Tag | Content |
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EnhancerAtlas ID | HS187-23473 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr8:8939360-8940160 |
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 | TCTTATGAAA AATAAGCAAT TTAATTATTC TATGTCTAGA CTTCTCATTA GCCTGCACTG 60 GAAGACCAAA TAAACCCATT AATATTGTTT TTCTGAGCAA AAGTTGTTCT CTCTGTATGA 120 AGAATTCTGC CTTCATCTTA GTCCATCTGG ACCCTGCAGC CAACTTTTAA AGTCACTGTG 180 TCCCCCCACC CCATTAGAAC TCTTAATATT TGTTTAACCT CAGAGTAGAA TGGAAAGCAT 240 GAATGGCAGA TATTTCTTAC GACTCCAGGA AGTGAAGTTT AGTCTCTTTC TAGAACCTTC 300 CATCAGGTGA GGTCCACTAT GAGCCTGGTT TAGAGGGGAA GGAGAATGGA GACCCTCACA 360 ATGTCCTAAG ACTCTTGTTT TCTTTGTTTT TCTTGTTTTC CTCTTACTCC TTTTACCAGA 420 ACTTCTGGCA AGTAACATGT TGACTCATGG TGTTTTATCA CTTCCTTCCT CTGGCTCACG 480 TCCAGTAGAC ATGCTAATGA GTTGCCAAGT CACCAGTAGG CAGGAAAAGA CAGAAGGGCT 540 TCTCTGCCAT GGAAACCTGA TCATCTGGTG TTAATATTCT GAAAATGACA TTCACAAAAT 600 GAGAGTTAAG CTGGATGAGA AGGTATCTCC TGCTTTCTGG CATGAAATCA TTCTTCCTTT 660 GTTTCCTTTG AAGTCCATAT CTGTGTAAAA GATGCAACAG CAGGAATGAT CTGTACTTCT 720 TGGGGGTCTT AATCTCTGCT GTGTTGAAAG GATATTGAAA GAAATGGATG AGGACCTACA 780 TCTGGGCTCC TCATCTTAGA 800
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