| Tag | Content |
|---|
EnhancerAtlas ID | HS024-10595 |
Organism | Homo sapiens |
Tissue/cell | Cerebellum |
Coordinate | chr20:61821770-61823240 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Myod1 | MA0499.1 | chr20:61822004-61822017 | AGAAACAGCTGCT | - | 6.28 | | RREB1 | MA0073.1 | chr20:61822642-61822662 | GCCCCAAACAACCCCACAGG | + | 6.24 | | Stat6 | MA0520.1 | chr20:61821995-61822010 | CTGTTCCAGAGAAAC | + | 6.26 | | TFAP2C | MA0524.2 | chr20:61822171-61822183 | TGCCCTGGGGCT | - | 6.11 | | Tcf12 | MA0521.1 | chr20:61822007-61822018 | AACAGCTGCTG | + | 6.32 |
|
| | 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 |
| GH20I063191 | chr20 | 61822824 | 61823030 |
|
Enhancer Sequence | CTGGACACCG AACCCAGGCA CTTCTCACCC CGAAGCACAC CATTGCCCAC CCCTGTGCCC 60
TGGACCCTCC ACAGGGCCAA GCGGGGGACG CTGTCCCAGA GAACCTGGAG CCTCCACAGG 120
GCCAAGCGGG GGACGCTGTC CCAGAGAACC TGGAGCCTCC ACAGGGCCAA GCGGGGGACG 180
CTGTCCCAGA GAACCTGGAC CCTCCACAGG GCCAAGCGGG GGATGCTGTT CCAGAGAAAC 240
AGCTGCTGCC CACCCACAGA AAGTCTCCTC TTCCAAGCCT GACAGTTCCA CAGGACTGAG 300
GCAACACTCT TCCTGGTCTC ACAAGTGGTG GCCAAAGCCC AAAGCCGCCA AGGGCCTCAT 360
CACCTGTGCA CCACCTACTC CACTCCCGTC CCCTCGGAAG CTGCCCTGGG GCTGCCCAGC 420
CTGCAGGGGC CCAGCCCTGT CCGTGGCAGC ATGTCAAGGC TGCCCTCGGC CCTGAAGGAG 480
ACCCTTCCTA CCCCACAGCT TCTCCTGGCA CCAAGCAGTG GCGCTGCGGT GTCCGAGCTC 540
CCCGTCTGCC CATAGGAGCC CCGCCATCAC CCACGGGAAG CAGCACTGCA ATCTCCGAGC 600
CTCACCCTCC GCAGGACACC AGGAGCGTCA GCATGCTGCC ATCCACAGAG CCCCGTGACG 660
GGCAAGTGCT GGGCTATGGC TTCCCATAGC TTAGGACCGA CTTCGGGCGG CTCGCCCTCT 720
CCACGGCCAC AGAGCTCGGA GGAGTGCCCA AGAGGCGCCT CTGTCCAGGA TACACTGGAG 780
GCCCCTGTGC CCAAGCTCTG CCCAGACATT AGCAGTTGCT GGTCCTTCTT TGACTCTGGG 840
TGGCCAGGAC ACTTGCGGGA GGGAGGGTGC TGGCCCCAAA CAACCCCACA GGCCGTGTGG 900
ACTCCCCAAA GGCAAAGGGG CCCTGTGGCA GACCTGTCCT GAGATAGGAG CCTCAGCCCT 960
GGGCCACAGC AGGAAGCCAG CAGGTCTGGT GGGCACCCCT GGAACTCACT GGAGTTGAGG 1020
CCTGGTCCTG ATGCTCATTC CGACACCTGA AGCCTGATTA GCTTGGCAAG TCTAGCTCCC 1080
TCTTGCACGA GCTGAGCGAC GCAGCAGGGC GAGGCCTGGC CCGTGCCCAA CGCTGACGCT 1140
TCCGCCTGGT CCAGCTGGTG ACAACGTATG AGACACCTAG GCCTGTGGCC GGCTGCCAGG 1200
AAAGGAGGGA ACCTAGACTG CTGTTCACCA TCTGAATACC CCGTGACTTA CCAGCAAGCA 1260
GGCCACTCTC TCACACCTCC ACCAGGGTCG CCTCCCAGAT AATCCTTCTC AGTCATAAGG 1320
AGGAACTCTT GAGAAGAGAC CTTCCAGGGA GGAGCCTGGT GGCTCGAGGA GCCTCTGAAC 1380
CGGGCTTTTT TTTGCTGTTT CTTTTTTTTT TGAGACGGAG TTTCACTCTT GTTGCCCAGG 1440
CTGGAGTGCC ATGGCGCGAT CTCAGCTCAC 1470
|
