Tag | Content |
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EnhancerAtlas ID | HS136-03892 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr11:102628360-102629850 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SPI1 | MA0080.4 | chr11:102628783-102628797 | GAAAAGGGGAAGTG | + | 6.64 | SPIB | MA0081.2 | chr11:102628785-102628797 | AAAGGGGAAGTG | + | 6.07 | Stat6 | MA0520.1 | chr11:102628802-102628817 | ATTTCTCAGGAAAAC | - | 7.64 |
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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 |
GH11I102757 | chr11 | 102628716 | 102629650 |
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Enhancer Sequence | TCTCTTCATG AAGTCTCAGA GCTTCCTCCT CTTCAGTAGA GTAGCCAGAT TTTTTTCTTT 60 ACTACATTTA GTAATACTTT CTCCATGAAT GCTTGAACAC ATTTAATCCA GGGGACTAGG 120 CTGTATTTAT CCATTCATAT ATGTCTTCCT CCATTCAACA AATATTTTCT TAATATTTCC 180 AGTCACTTAG GCTGGAGAAA GGAAAAATAG GCCAGCAGAT TATTCATGCA TGGTACCTTT 240 AATTTGTGCT GTAAGAGATT CATACAAAGT GCTGCAATTA CACAGAAGAC AGTGACCTTA 300 TGTACGATAG AGATGTGTGT ACAAACTTCC AACACATGAT GGATAAGAAC ACATTCTCCT 360 CTCTCAATTT AATTTTTAAC CACAACTTCC CCATCTAAAT GGAGTATCAC ACTAATGCAA 420 ACAGAAAAGG GGAAGTGAAT GAATTTCTCA GGAAAACCCA AATTCTCTCT TTCCCACAGG 480 ACTTCTGATG CCTGCAGAGG CAAGGGAAAT AAGAAAAGGA GGCATTTTCT AGGACAAATG 540 GAATATAGGT CATCTTTTCC CAGCCAAAAT GAGGCTGGAA CTCCCCGACC ACCATAGGGT 600 GCATACACTA GCTGTGGAGA AGCCATCCCC TCAGTGCTCC TGGTGCTTCC TGCCAGGAAT 660 CCCCTAGTTC ACTCAGTAGC CTCAGAAACA GGAAAGGGGA ACTCCTGAAA AACTGAGGAA 720 ACCACCATTG TGATAACTGG GATTGAGCAA CAAATTACAC ATGATGTCAT CTTCATGAAG 780 ACTCATACAA TAAGAAATCT GGTGGTTATT CAGTATAGTG CTTGACAACA ATTATGTCAT 840 AATACTGAAT GCTTTACTGA AAGAGCAATC TGTGTGTATG TCCAGCAAAC AGATCAAATT 900 TGCAAACAGA TAAAAAAGCA AAGCATGATA GTAGTGCTTA AAGTAGAAGC ACTGAACTCT 960 AGAGACTCAC CTTCATCCTA CTACCTCTCT CTTTGTCCCC TCTAACATAA CCCCCAAATA 1020 CCATGGAAGA ATGCAGCAAG TTTAAAAATC ACCAATCTAA TAGAAACCTC TTACTTGTCA 1080 AATGAGAAAA CTTAGAGACA TGGGCCTTCC ATCACTTGTT CCAGATCATG CATCTAGTGA 1140 AGAGCACTAG AATTAGAGCT GTTGCTTTCT ATTTCCAAGT CTAAGCCTAC TACACTAAGA 1200 ATTTCATTTC ATGTCAATGA ATCTAACATG GATTAGATTT TGTTTTCTGT CAAACATCAT 1260 ATTGTTTAAC TTATTGGAAT TCTGTGGTAT TTTGTAGCTT TCTTAAAGGA CTTCTCATAT 1320 TTTGCCTTAT GCTTGACTAT TTGTCTTCCT TTATGTATGA AATTTTTTTT ATAGGGTAGA 1380 GATATACTGT TATAGACATG TGTTTTATAA ATTGCACTAA TACAACAGTA ATCATTATTT 1440 CCCTGACATC AAAAACTTAC ACTGTGATCA GGTATTATAT GGAATAAAAG 1490
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