Tag | Content |
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EnhancerAtlas ID | HS017-02928 |
Organism | Homo sapiens |
Tissue/cell | CD14+_monocyte |
Coordinate | chr1:212947630-212948780 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFE2L1 | MA0089.2 | chr1:212948140-212948155 | ACATGACTCAGCAGT | + | 7.26 | Nfe2l2 | MA0150.2 | chr1:212948138-212948153 | CCACATGACTCAGCA | + | 6.75 | SOX10 | MA0442.2 | chr1:212947858-212947869 | AAAACAAAGGA | + | 6.32 | Sox3 | MA0514.1 | chr1:212947858-212947868 | AAAACAAAGG | - | 6.02 |
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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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| Number: 1 | ID | Chromosome | Start | End |
GH01I212774 | chr1 | 212948081 | 212948230 |
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Enhancer Sequence | GGATATCTTA AATACCTGTT TTGATCATTA CACATTGTAT ATATGTATCA AAATATCACA 60 TGTACCCCAT AAATATGTAC AAATATTATG TACCAATTTA AAAAAAATTT AAGGAAAGTG 120 AGAATGAGAG AAAATATCTG CAAATCATAT ATCTGATAAG GGACTAGCGT CCAGAATACA 180 TAAAGAACCA GTATAACTCA ACAATAAAAA GACAAATACC TCCCTCAAAA AACAAAGGAT 240 CTGAATAGAT ACTTCTCCAA AGAAGATATA CAGATGGCCA ATAAGCACAT GAAACGATGC 300 TCAACATTGT TAGCCATTAC AGAAATTCAA TTTAAAATCA CAATAAGATA CCACTTTATA 360 CCTACTAGGT TGATAAAAGA GCAGACAGTA ACAAGAGTTG GTGAGGGCAT AAAGAACTGG 420 AACCCCTACA CACTGAGGGA GGAATGTAAA TGGTGCAGGC ACTTTAGAAA ACAGTCTGGC 480 AGTTCCTCAA AAGCTACATA AAGAGTTGCC ACATGACTCA GCAGTTCCAT TTGTGGGTAT 540 ACATACTCTG GAGAACTGGA AACATATCCG TACAGGAACT TGTACATGAA TGTTCACAGC 600 AGCATCATTC GTAGTAGCCA AAATGAGTAA AATGTCATTG AGTAAAATGT CTGTACATTC 660 TAGTGTTAAC AAGTGACAAG AAGAAAAGTT TTTTTAAAAA GTCTGTATAC TCATGAATAT 720 ATAAATATAT AAAATACATA GTATATGTCC ATACAATGGA ATATTATTTT GCAATAAAAA 780 GAAATGAAGT ACTGATACAT ACTACAACAT AAATGAACTT TGAAAGCATT ATGCTAATTG 840 AAAGAAGCTG ATCACAAGGG ACCACATACC ACATGATTCA ATTTATATGA AATGTCCAGA 900 ATAGTCAGGT CTATAGAGAT AGAAAGTACA TTAGTGGCCG CCTAGGACCA GGGAAGCAAG 960 ATGAGAGACT GGAAATAATG GCTAAGGAGT GTTGGGTTTC TTTTCAGAAT AATAAACCAT 1020 TTTTAAAATT GATTATCATG ATGTTGCATA ACTCTGTGAA TAAACTAAAG CCACTGAGTT 1080 GTACACCTTA AGTGGGTGAA CTGTATGGTA TATGAATTAT ATCTTGATAA AGCCATTTAT 1140 AAAGAGTGTC 1150
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