| Tag | Content |
|---|
EnhancerAtlas ID | HS121-19901 | Organism | Homo sapiens | Tissue/cell | LNCaP | Coordinate | chr19:18671360-18672840 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr19:18672051-18672063 | AAACAAACAAAC | - | 6.32 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 2 | ID | Chromosome | Start | End |
| GH19I018560 | chr19 | 18671211 | 18671610 | | GH19I018561 | chr19 | 18672363 | 18673892 |
| Enhancer Sequence | GTGAGTACCT GCAATTCTTG GCTTTAATTT GCTAATAAAA GTGTCACGTC AGAGCTGAGT 60
TTGAAAAGTT CTGTTGCCCT TCCCCACAAC AACATTCTGG CAGCCCCTTG CTATGAGCCA 120
GACTCCGGGT CGGGTTCTGG TGACAGACAC ACCTCTACTC CTTCTTTTTT TTTTTTGAGA 180
CGGAGTCTCT CTGTTGCCCA GGCTGGAGTG CAGTGGCACA GTCTTGGCTC ACCACAACCT 240
CCGCCTCCTG GGTTCAAGTG ATTCTCCTGC CTCAAGCTCC CGAGTAGCTG GGACTAAAGG 300
TGCCCACCAC CATGCCTGGC TAATTTTTGT ATTTTTAGTA GAGATGGGGT TTCACTATGT 360
TGGCCAGGCT GGTCTCGAAC TCCTGACCTC GTGATCCACC TGCCTCGCCC TCCCAGAGTG 420
CTAGGATTAC AGGCGTGAGC CACAGCACCT GGCCACCTCT GCTCTTTTGG AGCTGACGTT 480
GTGGCGGTGA CAGGCAAACG GGTTAGCTGA TAACTAGGAT AATTTCATGA AGAGGTGAAC 540
CAGTGAAGCA GTTAAATCAA GGTAAAGGGT GGCTGGGCGC AGTGGCTCAG GCCTGTAATC 600
CTAGCACTTT GGGAGGCCAA GGCAAAAGGG TCGTGTCAGC CTAGGAATTT AAGAGCAGCC 660
TAGGCAACAT AGCGAGACCC TGTCTCTTAA CAAACAAACA AACAAAAACA AGGTAAAGTA 720
GCCTGGGCGC GGTGGCTCAT GCCTGTAATC CCAGCACTTT GGGAGGCTGA GGCGAGTGGA 780
TCACCTGAGG TCAGTAGTTC GAGACCAGCC TGGCCAAAAT GGTGAAACCC CGTCTCTACT 840
AAAAAATACA AAAATTAGCC AGGCGTGGTG GCGGGCACCT GTAATCCCAG CTACTTGGGA 900
GGGTGAGGCA GGAGAATCGC TTGAACCTGG GAGGCGGAGG TTGCGCTAAG CCAAGATCGC 960
GCCATTGCAC TCCAGCCTGG GTGACAGGAG TGAAACTCTG TATCAAAAAG AAATAAAAAA 1020
ACGAGGTCAA GTAGTAAGAG AAGCGGTAAG AGTGACGGGA ACAGGAGTCA TTGACCTCTT 1080
GGGAGAGGAG ACATTGGAGG TGGTGATGAT TTGCTGAAGC AGCCACACAC GTTCAGCTTG 1140
TGAGGACAGC AGTTGTTAGG CAGGGGATGA GGGAGGAAGC TGGCAGATCT GTGCAGGTGA 1200
GAGGTACCTG TGGCCTTGGG CTCATGGAAG TGGGAGGTGA TGGGATTCTA ATGTGCTTGG 1260
GTACAGTTTA CAAATACAAC CTCTCTTAGT TTGCCCAATA CCTCCAAATT CCTGGGGTGG 1320
CACACCTGAG GTTCAGGTGG CATGACTGAG CCACAGTCAC ACATCCCCAC TGTAGGATAC 1380
CACCACGGTT GGGTTAGGTT CCAGCACATG GCGGTCCCGG CCTGGCCTCT TGGTCCCACC 1440
TCACCTGGTG ACTAGTGCAG ACCACTCTGT TCTTGCCTGT 1480
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