| Tag | Content |
|---|
EnhancerAtlas ID | HS182-20623 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr8:22604740-22606300 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| TEAD1 | MA0090.2 | chr8:22605839-22605849 | ATGGAATGTG | - | 6.02 | | ZNF263 | MA0528.1 | chr8:22606178-22606199 | GAGGGAGGGTGGGGAGGTGGG | + | 6.82 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr8 | 22605286 | 22605400 | | chr8 | 22606038 | 22606156 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH08I022741 | chr8 | 22599459 | 22607261 |
|
Enhancer Sequence | ATAGTGGACA TCAGAGCTGT GGGTGATAAT AAGTGCTGGA TTCCTGGGAA GTCCCTGGGG 60
GTGCCCCCAC CCTTGTTCAG GCTCTGTCCC TTCCTCAAGT GCCACTGTGT AGATCCAGGG 120
TCTCTGCTGT GCCCAGCCTC CTGTACAGCA CCCGAGAGAG GCCACAGACG ACTGGGTTCT 180
GGACTTGAAC CTGGGTGACC TTGGGCAAGT CACCAGATCT GTGGGTCTCT GTGGCCTCTT 240
CAGTAAAATA ATGAAGATGA TTTATTGCAA GCCTCAAGGT TTGTGTTTCT TTGGGCAGGA 300
GCCTACTGTG ATCAGAGCTG GGGGAGCCAG TGTGAGCAGC AGGGTGAGTG GGGTGTGCAT 360
GGGTGTGCAC GCTCAGGGGG GTGGGGGGCT TGAGGGGTGG CAGGGGGACC CTACGGGATG 420
TTGCTTTTCA GCCTGGCGCT GCCTCGCTGA GTAGCCTGAG ACTAGGAAAA GGCTTAAAGA 480
ATTCACAGTG GGAAGGCTGC AGCCTGACTC TGCTCCTGGC CGGCGTTTGC CCGCTGCCTG 540
GCCCTGGCTG TTCCAACGAT GGACTTCCTT CCTCTTTGGC CATAAAAGTC TCCCGGAAAG 600
CCTTCCCACA GAGGCCCCGG GGGCTTTCTC AGGGAATGTG TGAGTGTGTG CTCACACAAG 660
CACTGTGGAG CAGGAGCCCA GGGCCGCGTG CAGGCTCTCC CACAGAGCTG TGGGTCCTGG 720
CGCTGGAGGA GAGGTTCGTC CCAGCCTGGG TGGAGAGCGG AGGAAAGGCT GGCCCTTGCC 780
TGGACTTGGG CCCTGGCTTA TGCAATGCTC AGACTCTTAG TCAACTTCAG CAACTGGGGC 840
ACATCCACAC GCATGTGCAC ACACGTGCAG GCACACACCC GGGCAGGGAG GTGTGAGGAA 900
GGGAGACCAA TGAGCCTGTG CCAAGCTCTG CTTACAGATC TCCCCAGATC TGGAGAGAAA 960
AGGGGAGCCC TTCTCCAAGA GGGGGCTGCG CTCAGGCTGC TAGGGTATGA TGATGGCTCC 1020
AAGCCTGTGG CTGAGGTTGG ATGGACCATT GAGAGGAGCC CTCCAGGGTG AGGGGACAGA 1080
AGCCCATCAG TCCGTATTGA TGGAATGTGG CTACAGTGTG GAGAGAAGAA GATACTTTCT 1140
CTTCCTGCCC CAGAAGGTAC CCAAGCCTCC GGGATGCTGG GTCACAGAAC CCGCCTGGCA 1200
GAGAGTTGCA TCAGAGCGAA ACTGCATGCT AGATGCCTGA GGGGAGAGGG CACTGAGGAC 1260
TTGTGATCCT AATTTCCCAA CCTTCAGCTG CTCAGGGTCA AGTCCTTAGG CTCCACTTGC 1320
TCTTCTCCCC TCCCCAGCAT TCTTCTGTAC TAGGTTGCAC ATGATGAGGG TGGTCTGAGG 1380
GGAGAACAAG GAGGGGGTGT GACTCAGAGT TCACCCGGCT GTCAGCAGCC CTGAGTCAGA 1440
GGGAGGGTGG GGAGGTGGGT GGAACAGCTT TTGGTAGTCT TGGGGTTCCC TATAAGCAAG 1500
AGCATCCCAG AAAAATAGAA GAGAGCCCCC CAGAAGCTAC GAGGCTCCCA CATGCAGGGT 1560
|
