Tag | Content |
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EnhancerAtlas ID | HS190-00006 |
Organism | Homo sapiens |
Tissue/cell | Treg_cell |
Coordinate | chr1:1072660-1073100 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF16 | MA0741.1 | chr1:1072762-1072773 | GCCCCGCCCCC | + | 6.02 | KLF5 | MA0599.1 | chr1:1072762-1072772 | GCCCCGCCCC | + | 6.02 | SP1 | MA0079.4 | chr1:1072759-1072774 | TCAGCCCCGCCCCCC | + | 6.01 | SP2 | MA0516.2 | chr1:1072758-1072775 | CTCAGCCCCGCCCCCCG | + | 6.91 |
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| Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
SE_10678 | chr1:1070790-1073800 | CD19_Primary | SE_24460 | chr1:1069443-1073717 | Colon_Crypt_2 | SE_25166 | chr1:1069414-1073756 | Colon_Crypt_3 | SE_28002 | chr1:1070749-1073765 | Fetal_Intestine | SE_29232 | chr1:1070790-1073347 | Fetal_Intestine_Large | SE_52392 | chr1:1069885-1073770 | Small_Intestine | SE_56870 | chr1:1071113-1073708 | VACO_400 | SE_57937 | chr1:1071999-1072994 | VACO_9m |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 1072776 | 1072800 | chr1 | 1072831 | 1072994 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I001131 | chr1 | 1067197 | 1073723 |
|
Enhancer Sequence | GCCCAGAGCC CGGGACACGC GACGAGGGGC CGGACCCCGA GGATGCGAGG ATGCGGGGAC 60 CCTGCCCCCG CTGGGCCGGG TTTTGGGGGC CCGGGACACT CAGCCCCGCC CCCCGCAGGC 120 TCTCTGTGGC CCTGGGGTGG GAGGGCTGCG GTCGAGAACC CCCCACGCGG CCCCTCCCCG 180 GAACCCGCAG GCTGTGCACC CTCTGGACTG AAGTCACCCG TCAGTCCCGG CTGGGGGTTT 240 CCGGGAACAG GGCAGGTGCT TTAAAGCAGG GGTGGCCGAT CTTTTGGCTT CCCTGGGCCA 300 CATTGGAAGA ATTGTCTTGG GCCACACATA AAATACACTA ACGATAGCTG ATGAGCGAAA 360 AAAAAATTGC CAAAAAAATC CCATTATGTT TTATGTTTTA AGAAGGTTTA CAAATTTGTG 420 TCGGACCCCA TTCACAGCAG 440
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