Tag | Content |
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EnhancerAtlas ID | HS040-00855 |
Organism | Homo sapiens |
Tissue/cell | Esophagus |
Coordinate | chr1:21952970-21953790 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL2 | MA0478.1 | chr1:21953763-21953774 | GGGTGACTCAG | + | 6.02 | JUNB | MA0490.1 | chr1:21953763-21953774 | GGGTGACTCAG | + | 6.02 | ZNF263 | MA0528.1 | chr1:21953023-21953044 | AGAGGAGGGAGAGGAGGGGCT | + | 6.32 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_08200 | chr1:21949387-21953199 | Brain_Inferior_Temporal_Lobe | SE_31655 | chr1:21944407-21954108 | Gastric | SE_41934 | chr1:21952257-21953097 | LNCaP | SE_65280 | chr1:21952357-21954349 | Pancreatic_islets |
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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 |
GH01I021625 | chr1 | 21952154 | 21954748 |
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Enhancer Sequence | GGGGGATGTG AGGGAGGATA GACTTCACGG AGGAGAGGGT CATGGGTTCC CCAAGAGGAG 60 GGAGAGGAGG GGCTTCATTA GCAGGGCTAC CACACAGGCT TCTCCTTCCC CGGAGATCAG 120 AGACGTGGAC AGGGTCTCTC CCCAAGCTCT CCATTAGGCC TCCAGCCAAG CAGTGACCTA 180 CTCTGAAGAT GAGTAGACTG AGGCAGGGGC ACTGAGGGTT GCTGTGGAGG GTGAGCTTTC 240 TGGACTAAGC AGGGTGCCCC CGCCTCTACA ATGGACCCCT CCCTGAGCCT CTGGGAGTAG 300 CCGCCTTGGC ATTGAGGGGC TACCAGGGCT ACCGCTATTA CGAATGACAG TGACCGTGAC 360 CATAACTGAC GCTCATTGGG CCTACCACAT GCCAGGCCCT GTGCTGAGCC CTCGTTCTAG 420 GCCCGAGGGC ATGGCCTCCT CACCACACTG GTATTCCCAC TTTACAGACA GGACCCAGCT 480 GTGCACAGAG GTCACACGGC TGGCCGGCAG CAAAGCTAGC ATCTGCATGA GACCTGCCTG 540 AGTCTAAGCC CGGACTCTCT GCCCACACCA CACCCTTCCC TGAGGAAAGA AAGCAGGTCT 600 GGCGAGGGTG AAGTCAGCTC CTATCACCCT AAAAAGCCTG CCGAGGCCAC CTCTGGGGCA 660 GGGAGAGGAA ATGCCCAGTG GTTCCCGGGA TCCTGGGGCT GGGCAAGCAG GCCTGGCTTC 720 CGCTGCTGCC TAGGGCCACC CTGACGTGGC TGCACCTCTG CTCAGGTCCC ATCAAGAGAG 780 GCTGGTCCCT CGAGGGTGAC TCAGATGATC GCTGGTGGCC 820
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