| Tag | Content |
|---|
EnhancerAtlas ID | HS192-04422 |
Organism | Homo sapiens |
Tissue/cell | U2OS |
Coordinate | chr16:627400-628370 |
Target genes | | Number: 40 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EN2 | MA0642.1 | chr16:627462-627472 | GCTAATTGGG | - | 6.02 |
|
| | 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 |
| GH16I000577 | chr16 | 627637 | 630156 |
|
Enhancer Sequence | TCCCGTCTCT ACTAAAAATA CAAAAAATTA GCCAGGTATG GTGGTGGGCA CCTGTAGTCC 60
CAGCTAATTG GGAGGCTGAG GCAAGAGAAT GGCGTGAACC CGGGAGGCAG AGCTTGCAGT 120
GAGCCGAGAT CTCACCACTG CACTCCAGCC TGGGCGACAA AACAAGACTC CGTCTCAGAA 180
AAAAAAAAAA AAAAAAGTGT TCTTTTCTCC TTCTTGCCAG TCCTGCTGTG GCTGAGGCCT 240
TGGCCCAGGC TTGGAAGGGG CCTGCGCAAT GGGCAAGTGG GGGCCAAGGT GTCACTCACT 300
GTCTCCTTAG TGGGGAGGCT GAGGCTCCCT TGGGGTCTGC CCGCTGGGGC ACAGCCTCTG 360
GATGCTGAGT TTCTTCCTGG GCGGCCAAGA CCCTGCTTCC CTGTTTGCTC TTGGGGGTGC 420
CTGTGCCCTC AACTTGACGC CATCCTCCCT CTGGGGACCT GTCCTCCTGC CTGGTCGCTG 480
TGGCCCTGAT GGGCTTGGCA CTGTCTCGCT CACCTGTGGT CATCCCGGGC AGCCCCCAGC 540
CTCTGCGATG GGGTGGGGCC TCTGGAGGGG ACTGTGTCAG CTGTGGGCTT CCCTGCAGGG 600
CTGGAGCCGA ATCAGGGTCT GCCAGGCCTC AGTGCGTCCA CGTGTTTGGG GCCGAGGGCT 660
CCAGTGGGTC CTGTGGCCGA GGTAGTGAGA GGGGAGGAAG ATGGTAGAGG TGGGTGCAGG 720
CAGGGGGCCA CGCGGATGCC CTGTGGGCCC GGCCATGTCA CCCAGGCCTG CAGAGAGAGG 780
CCTCCAGACC AGCCTCCTCA GACCCCAATC CCGGAGCCAT CTGTGAAGGG GAGCCCGTGT 840
GCTGTCCACG CTAGGACGCG GTAGACCCTG GAGGAGGGAA GGCTGGCCAA GGTGGGAGCC 900
CATCACGAAA GAGCCTGGGG AGATGCAGGT GCTGAGCCTG GCTGCCCCCG CCCCAGCGTG 960
GCCCCTGTGT 970
|
