| Tag | Content |
|---|
EnhancerAtlas ID | HS187-23482 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr8:10568300-10569240 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr8:10568504-10568515 | AGTGACTCATG | + | 6.14 | | Nfe2l2 | MA0150.2 | chr8:10568881-10568896 | TGCTGACTCACTCTG | - | 6.69 |
|
| | Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
| SE_27229 | chr8:10568103-10569324 | Esophagus | | SE_34980 | chr8:10563777-10574930 | HeLa | | SE_38608 | chr8:10567056-10571208 | HUVEC |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH08I010709 | chr8 | 10567484 | 10570956 |
|
Enhancer Sequence | TCCGGTCCAG TTGGTAGGAA GCCTCTGAGA TTCCAAGATG GGCAATGACA GGACAAAGCA 60
GGAGGAAAAG TGCCCATTTA TGGAGCAAGC ACTTGCTTTG AGTCATTTGA CCACAGTGTG 120
AAAGTCATTG CACCTCTCCA CTGGGTGAGG GGGTCTCAGG ATCCCAATTC CTCCAAATGA 180
GGAAGCCGGG GCTCAGGGGA ATGCAGTGAC TCATGTGGGT CTCAGCTAAC AAGGTGGAGG 240
AGCTGCGCAC TGGGCCTAGG TCGCTCCCCT TTGAATCGCA CTTCCCTTCC CCTCAGCAGT 300
GAGCTGGATG GGGCTCCACC TTGGGGCATA GGAACCAGGA AGACCACATG CTGCAGGGCC 360
ACAATCCAGC TGGACAGGAG AGACACACTT AGGAAAATGC CCACCACAAG CCTCCTGTGC 420
AGTTTCTAGC AAAGGGAGGC ATCTCCAGGC CAGGGGCACC CCGGGGCCTT TGCCCCTCCT 480
CCCCAGGAAG ACAGGTTTCC GCCCTGAGCA AGACGGCACA CGTCAGAGGC TGAGGCCAAC 540
CCGGGGCCAG TTCCCAGCAC TCGGGGTAGC TGGGGCCAAG CTGCTGACTC ACTCTGTAAC 600
CCTCAGACAA GTCACTTCCC TCCTGGGTAC CCAGCATGGA ATTGAAAGTG GGCATCCCTA 660
TGTCCCAGGC TGCCAGAGAG GCCTTTCCAA CCAGGGCTGA CTGGCTGGGT GGGGAGGGGA 720
TCGGATGATT GTGAGCAGAA TGGGAAACAT GTTCTTTGGA AACGGATATT CAATGGAATA 780
ACAGAACTTA ACATTTAGAA AGTGAGCAGT GGCTCAAGCC TGTAATCCCA GTACTTTGGG 840
AGGCTGTTTG AGTCCAGGAG TTCAAGACCT GGGTCTGAGC AACATAGCAA GACTCCGTCT 900
CTACAAAAAA TTAAAAAATT AGCCAGGTAT GGTGGCACAC 940
|
