| Tag | Content |
|---|
EnhancerAtlas ID | HS053-40559 | Organism | Homo sapiens | Tissue/cell | Foreskin_keratinocyte | Coordinate | chr9:88128810-88130390 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr9:88130356-88130371 | GAGGTCAGGAGTTCA | + | 6.22 | | Nr2f6(var.2) | MA0728.1 | chr9:88130348-88130363 | CAGATCAAGAGGTCA | + | 6.43 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TACAAATTCA CTCTCAGTCA TCCTTCCAAA GAAAAGAAAG TTTTAAATAA TCTGAAAAAA 60
AGTCGCTGAT TATCTGAACT AATTCATCCG TGGGCATCAG GTTTCTTTGC AACATACTCC 120
AAGAATTGGG ACTCTAAGGG GTAGTCATCT GTCTGCCATG GAGCCAATCT TACATGTGGC 180
TAATGAATAC ATGTATGTGC ATTTGGTTTC CATAAGGAAG TAGCAAAATA AATATTATTC 240
CCACGGCATC CTAAAAGTCA TTTATGGAAA CTTCCAGAAA CCACTGGAGT AGGCAGGGTT 300
AGGCCCCAGT CACCAATCAG TAGGTCCAGG CCAAGAGTAC CACTTACTCT TCAGAGCAGT 360
ATCAGTCCAC AGACTGCCGC CCTGCCCAGT CATCCTTCCA GCAGGTCATG GCGGCAGGAG 420
AGCCTTGCCA GAGTGGTGAG CAGCCTCATG GCCTTCCAGG GCTTCTGCTG CCCTCCCCGC 480
TGTATGGCTC ATCCTTCCTG CTGTATGGGA CAGGCTGGAA CCTGAACGCC AGCCTTAGGA 540
CTCAAGGCCC CACCCCCTCT AGTCACTGTT TCCAAGACTG CAGCTGCCTC CCTGCTGAGA 600
GGCCAAGGCT AAAACTCCAT GACCCTCTCT CCTCTCGGGC CTCCCTGCAG CCCCTGCCTG 660
CTCCCATCAG CCTCCCACAC TGCTCAGCGG TGAGCTCTGA ATTACGTAAA TGACCTGGTC 720
ACCCTGTTTA AAAATTCCTA CGGGTCACTT GAAATTCAGT CTACAGCACC ATGGCATTCA 780
AAGACTCAGC CAGAGCTTCC CAGCATCATT TCTATGCCAT AGATGCCTTC CCTGCCACAC 840
ACACACACAC AAACACACAC ACATATGCAT ACAACACACA CAGTTATAAA CATACACTCA 900
TACCGCATAA ACACACGCAA CACACAAACA CAAAACCCAC ACATTAACAT ACTAAGTCAC 960
AAACTCATAC ACAATCACAC ACCCACTCAT AAATACATAT GACACAAACA CGCAGTCACA 1020
AACTCATACA CAAACATATA TTCTTACACA TATGCACAAA ACACACAATC ACAACACACA 1080
CATAAACACA GATGTGAAAG AGACATTTGG CAAATGAACT TGAACCTGAA CTTGAACCCA 1140
AGAAGAGGGG TTCCAGCCAT CTCACCAGCA TATAGAGCCT TTGAATTAAC ACACAAGTTG 1200
GGAAGAAACC AAGAACTAAC AATATCCCTT GAGCCTCTGG ATCAAGCCAC ACCTGAAGCT 1260
AGACTTACCC CATGGGCATT TCATTATGTA AGCCAATAAA CTCCCTTCTT TATTGTGGTT 1320
CTTTTATTGA GGTTTAGCCA AGCTGGGTTT TCATCACTTG CCAACTAAAG ATCCAGACTG 1380
AATAGACACC CAGGAATCAA GCACCTGACA TTCGGAAACA ACCTCAATTA GTCATACTCT 1440
GCCTCCAGGG CTCAGTTGAG TTTCTTTAAA AACTAAGGCT CGGGCCAGGC GCCGTGGCTC 1500
ATGCCTGTAA TCCCAGTACT TTGGGAGCCT GAGGCAGGCA GATCAAGAGG TCAGGAGTTC 1560
AATACCAGCC TGGCCAACAT 1580
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