| Tag | Content |
|---|
EnhancerAtlas ID | HS073-14779 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr9:133803120-133804180 |
Target genes | |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Nr2f6(var.2) | MA0728.1 | chr9:133803266-133803281 | TGAACTCCTGACCTC | - | 6.22 |
|
| | 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 |
| GH09I130927 | chr9 | 133802878 | 133804860 |
|
Enhancer Sequence | TCTCGGCTCA CTGCAACCTC TGCCTTCCGG GTTCGAGCAA TTTCCCTGCC TCAGCCTCCT 60
GAGTAGCTGG GATTACAGGC GCCCGCCTGG CTAATTTTTG TATTTTTAGT CGAGACGGGG 120
TTTCACCATG TTGGCCAGGC TGGTTTTGAA CTCCTGACCT CAAGTGATCT GCCCGCCTCG 180
GCTTCCCAAA GTGCTGGGAT TACAGCATGA GCCACTGCAC CTGGCCGGGA AGCTGCCTTT 240
TAACAAGCAC CTCTGGCGAT TCCAACCCAG GCTGCCTGTA GGCACAGCTT TGAGAAACCC 300
ACATCTGTGC TGATCAGCTG AGGGTCTGGG AAGCTTGGAA GGGAGGAGTT AGGAGCACGG 360
CTCGCTGCCT CTGAATGAAA CATAAAGACC CACTGTCTCT TGAATCATCC AGTCTGTGGG 420
GAATGAGTCA AATCAAACAT TTTTGGGGAA GTAAATATGT CAGGTGAGCT GGCACTCCTG 480
GGCCCAGAAA GGCTGTTAGT CTTGTGGGAA TACTCTGTAC CTCTGCGCAG GCTATTGGGA 540
GGGCAGGACT CTGGGGTCCC TCCTTCTAAA TACCCCACCC CAGCTCTAAG GGTGGGCCTT 600
CATGAACTGG GCCTGAGCTG ACCAGGGGCT GAGCAATTTG GAGTGAGGTG GGGGTCCCAG 660
GTCAGCCAGA AAGTCAGGAG GTACCCCCAG CCCCCAGCCC TGCTGATGAG GCCTGGGGAA 720
GTTGCACATG GAGGGGCAGC TGGAAGGCGG TCTAAACATC CCTCTACCCC GGGAGGGGGA 780
AGCCACCTTC CCATCAGTCA CCCAGACAGG GTGATGAGGA CTGTAATTTC TCCAGCTGCT 840
GCCTTCAAAG GGAGGGAAAG GGCCCATTGC TCATGAGCAG CTGAGTGACC AAATGCCTGG 900
ATCTCTCAGT GGCTGCTGGG GGCGGTGGGG CGGAAGGGGC TTGGGCGCCC GTGGGGGCAG 960
GGGCTTGGCT CCTAGCCTCC AGGGATCTGA GTCACCGGGA GAACGTGGCA CAGGGCCAGG 1020
GGCCGGGCAG GGCTCCAGCA GGGGCTGGAT TCCAGGTCTG 1060
|
