| Tag | Content |
|---|
EnhancerAtlas ID | HS042-17327 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr16:27770830-27772110 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BHLHE40 | MA0464.2 | chr16:27771088-27771098 | ATCACGTGAC | + | 6.02 | | MITF | MA0620.2 | chr16:27771084-27771102 | GCAAATCACGTGACCCAG | + | 6.08 | | MITF | MA0620.2 | chr16:27771084-27771102 | GCAAATCACGTGACCCAG | - | 6.08 | | Pou2f3 | MA0627.1 | chr16:27771886-27771902 | GCCAATTTGCATAAAA | - | 6.6 | | TFEB | MA0692.1 | chr16:27771088-27771098 | ATCACGTGAC | + | 6.02 | | USF2 | MA0526.2 | chr16:27771086-27771102 | AAATCACGTGACCCAG | - | 6.24 |
|
| | 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 |
| GH16I027759 | chr16 | 27770334 | 27772150 |
|
Enhancer Sequence | TCTTGGCTGG GCAGCTCTGG GTGAGCCAGC TTGGTTGGCC TCTACTGGGC CTGCTCGAGT 60
TCCTGATCAG CAGGGAGGTG GACCAGCAGC TGAATGACCT AGGACATCTT CACCCACCCG 120
TCTGGCAGTG GGGAGGCTGC TGGCCAGAGA GACAGGTGTC TGGGTTAGCT GGGCTGCCTC 180
GCATGGCAGT CTCAAGCCCC GAGTGCTTTA CAGGCTCTGC TTGCCTCACG TGGGCTTCTG 240
TCCCAGTGTT CAAAGCAAAT CACGTGACCC AGAGTCAGGA GCAGAGAAGG AAACTCCAAC 300
TCTGGATGGG ATGAGGGGCA AAATCACATT GCAACAGCAG GGACACGGGA TGGGACGAGC 360
TTGTAGCCAC TTTGCACGTG AATGATGCGG CGAGAAGCCC ATGTGCAGGG TGCCGTGCTG 420
GCCACATGTT TTTTTCATCT GCCCCAGAGA TGCTCAGAGT TACCTTGGCA CCACGAAGGA 480
GGAAAAGGAT CTGAGGGCTA AGTTACAAAA AGTATGTTGG GAGATGTCAG GGGCGTGGGA 540
GAGAAAACCA AGCTCCAGGG AGGTCAGGTG ACCCAGCCCC TCTTCATGGC CACAAAGAAG 600
TCCTTTCACC TCTCTGGGCT TCCAGTTCCT CATCTGAGCT GCAAGGGGGT GGTGCCAGAT 660
GACACCCTGC TTCCTTCTGC CTGCTCTGTG GTGCTGGCAT TTCTGTGAAC GCTGCAAAGA 720
GTGAGTCTTA CACTTAGCTA CCCAAAAGGG TGCTAAAATA TGCGGCAAAT TCTCTAAGGG 780
CAGAAGGGTT TATTGTGTTT GGTCTTGCTC TAATGAGACA CCGTTAAGGA AAGAGACGTT 840
CCAGCCAATT ATCTGACAGG GCTTGATCAA GAGATTCATT CCATTTGAGT TTCCTGGGCA 900
AATGAATGAC ATCTGGGCTG TTTTGCCCCA GGGCCACAGA AGGTCACTTC TAAATGGTCT 960
CTGATCGAGA GAGGATGGGA GCAGAGGCAA AAGGATGGCG GTATCACCCT AGGTCACTTC 1020
CTTTACTCTG AGCCCACGTG AATGTTTGTG ATAGCAGCCA ATTTGCATAA AATGTCAGTT 1080
TCCAGCGCTG GGGCTTACTG ATACAAGTCT CCATGTAGTT GCTGGTTTAA TCATTCCATC 1140
TGTACTGAGC TCCTACTGTG TGCCAGGCAC CATGCCAGGC TCAGGACACA GTGGTTTAGA 1200
GAAACAGATG GGGTTTCTCC CTCAAGGAGT TAGGCATCTG GCGGGGCAAG TGGGTATTTA 1260
CCAAGATCAC GCGATTACAG 1280
|
