| Tag | Content |
|---|
EnhancerAtlas ID | HS184-12702 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr16:81437000-81438090 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CDX2 | MA0465.1 | chr16:81437292-81437303 | AGGCCATAAAA | + | 6.02 | | CTCF | MA0139.1 | chr16:81437304-81437323 | CGTCCAGCAGAGGGCGCCC | + | 7.3 |
|
| | 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 |
| GH16I081403 | chr16 | 81436774 | 81441457 |
|
Enhancer Sequence | TATTTGAATA ATTTGAATAA ATAATATTAT TTTAATTGAT TATTGTGGGA TCAATGAATT 60
CTAAATAAAA AATGCACTAA AAGTCTGTAG TGGGTGATGG GGTGGGGGAT TTAGGGGTGC 120
CGACGGGGTA GACCCCTATT GAAAGAGGCA CGAAAACTGG GAGATGAAAA GCATAGGCTC 180
GTTTGCCCTG TGTCTTCCTT CTCACGGCAG GGGATCGGCC GGCCACCTTC TCCCTGTGAC 240
TTCCTCCCAG TCCCGTCACC AAACCCCTGA GGCCGTCCTG GCATCAGACC GCAGGCCATA 300
AAAGCGTCCA GCAGAGGGCG CCCCAAACCC ACGAGGGCCG CGGCGAAGAA GAAGGTAGCG 360
GCCGCTGTCC TCTCCCCTCC CAGGCAGGTC CGGTGCGGAA GGGATCGCTG GACACTGGCG 420
ATGGTGGAGA GGCATGGTGG GCCGGGTCCC CCGCACCCTT CATGGCCCTG ACTCGGGGCT 480
GCCCATGACC TTCAGCGTCA GAGCTCGGTC TGGTCCATGC CTGCCTTGGG GAAGCTGCGC 540
CGCCTCTGCA CCCACCCAGG TCAGGGCCAC CTTCCCTCCA TTTGCAGCAT GAGCAGGTCT 600
GAGGTGGCGG CTCCGGGCTG AACAGCAGGA ACTGAGTTCT TTGTCCACAT GTGAGGGTGG 660
GCAGCCCATG AACAGTCCAC CCAGACACAA GTTACCCTGC CCCCGAGCCG GAATCCAGCC 720
CTGAGACCCC ACAGTGCTGC CTCTGAAACA GTGCTGGGAC GTCTCTCTGA GCCTGAGCTC 780
AGACTTTGGT GTCCCGCTGC TGAGGCCGGG GTCCCGCCGC TGTGACCGTG GCAAGGGTAA 840
GCCCTTTGTG CACCTGTGCC GTTGCCTGTA AAATGCTGGC AGTAATCACA GTGGAGCTAC 900
CCTAGAGGTT TGCTAGGAGG GTTACATGAG CCGTGCCTGG CACGGGCCAC AGAGGGTAGG 960
TTGCACATGG CTCTTTTCCC CACTGCCCAG TTATTAATCC AGGTCACAGT TACTTCTTCC 1020
CCCAGCCTCA CAGAAGATGG GGGCCACTGT AAACCCCACC CCATCCCAGA TGAATCAAGC 1080
CATCACCATA 1090
|
