| Tag | Content |
|---|
EnhancerAtlas ID | HS073-03623 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr13:21049760-21050810 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
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 | GGATGCACAG TAGTTCCCAT TAGCTGCGGG TCATAGGCCA AGACTAAAGA AGAGCCATAT 60
CAGCCTCAGG AGGCCTTGGG AACAGAGGGG AATCACCTGA TGCTGTGCAA CTGGCTCTGG 120
CCAGGCTCAG AGAAACCAGG GACCCTTTCA GCGGAAGATT CCCACCCACC ACCTACCAAC 180
TAGGATGGCA AGATAGCAAG TGCCTTCAAA CGCGAGCAAA GCAAGAAGCA AAAGGCCGCA 240
GGACGAGTCC CGGTGACATA TCCACAAATC ACAGGCAGAG AGCCTGTTAA AGGAAGGCTG 300
TGTAAGTGTA CTCAGTCAGT GGAAAGTGGA CTTGCTCCAG GAAGGCCACA GCCTCATCCT 360
GGCCTGTGTC ACCTGCCCCA CGCACACGGC AGTTCCGGGG CAGGTCCTGC GCACGCGGCA 420
GGAAGGAAGG AAACCACAGT AGGTCTCTCA GAGGAAACCA CAGTAGCAGC CTCCTCTGCC 480
AAAACAACAG AAATAGCTAC TCCAGTGTCC CAGGTGTCTT CCCACACACA AATGTGCAAT 540
GCGATACTTG CTGAACGCCA GGGCCTCTGA AAGGCAGGAA GGTAATTAGC TGGGAGTGGT 600
GGCATGTGCC TATAATCCCA GCTACCAGGA GGCTGAGGCA AGAGAATCAC TGGAACCCGG 660
GAGGCAGAGG CTGCAGTGAG CCAAGATCGC GCCACTGCAC TACAGCCTGG GTGACAGAGC 720
AAAACTCCAT CTCAAAAAAA AAAAAAAAAA GGAAAAACGA AAGGCAGGAA GGTCTCTGCT 780
GGGCAGCAGG GACTGATACA GGTCAACCAG ACCCATAAGA GGTGAAAGGC CGCCCCTTGA 840
AAGAAACCTT TTGATTTCCC CCAGTGGTTC AAACAGACTT ACTGGGCAAC AAGTCTTTGA 900
ATATTGACTT TCAAATGAAA ATAAACACAG CAAGGCAGCT CTGCGTCAGC AGATATGCTC 960
CCAGCGTGCT GATACCGCTA GGTGAGCAGC AGGGAGCCCA AGCCGGAAGA AAAACATGCA 1020
GCAGGGCCAG CACCGAGTTC TGCAGGTGTC 1050
|
