| Tag | Content |
|---|
EnhancerAtlas ID | HS184-20783 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr3:120277180-120278210 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr3:120277914-120277933 | GAGCGCCCCCTGCTGGCCA | - | 9.23 | | FOXP1 | MA0481.2 | chr3:120277196-120277208 | ATGTAAACAGAG | + | 6.32 | | FOXP2 | MA0593.1 | chr3:120277196-120277207 | ATGTAAACAGA | + | 6.02 | | RUNX3 | MA0684.1 | chr3:120277833-120277843 | AAACCGCAAA | + | 6.02 |
|
| | 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 |
| GH03I120558 | chr3 | 120276960 | 120280646 |
|
Enhancer Sequence | AAAACGAAAC AAAAACATGT AAACAGAGGT ACGGTCATTC TGGAGTTGGT ATCTTCTCTA 60
AAAGACCTGG AAGACCCGTC CTGCTGGCCA GGGAGGAGCT GACCATTGGA GGTCAGGGGT 120
TTGGGGGAGG TGGGCAAGAG CGGCGGCAGC CAAGGGGAAG AGGCAGCTGT AGGGTGGCAC 180
GGCAGCCCAC TCCGAGAACA GAGACGGGGA AAAGGAAAGA CATGACTGCA CAGCCAAATG 240
TGGCAGAGTT AGCCACTTTT GCAGTATGTT TTAAATTTTA TTCAAAGTGT TATATTCTGC 300
CAGATCTTGA AATATTTCAG AGCTCAGCCT GTGGGTGGGT TCAGCTCCAT ATATTTTTCA 360
TTAACATCTA CTAGTAGGCC TAGGATAGTA CAGAGAGAAA AGAAAGAACC ACGCCAGAAA 420
CACAGATAAC GAAAAAAAAC CAGGCTGACA AAAAGATACA TAGGGAAAGA TACAGGGAGA 480
TGCTGAGAAA AGCCGTTTTC TAGGTGCGGA GGAACACAGA GTTCTAGGAA GCAATTTAGT 540
CAAGAGATTC AGGAAAGCCT ATTAAGACGG TGTCCTGCGA GACGCTAGTT GCTACCCCAG 600
GTTAGAGATC AGGCGGTCCT GGATTAAGCC TCCCCGAACT GAAAACCGAA CAGAAACCGC 660
AAAGCTGCAT TGTTTTGTTT GTCCCTTGGT TGGGCTCCGG GCAACCAGCG CGCTGGGGTT 720
CTGACACACT GCCTGAGCGC CCCCTGCTGG CCACTGTGCA GAACTTCACC GTCTGGGCCC 780
AAGGTGAAAT CGAATTACGT AATTTCTCGA GCTTTGCACA CCCCATTTTT ACATTTTTAT 840
TTATTTTTTA TTTATTTTTG TATTTTCCCA AGCTCCTGGC TTCACTGAAG CCTACTGTCT 900
AATGCCAGCG CTTGAATGCT CTGACTGCCA AGGTCCTAAG GCCCAGTGAG GGCAGTCCTG 960
AGAGACCCAG CCTAATGAGA GTGCACGCAG GGGCTTGGCT GAACATTTAT GAAACACGTG 1020
CCACATACAA 1030
|
