Variant report

Variant	rs6925165
Chromosome Location	chr6:53713174-53713175
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:53668450..53670040-chr6:53712921..53715850,2	MCF-7	breast:

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10498795	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1543356	0.88[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes]
rs16884427	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs17748452	0.87[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2223617	0.89[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2473599	0.82[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs2473603	0.86[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2494087	0.84[AMR][1000 genomes]
rs2494090	0.82[AMR][1000 genomes]
rs2820217	0.88[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2820218	0.89[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs3000998	0.85[CHB][hapmap]
rs4077760	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.86[EUR][1000 genomes]
rs4131378	0.83[EUR][1000 genomes]
rs4272222	0.88[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4276504	1.00[CHB][hapmap];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs4357137	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4380749	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4397225	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4476827	0.88[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4580851	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6905927	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[YRI][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6908101	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6919924	0.86[EUR][1000 genomes]
rs761135	0.82[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes]
rs7752696	0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9464005	0.80[AMR][1000 genomes]
rs9474672	0.88[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.87[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	nsv1034955	chr6:53447607-53931055	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	nsv1021506	chr6:53600338-53770482	Flanking Active TSS Weak transcription Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
3	nsv830664	chr6:53698021-53825270	Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:46 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:53680400-53721600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr6:53693400-53720000	Weak transcription	Left Ventricle	heart
3	chr6:53695000-53719800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr6:53695000-53743200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr6:53697200-53718600	Weak transcription	Duodenum Mucosa	Duodenum
6	chr6:53698000-53715600	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr6:53703000-53718600	Weak transcription	Pancreas	Pancrea
8	chr6:53703200-53720000	Weak transcription	HSMMtube	muscle
9	chr6:53703200-53720200	Weak transcription	Aorta	Aorta
10	chr6:53703200-53726400	Weak transcription	Fetal Stomach	stomach
11	chr6:53703800-53717200	Weak transcription	Primary hematopoietic stem cells	blood
12	chr6:53703800-53727600	Weak transcription	Stomach Smooth Muscle	stomach
13	chr6:53705400-53718800	Weak transcription	NHEK	skin
14	chr6:53706000-53720200	Weak transcription	Esophagus	oesophagus
15	chr6:53706000-53722400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr6:53706200-53722000	Weak transcription	H1 Cell Line	embryonic stem cell
17	chr6:53706400-53714400	Weak transcription	Fetal Muscle Trunk	muscle
18	chr6:53706400-53720200	Weak transcription	Fetal Muscle Leg	muscle
19	chr6:53707600-53718800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr6:53707800-53718800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr6:53709400-53718600	Weak transcription	Gastric	stomach
22	chr6:53709600-53719800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr6:53709800-53719800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr6:53709800-53762200	Weak transcription	Primary B cells from cord blood	blood
25	chr6:53710200-53713200	Enhancers	Brain Cingulate Gyrus	brain
26	chr6:53710400-53720400	Weak transcription	Rectal Mucosa Donor 29	rectum
27	chr6:53711000-53715600	Weak transcription	Fetal Intestine Small	intestine
28	chr6:53711200-53718800	Weak transcription	Fetal Intestine Large	intestine
29	chr6:53711200-53719800	Weak transcription	Rectal Smooth Muscle	rectum
30	chr6:53711200-53720400	Weak transcription	Cortex derived primary cultured neurospheres	brain
31	chr6:53711400-53719600	Weak transcription	Thymus	Thymus
32	chr6:53711800-53713400	Enhancers	HepG2	liver
33	chr6:53712200-53713200	Enhancers	Brain Hippocampus Middle	brain
34	chr6:53712400-53713200	Enhancers	Small Intestine	intestine
35	chr6:53712600-53720400	Weak transcription	Sigmoid Colon	Sigmoid Colon
36	chr6:53712800-53715600	Weak transcription	Brain Angular Gyrus	brain
37	chr6:53712800-53719600	Weak transcription	Colon Smooth Muscle	Colon
38	chr6:53712800-53720000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr6:53712800-53721600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr6:53713000-53717200	Weak transcription	Brain Substantia Nigra	brain
41	chr6:53713000-53719000	Weak transcription	Primary T cells from cord blood	blood
42	chr6:53713000-53719800	Weak transcription	Brain Inferior Temporal Lobe	brain
43	chr6:53713000-53719800	Weak transcription	Fetal Thymus	thymus
44	chr6:53713000-53720000	Weak transcription	Brain Anterior Caudate	brain
45	chr6:53713000-53720200	Weak transcription	Dnd41	blood
46	chr6:53713000-53722000	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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