Variant report

Variant	rs73881606
Chromosome Location	chr22:32495970-32495971
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	22:32012966-32043914..22:32494662-32499630	K562	blood:
2	22:32494662-32499630..22:32860159-32865649	K562	blood:
3	22:32494662-32499630..22:32764253-32784733	K562	blood:

Variant related genes	Relation type
ENSG00000205853	Chromatin interaction
ENSG00000230736	Chromatin interaction
ENSG00000232218	Chromatin interaction
ENSG00000241878	Chromatin interaction
ENSG00000241954	Chromatin interaction
ENSG00000243519	Chromatin interaction
ENSG00000184459	Chromatin interaction

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs33968460	1.00[AMR][1000 genomes]
rs55788758	1.00[AMR][1000 genomes]
rs56131484	1.00[AMR][1000 genomes]
rs57518663	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60666969	1.00[AMR][1000 genomes]
rs60686589	1.00[AMR][1000 genomes]
rs61029609	1.00[AMR][1000 genomes]
rs61186856	1.00[AMR][1000 genomes]
rs61699774	1.00[AMR][1000 genomes]
rs73881605	1.00[AMR][1000 genomes]
rs73881608	1.00[AMR][1000 genomes]
rs73881612	0.86[AFR][1000 genomes]
rs73881613	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73884237	1.00[AMR][1000 genomes]
rs73884242	1.00[AMR][1000 genomes]
rs73884243	1.00[AMR][1000 genomes]
rs73884247	1.00[AMR][1000 genomes]
rs73884248	1.00[AMR][1000 genomes]
rs73884251	1.00[AMR][1000 genomes]
rs73884253	1.00[AMR][1000 genomes]
rs73884254	1.00[AMR][1000 genomes]
rs73884263	1.00[AMR][1000 genomes]
rs73884268	1.00[AMR][1000 genomes]
rs73884269	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1060529	chr22:32370432-32525699	Flanking Active TSS Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
2	nsv834177	chr22:32416679-32594663	Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	37 gene(s)	inside rSNPs	diseases
3	esv1803811	chr22:32441022-32509431	Enhancers Flanking Active TSS Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
4	nsv948789	chr22:32462505-32764760	Enhancers Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
5	nsv1065175	chr22:32467617-32761093	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
6	nsv544680	chr22:32467617-32761093	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
7	esv2830423	chr22:32477718-32767825	Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases
8	esv2422247	chr22:32486448-32788258	Strong transcription Flanking Active TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
9	nsv834178	chr22:32490449-32677521	Bivalent/Poised TSS Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
10	nsv3596	chr22:32491329-32507091	Weak transcription Strong transcription Enhancers Genic enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:32476600-32499400	Weak transcription	Pancreas	Pancrea
2	chr22:32485600-32498400	Weak transcription	Small Intestine	intestine
3	chr22:32486400-32508400	Weak transcription	Rectal Mucosa Donor 29	rectum
4	chr22:32490200-32504000	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr22:32491200-32511400	Strong transcription	Duodenum Mucosa	Duodenum
6	chr22:32493200-32515400	Weak transcription	Right Ventricle	heart
7	chr22:32494800-32498800	Strong transcription	Fetal Intestine Small	intestine
8	chr22:32495000-32498400	Strong transcription	Left Ventricle	heart
9	chr22:32495200-32496200	Strong transcription	Fetal Heart	heart
10	chr22:32495200-32498200	Strong transcription	Fetal Intestine Large	intestine
11	chr22:32495600-32496200	Strong transcription	Rectal Mucosa Donor 31	rectum
12	chr22:32495800-32496000	Enhancers	Stomach Mucosa	stomach

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links