Variant report

Variant	rs736218
Chromosome Location	chr18:29899067-29899068
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr18:29891994..29893877-chr18:29897571..29900006,2	MCF-7	breast:
2	chr18:29895037..29897248-chr18:29897872..29900366,2	K562	blood:

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs10502592	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs11665147	0.82[CEU][hapmap]
rs11665150	0.82[CEU][hapmap]
rs11665190	0.82[CEU][hapmap]
rs11876773	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs16963285	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs16963289	0.82[CEU][hapmap]
rs1824304	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2034968	0.81[CEU][hapmap]
rs41527551	0.81[CEU][hapmap]
rs616601	0.88[CHB][hapmap]
rs618004	0.88[CHB][hapmap]
rs625361	0.88[CHB][hapmap]
rs638142	0.88[CHB][hapmap]
rs656946	0.88[CHB][hapmap]
rs657479	0.88[CHB][hapmap]
rs668857	0.88[CHB][hapmap]
rs681347	0.88[CHB][hapmap];0.81[YRI][hapmap]
rs7230250	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs8097263	0.81[CEU][hapmap]
rs968099	0.90[CEU][hapmap]

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	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

No data

Chromatin state (count:53 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:29868200-29923800	Weak transcription	Gastric	stomach
2	chr18:29889400-29904200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr18:29890200-29902200	Weak transcription	Spleen	Spleen
4	chr18:29890400-29904000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr18:29891000-29905800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr18:29891000-29914000	Weak transcription	Fetal Brain Female	brain
7	chr18:29891200-29905600	Weak transcription	Rectal Smooth Muscle	rectum
8	chr18:29893400-29903200	Weak transcription	Pancreas	Pancrea
9	chr18:29896000-29899200	Enhancers	Brain Substantia Nigra	brain
10	chr18:29896400-29899200	Enhancers	Fetal Muscle Leg	muscle
11	chr18:29896600-29900000	Enhancers	Adipose Nuclei	Adipose
12	chr18:29896800-29899800	Enhancers	HepG2	liver
13	chr18:29897200-29899600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr18:29897200-29903200	Weak transcription	Psoas Muscle	Psoas
15	chr18:29897200-29903400	Weak transcription	Right Ventricle	heart
16	chr18:29897200-29918800	Weak transcription	Fetal Intestine Large	intestine
17	chr18:29897200-29926400	Weak transcription	Fetal Stomach	stomach
18	chr18:29897400-29899600	Enhancers	Brain Hippocampus Middle	brain
19	chr18:29897400-29909000	Weak transcription	Left Ventricle	heart
20	chr18:29897400-29923800	Weak transcription	Esophagus	oesophagus
21	chr18:29897400-29923800	Weak transcription	Skeletal Muscle Female	skeletal muscle
22	chr18:29897800-29901800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
23	chr18:29898000-29899200	Enhancers	HSMM	muscle
24	chr18:29898000-29899800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr18:29898000-29906000	Weak transcription	Duodenum Smooth Muscle	Duodenum
26	chr18:29898000-29906400	Weak transcription	Small Intestine	intestine
27	chr18:29898000-29906600	Weak transcription	Brain Angular Gyrus	brain
28	chr18:29898000-29918600	Weak transcription	Fetal Intestine Small	intestine
29	chr18:29898200-29899200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
30	chr18:29898200-29899400	Enhancers	Brain Inferior Temporal Lobe	brain
31	chr18:29898200-29901400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr18:29898200-29902000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr18:29898200-29915400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr18:29898400-29899200	Enhancers	Muscle Satellite Cultured Cells	--
35	chr18:29898400-29899200	Enhancers	Stomach Mucosa	stomach
36	chr18:29898400-29900000	Enhancers	Fetal Heart	heart
37	chr18:29898400-29903800	Weak transcription	Fetal Kidney	kidney
38	chr18:29898400-29904000	Weak transcription	Brain Anterior Caudate	brain
39	chr18:29898600-29899600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr18:29898600-29904000	Weak transcription	Brain Cingulate Gyrus	brain
41	chr18:29898800-29899400	Weak transcription	Pancreatic Islets	Pancreatic Islet
42	chr18:29898800-29900000	Enhancers	Liver	Liver
43	chr18:29898800-29901800	Weak transcription	Ovary	ovary
44	chr18:29898800-29903400	Weak transcription	Fetal Muscle Trunk	muscle
45	chr18:29898800-29904000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
46	chr18:29898800-29904000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr18:29898800-29904000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr18:29898800-29904000	Weak transcription	Fetal Lung	lung
49	chr18:29898800-29904000	Weak transcription	Osteobl	bone
50	chr18:29899000-29899600	Enhancers	Sigmoid Colon	Sigmoid Colon

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