Tag | Content |
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EnhancerAtlas ID | HS136-01620 |
Organism | Homo sapiens |
Tissue/cell | Monocyte |
Coordinate | chr1:205673290-205674930 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
GATA2 | MA0036.3 | chr1:205673522-205673533 | TTCTTATCTTC | + | 6.02 | MEF2C | MA0497.1 | chr1:205673753-205673768 | ATCTATTTTTGGTCA | - | 6.23 |
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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 |
GH01I205704 | chr1 | 205673929 | 205674128 |
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Enhancer Sequence | GTCTGAAGCA AGGCACCCAG GGAGGCACAG AGGAACGCAG GAGCGCTGAG ACATGGTGGA 60 TGGTAGGATT CCAACCTGCC CTCCTTTCCC CTTATTTACC CAGTTTGCGC CATCATCCCA 120 CCCTCCAGAG AAAATACGGA GACAGGGAAC GTCCCTCGGC AGCAAGAATG AAAGGTACGG 180 TGGCTCAGCA ACCAAGGCTG CTCCTTGTTT CTGCTACTGA TGTCCTATTA ACTTCTTATC 240 TTCCAGGGTG AAGATATTAC TGCAAGGCCT TTTGCCAGGC AGTTTCATGT ATGATCCTTA 300 CTACAACCCT GAGAAGTAGA TGTTACTGAC CTGGTTAACA GTCTCAGAAA CTGAGACTCA 360 GAGAGATTGT GTTCCCAAAG ACCCAGCTGG TTAGCAGAGA GCCAGAACTC AGACCTAGGT 420 CCCTGACTTT CTGTCTAGAG TTTTTCCCAC TGTTTCTCTT TTCATCTATT TTTGGTCAAT 480 TCACTGCTCC CTGATGCTTC TGCTGGAGGC TCTATATTCT GGGAAACAAG CGAAGGCAAG 540 CAAAATGCAG CCAATCAGTG CTGACCTTAG TCAATAAAAA GGTTGCAGAC AGTTGTGGTT 600 GTCAGGCTTT GTTGCTTAAC CATCTCTAGA CCTCTGTTTC TTTCTCTGTA GATTGGGGAC 660 AGTAATATTA CCTGTATCTC ATGGGACTGT GGTGAGGATT CAATGATAAA AGGCAGGACA 720 AGTGCTCAAG AGGATGCCTT GAACATAGTA AGCCCTCAAT AAAGGGGAGC TGCGGTTACT 780 ACTAAGACAG TGTTGGAGAA AGTACAAGAG CCACAGTTTT TCCAGGGTAA GAGGTAGATT 840 ATTAAAGGCT GATACTGTAT ATGTTCTCTT AGCTCCTCTC TTGAACATAA ACATCTGTGG 900 TTTGTCAAAG ACATTTTCAG GATCCGGTTT TCTTTTTAGA AAGAGGAAGG AAAAAAAACC 960 CAAGGCCTGA ATCTATAGGA AGTCCAAATG CACCCAGGAT TCTTAAGTCA CAAGATAAAA 1020 AGTGGAGATG CTTGAAGAGG CATCTGATAG TGGAATTCAT GGAAGAGGAA AAGGTCAGTT 1080 CCATCTCTAG TGACTCCAAC AGAGGGATGA AACATCCAAG AATGAAGAAA ATTATTTCCA 1140 GGAATGGCAA ATGAGGATGG AACCATAGGA TATAGTTATT ATTGTTAAAC CAAACCCAGT 1200 GCAATAATTG GTCTGTCTCA ATAACATCAC TCCGGCCAAG TTGCCGTTTC CAAGAAGGAA 1260 AGAATAAGAA TTTAGTCCAG CTGATTCTTC GGCATGATTT AAACCAGCAG TGGTTGTCAA 1320 ACCTTAGTGT GCCTCAGAAT CAACTGGAGG GCTTGTTAAA TCCAAACTGC GAAGTCTCAT 1380 CCCGAGTTTC TCATTTAATG GATTGGGGGT GGGACCCGAG TTTGCATTTT GAACAAGCTA 1440 CCAGCTGATG CTGAGACTGC TGGTCCATCC AGGGACCACA TTTCGAGAAC CACTGATTTA 1500 AAGCACTTTT CTATGGGCAA TCAAAGAATA TCAAATTGCA TAATTCTTTT TTATTTTTAT 1560 TTTTGAGACG TAGTCTGGCT GTCGCCCAGG CTGGAGCGCA GTGGTGCGAT CTCGGCTCAC 1620 TGCAAGCTCC GCCTCCCGGG 1640
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