| Tag | Content |
|---|
EnhancerAtlas ID | HS177-11764 | Organism | Homo sapiens | Tissue/cell | SK-N-SH_RA | Coordinate | chr2:39470500-39471870 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| REST | MA0138.2 | chr2:39471547-39471568 | CTTAGCACCCGGGCCAGCGGC | + | 6.38 |
| | | 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 |
| GH02I039243 | chr2 | 39470743 | 39471341 |
| Enhancer Sequence | ACCTGTTTAT AAACCTGTCC AGTTGACAAT ACAATCAGAC TAATTAAAAG CATCCCCAGA 60
AAACCAGAAT ACCACATAAT TATACAAAAT CCGATAAAGT AATTTTGTTT AAATATATCA 120
CATTTCGTGT GTGCACATAA CAGATCTGCA AGTCAAGCAC AAATCCACTT TATTTCCAGG 180
CCTCTGGTCT TCAGCCTTCT TCATTTAATG ACAGTTCTCT TTCTCGGCCA TAGGTAGGCC 240
TCCGCCTTGC GCGCTCCTCG GCCCCCGCCG CCGCCCACTC CCTGGGCAGC ACCATTTCCG 300
CCCCGAGGGA CCCTCACCGG GTCAGTGCTG CCACCTCGAA TCCGCCCCTT CCCTTCCAGG 360
GGCCACCGAA GCGGAAGGCG GTCCCGCTTT TCTTTCGGGG AACTTTTCTT GGTTCCTGCA 420
ACTGGGATCC GCAGTCTAGA CCTCGCGGCT CACCCCATCA ACCCCGCACG CTGCCCGCAG 480
TTCCCCCGCC ACCGGCAGAA TCCGCACTTA CTGCACCCAC AGGGCGACGG TGACGAAGCT 540
TCGAGCAGCG CCGAACAGCC CCAGCCCCAG CTCCCGCGCG TGTCGCTCGG AGGAGGCGCC 600
GTGTACCCAG CGACTTCGGA GCCAGCGGAA CCGCCGCAGC GTCTCCCGGG CAACCGGAAC 660
GCTAGGGCGC GCGGGGCACT GCGGCTTCCG GAGCGGGTTC CCCTGGCGCT GGCAGCCCCA 720
GCCCTGATCC TTCTGAGAGG TGACAGCGTG CTGGCAGTCC TCACAGCCCT CGCTCGGTCT 780
CGACGCCTCC TATGCCTGGG CTCCCACTTT GGCGGCACTT GAGGAGCCCT TCAGCCCACC 840
GCTGCACTGT GGGAGCCCCT TTCTGGGCTG GCCAAGGCCG GAGCCCACTC CCTCAGCTTG 900
CAGGGAGCTG TGGAGGGAGA GGCGCGAGCG GGAACCGGGG CTGCGCACGG CGCTTGCGGG 960
CCAGCTGGAG TTCCGGGTGG GCGTGGGCTT GGCGGGCCCC GCACTCTGAG CAGCCCGCCG 1020
GCTCTGCCGA CCCCGGGCAA TGAGGGACTT AGCACCCGGG CCAGCGGCTG CAGAAGGTGT 1080
AATGGGTCCC CCAGCAGTGC CAGCCCACCG GCGCTGCGCT CGATTTCTCA CTGGGCCTTA 1140
GCTGCCTTCC TGCGGGGCAG GGCTTGGGAC CTGCAGCCCG CCATACCTGA GCCTCCCACC 1200
CCCTCCATGG GTTCCTGTGC GGCCGGAACC TTCCCGACGA GTGCCACCCC CTGCTCCACG 1260
GCGCCCAGTC CCATCGACCA CCCAAGGGCT GAGGAGTGCG AGCGAACGGC GCGGGACTGG 1320
CAGGCAGCTC CACCTGCAGC CCCTGTGCGG GATCCACTTG TTGAAGCCAG 1370
|
| |
|
|
|
