Variant report

Variant	rs4714009
Chromosome Location	chr6:36726223-36726224
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:36725564..36727264-chr6:36727766..36730682,2	K562	blood:
2	chr6:36561839..36564756-chr6:36723772..36727529,4	MCF-7	breast:
3	chr6:36692374..36694188-chr6:36726056..36729043,2	MCF-7	breast:
4	chr6:36645102..36656546-chr6:36717974..36730993,29	MCF-7	breast:
5	chr6:36644838..36653438-chr6:36718524..36730954,23	MCF-7	breast:
6	chr6:36590960..36591893-chr6:36725819..36727563,13	K562	blood:
7	chr6:36656125..36657871-chr6:36725735..36728109,2	MCF-7	breast:
8	chr6:36724390..36726745-chr6:36953555..36956553,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000124762	Chromatin interaction
ENSG00000137409	Chromatin interaction
ENSG00000112081	Chromatin interaction

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs10807175	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10947628	0.88[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];0.91[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12198675	0.95[JPT][hapmap];0.91[ASN][1000 genomes]
rs13193217	0.89[CEU][hapmap];0.91[EUR][1000 genomes]
rs13203743	0.96[CEU][hapmap];1.00[CHB][hapmap];0.96[JPT][hapmap];0.93[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs236426	0.88[ASN][1000 genomes]
rs236445	0.96[CEU][hapmap];1.00[CHB][hapmap];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4557518	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs763047	0.86[YRI][hapmap]
rs763048	0.96[YRI][hapmap]
rs916295	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs916297	0.86[CHB][hapmap];0.95[JPT][hapmap];0.88[ASN][1000 genomes]
rs916304	0.82[CHB][hapmap];0.95[JPT][hapmap];0.86[ASN][1000 genomes]
rs9380596	0.90[YRI][hapmap];0.80[AFR][1000 genomes]
rs9380598	0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1023171	chr6:36686935-36880899	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
2	nsv538202	chr6:36686935-36880899	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases
3	nsv1033261	chr6:36687424-36837315	Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
4	nsv524053	chr6:36695223-36747406	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	11 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:69 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:36709200-36727000	Strong transcription	Cortex derived primary cultured neurospheres	brain
2	chr6:36718600-36726600	Weak transcription	Brain Cingulate Gyrus	brain
3	chr6:36718800-36726800	Weak transcription	Brain Hippocampus Middle	brain
4	chr6:36718800-36727400	Enhancers	Primary monocytes fromperipheralblood	blood
5	chr6:36718800-36727400	Enhancers	Primary T cells fromperipheralblood	blood
6	chr6:36719600-36727000	Enhancers	Sigmoid Colon	Sigmoid Colon
7	chr6:36720200-36726400	Weak transcription	Pancreas	Pancrea
8	chr6:36720600-36726400	Weak transcription	HMEC	breast
9	chr6:36721200-36726600	Weak transcription	Brain Anterior Caudate	brain
10	chr6:36721200-36726600	Weak transcription	Fetal Heart	heart
11	chr6:36721200-36726600	Weak transcription	HSMMtube	muscle
12	chr6:36721400-36726400	Weak transcription	Fetal Intestine Large	intestine
13	chr6:36721400-36726600	Weak transcription	Fetal Intestine Small	intestine
14	chr6:36721400-36728600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr6:36721800-36726600	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr6:36721800-36726600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr6:36721800-36733200	Weak transcription	Duodenum Smooth Muscle	Duodenum
18	chr6:36722800-36727600	Enhancers	Stomach Mucosa	stomach
19	chr6:36722800-36748200	Weak transcription	Fetal Kidney	kidney
20	chr6:36723600-36726600	Enhancers	Placenta	Placenta
21	chr6:36723800-36726600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
22	chr6:36723800-36726800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr6:36723800-36727400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
24	chr6:36723800-36736200	Weak transcription	Right Atrium	heart
25	chr6:36724000-36726600	Weak transcription	Muscle Satellite Cultured Cells	--
26	chr6:36724000-36728200	Weak transcription	Fetal Stomach	stomach
27	chr6:36724000-36736200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr6:36724200-36727200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr6:36724400-36726600	Weak transcription	A549	lung
30	chr6:36724400-36726800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
31	chr6:36724800-36726400	Weak transcription	Esophagus	oesophagus
32	chr6:36724800-36726400	Weak transcription	Skeletal Muscle Female	skeletal muscle
33	chr6:36724800-36726600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr6:36724800-36727000	Enhancers	Monocytes-CD14+_RO01746	blood
35	chr6:36724800-36734400	Weak transcription	Right Ventricle	heart
36	chr6:36725000-36726600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr6:36725000-36726600	Weak transcription	Rectal Smooth Muscle	rectum
38	chr6:36725000-36727400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
39	chr6:36725200-36726400	Enhancers	Rectal Mucosa Donor 31	rectum
40	chr6:36725200-36726600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr6:36725200-36726600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr6:36725200-36726600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
43	chr6:36725200-36726800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
44	chr6:36725200-36727600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
45	chr6:36725400-36726400	Enhancers	Duodenum Mucosa	Duodenum
46	chr6:36725400-36726600	Enhancers	Rectal Mucosa Donor 29	rectum
47	chr6:36725400-36726600	Weak transcription	Skeletal Muscle Male	skeletal muscle
48	chr6:36725400-36726600	Weak transcription	NHEK	skin
49	chr6:36725400-36726800	Weak transcription	Hela-S3	cervix
50	chr6:36725400-36727600	Enhancers	Primary B cells from peripheral blood	blood

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