Variant report

Variant	rs73228762
Chromosome Location	chr3:142325220-142325221
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:142322302..142325692-chr3:142327995..142330616,3	K562	blood:
2	chr3:142319541..142323718-chr3:142324179..142327610,6	MCF-7	breast:

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs11711434	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13316756	0.82[ASN][1000 genomes]
rs1403726	0.81[EUR][1000 genomes]
rs17623058	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2140433	0.82[ASN][1000 genomes]
rs2140434	0.82[ASN][1000 genomes]
rs2140436	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes]
rs2177397	0.82[ASN][1000 genomes]
rs28365824	0.86[ASN][1000 genomes]
rs28378300	0.80[ASN][1000 genomes]
rs28647471	0.84[ASN][1000 genomes]
rs28709617	0.84[ASN][1000 genomes]
rs4398471	0.84[ASN][1000 genomes]
rs4582093	0.82[ASN][1000 genomes]
rs55655603	0.86[AFR][1000 genomes]
rs55994893	0.83[ASN][1000 genomes]
rs56161530	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs56246347	0.86[AFR][1000 genomes]
rs56328361	1.00[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs56383228	0.84[ASN][1000 genomes]
rs56397702	1.00[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs58910647	0.82[ASN][1000 genomes]
rs60001529	0.81[ASN][1000 genomes]
rs6440095	0.85[ASN][1000 genomes]
rs6440096	0.84[ASN][1000 genomes]
rs6440097	0.84[ASN][1000 genomes]
rs73228752	0.82[EUR][1000 genomes]
rs73228757	0.89[ASN][1000 genomes]
rs73228758	0.89[ASN][1000 genomes]
rs73228759	0.90[EUR][1000 genomes]
rs73228782	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs73228788	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs73230583	0.86[AFR][1000 genomes]
rs73230587	0.86[AFR][1000 genomes]
rs73230588	0.86[AFR][1000 genomes]
rs73240323	0.81[ASN][1000 genomes]
rs7633021	0.84[ASN][1000 genomes]
rs7638338	0.84[ASN][1000 genomes]
rs7647212	0.85[ASN][1000 genomes]
rs7647497	0.85[ASN][1000 genomes]
rs9683274	0.98[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9816128	0.84[ASN][1000 genomes]
rs9816275	0.84[ASN][1000 genomes]
rs9826463	0.84[ASN][1000 genomes]
rs9847445	0.82[ASN][1000 genomes]
rs9857567	0.82[ASN][1000 genomes]
rs9862686	0.82[ASN][1000 genomes]
rs9868309	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv877556	chr3:141898980-142331360	Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
2	nsv877558	chr3:142123841-142331360	Weak transcription Strong transcription Flanking Active TSS Enhancers ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
3	nsv877559	chr3:142132749-142331360	Active TSS Enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
4	nsv877560	chr3:142132749-142362179	Strong transcription ZNF genes & repeats Weak transcription Active TSS Enhancers Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
5	nsv877561	chr3:142152925-142331360	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
6	nsv932989	chr3:142204208-142423305	Weak transcription Strong transcription Active TSS Flanking Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	33 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:142316200-142331000	Weak transcription	Small Intestine	intestine
2	chr3:142317000-142327600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr3:142317200-142337600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr3:142317400-142327400	Weak transcription	K562	blood
5	chr3:142317400-142337800	Weak transcription	HepG2	liver
6	chr3:142319400-142330000	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr3:142321800-142333200	Weak transcription	Colonic Mucosa	Colon
8	chr3:142323400-142327000	Weak transcription	Duodenum Mucosa	Duodenum
9	chr3:142323800-142325800	Enhancers	Rectal Mucosa Donor 29	rectum
10	chr3:142324200-142327400	Weak transcription	Stomach Mucosa	stomach
11	chr3:142324400-142326000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr3:142325000-142325600	Enhancers	Rectal Mucosa Donor 31	rectum
13	chr3:142325200-142327200	Weak transcription	Fetal Intestine Small	intestine

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