| Tag | Content |
|---|
EnhancerAtlas ID | HS121-07725 |
Organism | Homo sapiens |
Tissue/cell | LNCaP |
Coordinate | chr11:113568140-113569620 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| GFI1 | MA0038.2 | chr11:113568142-113568154 | GAAATCACAGCA | + | 6.22 | | Gfi1b | MA0483.1 | chr11:113568143-113568154 | AAATCACAGCA | + | 6.62 | | RREB1 | MA0073.1 | chr11:113568606-113568626 | CCCCCAAACACACACACACA | + | 7.55 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | CTGAAATCAC AGCATGAAAA CCACATGGGA GAGGATGGTG GTGGTAGGGT GGGACAGGAA 60
GAGCTGGACC CAGGATTCTG TAGTACTTGA AGAGGCCTTA ATGACAGCAT CTGGATCACC 120
CAGTGCCAAG TTCCCTGCTC CCCGGAGAGT GAGACCAGTC CCAAGAGCAG TATCACCCCT 180
TTTGGTAGAG CATTTCAGTT TTCTATTTTA ACCATGTGTT TTTAAGCGTG GTCTACCATT 240
CATTGTCACA GCAGCCCTGT GCAATGAGTA CTGCCATCCT CTCCATTCTG CAGAAGGAGA 300
ACTAAGGCAT GGAGTTTAAG CAACTTCCCC AAGATCACAG TGTCAGGAAA TGATGGATCC 360
AGGACTTAGA TCCAGGTCTT CTGATTTCAA ATCTTGTGAT AATAATAATT ACCAGTTGTT 420
GAGTGTATGC TTTTTCCAGG CTATTATGGA CTGACTCATG TCCCCGCCCC CAAACACACA 480
CACACAAATT CATATGTTAA AGCCCCAACC CTCAATGTGA CTGTATTTGG AGACAGGGCC 540
TTTAAGAAGG TGATTAAGGT TAAATGAGGT CACGAGGGTG ACGCCCTGAT CCAATAGAGC 600
CAGTGTCCTT ATAAGAAGAG GAAGAGACAC CAGAGAGCTC CCTCTCTCCT CAAGAGCAGA 660
GGAAAGGCCC GGGGAGTACA CAGGCAGAAG ACAGCCATCT ACAATCCAGG AAAAGAGCTC 720
TCTCCTGAAA CCGAATTCCA CAGCACCTTG ATCTTGGACT TCTAGCCACC AGAACGGTGA 780
GAAAATAAAT GTGGTTTAAA CCACCCGGTC TGTGGTACTT AGTCATGGCA AACCAAACAG 840
ACTACTACAC AAGTTCTGTG CTGATATCTT TTCTTAGATT AGTTTGTTTT ATCCTTAAAC 900
AATTTGTGCA GTAAATATTT ATATTTCCAT TTTATGGAGA AGGAAACAGA AGCAACAAGA 960
AGTAATGTGC CCAAAGTCAC ACAGTCAAAG ACAGACTCCA ACCTTATTCT AATGAGGTTA 1020
TTCTAAGCCC CAGCCTCTGG ACAGCATTGT ACCTTCTGAT CCCCAACTCT TACCTGGAGG 1080
GGAGGGGACA ATCAGGAGAG GGAGAGTGGG GATGAGGTGG GCTGATGTTC CCAGGTCCCT 1140
AGGTGGCCCT GCTGGTCACA CACTGGCTCC CACACACACA CACCTGATCC CTCCTCCCCC 1200
ATGTCCCTGG CTCACTCTGC CCCAAATGGC AAGTTTCCAT CCCTCCTGCC AGCCTGGTCT 1260
CCGGACCTTG CCCCAGCTAG AGATCAGGAC AGTCCTCAGG CAGTGCTGAA AGCCCCAAAT 1320
CAGAGATCAC TGCAAGGTGA CACCTTGTCA CTGCCCTCAC ACTAGAGGAG GGAAACACAT 1380
ATGGTTGGCA GTGAACAGAT GGCCCTTCAG TGTCGGTTCT CTTGCCCTCA GCTGTGACAG 1440
GTCCCTGCTG GGGAGGGAGG CCCGTAGCCT TAGGGGTGCA 1480
|
