Tag | Content |
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EnhancerAtlas ID | HS073-07018 |
Organism | Homo sapiens |
Tissue/cell | GM19238 |
Coordinate | chr19:877510-879930 |
Target genes | Number: 14 | Name | Ensembl ID |
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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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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_47773 | chr19:879665-880011 | Pancreas |
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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 | CTGTGAGCCA CCCCACTGAC CTCGCTCAAC AAGACGAACC CATCACACAG ACAAGGCAGC 60 GCAGGCAGGG GCTGGCGAGG GGCTTGCACC TGTGGTCCCT TCCCCCGGGG GCGCCTCCCT 120 CTGGCACCCT CCCAGCCCCA GCCCCAGCCC CAGACCCACG TGCCCCAGCA GCTCGCCTTC 180 CCCTGGTTGT CAATGCCCAC CAGCCCCTGC CCCACGTGCC CCAGCAGCTC ACCTTCCCCT 240 GGTTGTCAAT GCCCACCAGC CCCAGCCCCA GCCCCAGCCC CAGCCCCACG TGCCCCAGCA 300 GCTCGCCTTC CCGTGGTTGT CAATGCCCAC CAAGCCCAGC CCCACATGCC CCAGCAGCTC 360 GCCTTCCCCT GGTTGTCAAT GCCCACCAGC CCCAGCCCCA CGTGCCCCAG CAGCTCACCT 420 TCCCGTGGTT GTCAATGCCC ACCAGCCCCA GCCCCAGCCC CAGCCCCACG TGCCCCAGCA 480 GCTCACCTTT CCGTGGTTGT CAACGCCCAC CAGCCCCAGC CCCAGCCCCA CGTGCCCCAG 540 CAGCTCGCCT TCCCCTGGCT GTCAATGCCC CCCAGCCCCA GCCCCAGCGC CACGTGCCCC 600 AGCAACTCAC CTTCCCCTGG TTGTCAATGC TCAGCAGCTC ACCTTCCCGT GGTTGTCAAT 660 GCCCACCGAG CCCAGCCCCA CGTGCCCCAG CAGCTCACCT TCCCCTGGTT GTCAATGCCC 720 ACCAGCCCCA GCCCCAGCCC CAGCCCCACG GGCCCCAGCA GCTCGCCTTC CCCTGGTTGT 780 CAATGCCCAC CAGCCCCAGC CCCACGTGCC CCAGCAGCTC ACCTTCCCGT GGTTGTCAAT 840 GCCCACCAGC CCCAGCCCCA GCCCCAGCCC CACGTGCCCC AGCAGCTCAC CTTTCCCTGG 900 TTGTCAATGT CCACCAGCCC CAGCCCCGGC CCCGGCCCCG GCCCCACGTG CCCCAGCAGC 960 TCACCTTCCC CTGGCTGTCA ATGCCCACCA GCCCCAGCCC CACGTGCCCC AGCAGCTCAC 1020 CTTCCCGTGG TTGTCAATGC CCACCAGCCC CAGCCCCAGC CCCACATGCC CCAGCAGCTC 1080 ACCTTCCCGT GGTTGTCAAC GCCCACCAGC CACAACCCCA GCCCCACGTG CCCCAGCAGC 1140 TCACCTTCCC CTGGTTGTCA ATGCCCAACA GCCCCAACCC CACGTGCCCC AGCAGCTCGC 1200 CTTCCCCTGG TTGTCAATCC CCACCAGGGC CAGCCCCACG TGCCCCAGCA GCTCCCCTTC 1260 CCCTGGTTGT CAATGCCCAC CAGCCCCAGC CCCACGTGCC CCAGCAGCTC CCCTTCCCCT 1320 GGTTGTCAAT GCCCACCAGC CCCAGCCCCA GCCCCAGCCC CACGTGCCCC AGCAGCTCAC 1380 CTTTCCCTGG TTGTCAATGT CCACCAGCCC CGGCCCCGGC CCCGGCCCCG GCCCCGGCCG 1440 CAGCTCCACG TGCCCCAGCA GCTCACCTTC CCCTGGCTAT CAATGCCCAC CAGCCCCAGC 1500 CCCAGCCCCA CATGTCCCAG CAGCTCACCT TCCCCCGGTT GTCAATGCCC ACCAGCCCCA 1560 GCCCCAGCCC CACGTGCCCC AGCAGCTCGC CTTCCCCTGG TTGTCAATAC CCCCCAGCCC 1620 CAGCCCCAGC CCCAGCCCCA CGTGCCCCAG CAGCTCGCCT TCCCCTGGTT GTCAATGCCC 1680 AGCAGCTCAC CTTCCCATGG TTGTCAATGC CCACCAAGCC GAGCCCCACA TGCCCCAGCA 1740 GCTCGCCTTC CTCTGGTTGT CAATGCCCAG CAGCTCACCT TCCCATGGTT GTCAATGCCC 1800 ACCAAGCCCA GCCCCACGTG CCCCAGCAGC TCACCTTCCC CTGGTTGTCA ATGCCCACCA 1860 GCCCCAGCCG CACATGCCCC AGCAGCTCAC CTTTCCCTGG TTGTCAATGC CCACCAACCC 1920 CAGCCCCACG TGCCCCAGCA GCTCGCCTTC CCCTGGTTGT CAATGCCCAC CAGCCCCAGC 1980 CCCACGTGCC CCAGCAGCTC GCCTTTCCCT GGTTGTCAAT GCCTACCAGG GCCACGCCCC 2040 AGCAGCTCGC CTTCCCCTGG TTGTCAATGC CCAGCAGCTC ACCTTCCCGT GGTTGTCAAT 2100 GCCCCCCAAG CCCAGCCCCA CGTGCCCCAG CAGCTCACGT TCCCCTGGTT GTCAATGCCC 2160 ACCAGCCCCA GCCCCACGTG CCCCAGCAGC TCGCCTTCCC CTGGTTGTCA ATGCCCAGCA 2220 GCTCGCCTTC CCCTGGTTGT CAATGCCCAC CAGCCCCAGC CCCACGTGCC CCAGCAGCTC 2280 GCCTTCCCCT GGCTGTCAAT CCCCACCAGG GCCAGCCCCA CGTGCCCCAG CAGCTCACCT 2340 TCCCCTGGTT GTCAATGCCC AGCAGCTCGC CTTCCCCTGG TTGTCAATGC CCACCAGCCC 2400 CGGCCCCACG TGCCCCAGCA 2420
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