Tag | Content |
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EnhancerAtlas ID | HS091-22404 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chr18:55297750-55299280 | Target genes | | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Gfi1b | MA0483.1 | chr18:55298939-55298950 | AAATCTCAGCA | + | 6.32 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GTAAGAGAAC AGGCAAACAT CACTGCGGGC GCCTCTAGGG CTCGTTTCCC TGTCCCAGTA 60 CCGGGAATCG GGGAGGGGTC CAAGCAGAGT TCACTTAGTT AACAAATCAG TGAAGCAGTT 120 GGAAAATCTC AGTTATATTT TAAATGAGAT CGAGGGCGGT GACTCACGCC TGTAATCTCA 180 GCACTTTGGG AGGCCGAAGC GGAGGTGGAG GGTCGCTTGA GGCCAGGAGT TCGAGACCAG 240 CCTGGGCAAC GTGGTGAGCC ACCCCCGCCC CCGCCCCTCT ATAAAAAATA CAAGAATTAG 300 CCGGGCTTAT TGGCATGGGA TTGTGGTCCC AGCTACTTAG GAGGCTGAGG TGGGAGGTCG 360 CTTGAGCCAT GGAGGTCGAG GCTGCACTGA GCTGTGATCA CGCCACTGCA CTCCAGCCTG 420 AGGCTACGGA GAGAGACCCT GTCTCTAATT AATAAATAAA TTATAGATAG ATGATAGATA 480 GATGCAATAA AAAATAAAAT TGGCTTGTAA ACGGCAAACT AAAAGTGGAA ATTATCATTA 540 CAATGAAAAT ATTAATTTGA GGAACCGAAA ACTTAACTTT CCTTTTCCTG TAGTTAAGTT 600 TAAGCACTTA GATTTGCTTC AGTGATTCCC AGGCTTCATG ATTGCAAGCT GCTTGCTTGT 660 AAGCACCTTG TCTCTCACTA AAAAAAATTA CAGTTATTTT AAAGTCCCGC TGGATGCTCA 720 TTCTTTAAGG AGGGTGAACA ATGGTAACTC CTGTACCGTT AGAGCTCTGA ATGAAGCCAG 780 ATACGTTCCA TAGATCACAG AACTCATTTT CTGGCTTGGT GAGCCTGGTC AAGTTTCTTA 840 ACCTTTCTGA GCCACAGATG TTTCAATTAT AAAGTGATAA TAACCCTTCA CTGGGAAGGT 900 TATTGTGAGG ATAATATGAG ATCAGCTATA CCAAAATATG CCTAACATGT ACTTGACATC 960 CAGTAAGCTT TCTGAATTAG GATATAAATG GCATTAATGG TTAATCATTG TTATTCTTTT 1020 GTTCCATGAT ATGCATGAAT AACAACTTGA AGCCTTCAAA CTGCTGAGAG CTGCTTGGTG 1080 GACCTCGTCT CTCAATTTGC CCTTCCCACT AAACCTGTCT TCCCCCAACA GTGGGCTTTC 1140 TGGTCAGCAT TTCAGAATGT CTCAAACCGT AGGTCCTTCC CACAGCCCCA AATCTCAGCA 1200 AATGACCAGT CTCTTGCTTC AAGCTATTAA ATGGATGCTG TCTGACAGCC CTCCCTTGAA 1260 ACCTGCAAAC TCTCGTGCTT TGGCATCCAT CCTTTCCCTC TAGTGCAATG CAAGTCACAT 1320 CCTCCCTCTG GCTAACCTCT CCACCCATCT TCTGGATTCC CCACACCTCT CCAATCTAAT 1380 CTTCACACTC CAGCCAGGGC GAACACTTAC AAATATAAAC ACAGTCATTT CATTCTCTAT 1440 CTAGCAACTT TCCATGGACT TCCTTTTGCT CTCAGGGTTC ACCTCAACAT CCTTACAGGC 1500 TTTCCAGGCT GTGTATGCTC TGGCTTACCA 1530
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