| Tag | Content |
|---|
EnhancerAtlas ID | HS087-14175 |
Organism | Homo sapiens |
Tissue/cell | HEK293T |
Coordinate | chr22:44340680-44342030 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr22:44341932-44341951 | TGGTGCCCTCTACTGGCCG | - | 8.22 | | NFIC | MA0161.2 | chr22:44341402-44341413 | TACTTGGCACA | + | 6.32 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr22 | 44341640 | 44341710 | | chr22 | 44341338 | 44341408 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH22I043945 | chr22 | 44341841 | 44342030 |
|
Enhancer Sequence | TACTTTGGCT GTGGGTGTGT GGGCCGGACG GGCACCTCTC TCATCTGATG AGGCCTCACA 60
CGACATTCTA GAAACAGCTG GCTGAACACC AAGCAAGGAG CTTGCCCTTG GGTGTGGGGA 120
CCCTGTCTCA TGGGAGGCAG CTGAGTCAGT CAGAGGTCCT GGCACACCTG CTGAGAGCTG 180
CCACCCAGGC CAACCTGAAC CGGAGCCTGG GAAGACTTCC CGTCGGATGA GTCTCTTTGA 240
GTGCAGCATT GATGGTGGAA GAGCAGAGAG GCCCCAGATA AGCAGGGAAA GGTGCTTCAG 300
ACAGAGTGGC TGGGATGAGG ACTGGGGAGT GTCAGATAGC GCTGGCGTGT CTGAGCGAAG 360
GAGCTCTGGC ACCCATGGCA CAGGAAGGAG GTGGGACCCT GGAGGGGCAG GGCTAGCAGA 420
GCTCCTCGGA GCGTGTGGCT AGGTGCCTGG TAATGCAAGC CCCCTGTCCT CCACCCTCTG 480
TTGTACTGAG TCACAGTCTC CGGGGTGAAG CCTAGCAGTC TGCGTTGACA GGCCCCAGGG 540
GATGCCGCTA CTTCCTGAAT TCTGAATTCT GGAAACTGAG CCGGAGTTCA GGGCCTGGCT 600
CCCATTACCA GGGTTGGGCG TTATCCTGAA AATCATAGGC CTTGGTTTCC TCACTTGGCT 660
AACAGGGGTG ATCCCCATCC CCTCAATGGG TTTCCGTGAG CTCCTGAGAG CCCGTAGCAT 720
GGTACTTGGC ACATGCTGGG CATCAGGAGG TATGGCCTCT CTTGCTATTG TTGTTATTGG 780
TAGACACAGA AGGATTTAAA AGTAGGGGAA TGCAAAGATC CGATTTGCTA GGGAAGAGGG 840
CAGTAGTGGC CAAGTAGAGG GTGGATCCTG GGCCCTGGCT GGCAGCAGGC AGCAAGGGGG 900
GCTGCCAGGG CCCAGGCAGG GACGATCTGT AGACCGAGAG GCTTCCTAAG GCTCTTGGAC 960
AGGAGGAGGT GTCGGTTCCA AGCCTAAGGA GTGGGGCAGC CCTGGTGACT GGTGGTCAGT 1020
GGTGCCAGGC GGTGGGTGGT AGGACACCCT GGCAGGCAAG TAGGTTTGTG TGGGGGAAAC 1080
TGATAGGCCC CTCCAGGGAT TCGTTGGTGG ACAACACCTG TGATGTCCAG TGGGAGGTGT 1140
CCAGGTAGCT GGGAGGGCCA CAGGCTTGGA AGACCTAGGT GGTGACATCA GCCCAGCACT 1200
GAGGGCTAGA AGAAGCTGTG TCTCTGGCTG TGACGGCACC CTAGAGTGTG TGTGGTGCCC 1260
TCTACTGGCC GGCAATGTGG GTCCACCGTA GCTCAGACTG CACACTGCAG CAGCGGGAAC 1320
GGCCTCTAAG CCAACTTCCT CCATGTGTTT 1350
|
