Tag | Content |
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EnhancerAtlas ID | HS108-02172 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr1:85170510-85171190 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXH1 | MA0479.1 | chr1:85171052-85171063 | TGTGGATTGGA | - | 6.62 | HNF1A | MA0046.2 | chr1:85170909-85170924 | AATTAATGATTTACA | + | 6.76 | HNF1B | MA0153.2 | chr1:85170910-85170923 | ATTAATGATTTAC | - | 6.67 | SPI1 | MA0080.4 | chr1:85170720-85170734 | AAAAAGAGGAAGCT | + | 6.24 |
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| Number of super-enhancer constituents: 3 | ID | Coordinate | Tissue/cell |
SE_27979 | chr1:85169473-85172789 | Fetal_Intestine | SE_28841 | chr1:85169244-85173420 | Fetal_Intestine_Large | SE_63335 | chr1:85154996-85182414 | NCI-H82 |
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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 |
GH01I084703 | chr1 | 85169245 | 85173420 |
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Enhancer Sequence | CAATTCCATT GCTTAAAAAA ATGAAGTAAT ATATTCATAG AGTATAAAAT TCAAAATGTA 60 CAAAAGGACA TGCTGTGAGA AGCTTCTCTT CTACTCCTCA CCAAGCCACC CAGTTTCTCT 120 TCTCAGGAAC AACCAGGAGT GTCTGTTTCT TGTTTATTCT TTCAGGGACT TGAATTATTT 180 CTTAAAAGAT GTATGCAAGG TACTCAAGTG AAAAAGAGGA AGCTGAGCAT TGCAGACAAA 240 GAGAACAGCA TGAGACTGTT GGGGAGTAGG ACCCATGAGG CGGAAGGCAG TGAGAGAGTC 300 CTCTCCAGGA GGGGCCTTAC CATGCTAAGG AATTTGGATC TGATCCTGAA GCATTAGGAA 360 AGCCATTAGT AGATTTAGAG CAGAGGATCT GCCTGATGAA ATTAATGATT TACAAGGAAC 420 ACTCTGGCAG AAATGTGAAG AATGGATTGG AGAGAGGCGA GATCAGTGAA AGATACCAGT 480 TAGGAGGCAA TTGTAATTGT CCAAGGAAGA ACTAATGAGG ACTTAAATCA AGACAGAATC 540 GGTGTGGATT GGAAGGGGGG CCAACTCTGG TTGTTAAGGA AGAAGGATGA ACAGCATTTT 600 TGGATCAATT GGATTCCAAT GAATTTAATT CCTGTTCTCT CCTTATCTAA GAATTGCCTA 660 AGAGTCACAT GCCAAGAATA 680
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