Tag | Content |
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EnhancerAtlas ID | HS099-21293 |
Organism | Homo sapiens |
Tissue/cell | HSMMtube |
Coordinate | chr8:8939460-8940340 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
HSF1 | MA0486.2 | chr8:8939647-8939660 | TTCTAGAACCTTC | + | 7.12 | SOX10 | MA0442.2 | chr8:8939739-8939750 | TTCTTTGTTTT | - | 6.62 | TCF7L2 | MA0523.1 | chr8:8940022-8940036 | TTCCTTTGAAGTCC | - | 6.11 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_27764 | chr8:8931616-8940631 | Fetal_Intestine | SE_28660 | chr8:8931504-8940665 | Fetal_Intestine_Large | SE_38116 | chr8:8937421-8942637 | HUVEC | SE_56603 | chr8:8938338-8941106 | u87 |
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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 |
GH08I009073 | chr8 | 8931488 | 8940483 |
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Enhancer Sequence | AAGTTGTTCT CTCTGTATGA AGAATTCTGC CTTCATCTTA GTCCATCTGG ACCCTGCAGC 60 CAACTTTTAA AGTCACTGTG TCCCCCCACC CCATTAGAAC TCTTAATATT TGTTTAACCT 120 CAGAGTAGAA TGGAAAGCAT GAATGGCAGA TATTTCTTAC GACTCCAGGA AGTGAAGTTT 180 AGTCTCTTTC TAGAACCTTC CATCAGGTGA GGTCCACTAT GAGCCTGGTT TAGAGGGGAA 240 GGAGAATGGA GACCCTCACA ATGTCCTAAG ACTCTTGTTT TCTTTGTTTT TCTTGTTTTC 300 CTCTTACTCC TTTTACCAGA ACTTCTGGCA AGTAACATGT TGACTCATGG TGTTTTATCA 360 CTTCCTTCCT CTGGCTCACG TCCAGTAGAC ATGCTAATGA GTTGCCAAGT CACCAGTAGG 420 CAGGAAAAGA CAGAAGGGCT TCTCTGCCAT GGAAACCTGA TCATCTGGTG TTAATATTCT 480 GAAAATGACA TTCACAAAAT GAGAGTTAAG CTGGATGAGA AGGTATCTCC TGCTTTCTGG 540 CATGAAATCA TTCTTCCTTT GTTTCCTTTG AAGTCCATAT CTGTGTAAAA GATGCAACAG 600 CAGGAATGAT CTGTACTTCT TGGGGGTCTT AATCTCTGCT GTGTTGAAAG GATATTGAAA 660 GAAATGGATG AGGACCTACA TCTGGGCTCC TCATCTTAGA AAGTAGGCAC CTGCTTGGGA 720 ACACTTAGGC AAATGGATTC TCTCCTTCCC CATTTCCCTT CAGGGGCCAG AAGGTCGGAC 780 AGAAAGTCCA CCCTTGAACC TATCTAACGT CTAGGAGAAA GTCTTTCTAG AAACATAGAG 840 AAAGTGAATG ATGAGATGCC CGAAGAGTCA TAATAGCAAG 880
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