| Tag | Content |
|---|
EnhancerAtlas ID | HS026-01394 |
Organism | Homo sapiens |
Tissue/cell | CNCC |
Coordinate | chr1:62802330-62804640 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr1:62803502-62803520 | GAAAGGGAGGGAGGGAGG | + | 6.13 | | NFYA | MA0060.3 | chr1:62803790-62803801 | TCTGATTGGCC | - | 6.02 | | NFYB | MA0502.1 | chr1:62803791-62803806 | CTGATTGGCCCGGCT | - | 6.16 | | SOX10 | MA0442.2 | chr1:62803136-62803147 | AAAACAAAGAC | + | 6.14 | | ZNF263 | MA0528.1 | chr1:62803504-62803525 | AAGGGAGGGAGGGAGGGAGAG | + | 6.58 |
|
| | 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 |
| GH01I062336 | chr1 | 62802093 | 62804728 |
|
Enhancer Sequence | GTCTCTCTTA AGATATTCAG AACAGAGGAA AAAGCAGGAG TTAGATGGGT CTTGAGTGAC 60
TCTTTCTAGG CCAGCGTCCT TGTTTCCCAA GTCCAGTTCT CTTCCCCCAG GCTCCTCCCC 120
TGGGAGCCTG GAGGCCCCTA CACCTGGAGG AGCCGGGCCA AGGTTGGATG GCTGCCTGCC 180
TGCCGAGGGC ACTGTAGAGC GGGTGGTGGG TAGTGGATGA GGGTGGCACT TGACGCTGAG 240
ACCCCGCCGA CAGCCTGGGC ATCCTTGACT CGGGAAGTTA CACAGAGTGA TGGACCTTCC 300
TGTTAGGACT GTTTTACTAT AAATGAAACA GGAAAATATG AGAGAGTTCT TGAACTCTCC 360
TGGGAGGAAG ACAGTAACAA GCCATCTGAC CACCCAACTG CAGCTCACTT TAAATAACTT 420
TCTATGGCTA TTTTAAGACA GAAATGGACA TTCTCCTATT AATAAGCCTG GCTAAGTAAG 480
GCTGATCTGC AGCCAGGGTG AATCTGAAAG CCTCCTTCCC CACAGAGTCC CCAAGGGCAA 540
CAGACAGAGG GGCGTGCTCT TGTCGATGGA CAGGCCCACA CTGGTCATTT CGGGCAGGAA 600
ATTCTGTAGG GGAAGAGATT CCTCAACCTC TTATGCCTGC TCTTGCCCTT CTTGGAGGAG 660
CTCAAAAGCA GAATTTCTGT GGCTGAAAGG AGGATTTCCC CAGGGCCAGG CGTTGCCTCT 720
CCCAGGCTCC GCACTGACAC TCCTGGACAC TCCCACAGCC TAAGGAAGGA GGGTCTATTC 780
TTATTCCCTC CTTCCTTATA GATGTGAAAA CAAAGACAGG GGAGAGTTCA TTCTTCTCCA 840
AGTTCTCACA GTTAGAAAGG GAAGCTGGGA ATTGAGAGGG TTGCAAGTCA CCACTCCCCA 900
CCGTGCCTGC CCTCCTGAGG CACGGTTTAG ATGCTGCCCA GGCCTTCGAA GCCAACTTCT 960
TGCTTTGCCT GGGCAGTGGT GGGAGGCGGC TGCTCATCAC CGCTGGGCTC TCCCTTTCTT 1020
GCTCACTTGG CTCTTTGGTG TCCTTGTCAT AACTGAAAAA GCCATCATGG GCTGACGACC 1080
AGGTCCCCTT CACCCCAGAA CCATTTTGTG GGAGTGGTCA CTGCCCGGCT CCCCTCCCCT 1140
CCTGTGTCAT CAGACACTCA GTCACCCAAA GAGAAAGGGA GGGAGGGAGG GAGAGCCTGG 1200
GGCAGGGGCA GAGGCGCCTC AGCCTGACAT CATGGCTTCT GTCTGTGTCA CTGCCTTTCT 1260
CCTGCCTTTC CCAGTCTGAC TTCTCACTGT AAGGCTTCTA CTAGCCAGTT CTCTGCTTCC 1320
CCCATCTCTC TCTTCCTCAT AGGCCCCCCA GCTCTAGCTC CACCATCTGG AATCTTCCGA 1380
GGAGTTCCTG TGGCCTCCAG TCCCGCAGCG GACAGACTGC ATGTCTCAGC ATTTCTTGGT 1440
TCAAATTCCT GAGGCAGGAA TCTGATTGGC CCGGCTCCCT TTTCGTGCTG GGCCACAGGT 1500
CATAGGTTGC TGGCCAGCCT CAGTTGGCTG TCCACGGACA GCCAGAGTTG AGTGGGACAA 1560
AACACAGCTG AGGAATGTCC CCTCCTTTCA GCCGAGGCTG TTTGTTGAAT TGTTCCTTTT 1620
AGAAGGGACA ATGGCCAACA TTTGTACTGT GCTTCTAAAG CCTCTGCTGG CCTGAGGCAG 1680
GAACACAGTC TTTTGGGTCC TTTATAAATA ACTGTTTTAA CTGCTAGAAC AACTTACAAT 1740
ACGAAGGCTC TCACTCCAGC TTTCACTACG GCGTACCCCA TCTCTTTCAG ACTCCTCTCC 1800
TTGCCCCAAA TCTGTCCCTG GGAGCCCCCA GTGGTGACTC AGGGGTGAGT CCAGTCTGCA 1860
GCCGACTGCC TCCCACCGCA AATACTGCTG GCCCCACGAC CTTTGACACT TGGATTTTAG 1920
CAGCGGTCAC TCTATCTCCC GGCCCCAGAG TCGCCTCTGC CGACGGCCTC AGCATACCCA 1980
AGCCCTGCCA TGATTCAAGG AATAGCCACA GGGAGAGCTC TTCTCCCTGT TTGTGGGCCT 2040
CACCCCCTAT TAAATAGGAT TTTAATACTC GGGCCCCGAT GGCTTAGGGG CCGGAATGCC 2100
TAGTTTTTGC TCGAAGGCCA CTACGCCCAG GATCCAGCAC AAATGCCTGT GAGGCCAGGA 2160
CTGGGGATGC AGGGGCAAAG TTAAGGGGGG GACAGCAGGA CTTCCCTTGC CTGGGCCTGG 2220
GGGTGACCGC ACTTGACTTG ATTCCCCTGG GAGAAGTTAT TTCCCCACAG ACTCCTTGGT 2280
CTCTTGGGCC GTAGACTTGG GTGGGCCTCC 2310
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