| Tag | Content |
|---|
EnhancerAtlas ID | HS026-20831 |
Organism | Homo sapiens |
Tissue/cell | CNCC |
Coordinate | chr20:61645550-61646970 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr20:61645787-61645798 | GGTGACTCATC | + | 6.32 | | JUND | MA0491.1 | chr20:61645787-61645798 | GGTGACTCATC | + | 6.62 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr20 | 61645800 | 61646107 | | chr20 | 61646020 | 61646413 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH20I063014 | chr20 | 61645671 | 61646943 |
|
Enhancer Sequence | TTTGTTTGCA TTCCAAGCAA ATATTTTTAA CATTTTGCTC AGCTTTTGTA GTCACCATCA 60
GAAAAGTGAT GGGTCCAGAT TAACTAGTCC CTAATAACCA GAAACTGGAA GTCTGATGGT 120
TGTTTTCAGT CTTGAACAAC ATTGATTCTG CGGTGACCAG TTTAGAGTTC ATGCAATAGA 180
CCTTCCTCCC CCTTGTAAAA TCATCACTAT TTCAGCTAAT ACTTAGAGTG ACCTCCTGGT 240
GACTCATCCT CAGCCCCCTT TGCCGGTTCT TCTTTTCCCC GACATTTTCA TTCTGGAGGG 300
CTTGGGATTC AGTCCTTTGG CCTTTTTCCT AGCTGTGTCT GCCCCCTCGG GGATCTCATC 360
CAATACCCTT CCCACAGCCT ACCCAGACCC CAGTGCTGAA CTCCAGACTC ACGGATTCAG 420
CGGAGCGCAG AATGTCAGAT GTGTGAGGGC CGCCTCCGAT GCAGCGCGTT CCAGATGGAG 480
CTGCGGCCTC CCCCAGACCC GCCCACCCCC ACCCCCAGAT TCTGTTGAGG GCAAATCATG 540
CTTCCTCGCA GCTCACACCC TGTTGGTTCT CCCTCCCACG TTCATCTGGA ATGCGGCCGC 600
TCCCCACCTC TTCCCGCCTG CCCTCAGTCA GCACAGCAGC CTTCTAATGG CTTCTGCCCT 660
CCCATCATCC CCAGACCCTC CCTTTCACAC AGCAGCTGTG AGGTCCTCCT CAGGCAGGGT 720
CAGGTCACGC CTCTCCCTCT CAGAGTCCTG CCTCAGCCCC TCCCCTGTCA TCAACAAAGA 780
CTAGACTGTG AATGGCCCCA TCTGCCTCCT GCCTCCCGAG CTCACAGCCT CTGAGGTCCC 840
GGATGGGAAA TCCCACCAGG CAGTCTGTGG ACGCCGCACT GCAGGCGAGT GGGGTCTATC 900
TTTTCAAAGC TGATGCCCAC GCCCAGAGAG GGTGTCTTCC ATGAGAGACG TGGCCTGGCA 960
GCTGCTGCTG TGGGCCCTGG GCCCGGGGAC ACACCCGGCC CTCATTGAAG ACAGGAGGCA 1020
TCCCGCTGGG GGAGTCAGAT GAGATGTCCA GCCCCACGTC ACCTCCCTGT GCTCGGCCGT 1080
GCTCCGTGAA TGGCCTGGTG GGTTTCTGTG TGTGGAGAGC TGGGTGGGCT TCTAGGGTCT 1140
TGACTACGGG GCTGGATGTA GAGTACTCTA GAGAGGCTGG GGATGAGATG AGGCAGCTGC 1200
AGGTGGCCCC TCCTCACCGC CTGAGGACGC GGGACCACGC CAGGCTTTTC TGGGCAGGGT 1260
GCCCCTGGCT GTGTGGCAAC AGATATGCAC AGAAATGCCA CATGGGCTCC TGAGGCAGCC 1320
TCATGTCTCC ACTGGTGGGT GGTGTGGGAG AGGGGACCTG AGATTTTGCC TGGCTCCTTG 1380
CTATTTGGGG GACGGGTGTG CCTCTGGGGT CCCAGCTGTG 1420
|
