Tag | Content |
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EnhancerAtlas ID | HS121-10468 |
Organism | Homo sapiens |
Tissue/cell | LNCaP |
Coordinate | chr13:113824840-113825900 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Gfi1b | MA0483.1 | chr13:113825069-113825080 | AAATCACAGCC | + | 6.02 | IRF1 | MA0050.2 | chr13:113825232-113825253 | TATTTCTTTCTTTTTTTTTTT | + | 6.2 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr13 | 113824882 | 113825230 | chr13 | 113825595 | 113825664 |
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| Number: 1 | ID | Chromosome | Start | End |
GH13I113169 | chr13 | 113823802 | 113826149 |
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Enhancer Sequence | ACATGTAAGT ATTTTATCAT GAGTTTTTAT AAAACCACAT TGGAAATACA CTATCCTATG 60 TAAGAATGAA ATGACAAATT TAAAACTGGA CTGTTTCTAA TGCAACATAG AACTGAATTT 120 ACTGTCAATA AAACTGAGAT ACTTATCAAC TCAGGAAGCA TATGTAAAAT ACCAGCAGAA 180 GCCTGGGCCC AGCGACAGGC AAGTGCTAAC TCACACTCGG CAAGGGAGGA AATCACAGCC 240 TACATAAGGA TGACTTCATT TCCCACTGAA ATTGAGCAGT TGTGGCATAA GAGATGGATA 300 ATTGGCTAAA AATCGGAAGA ATGGGGCTCG AATCCCCCAG CAGTTGAGAC CTCAGGCTGA 360 GGCAGTGGCC TTCTCATCGG CTTATCTGTG CCTATTTCTT TCTTTTTTTT TTTTGAGACA 420 GAGTCTCACT CAATCCCTCA GGCTGGAGTG CAGTGGCATG ATCCAGGCTC ACTGCAACCT 480 CTGCCTCCTG GGTTCAAGCG ATTCTCATGC CTCAGCCTCC CGAGTAGCTG GGACTACAGG 540 CATGCACCAC CATATCCCAC TAATTTTTTG TATTTTTAGT AGAAATGGGG TTTTGCTATG 600 TTGGAAAAGC TGGTCTTTAC TCCTGGCCTT AAGTGATCGA CCTGCCTCGG CCTCCCGAAG 660 CGCTGGGATT ACAGATGTGA GCCACTGTGC CTGGCCCTTA AATATTTTTC AATCAACAAA 720 ATAACGTGAA AACCACTTCT CAACAGCCAA TGTTTGACTG GCCTGGAGAC GTTCCACATC 780 ACTGCTTCCT GCTTTTTAAT CATTTCACCA CACCCCACTG CACTCCAAAA CAGAAGAACT 840 AACCTTGACT GTTTTTAAAG GCTGTGGCAC TTGGTTGCAA TCGTGCAATC TGTGAGTGGC 900 CTTTCTGTCC GCAGAAAGGC ACAGTGTCCA CACCACGGGG CGGTGAGCCT GCGGGTCCTC 960 CAGGGCCGGT CTCTCCCTCC TCACGTGGCT CCCTGAGAAG CTCGTTTGAG CATTATGTCC 1020 CCTTGAAAAT CAGACTGTAA AGAACTGACG ATTGTTCATG 1060
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