| Tag | Content |
|---|
EnhancerAtlas ID | HS182-18635 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr6:30059270-30060270 |
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 | chr6:30059675-30059693 | TCTCCCTCCCTCCCTTCC | - | 6.25 | | EWSR1-FLI1 | MA0149.1 | chr6:30059683-30059701 | CCTCCCTTCCTTCCTCTC | - | 6.88 | | EWSR1-FLI1 | MA0149.1 | chr6:30059679-30059697 | CCTCCCTCCCTTCCTTCC | - | 8.13 | | ZNF263 | MA0528.1 | chr6:30059684-30059705 | CTCCCTTCCTTCCTCTCCTCT | - | 6.3 | | ZNF263 | MA0528.1 | chr6:30059678-30059699 | CCCTCCCTCCCTTCCTTCCTC | - | 6.74 | | ZNF263 | MA0528.1 | chr6:30059679-30059700 | CCTCCCTCCCTTCCTTCCTCT | - | 6.81 | | ZNF263 | MA0528.1 | chr6:30059675-30059696 | TCTCCCTCCCTCCCTTCCTTC | - | 7.48 |
|
| | 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 |
| GH06I030090 | chr6 | 30058573 | 30060526 |
|
Enhancer Sequence | CATTTTAACA CAGTAATAAT TTTATAATTT TATAATTTTC AAATCATTAA AGATTTTACT 60
ACTTTCTTAA CTACTCCAGG AGCCTGTGTC ACATTCCAGT CACAGGGAGG AAACTGGGGG 120
CCATGCAGGA TAAAGGTCAA AGCCTGCATG CTGGGACTCA AGTGCTTCCT CCCCAACAGT 180
ATTAGAACAC CAACTCCCAG GAGCACAGAG ACTTGAAGAG AGTGTCCGGG TCGTGGACTA 240
TGAGTCAGAG AAACCAAGCC AGGGGCATGC AAGGCAGCAC GAGGCAGAGC AGGGAAACCC 300
AGCAAGGGAG GTGGCAACGC ACAGTGACCT AGAAAAGCCT GATGAGCTGA GAGCCAGCCG 360
ACAACAGGCC CCATGTGCCT CTGTGTCTTG GTCCACATGA TAGACTCTCC CTCCCTCCCT 420
TCCTTCCTCT CCTCTGGTGA CCAGTAGCTA AAACATCACT GGCACGCTGC TGGCATCCAG 480
CCTGCCAATT AGTTCAGGAG CCACTCCCTC TGACTGCCTC CTGAGCCTCA GATGTTACCT 540
CCCCTGTCTC CCAAACACAC CCCTCCAGCT CTGTCCTGCC TGCCCTGAAT CTCTGGAAGG 600
AAAACTTGCC CTGGGACCTG CCTTGGACTC TCTGGTTCCC CTCATCCAGC CCCTCCCTGC 660
GCAGAACATG GCATCTCGTG CCCTTTTATC TGCCATTTCT GGCCACCTTT GCAAGCGTCC 720
TTGAAACCAG CGCTTGGTAG AGTTATCCAC GCCCATGTGA GGCTCCCCTG CCCCCTGGGT 780
GGTGTATGTG GCAGGAGGAG CAGGGAGGAG CTTCAAGGAA GCAGAGGGAA AGGAACCTAT 840
AAGAGTTCTT GGGATGGCTT CCAGGAAGCT GTGAGGACAG AGCTATGCTG AAAGGAGAAA 900
GGCAAAGGCT ACAGAAAAGT GAACACTGAA GAGGAATTAG GCAAGAACAA AGCCTACCAA 960
GTTAGAAGAA GGGAATGAGA GGGCGAAACA ACAGCACCAG 1000
|
