Tag | Content |
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EnhancerAtlas ID | HS017-29362 |
Organism | Homo sapiens |
Tissue/cell | CD14+_monocyte |
Coordinate | chr6:149021540-149022950 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
IRF1 | MA0050.2 | chr6:149022150-149022171 | AGTTAGTTTCATTTTCATTTT | + | 8.57 | IRF9 | MA0653.1 | chr6:149022154-149022169 | AGTTTCATTTTCATT | - | 6.03 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr6 | 149021872 | 149022507 | chr6 | 149022109 | 149022176 |
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| Number: 1 | ID | Chromosome | Start | End |
GH06I148700 | chr6 | 149021434 | 149022736 |
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Enhancer Sequence | ATATTTATTT CACATACAGA GAAATTAGTC ACTCTGTTTT CATTGTTCCT TTATTTTTAC 60 ATCTCTAATT TAATCTTGTA TTAATTCCCA AAAGCAATTG TGCAATTTTG GGTTTTTCTG 120 AAATACGTCT CATTCATTCC CTAAAGCTTT GGAAATGCTC CATGGTGCTC CTTTCCCCAA 180 GCCTTTTTGC ATTTTAAAAA ATTCCCTTTC TGTTTTAGAG CCAAACTTTG CCCTTGTCCC 240 AAACTTCTAT ATTTTAAAAA TACTCTTGTC TTATTTTCTA ATGATTGGGT GAATTTCATT 300 TCTACCACTT TTCTATTTTT TTTTCCCTGG ATTGTTTTGG TGATTCAATT TCTGGGCTCC 360 AAATATATAG TTGCCAGATT TTTACTGCTA TTGGCCATAA AATCCTGCCC AGTCACTGGG 420 CTGTAAAAAA GCAGATGCAA AATTGCTCCT ACTGTCGGCT GCCAGCTGTG TAGTCCCGCA 480 GCCAGAGGCA GAGAGGCCGT ATTCCCCCCA CTTTCCTTAG ATTCAGGAGC CTGTTCAATA 540 CGCATTGCCT ATGTCACGAC CTGCATAGCT GCCTGTCAGT AACCGCCTAG GGCTCTTATT 600 TGTGTAAATA AGTTAGTTTC ATTTTCATTT TGTTTGAACT TCCACATTGC CACTACATAG 660 AGAATGTTTT CTTTATCTTT TCCTACTGAG TTGTAAATAA TTGTTACCCT AATCTTGCAG 720 ATACAATGAT GCTGCCTTGA TTCTGGTGTG TTAGGTTCAG TTCACAGGAG CTACTCTCCT 780 TTTCAAAGCA AGCAGCATCA GCACACTGAT TCTTGGCTGG AATTCGGAGA CCCGGAGACC 840 TGGGCAGGAG ACAGAAGCAG CATTGTATGA AAGGATGAAA GAGAGACAAG AGGCAGCATC 900 CTGGGTGTGA AACGAAAATA ATATCATCTG TCTTGTCCAA ATGAACTGGC AATGCAAGGG 960 GGCCAACCAT AGAAAGAATC TATGTGGTAA GCAATGGAGT AGAAACCAGA TCAGATGAAC 1020 GGCCAAAATG CATGTTTATT TTCTCATTGG ATTCTCATGG TCTCACCTCC ATGGAGAGAC 1080 AGAACTAGAA TTTGACCCAT GCAGTGTGAC CAGAGGGCCT GGACGCCAAG TCTCTGCTTG 1140 ACTGCCCTGG TTTACGGTCT TTGAGAGGTT ATTTTCTGCC CAAGAGCATC CATTAGTACA 1200 TGGGAATCCA GACTTGGAAC ATGCTCTGTC TGGCTCCAGA GTCCTCTAGG TTTTCAAATA 1260 TTCTACTGAG ATTGAGGCAA AGGCTCAGGA AGCATCCCCT GAGCTGGAAA GGGCTGCTGT 1320 AATTGGTTTT CATAGGACAC CTGTATAGTG GGCTGTTGAC CCAGCTTGTA CACAGTCTCA 1380 GTGAGGGTGA TTTTTTTAAG GCTTATTTGT 1410
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