Tag | Content |
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EnhancerAtlas ID | HS060-11366 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr15:59529390-59530600 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Foxa2 | MA0047.2 | chr15:59530517-59530529 | ACAATGTAAACA | - | 6.04 | IRF1 | MA0050.2 | chr15:59529993-59530014 | AAAAGGAAACTGAAATTTGAA | - | 6.15 | MEF2C | MA0497.1 | chr15:59529417-59529432 | TGCTATTTTTGTAAT | - | 6.35 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_28166 | chr15:59528482-59529636 | Fetal_Intestine | SE_28782 | chr15:59528260-59529694 | Fetal_Intestine_Large |
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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 |
GH15I059236 | chr15 | 59528538 | 59530673 |
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Enhancer Sequence | TAGTTTTCAA ACATTTTATA ATGCATATGC TATTTTTGTA ATTTAAAAAA AGAAAAGAAA 60 AAGTGGGCAC TCTGAGGTTT CAAACCATGT GCCTTGAATT GATGCAAGCT TCCTTATTTT 120 AGAAGTTCTA AAATTAAACC TTGAAGCAAT ATTAATCACA TCCGGAGTAA CAAAGGCCAC 180 CTTCCGCTGG GTAGCCTTCC TGCATGGGGA GAGCCTTTTG TTAATAATAT ATAGTCTGCT 240 CTTCAAAATC CCCATTCTTC CTACAAAATC CCCCTGAATT GATAATGACC TCAATTCAAA 300 ACATGCTTAA GTCAGTCAGA TTTTTCATCT TTCTATTGGT ACCCTTTGTG TTACCAGGAT 360 AGAATTAAAG AACCCCATAT CATATAAAAT GATGGTGGGA GTTAGTATGA AAAATGCAGA 420 CTGCTACAAG TTCATAGGAC AATATTTTTG TTCGCGCTTC GCGATAAAAA ATTTTAGGGC 480 GCAGAGCAAA TGTTCTTCTA TGAATATCCA GCCCAAATTA ATTGTTATCG ATTGCTGAGT 540 TACTCAAGGA AAGAGAAAAC ATTTGCTTGG GGAACAACCA AGCAAGGTGA CACTCCTATT 600 CCCAAAAGGA AACTGAAATT TGAAATAATT TTACATTTCA AAACAAAACA AAAGAAACAA 660 ATGAACAGAG AATTGAGCTG GCCATATAGC GAAACTCAGA ACTTTGCTGA ATTTCCTTGA 720 ACTAATAATA CGGTTTTAAA GAAATTATGG GGAGGCGGGA ACCATCCTCT GTTCAGAGCT 780 CATGACCTGC AAAAGTCTGA ACCCACCTAT GCAAGTCACT CACCATCCTA GTGCTATGCT 840 CCTGGCTTCC TGGTCACATG AATAAGAAAA CCAAACTGAA ATTTCGTAAG CTACAGTAGC 900 AAGTAGAAAA CCAGCAAGCC TGGGACGAGG TGTCACACTC TTCCAGAGGA CATGCTTACT 960 CACAGGCAGC AACTAGGTCG GGCAAATTCA ACTCCATGGG GAAATTATCT TTTCAAATGG 1020 TTGACATACT CAGATGATGT ATTTACTAGA TCCAGGGTCA ACACACACAC TCTCTCATTG 1080 GAATTACACG GTTTGGCAAC AATGAAACTC CATTTTAGAA GTTGTAAACA ATGTAAACAT 1140 TCAAGAATAT TGGAAAGTCC AAGCTTACAA TGGCACAACC ACCCAATATA ATACTGCACA 1200 GGCATTTGAA 1210
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