Variant report

Variant	rs4714136
Chromosome Location	chr6:38228126-38228127
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:23)

rs_ID	r²[population]
rs1475761	1.00[CEU][hapmap];0.95[JPT][hapmap];0.93[YRI][hapmap];0.87[AFR][1000 genomes];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1931767	1.00[CEU][hapmap];0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs228181	0.95[CEU][hapmap]
rs228182	0.91[CEU][hapmap]
rs228184	0.87[CEU][hapmap]
rs228185	0.91[CEU][hapmap]
rs228187	0.91[CEU][hapmap]
rs4711527	0.92[YRI][hapmap];0.84[AFR][1000 genomes]
rs4711529	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4714140	0.95[CEU][hapmap];0.83[EUR][1000 genomes]
rs4714144	0.95[CEU][hapmap]
rs6905637	0.95[CEU][hapmap]
rs6922620	0.91[CEU][hapmap]
rs9349067	0.81[EUR][1000 genomes]
rs9380737	0.83[CEU][hapmap]
rs9462424	0.84[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9462425	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9470833	0.92[YRI][hapmap];0.84[AFR][1000 genomes]
rs9470847	1.00[CEU][hapmap];0.83[CHB][hapmap];0.91[JPT][hapmap];1.00[YRI][hapmap];0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9470848	1.00[CEU][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];0.87[AFR][1000 genomes];0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9470849	0.84[YRI][hapmap];0.84[AFR][1000 genomes];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9470851	1.00[CEU][hapmap];0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9470856	0.95[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1028825	chr6:37495154-38278320	Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
2	nsv1021991	chr6:37893949-38738720	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
3	nsv885817	chr6:38036420-39019503	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
4	nsv534620	chr6:38049585-38602064	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
5	nsv885818	chr6:38147745-38436317	Enhancers Weak transcription Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv885820	chr6:38166511-38468887	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:81 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:38181400-38229400	Weak transcription	Fetal Intestine Small	intestine
2	chr6:38194400-38230200	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr6:38204800-38229400	Weak transcription	Rectal Smooth Muscle	rectum
4	chr6:38205200-38228800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
5	chr6:38207800-38229400	Weak transcription	Brain Hippocampus Middle	brain
6	chr6:38208200-38236600	Weak transcription	Gastric	stomach
7	chr6:38208200-38255000	Weak transcription	Ovary	ovary
8	chr6:38209000-38229000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
9	chr6:38213400-38228800	Weak transcription	Cortex derived primary cultured neurospheres	brain
10	chr6:38213400-38232400	Weak transcription	Right Ventricle	heart
11	chr6:38215200-38229400	Weak transcription	Brain Angular Gyrus	brain
12	chr6:38215600-38229000	Weak transcription	Brain Substantia Nigra	brain
13	chr6:38216000-38229000	Weak transcription	Brain Cingulate Gyrus	brain
14	chr6:38216000-38238000	Weak transcription	Fetal Muscle Trunk	muscle
15	chr6:38218000-38229600	Weak transcription	Stomach Smooth Muscle	stomach
16	chr6:38218000-38229800	Weak transcription	Spleen	Spleen
17	chr6:38218800-38232200	Weak transcription	Small Intestine	intestine
18	chr6:38219400-38229600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr6:38220000-38238200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr6:38220200-38229400	Weak transcription	Colon Smooth Muscle	Colon
21	chr6:38220400-38229400	Weak transcription	Brain Anterior Caudate	brain
22	chr6:38220600-38228800	Weak transcription	HSMMtube	muscle
23	chr6:38220600-38241600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
24	chr6:38222000-38229600	Weak transcription	Aorta	Aorta
25	chr6:38222000-38234600	Weak transcription	Esophagus	oesophagus
26	chr6:38222600-38229400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
27	chr6:38222600-38229400	Weak transcription	Fetal Muscle Leg	muscle
28	chr6:38222600-38232400	Weak transcription	Lung	lung
29	chr6:38223000-38230000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr6:38223000-38231600	Weak transcription	Fetal Intestine Large	intestine
31	chr6:38223400-38229400	Weak transcription	Brain Inferior Temporal Lobe	brain
32	chr6:38223600-38229400	Weak transcription	Skeletal Muscle Female	skeletal muscle
33	chr6:38223600-38229800	Weak transcription	Rectal Mucosa Donor 31	rectum
34	chr6:38223600-38256000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
35	chr6:38223800-38229600	Weak transcription	Duodenum Smooth Muscle	Duodenum
36	chr6:38223800-38229600	Weak transcription	Skeletal Muscle Male	skeletal muscle
37	chr6:38223800-38229800	Weak transcription	Fetal Lung	lung
38	chr6:38223800-38230000	Weak transcription	Primary hematopoietic stem cells	blood
39	chr6:38224000-38228800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr6:38224200-38230000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr6:38224400-38228800	Weak transcription	Left Ventricle	heart
42	chr6:38224400-38229200	Weak transcription	Adipose Nuclei	Adipose
43	chr6:38224400-38239000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
44	chr6:38224400-38267600	Weak transcription	Primary T cells from cord blood	blood
45	chr6:38224600-38230200	Weak transcription	Rectal Mucosa Donor 29	rectum
46	chr6:38224600-38231800	Weak transcription	Duodenum Mucosa	Duodenum
47	chr6:38224600-38255200	Weak transcription	Primary B cells from cord blood	blood
48	chr6:38224800-38229400	Weak transcription	Fetal Stomach	stomach
49	chr6:38224800-38256400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
50	chr6:38225000-38255800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood

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