Variant report

Variant	rs747107
Chromosome Location	chr16:55695721-55695722
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr16:55684943..55687258-chr16:55695232..55697470,2	K562	blood:
2	chr16:55695466..55697327-chr16:55702123..55704926,2	K562	blood:

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs11076111	0.95[CHB][hapmap];0.95[JPT][hapmap];0.99[ASN][1000 genomes]
rs12232407	0.95[CHB][hapmap]
rs13333066	0.95[CHB][hapmap]
rs1362620	0.84[ASN][1000 genomes]
rs1362621	0.84[ASN][1000 genomes]
rs1532701	0.95[CHB][hapmap]
rs17247999	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17307096	0.95[CHB][hapmap]
rs17307291	0.95[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs17841327	0.95[CHB][hapmap]
rs2062723	0.95[CHB][hapmap]
rs2242446	0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs2397771	0.95[ASN][1000 genomes]
rs28501300	0.95[ASN][1000 genomes]
rs28665972	0.98[ASN][1000 genomes]
rs28693487	0.97[ASN][1000 genomes]
rs28811645	1.00[EUR][1000 genomes]
rs3760019	0.84[ASN][1000 genomes]
rs3785147	0.98[ASN][1000 genomes]
rs9937434	0.95[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv906673	chr16:55631035-55798370	Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv431501	chr16:55639454-55789570	Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv517827	chr16:55656355-55698027	Flanking Bivalent TSS/Enh Bivalent/Poised TSS Enhancers Bivalent Enhancer Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	esv2758426	chr16:55669396-55983590	Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	esv2758649	chr16:55669396-55983590	Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:55692600-55705400	Enhancers	Placenta	Placenta
2	chr16:55693600-55699400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr16:55693600-55699400	Enhancers	NHEK	skin
4	chr16:55693800-55699000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr16:55694200-55695800	Enhancers	HepG2	liver
6	chr16:55694200-55698400	Enhancers	Fetal Muscle Leg	muscle
7	chr16:55694200-55698400	Enhancers	Fetal Stomach	stomach
8	chr16:55694400-55696000	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr16:55695000-55696200	Enhancers	Fetal Muscle Trunk	muscle
10	chr16:55695000-55697400	Enhancers	Brain Germinal Matrix	brain
11	chr16:55695000-55697400	Enhancers	Brain Hippocampus Middle	brain
12	chr16:55695000-55699400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr16:55695200-55697600	Enhancers	NHDF-Ad	bronchial
14	chr16:55695200-55698200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr16:55695400-55699600	Enhancers	HMEC	breast
16	chr16:55695600-55696000	Enhancers	Stomach Smooth Muscle	stomach
17	chr16:55695600-55696200	Enhancers	Adipose Nuclei	Adipose
18	chr16:55695600-55696200	Enhancers	Right Atrium	heart
19	chr16:55695600-55696800	Enhancers	Brain Inferior Temporal Lobe	brain
20	chr16:55695600-55696800	Enhancers	Brain Substantia Nigra	brain
21	chr16:55695600-55697200	Enhancers	Fetal Brain Male	brain
22	chr16:55695600-55703800	Enhancers	Breast Myoepithelial Primary Cells	Breast

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