| Tag | Content |
|---|
EnhancerAtlas ID | HS091-41681 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chr6:84588250-84589900 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| KLF13 | MA0657.1 | chr6:84589654-84589672 | CTCAGAGGGGCGTGTCAT | - | 7.25 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GAGACGGGGT TTCACAGTGT TAGCCAGGAT GGTCTCGATC TCCTGACCTT GTGATCCACC 60
TGCCTCGGCC TCCCAAAGTG CTAGGATTAC AGGCGTGAGC CACCGCGCCC AGCCGTGTTT 120
TGTAATTTTT GAATGAATGT CACACATTAC ATATAGAAGA ATAATAGAAA CTGTGGTATT 180
TACACTCAGA CATGTAGTAC ATTTTTTTTT TTCTGGCAGG TAGTTAGGTT GAATCAATCT 240
AGTAAGTAGT TGAGCTAGAT TTGGAGTGTA TTTTGCTATT GTTACCATCA GTGTACCACA 300
GACTTCAAAT TCCTCCAGTG GTGGGCCACT GCTACCTTGG TTTTAATTCA GGGCCTGCAA 360
TGCTAGAGGG TTTTTTTCCC CCATTGTTCT TGTTCTACTC TTAGCTGACA CCTTACCCTA 420
TATATCTTTG CAGGATCTTT CTCCATTGCT CTTCCCCCTC TCCAAAAGGC AGTGCTGTTA 480
CTTATTACTT GGTGTAAGAC TTGTAGTGGG GGCAGAAGGG GTTTTGCAGT TTTCCTGTTT 540
CAGCCTCAGT CTTAGACAGG TTTTATGCAC CTGAGCCCCA GGGGCTGAGC TTTCTCATTG 600
CTTTTGTACT TCCCCAAGGG CAGATAACTC CTGCATCGTA CTCAATGCAG CATCTAGAAT 660
GCAGGCAGGT TTCATGAGCC TCTTCCCTTT GTGGCAGCTG GACTTTGCCT TGTATCAGGT 720
GGGGAGGGCA GGGCAAAGGG TCTAGGATGT GAGCAGTTTC CCTGTCTCTT TTCCAGTGTG 780
AGAGTATCAG TGTTTTGTAT TCACACCGAA TCTGGGTCTG AGTACATTTT CTGTTCTTTC 840
CCAGTATTTA GCTAGCATTT GCCTAGTGTC AGTGCAGGAT AAGGGAGCGT GTGTGTTTTA 900
CACTCTTTCC AGCAGCAGTT AGTATTTGCC TCCTGTCAGT ACAGGGACCG GTGGTGGGAG 960
GCTTTACTGC CCCTTTCCAT CAATAGATGG CTTTTGCCTC CAGATAGGAT CTGTGGTATG 1020
GGTGAAATTT TCCCTTTACC CTGGCAGTAG CTCATTAACA CCTTGTACTC CTGTAGGCCT 1080
TAAACTATGG ATGGACTTTT CTTTGTACTC TTGCACTACC CTCTAATCTT GCTGCAGATA 1140
TTACACAGCT GTGCTACCAG TGGGCCTTTC TCGTGTCTGC TTTGCCTATA GTATTTCTCA 1200
TGAGCATCTC AAGAGGTGAA AGATTATGAA AAAAGAGTTG GCAAGTGGGG ACAGAATCCC 1260
CTTGTGTCTG AGGTTCTCAG GGATTCCAAA TTGGCTCTAG TGCGCACTTG GCCCTTAAAG 1320
TTTGTTAAAA TTTCAGTTGT TTTGTGGTGA CGTCTCATTT TTCTGTGCTC TGCTGAAGCT 1380
GAAGGGGTTC ATGTGGTTCA TCTCCTCAGA GGGGCGTGTC ATCCTTTGGA ATTTAGATCA 1440
TCTGGTTGCC TTATGACCTC ACCTCTCTGA TGGGCTCAAA ATTTTATGAT TTTTTAATGG 1500
ATTGTCTGCC TTGTTGTTAA GGGTGAGAGC AGTGTTTTCT TGTGGCCTTC TACTGTTTTC 1560
CCACTTTTTA AATTTTTGTT TTTTATTGAC ACGTAATTGT ACATATTTAT GGGCTACCAT 1620
GTGTCATTTT AGTACATGTA TACATTGTGT 1650
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