Variant report

Variant	rs7745460
Chromosome Location	chr6:119396199-119396200
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:119253156..119256806-chr6:119394976..119399977,7	K562	blood:

Variant related genes	Relation type
ENSG00000253194	Chromatin interaction
ENSG00000111877	Chromatin interaction

Extended variants
information (count: 58 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs10456919	0.87[ASN][1000 genomes]
rs12189950	1.00[CHB][hapmap];0.89[JPT][hapmap];0.98[ASN][1000 genomes]
rs12190491	0.94[ASN][1000 genomes]
rs12190974	0.84[ASN][1000 genomes]
rs12191819	0.93[CHB][hapmap];0.87[CHD][hapmap]
rs12193093	0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12195153	0.83[ASN][1000 genomes]
rs12195334	0.87[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.85[MEX][hapmap];0.90[MKK][hapmap];1.00[TSI][hapmap];0.97[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12195400	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12197931	0.93[CHB][hapmap];0.82[CHD][hapmap]
rs12204929	1.00[CHB][hapmap];0.89[JPT][hapmap];0.98[ASN][1000 genomes]
rs12206826	0.93[CHB][hapmap];0.82[CHD][hapmap]
rs12214184	0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12214265	0.97[ASN][1000 genomes]
rs1342793	0.84[ASN][1000 genomes]
rs1407205	0.93[CHB][hapmap]
rs1418712	0.84[ASN][1000 genomes]
rs1591368	0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1591369	0.92[ASN][1000 genomes]
rs1775619	0.86[CHB][hapmap];0.88[CHD][hapmap];0.81[ASN][1000 genomes]
rs2357022	0.83[ASN][1000 genomes]
rs2357161	0.80[ASN][1000 genomes]
rs2782574	0.83[ASN][1000 genomes]
rs2797355	0.83[ASN][1000 genomes]
rs284914	0.93[CHB][hapmap];0.82[CHD][hapmap]
rs3798595	0.93[CHB][hapmap];0.82[CHD][hapmap]
rs4946384	1.00[CHB][hapmap]
rs4946391	0.89[GIH][hapmap];0.88[TSI][hapmap]
rs55810806	0.87[ASN][1000 genomes]
rs55919736	0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs56347939	0.97[AMR][1000 genomes];0.91[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs603770	0.84[ASN][1000 genomes]
rs706978	0.86[CHB][hapmap];0.88[CHD][hapmap];0.83[JPT][hapmap];0.84[ASN][1000 genomes]
rs706979	0.87[ASN][1000 genomes]
rs72953079	0.98[ASN][1000 genomes]
rs72953080	0.95[ASN][1000 genomes]
rs768996	0.92[CHB][hapmap]
rs7768348	0.83[ASN][1000 genomes]
rs794250	0.84[ASN][1000 genomes]
rs794252	0.84[ASN][1000 genomes]
rs794253	0.82[ASN][1000 genomes]
rs794254	0.84[ASN][1000 genomes]
rs794255	0.84[ASN][1000 genomes]
rs794259	0.83[ASN][1000 genomes]
rs794607	0.93[CHB][hapmap];0.87[CHD][hapmap]
rs797002	0.84[ASN][1000 genomes]
rs797017	0.92[CHB][hapmap]
rs811201	0.92[CHB][hapmap]
rs811584	0.87[ASN][1000 genomes]
rs9481870	0.93[CHB][hapmap]
rs9481871	0.92[CHB][hapmap]
rs9489535	0.93[CHB][hapmap]
rs9489536	0.93[CHB][hapmap];0.82[CHD][hapmap]
rs9489537	0.93[CHB][hapmap];0.82[CHD][hapmap]
rs9489543	0.92[CHB][hapmap]
rs9489544	0.93[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1030400	chr6:119320153-119433830	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region miRNA	30 gene(s)	inside rSNPs	diseases
2	nsv528632	chr6:119380885-119397860	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA	27 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:119385000-119397200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr6:119393200-119397400	Weak transcription	HepG2	liver
3	chr6:119393600-119398200	Weak transcription	Fetal Intestine Large	intestine
4	chr6:119393600-119398400	Weak transcription	Fetal Intestine Small	intestine
5	chr6:119394400-119396800	Enhancers	Primary T helper cells PMA-I stimulated	--
6	chr6:119394400-119397400	Enhancers	Primary T helper naive cells from peripheral blood	blood
7	chr6:119394600-119397000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
8	chr6:119394600-119397200	Enhancers	Breast Myoepithelial Primary Cells	Breast
9	chr6:119394800-119396200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr6:119395000-119397200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
11	chr6:119395000-119399000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr6:119395400-119396400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
13	chr6:119395400-119396600	Weak transcription	K562	blood
14	chr6:119395800-119396200	Enhancers	Fetal Brain Female	brain
15	chr6:119395800-119397200	Enhancers	Primary T killer memory cells from peripheral blood	blood
16	chr6:119396000-119396200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
17	chr6:119396000-119396200	Enhancers	Primary T helper cells fromperipheralblood	blood
18	chr6:119396000-119397200	Weak transcription	Brain Inferior Temporal Lobe	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links