Tag | Content |
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EnhancerAtlas ID | HS109-13312 |
Organism | Homo sapiens |
Tissue/cell | Kasumi-1 |
Coordinate | chr2:231321890-231322580 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RUNX1 | MA0002.2 | chr2:231322246-231322257 | TTCTGTGGTTT | + | 6.32 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_09384 | chr2:231320724-231324992 | CD14 | SE_10266 | chr2:231321351-231322930 | CD19_Primary | SE_10885 | chr2:231272649-231341656 | CD20 | SE_18487 | chr2:231320965-231325165 | CD4p_CD25-_Il17-_PMAstim_Th | SE_22757 | chr2:231321449-231322907 | CD8_primiary | SE_53670 | chr2:231321492-231324812 | Spleen | SE_62343 | chr2:231275151-231339482 | Tonsil |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH02I230456 | chr2 | 231321647 | 231323115 |
|
Enhancer Sequence | GGCAGGTCTG TGCTGGGGGA AACCTTGAGC CAGAATCTGC AGGGCTCTAC ACCACTGATG 60 CAGGCTTCTT CAGGCACTTC AGTAGGCATG AAGCCCAGTG CTATTGAAGC CAGCTTGCTG 120 CTAGGATGGG CCTCAAGCCC AGTGCCACTT GGTCCAGTTT GGCACTCGGT CTGGTCTGGA 180 TCATGGGTTC ACTGAGGCTG AAATAGTGCT GTAGGAGGCT GAAGACTGAG TTCGCAGGGC 240 TGGCCTGAGT CCTGGGGCTG CAGGATTTAG GTTGGGGTCA GAGTGAGCTT GGAGGTTCAG 300 ACCATGGGTA CTGGCTAGAG TCTGGGGCTT TGGGAGCTGG GTTTTACTGA AGTCGGTTCT 360 GTGGTTTGGG TGTAAGGCAA AGTCTGGTGC TCACTTCCTT CTCCTTTCCC CAAGCATATT 420 GTATCTTGCT CAATGCTGTG CTTCCTGGAG TTGGGGAAGA TGACACAGTG AAACTTTTCT 480 TCCTGCCCTT TTCAATGTGC TCTTTCTTAT TTCTGTGTTT CACTCAGGTG CTGTGATCTT 540 TCATCTGGTT TCCTCAGCTC TTGCAAAGGT ATTTTCATGC ATAGGTCGTT GTTCACATCA 600 GTGTTTCTGC AGGGGATGGA GGGCTGGAGA GTCCTATTCT CCCATCTTGC TCTACTTCTC 660 CCCAATTTTC TAATTATATC TTTATTTTTC 690
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