Tag | Content |
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EnhancerAtlas ID | HS091-16947 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr16:29731750-29733310 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Gata4 | MA0482.1 | chr16:29732476-29732487 | AAGAGATAAGA | - | 6.02 | IRF9 | MA0653.1 | chr16:29732068-29732083 | AACAAAAGTGAAACT | + | 6.15 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr16 | 29732800 | 29733140 | chr16 | 29732182 | 29732600 | chr16 | 29732946 | 29733211 |
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| Number: 1 | ID | Chromosome | Start | End |
GH16I029721 | chr16 | 29732522 | 29733320 |
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Enhancer Sequence | GGCGTGAGTC ACTGCGCCCA GCCTACACAC ACTTTTTTTT TTTTTTTAAT TAGCTGGGCC 60 TGGCTGAGCA CGGTGGCTCA TGCCTGTAAT CCCAGCACTT TGGGAGGCCA AGGCGGGCGG 120 ATCAACTGAG GTTGGGAGTT CAAGACCAGA CTGACTAACA TGGAGAAACC CCGTCTCTGA 180 AAATACAAAA TTAGCCGGGC ATGGTGGCGC ATGCCTGTAA TCCCAGCTAC TCCAGAGGCT 240 GAGGCAGGAG AATGGCTTGA ACCTGGGAGG CGGAGGTTGC TGTGAGCTGA GATGGCGCCA 300 TTGCACTCCA GCCTGGGCAA CAAAAGTGAA ACTCTGTCTC AAAAAAAAAA AAAAAAAAAT 360 TAGCTGTGCC TGTAGTCCTA GCTACTGTGG AGGCTGAAGC AGGAGGACTG GTTGAGCCCA 420 GTTCAAGGAC GCAGTGAGCT ATGATTGCAC CACTGTACTC CAGTCTGGGC AACAGAGTGA 480 GATGTTATCT AAAAAAACAG AGTACAATTC AGTGGTTTTT AGTATATTCA CAAAGTTGTG 540 CAATCTATGC CACTATCCAG ACATTTTAAT CAACCCAAAA CGAAACTCTA TGCCGAATAG 600 TCACTGCCCA TTCCCCTCTC TTCCCTAGCC CTGCCAACCA CTAATCTGTA GGGACCAGCC 660 CCACAGGGTC GGTGGGTCTC TCCCTGTGTG CGGCGACGAG AGAGTGTAGA AATAAAGACA 720 CAGACAAAGA GATAAGAGAA AAGGCAGCTG GGCCCGGGGG GACCACTACC ACCAATGCCC 780 GGAGACCGGT AGTGGCCCCG AATGTCTGGC TGCGCTGTTA TTTATTGGAT ACAAGGCAGA 840 AGGGGCAGGG TAAAGAATGT GAGTCACCTC CAATGATAGG TAAGGTCACG TGGGTCATGT 900 GTCCACCGGA CAGGGGGCCC TTCCCTGCCT GGCAGCCGAG GCAGAGAAGG AGAGGAGACA 960 GAGAGAAAGA GAGCTTATGC CATTATTTCT GCATATCAGG GACTATTTGT ATTTTCACTA 1020 ATTTACTACT GCTATCTAGA AGGCAGAGCC AGGTGTACAG GATGGAACAT GAAGGCGGAC 1080 TAGGAGTGTG ACCACTGAAG CACAGCATCA CAGGGAGACG GTTAGGCCTC TGGATAACTG 1140 CGGGCGAGCC TGACTAATGT CAGGCCCTCC ACAAGAGGTG GAGGAGCAGA GTCTTTTCTA 1200 AACTCCCCCG GGGAAAGGGA GACCCCTCCC CCCACTTTCC CGGTCTGCTA AGTAGTGGGT 1260 GTTTTCCCTT GACACTTACG CTACCGATGG ACCACAGTCC GCCTGGCAAC GGGCGTCTGT 1320 CTTCCCAGAC GCTGTCGTCA CCACTAGACC AAGGAGACCT CTGGTGGCTC TGTCCGGGCA 1380 TAACAGAAGG CTCGCACTCT TGTCTTCTGG TCACACTTCG CTATGTCCCC TCAGCTCCTA 1440 TCTCTGTATG GCCTGGTTTT TCCTAGGCTA TGATTATAGA GCGAAGATTA TTATAATATT 1500 GGAATAAAAA GTAATTGCTA CAAACTAATG ATTAATGATA TTCATATATA ATCATATCTA 1560
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