Variant report

Variant	rs71526391
Chromosome Location	chr7:22279657-22279658
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10499541	0.87[AFR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11761102	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11766435	1.00[ASN][1000 genomes]
rs11766861	0.87[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11773706	0.90[AFR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12534735	0.90[AFR][1000 genomes];0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12700363	1.00[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12700364	0.90[AFR][1000 genomes];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13222400	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13230638	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13237958	0.90[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1419764	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1419765	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17711941	0.97[AFR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17773555	0.87[AFR][1000 genomes];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34167821	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34401570	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35430878	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35979304	0.81[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs56073345	1.00[ASN][1000 genomes]
rs71526392	0.80[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71526393	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73683342	1.00[ASN][1000 genomes]
rs73683348	1.00[ASN][1000 genomes]
rs73683355	1.00[ASN][1000 genomes]
rs7803094	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:22243400-22307200	Weak transcription	Thymus	Thymus
2	chr7:22259800-22281600	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr7:22260800-22281400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr7:22262200-22329000	Weak transcription	Primary B cells from cord blood	blood
5	chr7:22263400-22281600	Weak transcription	Fetal Intestine Large	intestine
6	chr7:22264400-22291000	Weak transcription	Lung	lung
7	chr7:22267800-22280600	Weak transcription	Brain Hippocampus Middle	brain
8	chr7:22269400-22281800	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr7:22270200-22283800	Weak transcription	Duodenum Mucosa	Duodenum
10	chr7:22271800-22289400	Weak transcription	Brain Cingulate Gyrus	brain
11	chr7:22271800-22290000	Weak transcription	Brain Anterior Caudate	brain
12	chr7:22272000-22290000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr7:22274200-22285800	Weak transcription	Gastric	stomach
14	chr7:22274200-22289400	Weak transcription	Brain Angular Gyrus	brain
15	chr7:22274400-22282600	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr7:22274400-22288000	Weak transcription	Brain Substantia Nigra	brain
17	chr7:22274400-22291000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
18	chr7:22275000-22290800	Weak transcription	H1 Cell Line	embryonic stem cell
19	chr7:22275600-22286000	Strong transcription	Dnd41	blood
20	chr7:22276200-22285800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr7:22276600-22295600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr7:22276800-22281600	Weak transcription	Esophagus	oesophagus
23	chr7:22277400-22280400	Weak transcription	Rectal Mucosa Donor 31	rectum
24	chr7:22277800-22280400	Weak transcription	Fetal Thymus	thymus
25	chr7:22278200-22279800	Strong transcription	HepG2	liver
26	chr7:22278600-22325800	Weak transcription	Liver	Liver
27	chr7:22278800-22310800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr7:22279000-22281600	Weak transcription	Spleen	Spleen
29	chr7:22279000-22297000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr7:22279200-22281600	Weak transcription	Fetal Intestine Small	intestine
31	chr7:22279200-22281600	Weak transcription	Pancreas	Pancrea
32	chr7:22279200-22283600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links