| Tag | Content |
|---|
EnhancerAtlas ID | HS030-00894 |
Organism | Homo sapiens |
Tissue/cell | CyT49 |
Coordinate | chr1:46985100-46986680 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL2 | MA0478.1 | chr1:46985120-46985131 | GGGTGACTCAG | + | 6.02 | | JUNB | MA0490.1 | chr1:46985120-46985131 | GGGTGACTCAG | + | 6.02 | | STAT3 | MA0144.2 | chr1:46985789-46985800 | CTTCTGGGAAA | + | 6.62 |
|
| | 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 |
| GH01I046519 | chr1 | 46985499 | 46989059 |
|
Enhancer Sequence | CCAGGTCCAG CCTGCTTCCT GGGTGACTCA GAGGAGGTAA AAAGGAGAAG GCACTGGGGA 60
GGCTGAGAAG CTGAGCAGTT CTAGGCCCAG CATGCCGTTG GTGCTCAGAT AGCCCATGGT 120
GGGGGAAATG GGAAAGGTAG GGGGCTCCCC GAAGCTTCTC TCCAAATTCC CCATGTTCTC 180
TCTTTCTTTT TTTTGAGATG GAGTTTTGCT CTTGTTGCCC AGGCTGGAGT GCAATGGTGC 240
GGTCTTGGCT CACTGCAACC TCCACCTCCC GGGTTCAAGG GATTCTCCTG CCTCAGCCTC 300
CCCAGTTGCT GGGACTACAG GCGCTGACCA CCACTCCTGG CTAATTTTTT GTATTTTTAG 360
TAGAGACGGG TTTCACCATG TTGGCCAGGC TGGTCTCAGA CTCTTGACCT CAGGTGATCC 420
ACCTGCCTTT GCTTCCCAAA GTGCTGGGAT TACAGGCGTG AGCCACCGCC TGGCTGAGCC 480
ATGGCGCCCG GTAGTTCCCC CTTCTCTTAG GCCTTGGCCA ATGTTCTTGC AGCTCAGGGG 540
TCTGGTTCCT TAGGGGCCCT CAGGGAAGGG GCCCCTGCTG AGAGGGTCTG GGGAATGGAC 600
CCCTTTAGGG CTGGGCACTT CCCTCATCTC TTTCCCACAG AGCTGCTCTG GGCTGGAGCC 660
CTCCACCCCC ATCACTCATT CTCCTTTAGC TTCTGGGAAA GCCGATTAGG AGGTGGCCTT 720
CTACCCGCCC CCCTGACAAG TGTGTCTGAA CTTCCAACAA AGGCCCTCAG AGGGTTGCAG 780
AGGGAGGGCT CAGCACTGGG AACCTGACAC CACTGGCCAG GGATCACCCC AGCAGCCTAG 840
GAGGCAGCTC TGTGGGGCTG CCCACCCCAC GGCAGGCAGG AATGTCGCTC TGAGAGGGGA 900
CCTGGTCCCA CAAAGGCCTG GGGGCTGGGC TGAGGCAGGC TGGAGAGGTC TTCACCTGGG 960
AGGCCTCACA ATAAGGAAGA CAGCAAGGGC CAGCACCCAG GAAGGCACGT GGGAATAGGC 1020
ATACACGCCC CCACACACTG ACAGCCTCTC ACACACATTC CCCATACATT CACAGCACAC 1080
ACGCACACAC GCATCCTCTC ACACCCCTGG GACATGTTGA CTTCTGCACT GGACCACACA 1140
ATCCCAGGGT GTCTGTCTCC CTGTCTCTCA TGCCTGTGTA CACAGCCCCA CTGCAAACCG 1200
GCAGACACAC AGCCACGCTC TGTCGCCTGA TGCTCCACAC ACCCGCTCCA CCCCCAGACA 1260
TGCATTCTTC CCGGCTTGCT CACACTCCAG ACAGCCCCTG AATGCTCAGT GGCACCAGCT 1320
CCCCTGTACA GACAGCCTCT CGAGCCAAAC TGCTGGCCTG GTGCCCACAG AGACTTGGTG 1380
GCGGCTGCCC TGTGATTGTG GAAGATGCCA CCCAAATGCC CACATAAGAG TCAGACACTG 1440
GTCCCAGCTG CCATGTGAAC ACCCATGTGC ACCAACCCAC ACATCCACCC CAAGGGGCTG 1500
CCTTGAGCCC ACCTCTTCAC AGCATGCTCC CTCCTGCAGC AGCCTCATGG GCGTGTGACC 1560
CATGCAGTCA CACAGGGCCC 1580
|
