| Tag | Content |
|---|
EnhancerAtlas ID | HS060-12103 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr16:391390-392570 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NFYB | MA0502.1 | chr16:391965-391980 | AAACGCACCAATCAG | + | 6.73 | | REST | MA0138.2 | chr16:391394-391415 | CTTAGCACCCGGGCCAGCGGC | + | 6.38 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 3 | Chromosome | Start | End |
| chr16 | 392396 | 392510 | | chr16 | 392275 | 392350 | | chr16 | 392055 | 392128 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH16I000342 | chr16 | 392161 | 393428 |
|
Enhancer Sequence | GGGGCTTAGC ACCCGGGCCA GCGGCTGCGG AGGGTGTGCT GGGTCCCCCG GCAGTGCCGG 60
CCCACCGGAG CTGCGCTCAA TTTCTCGCTG GGTCTTAACT GCCTTCCTGC AGGGCAGGGC 120
TCGGGAGCTG CAGCCCGCCA TGCCTAAGCC CCCCACCCCC TCCGTGGGCT CCTGTGCGGA 180
CCGAGTCTCC CCGACGAGCG CCCGGTCCCA TTGACCACCC AAGGGCTGAG GAGTGCGGGC 240
GCACGGCACG GGACTGGCAG GCAGCTCCAC CTGCAACCCC GGTGCGGGAT CCACTGGGTG 300
AAGCCAGCTG GGCTCCTGAT TCTGGTGGGG ACGTGGAGAA CCTTTATGTC TAGCTCAGGG 360
ACTGTAAATA CACCAATCGG CACTCTGTAT CTAGCACAAG GTTTGTAAAC ACACCAATCA 420
GCACTCTGTG TCTAGCTCAG GGTTTGTGAA TGCACCAATC GACACTCTGT ATCTAGCTAC 480
TCTGGTGGGG ACTTGGAGAA CCTTTGTGTG GACACTCTGT ATCTAGCTAA TCTGGTGAGG 540
ATGTGGAGAA GCTTTGTGTC TAGCTCAGGG ATTGTAAACG CACCAATCAG CGCCCTGTCA 600
AAACAGACCA CTGGACTCTA CCAATCAGCA GGATGTGGGT GGGGCCAGAT AAGAGAATAA 660
AAGCTGGCTG CGGGAGCCAG CAGTGGTAAC TCGCTCGGGT CCCCTTCCAT AGTGTGGAAG 720
CTTTGTTCTT TCTCTCTTTC CAGTAAGTCT TGCTGCTGCT CACTCTTTGG GTCCACACTG 780
CCTTTATGAG CTGTAACACT CACCGCGAAG ATCTGCAGCT TCACTCCTGA AGCCAGTGAG 840
ACCACGAACC CACCAGAAGG AAGAAACTCC GAACACCTCC GAACGTCAGA AGGAACAAAC 900
TCCGGACAGG CCGCCTTTAG GAACTGTAAC ACTCACGGCA AGGGTCCGCG GCTTCATTCT 960
TGAAGTCAGT GAGACCAAGA ACCCACCAAT TCCGGACACA CCGGGACGAC TAACCGGCTC 1020
TCCACAGGAT ATGCATCCCC TAACACGTGA GGCCTAAGCT CCAGGCCCTG CTGTGGTAGC 1080
AATGCTCACC AGCCGCCTGT TCAGTACCCA CTCTCCTTTT CCCTTTGCAT TACCCGCAGC 1140
CTTCCTTTGG AGGACTGCCC CCAGCTCCCC ACTGGGGAGC 1180
|
