Tag | Content |
---|
EnhancerAtlas ID | HS092-27525 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr22:41405070-41406000 |
Target genes | |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
E2F6 | MA0471.1 | chr22:41405697-41405708 | GGGCGGGAAGA | + | 6.14 | ESR2 | MA0258.2 | chr22:41405669-41405684 | GGGCCAAGCTGACCT | - | 6.52 |
|
| 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 |
GH22I041008 | chr22 | 41404931 | 41406002 |
|
Enhancer Sequence | TAAGTGTCCC TGTGGGCTTC ATTTTTGTTT TCTATTTTTT AAGAGACAGG GTCTTGCTCT 60 GTTACCCAGG CTGGAGTATA GTGGTACCAT CACAGCTCAC TGCAGCCTCA AACTCCTGGG 120 CTCAAGTGTT TCTCTTGCCT CAGCCTCCCA AGTAGCTGAG ACTATAGGCA TGCACCTCCA 180 CGCCTGGCTA AAGTTTTGTT TTGTTGGTTT TTTTTTTTTT TTTTTTTTTG AGCCTCTATG 240 CCCCAGGCTC AAGCAATCCT GCCTATGTTG CTCAGGCTGA CCTCACACTC CTGGGCTCAA 300 GCCATCTTCC ACCTCAGCCT CCCAAAGTGC TAGGGTTACA TGCATGAGCC ATCACATCTG 360 GCTCCCACGG GGGGTTTTGT AAACTGAACA AAGGGAGCTC CCTTTCCCCA GCAATTCATC 420 CCTGGAGTCC ATATGAACCA ATGTTCCTCA TTTACAGCAG AAAAAGCAGC TTCCCATGCT 480 CTAACCCCTG CCTGCTCCTC AGCTGAATGA GGCTGACAGG TGCACACCCT GCAGCATCCT 540 GCACCTCACC AGGTAAACAG GCCTGAAAGA GGGAGGCCAT GGGTGTGGGC ACAGGCTCAG 600 GGCCAAGCTG ACCTCGCAAA GGCTGAGGGG CGGGAAGAAC AGGAGGAAGT GTGGGCAATG 660 GGGAGCTGCT GGGTCTGGAG CAATTACCAT TGCCACATGG TGAAGACACC AGCCCAGAGG 720 CTGACCTGGG GCTGAGCAGA GCCCAGCAGT AGGGTAGGAA GGGGCCCACC CTTGCTCCTC 780 CAGCTCCCTT TTCTCCCCAC CCCTCAACCC CAAACTCTGT CCCTCCTCCT CACTGCCCTG 840 CTGTCAGTTC ACCTCCTTTA ACCCTTTCCT CCCGTGCCTC CCAAGGAAAA GGGGAAACTA 900 ACAGGCCAAC TGATCTTCAA CGGCCATGGA 930
|