Variant report

Variant	rs16987446
Chromosome Location	chr22:32532668-32532669
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	22:32529813-32538538..22:32740683-32750950	H1-hESC	embryonic stem cell:	embryo
2	22:32529813-32538538..22:32868055-32872511	K562	blood:
3	22:32529813-32538538..22:32878464-32886640	K562	blood:
4	22:32529813-32538538..22:32860159-32865649	GM12878	blood:
5	22:31836635-31847259..22:32529813-32538538	K562	blood:
6	22:32529813-32538538..22:32750950-32761732	K562	blood:
7	22:32012966-32043914..22:32529813-32538538	K562	blood:
8	22:32529813-32538538..22:32764253-32784733	H1-hESC	embryonic stem cell:	embryo

Variant related genes	Relation type
ENSG00000271093	Chromatin interaction
ENSG00000184708	Chromatin interaction
ENSG00000241878	Chromatin interaction
ENSG00000230736	Chromatin interaction
ENSG00000100225	Chromatin interaction
ENSG00000128276	Chromatin interaction
ENSG00000243519	Chromatin interaction
ENSG00000232218	Chromatin interaction
ENSG00000184459	Chromatin interaction
ENSG00000205853	Chromatin interaction
ENSG00000241954	Chromatin interaction

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:5)

rs_ID	r²[population]
rs16989711	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs28433835	0.81[EUR][1000 genomes]
rs33943816	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs56350448	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs8140700	1.00[CEU][hapmap];0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	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
2	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
3	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
4	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
5	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
6	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
7	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
8	nsv962788	chr22:32528613-32537754	Active TSS Flanking Active TSS Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr22:32515800-32533600	Weak transcription	Right Atrium	heart
2	chr22:32529200-32533000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
3	chr22:32529200-32533600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr22:32529400-32533000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
5	chr22:32529600-32533000	Weak transcription	Primary T cells fromperipheralblood	blood
6	chr22:32529600-32533000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
7	chr22:32529600-32533600	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
8	chr22:32531400-32532800	Enhancers	HMEC	breast
9	chr22:32531800-32532800	Enhancers	HUVEC	blood vessel
10	chr22:32531800-32533000	Enhancers	Left Ventricle	heart
11	chr22:32532200-32533000	Weak transcription	Spleen	Spleen
12	chr22:32532200-32534000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr22:32532400-32532800	Weak transcription	Dnd41	blood
14	chr22:32532400-32533600	Weak transcription	Muscle Satellite Cultured Cells	--
15	chr22:32532400-32533600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr22:32532400-32533600	Weak transcription	Rectal Mucosa Donor 29	rectum
17	chr22:32532600-32533000	Enhancers	K562	blood
18	chr22:32532600-32533600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr22:32532600-32533600	Weak transcription	NHEK	skin
20	chr22:32532600-32533800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr22:32532600-32533800	Weak transcription	Stomach Mucosa	stomach

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