Tag | Content |
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EnhancerAtlas ID | HS101-16382 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr16:4997130-4998310 |
Target genes | Number: 17 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr16:4997847-4997865 | GGAAGGGAGGAGGGACAG | + | 6.04 | ZNF263 | MA0528.1 | chr16:4997252-4997273 | CCCTCCCTTCCTCCATCCATC | - | 6.06 | ZNF263 | MA0528.1 | chr16:4997244-4997265 | CCCTCTCTCCCTCCCTTCCTC | - | 6.08 | ZNF263 | MA0528.1 | chr16:4997240-4997261 | TCTTCCCTCTCTCCCTCCCTT | - | 6.84 | ZNF263 | MA0528.1 | chr16:4997245-4997266 | CCTCTCTCCCTCCCTTCCTCC | - | 7.13 | ZNF263 | MA0528.1 | chr16:4997248-4997269 | CTCTCCCTCCCTTCCTCCATC | - | 7.21 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_26593 | chr16:4997107-4998746 | Esophagus | SE_65358 | chr16:4991965-4999969 | 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 |
GH16I004947 | chr16 | 4997550 | 4998710 |
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Enhancer Sequence | CTCCATCCAT CCATCCATCC ATCCATCCAT CTCTTCATCC CTCCATTCCT CCATCCATCT 60 CTTCATCCCT CCATTCCTGC ATCCATCCAT CCATATCTTC ATCCCTCCAT TCTTCCCTCT 120 CTCCCTCCCT TCCTCCATCC ATCCATCCAT CCATCTATCC ATCCATCCAT CCATCCCTTC 180 ATTTGTCAAA TATTTACTAA GCACCTGCTA CGTGACAAGT CCTGTTCTAG GCACTCAGGA 240 TTCAAGATCA AGTACAATAG ACTCAGGTTC CTGCTCCCAG GGAGCTTGCT GTGGGAGACA 300 GGAGTGGGAA TGGACAAACA ATGTAAGTTT GAGGTCCCCT TGGGTGGATC ATGGCGCCTC 360 TTCTGTGTGC CCCAGGAGAC AAAGTCTGCA GTCGGCACAG AGTCACCGTC AGGTGGGGGC 420 CCAGGGACAC TATGAGGAAA GTGGCCAGAC TCCAGTCTGA GGGTGGTTGA GGACCCGGTG 480 AGGAAGGGGA GGCCTTAGCT TGCAGGGCGT CAGGTTCCCT CATCGTGTTT TCTGCATCAC 540 TGACATTTCC CAGGAGCCAG GCTCCTCCCC AACCCCCGTG GAGGATCTCG ACCTCTTGCC 600 CCCACAATAC CTCCCACAAG TCACTCATCC ATTTATTGAG CACCTACTGT GTACCCGGCT 660 CTGGGGATAT AGTAGCAAAC ACGATACATC CCTCACATCC TGGGGGCCCC CTGTCTTGGA 720 AGGGAGGAGG GACAGAAAAG CAAACAGATA ACCACATTTT TTACAAATGA AATAACCTAA 780 GTGCCCATCA GTGGGGGAAG CGGTGGTAAA TTACAAAACT GCCCTAGTCT GGGAGGAATT 840 CGGGGAGGCC TGTGGGCCTC ACAGGGAAGC TGAGGGTGTA GCAAGTGAAA AAAGGAAGCT 900 GCCTGCTATT AGGTGTCGTG TTTTGCCATT TCCGCTTCAG AACGGAGCTG CCCTGTGTCT 960 CCGTGAGCTC GTCCTCCACC TGCCTGCCTG CCTGGCTCTG CCTCCACTCT TTGTTCACGC 1020 TCTCTGCTGA GCTCAAACAT TCCTGCTGGG CCCAGGCAGC CAAGCCCCCA TCAGCCGCCT 1080 CCCAGGCCAT TCTCTAATCA CAAGCTCAGG CTTAATCCCC ACACACGCCC AGGACTCCGC 1140 TCTGGGCAAA TACTCCTCCT TTCAGCCCTG GAGTCCCTGA 1180
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