| Tag | Content |
|---|
EnhancerAtlas ID | HS091-40647 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr6:29663350-29665070 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr6:29664495-29664514 | GAGTGCCCTCTGCTGGTTC | - | 6.45 | | EBF1 | MA0154.3 | chr6:29663661-29663675 | TTTCCCATGGGAGT | - | 6.03 | | Nkx2-5(var.2) | MA0503.1 | chr6:29664646-29664657 | CTTGAGTGGCT | - | 6.62 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | ATTGTTTTTG TAGTTTTAGT AGAGACAGGG TTTCTCCATG TTGGTCAGGC TGGTCTCGAA 60
CTCCTGACCT CAGATGATCC GCCCACCTCG GCCTCCCAAA GTGCTGGGAT TACAGGCGTG 120
AGCCACCGCG CCTGGCCTGC ACATAGCTTT TCAGCTTTCC TGCTCTCCAC TGCAGGAATG 180
CTAGCACTCC CTGTAGAGAG GGGAAAGGGC CCTGTCTTTC ACACAAGCCT GGCCCAAATG 240
GCCACACTGC CAGTGGAAAC ACAGTCACCC CTGATAGCCC TAGAAAGGCT CTTCTCTGGC 300
ACACGTGCCA ATTTCCCATG GGAGTGGCCA TGCTGTGTTT GAAGCAGTGG TGGATGGGGG 360
AAGGGCAGGA GAATTTCCCC TTTCCATGCC TGATTCTAAG CACTGGGGCT GCTTGGCTGC 420
TGGGATGGAA CTACACTCCT TCAGCGCAGA GCTGAACACA GTGTCCACGA CTCTGCTGGA 480
AGTGGTGCAG TCACTCAGCC CACAAACAAG GAGCTCTTGG ACACAGATGA GTACATGGTC 540
TGGCCTCCTT TGTCCCAACT GGTACTTTTT TTGTGTACTG CAGTCTCCCT TTCCTTAGGA 600
GCAGCAATCC CTGATGGCTA GACCACTGGG AACCCTGCAG CTCCACTGGG TCCAGCCAGC 660
CCTGTGTGGC TGCCACAATC CAAGTGGGCA CTGGGGGCAT GGCTGCAGGA GCTTCTGTGA 720
TGTGAATATA CAAAGGTTGG GGTTCCCTGG GAAGGACACA GTCCCCTGAT GGCTACACTC 780
CTAATATGGC ACCCTGCCAA CACTGCCCGA GTCTGGAGGA GGGACAAGTG ACCCAGCGCA 840
AGTTGGTTGT CTGGTGTGAT GCCCTCCAGA AGTTCCCAAA TCGCCATGCA CATCAGTGTT 900
TGGCTTTGTG AGGGCAGAGG AGCTCTCCGA CAGTTCAGAT ACTGGTGGTC TTCCTTAGGG 960
ACGACGGGAG TCAAAACACT CCTATCTTAC CTTTCAATGA AATACCAAGT CTCTCAAGGT 1020
TCCTAGCTGA TTTCTGCCAG CTTCTTACTT TCTTCTTTTT TTCTGTCTCA GCTTTTCCCC 1080
ATGAGTTCTG AAACATTCTG ATGTGATTCT GACAGCTATT TCCACACTCA GGCTGGGCCC 1140
TGGAGGAGTG CCCTCTGCTG GTTCTCTGAG ACCTGTGGCT GGGATCATCT CTGATAAGGT 1200
TTGGGTGTTT GTCCCCTCCA AATCTCATGT TGAAAGATCC CCAGTGTTGG AGCTGGGGCC 1260
TAGTGGGAGG CGTTTGGGTC ATGGGACCGG TTCTCTCTTG AGTGGCTTAG TACCCTGCCC 1320
ATGGTAATGA GTGAGCTTTC ACTCTATTCG TTCACACGAG AGCTGATTAT TTAAAAGAGC 1380
CTAGCAGCTC TCTTGCTCTT TCTCTCTCCA TGTGACACAC CTGCTCTTCC TTTGCCTTCT 1440
GCCACAAGTA AAAGCTTCCT GAGACTTCAC CAGAATCCTA GTGGAGCTGG CCCCATGATT 1500
GTACAGCCTG CAGAACTGTG AGCCAAATAA ATCTCTTTTC TTTATAAATT ACTTAAACCC 1560
AGGTATTCCT TTACAACAAC GCAAATGGAC TAATACAGTC TCCCTCTGCT GCCTCCAAGG 1620
TCACTCCTTG ATCTTCACTG CTTTAGGCAG CCTTTTACCC TACTTTGTAG TTGGAGCTTC 1680
AGGGGCTTAA CATCTTAAAA GTTTTATTTT ATTTTTTAAT 1720
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