| Tag | Content |
|---|
EnhancerAtlas ID | HS095-08126 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr13:21049770-21050490 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr13:21050176-21050194 | GGCAGGAAGGAAGGAAAC | + | 7.53 | | NFKB1 | MA0105.4 | chr13:21049845-21049858 | AGGGGAATCACCT | - | 6.22 | | NFKB1 | MA0105.4 | chr13:21049845-21049858 | AGGGGAATCACCT | + | 6.5 |
|
| | 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 |
| GH13I020474 | chr13 | 21048535 | 21051757 |
|
Enhancer Sequence | TAGTTCCCAT TAGCTGCGGG TCATAGGCCA AGACTAAAGA AGAGCCATAT CAGCCTCAGG 60
AGGCCTTGGG AACAGAGGGG AATCACCTGA TGCTGTGCAA CTGGCTCTGG CCAGGCTCAG 120
AGAAACCAGG GACCCTTTCA GCGGAAGATT CCCACCCACC ACCTACCAAC TAGGATGGCA 180
AGATAGCAAG TGCCTTCAAA CGCGAGCAAA GCAAGAAGCA AAAGGCCGCA GGACGAGTCC 240
CGGTGACATA TCCACAAATC ACAGGCAGAG AGCCTGTTAA AGGAAGGCTG TGTAAGTGTA 300
CTCAGTCAGT GGAAAGTGGA CTTGCTCCAG GAAGGCCACA GCCTCATCCT GGCCTGTGTC 360
ACCTGCCCCA CGCACACGGC AGTTCCGGGG CAGGTCCTGC GCACGCGGCA GGAAGGAAGG 420
AAACCACAGT AGGTCTCTCA GAGGAAACCA CAGTAGCAGC CTCCTCTGCC AAAACAACAG 480
AAATAGCTAC TCCAGTGTCC CAGGTGTCTT CCCACACACA AATGTGCAAT GCGATACTTG 540
CTGAACGCCA GGGCCTCTGA AAGGCAGGAA GGTAATTAGC TGGGAGTGGT GGCATGTGCC 600
TATAATCCCA GCTACCAGGA GGCTGAGGCA AGAGAATCAC TGGAACCCGG GAGGCAGAGG 660
CTGCAGTGAG CCAAGATCGC GCCACTGCAC TACAGCCTGG GTGACAGAGC AAAACTCCAT 720
|
