Tag | Content |
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EnhancerAtlas ID | HS091-11230 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr12:123651340-123653500 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr12:123652878-123652899 | CATGACTTTCTTTTTTTTTTT | + | 6.05 | NFAT5 | MA0606.1 | chr12:123652627-123652637 | ATTTTCCATT | + | 6.02 | NFATC1 | MA0624.1 | chr12:123652627-123652637 | ATTTTCCATT | + | 6.02 | NFATC3 | MA0625.1 | chr12:123652627-123652637 | ATTTTCCATT | + | 6.02 | SOX10 | MA0442.2 | chr12:123652073-123652084 | GTCTTTGTTTT | - | 6.14 |
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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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Enhancer Sequence | TAGAATGAAA ACGGTCAGGC ATTATAAAGG TCTGCACTTC ATTTCAGACT GCATGTGCAT 60 ATAAAACAAT CTGCTCTCAA ACAGTATTTA CACATTTGTA CACTAATTTA AAAATCACAT 120 GTAACAATCT ATATTTTGGA TACAATTTAT TTTACAGTTT TATGATTCAA CTTAACTGTT 180 GTTCTAGGTT TCTGTTACTT CTGAATCTCA GTCAAGATTC AGGTACTTGC GGCTCTGAAC 240 ATTCCCCTCA CTGTCTCTCA GGCATTTCAC ACCCTTTACA CTCTGTGCCC CTACTGTAGC 300 TGAGGGTAAA GTGCTGAAGG AAGCAGGGCT GCCCTTCTTG TTCCCTTCAG ACCAGCACTG 360 TCCAACAGAA TCTTCTGCAA AACCAGAAAT GCTATCTGCA CTGTCCAATG CAGCAGTCAC 420 AAGTCAGGTG TCACTACTGA ACACCTGAAA TGTGGCTGCT GAGACTGAAG AACCAATTAT 480 AAAACGTTAA TTTTAATAAT GAAAGTTTTC AGTATCAAAA TGGAGTCACT AATGTCAAAC 540 TCCCAAAAAA TGGAGCTGGG AGGCACAAAG GAGCAGCCTC TCACACAGAT GCTGATTATG 600 GGAACTATTC TGAATTCCTC AGAACGACAG TATTCCAGAT AATAAGCTGC TTGTACAAGG 660 AAACATCCCT AACAAGGGAT GTCTCCACCA CTGAGCTAAT GCTAATGCCT GCAACATGCT 720 CCTGTAACCA GTGGTCTTTG TTTTAAAATA GCTTAGTGGA CTGTGGACTG CCCTTTGTCT 780 TTTAAAGTTT CCTGTGTCCC AACCCCTTTG GACATGCTTA TGGTTCACCA CAGCATGCGT 840 ACTCCAGCTT GCAAACCCCC AACATTTCCA AATAAATTTC TTTGGAGAGT CAGTCTCTGT 900 CACTGATTTT AGGTTGACAT GATTGATTTA AATAGTAATA GTGGCTGTTG GCAGGACTGT 960 ACTGAACAGC GCAATTCTAG ACATTGCTCC CCCAGCTCAT CTGAGGTTCC CACCATCATG 1020 TTAACCCCCA GTCATTCCCC AGACTTTAGA GCCTGCCTTG TTTTCTCCAC ACCTATGCCT 1080 GTTCTCACAC TAGGCAACTT CCTGACCACT CTCTCCAGTG AGGTGACCCT CTACTCCTCA 1140 GCCAGCCACC TCAGAGGGTA CTTGCTGGCT TTTGTCAAAA CCAGAGAACA CACTCCCCTT 1200 AAGAAACCAA TACTCCAAAG ACTGTGCCCC TATTCTGCCT CCCGCCCTCA AGCTTCAGCA 1260 ACGTGACCTA CGATCCTTGG CCTCTCCATT TTCCATTTAT CAACCCCTCC TAGTCTGACT 1320 AGGTCCTCTT GATCTACCCT GAAGTCCACA CTCACGATAC TTTCTCTCTC ACCTTTCACC 1380 ACACCTGACT GGCAGCAAAA TCTGAGGACT GGCTGACTAC AAAGGCCGCG CTTCAGGTCT 1440 CAACTCCTAC CACTGAGCTT TGCTGGAAAA AAGCCACCAG CTGGGCAGAC TCATCACCAC 1500 CTCAAGCGGA CACCCCAAAC CGCCTGACCG CCTGGCAACA TGACTTTCTT TTTTTTTTTT 1560 TTTTTTGAGA CGGAGTCTCG CTCTGTCACC CAGGCTGGAG TACGGTGGCG TGATCTCGGC 1620 TCACTGCAAG CTCCGCCTCC CAGGTTCAAG CGATTCTCCT GCCTCAGCCT CCCAAGTAGC 1680 TGGGACTACA GGCGCCTGCC ACCACGCCCG GCTAATTTTT TTGTATTTTT AGTAGAGACG 1740 GGGTTTCACC GTGTTAGCCA GGATGGTCTC GATCTCCTGA CCTCATGATC CGCCCACCTC 1800 AGCCTCCCAA AGTGCTGGGA TTACAGGTGT GCGCCAACGC ACCCGGCCGG CAACATGACT 1860 TTCTGTAACC AGCAAGCTTC AGTTCTCCAA ACATGACTAT CTCACACCCT TTCCACCCTC 1920 CTCAAACCTC CCATCCCACC TTCGTTGACA GGTGAAACTT TTGAGTCAAA TTCAAAGAAA 1980 CACCAGAAAC CATGAAACAA CTCTTGTTTT CTCTCTGTCC CCTTTCACAA CCAAACATTT 2040 TAGAGGCTGC CTCTTCTATC TACATTCACT TCAACTCCAG TCACTCTTTC CCTCAGTTTT 2100 TTTTTTTTTG AGACAGAGTC TCACTCTGTC GCCCAGGCTG GAGTGCAGTG GCGCGATCTC 2160
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