Tag | Content |
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EnhancerAtlas ID | HS108-12356 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr14:75700770-75701700 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr14:75700959-75700980 | AAAAAAAAAAAGAAAGAAAGA | - | 6.25 | IRF1 | MA0050.2 | chr14:75700969-75700990 | AGAAAGAAAGAGAAAGTCAAG | - | 6.96 | RREB1 | MA0073.1 | chr14:75701313-75701333 | CCCCACCCCACCCGCCACAG | + | 6.18 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_25845 | chr14:75700606-75701838 | Duodenum_Smooth_Muscle | SE_26738 | chr14:75700953-75701671 | Esophagus | SE_28748 | chr14:75700247-75701790 | Fetal_Intestine_Large | SE_37398 | chr14:75700795-75702224 | HSMMtube | SE_50151 | chr14:75700862-75701786 | Sigmoid_Colon | SE_52363 | chr14:75700038-75701856 | Small_Intestine | SE_53348 | chr14:75700993-75701872 | Spleen |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr14 | 75700902 | 75701698 | chr14 | 75701379 | 75701456 |
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| Number: 1 | ID | Chromosome | Start | End |
GH14I075233 | chr14 | 75700420 | 75702502 |
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Enhancer Sequence | AAACCCTGTC TCTACTAAAA ATACAAAAAT TAGCTGGGCA TGGTGGTGTG CACCTGTAAT 60 CCCAGCTACT AGGGAGGCTG AGGCAGGAGA ACTGCTTGAA CCCGGGAAGC GGAGGTTGCA 120 GTGAGCAGAG ATTGTGCCAC TGCACTTCAG CCTGGGTGAC AGGGAGAGAT TCCATCTCAA 180 AAAAACAGAA AAAAAAAAAA GAAAGAAAGA GAAAGTCAAG AACAAAGTTT CTTCATGAAC 240 AAAGGGCATG AAGAAACCTG TTCAGTAGCA GCGGGGCTGT TCAGTGGGGC CAATGTTCAG 300 TGGGGATAGT GAGACCAGAG GTTGAAAGCC GGTAGAGAGT ACAGAAAAGG TGGACAGAAT 360 ACTAAGACAA AGTACCGTGT ACTTTCAATA AGCTCTTGGT CTCAACTCTT GGTGACTGTA 420 CAAGGTAGGC CAAAGACAAA AACTGTCCAA CGACAGAAAT TTCACTTTGA AGTTCCCTCC 480 ACTCCATTTC TCCACCCCCT TCCTTCCTAT CTCCTTTAGC AAAGTCCTTT CCTCAGAGAT 540 CTCCCCCACC CCACCCGCCA CAGCCCCACA GCCCTGTCGG TCTAGCAGGG TGAGTAGCCG 600 CACTGTCTCT GAACCCTTAC GCCTGGACTT TGAAGGGGGA ACAGATTCTT GCTTACTGAG 660 TCAGCCTCGG CTGCTTCCTT TTTGTGCTTG AAGAAGCCAA AGAGTGAGCA GATTGGAGAG 720 GACTAAAAGA AGCCAGAGAT GCTGGTCAAT TGACACAAAA ATAAAGAGCT AAGGGAGAGG 780 TTGAGAGAGG GAGAGCAATA TCTATGGGTG TCTGGAATTT TTAAAGGGCT CAGAGGAGGA 840 GGGGGCCGGG CGTGGTGGCT CACGCCTGTT ATCCGAGCAC TTTGGGAGGC CAAGGTGGGC 900 AAATCACGAG GTCAGGAGTT TGAGAGCAGC 930
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