Tag | Content |
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EnhancerAtlas ID | HS091-23114 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr19:8092720-8094950 |
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) |
HES2 | MA0616.2 | chr19:8094916-8094926 | GGCACGTGCC | + | 6.02 | HES2 | MA0616.2 | chr19:8094916-8094926 | GGCACGTGCC | - | 6.02 | HNF4G | MA0484.1 | chr19:8094112-8094127 | AAAGGCCAAAGGTCA | + | 7.01 | Nr2f6(var.2) | MA0728.1 | chr19:8093008-8093023 | TGAACTCCTGACCTC | - | 6.22 | Nr2f6 | MA0677.1 | chr19:8094113-8094127 | AAGGCCAAAGGTCA | + | 6.73 | RREB1 | MA0073.1 | chr19:8093678-8093698 | TGGGGTTGGGGGGTGTGGGG | - | 6.22 | Rxra | MA0512.2 | chr19:8094113-8094127 | AAGGCCAAAGGTCA | + | 6.09 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr19 | 8093129 | 8093432 | chr19 | 8093472 | 8094571 |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I008028 | chr19 | 8092970 | 8095351 |
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Enhancer Sequence | CACTGGCCTT CCTCGTCCTC CTCTTTATAC CATTGCACCC AGGTTTGTTT GTCTGTTTTT 60 AGTGACAGAG GCTTGCTGTG TCACCCAGGA TGGAGTGCAG TGGCACATTC TCAGCTCACT 120 GCAACCTCTG CCTCCCAGAT TCAAGCAATT CTCCTGCCTC AGTCTCCTGA GTAGCTGGGA 180 TTATAGGCAT GTGCCACCGC ATCCGGCTAA TTTTTGATTT TTTTTTTTTT TTTTTTTTTT 240 TTTTTTTTTA GTGGAGACGG GGATTCATTA TGTTGGCCAG GCTGGTCTTG AACTCCTGAC 300 CTCCAGTGAT CCACCTGCCT CGGCCTCCCA AAGTGCTGGG ATTACAGACA TGAGCCACTG 360 CACCCAGCCC CTGGGGTTTT ATTTACCCAG ATCCCCACTG CCTTTCCTTC CTGTGGCTGA 420 CATCTCCCTA CACTGTCCCC CAGAAACACA GCTGTTTTGC CCTCAACCAC AGCTCCTGCA 480 TCCAGTGCAG GGCCTGGCTC TTGACTGAGA CATCAGCAAA TGTGAGCCCT GCTCTCCTGG 540 GTCAATGCAG GCTCCTTCAG GAAGGAGGCG GGGATCTGTC CCCCTTGGCA TCCCCAGTGC 600 CCAGCATGGG GGGCCTGGCA CCCATGAGGC AGCCAAGGCT TTCAGACCAA ATGAACAAGC 660 AGTGAGCCCT GCCTTCGAGG GCCCGTCTTG AGGACACCAG GTGGGTTTAT GACATCCCAG 720 TGGACATGAG GCCCCCAGGG ACCAGTTCCT CTCCGGCATT GGCACCAGGG CCCCTGCCCC 780 ACTGGATCAG ACCTCCCAAG CTTGGGGTCC CTTTTCCAGT AGGCAAGAGA GGCACCCGAC 840 TCCTGCTTCA GCCCAAGGAG AACCTGCCGA CTCCAAGGGG TGGCCATTGA GGGGATCAGT 900 GACGTAAGTC CTTCAGAGGC AGCAGGGACA AGGAGCTGTA GGGAAAACAG GGCAGGCCTG 960 GGGTTGGGGG GTGTGGGGTG CTGACAAGGT GCAGACCCAC CACCCCAACC AAGCCCCTCC 1020 TCCGCAGATC CATCACCTCT GCCCCGTGCC CCATGAATGA ACCAGCTCAT TCCCCGGCCC 1080 AGTGACCAGC ACAGGCTCCA GACGTTTCCC TCGGACATTG TCTGCCTGAC CACCTCTTCC 1140 AGCACAGTGA GGGGCCTGGG ATCTGGAGGC CAGAGTGGGC CAGGCCTAGG GGTGGGGGGA 1200 AAAACGTCAC TATTCTTAGA TCCCTCGTCC TCCAGGGCCC AGGCCAGGCG GAGCAGTCAC 1260 ATTCCAGAGG TAGAAACCAT CAGCCCACAC AAATGCTTGT GTTCCCTGAG GAGGCCAAGG 1320 GTCACCAGGA ACTAAAATCA GCTTTTCCCA AGAAAGGCGG GAGACAGGGT GGGGGGCGGG 1380 GGGCAGGGTT AGAAAGGCCA AAGGTCACCC AATAAACCCT TCCAGCTGCC CCTGGTGGAA 1440 AGCCCCTCTG AGTCCGGAGG GATGAGGACA GAGGGATTCT CGCCCTCTAA GCTACTCTGC 1500 GGGCTGGCTG ATTCTTCCTG GTAGGGGGCG GTCCTGTGCA GTCTAGATTA TTTAGCAGCT 1560 CTCTGGCAGC CCACCGCCCC CCCAGCCTCC CAGTGGTGAC AGCCAAATCT CTCTCCAGGC 1620 ACGGGCCAGG TGTCCCCTGG GGAAAAATCG ACCCCAGATG AGAACTGTAC TTTCCCAAAC 1680 AGAGCTTCCA GGTGGCGTCT GGGGTAGATA TTTAGGATCC TGCTGTTCTA TGGACTCTGT 1740 TCTCTCAGCC TGGAATCCTC TTCCCGCATA GCACAATCCC CCACCAGCCC TGCAATCTTC 1800 CAGAACTAAA CCCACACATC ACCTCCCTCA GGAAGTGTCC TGTGGGCCCC CCATCTTATG 1860 ATTTTGGCCC CCACGGATGC TGTGGTAGGT AAAATAAAGC CCCTTTGGCC AGATATGGTG 1920 GCTTACACCT GTAATCCCAA CATTTTGGGA CGCCGAGGAG GGAGGATCAC TTGAGCCTAG 1980 GAGTTAGAGA CCAGCCTGGA CAACATAGCA AGACACAGTC TCTACAAAAA AAAATAAAAA 2040 AATTAGCTGG GGCTGGGCGC GGTGGCTCAC GCCTGTAATC CCAGCACTTT GGGAGGCCAA 2100 GGCGAGCGGA TCACAAGGTC AAGAGATCGA GACCATCCTG GCCAAGATGG TGAAACCCTG 2160 TCTCTACTAA AAATACAAAA ATTAGCTGGG CGTGTTGGCA CGTGCCTGTA ATCTCAGCTA 2220 CTCTGGAGGC 2230
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