Tag | Content |
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EnhancerAtlas ID | HS127-16994 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr2:85804770-85806130 |
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) |
MIXL1 | MA0662.1 | chr2:85806104-85806114 | TCTAATTAAC | + | 6.02 | ZNF263 | MA0528.1 | chr2:85804958-85804979 | TCTACTCCTTCTCCCTCCCTC | - | 6.12 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_13265 | chr2:85804112-85807430 | CD34_Primary_RO01480 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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Enhancer Sequence | TGGTGAGCCA ACTGGGAACT AGGAAAGGGC TGGTTTAAAG AGGAGCCAGA GGGGGCTTGG 60 GACTGGGGGT TGGCTGTGTC GGGGGAGGAG AGTTGGTGGC AAAGTTAGAG GGCTGGGCCA 120 GTGCTGCTAT GGCCTCTCTT CTTTGACAAC TTGGCTGCAA ATAGCTCTGA GCTGTCCTGG 180 CAGGTGTTTC TACTCCTTCT CCCTCCCTCC CCTGACCTCT GTGCTGGTGG GGAGCTGGGC 240 TTCCGTGCCA GCGCCGATGG GGGCTCCGAA TTCCAGGCAA AGAGTTGTTG TGCCTTCCTC 300 CTCCAGGGAG CCCGAGGCGG GTGTTGTGAC ACCACACCAG GCAGCGCCTG GGCAGTTCCC 360 AGTTCAGATT CCAGCCCAGC GGCAGAAGCT CTCCTCTCCG GCCTTTCACT TTATCCCCAC 420 ACAGAAACAC AAAGGATTTG TGTGTCCACT GAGTCCTTTG GGTGTCCTTT CTCCATTAAC 480 ATGGAGAAGA GAACTAAAGG TTTATAAGAG AACCAGAAGT TGGTTCTCTG TGATAATGTA 540 GTTCTGACCC ATGCCACTGG CCTATTTTTG GAGGTCAAGC GGGGAGGAGC TAAATACTAT 600 TTTTCTCTCC TTGTTCAAAA ACCTTGTCAT GAAGCCTCCG AGATGAGACA TCAGCCAGGG 660 AGGACTAGTC CTCCATTTCC CCCAACACCC AGGCGGGTAT TTTTATTTAA TATCTGCATA 720 AGCAGGCGGT TGCTTGGTGC CTGCACGTGT CGCCCAGTGG TGGGGAAAGC AGAAGTGTGT 780 GGCTCAACGG CTCCAGGCGC CTTCTGGGAT ACTTGGTTGC CTGTTGTTCT GGGTCACAGC 840 AATGGCATTG CGGCCAGGGC CGTGCTCCGG CAGCTGGCTT AGAGGGACAG ATGGGTGGGG 900 CTGGGTGAGG GTGTTCTGCT GGCCAGCACA GACACTTTCA ACCAGGGTCC CAAGAAATCA 960 GGAAAGGGGG GTGGCTCTGG GAATTGTAAA TAGTGGCGGG CTCTGCTCTG GAAGGGAACA 1020 TTGTGAGATG CTGGCCCTGC TGTATTCTAC GGCCCTCTCT AGGGAGCAAG GAAGCAGTGG 1080 GGAGGGATTT AGTGATGTGC TGCTTTTCCT TGTCAGGGGC CCTAATAACC CCAAAAGAAG 1140 TTTGATCTAG TCTGTTCAGC ATCACATCTC ACCTTCTGGG GCTTACAAAT GCATTTATTT 1200 TTGATTACAG AAGTAATACA TGAAAACATT CTCTTTGTAA ACATTTCAAG CATTTTACAA 1260 AAAGCTTAAG TCTGCCTGAG GCCTTACCCT CCCCAGATCT CTGAGCCCAA GTCTCCAGTT 1320 CCCCCACCAC TTGGTCTAAT TAACCCCGTG TTGCCGCACA 1360
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