| Tag | Content |
|---|
EnhancerAtlas ID | HS017-03665 | Organism | Homo sapiens | Tissue/cell | CD14+_monocyte | Coordinate | chr10:16857740-16858970 | SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| IRF1 | MA0050.2 | chr10:16858394-16858415 | AAAATGACACTGAAAGTGACC | - | 6.05 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | CTTCACAGAG GAGGGAAGGG ATATGTTAGC CTGGTGCAGA CGGATAAGGT TTTACACAGG 60
TGGTGATGTC TAAGCTGACT CTTAGAAGTA AAAGGATTTC AGGTGCAAAC GACTGAGAAA 120
GAGGGAAAAC AGAATTTGTA AAGGCACCAA GATCTGAACG AGTAGGCTCT GGTCCAGGAA 180
GGGCAACAGG TTCAGAATGG CTGGAATGCC AGCTGCATGG AAGGGTAAGG TTGTGTTCAG 240
ATTCAGAAAG GCCTTGTACA TCACGCCAAG AAACCTGGAG CATTACCGTC GATAATGGAC 300
AACCTGGAGA AGTGCGGAGA GGGTTTAAAC CAAAGCCACG TCAGCCTGAA GAACTGCTTT 360
AGCTCACTTA TCACAGGTTT TTCAAATATT AGAATTAGTA GCCAACATCT AAAAATTAGC 420
AAATTTCACA TAAAAATATA GAATCTTGGT TCCTTTAAGA AAATAATCTG GCACATTGGG 480
CCAACATTCC TATGGTGACA TGTGTCTGAG TAGCAGGTGC AGCAGCTGGC CCCTTCAAGT 540
GGGACACCTA TCACCTAGTT CATAACCGCC CCTGACCGCC CTCACTTGGA GGCATGTGAA 600
TCTGCAATCC CTGGTTTTAA GGGAGAGGGT AACACCATAG ACAGGGGTTA CAGGAAAATG 660
ACACTGAAAG TGACCCAGTG ATTAAACTGG GCAGTGAAAC TGAAGGCAAG AGGGCAAGTT 720
AGGAGGATTT CACCACAGCA TGAGGAGGTG ACAAAAGCCT GAACCAAGTT CGGAGAATAA 780
ATACTCAGAA GAATGTAAAG ATTCAAGAAA TGCTTAAAAC GCTCCAGGCA CAAGAATGCT 840
TATTAACCAT GGAACTTTTC TGTGTCATTT GTTCATGGAC AAAGACTGTA TTAGGAGACA 900
GGAAGAAGGA CTCAAAATTA ATTTTCAATT TATAATTAAA GTGACTATTA AGCAAACTGT 960
GGAAAATCCA CCTCAATGCC ATACAGCAGA GACAACCGAT GAGGCACAGC TGTCTGTGTG 1020
ATTCTCATCG TGGACTCTCA GGATCGTTTT CCAGGTGGAA CAGAACAAAT CCTACTGCAA 1080
ACCCTCTGCG CGAAGCCCCT GACAAGTGAG GTTTACAAGC AGGGGCTGGG GTCTAAACCA 1140
GTACAATCGC TCACAGCAGG ACCAGCAGTG AATTGGCAAA CTTAGAAAGC CTTCCAGCTC 1200
ATCCACGGGA GAGTCCTGCC CGAGAACTCA 1230
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