Tag | Content |
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EnhancerAtlas ID | HS091-23914 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr19:36180250-36181800 |
Target genes | Number: 30 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFYB | MA0502.1 | chr19:36181643-36181658 | CTGATTGGTGCGTTT | - | 6.73 | NFYB | MA0502.1 | chr19:36181594-36181609 | CTGATTGGTCCATTT | - | 9.03 |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH19I035689 | chr19 | 36180825 | 36181220 |
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Enhancer Sequence | TCTGTCACTC AGGGTGGAGT GCAATGGCAG GATCATGGCT CACTGCAGCC TCAACCCCCC 60 AGACTCAAGC GATCCTCCTG CTTCAGCCTG CCAAGTAGCT GGGACTACAG GTGCATAACA 120 CTATAACTGG CTAATTTTTA AATTTTTTGT AGAGACGGAA TTTTGCTGTA TTGCCCAGGC 180 TGATCTCAAA CTCCTAAGGC TCAAGTGATT CTCCTACTTC GACTTCTCAA AGTGCTGGGA 240 TTATAGGCAT GAGCCATTGT GCCTAGCTAG TTTTTTCCTT TAAAAACCAC ACTGCTGACC 300 AGGCGCAGTG GCTCACGCCT GTAATCCCAG CACTTTGGGA GGCCAAGGCA GGAGGATTAC 360 CTGAGGTCAG GAGTTCGACA CCAGCCTGGC CAACATGGTG AAACCCCGTC TATACTAAAA 420 GTACAAAAAA ATTAGCCGGG TGTAGTGGTG CACACCTGTA ATCCCAACTA CCCAGGAGCT 480 GAGGCACGAA AATCCCTTGA ACCCGGGAGG CGGAGGTTGC AGTGAGCTGA CATCATTCCA 540 CTGGACTCCA GCCTGGCCGA CAGAGCGAGA CTGTCTCAAA AAAAAAAAAA AAAAAAAAAA 600 CCCTGCAAAA GAATTTAATG GCATGAAAAA AATGCTTGGG AAATTGTGAC ATGAGAAAAA 660 CAGATTACAA TGTAGCATGC CAAGTATGAT TCCTTCCCTG ATAAAAATAT AAATATGTGC 720 ATGTTTGCAT TTTTTTTAAA AGAAAGTCTT CCAAAGGTTA TTGAGGAAGA GGACACATTT 780 GCAGGGGATC TTTACTTCAT TCCTTGGACA TTTTGGTATT TTGCAAATAT TTTATGATGA 840 CTATTGCCTT TGTCCTCTAA CAAAAAATCA AGAAATATAT CTTAGTTAAA ATGTCCCTGC 900 TGGACATAAA ATGTACATTG AGAAGAGAAT TATCCTACTA AATATTTTCA AACTTTATCT 960 GAGCAGTTAA GGTGTCCGGA ATTGGTGGGT TATTGGTCTC ACTGACTTCA AGAATGAAGC 1020 CGCGGACCCT CGCGGTGAGT GTTACAGCTC TTAAGGTGGC GTGTTTGGAG TTTGTTCCTT 1080 CCGATGTTCG GATGTGTCCG GAGTTTCTTC CTTCTGGTGG GTTCCTGGTC TCGCCGGCTC 1140 AGGCAGGAGT GAAGCTGCAG ACCTTCGCGG TGAGTGTTAC TGCTCATGAA GGCAGTATGC 1200 ACCCAAAGAG TGAGCAGCAG CAGGATTTAT AGCAAAGAGC AAAAGAACAA AGCTACCACA 1260 GCACGGAAGG GAACCCCAGC GGGTTGCCGC GGCTGACTCG GGCAACCTTC TTTTATTCTC 1320 TTATCTGGCC CCACCCACAT CCTGCTGATT GGTCCATTTT ACAGAGAGCC GAGTGGTCTG 1380 TTTTGACAGG GTGCTGATTG GTGCGTTTAC AATCCCTGAG CTAGACACAA AGGTTCTCCA 1440 TGTCCCCACT AGATTAGCTA GATACAGAGT GTCCACACAA AGGTTCTCCA AGTCCCCACC 1500 AGAGTAGCTG GATACAGAGT GTCGATTGGT GCATTCACAA ACCCTGAGCT 1550
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