| Tag | Content |
|---|
EnhancerAtlas ID | HS053-26344 | Organism | Homo sapiens | Tissue/cell | Foreskin_keratinocyte | Coordinate | chr3:10987440-10989140 | 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 | chr3:10987540-10987559 | CAGCCACCAGGTGGCGCTG | + | 8.3 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr3 | 10987447 | 10987821 | | chr3 | 10988144 | 10988547 |
| Enhancer Sequence | TCCTGCCCTT ATCCACTCTC CCCCACCCCC ACCCCTCCAT CCCAGTCCTG GGCTCAGAGG 60
GGCCTGTGGC TGGCAGATCC AGGCTCTGTT AGCAGCAAGT CAGCCACCAG GTGGCGCTGC 120
TGCTAAACCC AAGCCCCCTC CCTGTGGTCC TGGCTCAGGC CAGTGAGGTC AGGACTAGAG 180
CTGGGACCCC ACAGTTGAGA CTAGAGGATC CAGAGGTCTC ACTCTGGGTG CCCAGATGGG 240
GGACAGAAAG GCTGCCCTTG TCAAACGCGC ACAATTCATC CTTCTCACCC TGCCCCATCC 300
CTAGCTCACG TTTGCAGCAC TACCCTAACA GCCAGAAGTG AGGGTTCTTA ACTCTCTCAC 360
TCCTTTGCTG TGTGACCTTG GGCAAGTGAC TTTGCCTCTC TGACTTCAAC GTCCTCTTCT 420
GTACAAGTGG ACAGAATAAG CCACTCAGGG GTGCCGAGAG GATGAGATGA GATGATGGTG 480
TGTGTCAAGC GTCCGGCACA CAGGGAGAAC ATGGCTCTCC CAGTGAGCCT CCTTCCTCGG 540
GTCCATGGTC AGAAGGGCCC CAGCCGGTGT CAGGAGACCT GCACCCTAGC TCTGAATTCG 600
CTGTGTGCCT TCAAAAAAGA CATGCTGCCT CTCCAAGTCT CGGTTTCCTC ATCTGTAAAG 660
TGGCACTAAT CACAGGAACT TTCTTTTTGG TTATTCTGAG GATGAAATGA GAACATGGCT 720
ATATGGCATT TGTTTTATAA AGCCCCACAT GATCAGGAAA GGTGATTATT GAAAGCATTT 780
CTGCAGCAGC TTTCAGGGGG TGGGATTGGG TGAATGTGTA AATAGTGGTG AGGTGGGAGA 840
GGTGACCGGG CACATGGGAC AGGCTGCGGG TTTTGCTCTG TGTACCTACA ATGACACAGG 900
CCCCTTGTGC CACACCCTAC TTGGCATCTT CCCGGCCATG CCCCAAGCCC CTATCTTGCT 960
CCATCTATCC TGGAGTCTTG CCCCAACCCG TTTAAACACA AAAATGTCTG AGTGCCTGCA 1020
CGGAACAAAG ACGAGAGGCA GAACACGGAA ATGTCGATTG TGATTATCTC TGAATGATAA 1080
GGTTTGGGCT GATTTTTATT TTCTCCTTTT TCTTTTATTT TTTCTGTACC ATCTAATTTT 1140
TTTTTAACAA AGAACATCTA TTGCTTTTAT ATTCCAAAAA CCAGAATCAA TAAAGCTATT 1200
TTTAAAAATC CTTTCCTTGC CATCAAGAGG TTGGTTATAA ATGAAGGCTC CAGAGAAAGA 1260
AACAATGATT CTCCTGTGGC TGGAAGATGT GGCCAGAGGG AGATGGGAGG GGAGAGGAGG 1320
CGTCACCACG TAAGCTGCCT TCAGTCCTGT CTCCAGCCTC CCCTGGGAAG CCAAGGAAGA 1380
GGCAGATGCA GCAGGACCCC TCCTCCGGGC CACAGAGCTC CCCGTAACAT TTATGGGCCA 1440
GCATTCCAGG GGCCTTGAGC TTGCCGCTTG TCTCTGGGAG CTCGTCATGG TTGTTGAAGG 1500
AAGAAGGGAG CAAACAAGCC AGGAAGCCAT GCTTGGTGAG GGCTGACTAT GAACTAAGTG 1560
CTGCCACCTC TATTAACTCA TCAGACCTCC CTCCCCACAC TCCCCTGTTG AGGGAGCTGG 1620
GATTATCAGC CCAGGTTACA GATGAGAAAA CTGAGATATG AACTTACATA TCTGACTGCC 1680
TTCTGGATCT CTCCTCTTGA 1700
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