Variant report

Variant	rs7772436
Chromosome Location	chr6:33991368-33991369
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:33985452..33987578-chr6:33989477..33993498,4	MCF-7	breast:
2	chr6:33990582..33994151-chr6:33994836..33998218,3	MCF-7	breast:
3	chr6:33985161..33986783-chr6:33990060..33992314,2	K562	blood:
4	chr6:33955318..33960116-chr6:33987348..33992002,6	MCF-7	breast:
5	chr6:33989625..33994952-chr6:33996605..33998585,4	K562	blood:
6	chr6:33991283..33992902-chr6:33994714..33996515,3	K562	blood:
7	chr6:33984912..33989076-chr6:33989536..33992823,4	K562	blood:

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs2229901	0.87[YRI][hapmap];0.81[AFR][1000 genomes]
rs2306926	0.83[ASN][1000 genomes]
rs3778043	0.83[ASN][1000 genomes]
rs3778044	0.83[ASN][1000 genomes]
rs60279188	0.83[AMR][1000 genomes]
rs61423062	1.00[ASN][1000 genomes]
rs61457033	1.00[ASN][1000 genomes]
rs6457754	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6457756	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6901878	0.83[ASN][1000 genomes]
rs6902110	0.83[AMR][1000 genomes]
rs6934879	0.87[AMR][1000 genomes]
rs7745888	0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7762948	1.00[ASN][1000 genomes]
rs7772932	0.87[YRI][hapmap]
rs9296110	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9461941	1.00[ASN][1000 genomes]
rs9461942	1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs9461943	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9461945	0.96[ASN][1000 genomes]
rs9469671	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9469672	0.93[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9469673	0.96[ASN][1000 genomes]
rs9469675	1.00[ASN][1000 genomes]
rs9469677	1.00[ASN][1000 genomes]
rs9469678	1.00[ASN][1000 genomes]
rs9469679	0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9469681	1.00[ASN][1000 genomes]
rs9469682	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916210	chr6:33804111-34144062	Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	32 gene(s)	inside rSNPs	diseases
2	nsv462900	chr6:33932442-34195011	Bivalent/Poised TSS Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
3	nsv602843	chr6:33932442-34195011	Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Enhancers Genic enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases
4	nsv885777	chr6:33942228-33997375	Enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
5	nsv885778	chr6:33942228-34007054	Bivalent Enhancer Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
6	nsv462901	chr6:33953646-34050917	ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
7	nsv602861	chr6:33953646-34050917	Weak transcription Bivalent Enhancer Enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:33984000-33993600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr6:33984000-34010200	Weak transcription	Brain Anterior Caudate	brain
3	chr6:33984400-34023000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr6:33985200-34002200	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr6:33985800-34000400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr6:33986200-34009600	Weak transcription	Right Atrium	heart
7	chr6:33987600-33992000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr6:33988000-34013600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr6:33988600-33991600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr6:33990400-33992000	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr6:33990600-33991400	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr6:33990600-33992800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr6:33990600-33993200	Weak transcription	Fetal Brain Male	brain
14	chr6:33991000-33993400	Weak transcription	Fetal Brain Female	brain
15	chr6:33991000-34003400	Weak transcription	H9 Cell Line	embryonic stem cell

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