Tag | Content |
---|
EnhancerAtlas ID | HS007-00494 |
Organism | Homo sapiens |
Tissue/cell | BE2C |
Coordinate | chr1:53834010-53834980 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Crx | MA0467.1 | chr1:53834193-53834204 | AAGAGGATTAG | + | 6.62 | ZNF263 | MA0528.1 | chr1:53834508-53834529 | GACCCTCTCTCTTCCTCCTCC | - | 6.19 |
|
| 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 |
GH01I053367 | chr1 | 53832884 | 53834793 |
|
Enhancer Sequence | TGCTGTCTCT CAGGCTTTAG CCCGGGTGCA ACTTTGTATC TGCCTCCAGG GCTGCAAACA 60 CTCCCTGCCC AGCTGTCTCT TTGCTTTTAA TTGTCTATTT CCTCCACACT GCCAGTCCTC 120 AGTTTCCCTT CTGTTAAACA GGCTGTCCTA ACCATTCCAC GCAACGTACC GTGTGGGGAC 180 TAGAAGAGGA TTAGCCCAGC AGAGGCTTTG TGGGCATGTT GCTTCCTTCT TTTGCCCTTC 240 CAACTGCCTG CCCTTTCCAT CCCAGCAATG GATGGGCTGG GAGCCAGCTG GGCCCGGGTG 300 CCTAGGCTCA CCATGTGGCA TCGGCCTCAG CCATTCCTCC CAGGGCCGCA GCCACTCTTC 360 ACCCCTAGGA GAAACTGTGG GGTCCTGGCA GGGGCGGGAG GCGGCTCTAG GGACGCAGCT 420 CTGCCCTTGA CTGGGAATGA CGCCAAGGCT GCTGCTGCCT GCTGACAGTC TATCCTGCTG 480 CCCAGTCCGC TGGCGGCAGA CCCTCTCTCT TCCTCCTCCC ACAGTCCCAC CCACAGCCTG 540 AGCCCTGGGG TTCAGCCTGC TCAGGTCCAC TCTGACGGGG CTAAGCAGAG CTCCCCAGTC 600 CAGGAAGCCC AGACACCATC AGGCTCTGTG GCCCTGGCAA GTCCTGCCAG TGTTTAGGAG 660 GTGACCAGAA CCAGTTCTGA CAACCCAAGA AGCTGGAGCA CAAATACCCC TTCCTGAGCC 720 TGCCACCTGC AGTGTGAAGG GCCCGAGCAG TGACTCTGAA GCCAGCCTTC ACCACAATCA 780 GCTGTGTCTC TGGGCAAGTT ATCTAATCCT CCGTGCGTCT TTGTCTGTAA AGTGGAGTAA 840 CAGTGTCTAC CCCGCAGGGC TGGTATGTGG ACTAAATGAG GTAATACACA GGTGACTCTC 900 GGGACAACAG AGCCCCTGGG AAGCACTTCA TGAGGATTAG CCATTATTAT TTCACCTGTG 960 TTCTGCATGT 970
|