| Tag | Content |
|---|
EnhancerAtlas ID | HS037-03169 |
Organism | Homo sapiens |
Tissue/cell | ESC |
Coordinate | chr1:210031450-210032750 |
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 | chr1:210031585-210031600 | CTGATTGGTCCGTTT | - | 8.25 | | NFYB | MA0502.1 | chr1:210031537-210031552 | CTGATTGGTCCATTT | - | 9.03 | | Nr2f6(var.2) | MA0728.1 | chr1:210032596-210032611 | GAGGTCAGGAGTTCA | + | 6.22 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | TCCACACCAG GACAGAGTAC GAGGAGATGC CACTGCTGGC TCCAGCAGCC TGCTTTTATT 60
CTCTTATCTG GCCCCACCCA CATCCTGCTG ATTGGTCCAT TTTACAGAGA GCCGATTGGT 120
CTGTTTTACA AAGAGCTGAT TGGTCCGTTT TGACAGGGTG TTGATTGGTG CGTTTACAAT 180
CCCTAAGCTA GACACAGAAG TTCTCCAAGT CCCCACTAGA TTAGCTAGAT ACGGAGTGCT 240
GATTGGTGTA TTCACAATCC CTTAGCTAGA CATAAAGAGT CTCCAAGTCC CCATCAGATT 300
AGCTAGATAC AGAGTGCCCA TTAGTGCATC CACAAACCCT GAGGTAGACA CAGGGTGCTG 360
ATTGGTGTGT TCACAAACCT TGAGCTAGAT ACAGAGTGCT GATTGGTGTA TTTACAATCC 420
CTTAGCTAGA CATAAAGGTT CTCCAAGTTC CCCACTAGAC TCAGGAGCCC AGCTGGCTTC 480
ACCTAGTGGA TACCGCAGCG GGGCCGCAGG TGGAGCTGCC TGCCAGTCCT GCAGCGTGTG 540
CCTGCACTCC TCAGCCCTTG GGCAGTAGAT GGGACCAGGC GCCCTGGAGC AGGGGCCGGA 600
GCTCCTCGGG GAGGCTTGGG CAGCGCAGGA GCCCACGGCG GGGGTGGGGG AGGCGGCTCA 660
GGCATGGCCA GCTGTAAGTT CCGAGTCCTG CCCCGCGAGG AGGCAGCTGA GGCCCAAGAA 720
TTTGAGCGCA GCGCCAGCGG GCCGGCACTG CTGGGGGACC CAGGGCACCC TCCGCAGCTC 780
CTGGCCTGGG TGCTAAGCCC CTCACTGCCC GGGGCGGCGG CGCCAGCCGG CCGCTGCAAG 840
TGCGGGGCCA GCTGAGCCCA CGCCCACCCG GAACTCGCGC TGGCCCGCAA GTGCGGCACG 900
CAGCCCCGGT TCCCGCCCGC GCCGCTCCCT CCACACCTCC CGGCAAGCTG AGCGAGCCAG 960
CTCCGGCCTC AGCCAGCCCA GAAAGGAGCT CCCACAGTGC AGCGGTGGGC TGAAGGGCTC 1020
CTCAAGCGCG GCCAGAGTGG GCGCCAAGGC CGAGGAGGCG CCCAGAGTGA GTAAGGGCTG 1080
CGAGGGCTGC CAGCACGCTC TCACCTCTCA CCCAGGACTT TGGAGGCTGA GGTGGGTGGA 1140
TTCCTTGAGG TCAGGAGTTC AAGACCAGCC TGGCCAACAT GGCAAAACCC CATCTCTACT 1200
AAAAATACTG AAATTAGCTG GGTGTGGTGG TGGGCGCCTG TAATTCCAGC TTCTTGGTTG 1260
GTTGAAGCAC AAGAATCTTT TGAACCCGGG AGGCAGAGGT 1300
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