Tag | Content |
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EnhancerAtlas ID | HS127-06295 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr11:112050210-112051200 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
RUNX1 | MA0002.2 | chr11:112050419-112050430 | CTCTGTGGTTT | + | 6.14 |
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| 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 |
GH11I112179 | chr11 | 112049924 | 112050712 |
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Enhancer Sequence | CCTTGATTTT GGAGAACAAC TTGGATTTCT TGGCATGGGC TGGTTCTGTG GAATATGCAT 60 TAATATCTGC TTCCTCTGTG AGGTTAATAT TTCCATTCCA TCCCTTTGAT TACAGATAAA 120 GAAACTGTAG CCTAGAGGAG AAGAAAGGAG ACTTTTTAAA CAAAATGTCC TGCTTTTTCT 180 GCTCTGTAGA CTATTGTAAA TTTGAAGCCC TCTGTGGTTT GTACCAAAAG AAGAGAGGTG 240 TCAGAAGCTG TCAGTGTGGT GACTGAGCTG TTTCCCCACA AGTTCCTGAA GGAAGGGCAA 300 TGTCTCCTCA TACCACTCTC TCCCTCACCC AGCACTTGCC AGACACATGG TCTTTTTCAG 360 TTCCTCAAAC TGGGCACAGT TGTATCTTCT CAGCATCTTA GCATTAGTTC TCTCACCTAT 420 GTTCCCTAAT CTTCCCAAGA CTGGTCTTTT CATTCAGATG TCAACTCAAA TCTCATGTCC 480 TTTGAGCCTT TCCTGATCTC CCAACATAAA AATGCCAGCA CAGTCATCCC TCAGCATTCA 540 CAGGGCATTG GTTAGAGGAC CCCCTAAACA CCAGAATCCA AGTATGCTGA AGTCCCTTAT 600 ATAAAATGCT TTTATTTGCT TTTAACCTAC ATATATCCTC CCATTATCTT TTAAATCATC 660 TCTAAATTAC TCTATAATAC TTAATACAAT GCTTACACAT ACTTCATTCC CATGGATTTG 720 TCTTAGTACT CAGCAAATTC AAGTTTTGCT TTGCAGAACT TTGTGGCATT TTTTTCCCAC 780 AATATTTTTG ACTCAAGAGA TTGGTTGAAT CCACAGATGT GGAATATATG GATATGGAGG 840 GCTGACTGTA TTAATTATAA TTACCTATTT TAATTCTCTA CACAGTGTTA TCAGTGTCTG 900 GTATTTTTTA TTTGTTATTT GAGTGTTAAG CTCTGTTCCC CCACTAGAAT GTAATTTGAT 960 GAGGGTAGAG ACTTTTTCTA GTTCATCCTG 990
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