| Tag | Content |
|---|
EnhancerAtlas ID | HS121-15790 |
Organism | Homo sapiens |
Tissue/cell | LNCaP |
Coordinate | chr17:20353430-20354790 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr17:20353500-20353518 | CCCTCCCTCCCTCCCTCC | - | 6.03 | | ZNF263 | MA0528.1 | chr17:20353496-20353517 | CTCTCCCTCCCTCCCTCCCTC | - | 7.43 | | ZNF263 | MA0528.1 | chr17:20353492-20353513 | TCCTCTCTCCCTCCCTCCCTC | - | 7.5 | | ZNF263 | MA0528.1 | chr17:20353500-20353521 | CCCTCCCTCCCTCCCTCCTCA | - | 8.12 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I020450 | chr17 | 20354114 | 20354513 |
|
Enhancer Sequence | ACCTGTGCAG AGATTATGCC GTTTGCACTA CACTTGGGAA GTCCTCCACC CTCACTGCAG 60
CCTCCTCTCT CCCTCCCTCC CTCCCTCCTC AGTTGTTAAT AAGCCCCTCA CCTGCACTCT 120
ATCCCCACTG AGCGACCGGC TCTTCACTAA ACAGGCTGTG CGTGCTCCTT CCCCTGTACT 180
GTTCCCTGGC CTAGAATACT GTTCCCACGA CATCAGGGAC AGGAGCACTG GCCTGTGCCA 240
TCTGTATCCC TCGGACCCAG CACACAGGAG TGCTCTGGGC CTGGGCTCCT GCAGCATCAG 300
CCTCCTAACT TGTCTTTTCC ACCCCAATGC CTTCTCCATG AGGCAGTCAG GGTACAAATG 360
TTAAAACCTC CTGCCCTTTG CAATAGCTGA CACTCTTAAC ACACATGCCA TGTGTAAGGC 420
ACTGTCCTAA GCGTGCTACA GATACTGCCT CATTCCATTC TTACAGCTCT AGGAGATTCA 480
TATGATTATT AGCTCCATTT TGTAGATGAG GAAACTGAAG CACAGAGTAG CTAAGTCACT 540
TGCCCGAGGT CACACAGCTG TCCACAAATC AAAGAATGTT GCTCCCTGGC TCCATGGCTG 600
CAAAGCCCTA CATCAGTCAT TTTCAACTCT GATTGCAGAG TGTAATCACT TCAGGCATAT 660
TTTAAAAATA CAAATGCCCA GGCTGACCGC CTCATTGGCC TGGGCTGGGG TCCCAGCACC 720
TATATGTTCT TTGTAAGCTC TCTGGGTGAT TTGAATGTGT AGTCAGGGCG GAGCACGCCT 780
GCTGCTGTTC CTGGAGAGGC CACACCCGCA CCTCTGCATG TTGGCCCTAG CTGCCCCTCC 840
CAGGCTCGCT CTATCTCATC GCTCTGTTTT GCTTTCTGCG TGGCACTGTT GTTATCTGCA 900
ACAATCTGTT CATGCTTTAG TTTCCTTGTT CCTTCCCCCA GCTAAATTGT AAACTCTCTG 960
GAGGAAGGAC CCTATGTGTC TGCTTCATGA CTGCGCTCCC AGCACGTGGA GTGCTTCCTG 1020
CACAAAGCGG GCGACAGTGA AATCGTTGAA TGAGTCAGTG AAGAAATGAA TAACACCTCC 1080
TTCTTGGGTC TGATTTGACA CTTACTGACT GTGTGACCGC AAGCAAGTAA CCTGCACTTG 1140
TGAGTTTCTT TCCTCATCTA AAAAAGCAGA TCCCAACGCT TCCTTCATGC AGGACAGTAA 1200
TAATTATTAA TAATAATGAC AATAATTTTT TGGCCACCTT TTCTTCTGGG CCCTCATCCC 1260
AGAGGCATCA GCTTCCATCC TGTTCAAGGT GCCCCAGACC TCCTTTACCC CCTCCCCGTG 1320
TACCCATAGG AGCCTCCTCA AGCTCCAGGC TGCGGCGCCT 1360
|
