Variant report

Variant	rs16869710
Chromosome Location	chr4:20526326-20526327
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	chr4:20523924..20528814-chr4:20529979..20533710,4	K562	blood:

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs16869701	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16869711	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16869713	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16869714	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2292438	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35505999	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3756148	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs3775808	0.95[ASN][1000 genomes]
rs3822188	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs729919	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv878742	chr4:20473799-20527864	Weak transcription Active TSS Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv829875	chr4:20502895-20680956	Enhancers Genic enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA	89 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:20464600-20532600	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr4:20489200-20529600	Weak transcription	Fetal Stomach	stomach
3	chr4:20490800-20529600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr4:20492000-20534800	Weak transcription	Fetal Kidney	kidney
5	chr4:20492000-20599800	Weak transcription	Aorta	Aorta
6	chr4:20508800-20534000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr4:20511800-20576200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr4:20513200-20534600	Weak transcription	Fetal Brain Male	brain
9	chr4:20519400-20571000	Weak transcription	Adipose Nuclei	Adipose
10	chr4:20520600-20539600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr4:20521200-20535400	Weak transcription	Spleen	Spleen
12	chr4:20521400-20529600	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr4:20523000-20529800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr4:20523000-20530400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr4:20523000-20532600	Weak transcription	NHLF	lung
16	chr4:20523200-20530400	Weak transcription	Osteobl	bone
17	chr4:20523200-20534000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr4:20523200-20535800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr4:20523400-20529600	Weak transcription	HSMM	muscle
20	chr4:20523400-20529600	Strong transcription	NHDF-Ad	bronchial
21	chr4:20523400-20529800	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr4:20523400-20529800	Weak transcription	NHEK	skin
23	chr4:20524200-20555200	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr4:20524600-20527400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr4:20524800-20529600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr4:20525000-20536600	Weak transcription	Gastric	stomach
27	chr4:20525200-20555400	Weak transcription	Stomach Smooth Muscle	stomach
28	chr4:20526000-20529600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr4:20526000-20529600	Weak transcription	Colon Smooth Muscle	Colon
30	chr4:20526200-20528400	Weak transcription	Fetal Lung	lung

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