| Tag | Content |
|---|
EnhancerAtlas ID | HS053-17823 | Organism | Homo sapiens | Tissue/cell | Foreskin_keratinocyte | Coordinate | chr18:3888800-3890230 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Esrra | MA0592.2 | chr18:3889788-3889799 | TTCAAGGTCAA | + | 6.14 | | GCM1 | MA0646.1 | chr18:3889048-3889059 | TATGCGGGTAC | + | 6.32 | | TP53 | MA0106.3 | chr18:3889355-3889373 | AACATGTTCTGGCATATT | + | 6.07 | | TP53 | MA0106.3 | chr18:3889355-3889373 | AACATGTTCTGGCATATT | - | 6.33 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TAAACGATAA AATCTCCTAA TCTTATTTTG GACTGACAGA GTTCAAATAT GCCTGTGCTG 60
ACTCTATGGG ACCTCGGAGA TATGCTTCCT ATGGAATTGT TCTTATCTGG ATTTTCAGGA 120
GAGGGTTGGT TATCTCGGCT AAATGGACAG ATGAATTCCC TTGGGAGCCA GCTAGGAGAA 180
TGTGGTTACC TTAACCAGCC ATGGACAGTG CCCTTCAGGA GGTGCTGCAG CAGGGGGACA 240
GCCTGTCTTA TGCGGGTACA ATTGATGGGG GTAGAATATT CACAGAGAAG AGAAAAACCC 300
ATCAGCGTTT ACTCCAAAAA AAGTTGGGAA AAACTTGCAA ACTACTGATG AATCTAGGAG 360
AAAGAAGAAA TGATGACAGA ATAAACCTGT TTAATGGTAC CTAAAGACAG CCGTGATGGA 420
AGATGGAAAA ACACAAAAAC AATGACAATC AAAACAATAT GACAATACAA CTTGAAAAGG 480
AGCAGTGGAA ATAGCCTCTG ATGAAACCAA GTTATTTTTG TCTAGATTGC TCATGACTAG 540
CTGAGTAGTC TTGTGAACAT GTTCTGGCAT ATTCTATACA ACTTGTTTCA CAGCCAGATT 600
TTATATATAC ATACATGCAT ATATATATAT ATATTTACCT GAATCAAATT TTCTCTTATA 660
AAGTCTCTTT CTTTAAAAGC TGTTGCTCTT CTTACCAAGT TTGCTGTACA AATCTACTTT 720
CCTTAGTGCT GAGACCCCAA AAGTGCAGAC ATTAAGCCCT TTTGTGGTAG CTGTTCAGCT 780
GACACCTGCT TTTGGGAATT TCTTCCCTAC TCACAGCATC TCCTGGTGAC CCTGTGGCCA 840
GGACTGTTGA AGGTGATCAC CACATTTTCT GAGCTTATGG AAGACTGGAC TCAGGGGCAT 900
CCATGCAGAG CCTTCACTGA GCTAATGAGA TGCTCACTTT GGGAAATCTA GGTGGGGATG 960
TTCCTAGAAT CACTGGACTC TGGTAAGCTT CAAGGTCAAG TAAAGGAAGG GCCCATGTCG 1020
GCCCCACTGG AAGCCAGAGT TGATGCTATT GAACTGTGGG GCAGCGTTAG CCATGGGCCC 1080
TACAGAGGGA GTGTGTGTGG AGGGAAGAGA GGAGCCAGTC CAGAGTCCAT GGAACCCCAG 1140
CGAAAGAAAC AGACAGAAGC TGCCTAATGG CCTTGTAGGT CTAGTCAGGC CTGGCTCCCT 1200
GCCCAGAGGG TGAGACTCTG TGGTCATCTG CAGCAGAACC AAGGCAGGCC CACAAAAGCT 1260
TACTCATCCA AGTAAAGGGG ACCCTCCTGC CCAGTGGGTA ACTGCAAGCA TACAGAACCT 1320
CCACCACTGT GGTCTACATC CAAGTGGGGC CAATGTGAGT CAGTCTCTGA AGTGGCCCCA 1380
ACAGAATTGG CTAAGTTATC CTCATACAGC TTTATACCCA TTTAAGTATT 1430
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