Tag | Content |
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EnhancerAtlas ID | HS159-00390 |
Organism | Homo sapiens |
Tissue/cell | Pancreatic_islet |
Coordinate | chr1:159851160-159852770 |
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: 2 | Chromosome | Start | End |
chr1 | 159852272 | 159852569 | chr1 | 159851477 | 159851987 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I159881 | chr1 | 159851078 | 159852772 |
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Enhancer Sequence | ACTTTCAATT CTCTCTCCAT TTCTAAATTC TCTCTGCACT TAAGGTGGCG ACACACCTCT 60 TGCAAGGTGA TCATACACTG CCTTGCAGGT CCCCACTCAT TTCATATGTG TTCGCTCTGC 120 CCCAGTTACA GGACAAGGGA CCTTGTGTCA CACATCCTCT CTTCCCCAAC AACATGTAGC 180 CCAATGCAAG GAAAATAGCA AATATTCGAT AAACCATTGA TAAATGAGGC AGGAAAGGTA 240 GGACCAAAGT GAGAGGCATG TGAGAAAGGA AAGAAAAAAA GTTCTTAGAC ACAGGGAAAC 300 ATTTGACGGA GATCAGAGTA CCAATGTGAA CAAGGTCGTT TTTAAGGAAG GATCCCCCTG 360 CCTTTCCCAG ACCTGAGCCT TCAACAGCTC TCAATGATCA GACCACTTCT GAGCCAAGCA 420 CATTCTCAGG TGCAGAGGGG CATCGGAATT AGGGGAACAG CTGGCCCCCC AATCACCTCC 480 AATCAATCTC AGACTCCTTA AGTTCTTCTA TTGATTAACT CACCCCACCT CCCACACTGT 540 TTCCAGCTCC CTCCATTTCT CCAAAGACTA AATCCCTCCC TGGCCTTCCA GGTCTTCCTC 600 AGCCCAGCTG CTGCCCTGAT TCATCTAACC AAGGTAACTC TCCCTGTGTG TCTTCCTGTA 660 GTGCTGGCTC TCTGCCAGCT TGGCTCACTG CCCAGTTCAA GGCTTCTTCC TTCAGGAAGG 720 CTTCTGAACC AGAGCGGTAT GGCAACTCTC TGCCTCTGAG GTCCATGTGG TGCGTGAGTC 780 ACAGACATTC CCTCTCTCTC TCACCATACT CATTTCTTTG CTCACTCCAC TTTTCCCTTT 840 CTGCCCCTCC AACTCTCTCG CTCCTTTTCC CCCTTCTCCC TTTCTTCCTT TCCTTCCTAA 900 CTGCTTCTCA CTGATTTTAG GCCTGCTATT TGTATCCCAG ACATCATTTA ATCTCACTGG 960 CCCTCAAAGC TAAAGATGCT GTTGATTTCT GATGTATGAC ATACATACAA TCATGTATTT 1020 ATTTACTTCT TTCCCTATTT ATTTACTTTT TGGATTGTTG TTTTTGTTGG CTCATTTCAA 1080 TTCCAAGACA CCAAAGGACT TTCCCTGTTT CTTTTGAAGC CCTTCCAAAG CAACCCCAGA 1140 TAAATTCCCT TCACTCTTTC CCCCTTTGTT AGCAAGGTGG GAAACGCTGC CCTTCGTACC 1200 ACCATGAGAT GATACAGTAG GTCTAAAGCT GGGAAGGCAC AGGTTTCCTT GCTAAAGTTG 1260 CCCAATAATA CTTCCTGGAG ACTCAGGGAG TGCCTGTTAG AAGGACATTA AAAGGATAAT 1320 GACACAACAT CAACATAATG GTGCTGACTC ATGGACTCCT AGAACTTCCT CAGTGAGCCC 1380 ACTAATTCCC ACTCCCCACA TCTAGTTGGA TTTTCCTGCC CTCACTTCTC ACCCACTACC 1440 TTGCATATTT GCCCCATAAC TTTCCTTCTT GGCCCTTTCC CACTCTCTCT CCCCTGAGCC 1500 AGGAAATGGA GTAACTTGGC CAGGTCTCTC ATTGCCTTCA CCCTGCTATT CTCCTTCTCA 1560 TGCAGTTCAC AGAGCTGTGT GCCCCTTCAG TTTCCCAACT ACCCAGGTGA 1610
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