Tag | Content |
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EnhancerAtlas ID | HS091-34849 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr3:113345060-113346490 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
POU4F2 | MA0683.1 | chr3:113346294-113346310 | ATGAATATTTAATTGA | + | 6.33 | ZNF263 | MA0528.1 | chr3:113345425-113345446 | TCCTCCTCCTCCTCCTCCTCC | - | 12.34 | ZNF263 | MA0528.1 | chr3:113345428-113345449 | TCCTCCTCCTCCTCCTCCTCC | - | 12.34 | ZNF263 | MA0528.1 | chr3:113345419-113345440 | TCACATTCCTCCTCCTCCTCC | - | 6.78 | ZNF263 | MA0528.1 | chr3:113345422-113345443 | CATTCCTCCTCCTCCTCCTCC | - | 8.71 |
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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 | TGGTGAGTTC ATATCTATCT TTTTGTGACT TTCTTCTCTC TTTACATCTT GTACTCTCTT 60 TTTCTTCTGC TCTTCCTTAC TTTTTTTTAT ATTCCTCTCT AATTTTACTT TCCATTTCCT 120 CCTTGTAATT CAATGTACAG ACCATCTTAT TTCTTTCATA AATTTTATAT CCTTTGGTTA 180 GATCTTTAGT TTTTCTTTTA CTCTTCAATA TCTTTAGACA CAGAGGGACA AAATTACTTT 240 CCCTAAGTTG CACAGCACGT TTGTTCTGAA TTGGTTATTA GACCCACATG CCCAGAATTC 300 CCCCAGGAAC CACTTTTAGC AATTCCGATA ACATTGGGTT ATTCCTTCTT ATGCCATACT 360 CACATTCCTC CTCCTCCTCC TCCTCCTCCA GTCTCCCTGA ATATTTCACA AATATTTTAC 420 ATATTCCTTA AGTGGCTTGG GGTAGCAGCC ACGTGTCTGT TGCCTTCTGA CCAGTCTGTC 480 CCAAATCTCT CCTGTAGTTT CTCTATTTTT TTGCCCCAAC CCTTTCTCAG AAGCCATGAG 540 TATTTATATC AACCCTGGAT TATAGTTCCA TCCTTTAATC CTAACTTTGA TTTTTCCCAA 600 TTAAAAGTCC ATGGTGCCTG TAGGCAGGTT CAATTGACAA TTAACAACCC TACTAGACTC 660 CCGGGCTCCA GACCTACTAG ATGCCCGGGC TCCACGCAAA GCGGGCTCAG GCAGGCCATA 720 TGACTTCAAG AGTGGAGCAG GGCTATCCTC TAGTGGCCAG TTTGGGAAGC TTGGCCAATC 780 TGTATAAACA GTCCTTACGT CTTTTACTTT TGATCGTCAC CTTCATGAGA GAGACAGAGA 840 CAGCAAAAGT GGAACTAAAG ATTCCACGTG GGGCAGTAGT AGTCAAATGA ACTAGAAATG 900 GAGGAGGAGG GTACATTTCT TATATAGCAA TACTCTATCC AACAGGACTT TATTCCTTTG 960 ACTCTTGACC TAAATGTCCC CTAAGTAATG ACTTCCCAGG CCACCCTATC AAAATTTTTT 1020 ACCTCCCCAC ACCTGATACT TCCTGTATTT CCTCCCTTAT TTAACTTCTA TCCTTAGCAC 1080 TTATTACTAT CTAACATGCT ATATTTTACT CATGTATTTG TTTCACGTCT AAAGCCCTCT 1140 TTAGAATGTA AGCTACATGG AGAATAGGGA TTTTTGTCTC TTTCATTACC AACTATATCT 1200 CCATAGCATC TGGAATAGCA CATCATAAAC CTTCATGAAT ATTTAATTGA CAAATGAATT 1260 GTATAATTAT AATAAGTGCC TATTAAGAGC AAAGGATTGC AGAGAGCTGC AGAAGGCATG 1320 AGAATGAGAG GGAACTAACA GTTTCCAGTC TGTGTGCATC TCAGAGAGAA AACAGGACTT 1380 AGTGTGACAG TGACTGTCCA TTCCTTTCAT TTCTCTGTCC CTCTCACTTC 1430
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