| Tag | Content |
|---|
EnhancerAtlas ID | HS052-25138 |
Organism | Homo sapiens |
Tissue/cell | Fibroblast_foreskin |
Coordinate | chr22:41404700-41406100 |
SNPs | | Number: 2 | 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 | CCATGTAAAC CTCATAAGCA AGGTGGAATT TTTTTGCTTC CATTTTACAG TTAGGGAACC 60
TAAGGCAGAT GGTGTTTTAA GCGACTTGCC CAAATCAGCA GAGCTAGCTC CATAGCAGGG 120
AAGGATTTGA GCCCAGGTTT TTAGTTGCCT TTGGAACTCT TGGTCTTTTC TACTTCGCTC 180
AGTGTTCACT GTAGCTGCAT GTAACATGGC TCACTCATTC ATTCACTTGT TCATTTAGTA 240
AATATTTCCC AAGCCTCCTC CATCCCTCCG CCACCCAAAA TGCCAGGCCC TGTCCTGCAC 300
ACTGGGGACC CATACATCCA TGGGTCACGG ACCTTGCCCC AGAGGAGCTC TGGTCCCACG 360
GCCTGGGCAA TAAGTGTCCC TGTGGGCTTC ATTTTTGTTT TCTATTTTTT AAGAGACAGG 420
GTCTTGCTCT GTTACCCAGG CTGGAGTATA GTGGTACCAT CACAGCTCAC TGCAGCCTCA 480
AACTCCTGGG CTCAAGTGTT TCTCTTGCCT CAGCCTCCCA AGTAGCTGAG ACTATAGGCA 540
TGCACCTCCA CGCCTGGCTA AAGTTTTGTT TTGTTGGTTT TTTTTTTTTT TTTTTTTTTG 600
AGCCTCTATG CCCCAGGCTC AAGCAATCCT GCCTATGTTG CTCAGGCTGA CCTCACACTC 660
CTGGGCTCAA GCCATCTTCC ACCTCAGCCT CCCAAAGTGC TAGGGTTACA TGCATGAGCC 720
ATCACATCTG GCTCCCACGG GGGGTTTTGT AAACTGAACA AAGGGAGCTC CCTTTCCCCA 780
GCAATTCATC CCTGGAGTCC ATATGAACCA ATGTTCCTCA TTTACAGCAG AAAAAGCAGC 840
TTCCCATGCT CTAACCCCTG CCTGCTCCTC AGCTGAATGA GGCTGACAGG TGCACACCCT 900
GCAGCATCCT GCACCTCACC AGGTAAACAG GCCTGAAAGA GGGAGGCCAT GGGTGTGGGC 960
ACAGGCTCAG GGCCAAGCTG ACCTCGCAAA GGCTGAGGGG CGGGAAGAAC AGGAGGAAGT 1020
GTGGGCAATG GGGAGCTGCT GGGTCTGGAG CAATTACCAT TGCCACATGG TGAAGACACC 1080
AGCCCAGAGG CTGACCTGGG GCTGAGCAGA GCCCAGCAGT AGGGTAGGAA GGGGCCCACC 1140
CTTGCTCCTC CAGCTCCCTT TTCTCCCCAC CCCTCAACCC CAAACTCTGT CCCTCCTCCT 1200
CACTGCCCTG CTGTCAGTTC ACCTCCTTTA ACCCTTTCCT CCCGTGCCTC CCAAGGAAAA 1260
GGGGAAACTA ACAGGCCAAC TGATCTTCAA CGGCCATGGA GCTTCGTTTC TTAAAAATTC 1320
ATTAAGAGGC CAGGCGCAGT GGCTCATGCC TGTAATCCCA GCACTTTGGG AAGCCAATGG 1380
AGGTGGATCA CTTGTGGTCA 1400
|
