Tag | Content |
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EnhancerAtlas ID | HS145-11350 |
Organism | Homo sapiens |
Tissue/cell | NHBE |
Coordinate | chr19:877180-879930 |
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) |
MYC | MA0147.3 | chr19:877719-877731 | CCCCACGTGCCC | + | 6.07 | MYC | MA0147.3 | chr19:877793-877805 | CCCCACGTGCCC | + | 6.07 | MYC | MA0147.3 | chr19:877905-877917 | CCCCACGTGCCC | + | 6.07 | MYC | MA0147.3 | chr19:877973-877985 | CCCCACGTGCCC | + | 6.07 | MYC | MA0147.3 | chr19:878035-878047 | CCCCACGTGCCC | + | 6.07 | MYC | MA0147.3 | chr19:878185-878197 | CCCCACGTGCCC | + | 6.07 | MYC | MA0147.3 | chr19:878309-878321 | CCCCACGTGCCC | + | 6.07 | MYC | MA0147.3 | chr19:878377-878389 | CCCCACGTGCCC | + | 6.07 | MYC | MA0147.3 | chr19:878451-878463 | CCCCACGTGCCC | + | 6.07 | MYC | MA0147.3 | chr19:878507-878519 | CCCCACGTGCCC | + | 6.07 | MYC | MA0147.3 | chr19:878631-878643 | CCCCACGTGCCC | + | 6.07 | MYC | MA0147.3 | chr19:878687-878699 | CCCCACGTGCCC | + | 6.07 | MYC | MA0147.3 | chr19:878743-878755 | CCCCACGTGCCC | + | 6.07 | MYC | MA0147.3 | chr19:878799-878811 | CCCCACGTGCCC | + | 6.07 | MYC | MA0147.3 | chr19:878867-878879 | CCCCACGTGCCC | + | 6.07 | MYC | MA0147.3 | chr19:879077-879089 | CCCCACGTGCCC | + | 6.07 | MYC | MA0147.3 | chr19:879145-879157 | CCCCACGTGCCC | + | 6.07 | MYC | MA0147.3 | chr19:879321-879333 | CCCCACGTGCCC | + | 6.07 | MYC | MA0147.3 | chr19:879433-879445 | CCCCACGTGCCC | + | 6.07 | MYC | MA0147.3 | chr19:879489-879501 | CCCCACGTGCCC | + | 6.07 | MYC | MA0147.3 | chr19:879625-879637 | CCCCACGTGCCC | + | 6.07 | MYC | MA0147.3 | chr19:879681-879693 | CCCCACGTGCCC | + | 6.07 | MYC | MA0147.3 | chr19:879769-879781 | CCCCACGTGCCC | + | 6.07 | MYC | MA0147.3 | chr19:879825-879837 | CCCCACGTGCCC | + | 6.07 | MYC | MA0147.3 | chr19:879913-879925 | CCCCACGTGCCC | + | 6.07 | MYC | MA0147.3 | chr19:878097-878109 | CGCCACGTGCCC | + | 6.74 |
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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 |
GH19I000879 | chr19 | 879666 | 880011 |
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Enhancer Sequence | CTGCCAGAGA CAGAGCCCAA GGAGAGCCCG GTGAGATGGG GCTGCGCCCT CAGCCGGGAG 60 AGGAATGGGG CCCTGGGGCT GCGGCACGTG TGTGGATCTG TGTGCGCGCA CGCCCGTGTG 120 TGGGCCTGTG TGCGCGCATG TGTCTGTAGC GTCTGTACCT TTCTGTCAGG GTCATGCACA 180 ATGCCTCTGG GAACAGGGAA GGAAACCTCC CTGAGCCCCG ACTGCACTGG ATGCCGAGCC 240 AGGCTTACAC TCGTCTGCTT TACCTGAGGA GTCTACCCCG TGAAAGGCGG TCCTCTCAAC 300 AGCTCCTAGT TACGAAGCTC CTAATACGTG CTGTGAGCCA CCCCACTGAC CTCGCTCAAC 360 AAGACGAACC CATCACACAG ACAAGGCAGC GCAGGCAGGG GCTGGCGAGG GGCTTGCACC 420 TGTGGTCCCT TCCCCCGGGG GCGCCTCCCT CTGGCACCCT CCCAGCCCCA GCCCCAGCCC 480 CAGACCCACG