Tag | Content |
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EnhancerAtlas ID | HS127-17469 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr2:121307740-121310230 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CDX2 | MA0465.1 | chr2:121308010-121308021 | AAGCAATAAAA | + | 6.32 | ESR2 | MA0258.2 | chr2:121308900-121308915 | GGGTCACCCAGACCT | + | 6.64 | FOXP1 | MA0481.2 | chr2:121309189-121309201 | ATGTAAACAGAG | + | 6.32 | FOXP2 | MA0593.1 | chr2:121309189-121309200 | ATGTAAACAGA | + | 6.02 | MAX | MA0058.3 | chr2:121309787-121309797 | ACCACGTGCT | + | 6.02 | RREB1 | MA0073.1 | chr2:121309444-121309464 | ACCCAGCCCACCCACTCACC | + | 6.17 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr2 | 121308332 | 121309031 | chr2 | 121309130 | 121309553 | chr2 | 121309676 | 121310000 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I120550 | chr2 | 121308041 | 121311056 |
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Enhancer Sequence | GGCATCTGAG TGAACCATCC TCTTCCCATT TTCCAGAAGA GGAAGCCAAG GCTGAGAATG 60 AGGAGTGACG TGCTCAGAAT CACACAACAG GAAGGGTGGA GAATCTCTGC CTGGCACAAA 120 GTGCTTCTTT CTATGTTCTG CCTCGACTTG TCCCCAACCC AAGGGATTCT GAGCTGCTCT 180 GGAGGTATCT GGAATAAGAA GAGACAGATG CAGAGCAGGA CAGTTCCAGC TCTTTCTTGG 240 GAACAGCAGT ACAGAATGCG AAATGCTTTC AAGCAATAAA ACCCGTTATC TGTGCAGAAA 300 CCCATCTGTG CTAAGGAGAA TTCCGCAGGG ATTATTGTCC CCTGGAGACA GGAGAAGCCA 360 TTTGGTGGGC TAAAGCATCA AGACAAGACC TTGGCTGATT ATAAGTCACA TTAGACAATT 420 ACATTCTTAG CTCCTGGGAG TAATGATGGC TGGATTTGCT CTGATTTCTT CTTGTTGCAA 480 AATAATGCCT GTTTAGGATA TTTTGGCCTT CTGTGTAATA AACCTGTGTA TTGGATTGAG 540 TCGAAATATT TGGCACATTA AAAATTACTT TCAGTCAAGG TTTTTTAAAA GCCCCATTTT 600 TCTGTCCACA TTCTCCTTCA TTCCAGAGAC CCTAAATGTA CTCTATGTGG AGACTGATTA 660 GTCATCCCGG GTGTAGGACC AGCTCTGGGG CAAACAATTA GGGTTTTCAT TTTACTCTTT 720 CATACCCACC ATGTTGTGAG TGGGGAAGAA AAGCAGGACT GAGGGATGTT ATGGCTCAGG 780 CTAGCTATGT GTGCCCTCTT TATCTCTGAC CTTGGGAAGC CCACACACTG CAAAGAGGCC 840 AGCAGGGATC TGGGGACAGG CAGACTTGGA TTCTGATCTC TGCCCTGCCT CTTCCTAAAC 900 CTGTGACCTT GGGCAAGTTG CTCAACCTCT CTGAGGACTG ATCTGTTTCT CTGTAAAACA 960 GGGCAACTAA TTGAATTCTT AGGGGATTAA ACGAGGCAAT GGATACAAAA GCATTGTGAC 1020 TGTTCAGGAA ATGTTAACAT GTGGCTGGTA GTTGACAACT TCACTGTTGA GGAGTTCCCA 1080 GTCCCCAGCC ACAGAGACAA GATTAGCAGA GATTATCTCT CATGGGGCAG AGGAGAATAT 1140 GGGGGGAAAT ATGGGCTTTG GGGTCACCCA GACCTAACTT GTGCTCTCCT ATCTCTTTGT 1200 CCTGAGCCGT TACAATAGCT CTCAGTGCCT CTCTTTTCTT ATCTGCAAAA TGGGCTTATC 1260 ATAATACATG CCTGGCAAAA TGTGTTAAGA TAGCTCATGC CTGAGAGCCA GGTTTATATT 1320 AAGACTTTAT TGGATGGCGA CAAAACTGGT GCCCAGCAAG GGGGCCTGCC AGATAATTCA 1380 TCAGGGTCCC AGGCATTATC CATGGACAGA ATATATTCTC TCACACGCAC TTGTCTGCAT 1440 GGTTTTGAAA TGTAAACAGA GGCTATTGCA ATAAATGAAA TAAATTCTTG CCAAGACACT 1500 AGTGAATTCA TTTCCTCTCA GCCAATGGAT TCTAAGAGGC CGAAAAGGAG AAGTGAAAAT 1560 TTTGTTTTAG CACTACATAA GGCTTCTCGT ACTTGCAGCC AAAGAGGTCA GAGATTTGGT 1620 CCCAAGACCA ACTTAGAGTC ATGTGTGACA CTGGGATTCA GAGGCTAGTT GTGGGCCACA 1680 GGGAGGAAGC TGACCCCTGG GCTCACCCAG CCCACCCACT CACCAGCTCT CCTTTCCTTC 1740 CTGGGTCCCT TGGGGAGGAG AAGCCATCCA CCTCATGGAA AGTGCTTTAG AGGCTCCTCT 1800 GTGGGTGCCC TACTCTGCAC CCTTTGCGGG GACTCTCTGC TTCAGTTCGC AGGACAACCT 1860 TAATAGCTAA CTGCAGAGAG GACTGAATGG TTAAGTAGCT CCTCCAAGGA AGCAGAGCCA 1920 AGTATCAGAG GCCGGTTTCC ATCCAGGGAT TGAGAGAAGA ATCAGGAGCA CATAGGCTGT 1980 GGCAGTAAAA AGCAGATCCC AAAGACAGTA TAGGGCGGCT CGAAAGGGGC CTTCCTACAT 2040 AGCCACCACC ACGTGCTCCG GCGCTACCTC CAGGGGGCTG GGCGCAGCTG GAGGACACAG 2100 TTCGGCAGCT TGCTAGAAGC CTCCAGCTCT TCCTTTTCTG TATCCTTCAG GTGACTGTGG 2160 AAGGCTGGCC GTGCAGCCTG CCATCAGCCT GGCCTCAGCC GGGGAGGGGG ACCTTTCTCC 2220 TGGAGGCCAC AGAAACACTG AGGACCTCTC AGCTGAGAAG GTCAGATGGA GGTGCTGGAT 2280 GATTGGAGGA GATCAAACTG ATGAGGAAAA CGCAAATGGC ATCCTTCAGG AGCAAAAGCT 2340 GTCTCCTCTT TTACTTCACA TGTCCACCCA GCAGCTCTAT GAGTTCTGAT TCAGCATTGC 2400 ACTTACCACC CACCCTCCCC GCCTTTTACA GAAAAGGAAA CTGAGGCTCC GAGGTTGCGG 2460 AGTTGCTTGC TCCAGCTGAT GACAAAGGCA 2490
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