| Tag | Content |
|---|
EnhancerAtlas ID | HS184-04510 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr10:99461070-99462060 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Foxd3 | MA0041.1 | chr10:99461452-99461464 | GTTTGTTTGTTT | + | 6.32 | | MYB | MA0100.3 | chr10:99461128-99461138 | GACAGTTGGT | - | 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 |
| GH10I097701 | chr10 | 99461157 | 99461670 |
|
Enhancer Sequence | GGGACTGTGT GTCTTCTCAT TTTGGAGAGA GGATGAGAAC TTCTTCATTT ATAAGAAAGA 60
CAGTTGGTCT TCTTTAGGCG GAAATATGAA GTTGTTTCAA TATTGCATGG AAATTCAAAT 120
GTATATAGGA GTGGATATGG AAGCTGAGCG TTGATCCACT GTGCCAGTTA TCAACTTGTT 180
GCCTCTCAGC AACAAATGCA CCCTCTGTTG TACAGTTCCA TGATCCTGGA GAGGAGCCCT 240
GTACTTTTTC TTTTCCAGCT AACACAATGC TCAGCTTTGT CAGTAGAGGG AGCTAGCGGG 300
ACACTGTAGG AGGCAGGGGT TTAGGAGTTT CTCTCCTTGG TTCTTGTGTG CGCCTCTCAC 360
TAGGCTCCTG TGGGTTTTTT TGGTTTGTTT GTTTTTGAGA CAGGGTTTCA CTCTGTCACC 420
CAGGCTAGGG TGCAATGGTG TGATCATGGC TCAATGCAAC CTCAACCTCC CGGGCTCAAG 480
GGATCCTCCC ACTTCAGCCT CCCAAGTAGC TGGGACTACA GGCGTGTGCC AACATGCTCA 540
GCTAATTGTG TGCTGGGATT ACAGGTGTGT ACCACCATGT CCGGCCTCTT GAAACGTTTG 600
AGGTTCCTCC ATGGCCCGGC CCCTGGAGCA CATCTGGTTT TCCAGCCCAG GCTCCAGCAG 660
CGTGGGCTCC TGTGGTGTGA GCAGCTTCTT CAGTGCCTGG GTCCTACAGC GCGTGGCAGT 720
CAGCAACACA CCATGGCTAG GAGCTTCCCT CGGCACCTCT TTGGGTGGCT TTGCAGCAGG 780
TTTTGAGATG CAGTACCTCC CTGTGAGCAA CTTCCCCAGC ACACCTAAAT GGCAGATTTC 840
TAGCAAGTTC CACCGGTGCA GCACCACAAT GACTTTTTTG CCTTCCAGTG AGCCACAGCC 900
CCATCCTCTC CAATGAGGTC TGGATTTCAG CCCTGGGGGA AGGGTGGGGA AGGAGCTCTT 960
TTTTGGGTGT CTATCTCAGC CCTAGGGCCT 990
|
