| Tag | Content |
|---|
EnhancerAtlas ID | HS034-18021 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr2:233367550-233368530 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CREB1 | MA0018.3 | chr2:233367868-233367880 | CGTGACGTCACC | + | 6.32 | | CREB1 | MA0018.3 | chr2:233367868-233367880 | CGTGACGTCACC | - | 6.32 | | ZNF263 | MA0528.1 | chr2:233367630-233367651 | GGAGGAGAGGGGGGCGGGGAG | + | 7.08 |
|
| | 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 |
| GH02I232500 | chr2 | 233365404 | 233368709 |
|
Enhancer Sequence | ATGCGCCCAC AGAAAATACC ACCGAAGTAA GAGACGGAAG AGACGGGAGG TTGGGGGGAG 60
TGGAGCGGGG TGGTGTTGGG GGAGGAGAGG GGGGCGGGGA GGCAAGATCA GACGACAAAG 120
AAAGGGAAGG CAGAGGCGGG GGCGGGAGGG AGGTTTATCC GTAGGAGTCA GCCCAGTTGG 180
GTCAAACTAA GGACCCAGTG CAGACCCCGA GGCCCAGAGA CACAGGTGTG CGCACAAACA 240
CGCACTCTGC GGAAGGCCGG GGCGGGCCTG GCCGCTGCGG GACTCCTGGC CCGGCGCCCT 300
TGACGTCAGC GGCTGGGCCG TGACGTCACC TCACCGCCCC CGCCGCGCTC CCGCCCCCGC 360
CCGCGGGCAC TCAGTCTCCG CTAATGGCAG GCGACGGGGA ATGGCACATC TGTCTTGCCG 420
GGAATTAGTT CATTGAATCA GGCGGCCCGA GCTGCGGCAG CGACCTTAGC CCTGGCCCCA 480
GGGAGGGGTC TGGGCGGGCG GCGTGGGGGA GGTTCAGGCT GGAGGGCTGA GTGCGGGGAC 540
GGGAGGAGGG GACTCACCTG GACTCGCGAG GGGGACTGAG CGCTCTCCAA ATATAGGTCA 600
ATGTCCCGCT CAGCCTCCCT CCCCCAGCAC CGTGAGGACC GAGGCCTGGG GCCTGGCGCC 660
CGCCTGGTGG ACCTCGGGGG CAGGCTGGGG ACCGGGCCCC TGCGGGACGC GGCGCGGCAG 720
GACGCTCCCC GCGCCTTTCT TTCTGCACCT GCCCCTCGGG GTGGGTCCCC CTCTTTACCC 780
TCGCTTCCCC CCGCGGGTGC CGATAAAGGC GGCTAATTCC CGAGCCCGGG GAGGGAGGGG 840
GCGACTGTTC CAGTCAACAC TTCCCCGCGC TCTTCCCCGA CCCTCCCAGA GCGTTCCCGC 900
TGCTCAGGGC GAGGAGCAGC TGCGGCCAGT TTGTCCTAGC GGTTTAGGAG GCAGGGAGGT 960
TTCCTCCAGC CTGGAGCTCT 980
|
