Tag | Content |
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EnhancerAtlas ID | HS101-03855 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr1:209989520-209990220 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:209989737-209989755 | GGAAGGATGGGAGGGAAG | + | 6.13 | RREB1 | MA0073.1 | chr1:209990187-209990207 | TGTGTGTGTGTGTATTGGGG | - | 6.29 | ZNF263 | MA0528.1 | chr1:209989734-209989755 | GGAGGAAGGATGGGAGGGAAG | + | 6.81 | ZNF263 | MA0528.1 | chr1:209989731-209989752 | AGAGGAGGAAGGATGGGAGGG | + | 6.9 |
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| Number of super-enhancer constituents: 4 | ID | Coordinate | Tissue/cell |
SE_27309 | chr1:209987826-209990934 | Esophagus | SE_34153 | chr1:209987800-209991306 | HCC1954 | SE_35823 | chr1:209987333-209991619 | HMEC | SE_64223 | chr1:209987771-209991222 | NHEK |
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| 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 |
GH01I209814 | chr1 | 209987498 | 209991386 |
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Enhancer Sequence | CGGCAGCATT TCTAGTTCAG GCCCAGACCC GTCCTGGCAG CCTGGATTCC ACTGCCTAGG 60 CAGGAAGCTC ATCTCAGCCC AGTGACCTTT TCTCTCTGTT TTTTGTCACA GAGGAATTTC 120 CATGCCAGCA GTATGGGGCA ATGGGGGTGG GTGGCCAAAG GTTTCCCCCT TAAGCCACAA 180 GAGCCATGGA GTGGAGGTAA GCTAAGCAAA CAGAGGAGGA AGGATGGGAG GGAAGGATCA 240 GGAAGATTTA GAGAGTCCAT TCCTCAGGCT GCTTCATCCT CAAATTCCAA GGTAAATAAA 300 GGTGTTGGGA AGGATGCACT ATATGTCCAG CTGCCCAGCC CTGAAGATCC TCCCCCTAGA 360 GAACTGAGAC AGGAGTTTTC TCACATTCCC ACATGCAGGA GGGAAAGAGG CTGGGCCTGG 420 GCAGGTCTAG AGAGTTCTGT TCCCCTGCCC CAGGGGAACA CGCCTAGGCT TGCTGACCTC 480 TCAGGTAGGA GTCTGTCAGG TTGGAAGCTG GGCCTCTCAT TGTGTGTGTG TGTGTGTGTG 540 TGTGTGTGAG AGAGAGAGAC ACGTGTGTGT GTGTGTGTGT GTGAGAGAGA GAGACACGTG 600 TGTGTGTGTG TGTGTGTGAG AGAGAGAGAC ACGTGTGTGT GTGTGTGTGT GTGTGTGTGT 660 GTGTGTGTGT GTGTGTGTGT ATTGGGGGAG AGAAGCATAT 700
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