| Tag | Content |
|---|
EnhancerAtlas ID | HS121-18712 | Organism | Homo sapiens | Tissue/cell | LNCaP | Coordinate | chr19:2794910-2796070 | Target genes | | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ESR2 | MA0258.2 | chr19:2795544-2795559 | AGATCAGGGTGACCC | - | 6.13 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | GTGAGGGGGC CCTGCGGGGA GTGCAAATAG CCTCCCAAGT AACTAGGATT ACAGGCGCCC 60
GCCACCACAC CCGGCTAATT TTTGTATTTT TAGTAGAGAC GGGGTTTCAA CGTGTTGGTC 120
AGGCTAGTCT CGAACTCCTG ACCTCAAGTG ATCCGCCCAC CTCGGCCTCC CACAGTGCTG 180
GGATGACAGG TGTGAGCCAC TGTGCCCGGC CCATTTTTTG TATTTTTAGT AGGCACAGGG 240
TTTTGCCATG TTGGTCAGGC TGTTCTCAAA CTCCTGACCT CAGGTGATCC GCCCGCCTTG 300
GCCTCCCAAA GTGCTGGGAT CACAGGCCTG AGCCACCACG CCCGGCCACA CATGTGCACT 360
TTCATTTCCT TTCCTGGCCA TCCTAGTGTG ACCCAAACAC CCCATCCCCA CATGGCGTGA 420
GCTGGCAGGG CCTGGCGGCA TGGCTGCGTG GGCTCCTGCT CCCCCGGATG CTCCTCGCAG 480
TATGCAGTGG GGCCTTTGCT GTTGATGTCA CATGATCAGG AGAGACCCAG AGACCCTCCT 540
GCTGCTGTTC ATCCTCTTAG GCGAGGACCC CTGGGAATGT GCTGATGTGT CCCACAGTCT 600
CAGGATCATG CAGCCCTAGT GCTTTGGTAA ATCCAGATCA GGGTGACCCA TGATAGCCGT 660
GGATTGTTAT TTCTTTTTAT TTAAATACAG ACAGGGTCTC ACAACGTTGC CCACGCTTGT 720
CTCGAACTCC TGGGCCCACG CAATCCTCCC ACCTCCACTT TCCAGAGTTT CTGTTGAGAC 780
AATGAGAGGT TCCCATGCAG GTGCAGGAAA GAATCGAATG CCTTTGCCAA CTTTGCCCAG 840
GTCCCCAGTG ATGACGTTTT GCAAAACTAT GGTGTCATCT ACACCCCGAT ACCGACCTGG 900
AGACCACCAG CAATCTAATT CCCATTCAGC CATCGCACTG GTGAAGGAGC TCTGGACTGA 960
TGTCAGTGTG GGGCTCTTCC AAACAAAGCG AACGTTTGCA CAGGTTTTAT GTAGAGACAG 1020
GTCGTCATTT CTCTGAGATA AATGCCCAGG AGTGCAGTTG CCAAGTCACA CGGGGGCCGG 1080
ATGATCAGGT TTTTAAGAAA CTGCCAAACT GCTCTTTGGA GCGGCTGCAC TGGCCCACGT 1140
CCTACATGCT TTGATGTTTT 1160
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