Tag | Content |
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EnhancerAtlas ID | HS121-24843 |
Organism | Homo sapiens |
Tissue/cell | LNCaP |
Coordinate | chr21:42851210-42852400 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZNF263 | MA0528.1 | chr21:42852183-42852204 | GGAGGAGGCAGGGCAAGGTGG | + | 6.05 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_31458 | chr21:42851460-42853539 | Gastric |
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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 |
GH21I041479 | chr21 | 42851744 | 42852577 |
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Enhancer Sequence | TAAAAAAGAA AACCTTATTT GTGATAATGG TTAAGGCATA AGCAAACACA AATCCTATAC 60 TATGTCATAA TACCGCTCAT ACGACATTCA GAATAAGAGG GAAAAACCTT AGCATTTAGG 120 AAAAAAAATC ACACGTTCTA ACCAAGTGCT AGAATATTGT AACGATTTTT CGATTCAATA 180 ACCCTAAAGT GTCAGACAAA ATTCCTTCAT TGGTCGTGTT TCTTATCCAG GTTAGGATCA 240 AGAAACTATG AGAAGGACAT AGGATTGTAT AATCATACAC ACATTTAATC TAATAAAAGG 300 TACAGATGTT AACATGGCCC CAGTTATCAA TTCCACCAGG TTCCTGGACT GTGATGGGGG 360 GGCTTTGCTG TGTAATTCAC CCCTGCTGTT TAGGGATGTC ACAGTGACTA GCTAAGATGC 420 CAACTTTCTC ACCGAGTGGT AATTCATTCT GAAAACTGGC ATATTGAATA CCCTAAAGTT 480 GCATAGAAAT CACCTGGGGA CCCTCCCATG GAAAACAAAG TGGCAGTAGC ATCCTACCAC 540 CCTCTCCCCC GATGCCTGAG GGCTGCCGCA TCTCCCCAGG CAGTGCTGGT AAATGGTAAC 600 CACCGCCCCA CCCCCGTTAG GAATCACTGT CAGGCGACAC ACACCCTGTT AAGCCTTCCC 660 ACCTTCCCTC AGAGCTACGA GCAGGAATGA CATTTTTTAA GTATCAGTCT GATTGATTGA 720 TTCTCTCCCC AGCTCAAAAG GCTTCCATGG CTCCCGAATG AAGTGAAACT GGCACAGGAT 780 TTGTCTCTGC TGCTCTCCCC AGCCCAACCC TCCTCGCCAG CTGTTCTGGT CCAACCTCTA 840 CCCAGGGAGG TGAATGGACC CTGGCTGAGA GGCACCTTGG AAAAAGAGGC ACCTAACGCC 900 CTCAGCCTAC CCCTCTGACC AGATGACCAC AGCACTGGGC ACTCCCGAGC AACCAGGAGT 960 CTATAGAGGC CAAGGAGGAG GCAGGGCAAG GTGGCAGTGA GCCAAGGTCT GTGTGCTGGG 1020 CACAGCCCTA GCAGGACAAA TTCCACCTGC TGGTTATAGG GCTCAGCTTT TGGAAGGTGA 1080 CAATTGTCCC CAGCACTCAT GTGCCGGTGC TTTCACAGGG AGGCAGAGAG AGGGTCTTCT 1140 CGTGTTTCTG CTGTCTGTTA CTGTCACTCG GCGGGTGCTG CCCCATACTC 1190
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