| Tag | Content |
|---|
EnhancerAtlas ID | HS184-10315 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr14:74718120-74719110 |
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 | chr14:74718408-74718427 | AGCTGCCCCCTAGTGGGTA | - | 6.01 | | IRF1 | MA0050.2 | chr14:74719087-74719108 | CTTTTCTTTCTTTTTTTTTTT | + | 6.41 |
|
| | 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 |
| GH14I074251 | chr14 | 74717904 | 74718730 |
|
Enhancer Sequence | CCAGCCTGGG CAACAAGAGC GAAACTCTGT CTCAAAAAAG CAACAAAAAC AACAACAAAA 60
AATCAAACCT CTTCACGTTG GCATTTGTAT GCTTTTAAAT CTCTCTAGGT GATTCTGTGT 120
GCAGTGAATG TAAACACACT GGGTTGGAGG CTCAGGAGAG GGTTGTTTCT GTTCTGAGTG 180
GGTTAATATG AGTGGAAGAA AGTGGCGTTT TGGGTGGCAG GGGTTTGGGG TGAGGAAGGA 240
AATGGAATGT CAGTGCTCAG GCAAGAGGCT GTCTGGAAAT GTGGTCGGAG CTGCCCCCTA 300
GTGGGTAACA GAGGCTGCAG CAAGACTCCA CTTGTCTGAG CCTTAGGCTG GGCTGCACAG 360
AGCGCGCTGC AATAAACCGC GGGCGAAGTG CTGAGTGGGT GCAGAGTGTG AAGCCCTTAA 420
GTCACGCCAG CGATGAGCCC AAATTCATCA GCTTCCAGCC AGAGGGGAAG AAAGAGACTG 480
GGGGAAAGTG ATGGACGCTC ACCTGATGGC ATGTGGCAAG ATGGCAGGGC AGGGCCTGAG 540
GTAGCGAGGA GACCAGAATG TGCAAAGGGC ATCTGTCATG CACAATGTCT CCTTCAGGAG 600
GTATTTAGGA GGGCGATCCT GGAAGGACTG CAGAGGGTCT CCTGGGAGAT GATTGAGGGA 660
TGGAACCCTG GGCATGTTTT CTGGTGGCGA TGCCAGGGCG GGAGCTTGCA GGACAGCAGC 720
TATGTGATGA TGCAGAGACA AGAGGAGGTG TGAGGCATGG CCTCGGCTGT TCCTGCTGAT 780
TGCCCACGTC GAGAAAGAGC TGACAGGGTT TCCTGGCCTG CTAGCTGTGC CTTTGCATCC 840
ACTTGGCAAG AAGTCCTTCC CTGGGCCCAG TCTTTCCTTC GAGGCACAGG CACATTCTGT 900
GCCTGCTGTG GAGGCACCTG CCAGACAACT GTGGACAGCC ACAGTCTTTC CACACAACCT 960
GGGCTTTCTT TTCTTTCTTT TTTTTTTTTT 990
|
