Variant report

Variant	rs60658774
Chromosome Location	chr9:96962138-96962139
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:96942774..96945747-chr9:96959750..96962534,2	K562	blood:
2	chr9:96831171..96832871-chr9:96960343..96963086,2	MCF-7	breast:
3	chr9:96960924..96963618-chr9:96965476..96967579,2	K562	blood:

Variant related genes	Relation type
ENSG00000230262	Chromatin interaction

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs1421139	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16909702	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16909728	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73653440	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73653443	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73653444	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73653447	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73653451	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7466359	0.83[AFR][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	nsv482457	chr9:96813852-96996170	Strong transcription Flanking Active TSS Weak transcription Enhancers Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	217 gene(s)	inside rSNPs	diseases
2	nsv831655	chr9:96834042-97042009	Enhancers Weak transcription Genic enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	218 gene(s)	inside rSNPs	diseases
3	esv3394266	chr9:96935210-97045514	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	195 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:42 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:96931400-96965600	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr9:96942400-96964000	Weak transcription	Rectal Smooth Muscle	rectum
3	chr9:96946200-96962800	Weak transcription	Gastric	stomach
4	chr9:96946200-96965000	Weak transcription	NHLF	lung
5	chr9:96946800-96965400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr9:96947000-96966200	Weak transcription	Fetal Kidney	kidney
7	chr9:96955000-96964600	Weak transcription	Ovary	ovary
8	chr9:96955400-96962200	Weak transcription	Brain Cingulate Gyrus	brain
9	chr9:96955800-96962800	Weak transcription	Stomach Smooth Muscle	stomach
10	chr9:96956800-96963000	Strong transcription	HSMM	muscle
11	chr9:96956800-96963400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr9:96957000-96963000	Strong transcription	Muscle Satellite Cultured Cells	--
13	chr9:96958400-96962600	Weak transcription	Primary T cells from cord blood	blood
14	chr9:96958400-96963000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr9:96958400-96963800	Weak transcription	Primary B cells from cord blood	blood
16	chr9:96958600-96963400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr9:96959400-96963600	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr9:96959600-96964800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr9:96959800-96962200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr9:96959800-96963400	Weak transcription	Fetal Brain Male	brain
21	chr9:96960000-96964000	Weak transcription	Left Ventricle	heart
22	chr9:96960200-96962400	Enhancers	Skeletal Muscle Female	skeletal muscle
23	chr9:96960200-96965000	Weak transcription	Adipose Nuclei	Adipose
24	chr9:96960400-96962800	Weak transcription	Osteobl	bone
25	chr9:96960400-96964000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr9:96960400-96966000	Weak transcription	HSMMtube	muscle
27	chr9:96960600-96962600	Weak transcription	Aorta	Aorta
28	chr9:96961000-96965400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr9:96961200-96963000	Weak transcription	NHEK	skin
30	chr9:96961200-96964000	Weak transcription	Fetal Stomach	stomach
31	chr9:96961200-96966200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr9:96961200-96973600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
33	chr9:96961400-96962600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chr9:96961400-96962800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
35	chr9:96961400-96962800	Weak transcription	Lung	lung
36	chr9:96961400-96964000	Weak transcription	Fetal Muscle Leg	muscle
37	chr9:96961400-96964000	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr9:96961600-96962600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr9:96961800-96962200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
40	chr9:96961800-96962600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
41	chr9:96961800-96962600	Weak transcription	Fetal Lung	lung
42	chr9:96962000-96962600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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