Tag | Content |
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EnhancerAtlas ID | HS161-01298 |
Organism | Homo sapiens |
Tissue/cell | PC3 |
Coordinate | chr1:178499020-178500120 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Gata1 | MA0035.3 | chr1:178499984-178499995 | TCCTTATCTCT | + | 6.02 | SOX10 | MA0442.2 | chr1:178499811-178499822 | TTCTTTGTTTT | - | 6.62 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I178530 | chr1 | 178498781 | 178499981 |
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Enhancer Sequence | AGGCCTGCAA TGAAATGAAT TTTGATCTAC CTTAAAAAAT AAACAAATGA CTTACAGTTA 60 TTTTGAGAGG AGGTAGGAAA TAAAATAATA GGAAAACGTG AGTGGGTGGG GATCAGGACT 120 GGCTATTCTA GAGGACAGGG GTGGGTCCCT TGTAACACAG CATCTCACTC CTGTCAACCT 180 GGTGGCCAAT GACAACAGAG TGAGGGGCAG TTGGCTCACC CCAGCCCTCC CATAGGTAAC 240 AGGTGCGGCA GCCCCAGGCC TTGACGCATG TGGTCATCAG AGAAACATGA GGGTGAGTCA 300 TCTGGGAGCA ATTAAGAGGG GAGGCCCAGG AGGAGGCCAG ACTGTGTCAT CCATCCCATC 360 ACTGCCACAG CACTGGCCCA GTGCCCACTC ACAACATTCC TTCTCCTGGG TCACAGGCCA 420 CAGGCCAGCC CAGAAGGTGG CTGAGGATGG GCTCAGGCAT CCAACACTTC TGACTGGGGC 480 CCAGATCCAT CTCTCTTAAA CTCAGCAGCT CTGAGGATCC CCCAATTCCA TGGCAACGGG 540 CTGCCTACCC ACCTTCCCAA GGGGTGCTAC TCTGACTTGC CACAGTCTAG TCTCAGCAAA 600 CTGAAGCTGT CCTTTAAAAA CATAAATTAG AACATGTCAC TCTTCAGCTC AGAACTTTCC 660 AGTGTTTTCC CACTTCTCTC AGAGCAAAAT GCAAAGTCAA TGGTTCACAA AGCCCTACAG 720 GATCCGCCCT GCTGCCTTCC CCATCCCTAA CCCTGTACAG TATTTCACTT GCACTTTCTA 780 GCCATGCTGG TTTCTTTGTT TTTCTTCAAA CACAACACAT ACCCTCTTGC CTCAGGGCCT 840 CTGCACTTGC AAACCCTACC CCCTCTCACC ACCCTGCCAC CACCATCACT AGAATTCTCA 900 GCCTTCCAGT CGGCCAGCTC CCTCGCCTCA AAGTTACCTT CTCAGTGGCC CCCAGTCCCA 960 GCATTCCTTA TCTCTCTTAC TGTCTGCTTT ATTTTTCTCT CCAGCACTCT TGTCACCAAC 1020 TCACATACCA TACAGTTTAC TTATTTGTTT ATTGTCTGTC TTTTTCTACG AGAATCTAAG 1080 CTTTTTGAGT GTGGAGATTT 1100
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