| Tag | Content |
|---|
EnhancerAtlas ID | HS053-01467 | Organism | Homo sapiens | Tissue/cell | Foreskin_keratinocyte | Coordinate | chr1:54480900-54482620 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr1:54481546-54481561 | TGAACTCCTGACCTC | - | 6.22 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 54481793 | 54482552 | | chr1 | 54480902 | 54481047 |
| | | Number: 1 | ID | Chromosome | Start | End |
| GH01I054015 | chr1 | 54481563 | 54483001 |
| Enhancer Sequence | CCAAAATGCT GGGACAACAG GCGTGCACCA CTGTGTCTGG CCTGTTATTG CTTATTGAGG 60
ACTTACCATG TGCCGAGCCT TATTCTAAGC ACTATGGAGA TAGCAGTGAT AGGGGACGTC 120
CCTGCTCTTG TAGAACTGTA CTTTAATTCT CCTTTAATTC TCCCCTGCTT ACAAAATAAT 180
AAAAGAAGGC TTTACTGAGG ACCTCCTGGG TGCCCTGCTG TGCAGCTTGC CCTGGTCCTT 240
GCCCTCTGCA GCTTGTTATT GCACTTAGAA GGCAAGGCAT GGACATGCCT GAAGGGGTGT 300
GGGAGCTACT GACGTGCCCA GGCCACAGGT ACCTCAGAGA AAGGGGCAGG AGCAGGTGTG 360
ATTCATCCCT GTGACCCCAG GGCCCAGCCC AGAGCCAGGC ACGTGGTGGG GGCTTTTGTT 420
TTTTTTGTTT TTTTTGTTTT TTTTTTGAGG CGGAGTCTTG CTCTATTGCC CAGGCTGAAG 480
TGCAGTTGCA TGATCTCAAC TCACTGCAAC CTCTGCCTTC TGGGTTCAAG CGATTCTCCT 540
GCCTCAGCCT CCCGAGTAGC TGGGATGACA GGCGCCCGCC ACCATGCCTG GCTAATTTTT 600
GTATTTTTAG TAGAGACGGG TTTCACCATG TTGGCCAGGC TGGTCTTGAA CTCCTGACCT 660
CAGGTGATCC GCCCACCTTG GCCTCCCGAA GTGCTGGGAT TACAGGTGTG AGCCACCACA 720
CCGGCCTGGG GCTTTGTGAA CACTCTGTGA ATATGCCGAC CTGGGGGTCC AGGAGGCAAG 780
AGAAGGCCCC CAGTATGGGT CAGTCCAGGT TATTTCCAAT CCATTCACAT TTCTGATGCA 840
GTGTCCTCAG AAGCAGAATG GGATTTCCAC AGGCAGGTAA GGGGAGGGTG CAAAGAGAGG 900
GCATTCCAGG CAGAGGGCGT GGCAGGAGTA AAGGCCCAGT GGTTGCAGGT GGGGGAGCAC 960
AAATGGCCTG GGGTGGTGGG ACTCCAAGAT GGATGTGTAT TGGGAGGGGA GACAATAGCA 1020
GGAGAGGCAG CATAAATCTA AAACCTGTCA TCCCTACAGC CCTAGTTGGT GGCTCCTTGG 1080
CCATCAGCAA ACAGGGTAAA CTCAGGTAAC CAGGGAGGCA GCGTGACTCT GGGCAGGGAG 1140
AGGTGTCCTG ATCAGCCAAG CAGCTCCTCA AATATTTGTG CAGCACAGAC CATGCACAAG 1200
GTGGGGCCAT GGGAGAACCC GCAGAACCAA GGCTCCTGCC CAGGTGAAGC TGTTGCACTT 1260
CAAAGCCAGA AAGCCCTTAG GTGCCAGTCC TCTCCCTGTA CCGATGAGGA AAAGGAGGTG 1320
ATTCTTTCCA CAACCCCGCC CATCATGAGT CAGGACTTAG AAATAAACAA ACACCAGCTC 1380
GGAGCAACAA AAGCCCTGGG GCTTTGTAAC CAGAGAGACC TCAGTTCACA TTTGAACCCT 1440
GGCCCTCCAA CCTCCCTGCT GTGTGACCTT GGCCTGGTTA CTCAACCTCT CTTAGTTTCA 1500
GCTGTCTCAT CTGTTATTGC CCCATAACAG GGCCCCTGTC TCAGAGCTGT CCTGAGGATT 1560
AAAGAGATCA TGCAGTGCCA GGCACCTAAC TGGGGATGGA TTCTTTATAG CTGGTATTTT 1620
AATCTACCTC TCTGAGTGTG TTTCGTCATT GATCAAATGT GGGCCAAGCC AGGGCATATG 1680
CAAAGCTCAG TACATGTGTG TTTCTTCCTT CTTCTATTTT 1720
|
| |
|
|
|
