| Tag | Content |
|---|
EnhancerAtlas ID | HS091-18006 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr16:74493930-74495250 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Atoh1 | MA0461.2 | chr16:74494969-74494979 | AACATATGTT | + | 6.02 | | Atoh1 | MA0461.2 | chr16:74494969-74494979 | AACATATGTT | - | 6.02 | | Nr2f6(var.2) | MA0728.1 | chr16:74494273-74494288 | TGAACTCCTGACCTC | - | 6.22 | | ONECUT2 | MA0756.1 | chr16:74494630-74494644 | GGAAAATCAATAAA | + | 6.25 | | ONECUT3 | MA0757.1 | chr16:74494630-74494644 | GGAAAATCAATAAA | + | 6.72 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TTTTTTTAGA CAGAGTCTTG CTCTTGTTGC CCAGGCTGAA GTACAATGGC ACGATCTCGG 60
CTCACCGCAA CCTCTGCCTC TCATGTTCAA GTGATTCTCC TGCCTCAGCC TCCTGAGTAG 120
CTGGAATTAC AGGTATGTAC CACCATGCCC AGCTAATTTT GTACTTTTAG TAGAGACAGA 180
GTTTCTCCAT GTTAGTCAGG CTGGTCTCGA ACTTCTGATC TCAGGTGATT GCCCACCTTG 240
GCTTCCCAAA GGGCTGGGAT TACAGGGCAT GAGCCACCGC AACTGGCCTG ATTTTTGTAT 300
TTCTAGTAGA GATGGGGTTT CGCCATGTTG GCCAGGCTGG TCTTGAACTC CTGACCTCAG 360
GTGATCCTCC TACCTTGGCC TCCCAAAGTG CTGGGATTAT AGGCATGAGC CACCACACCC 420
GGCCTGAACT GACAGTTTCA AAAGCAGATG AGTCCGGTGA TTCCAATCAG CTCTGGACAC 480
CGCAGGATCT GTGCCCCCTC TTCACTGGCC TACTGCTGTT TTACAAGCCA GGGGCAGTAG 540
CACTGCTATC ACCAGAACCC TTGGTCTCTA AACATGTCAG TTTGATGATC GTCCCACACC 600
TGTGCCAGGG CTCATCACAA ACAGTTTCCT GGGGGTTTCG TGCCCCTCCT CCTATATTGG 660
ATGCCAGGCT TCATTCTTCA CAAGGACTGG CACACAGAGT GGAAAATCAA TAAATGTCAT 720
ATCTTTACAC TGTAAACACT GAGACTTGAG TCAGATCTCA GGACTTGTCA AAAAGAAGGC 780
TGCTACTTGA TTCCACAGGA GCAAGGTTAT ATATAACCAA ATCAAATACG AAAAGCAAAC 840
GCTTGACATT CACATAGGTT CAGGGTCAAA CCAGACTCTC AACTTGAAAG TGTGCACACG 900
CGCGTACCCG CACACACACG CACACATACA CAGGAGTTGA GAAACACAGC CCACAGCAAA 960
GACAAAAATA TTAAGTTTCT TTGGACAGTT TTATGAGTGA GCTTTTTTGT AACAGCTTTT 1020
GTTATGAGCT CCTGAAATTA ACATATGTTG AACACGCTCT CCACAAGGCC TTTTCTAGCT 1080
AAGAAGTCCA ATAATCTCCA AAGATGGGCA CTTCCTTACG GCCATTATAG AATTACTTTT 1140
TTTTTTTTTT TTTGAGATGG AACCTCGCTC TGTCGCCCAG GCTGGAGTGC AGCGGTGCAA 1200
TCTCGGCTCA CTGCAAGCTC TGCCTCCTGG GTTCATGCCA TTCTCCTGCC TTAGCCTCCC 1260
GGGTAGCTGG GACTACAGGT ATACGCCACC GGGCCGGGCT AATGTTTTTT TTTTTTAGTA 1320
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