| Tag | Content |
|---|
EnhancerAtlas ID | HS108-41619 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr9:131428500-131429340 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| FOSL1 | MA0477.1 | chr9:131429070-131429081 | GGTGACTCATG | + | 6.62 | | JUND | MA0491.1 | chr9:131429070-131429081 | GGTGACTCATG | + | 6.02 | | Klf12 | MA0742.1 | chr9:131428892-131428907 | TAGCTGGGCGTGGTC | - | 6.33 | | Nr2f6(var.2) | MA0728.1 | chr9:131428824-131428839 | GAGGTCAAGAGTTCA | + | 7.64 | | RARA | MA0729.1 | chr9:131428824-131428842 | GAGGTCAAGAGTTCAAGA | + | 6.45 |
|
| | 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 |
| GH09I128666 | chr9 | 131428705 | 131429450 |
|
Enhancer Sequence | AAAAGTTAGC CGGGCGTGGG CATGGTGGTG GGCGCCTGTA ATTCCATCTA TTTGGGAGGC 60
TGAGGCATGA GAATTGCTTG AACCTGGGAG GTGGAGGTTG CAGTGAACCA AGATCGTGCC 120
ACTGCTCTCC AGCCTTGGTG ACAGAGTGAG ACCCTGTCTC AGAAAAAAAA AAAAAAAAAA 180
AGCCAAAATA CATCCACACA TCATACTACA AAATTAATTC AGGTTGGTTA TAAACTGGAA 240
TGTTAAAAAT GAAGACAATG CCGGGCATGG TGGCCCACGC CTGTAATCCC AGCAGTTTGG 300
GAGGCTGAGG TGGGCGGATC ACTTGAGGTC AAGAGTTCAA GACTAGCCTG ACCAACATGA 360
TGAAACCCCA TCTCTACTAA AAACACAATA ATTAGCTGGG CGTGGTCAGT GCCTATAATC 420
CCAGCTACTC CGGAGGCTGA GGCAGGAGAA TCCCTTGAAC CCAGGAGGCA GAGGTTTCAG 480
TGACCTGAGA TTGTGCCACT GCATTCCAAC CTGGGTGACA GAGCAAGACT CCATCTCAAA 540
AAAAAAAAAA AAGAAGATAA GGCCTGGCAT GGTGACTCAT GCCTGTTGTA ATCCCAGCAC 600
TTTCAGAAGC TAAGGTGGAT GGATCACTTG AGCCCAGAAG TTCAAGACCA GCCTGAGCAA 660
AATGGCAAAA CCCTGTTGCT ACGAAATACA AAAATTAGGC CAGGCGCGGT GGCTCACTCC 720
TGTAATTCCA GCACTTTGGG AAGCAGAGGG GGGTGGATCA CGAGGTCAGG AATTCAAGAC 780
CAGCCTGGCC AACATGGTGA AACCCCATCT CTATGAAAAA TACAAAAATT GGCCAGGTGT 840
|
