Tag | Content |
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EnhancerAtlas ID | HS091-44429 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr7:99012680-99013520 |
Target genes | Number: 20 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
PAX5 | MA0014.3 | chr7:99013077-99013089 | GAGCGTGACCAC | + | 6.62 |
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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 | CCCACAGGGT CGGTGGGTTT CTCCCCGTGT GTGGAGACGA GAGAGCGTAG AAATAAAGAC 60 ACAAGACAAA GAGATAAAAG ACAGCTGAGC CTGGGAATCC CACCAAGACG CGGAGACCGG 120 TAGTGGCCCC AAATGCCAGG CTGCACTGAT ATTTATTGGA TACAAGACAA AGGGGCAGGA 180 TAAGCAGTGT GAACCATCTC CAATGATAGG TAAGGCCACA TGGGTCACGT GTCCACTGGA 240 AAGCGGGCCC TTGCCTGCCT GGCACCAAGG CAGAGAGAGA GAGACAGCTT ATGCCATTAT 300 TTCTGCTTAT CAGAGACTTT TAGTACTTTC ACTAATTTGC TATTGTTATC TAAAAGGCAG 360 AGCCAGGTGT ACAGGATGGA ACATGAAGGC GGACTAGGAG CGTGACCACC AAAGCACAGC 420 ATCACAGGGA GATAGTTAGG CCTCTGGATA ACTGCGGGCG GGCCTGACTG ATGTCAGGCC 480 CTCCACAAGA GGTGGAGGAG TAGAGTCTTC TCTAAACTCC CCCGGGGAAA GGGAGATTCC 540 CTTTCCCGGT CTGCTAAGTA GCGGGTGTTT TTCCTTGACA CTAACGCTAC TGCTAGACCA 600 AGGTCCGCTT GGCAACGGGC ATCTTCCCAG ATGCTGGCGT TACCGCTAGA CCAAGGAGCC 660 CTCTGGTGGC CCTGTCCGGG CATAACAGAA GGCTTGCACT CGTTTTCTGG TCAGTTCTCA 720 CTATGTCCCC TCAGCTCCCA TCTCTGTATA GCCTGGTGTT TCCTAGGTTA TGATTGTCGA 780 GTGAGGATTA TTATAATATT GGAATAAAGA GTAATTGCTA CAAACTAAGG ATTAATGATA 840
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