Tag | Content |
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EnhancerAtlas ID | HS180-18016 |
Organism | Homo sapiens |
Tissue/cell | Small_intestine |
Coordinate | chr16:11773900-11774760 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF4 | MA0039.3 | chr16:11773938-11773949 | CCACACCCTCC | + | 6.32 |
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| Number of super-enhancer constituents: 6 | ID | Coordinate | Tissue/cell |
SE_10434 | chr16:11773362-11779132 | CD19_Primary | SE_11208 | chr16:11762424-11786074 | CD20 | SE_43514 | chr16:11771151-11787464 | MM1S | SE_48190 | chr16:11760947-11777851 | Psoas_Muscle | SE_62988 | chr16:11758191-11785300 | Tonsil | SE_67152 | chr16:11771151-11787464 | MM1S |
|
| 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 |
GH16I011674 | chr16 | 11768221 | 11778156 |
|
Enhancer Sequence | ATGGCTTATC TGTTCCTGAA GCCAGAGCTC AGCTTCACCC ACACCCTCCA AGAAAGACAA 60 GAGCTCCTAG GCCCAGGCCT AAAGCCAGTG ATGCAGGGCC CCAGGAGTGT GTAGGCATGG 120 GGCCTCTGTG TGCTCGGAGA TGCCCAGCGG CTGTGTCAGG AAGAGCGTCC AGGGGAGGCA 180 GGAGTGTCCC ACCTATGTCC CTCTTGTGCC CACTGACAGT GCCCGGAGAA AAAGGAAGAA 240 CTTGAAAGAT ACCCAGTCTG TTTCTTCAGC AAGCATTTAT TACACATTCT CTAAGGCAGG 300 GGTTCTCAAC TGGGGGTGAC TGTACCCCCA TTCCCCAGGT ACATCTGGCT CACACCTGGC 360 AACCTGATAA CTGGCAAACA GCCCAACCAA AGGACTATGA ATTCAGGCTG CCCAGCCCTG 420 AGAGCACAGA ATAAGGAAGG AAGGTGACAT AGAAAGGGGT TTTCCCTACA GCTTTGTTCC 480 AGGTCCTGAT CTAGAGATCT AGAAAATTCC TCTTCAGAAC TTGTCATTTA ATCGTCTGAT 540 GATGTTTCTC TCACATATCT ATTTACCTGT GCCTGTACAG CCTGGCTGCA ATTGATCAAA 600 ACTACCAGCT TTATGCACTT AGGTATGAGG TGGGCCGGCA GCCGAGTTTG TCTCCCTCAG 660 GTGTTAACAG AATGGAAGTC AACAGCAGGG ACTCCAGAGC CTGGCTGCCC AGGGCCACTG 720 GACCCGGCCG TAAATTGTTT TATAATTTTG GGGTAAACAT TCAACCATCC CCTCCTTTAA 780 AGCTTAGTTT TCTTAACATA TAAGCTTTCT TCAAGTGGGG CCCAGCCATT CAAATGACAA 840 AGCTGGGTGT GGTGCTGTGT 860
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