Variant report

Variant	rs62522241
Chromosome Location	chr8:99199369-99199370
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:99197354..99201029-chr8:99202677..99207543,4	MCF-7	breast:
2	chr8:99197086..99199611-chr8:99306001..99308233,3	MCF-7	breast:

Variant related genes	Relation type
ENSG00000104361	Chromatin interaction
ENSG00000252558	Chromatin interaction

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

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10955157	0.96[ASN][1000 genomes]
rs10955158	0.91[ASN][1000 genomes]
rs12542592	0.96[ASN][1000 genomes]
rs12542593	0.96[ASN][1000 genomes]
rs12542608	0.96[ASN][1000 genomes]
rs12547555	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12549134	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs13263648	0.96[ASN][1000 genomes]
rs1901363	0.86[ASN][1000 genomes]
rs2122929	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3735883	0.84[ASN][1000 genomes]
rs3735884	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs55772672	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs55975205	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs56215918	0.93[EUR][1000 genomes]
rs58297506	0.81[AFR][1000 genomes]
rs59980805	0.81[AFR][1000 genomes]
rs62522239	0.87[EUR][1000 genomes]
rs62522242	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62522245	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62522247	0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62522248	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62522249	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs62524189	0.83[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6985720	1.00[AFR][1000 genomes];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6995263	0.96[ASN][1000 genomes]
rs6995983	0.87[AFR][1000 genomes]
rs7005911	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7016814	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72664827	0.93[EUR][1000 genomes]
rs73281898	0.81[AFR][1000 genomes]
rs73283715	0.81[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1032904	chr8:98756076-99476925	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
2	nsv539687	chr8:98756076-99476925	Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
3	nsv831405	chr8:99095239-99260934	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
4	nsv891216	chr8:99153160-99209248	Strong transcription Active TSS Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	esv14716	chr8:99169690-99199971	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:31 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:99191600-99203000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr8:99191600-99243800	Weak transcription	Spleen	Spleen
3	chr8:99192200-99201000	Weak transcription	Fetal Heart	heart
4	chr8:99192200-99205800	Weak transcription	Fetal Intestine Small	intestine
5	chr8:99192200-99210600	Weak transcription	Rectal Mucosa Donor 31	rectum
6	chr8:99192200-99214400	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr8:99192800-99210400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr8:99193400-99206400	Weak transcription	Pancreas	Pancrea
9	chr8:99194800-99216600	Weak transcription	Colonic Mucosa	Colon
10	chr8:99196400-99204800	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr8:99197000-99204800	Weak transcription	Fetal Intestine Large	intestine
12	chr8:99197000-99205000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
13	chr8:99197000-99209200	Weak transcription	HSMMtube	muscle
14	chr8:99197000-99210400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chr8:99197000-99219000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr8:99197400-99206200	Weak transcription	Aorta	Aorta
17	chr8:99197400-99206200	Weak transcription	Rectal Smooth Muscle	rectum
18	chr8:99197800-99204800	Weak transcription	Right Atrium	heart
19	chr8:99197800-99215400	Weak transcription	Fetal Stomach	stomach
20	chr8:99198000-99210400	Weak transcription	Osteobl	bone
21	chr8:99198000-99217000	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr8:99198200-99200800	Weak transcription	Right Ventricle	heart
23	chr8:99198200-99200800	Weak transcription	NHDF-Ad	bronchial
24	chr8:99198200-99201200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr8:99198200-99201200	Weak transcription	Left Ventricle	heart
26	chr8:99198200-99202000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr8:99198200-99207200	Weak transcription	Esophagus	oesophagus
28	chr8:99198200-99215200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
29	chr8:99198200-99239200	Weak transcription	Lung	lung
30	chr8:99198400-99201400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr8:99198400-99204800	Weak transcription	Ovary	ovary

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