| Tag | Content |
|---|
EnhancerAtlas ID | HS053-37389 | Organism | Homo sapiens | Tissue/cell | Foreskin_keratinocyte | Coordinate | chr7:116909240-116910770 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr7:116909563-116909576 | TTCCAGAAGGTTC | + | 6.15 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH07I117268 | chr7 | 116908781 | 116911605 |
| Enhancer Sequence | CTCTTTTTTG CTTAGAGAAT ATGATCATTG AACTGGTCAT TTTCAATAGC CAGTTGGACG 60
AATGAATACT CATTGAGTTC TAATCACAGG GAGCTCTGGT ATACTAGAAA GGACACTGGA 120
GTGAGAGTTA GAAGACAAAT ACTTGAGTTC AGGCTGTGCC TCTTATATGC TTATAAGTCT 180
TTTATTACCT GGAGCAAATT ACCATATCTG AAACTTGGCT CATCTCAATA TCCGTATCTA 240
AGGGTGGTTC TAAGCACCAA ATCCAATCCA AGTACTTTAC AAAGTGCTTG TCAAGTAAAA 300
GGAAAAGTGT TCGGTGTTAG TCCTTCCAGA AGGTTCTGAG CAAGTGTATG TTTGTCTTAG 360
TCACCATTAC ATTTCCAGTA CGTAGCACAG TGGTTGACTC ATAGGAGATG CTCAATACAG 420
CCTTACTGAA TGAATAATAA CTGTTCTTCC CTGAAGATGA TTCAGAGTGT CTTGCTCATA 480
TCACAGTTCG AATCATGAAG TTTCTTTTGT TTTCCCATGA ATAACATCTG GAGGTTGGAA 540
TAAATAATCT GCAAAGTTCC TTCCAAATGT GACATTCTGT GATGCCAGGA ATTTTCACTC 600
TCGGGATCCT GAAGTGTCAT GTAAACTCAC TGCTGTGTTG AAGTCCCATA TCTGTATGAC 660
AGAACAATAA TAATTTTCAG AAACTGTTTA ATTATCTGTC TACAATATAT AGATCAGGGG 720
AATCATCTTG ACTTGCTCAT TCCGTTGGTT CAGAAAAATT AAAAGAAATT TGCCAATGAA 780
TGGCTAATAG CCAAAGGAAA TATTCAAATT CATTTGTCTG TATAGACAGT CTGCTGAGTA 840
ATTCTTACTC CAGTTACTAA ATCCTGTAGA AGAGGAAAAT TTCTCATCTG TGAATCATGA 900
TTCTAATAAA ATCTCCAAGG GCTGGTGTAA ATACTTTTAA AAACACAAGT GCTTATTATT 960
TCATGAGAGT TGCTGAGAAG ATAAGGCATT GTTTATAGTT ACAGCAATAT ATAGGAAAAT 1020
TAAACCCGTA CTCCCTTCTC CTTCTAGTTG TACTCTTAGG CTGGGAATAT TTGTCTTGAT 1080
TAAGCACGAT TCCAAAATGA CAATTCAGGG TTCGAGGCCT TTCATGAAGC CTTCATTACT 1140
ATTGGAGAAT AATGATCCTG GGGCAGATGC CAAAGATTAT ATGGGTGGGT AGACTTTTGG 1200
AGACACCGAG TCAGATTTTG TTTTCTGTTT TTCCTGCTAT TTCTTCGGCT GGTGGGCGAC 1260
CTCCACCTGT AACCTGAAGC ACCTAAACAT TTACAGATGG GTTTGTGACG CTCCCCAGCC 1320
TCTGCTTAAG TCACCAGTGT GAGCAGTCCA GCTGAGTGAA TCCTGGTTGC ATCTTCGTCA 1380
TTTAATTATT TGAACTGGGT TTACGGGCAG TAATGTGACT CCTCTCGTCT GTGGAACTTA 1440
GGAAGGCCTA CGATGCTATT AAAAGAGGAC TGGGTGAACT GCCTGGGGAA ATCCAGGGCC 1500
TATGATTCAA TTACAGGGGC TTTCACGGGG 1530
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