Tag | Content |
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EnhancerAtlas ID | HS048-02533 |
Organism | Homo sapiens |
Tissue/cell | Fetal_small_intestine |
Coordinate | chr1:159851320-159852390 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr1:159852039-159852057 | CTTTCTTCCTTTCCTTCC | - | 6.06 | EWSR1-FLI1 | MA0149.1 | chr1:159852030-159852048 | CCCTTCTCCCTTTCTTCC | - | 6.13 | RREB1 | MA0073.1 | chr1:159851625-159851645 | CCCCCAATCACCTCCAATCA | + | 6.01 | ZNF263 | MA0528.1 | chr1:159852021-159852042 | TCCTTTTCCCCCTTCTCCCTT | - | 6.02 | ZNF263 | MA0528.1 | chr1:159852018-159852039 | CGCTCCTTTTCCCCCTTCTCC | - | 6.33 | ZNF263 | MA0528.1 | chr1:159852030-159852051 | CCCTTCTCCCTTTCTTCCTTT | - | 6.37 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_09609 | chr1:159849306-159853172 | CD14 | SE_27216 | chr1:159851194-159853009 | Esophagus | SE_34829 | chr1:159848784-159853407 | HeLa |
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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 |
GH01I159881 | chr1 | 159851078 | 159852772 |
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Enhancer Sequence | CTTCCCCAAC AACATGTAGC CCAATGCAAG GAAAATAGCA AATATTCGAT AAACCATTGA 60 TAAATGAGGC AGGAAAGGTA GGACCAAAGT GAGAGGCATG TGAGAAAGGA AAGAAAAAAA 120 GTTCTTAGAC ACAGGGAAAC ATTTGACGGA GATCAGAGTA CCAATGTGAA CAAGGTCGTT 180 TTTAAGGAAG GATCCCCCTG CCTTTCCCAG ACCTGAGCCT TCAACAGCTC TCAATGATCA 240 GACCACTTCT GAGCCAAGCA CATTCTCAGG TGCAGAGGGG CATCGGAATT AGGGGAACAG 300 CTGGCCCCCC AATCACCTCC AATCAATCTC AGACTCCTTA AGTTCTTCTA TTGATTAACT 360 CACCCCACCT CCCACACTGT TTCCAGCTCC CTCCATTTCT CCAAAGACTA AATCCCTCCC 420 TGGCCTTCCA GGTCTTCCTC AGCCCAGCTG CTGCCCTGAT TCATCTAACC AAGGTAACTC 480 TCCCTGTGTG TCTTCCTGTA GTGCTGGCTC TCTGCCAGCT TGGCTCACTG CCCAGTTCAA 540 GGCTTCTTCC TTCAGGAAGG CTTCTGAACC AGAGCGGTAT GGCAACTCTC TGCCTCTGAG 600 GTCCATGTGG TGCGTGAGTC ACAGACATTC CCTCTCTCTC TCACCATACT CATTTCTTTG 660 CTCACTCCAC TTTTCCCTTT CTGCCCCTCC AACTCTCTCG CTCCTTTTCC CCCTTCTCCC 720 TTTCTTCCTT TCCTTCCTAA CTGCTTCTCA CTGATTTTAG GCCTGCTATT TGTATCCCAG 780 ACATCATTTA ATCTCACTGG CCCTCAAAGC TAAAGATGCT GTTGATTTCT GATGTATGAC 840 ATACATACAA TCATGTATTT ATTTACTTCT TTCCCTATTT ATTTACTTTT TGGATTGTTG 900 TTTTTGTTGG CTCATTTCAA TTCCAAGACA CCAAAGGACT TTCCCTGTTT CTTTTGAAGC 960 CCTTCCAAAG CAACCCCAGA TAAATTCCCT TCACTCTTTC CCCCTTTGTT AGCAAGGTGG 1020 GAAACGCTGC CCTTCGTACC ACCATGAGAT GATACAGTAG GTCTAAAGCT 1070
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