Variant report

Variant	rs16962965
Chromosome Location	chr18:29860726-29860727
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	chr18:29853249..29854777-chr18:29860158..29863062,2	K562	blood:
2	chr18:29839871..29842778-chr18:29859077..29861521,2	K562	blood:

Extended variants
information (count: 56 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs10502593	1.00[CEU][hapmap]
rs10502597	1.00[CEU][hapmap]
rs10502598	1.00[CEU][hapmap]
rs10502599	1.00[CEU][hapmap]
rs11660076	1.00[CEU][hapmap];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11661174	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11661186	0.93[EUR][1000 genomes]
rs11661378	1.00[CEU][hapmap]
rs11664951	1.00[CEU][hapmap]
rs11665544	1.00[CEU][hapmap];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11873828	1.00[CEU][hapmap]
rs11877881	1.00[CEU][hapmap]
rs12052010	1.00[CEU][hapmap]
rs1380086	1.00[CEU][hapmap]
rs16962918	0.96[EUR][1000 genomes]
rs16962924	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs16962941	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs16962953	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs16962971	1.00[CEU][hapmap];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16962974	1.00[CEU][hapmap];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16962977	1.00[CEU][hapmap];1.00[EUR][1000 genomes]
rs16963129	1.00[CEU][hapmap]
rs16963184	1.00[CEU][hapmap]
rs17743799	1.00[CEU][hapmap]
rs17743907	1.00[CEU][hapmap]
rs17744164	1.00[CEU][hapmap]
rs17805881	1.00[CEU][hapmap]
rs17805905	1.00[CEU][hapmap]
rs17805953	1.00[CEU][hapmap]
rs17811420	1.00[CEU][hapmap]
rs17811474	1.00[CEU][hapmap]
rs17811780	1.00[CEU][hapmap]
rs28394787	0.84[AFR][1000 genomes]
rs28482447	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28540269	0.96[AFR][1000 genomes]
rs28673618	0.96[AFR][1000 genomes]
rs3859366	0.96[EUR][1000 genomes]
rs41535045	1.00[CEU][hapmap]
rs4462681	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs60291556	0.96[EUR][1000 genomes]
rs60694040	0.82[EUR][1000 genomes]
rs7243861	0.93[EUR][1000 genomes]
rs7243963	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs73419859	0.96[AFR][1000 genomes];0.96[EUR][1000 genomes]
rs8086611	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8086990	1.00[CEU][hapmap];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs8087394	0.96[EUR][1000 genomes]
rs9916917	0.93[AFR][1000 genomes];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9947150	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9950965	0.90[EUR][1000 genomes]
rs9953127	1.00[CEU][hapmap];0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9960751	1.00[CEU][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9962307	1.00[CEU][hapmap];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1056007	chr18:29711974-29899564	Enhancers Weak transcription Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
2	nsv833616	chr18:29792336-29964212	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
3	nsv528846	chr18:29832147-29890042	Strong transcription Enhancers Weak transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA target site	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:59 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:29835200-29861600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr18:29837400-29867200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr18:29839800-29871800	Weak transcription	HSMMtube	muscle
4	chr18:29843000-29867000	Weak transcription	Brain Angular Gyrus	brain
5	chr18:29846000-29867000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr18:29848200-29863600	Weak transcription	Muscle Satellite Cultured Cells	--
7	chr18:29848600-29867200	Weak transcription	Lung	lung
8	chr18:29848800-29866600	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr18:29849400-29867000	Weak transcription	Esophagus	oesophagus
10	chr18:29849800-29867000	Weak transcription	Skeletal Muscle Female	skeletal muscle
11	chr18:29850000-29877600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr18:29850200-29866600	Weak transcription	Fetal Lung	lung
13	chr18:29850200-29867000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr18:29850200-29867000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr18:29850400-29865800	Weak transcription	Fetal Muscle Trunk	muscle
16	chr18:29850400-29866600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
17	chr18:29850400-29867200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr18:29852200-29865000	Weak transcription	Fetal Stomach	stomach
19	chr18:29855000-29861000	Enhancers	Fetal Intestine Small	intestine
20	chr18:29855200-29860800	Enhancers	Fetal Intestine Large	intestine
21	chr18:29857000-29863200	Weak transcription	Right Atrium	heart
22	chr18:29857400-29861000	Enhancers	Duodenum Mucosa	Duodenum
23	chr18:29857400-29862400	Weak transcription	Right Ventricle	heart
24	chr18:29857800-29861000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr18:29857800-29863400	Weak transcription	Brain Hippocampus Middle	brain
26	chr18:29858200-29865000	Weak transcription	Sigmoid Colon	Sigmoid Colon
27	chr18:29858600-29862400	Weak transcription	Fetal Heart	heart
28	chr18:29858600-29877600	Weak transcription	Fetal Kidney	kidney
29	chr18:29859000-29860800	Weak transcription	Brain Cingulate Gyrus	brain
30	chr18:29859000-29864000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr18:29859000-29865200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
32	chr18:29859000-29866600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
33	chr18:29859000-29867600	Weak transcription	Colonic Mucosa	Colon
34	chr18:29859000-29870400	Weak transcription	HepG2	liver
35	chr18:29859400-29867200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr18:29860000-29861200	Enhancers	Ovary	ovary
37	chr18:29860000-29861400	Enhancers	Liver	Liver
38	chr18:29860200-29861000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr18:29860200-29861000	Enhancers	Left Ventricle	heart
40	chr18:29860200-29861000	Enhancers	Rectal Smooth Muscle	rectum
41	chr18:29860200-29861200	Enhancers	Aorta	Aorta
42	chr18:29860200-29861400	Enhancers	Pancreas	Pancrea
43	chr18:29860200-29861600	Enhancers	Colon Smooth Muscle	Colon
44	chr18:29860200-29861600	Enhancers	Stomach Mucosa	stomach
45	chr18:29860200-29861600	Enhancers	Stomach Smooth Muscle	stomach
46	chr18:29860400-29860800	Weak transcription	Brain Inferior Temporal Lobe	brain
47	chr18:29860400-29861000	Enhancers	Small Intestine	intestine
48	chr18:29860400-29861200	Enhancers	Skeletal Muscle Male	skeletal muscle
49	chr18:29860400-29861400	Enhancers	Psoas Muscle	Psoas
50	chr18:29860600-29861000	Enhancers	Adipose Nuclei	Adipose

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