Variant report

Variant	rs10967742
Chromosome Location	chr9:27157144-27157145
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:2)

rs_ID	r²[population]
rs10967740	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10967741	1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv892862	chr9:26956663-27190655	Enhancers ZNF genes & repeats Weak transcription Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
2	nsv1016733	chr9:27073650-27264576	Enhancers Weak transcription Genic enhancers Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1022313	chr9:27083369-27250505	Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1017802	chr9:27088160-27262682	Weak transcription Flanking Active TSS Enhancers Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv1019104	chr9:27088160-27358206	Enhancers Weak transcription Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
6	nsv892863	chr9:27138898-27170934	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
7	nsv6512	chr9:27155677-27200455	Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:27150800-27158000	Weak transcription	Spleen	Spleen
2	chr9:27151000-27158000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr9:27151000-27172800	Weak transcription	Left Ventricle	heart
4	chr9:27151000-27229200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr9:27151200-27164800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr9:27151800-27158000	Weak transcription	Lung	lung
7	chr9:27151800-27165000	Weak transcription	Stomach Smooth Muscle	stomach
8	chr9:27152000-27174600	Weak transcription	Fetal Muscle Leg	muscle
9	chr9:27152200-27165400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr9:27152400-27157800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr9:27152400-27181600	Weak transcription	Adipose Nuclei	Adipose
12	chr9:27154400-27158000	Enhancers	Osteobl	bone
13	chr9:27155400-27157600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr9:27155400-27157600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr9:27155400-27157800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr9:27155400-27157800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr9:27155400-27159000	Weak transcription	Colon Smooth Muscle	Colon
18	chr9:27155400-27161400	Weak transcription	Fetal Lung	lung
19	chr9:27155400-27164600	Weak transcription	Fetal Stomach	stomach
20	chr9:27155600-27159000	Weak transcription	Fetal Heart	heart
21	chr9:27155800-27157200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr9:27155800-27157600	Weak transcription	HUVEC	blood vessel
23	chr9:27156200-27158200	Enhancers	Placenta Amnion	Placenta Amnion
24	chr9:27156400-27157800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr9:27156600-27157800	Enhancers	Hela-S3	cervix
26	chr9:27156800-27157200	Enhancers	Muscle Satellite Cultured Cells	--
27	chr9:27156800-27157400	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr9:27156800-27157600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
29	chr9:27156800-27157800	Enhancers	HMEC	breast
30	chr9:27157000-27158000	Enhancers	NHEK	skin

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