Tag | Content |
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EnhancerAtlas ID | HS051-18478 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr22:31709100-31710020 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr22:31709431-31709450 | TGGCTCCCCCTGCTGGTCG | - | 7.37 | NKX2-3 | MA0672.1 | chr22:31709129-31709139 | TTCAAGTGGT | - | 6.02 | SOX10 | MA0442.2 | chr22:31709513-31709524 | AAAACAAAGCA | + | 6.02 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_41921 | chr22:31709432-31710068 | LNCaP | SE_62272 | chr22:31668337-31710103 | Tonsil |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr22 | 31709586 | 31710000 | chr22 | 31709138 | 31709209 |
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| Number: 1 | ID | Chromosome | Start | End |
GH22I031312 | chr22 | 31708950 | 31710130 |
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Enhancer Sequence | TCGGCTCACT GCAACCTCCA CCTCCAGGGT TCAAGTGGTT TTTGTACCTC AGCCTCTGGA 60 GTAGCTGGGT CTACAGGCGC ATACCACCAT GCTTGGCTAA TTTTTGTATT TTTTGTAGAG 120 ACAGGGTTTC ACTGTGTTGC CCAGGCGGGT CTCAAACTCC TGGCCTCAAG TGATCTGCCC 180 AACTTGGCCT CCCAAAGTGC TGAGATTAAA AGTGTGAGCC ACCACACCCA GCCGGTTCTC 240 TGTAACTTAA ATGAGGAGAA AATTACCTGG GCCTTGAGAA ACAACTTTTA TCCTGGACCT 300 CTTTTGTCTA GCTGAAAAAT CTAAATTTTT CTGGCTCCCC CTGCTGGTCG CTCCTGGGCA 360 GTTGCGTACA AGTGCCCTGA TAGGATTGGA GCCAGAGCCA AGTTTGGGAA GGGAAAACAA 420 AGCATTGTTG GTAGAGTGCC CTGACCAGTC CAGGCAGGTT TGAGGAGGAG GAAAGCAGCT 480 TGTTGAAAAC AGTTCTGGGA AGTGCAGCTT TCTGTGTAAA GGGCAAGGAA GGTGGCCCAC 540 TGCCAGCCAA AATCAGGAGA GCAGGGATTG GGGCTACAGC TTCCTGGTCT GCAGCACTGT 600 AGACCATGAG AATCGTGACC ACACGAGCCC ATAAGTGAGC TGGTCATTAT GTGAGGATCA 660 GACCCTATCT TGAGAATGGA GATGGGCTCC TTTTCTAAGA CAAAGCAGTC TGGGGTCAGA 720 CATAGTCACC ATGCAGGCAT AGTACCTACA GTGTTTGTTT TATTTTGGTA AGAATGGTGG 780 TGAATGTAGA TGGGAGCATC CCCAGAGTTC ACAGTCCTGC GTTGGCTACA TGACCGTACT 840 ATCTCCCAGT TCTTAAGACC ATTAACAACT CTGTGGAGCT CTGGGTGGAG CTTCTGCCAG 900 GGCCTTCCTT CTCCACCCTC 920
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