| Tag | Content |
|---|
EnhancerAtlas ID | HS108-00021 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr1:1000700-1001550 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| BHLHE40 | MA0464.2 | chr1:1001171-1001181 | GTCACGTGAT | - | 6.02 | | MITF | MA0620.2 | chr1:1001167-1001185 | GCAAGTCACGTGATCACA | + | 6.31 | | MITF | MA0620.2 | chr1:1001167-1001185 | GCAAGTCACGTGATCACA | - | 6.31 | | TCF3 | MA0522.2 | chr1:1000949-1000959 | AGCAGGTGTT | - | 6.02 | | TFEB | MA0692.1 | chr1:1001171-1001181 | GTCACGTGAT | - | 6.02 | | USF2 | MA0526.2 | chr1:1001167-1001183 | GCAAGTCACGTGATCA | + | 6.05 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr1 | 1000831 | 1000953 | | chr1 | 1000736 | 1001492 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH01I001061 | chr1 | 996971 | 1001049 |
|
Enhancer Sequence | CTAAGCTTAG ATGCAGGTCT CTCCCTGGCA GCCCCTCAAG GCCACGAGGA TCAGTGCTCG 60
GAGCCTGGAG GGCTGTGTGC AGGAGTAGCA GGGCCACTGA TGCCAGCGGG AAGGCCAGGC 120
AGGGCTTCTG GGTGGAGTTC AAGGTGCATC CTGACCGCTG TCACCTTCAG ACTCTGTCCC 180
CTGGGGCTGG GGCAAGTGCC CGATGGGAGC GCAGGGTCTG GGACTGTAGG GTCCAGCCCT 240
ACGGAGCTTA GCAGGTGTTC TCCCCGTGTG TGGAGATGAG AGATTGTAAT AAATAAAGAC 300
ACAAGACAAA GAGATAAAGA GAAAACAGCT GGGCCCCGGG GACCACTACC ACAAAGACAC 360
GGAGACCGGT AGTGGCCCTG AACGGCTGGG CTCGCTGATA TTTATTGCAT ACAAGACAAG 420
GGGGCAGGAT AAGGAGGGTC AGTCTTCTAA GTGATTGACA AGGTGAAGCA AGTCACGTGA 480
TCACAGGACA GCGGGCCCTT CCCTCTTAGG TAGCTGAAGC AGAGAGAGAA GGCGGCAGGC 540
ATCAGCGTTT TCTTCTATGA ACTTATAAGA TCAAAGACTT TAAGACTTTC ACTATTTCTT 600
CTACCGCTAT CTACTACGAA CTTCAAAGAG GAACCAGGAG TACGGAAGGA GCATGAAAGT 660
GGACAAGGAA CGTGACCATT GAAGCACCAC AGGGAGGGGT TCAGGCCTCC GGATGACTGC 720
AGGCAGGCCT GGGTAACATC CAGCCTCCCA CAAGAAGCTG GTGGAGCAGA GCGTTCCCTG 780
ACTCCTCCAA GGAAAGGAGA CTCCCTTTCC CGGTCTGCTC AGTAACGGGT GCCTTCCCAG 840
ACACTGGCGT 850
|
