| Tag | Content |
|---|
EnhancerAtlas ID | HS017-28467 | Organism | Homo sapiens | Tissue/cell | CD14+_monocyte | Coordinate | chr6:41861880-41863060 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr6:41861895-41861916 | CCCATCTCTTCCTGCTCCTCT | - | 6.05 | | ZNF263 | MA0528.1 | chr6:41862602-41862623 | TTCTCCCCTTAATCCTCCTCA | - | 6.26 | | ZNF263 | MA0528.1 | chr6:41863024-41863045 | ACCTCCTCCGTCCCCTCCCCC | - | 6.33 | | ZNF263 | MA0528.1 | chr6:41862599-41862620 | CCTTTCTCCCCTTAATCCTCC | - | 6.53 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTTTAAATTC TGGGGCCCAT CTCTTCCTGC TCCTCTCACC ATTTGCTTTT AGCCCTGTCT 60
CTTTACCTCA CTGTTTTCAC CTTGGATCTT GCTGAACCTC TTCAATTAAC GTAATTACCC 120
AGTTATCCTT GTCCCAGATG GCCATCACTT CTTACACCCT AACTCTAGTC TCCTTTCAGC 180
TCTTCTGGTC CCAGAATCGT CCTACAGACA CCCATCTCTT ATCTGTTTCC TTTCGCCCTT 240
CCACCACACT CTTATTCCTG ACTCCACCTG GTTCCAGTCC AGGTCTCATT TGCCCTCCCT 300
CACTTTACAG AATTTACATC CATCGCCCAC CCACTAACCC ATTCCTTTCT CAGAACCTCG 360
CCAGCAGTTC CCACCACACC GTTGGTCCCA GTCCTTCAGC TCATCTCGCT CCGCACTAGT 420
TCACACCCTC GTCACGTCTG GCTCTTAATC ACTCTCTCTT TCCTACTCCC AACTATTACC 480
CCAGCTCTGC CCCTCCTTGT CTTCCACTTC CAACACTTAC CCCGGTACCC CTCACCCCAA 540
CACCACCCGC TACGAAGATT TCCCCTTCAA ACCCCTGCTC TTACACCTAA CCCCAGGATC 600
CCTTTCCCCA GCCCTAACCT CATTCCCTGC CCGGCTTCCT TAACGCCCAC CCTGGCTTTT 660
GCCTCCTTCC TATCTCCTTG GCTGGCTTTT TCTCACTCCT CCTCTCCCTG GCTTCTAACC 720
CTTTCTCCCC TTAATCCTCC TCATCTCATT CTCAACCCGG TTCCCCTCAT CGCCTCCAAG 780
CCTTCCTTTC CCTCTCCCTT CAACGCTTTT GCCCCAACCC AGCCGTCGCC CACCCCGCCA 840
AAATAAGGCG CCCGCGCGCC CCGACTCCCG GCTCTCGCCT CCCGCCGCCC CCGCCCCGGG 900
CGCCCCCAGC CCGCCGGCGC CGCGGTCCCG CCCCCTGCCG CCGCTCCTCC CGCCCGCGAG 960
GCGCGCGCTG CCTTTGTCGC CCCTCACCCG GTGTGTGAGG ATTTTGCTTC TTTAAAGGGG 1020
AGGGCTAGTG AGCCGGAGAC TCCTATCCCC GCCTCCGAGT CTTAGAATGG GCTCCCTGGC 1080
CGTCGCGGCC TCCCCGGCCC CCGTTCCCCC TACCCCCTGG AGCTACCCAC TTTGCTGCCT 1140
CCCCACCTCC TCCGTCCCCT CCCCCGGCCC CCTCTATTTA 1180
|
| |
|
|
|
