AGCCAGGCGT GGTGGTGCAC GCCTGTAACC CCAGCTACTC 660 GGGAGGCTGA GGCAGGAGAA TCACTTGAAC CCAGAGGTTG CAGTGAGCCG AGATCGCGGC 720 ATTGCACTCC AGCCTGAGCA ACAGGAGCAA GACTCCATCT CAAAAAAAAA AAAAACCTGA 780 GAGAAGCCCC TTGGTCCCAG CCTTTCTCTG ACAGCAGTGG TGACAGGCTC AGCTCTCCTC 840 CGAGTGCAGC CCTGTCACTG ACCTTGCTCC TGTCTCAGGG CTGGGAAGAC TGTTGATGTT 900 GTCATTCCAA AGATCCCACC TGGATCAGGG GAACATCCCC CACAGAAGGG TTAGCCATAC 960 AGTGCCAGAT TCTCCAGGAG AAATTCACCA AAGAAATGGA GTCCCCTTGG GGACAGATTC 1020 AACTTGTATT GTCAGCCAGG AGCTGACGTG GCACTTCTGA GAAGAGGCCG GCGCACCTGC 1080 TGGCGGGTGC TTTGTGCACT TTTCAGACAG GTCAGGATCC AGCCTGTAGG CAAATTTACT 1140 TTTGCTTTGA CCTGTAAAAC CGGATCTGCC CAGCCTTCAT TCTCTCCCTG GAGAACGCCT 1200 GCGGCCCCAA AGCCAGGCCT ACTGATTTCC AGTGAGGCCA CAAATCCCCT CCCTGGTTAG 1260 CAATTCAGTT TTCACCGCCT TGGGGGAGAG GGCCTGCCCT TCCTTGAGGG GAAGAACCTG 1320 GAAGGCTCGG CTCAGTGTCT TCTCTTGGAA GAGAAGAGTG TGCATGCAGA AGGGTGTAGA 1380 AAATGCTAGA CGTGTTTCAT CTTCTTGACA AAATGACATT GTAAGATGTG TGTATATGTT 1440 TTTAAAAATA TTACATAGGG GCTGAACATG GTGGCCCACT CCTGTAGTCC AGCACAGGGA 1500 GGCGGAGGTA GGAAGATTGC TTGAGGTCAG GAGTTCAAGA CCAGCCTGGG CAATGTAGGA 1560 AGACTTCATG TCTACAAAAA AAAAAAAAAA AAATTTCATT AGCCAGGCAT GGTGATGCAT 1620 GCCTATAGTT CCAGCTACTT GAGAGGCTGA GGTGGGAGAA CCCCCTGAGC CTGGGAGGTC 1680 GAGGCTACAA GAAGCTGTGT TCATGCAACT GTACTCCAGC CTGGGCAACA GAGCAAGACC 1740 CTGTCTCAAA AATATATATA GGCTGGGCGT GATGGCTTAT GCCTGTAATC CCAGCACTTT 1800 GGGAGGCTGA AGCAGGCGGA TCACTTGAGG CCAGGAGTTG GAGACCAGCC TGACCAACAT 1860 GGTGGAACCC TGTCTCTACT AAAAATACAA AAAAAGTTAA CCAGGCATAG TGGCTCACAC 1920 CTGTGTAATC CCAGCTACAC GGGAGGCTGA GGTGGCAGTG AGCTGAGATC GCGCCATTGC 1980 ACTCAAGCCT GCACTCGAGG TGACAGAGTG ACTCCATCTC AAAAAAAAAA AAAAAAAAAT 2040 ATATATATAT ATATATATAC ACACACACAC ACACAGACAC ACACACACAA TACATATATA 2100 TATGTGTGTA TATATATATA TATAACATGG TTATGTGAGT ATTTGTATGT ATTTTATTAA 2160 CAGTAATGTT ATCATTGTTT 2180
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