Variant report

Variant	rs1336655
Chromosome Location	chr6:69724069-69724070
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:52)

rs_ID	r²[population]
rs1007921	0.81[AFR][1000 genomes];0.83[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12194774	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12194946	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12213405	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs13191563	0.85[ASN][1000 genomes]
rs13192798	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13197569	0.85[ASN][1000 genomes]
rs13205016	0.85[ASN][1000 genomes]
rs13205140	0.85[ASN][1000 genomes]
rs13219339	0.85[ASN][1000 genomes]
rs1336635	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1336636	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1336651	0.85[AFR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1415029	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1415036	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1556756	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1889877	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1889878	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2210867	0.85[AFR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2225803	1.00[ASN][1000 genomes]
rs2343396	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35797298	0.90[ASN][1000 genomes]
rs3734465	0.81[ASN][1000 genomes]
rs3757046	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3757047	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3798996	0.85[ASN][1000 genomes]
rs3799002	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs3799007	1.00[ASN][1000 genomes]
rs3799016	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3799017	0.98[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3799021	0.90[ASN][1000 genomes]
rs3799023	0.81[ASN][1000 genomes]
rs3823066	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3823067	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs602406	0.85[ASN][1000 genomes]
rs62416781	0.85[ASN][1000 genomes]
rs62416803	0.81[ASN][1000 genomes]
rs6903686	0.85[ASN][1000 genomes]
rs6904267	0.81[AFR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6908180	0.85[ASN][1000 genomes]
rs6934473	0.85[ASN][1000 genomes]
rs7741493	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7743332	0.85[AFR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7756040	0.85[AFR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7756637	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7760307	0.80[AFR][1000 genomes];0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7761270	0.85[ASN][1000 genomes]
rs7764479	0.81[AFR][1000 genomes];0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7767118	0.82[AFR][1000 genomes];0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9446085	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9454674	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs947221	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv886137	chr6:69684850-70095690	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:69685800-69758800	Weak transcription	Fetal Brain Male	brain
2	chr6:69701000-69737600	Weak transcription	Brain Hippocampus Middle	brain
3	chr6:69701200-69724400	Weak transcription	Brain Germinal Matrix	brain
4	chr6:69702400-69728600	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr6:69702400-69737600	Weak transcription	Brain Angular Gyrus	brain
6	chr6:69718600-69726200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr6:69719400-69725800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr6:69720400-69758600	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr6:69721400-69728600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr6:69721400-69728800	Weak transcription	Left Ventricle	heart
11	chr6:69721600-69752200	Weak transcription	Fetal Lung	lung
12	chr6:69722400-69725800	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr6:69723000-69725400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr6:69723000-69725600	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr6:69723000-69725600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
16	chr6:69723000-69726000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr6:69723400-69742600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr6:69724000-69725000	Enhancers	HUVEC	blood vessel
19	chr6:69724000-69725200	Enhancers	Fetal Adrenal Gland	Adrenal Gland

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