Variant report

Variant	rs7869097
Chromosome Location	chr9:16719631-16719632
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 37 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10738452	1.00[CHB][hapmap];0.84[ASN][1000 genomes]
rs10756791	0.86[CHB][hapmap]
rs10810597	0.86[CHB][hapmap]
rs10962579	1.00[MEX][hapmap]
rs10962581	1.00[MEX][hapmap]
rs10962602	1.00[MEX][hapmap]
rs12002953	1.00[EUR][1000 genomes]
rs12004872	1.00[EUR][1000 genomes]
rs12236540	1.00[MEX][hapmap]
rs1330302	0.86[CHB][hapmap];0.87[YRI][hapmap]
rs1411429	0.86[CHB][hapmap];0.87[YRI][hapmap]
rs1411430	0.86[CHB][hapmap]
rs1537004	0.86[CHB][hapmap];0.87[YRI][hapmap]
rs1544103	1.00[CHB][hapmap];0.84[ASN][1000 genomes]
rs16934964	1.00[EUR][1000 genomes]
rs1888205	0.86[CHB][hapmap]
rs2150090	0.86[CHB][hapmap]
rs2183408	0.86[CHB][hapmap];0.87[YRI][hapmap]
rs2210104	1.00[CHB][hapmap];0.84[ASN][1000 genomes]
rs2275255	0.86[CHB][hapmap];1.00[EUR][1000 genomes]
rs3850446	0.86[CHB][hapmap];0.87[YRI][hapmap]
rs3850447	0.86[CHB][hapmap];0.87[YRI][hapmap]
rs3904154	0.86[CHB][hapmap];0.87[YRI][hapmap]
rs4626704	0.82[CHB][hapmap]
rs7029771	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7031782	1.00[MEX][hapmap]
rs7035869	1.00[EUR][1000 genomes]
rs7855308	0.82[AFR][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	nsv530933	chr9:16251206-16830845	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv530934	chr9:16281246-16779432	Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv1032856	chr9:16465330-16773471	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
4	nsv540073	chr9:16465330-16773471	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	nsv1024799	chr9:16631890-17431827	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
6	esv2758627	chr9:16641966-16809203	Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
7	esv2759673	chr9:16641966-16809203	Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Strong transcription Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
8	nsv892649	chr9:16677221-16761597	Enhancers Flanking Active TSS Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
9	nsv892650	chr9:16696187-16950860	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:44 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:16709000-16726000	Weak transcription	Duodenum Smooth Muscle	Duodenum
2	chr9:16709600-16725800	Weak transcription	Fetal Stomach	stomach
3	chr9:16711400-16726600	Weak transcription	Psoas Muscle	Psoas
4	chr9:16711800-16720800	Weak transcription	HSMM	muscle
5	chr9:16713200-16725800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr9:16713200-16726600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr9:16714200-16721000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr9:16714200-16722000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr9:16714200-16722000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
10	chr9:16714400-16722200	Enhancers	NHDF-Ad	bronchial
11	chr9:16715400-16720400	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr9:16715800-16720600	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr9:16715800-16720600	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr9:16716600-16720400	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr9:16716600-16721800	Weak transcription	NHLF	lung
16	chr9:16717000-16720400	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr9:16717000-16720600	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr9:16717400-16720200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr9:16717600-16721800	Enhancers	Colon Smooth Muscle	Colon
20	chr9:16718000-16720800	Enhancers	Muscle Satellite Cultured Cells	--
21	chr9:16718000-16721000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr9:16718000-16721400	Enhancers	Ovary	ovary
23	chr9:16718000-16722200	Enhancers	Fetal Lung	lung
24	chr9:16718000-16722400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr9:16718200-16720400	Genic enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr9:16718400-16720000	Enhancers	A549	lung
27	chr9:16718400-16721400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr9:16718600-16720400	Enhancers	H1 Cell Line	embryonic stem cell
29	chr9:16718600-16721200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr9:16718600-16722000	Enhancers	Rectal Smooth Muscle	rectum
31	chr9:16718800-16719800	Enhancers	Adipose Nuclei	Adipose
32	chr9:16718800-16720000	Enhancers	HUVEC	blood vessel
33	chr9:16719000-16720000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
34	chr9:16719000-16720200	Enhancers	Osteobl	bone
35	chr9:16719000-16722400	Enhancers	NH-A	brain
36	chr9:16719200-16722000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
37	chr9:16719200-16725400	Weak transcription	Stomach Smooth Muscle	stomach
38	chr9:16719200-16726000	Weak transcription	H9 Cell Line	embryonic stem cell
39	chr9:16719400-16721000	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr9:16719400-16721400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr9:16719400-16721400	Enhancers	Hela-S3	cervix
42	chr9:16719400-16721800	Weak transcription	Right Atrium	heart
43	chr9:16719600-16720200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chr9:16719600-16721600	Weak transcription	HSMMtube	muscle

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