| Tag | Content |
|---|
EnhancerAtlas ID | HS184-18008 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr20:32065030-32065900 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| RREB1 | MA0073.1 | chr20:32065154-32065174 | CCCCACCCCACCCCCACTGT | + | 6.35 | | TFAP2C | MA0524.2 | chr20:32065338-32065350 | TGCCCTGGGGCA | + | 6.44 | | TFAP2C | MA0524.2 | chr20:32065338-32065350 | TGCCCTGGGGCA | - | 7.22 | | ZNF263 | MA0528.1 | chr20:32065437-32065458 | GGAGGTGGACGAGGGAGGGAA | + | 6.42 |
|
| | 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 |
| GH20I033477 | chr20 | 32064819 | 32066273 |
|
Enhancer Sequence | GGATAGTGCT GATTCAAACC CTCTAATTCT CCAGAGTTTT TCTCCCTTTT CAGAATAGGG 60
CTCTCTTCTC TGCAGCCTTT CTTCCCCTCA CCCCCAACAA GGCCCATCGA GGCACAGTAA 120
TCTGCCCCAC CCCACCCCCA CTGTATCCTC TGGGCATAGA TTCCAAAACC CCCAGTGGGT 180
GGCTGAAACT GCAAATAGTT CCTAACCCTC CATAGTTTGT ACTTGCAATG ACCTTGGTGC 240
GAAGGTGTTC TTTTGTTCTC TGCAGGGCCT GCACCTGGGA TGGAGGCTGG AGAACAGGTG 300
TGGAGCTGTG CCCTGGGGCA CCGAGGGGAT AGGCTCAATT GTTGGTGTTG TAAAGCAAAC 360
AACTGCACCC AACTCTGTCC CAGGCGCCAG CAGAAGCCTC CACCTTCGGA GGTGGACGAG 420
GGAGGGAAGC CCTGGGGAAT TGTGGGCCCT GTCCCCACTA TCTCCCAGAG GCAGTTTAAG 480
ATCACATAAT AAGTCTGGGC CTGGAATGAA CAGTTTCCAG CACAGCTGAC ACCTGGGGCA 540
GGTGCTCCAG ATGGGAGGCC CAGAGTGCAG GGGGAGGAAA GGCTTGGCAA CCTCACAAAG 600
GCCAAGGCTC ATCTGCACTG GAGGCTGTGG AAGGTGCGAA TAAGTCACAT TCAGATTATT 660
TCAACCTATA CACATTCCAC ATCCACTGTG GCCCCAACAC CACCAGCAGA GAAAAGCAGG 720
AGTGGAGAAA CCCCAATCCT ATCTACACCC TCATGCAGAC ATCCCAAAGT TAACATCCCC 780
AGACCTGAAC TCCTGCTTTC GCCCTTGGCA TGTGTTTGTT CATCCCACAG CTGTCACCAC 840
CTCAGCCTGT GGCTGCTCCA TCCTTTCAGC 870
|
