Variant report

Variant	rs7607170
Chromosome Location	chr2:100903008-100903009
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:100901888..100904596-chr2:100917454..100919195,2	MCF-7	breast:
2	chr2:100893699..100897169-chr2:100899587..100903259,4	MCF-7	breast:
3	chr2:100885071..100887270-chr2:100902977..100904501,2	MCF-7	breast:
4	chr2:100901321..100904489-chr2:100937079..100940896,4	K562	blood:
5	chr2:100898902..100903882-chr2:100937164..100940384,5	K562	blood:
6	chr2:100900693..100917248-chr2:100932005..100942326,51	MCF-7	breast:

Variant related genes	Relation type
ENSG00000170500	Chromatin interaction

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs10865038	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10865039	0.89[CEU][hapmap];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11123825	0.80[EUR][1000 genomes]
rs12464505	1.00[JPT][hapmap]
rs12467008	1.00[JPT][hapmap]
rs13008568	0.86[YRI][hapmap];0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13024601	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13031270	0.86[YRI][hapmap];0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13031493	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13031712	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13033057	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2033748	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2033749	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2309815	1.00[JPT][hapmap]
rs2309817	0.96[CEU][hapmap];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2309818	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2309819	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2309820	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2309821	1.00[CEU][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2309822	0.96[CEU][hapmap];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2309823	0.92[CEU][hapmap];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2309824	0.96[CEU][hapmap];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2309825	1.00[CEU][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2309826	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2871341	1.00[JPT][hapmap]
rs4851281	1.00[JPT][hapmap]
rs4851282	1.00[JPT][hapmap]
rs4851284	0.81[EUR][1000 genomes]
rs4851285	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4851286	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4851287	0.89[CEU][hapmap];1.00[CHB][hapmap];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs6542923	0.85[CEU][hapmap];1.00[JPT][hapmap]
rs6542924	0.82[CEU][hapmap]
rs6754867	0.81[CEU][hapmap];1.00[JPT][hapmap]
rs6755791	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.94[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7421891	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7557575	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7557660	0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7557977	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7559464	0.96[CEU][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7562372	0.96[CEU][hapmap];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7582180	0.89[CEU][hapmap];1.00[CHB][hapmap];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7588623	0.89[CEU][hapmap];0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7601442	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7601873	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap]
rs7606277	0.84[EUR][1000 genomes]
rs7607676	0.93[AFR][1000 genomes];0.99[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7609376	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][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	nsv1007777	chr2:100816913-101308914	Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
2	nsv535844	chr2:100816913-101308914	Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
3	nsv834311	chr2:100816917-100990036	Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:66 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:100891800-100907600	Weak transcription	Rectal Smooth Muscle	rectum
2	chr2:100892000-100904000	Weak transcription	Gastric	stomach
3	chr2:100892200-100909800	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr2:100896600-100907000	Weak transcription	Spleen	Spleen
5	chr2:100896600-100907600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr2:100897600-100903600	Enhancers	Dnd41	blood
7	chr2:100898400-100906800	Weak transcription	Placenta	Placenta
8	chr2:100898400-100908200	Weak transcription	Fetal Lung	lung
9	chr2:100898400-100915600	Weak transcription	Right Atrium	heart
10	chr2:100898800-100915000	Weak transcription	Adipose Nuclei	Adipose
11	chr2:100899000-100907400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr2:100899400-100903200	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr2:100900000-100903600	Strong transcription	Skeletal Muscle Female	skeletal muscle
14	chr2:100900000-100904200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr2:100900000-100905600	Strong transcription	Aorta	Aorta
16	chr2:100900200-100903200	Enhancers	NH-A	brain
17	chr2:100900200-100903600	Genic enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr2:100900200-100903600	Strong transcription	Left Ventricle	heart
19	chr2:100900200-100905200	Strong transcription	Brain Germinal Matrix	brain
20	chr2:100900200-100919000	Strong transcription	Fetal Brain Female	brain
21	chr2:100900600-100904200	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr2:100900800-100906800	Weak transcription	Fetal Thymus	thymus
23	chr2:100900800-100907000	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr2:100900800-100907800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr2:100900800-100926600	Weak transcription	Right Ventricle	heart
26	chr2:100901000-100904800	Weak transcription	Brain Cingulate Gyrus	brain
27	chr2:100901000-100937000	Weak transcription	Fetal Brain Male	brain
28	chr2:100901200-100903200	Weak transcription	Brain Hippocampus Middle	brain
29	chr2:100901600-100903200	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr2:100901600-100903400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr2:100901600-100903600	Enhancers	Hela-S3	cervix
32	chr2:100901600-100904200	Enhancers	Pancreas	Pancrea
33	chr2:100901600-100904200	Genic enhancers	K562	blood
34	chr2:100901600-100907200	Strong transcription	Brain Inferior Temporal Lobe	brain
35	chr2:100901800-100903200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
36	chr2:100901800-100903400	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr2:100901800-100903400	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr2:100901800-100903600	Enhancers	Fetal Kidney	kidney
39	chr2:100901800-100903600	Enhancers	Stomach Mucosa	stomach
40	chr2:100902000-100903200	Enhancers	HUVEC	blood vessel
41	chr2:100902000-100903400	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr2:100902000-100903600	Enhancers	H1 Cell Line	embryonic stem cell
43	chr2:100902000-100903600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr2:100902000-100903600	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr2:100902000-100903600	Genic enhancers	Cortex derived primary cultured neurospheres	brain
46	chr2:100902000-100903600	Genic enhancers	Brain Angular Gyrus	brain
47	chr2:100902200-100903800	Enhancers	H9 Cell Line	embryonic stem cell
48	chr2:100902200-100907000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
49	chr2:100902400-100903200	Enhancers	Liver	Liver
50	chr2:100902400-100903400	Enhancers	Fetal Intestine Small	intestine

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links