Tag | Content |
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EnhancerAtlas ID | HS091-11415 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chr13:21682750-21684220 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ESR2 | MA0258.2 | chr13:21683332-21683347 | AGGTCAGCCAGCCCT | + | 6.52 | Nr2f6(var.2) | MA0728.1 | chr13:21682798-21682813 | TGAACTCCTGACCTC | - | 6.22 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GTATTTTTAG TAGAGATGGG GGTTTCACCA TGTTGGTCAG GCTGGTCTTG AACTCCTGAC 60 CTCAGGTGAT CTGCCCGTCT TGGCCTCCCA AAGTGCTGGG ATTACAGGCG TGAGCCACTG 120 CGCCTGGCCC ACGTTTTTAC AGTTAGTTTA TATCTTACAA TTTTCATTGG CAGTTTCATT 180 GTAGGTTTAA GTAATAAACC AGGAAACTTT AAAAAATAGA TGATAGATAA ATCCCTCAAG 240 TGCTTCCCGG TGCCCTCGGG ATAACATACA ACTTTCTTAC TGGGACTTCC TATGTTCTTT 300 ATAACTGGCT CCTGCTCACT CGCCAACCCC AACTCTCCTC TGTAGCCAGC CCCCTAAGCA 360 TTCCATCCTC TGTCCTTTGC ACATATATTC AACTCTGTCT GAAGGCCAGC CCTGCACACC 420 TTCCCCCAGC AATCTCTATT TATCCTTTAA GTCTCGATGT AGAATCATTT ATTCCATGAA 480 GCTGCCCTGG TGTTCCCCTC CCCCAACCCC ACACTTTGAA CTTCCCTAGC ATAGCGCTTT 540 TCACCCGATG ACAATTGTCT ACTTGTTTGA TGTCTTCTGA GGAGGTCAGC CAGCCCTGTG 600 ACCAGAAGGC ATCAGCCCTG AGTTAAGTCT TGCTCACTGT TCTGTTCCTA GCCCCTAGCA 660 GAGGAAGCCC AGCTCCACCA TGGGCTCTGG CCAAGTGTCT GTTTTCTGAG TCCTTCTTGT 720 CCCTATCGTA AGGCCCCTCT CTCAGCCACC TCCACATGCC TTTCACGGGG CCCAGGCTCC 780 TTCAGGCGCT CTCCCCATGG CATGCAGGGT GTGCAGGACA GCACGAGGCT GCTCGGGTCA 840 CATGCTCGGG AGCCTCAACC TACCACGGCC TCTGTACTAC CCTTGTGCCC TGAGGAGCTC 900 TGGGCTCCCT GAGCTGTGGG ATCCCTTCAG CCTTTTCTGA GGTTTCTACC AGCCTTTATC 960 TAGTCTGAGT CAGGTTGCTT TTCAGAGACA TCGTCAAAGT TTAATTCTAT CAACATCACC 1020 AATTAGGATG GCCCAAATCC AGAGCACAGA CTTATGACCT GGAGAGGATG TGCAGCAACA 1080 GGAACTCTCA TTCACTGCTG GTGGAATGCA AAATGGTGCA GCCACTCTGG TCTTTTTGTT 1140 TGTTTTTTAG AGACAAGGTC TCTCTCCCTT GCCCAGGCTG GAGTGCAGTG GCATGATCAT 1200 AGCTGACTGC AGCCTGGAAT TCCTGGGCTG AAGCGATATC CTCCTATCTG AGCCTCCCAA 1260 GTAGCTGGGA CTACAGGTGC ATACCACCAC ACCCGGCTAA GTTTTGTTTT GTTTTTTTTT 1320 TTTTTTTTTG AGACCGAGTC TGGCTCTGTC GCCCAGGCTG GAGTGCAGTG GCGTGATCTC 1380 GGCTCACTGC AAGCTCCGCC TCCCAGGTTC ACGCCATTCT CTGGCCTCAG CCTCCTGAGT 1440 AGCTGGGATT ACAGGCACCC GCCACCACGC 1470
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