Variant report

Variant	rs35973114
Chromosome Location	chr6:76318102-76318103
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:76316605..76319587-chr6:76326249..76328171,2	MCF-7	breast:
2	chr6:76316110..76319023-chr6:76339771..76341687,2	K562	blood:
3	chr6:76316195..76318634-chr6:76459170..76461001,2	K562	blood:
4	chr6:76316156..76318537-chr6:76328526..76330839,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000112701	Chromatin interaction

Extended variants
information (count: 72 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:54)

rs_ID	r²[population]
rs10806047	0.88[ASN][1000 genomes]
rs10943277	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10943278	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10943279	0.81[AFR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10943287	0.88[ASN][1000 genomes]
rs12192223	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12196105	0.88[ASN][1000 genomes]
rs12199494	0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12201305	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12203148	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12205818	0.81[AFR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12208368	0.81[AFR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12209039	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12212123	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12212171	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12213476	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12214738	0.93[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12215914	0.87[AFR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13196164	0.88[ASN][1000 genomes]
rs13205073	0.88[ASN][1000 genomes]
rs17792773	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28480026	0.92[ASN][1000 genomes]
rs33997653	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34636573	0.81[AFR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3798455	0.88[ASN][1000 genomes]
rs57268793	0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58570618	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66632417	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs67016585	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71561434	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs71561437	0.81[AFR][1000 genomes];0.96[ASN][1000 genomes]
rs71561438	0.92[ASN][1000 genomes]
rs72886845	1.00[ASN][1000 genomes]
rs9341531	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9341534	0.88[ASN][1000 genomes]
rs9341535	0.84[ASN][1000 genomes]
rs9343315	0.81[AFR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9343320	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9350596	0.87[AFR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9352224	0.88[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9352228	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9352229	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9352231	0.87[AFR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9352232	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9352241	0.88[ASN][1000 genomes]
rs9359133	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9359135	0.87[AFR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9360924	0.93[AFR][1000 genomes];0.93[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs9360926	1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9360930	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9360932	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9360939	0.81[ASN][1000 genomes]
rs9360942	0.88[ASN][1000 genomes]
rs9447540	0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:18 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1027915	chr6:75893542-76510113	Active TSS Enhancers Strong transcription Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
2	nsv538311	chr6:75893542-76510113	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
3	nsv1022428	chr6:76023118-76575620	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	48 gene(s)	inside rSNPs	diseases
4	nsv538312	chr6:76023118-76575620	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	48 gene(s)	inside rSNPs	diseases
5	nsv1032245	chr6:76045537-76545703	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	47 gene(s)	inside rSNPs	diseases
6	nsv538313	chr6:76045537-76545703	Strong transcription Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	47 gene(s)	inside rSNPs	diseases
7	nsv1019328	chr6:76154751-76604197	Enhancers Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
8	nsv538314	chr6:76154751-76604197	Enhancers Strong transcription Active TSS Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
9	nsv1023331	chr6:76238459-76482117	Strong transcription ZNF genes & repeats Active TSS Weak transcription Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
10	nsv538315	chr6:76238459-76482117	Enhancers Strong transcription Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
11	nsv1017542	chr6:76238459-76537447	Strong transcription Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
12	nsv1031745	chr6:76257913-76493355	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
13	nsv538316	chr6:76257913-76493355	Strong transcription Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
14	nsv533100	chr6:76257914-76493354	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
15	nsv1023749	chr6:76287578-76482117	Weak transcription Flanking Active TSS Genic enhancers Strong transcription Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
16	nsv538317	chr6:76287578-76482117	Strong transcription Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	38 gene(s)	inside rSNPs	diseases
17	nsv1021090	chr6:76306100-76759397	Weak transcription Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers 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	40 gene(s)	inside rSNPs	diseases
18	nsv538318	chr6:76306100-76759397	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	40 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:116 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:76313600-76320200	Weak transcription	Stomach Mucosa	stomach
2	chr6:76313800-76318800	Enhancers	Primary neutrophils fromperipheralblood	blood
3	chr6:76313800-76320200	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr6:76313800-76320200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
5	chr6:76313800-76322200	Enhancers	Primary T helper naive cells from peripheral blood	blood
6	chr6:76313800-76322200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
7	chr6:76313800-76325400	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr6:76313800-76331600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr6:76314000-76320200	Weak transcription	Aorta	Aorta
10	chr6:76314000-76321800	Weak transcription	Fetal Intestine Large	intestine
11	chr6:76314000-76323400	Enhancers	Primary T cells from cord blood	blood
12	chr6:76314000-76324600	Weak transcription	Fetal Stomach	stomach
13	chr6:76314000-76325600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
14	chr6:76314000-76325800	Enhancers	Primary T killer memory cells from peripheral blood	blood
15	chr6:76314000-76326000	Enhancers	Primary T helper cells fromperipheralblood	blood
16	chr6:76314000-76343200	Weak transcription	Fetal Kidney	kidney
17	chr6:76314200-76318200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr6:76314200-76318200	Weak transcription	Brain Cingulate Gyrus	brain
19	chr6:76314200-76318200	Weak transcription	Fetal Lung	lung
20	chr6:76314200-76318600	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr6:76314200-76318600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr6:76314200-76318800	Weak transcription	HUES6 Cell Line	embryonic stem cell
23	chr6:76314200-76318800	Weak transcription	Osteobl	bone
24	chr6:76314200-76319000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr6:76314200-76319000	Weak transcription	NHLF	lung
26	chr6:76314200-76319800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr6:76314200-76320800	Weak transcription	HSMM	muscle
28	chr6:76314200-76321000	Weak transcription	Thymus	Thymus
29	chr6:76314200-76321800	Weak transcription	Fetal Thymus	thymus
30	chr6:76314200-76322000	Weak transcription	Placenta	Placenta
31	chr6:76314200-76322200	Weak transcription	Fetal Muscle Leg	muscle
32	chr6:76314200-76324800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr6:76314200-76325200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
34	chr6:76314200-76325200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr6:76314200-76329000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr6:76314400-76318400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
37	chr6:76314400-76318800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr6:76314400-76318800	Weak transcription	NHEK	skin
39	chr6:76314400-76319000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr6:76314400-76319200	Weak transcription	Muscle Satellite Cultured Cells	--
41	chr6:76314400-76319200	Weak transcription	HMEC	breast
42	chr6:76314400-76319400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr6:76314400-76320000	Weak transcription	Stomach Smooth Muscle	stomach
44	chr6:76314400-76320000	Weak transcription	Hela-S3	cervix
45	chr6:76314400-76321800	Weak transcription	Left Ventricle	heart
46	chr6:76314400-76323600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr6:76314400-76324600	Weak transcription	Esophagus	oesophagus
48	chr6:76314400-76327600	Weak transcription	Cortex derived primary cultured neurospheres	brain
49	chr6:76314400-76334800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr6:76314400-76336800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links