TGCCCCAGCA GCTCGCCTTC CCCTGGTTGT CAATGCCCAC CAGCCCCTGC 540 CCCACGTGCC CCAGCAGCTC ACCTTCCCCT GGTTGTCAAT GCCCACCAGC CCCAGCCCCA 600 GCCCCAGCCC CAGCCCCACG TGCCCCAGCA GCTCGCCTTC CCGTGGTTGT CAATGCCCAC 660 CAAGCCCAGC CCCACATGCC CCAGCAGCTC GCCTTCCCCT GGTTGTCAAT GCCCACCAGC 720 CCCAGCCCCA CGTGCCCCAG CAGCTCACCT TCCCGTGGTT GTCAATGCCC ACCAGCCCCA 780 GCCCCAGCCC CAGCCCCACG TGCCCCAGCA GCTCACCTTT CCGTGGTTGT CAACGCCCAC 840 CAGCCCCAGC CCCAGCCCCA CGTGCCCCAG CAGCTCGCCT TCCCCTGGCT GTCAATGCCC 900 CCCAGCCCCA GCCCCAGCGC CACGTGCCCC AGCAACTCAC CTTCCCCTGG TTGTCAATGC 960 TCAGCAGCTC ACCTTCCCGT GGTTGTCAAT GCCCACCGAG CCCAGCCCCA CGTGCCCCAG 1020 CAGCTCACCT TCCCCTGGTT GTCAATGCCC ACCAGCCCCA GCCCCAGCCC CAGCCCCACG 1080 GGCCCCAGCA GCTCGCCTTC CCCTGGTTGT CAATGCCCAC CAGCCCCAGC CCCACGTGCC 1140 CCAGCAGCTC ACCTTCCCGT GGTTGTCAAT GCCCACCAGC CCCAGCCCCA GCCCCAGCCC 1200 CACGTGCCCC AGCAGCTCAC CTTTCCCTGG TTGTCAATGT CCACCAGCCC CAGCCCCGGC 1260 CCCGGCCCCG GCCCCACGTG CCCCAGCAGC TCACCTTCCC CTGGCTGTCA ATGCCCACCA 1320 GCCCCAGCCC CACGTGCCCC AGCAGCTCAC CTTCCCGTGG TTGTCAATGC CCACCAGCCC 1380 CAGCCCCAGC CCCACATGCC CCAGCAGCTC ACCTTCCCGT GGTTGTCAAC GCCCACCAGC 1440 CACAACCCCA GCCCCACGTG CCCCAGCAGC TCACCTTCCC CTGGTTGTCA ATGCCCAACA 1500 GCCCCAACCC CACGTGCCCC AGCAGCTCGC CTTCCCCTGG TTGTCAATCC CCACCAGGGC 1560 CAGCCCCACG TGCCCCAGCA GCTCCCCTTC CCCTGGTTGT CAATGCCCAC CAGCCCCAGC 1620 CCCACGTGCC CCAGCAGCTC CCCTTCCCCT GGTTGTCAAT GCCCACCAGC CCCAGCCCCA 1680 GCCCCAGCCC CACGTGCCCC AGCAGCTCAC CTTTCCCTGG TTGTCAATGT CCACCAGCCC 1740 CGGCCCCGGC CCCGGCCCCG GCCCCGGCCG CAGCTCCACG TGCCCCAGCA GCTCACCTTC 1800 CCCTGGCTAT CAATGCCCAC CAGCCCCAGC CCCAGCCCCA CATGTCCCAG CAGCTCACCT 1860 TCCCCCGGTT GTCAATGCCC ACCAGCCCCA GCCCCAGCCC CACGTGCCCC AGCAGCTCGC 1920 CTTCCCCTGG TTGTCAATAC CCCCCAGCCC CAGCCCCAGC CCCAGCCCCA CGTGCCCCAG 1980 CAGCTCGCCT TCCCCTGGTT GTCAATGCCC AGCAGCTCAC CTTCCCATGG TTGTCAATGC 2040 CCACCAAGCC GAGCCCCACA TGCCCCAGCA GCTCGCCTTC CTCTGGTTGT CAATGCCCAG 2100 CAGCTCACCT TCCCATGGTT GTCAATGCCC ACCAAGCCCA GCCCCACGTG CCCCAGCAGC 2160 TCACCTTCCC CTGGTTGTCA ATGCCCACCA GCCCCAGCCG CACATGCCCC AGCAGCTCAC 2220 CTTTCCCTGG TTGTCAATGC CCACCAACCC CAGCCCCACG TGCCCCAGCA GCTCGCCTTC 2280 CCCTGGTTGT CAATGCCCAC CAGCCCCAGC CCCACGTGCC CCAGCAGCTC GCCTTTCCCT 2340 GGTTGTCAAT GCCTACCAGG GCCACGCCCC AGCAGCTCGC CTTCCCCTGG TTGTCAATGC 2400 CCAGCAGCTC ACCTTCCCGT GGTTGTCAAT GCCCCCCAAG CCCAGCCCCA CGTGCCCCAG 2460 CAGCTCACGT TCCCCTGGTT GTCAATGCCC ACCAGCCCCA GCCCCACGTG CCCCAGCAGC 2520 TCGCCTTCCC CTGGTTGTCA ATGCCCAGCA GCTCGCCTTC CCCTGGTTGT CAATGCCCAC 2580 CAGCCCCAGC CCCACGTGCC CCAGCAGCTC GCCTTCCCCT GGCTGTCAAT CCCCACCAGG 2640 GCCAGCCCCA CGTGCCCCAG CAGCTCACCT TCCCCTGGTT GTCAATGCCC AGCAGCTCGC 2700 CTTCCCCTGG TTGTCAATGC CCACCAGCCC CGGCCCCACG TGCCCCAGCA 2750
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