Variant report

Variant	rs28513111
Chromosome Location	chr9:18331122-18331123
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs10113897	0.82[ASN][1000 genomes]
rs10115400	0.91[ASN][1000 genomes]
rs10115405	0.91[ASN][1000 genomes]
rs10117176	0.84[ASN][1000 genomes]
rs10119710	0.92[ASN][1000 genomes]
rs10124318	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10125689	0.98[ASN][1000 genomes]
rs10217257	0.88[ASN][1000 genomes]
rs10738507	0.84[ASN][1000 genomes]
rs10810954	0.92[ASN][1000 genomes]
rs10810955	0.87[ASN][1000 genomes]
rs10810956	0.82[ASN][1000 genomes]
rs10963573	0.84[ASN][1000 genomes]
rs10963577	0.92[ASN][1000 genomes]
rs12339435	0.85[ASN][1000 genomes]
rs12349149	0.94[ASN][1000 genomes]
rs12555902	0.89[ASN][1000 genomes]
rs1329724	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1340047	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs16936603	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2226017	0.91[EUR][1000 genomes]
rs35016784	0.84[ASN][1000 genomes]
rs3924761	1.00[ASN][1000 genomes]
rs4268217	0.96[ASN][1000 genomes]
rs4382567	0.99[ASN][1000 genomes]
rs4395986	0.90[ASN][1000 genomes]
rs4436218	0.91[ASN][1000 genomes]
rs4524897	0.90[ASN][1000 genomes]
rs4526458	0.89[ASN][1000 genomes]
rs4554575	0.89[ASN][1000 genomes]
rs4582650	0.92[ASN][1000 genomes]
rs4606157	0.89[ASN][1000 genomes]
rs4961461	0.90[ASN][1000 genomes]
rs4961633	0.88[ASN][1000 genomes]
rs4961634	0.90[ASN][1000 genomes]
rs4961635	0.85[ASN][1000 genomes]
rs4961639	0.91[EUR][1000 genomes]
rs4961640	0.91[EUR][1000 genomes]
rs4961641	0.91[EUR][1000 genomes]
rs7023268	0.91[EUR][1000 genomes]
rs7023546	0.84[ASN][1000 genomes]
rs7038607	0.99[ASN][1000 genomes]
rs7855772	0.83[ASN][1000 genomes]
rs7856108	0.90[ASN][1000 genomes]
rs9298791	0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831522	chr9:18231982-18459492	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv491807	chr9:18243672-19009770	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
3	esv2764161	chr9:18247433-18443060	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv892684	chr9:18261485-18401585	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv525659	chr9:18288212-19009041	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
6	nsv1019127	chr9:18288271-18996288	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
7	nsv430001	chr9:18301116-18346392	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
8	nsv892687	chr9:18303691-18430297	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	nsv525743	chr9:18312578-18359014	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:18323600-18332000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr9:18325600-18334200	Weak transcription	Fetal Heart	heart
3	chr9:18326000-18333200	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr9:18327600-18331800	Weak transcription	Osteobl	bone
5	chr9:18327800-18331400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr9:18327800-18333400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr9:18327800-18333800	Weak transcription	NHDF-Ad	bronchial
8	chr9:18330200-18331400	Enhancers	HUVEC	blood vessel
9	chr9:18330200-18332600	Enhancers	Colon Smooth Muscle	Colon
10	chr9:18330200-18332600	Enhancers	Fetal Lung	lung
11	chr9:18330400-18331600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr9:18330400-18332000	Enhancers	Duodenum Smooth Muscle	Duodenum
13	chr9:18330400-18332600	Enhancers	Sigmoid Colon	Sigmoid Colon
14	chr9:18330600-18331400	Weak transcription	Stomach Smooth Muscle	stomach
15	chr9:18330600-18331600	Enhancers	HMEC	breast
16	chr9:18330600-18332400	Enhancers	Fetal Kidney	kidney
17	chr9:18330800-18331600	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr9:18330800-18331800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr9:18330800-18331800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr9:18330800-18332200	Enhancers	Breast Myoepithelial Primary Cells	Breast
21	chr9:18331000-18331200	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr9:18331000-18331200	Enhancers	Fetal Stomach	stomach
23	chr9:18331000-18331400	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr9:18331000-18331400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
25	chr9:18331000-18331400	Enhancers	Right Atrium	heart
26	chr9:18331000-18331600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr9:18331000-18331600	Enhancers	Rectal Mucosa Donor 31	rectum
28	chr9:18331000-18332600	Enhancers	Ovary	ovary
29	chr9:18331000-18333000	Enhancers	Hela-S3	cervix
30	chr9:18331000-18334400	Enhancers	HUES64 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links