Variant report

Variant	rs6969521
Chromosome Location	chr7:108042910-108042911
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:108037200..108040749-chr7:108041126..108043530,3	MCF-7	breast:
2	chr7:108042175..108044661-chr7:108050644..108052443,2	K562	blood:
3	chr7:108040975..108043949-chr7:108092664..108095074,2	MCF-7	breast:

Extended variants
information (count: 68 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:65)

rs_ID	r²[population]
rs10245718	0.87[CEU][hapmap];0.82[AMR][1000 genomes]
rs11971972	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11973105	0.84[EUR][1000 genomes]
rs11973823	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11976021	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11979596	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11983900	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12669879	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12705470	0.84[EUR][1000 genomes]
rs13222628	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs13227836	0.86[CHB][hapmap];1.00[JPT][hapmap];0.80[YRI][hapmap];0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13228190	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs13238841	0.85[EUR][1000 genomes]
rs13245101	0.84[EUR][1000 genomes]
rs13245242	0.83[CEU][hapmap];0.84[EUR][1000 genomes]
rs17155637	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17338441	0.84[EUR][1000 genomes]
rs17338462	0.84[EUR][1000 genomes]
rs17421351	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17423043	0.84[EUR][1000 genomes]
rs17423119	0.84[EUR][1000 genomes]
rs2108252	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2108253	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2214913	0.84[EUR][1000 genomes]
rs2300036	1.00[CEU][hapmap];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2300040	0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2300048	1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[YRI][hapmap];0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2300052	0.84[EUR][1000 genomes]
rs2395995	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34218460	0.83[EUR][1000 genomes]
rs35429156	0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35436957	0.85[EUR][1000 genomes]
rs35617326	0.84[EUR][1000 genomes]
rs56145857	0.84[EUR][1000 genomes]
rs59458537	0.85[EUR][1000 genomes]
rs60398019	0.83[EUR][1000 genomes]
rs6466224	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6466225	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6466226	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6466233	0.80[CEU][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes]
rs66461825	0.84[EUR][1000 genomes]
rs67027479	0.84[EUR][1000 genomes]
rs6949637	0.84[EUR][1000 genomes]
rs6954366	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6959023	0.83[EUR][1000 genomes]
rs6959409	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6960478	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6966107	0.95[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6976309	0.84[EUR][1000 genomes]
rs6976649	0.83[EUR][1000 genomes]
rs6976659	0.84[EUR][1000 genomes]
rs6976752	0.84[EUR][1000 genomes]
rs6976776	0.84[EUR][1000 genomes]
rs6976804	0.84[EUR][1000 genomes]
rs6978552	0.80[CEU][hapmap];0.85[EUR][1000 genomes]
rs71213282	0.84[EUR][1000 genomes]
rs7784170	0.80[CEU][hapmap];0.85[EUR][1000 genomes]
rs7786947	0.80[CEU][hapmap];0.84[EUR][1000 genomes]
rs7790875	0.85[EUR][1000 genomes]
rs7792321	0.86[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs7797885	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7806869	0.80[CEU][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7807737	0.84[EUR][1000 genomes]
rs7807941	0.84[EUR][1000 genomes]
rs9649307	0.84[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	esv3348839	chr7:107377311-108286538	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
2	nsv888942	chr7:107893695-108055858	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
3	nsv888943	chr7:107893695-108058574	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs6969521	THAP5	cis	normal skin	skin_eQTL
rs6969521	THAP5	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:108014800-108043200	Weak transcription	Brain Cingulate Gyrus	brain
2	chr7:108021400-108043000	Weak transcription	HMEC	breast
3	chr7:108024000-108045600	Weak transcription	Brain Anterior Caudate	brain
4	chr7:108027800-108043000	Weak transcription	HUVEC	blood vessel
5	chr7:108034800-108043000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chr7:108035000-108046600	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr7:108036400-108049200	Weak transcription	Spleen	Spleen
8	chr7:108036600-108043000	Weak transcription	Fetal Intestine Large	intestine
9	chr7:108036600-108044600	Weak transcription	Brain Substantia Nigra	brain
10	chr7:108036600-108045600	Weak transcription	Brain Inferior Temporal Lobe	brain
11	chr7:108036600-108046600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr7:108036600-108048000	Weak transcription	Brain Angular Gyrus	brain
13	chr7:108036600-108048000	Weak transcription	Pancreas	Pancrea
14	chr7:108036600-108054200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr7:108036800-108046600	Weak transcription	Brain Hippocampus Middle	brain
16	chr7:108037000-108044000	Weak transcription	Fetal Brain Male	brain
17	chr7:108037000-108046800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr7:108039000-108043000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
19	chr7:108039200-108045000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
20	chr7:108040000-108048000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
21	chr7:108040200-108048800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr7:108040600-108046400	Weak transcription	Fetal Muscle Leg	muscle
23	chr7:108041000-108043000	Weak transcription	A549	lung
24	chr7:108041000-108043200	Weak transcription	Pancreatic Islets	Pancreatic Islet
25	chr7:108041800-108044400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr7:108042000-108043400	Weak transcription	Fetal Lung	lung
27	chr7:108042600-108046600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr7:108042800-108044200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr7:108042800-108044800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links