| Tag | Content |
|---|
EnhancerAtlas ID | HS184-25239 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr5:158938290-158939570 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| HSF1 | MA0486.2 | chr5:158938679-158938692 | TTCTGGAACATTC | + | 6.67 | | Myog | MA0500.1 | chr5:158938455-158938466 | CAGCAGCTGTC | - | 6.14 | | Tcf12 | MA0521.1 | chr5:158938455-158938466 | CAGCAGCTGTC | - | 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 |
| GH05I159511 | chr5 | 158938695 | 158938959 |
|
Enhancer Sequence | AGAGGCTCAG TTACTTGCCC AACAGCTCAT TGTTCAAAGG TAGCAGTGCT GGGATTTGAA 60
CCCAGGGTCC ACTTGATTCT AAAGCCTACA TTCTCACCTC CTCCGTTATC AGGTAGGTGA 120
GAGGTGCCTT CTACTTTCTG CTGTGAAAGT GCAGATACAG AGGAGCAGCA GCTGTCCACT 180
TGCTTCTCCA GTGTTCATAT GTCATAAATC CCTCAGGGAT GTAGCCTTAG ACTTATTGTT 240
CCTACCCCAT TACTGGCCAT TCCCTACCAT CCCCACCAAA CCCATGCTCC TTCTCCACTC 300
ACCACTTCTC CACAGGTCAC AGTGGTCTGT GCCTCAGAGC CTTCATAGGT GCTGGTCCTT 360
GTTCTTGAAA CCCTAGTCAT CTCTCTTACT TCTGGAACAT TCCTACTCGG CAAGGTTCAG 420
ATGCCGTCTC CCTTTTAAAA GATGCTCTGA TTTTCAAATA GCCACAGCCC ACTTTTGCTT 480
CTGTCATAGT CTGTATCATG TTCTGTAATT ATTTGTTTTA GTCAACTCTC ATTCAATAAA 540
TATTTGCTGA GTGACTCTTT GTGCTTGGCA CTGTGTTAGG TGCTGGGGAA TTTTCTCCTG 600
TCCACTTTTC CTGTCCTCTA GACACCCATC ACACAATCAA ACTCATAGTT TTTTTTTTTT 660
TTTTTTTAAC AGAGATGTGC CTTATTTCCC CCGAATCCCA GGTAACTGAC AAAGCCTAAT 720
ACATAGAAAA TGCTCAATAG CCACTTGATG AGTGGATCCA TGACCCAGTA CTTATCTTAC 780
CTTTGAATAA TTGCCTCTTT CTTTCCATCC TCTACTAGAT TCTTAGACTC TTGTGGACAG 840
GGGTTGGGAC TTATTTTGCT TTTGTCCCTG TTGCTTAGCA CAGAGAAGTA ATTTAATATG 900
GTTTGTTGAA TGAACGATTA TGAGAAGTGT GAGTTCTGGG AGTGGATATG CTAATTCTAC 960
AAGCATATGC TAATTTGGGG AGTGGATATG TTCTGGGTTC TGGGAGTGGA TATGGTAATT 1020
CTACAAGCTA ATTCTACAAG CATGTGACCC ACTGTGTATC TAGTGCCAAT CATTGCTTGG 1080
GTGGGCACCA TGAAAAGCAA ATACCATGCA GATCTCACAC CCTCAGGATC CTGAGTGCAT 1140
GGTGACCGGG CGTATACACA CAAAGTTGCA AGAGAAAGAT TCAGCAGGGG AAGAGCCCAG 1200
GTGCCAACCA GACAGTCACC TTGTCCAGAA TCTCTGCTGG TCCCTGGCCC TGTCCTCAGC 1260
CGCCTGTGGC TCTAATTTCG 1280
|
