Tag | Content |
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EnhancerAtlas ID | HS051-26496 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr8:101913400-101914360 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Esrra | MA0592.2 | chr8:101913941-101913952 | ATGACCTTGAG | - | 6.02 | Esrrg | MA0643.1 | chr8:101913941-101913951 | ATGACCTTGA | - | 6.02 | Gata4 | MA0482.1 | chr8:101914235-101914246 | GGGAGATAAGA | - | 6.62 | HNF1A | MA0046.2 | chr8:101914335-101914350 | GGTTAATCATTAGCA | - | 6.04 | HNF1A | MA0046.2 | chr8:101914335-101914350 | GGTTAATCATTAGCA | + | 6.12 | HNF1B | MA0153.2 | chr8:101914336-101914349 | GTTAATCATTAGC | + | 6.17 | HNF1B | MA0153.2 | chr8:101914336-101914349 | GTTAATCATTAGC | - | 6.32 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_10716 | chr8:101911992-101915431 | CD19_Primary | SE_11102 | chr8:101911654-101916492 | CD20 |
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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 |
GH08I100899 | chr8 | 101911621 | 101915177 |
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Enhancer Sequence | AGAAAACATC ATTTAAATTA ATTTCAGGTT AGGTGAGGTG GCTCATGCCT GTAATCCTAG 60 CACTTTGGGA GGCCAAGGCA GGAGGATTGC TTGAGCCCAG GAGTTTGAGA CCAGCCTTGG 120 CAACATAGAG AGACCCTGTC TCTACAAACA AAAAACAAAA CAAATAGCCA GGTGTGGTGG 180 TGGAGATATT TTGCATTCTT TTTTTATAGT AAGTCTTCAA AATCTAGCAC ATCTCAGTTT 240 GGACCAGCCA CATTTCAACT TCTTAAGAGT CACATACAGT GAGTAGCTAC CATATTGAGC 300 AGTGCAGGTT TCGATCCTAT GCTTAGAAGG ATCATGACCA ACAAATAAAG GCAGTTCAAG 360 TTCTCTAGTG TTCCAGTGTG AGCTGGAAGG CAGTTGTCTC TACAAAGGGA TCTTTTTCTA 420 TCCAAGGCAA CCACAGGGCT GGGGATGGTA GGTGTGGAGC TGTACCTTAA AGCATATGTT 480 AATGCTCTGG AAATCCATGT CTTTCCTTCA GACATTTCCC TCCTCTCTGT TCATAAGCTA 540 CATGACCTTG AGCAAATCAC CTCCTCTCTT GGGTTCTCAG CTTCCTCATT TGCAAAATGA 600 GAGGGTTGAA CTTGAAGATG AGGCCCCTTC TGTCTTTGAT GTGTCATCAT TCTCTGAACC 660 ACCACTCGGG CAGCATCCTC TGGGGAGCAG CCACCCACTC TTGGGAGCTC TCAGGCACTT 720 CCCAGAGCTG CCACCTGCTC TGAGCTACCT CTAGAGTAAG TGGTGCTCGG AGGCTGGGAA 780 ATGAATATTA AGCTGCCTAC CCAACCTAAG AGTAGCTGCT CCCTTTGGAG AGGTGGGGAG 840 ATAAGACTTT GGATGTGTAG AATTCTAGGC GTACCTTTCT TTTTGGCCTA CGCATGTATT 900 TTTAAGGGGC ACCTCTTGCT TCCTGGAGCT GCTGTGGTTA ATCATTAGCA ATAGAAGATA 960
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