Variant report

Variant	rs474159
Chromosome Location	chr6:13383133-13383134
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:13382356..13383974-chr6:13614219..13616340,2	MCF-7	breast:
2	chr6:13379880..13381834-chr6:13381972..13383883,2	MCF-7	breast:
3	chr6:13355357..13357068-chr6:13380690..13383506,2	MCF-7	breast:
4	chr6:13381851..13383974-chr6:13486160..13487948,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000145990	Chromatin interaction
ENSG00000237786	Chromatin interaction
ENSG00000187461	Chromatin interaction
ENSG00000261071	Chromatin interaction
ENSG00000225921	Chromatin interaction

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:38)

rs_ID	r²[population]
rs10807431	0.93[AFR][1000 genomes];0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs10807432	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10948650	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12153966	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2439536	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2496139	0.83[EUR][1000 genomes]
rs2496160	0.81[EUR][1000 genomes]
rs2496161	0.81[EUR][1000 genomes]
rs2496173	0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs28813108	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs4711978	0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs476904	0.88[EUR][1000 genomes]
rs489396	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs491278	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs492433	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs501987	0.85[EUR][1000 genomes]
rs510932	0.86[EUR][1000 genomes]
rs516003	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs517803	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs524118	0.83[EUR][1000 genomes]
rs531256	0.85[EUR][1000 genomes]
rs548119	0.85[AFR][1000 genomes];0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs552655	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs553671	0.89[AFR][1000 genomes];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs553948	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs560396	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs564174	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs570315	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs573109	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs575709	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs579028	0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs61492644	0.83[AMR][1000 genomes]
rs7760579	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7770078	0.87[AMR][1000 genomes];0.83[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs821276	0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs821277	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9357708	0.85[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9367440	0.89[EUR][1000 genomes];0.84[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	nsv532021	chr6:13232627-13805381	Active TSS Genic enhancers Strong transcription Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	74 gene(s)	inside rSNPs	diseases
2	nsv1028533	chr6:13239059-13484814	Enhancers Strong transcription Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
3	nsv538136	chr6:13239059-13484814	Strong transcription Weak transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
4	nsv1034016	chr6:13248122-13418225	Enhancers Flanking Active TSS Strong transcription Weak transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:56 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:13355600-13383400	Weak transcription	A549	lung
2	chr6:13365800-13385400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr6:13366000-13386800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr6:13368000-13404600	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr6:13368400-13386600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr6:13376000-13383400	Weak transcription	Psoas Muscle	Psoas
7	chr6:13376800-13386600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr6:13376800-13395200	Weak transcription	NHEK	skin
9	chr6:13377800-13383400	Weak transcription	Skeletal Muscle Male	skeletal muscle
10	chr6:13377800-13395600	Weak transcription	Aorta	Aorta
11	chr6:13378600-13383200	Weak transcription	Primary monocytes fromperipheralblood	blood
12	chr6:13378600-13383600	Enhancers	GM12878-XiMat	blood
13	chr6:13379200-13386600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr6:13379400-13383600	Weak transcription	Spleen	Spleen
15	chr6:13379800-13383200	Weak transcription	Primary neutrophils fromperipheralblood	blood
16	chr6:13380200-13383600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr6:13380200-13389400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr6:13380400-13383400	Weak transcription	Pancreatic Islets	Pancreatic Islet
19	chr6:13381000-13383400	Weak transcription	Fetal Lung	lung
20	chr6:13381000-13385800	Enhancers	Primary B cells from peripheral blood	blood
21	chr6:13381200-13383400	Weak transcription	Gastric	stomach
22	chr6:13381200-13383600	Weak transcription	Brain Inferior Temporal Lobe	brain
23	chr6:13381200-13383600	Weak transcription	Fetal Kidney	kidney
24	chr6:13381200-13384000	Weak transcription	Right Ventricle	heart
25	chr6:13381400-13383200	Weak transcription	Duodenum Mucosa	Duodenum
26	chr6:13381400-13383600	Weak transcription	Brain Angular Gyrus	brain
27	chr6:13381400-13383600	Weak transcription	HepG2	liver
28	chr6:13381600-13383400	Weak transcription	Colon Smooth Muscle	Colon
29	chr6:13381800-13383400	Weak transcription	Brain Anterior Caudate	brain
30	chr6:13381800-13383400	Weak transcription	Brain Substantia Nigra	brain
31	chr6:13381800-13383400	Weak transcription	Stomach Smooth Muscle	stomach
32	chr6:13381800-13383600	Weak transcription	Rectal Mucosa Donor 29	rectum
33	chr6:13381800-13383800	Weak transcription	Primary T helper cells fromperipheralblood	blood
34	chr6:13381800-13384600	Enhancers	Primary B cells from cord blood	blood
35	chr6:13381800-13395400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
36	chr6:13382000-13383800	Weak transcription	Colonic Mucosa	Colon
37	chr6:13382000-13383800	Weak transcription	Skeletal Muscle Female	skeletal muscle
38	chr6:13382000-13385200	Weak transcription	K562	blood
39	chr6:13382000-13386600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr6:13382200-13383400	Weak transcription	Fetal Heart	heart
41	chr6:13382200-13383600	Weak transcription	Small Intestine	intestine
42	chr6:13382200-13384200	Weak transcription	Left Ventricle	heart
43	chr6:13382200-13384800	Weak transcription	Right Atrium	heart
44	chr6:13382400-13383400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr6:13382400-13383400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
46	chr6:13382400-13383400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr6:13382400-13383400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr6:13382400-13383400	Weak transcription	Adipose Nuclei	Adipose
49	chr6:13382400-13383400	Weak transcription	Rectal Mucosa Donor 31	rectum
50	chr6:13382400-13383400	Weak transcription	Stomach Mucosa	stomach

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links