| Tag | Content |
|---|
EnhancerAtlas ID | HS017-31847 |
Organism | Homo sapiens |
Tissue/cell | CD14+_monocyte |
Coordinate | chr8:59050000-59051150 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ETV6 | MA0645.1 | chr8:59050668-59050678 | AGCGGAAGTG | + | 6.02 | | Nr5a2 | MA0505.1 | chr8:59051087-59051102 | GGTGGCCTTGAATTC | - | 6.44 |
|
| | 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 |
| GH08I058138 | chr8 | 59050061 | 59051013 |
|
Enhancer Sequence | TCCCAGCTAC TCAGAAGGCT GAGACAGGAG AATCATTTGA AATAGGAGGC GGAGGTTGCA 60
GTGAGCTAAG ATTGCGCCAT TGCACTCCAG CCTGGGCAAC ACAGTGAGCC TCCGTCTTAA 120
AAAAAAAAAC AGCTTACGTT TACTGAACAA TTTCTGGGCT GAGCTCCTGA CCAAGCACTT 180
TCATGTGTCA CCTCAAGGAA TTCTCACCCC AGCCAGTGAA GTGTAGGAAT CATGGTTATC 240
AATGTTCCAT AAATGAGGAA ACTCAGGTAC ACTAGCTGGA GAAACTTGCT CAGGGTCAAG 300
TGTCCTGTGT TCTTTTTCCG TGCCCTAAGC ATTTGCCCCA CTGAATTCTC ATTTCTTTGC 360
CTGGATGAAA TCTCAGACAG GACCTGTAGC CTTTTCAGTT CGTCTTCAAT AATTTAGTCC 420
CCAGATCAGT TTCAGACCTG GAAGAGTGCT GCCTCACATC AAGATCAAAA CTCCACCTCT 480
GGTCCAGTTA AACTGGTTTC TCTTCTCCCA GCTCAGGGCC GCATTGGCTT GGAGACCCTG 540
TGAAGAAGAA GCATCATTTT CCCCTTTACT TGCTCCAGCT CCTCTCCTGC TCCTTATCAG 600
ACGGCTCTAC CAGCCTCTAC TGGGCAGACC CTGCATTGCG TAATGAGCAA GGGACGGACA 660
GAGCATTCAG CGGAAGTGAC AAGGTTTCTC TCCCTGGCTC TTGCAGTGGG AATCAATGTC 720
CCCTGGGCAT GGCACATTTC AGAGCTGGTT CTCTCTGGGA GCTTTTGGGT TCCGTGGAGG 780
CAGCCACGCC TCTGCTCAGC TAGTGGATGC CCCCAGCCTT CTCAGAGGAG GGCTTTGGGC 840
AGACATTGTT TTCTGTTGGC CTCCTTTGAG GGGACTTCTT TGAGAATACT CCTAGACCAC 900
CTTTCCCCGG CACATGTGTG GGCCGAGCAA ACCCTCATTT TTGTGCCTGT GGAAAGGCAG 960
CTTCATCCTG CCTGTGTGAT CTGGTTAGAG AGTCCATTAC AGACTCTGCC CTTAGACTTC 1020
TCAGACTGGA GGTATAAGCC AGTTCCCAGG CTCCTCAGCT CCAAGGGGCC TGTGTTGGGC 1080
TTTTTTGGGT GGCCTTGAAT TCAGCCCCAG CCAGTGTGAG ATGAGAGGAG GCTATGGCCA 1140
CCATTGTGTA 1150
|
