| Tag | Content |
|---|
EnhancerAtlas ID | HS184-02690 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr1:225039040-225039960 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr1:225039360-225039379 | TAGTGCCCTCTGCTGGTGA | - | 7.82 | | Myod1 | MA0499.1 | chr1:225039155-225039168 | AGTGACAGCTGCC | - | 6.04 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 2 | ID | Chromosome | Start | End |
| GH01I224851 | chr1 | 225039281 | 225039450 | | GH01I224852 | chr1 | 225039561 | 225039830 |
|
Enhancer Sequence | CTTGGAATGG GGGTCGTTCC AAGGTGTCCA CAGTCAGACC CACCTGCTCC AGGGTGGCTG 60
AGAGCATGAG AAAAGGTAAC TTGCTCAGAG TGCTCAGTAC TGACCTATGC TGGTCAGTGA 120
CAGCTGCCAA TAAACAAGGG GGTGGGGACT GTGCCTCCCA AGGTAGGCCA GCCTAACTCT 180
GTAAAGCACT GTTAGTTTAA CTGTCCCAAA GCGAGCTATG GACAAGAGCC TTGAAGTCCA 240
GTGTTTTATA ATGGGCATAA ACACAAGGTG CCAGCTTGGA GGACTTTCTG CTGATGCCCT 300
CAACAGAGCC AGCTCTGGCA TAGTGCCCTC TGCTGGTGAT GTGGATCCAT GCTCGGCAAG 360
CCCGGGAAAA AAGGCAGGTC AAGACACTTT GAGACTCCTT CTCAGGCCAC CACATGGTGT 420
TTAATGATTA TTGTTATATT CTAAGTTGAT AGAAGTGCAC TCTGGCCCTT AGCTGGGGAC 480
CAAAGCAAAG GAGTGGAGAG GAGCTAGGAG GGCAGTAGCA ACACGGGGAC ACCCTCTAAG 540
CAGCAGCTCA GCCCGTCCCT GCCCTGGCCT TTCAGCCCCT CACTCCTCCT GAGTCCTCTC 600
AGCTCACTGC CATGAGGTGT TCTATGTTTC CTCCACGGGG CTGGGGGATC CGAAGGCAGG 660
CACTACTTTG ACTTTCTGCA TCTGGAGGCC ACAGTAGGTA CTGAATACAC CTTTGATGGA 720
AGGGCTCATC ACCTGTTCCG TTCCCACACT GTTTCCATGA CAAATGACTG AATGCAGACT 780
GTGCTCGAGA GGCTCGCACA GCAGGGCCGC TCCCACTGCT CTGTTGCTTA AACAGGAAAG 840
GGTCCAGCCT AGGGCACCGA AGGCAAAGGA GCAGAGGGGG GTTCTCTCAA TTCAGTGAGG 900
GGCACAAAAG GCAACCCACC 920
|
