Tag | Content |
---|
EnhancerAtlas ID | HS082-07498 |
Organism | Homo sapiens |
Tissue/cell | HCASMC |
Coordinate | chr12:291200-292310 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Crx | MA0467.1 | chr12:291882-291893 | CTAATCCCCTT | - | 6.32 | ZNF263 | MA0528.1 | chr12:291625-291646 | TCCTCCCCTGCGCCCTCCCTC | - | 6.11 |
|
| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr12 | 291440 | 291523 | chr12 | 291572 | 292069 |
|
| Number: 1 | ID | Chromosome | Start | End |
GH12I000182 | chr12 | 291400 | 292062 |
|
Enhancer Sequence | CGACTACCCT GTGCACCAGG TCCCCTCACT CACCTTCCTC GGGGTGAGCC ACATGGCCCC 60 CGGTGTCACA GATGAAGGTC TGAAGACGCC CAGGCAAGAA GGACGCTCCG TCCAGGGCGG 120 AGCCTTGGGA GCAAAGGCAG ACCCCGTGGA GGGCAAGGGA GGTGGTCCTT CCAGGAGAAC 180 GTGAGGCCCA GCCAGCGCCC AGCGGCCTGG AGCCGCAGGC TGAGTTCTGA TCTGCTCCCC 240 TTCCCGTCCC AGGACGGCAG CCAGGCCCCA AGATAGACCA AGCCCAGGTC AGAGTCAGGG 300 AGGTTAAATG AGGGCGCAGG AATGGGGGGT GCAGAGGGAC AGGTCCAGAA GTGGTTCTGC 360 CAGAATTCCC TTCTGGATGG GCTGGAGGAG AGGGAGCTGG AGCTCAGCGG GTGGGCGGAG 420 TGCTCTCCTC CCCTGCGCCC TCCCTCCCGT GCCCCTGCAG GGCTGCACGG GTTCCCTCCC 480 TAGGGAACCA GGCTGCCTAA CCCACCAGCC GGCCCCTAGC ACCTCAGCGC TTCCTGCTCC 540 CATGACCCTA AGGACTAAGT GACCTCAAGC CTGGCTCTGG GAAAACTGTG GGAACCGGCT 600 GCTGGGAAGA CGACCTGGCT GTTACTCCCA CGTTTCCAAC TGCCTAGACA GACCTGCCCT 660 GCCCTCCTTT CCTCAAGAAA CCCTAATCCC CTTTCCTTCT GAGACATCTA GGGTAGGAGT 720 CAGCCTCCCT CCCTGCACCC TCAGAGGGAA TGGAAGGCAG GGGAGTCATA CAGCAGTGCC 780 AGGCCTGCAG GCTGAGTCAC AGGCCAGTCA TCCTTCTATG GCTAAGGGGA CTACTTCACT 840 TAAGAGGTTA AAAAAGAAGA ACAGAATAAG CCCAAAGGAA AGAAACAATA AAGACAAAAG 900 CAGAAGTAAT AAAATAGAAA ATATATATAC AATAGAAAAG ATTAACACAA CCAAAAGTTA 960 GTTCTAAGAA ATGACTAATA AAGTTGACAA ACCTCTGATA AGACTGATCA CGAAGAAGAG 1020 AGACGGCACA AATGAATAAC CTGAGGACCA ACAGGGAGAA CGTAACTATG AATGCTGCAG 1080 AGATTTTCAA AATAAAATAC TTCAAATAAA 1110
|