Tag | Content |
---|
EnhancerAtlas ID | HS105-44000 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr2:71098450-71099450 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr2:71098795-71098814 | CGACCAGCAGAGGGCAGCA | + | 7.76 | Myog | MA0500.1 | chr2:71098844-71098855 | GACAGCTGCAG | + | 6.62 | Tcf12 | MA0521.1 | chr2:71098844-71098855 | GACAGCTGCAG | + | 6.14 | ZNF263 | MA0528.1 | chr2:71099412-71099433 | AAAGGAGGGTGGGGCAGGGGG | + | 6.08 |
|
| 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 |
GH02I070871 | chr2 | 71098549 | 71099186 |
|
Enhancer Sequence | TGTTTTCATT ATCATTGTAC CCCCAGTACT CAGGGAGTAT TCCGGGAGCA TAAAGGACTC 60 CTCTTGGGTT TCCCATCCTA ATGGGGCTGT CCGTCCTGCC CCTTCCCTTA TGGACCAGGA 120 TTAGGGAGCG TGGACTGCTG CACTGGGCAC GAACAGGTGT AACCAGAGAA ATTAGACACG 180 CGGCCAGCTT CCCGGGCCTG GCCTCGTTGG AGACATCCCC CACTCTCCCT CCTTTTCCCA 240 CCCCCATCCA CCCATTTCTG GACCCTAGGG AGCCATAGCC CACCACCCGG GGTGCCTGCG 300 CAAGGAAGTC GGCGAAGAGC GAAACCCCTC GGTGCTGTAA GTTTGCGACC AGCAGAGGGC 360 AGCACAAGGC CGCTTCCCTG GAGGTGGCCG GCAGGACAGC TGCAGCACTA CTGGAGGCGG 420 GCGGGCACCG ACTGGCGGCG GCCAGGGTAG GAGAGCCCTG TCAGTGTGAA ATTAGCCTGA 480 AGACTGGGGC GTGGTATTAG TGCGTACGCC AGGGGCACGT CCCGGTCCCT GACACCCAGG 540 ACACTGTCGT TACCGCCGCC TTCCTCCATC AGTGTGGTAC CAAGGGCCGT GTGGTGCAGT 600 GATGGGGGCA CAGGCTCTGC CATGAGGCTG AAAGGATGTT TCCACTCCAC CGTTTACTGT 660 GTGGCGTTGG GAAAGTTACC TGACCTGTCT GAGCCTCAGC TTCCCCATCT ATTACATGGG 720 GTAATACGGC CCACCTCACT GGGTCGTTAG GGAGCTCATA GGCACACCGG TAAGTGCTTA 780 ATATTCACCT TCATCAGCAC TTTTCTTATT GCGTCATAAT TGCCCAACTG TGTATCTCTC 840 CTTGTACAGG TTTCCTTAGC ACTTGTGGGA GATTATGTTT GGGATCTATA TCCAGGAGTG 900 GAATTTCTGG GTCACATGGC ATGAAAAAGT TCCCAGATGC CTGAGCTGCC TGGTCCTCAG 960 GAAAAGGAGG GTGGGGCAGG GGGGTGTCTC CAATCTCAAA 1000
|