Tag | Content |
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EnhancerAtlas ID | HS127-25367 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr5:127675460-127677910 |
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) |
EWSR1-FLI1 | MA0149.1 | chr5:127677414-127677432 | TCTGCTTTCCTCCCTTCC | - | 6.3 | EWSR1-FLI1 | MA0149.1 | chr5:127677418-127677436 | CTTTCCTCCCTTCCCTTC | - | 6.42 | KLF4 | MA0039.3 | chr5:127676568-127676579 | GGAGGGTGTGG | - | 6.32 | Klf1 | MA0493.1 | chr5:127676570-127676581 | AGGGTGTGGCT | - | 6.02 | SOX10 | MA0442.2 | chr5:127677723-127677734 | AAAACAAAGAC | + | 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 |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I128341 | chr5 | 127676693 | 127677177 |
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Enhancer Sequence | TGAAGGCAGG GCCCCTGTCT CTGTGCAGGA GGGACTGGCA AACCCCAGAG AGACAGGCAG 60 CCACGACGGA CCAACCCTGA GCCAGAGAGC ACACATAGGG CAGGGCCATG GTGTGTGCCC 120 CAATTTGTGT TTTTGTGTCA TATTCAGATG TAAAGAGCTT ATTGATTTAG TAAGCCCTTT 180 GGTGACATGA GCTGTCACCA ACACCTGAGG ACTGTGTGGG TGAGTTTGTT TCCTCTTTTT 240 ATATATTACA GTAAATAATC TTCAGCAACT ATATTCTCAA ACACAGGGTT CTCTGAGAAA 300 TCTCCTATGC TTATAACTAA GATTTTTAAT AGAGAAGTCA TGTCTATATA AAATATGTTT 360 AAGAAAACAT GACCTATTTA CAAATGTTTT AGTCCAAAAA TCAAAAGTTT TTAATCTAAA 420 AATCTGTCAG TGGGGAAAAA TGCCCCACTA CGATCTCTTT ATTTTGATGA ACTTAATTTT 480 GAAGTTTTAA AATCACAGGA TTTAGTGCAT AATTTGTGCA TGTTCTCTTG AGAGGGGGGT 540 CTCAGTCTCT GCTTTCTGCC AGCTTTTACT TAGTTTTTCT GTATTTATTT CTCCAATTAC 600 AGGAGTCTTT ATTTATTTCC CTCATTACTG GCCATGTGAA AAAAATGTAA ATACTTTCTT 660 TTAAACAAAC ATATTAACAG AATTTATTGA TTCAATTAAG TAGCTAACAA TATGTATATT 720 AATTTTCTTT CTATCTATCA GTATCTAGGA CTGGTGTTAA GAGTCATATG AGGAATGTGT 780 TCTAGGGTGG AGCAGGGACA ATCTTTGGCT AATGTGATGT GGTGGGAGTT TCATAGTATA 840 AACAGTGTGG ATTCTAGAAC CAGATACCTG GCTACAAATC CCAGTCTGTC ATCTACTGAG 900 AACAGGGCCT TGGGAAAATC ATTTAGTCTC TCTGTGCCTC AATTTCCTTA TTTGTCATAG 960 AATCCACCTC ATAGAGTTAA ATGACTATTT GTTAAGTGCT GAGAACAGTG CCTGTCTCAT 1020 AGAAAGTGCT CTCTCTTTCT CTCTCTCTCC CTCTCTCTCT CTCTCTCTAT ATATATATGC 1080 AAACTTCTCT GCTAAGAATG GGTAATTTGG AGGGTGTGGC TTTTGAATTG GTTCTTGAAG 1140 GTTGTACAGA AATGCTAGCT TTAAAGATAC AGAATAGAGA GGCAAGAGAT GAAGCGCACC 1200 GGTGAAGAGA AAGGAAGCAT TTCAGGGAGC AGTAAGCCAC AGATTGGCTG GACTGGAGAG 1260 GCTGACAATG AGTGTGGGTA CAGGACGGAC CGGTAGGATT ACTAAAAGCC CCCAGCATGG 1320 GAGGAGACCG GCCCTTCCTG CTGTGAAGAT GAGAGCCAAC AATTTTCCAC AGAACTTCAC 1380 AGTATATCCA GAGCAATGCA GCCCTGTCAA TGTGTTAGAG ACATTAAGCA ACTTTGGCTA 1440 ATTTCACAAC AAAGGAAGAG GTGGGGTCAG AACTGGAAGA ACCCTGAGCT TCTTTATCCA 1500 GCACCAGGAT TGCCTATACC AGTGGAAGTT GTTCAGTGGG AAGTTACACA ATCCAGCCCT 1560 GCTTGGATGG TTAACCTGGG TTGTGGCAGT GAAGGATTTG ACCGTGGGAA CTTAACAGGT 1620 TGGGAGATCC TGGAGGAGTC TGTGATACAG TAGATACTGT GACATGTCAC CCAGGTCCCT 1680 CTTCAGGAAA GAAGGACTTA CTCCCCCTCC CCGTCAGCTA TTGGTAGTGT CGCTGGCAGA 1740 AAGCCCTCAG ATGCCCACTA TTCTAAGAGG ACCTCTTCCC CCATTCCCTG GGCAGCTGTA 1800 TCCCAAGATT GGTCCTGCAG GTACCTAACT GCATGGCTTC CATGCCCTAC TCAAGGCAAC 1860 TCTGATGGGC CATCCCAGTT CCAGAACTCC CAGTGGCATG GGCTGAGGAC TTCAGTGGGA 1920 CTGCATCATA GCCCCATTTC TTTCTCTGCC CACTTCTGCT TTCCTCCCTT CCCTTCCTCA 1980 TTGTTCATCC CAGGAGCAAG CCCCGATAAA CTTCCTGAAT GCTCTTCTCT GCCTTGGAGT 2040 CTGTTTCCTG AGGAGCTTAA CCTGCCTCTG TCTGAAGAAA TATCACAGGT AATTGAAATA 2100 GCCAGTTTAA TGAAAGAATT CGCATAACTT TTTCACTTTG GGAGAGAGAG ACATCAAAAT 2160 TCAATTGGAG GCTTCAATCC TGTTCAAAAT TATACTCCTA ATGCATACAG GGAAGTCCCT 2220 AGTAGGATAA AGTACAGGGT AGGGGGAAGA GCAAAGAAAG ATCAAAACAA AGACAAACTT 2280 TCCAGATGGG AAGTTATAAA TGTGGGAGTG AAACTCAGGA AGAACAGAGA GAGTTAGAGA 2340 CAGGGTCTGG GAGTCAGCTC AGCAGAGGCC ATCTCTGAAG TCATGATGGT AGATGAAACT 2400 CTGAGAGGCA AGACGCTGAG TAGAGGACTC TGGCAACACC CAAGAAATGG 2450
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