Variant report

Variant	rs10992061
Chromosome Location	chr9:94483954-94483955
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10820899	0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10992057	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10992058	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10992059	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10992060	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10992063	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13292198	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs41308940	0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67857232	0.91[ASN][1000 genomes]
rs7467403	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1045332	chr9:94352661-94656016	Active TSS Bivalent Enhancer Enhancers Strong transcription Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
2	nsv1047426	chr9:94363211-94758114	Weak transcription Bivalent Enhancer Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
3	nsv531631	chr9:94373847-94633213	Weak transcription Enhancers Bivalent Enhancer Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:40 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:94458000-94489800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr9:94474200-94486000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr9:94476400-94485400	Weak transcription	Fetal Lung	lung
4	chr9:94477000-94487000	Weak transcription	Rectal Smooth Muscle	rectum
5	chr9:94477200-94484600	Weak transcription	Ovary	ovary
6	chr9:94477200-94489800	Weak transcription	Right Atrium	heart
7	chr9:94477200-94496800	Weak transcription	NHLF	lung
8	chr9:94477200-94533000	Weak transcription	Fetal Kidney	kidney
9	chr9:94478800-94484400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr9:94478800-94484600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr9:94479400-94484400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr9:94480600-94484400	Weak transcription	Gastric	stomach
13	chr9:94481200-94484400	Weak transcription	Fetal Intestine Small	intestine
14	chr9:94481800-94484000	Enhancers	Primary hematopoietic stem cells short term culture	blood
15	chr9:94482000-94484400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
16	chr9:94482000-94484400	Weak transcription	Fetal Intestine Large	intestine
17	chr9:94482400-94484000	Enhancers	Primary B cells from peripheral blood	blood
18	chr9:94482400-94484400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr9:94482400-94491600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr9:94482600-94484200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr9:94482800-94484400	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr9:94483000-94484600	Enhancers	Placenta	Placenta
23	chr9:94483000-94496600	Strong transcription	Fetal Stomach	stomach
24	chr9:94483200-94484000	Enhancers	GM12878-XiMat	blood
25	chr9:94483400-94484600	Enhancers	K562	blood
26	chr9:94483400-94486000	Weak transcription	HUES6 Cell Line	embryonic stem cell
27	chr9:94483400-94486800	Strong transcription	Colon Smooth Muscle	Colon
28	chr9:94483400-94489800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr9:94483400-94501600	Weak transcription	Rectal Mucosa Donor 29	rectum
30	chr9:94483600-94484400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr9:94483600-94484400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr9:94483600-94484800	Weak transcription	Placenta Amnion	Placenta Amnion
33	chr9:94483600-94487600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr9:94483600-94504000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr9:94483600-94519400	Weak transcription	HUES64 Cell Line	embryonic stem cell
36	chr9:94483800-94484000	Active TSS	Spleen	Spleen
37	chr9:94483800-94485400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr9:94483800-94485800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
39	chr9:94483800-94486200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
40	chr9:94483800-94489400	Strong transcription	Stomach Smooth Muscle	stomach

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