Tag | Content |
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EnhancerAtlas ID | HS017-16201 |
Organism | Homo sapiens |
Tissue/cell | CD14+_monocyte |
Coordinate | chr19:16444690-16445900 |
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) |
PLAG1 | MA0163.1 | chr19:16445048-16445062 | CCCCCCTTGGCCTC | - | 6.06 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_20477 | chr19:16444793-16446912 | CD56 | SE_22931 | chr19:16445721-16446821 | CD8_primiary | SE_38557 | chr19:16444606-16446278 | HUVEC | SE_61491 | chr19:16432573-16510994 | Toledo | SE_62295 | chr19:16434424-16512260 | Tonsil |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr19 | 16444890 | 16444986 | chr19 | 16445135 | 16445285 |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I016334 | chr19 | 16445319 | 16445495 |
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Enhancer Sequence | GTAGAGCCTG AGTCTCACTG TGTTACCCAG GCTGGTCGCA AACTCCTGGG CTCAAATGAA 60 CCATCCACCT TGGCCTCCCA AAATGCTGGG ATTACAAGAG TGAGACATTG TGCCTGGCTA 120 AAATTCACTT TTTTTTTTTT TGTGACAGAG TCTTGCTCTG TCACCCAGGC TGGAGTGCAG 180 TGGCACGATC TCGGTTCACT GCAACCTCCC ACCTCAAGTG ATTCTCCTGC CTCAGCCTCC 240 CGAGTAGCTG GGATTACAGG CGCACGCCAG CACAGCCGGC TAATTTTTAT ATTTTCAGTA 300 GAGACGGGGT TTCACCATGT TGGCCAATGG TCTCAAACTC CTGACCTCAG GTGATCCGCC 360 CCCCTTGGCC TCCCAAAGTG CTAGGAATAC AGGCGTGAGC CACCACACCC AGCACAAAAT 420 TGGTTATTTT TAAGTGTTCA GTTCAGCAGC ATTCACAGCA TTGTGCCACC TTCACCACCA 480 CCCATCTCCA GAGCTTTTCC CTTCTTCCCA AACTGAAACT TTGATCCCAT TAAACACTCA 540 CTTCCCATTC TCCCTCCCCA GCCACTGGCC CCCACCCTTC TTCCTTCTGT CTCTACAAAT 600 TTGAGCACTC TGAGGACCTC CTAGGAGTGG AATCATACAG TATCTGTCCT TTCCTGTAGT 660 TTATTTCACT CAGCATAATG TCTTCAAGAT TCATCCACGT GGTAGTGTGT GTCAGAATTT 720 CCTTCCTTTT TATGACTCAG TAATATTCCA TTGTGTGGAA GGACCACATT TTGTATGTCC 780 ATTCATTCCT TGATGAACAC TTGGTCATTT CCACCCCTTG GCTGCTATGA ACATGAGTGT 840 GCAAATACCC ATTCCAGCCC CTGCTATCAG TTTTTTGGGG CTGTGTCCCT AACAGTGGAA 900 TGGCTGGATA CCCTTTTTTA CTTTTTACTG TTAGTATTTT TTGAGACAGA GTCTCACTCT 960 CTCGCCCAGC CTGCAGTGCA GTGGTGCAGT CTCAGCTCAC TGCACCCTCT GCCTCCCGGG 1020 TTCAAGTGAT TCTCCTGCCT CAGCCTCCCA AGTAACTGGG ATTACAGGCG TGCACCACCT 1080 CACCCAGCTA ATTTTTGTAT TTTTAGTAGA GACGACGTTT CACCATGTTG GCCAGGCTGG 1140 TCTCGAACTC CTGACCTCAA GCGATCCTCC TGCCTCGGCC TCCCAAAGTG CTGAGATTAC 1200 AGGCGTCAGC 1210
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