Tag | Content |
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EnhancerAtlas ID | HS017-32856 |
Organism | Homo sapiens |
Tissue/cell | CD14+_monocyte |
Coordinate | chr9:15430620-15432120 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MAFG | MA0659.1 | chr9:15431069-15431090 | GATGTGCTGGCTCAGCAGGAT | + | 6.13 | POU2F2 | MA0507.1 | chr9:15431915-15431928 | TGAATTTGCATAT | + | 6.67 |
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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 |
GH09I015430 | chr9 | 15430141 | 15431481 |
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Enhancer Sequence | GTGTTCAATA CTTACTAGTG ATGTTTAGCT TGTTTCTGTC TGCTTGTTAT TCCTTGCAGT 60 ATTGTTTGTA ATTGCAAAAT ATTTGAAATA CCTTAAATAT ACAGACGTAG GAGAGGAGAG 120 TGTTGAATAC GCTATGGGAA ATCCACACGG TAATATTTTG CAGCTAGAAT AAAGGATGAG 180 GAAGGATTAA TTCAGAGTAA TTTCCAGTAC ATTCTATTAA GTGAAAAAAG CAAAGTCCCA 240 AAGTATATGC CACCTTTCAT GTAAGAAAGG TGTGCCAGGT GTAGTTTATT GGCTCTCATC 300 TTCAAATTTA CCTCTTTTTC CTGCTCTGTA AAAATGGACC TTGGCCTTTT AAATACTTTT 360 CTTTTGCCAA CTAGCACATC CTTAAGCTTT GTCAGTGAAG GGCAATGGAG AGACTTCTCA 420 GGAGTCTCAA AGGTTTTGCT TCCTGATCTG ATGTGCTGGC TCAGCAGGAT CCTGCAGTGC 480 ACACAGCTTC CCCAGTGCCC AGCTCCTGCA ATACACTGCA GTCTGAAGCA CCCCGCGCCC 540 AGCAGCTTTC CTGCCAACCC CATTTCCCTC CACAGCTCCC CTGAACAGGT TTTCCTAGTG 600 CCCTTGAGGG TGGATTTCCA GCAAGTTCCA CTGATGCAGT ACCATAGCAA CTTCTTTCTC 660 CAGCTCGTCT GGATCTCTGT CCAGGAAGAA AAAAGGACTT CCCTGCGCTC TTTCTCAGCC 720 CTAGGGGTAG GGTGCTCCTT CTGTTTGCTA TTATTCTATA CTTCAGTGTT CCCTTTTACT 780 GCTTCCTTGC CAATCCCTCA TTATTCCAAT CCTCTGTTAA AGTTATTGAA TCCTTAACCT 840 TTGTTCAAAT TGCTGTTCTT TTTTTCTTCC TAATTGAACT CAGATTGATA CAGGAGATAA 900 CAGAGTATAC ACAAATATCT GTTTATTTGA ACAAAGGAAA TGGAAAGGAC AAACCAAAAC 960 TATAGAGACT GATTGCCTGC AGGGGTGGGT GGGAAAGGGG TGGAAAGAAG GGAGGGAATG 1020 GGAACAGGTT AGTAGGAACA AAGAGGGAGT GACACTTTTG ACTCTTAGGA TCATAGTAAT 1080 GTGTCACATA TTTTTCACAC ACCCCAAATG TAATCAGACA ATTAAAACCA ACTAGGATGT 1140 AGGGGGAACC CAAAACTGAA TTCAAAAACT AAAAAATAAG GCTAGTTGTA TTACGGATGT 1200 GTAATATAAC ACCACTGAAA AGGGTGGGGA AGAAAGAACT AAAGTCTGTA TTAAAGCCTG 1260 TCTTTTTTTT TTTTTTTTTT TTTTTGAGCA CTTCATGAAT TTGCATATCA TCCATGCACA 1320 GGGGCCGTGC TAATCTTAAA TATATTGTTC CGATTTTTAA ATAATAAAAT GCTACCAAAA 1380 GCGTATCTTG ATATAATGTA AAGGTGAAGA CAGAACTGTT TATAATTTAG TGTTTCTCAC 1440 AGGGGTATAG GTTAGCAATT CTGTAACTAT TTTATGTATT TACTAGAATT GAACAAATCA 1500
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