Variant report

Variant	rs73701095
Chromosome Location	chr8:108342481-108342482
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr8:108306316..108309008-chr8:108341130..108342850,2	K562	blood:
2	chr8:108315162..108317666-chr8:108340503..108343303,2	K562	blood:

Variant related genes	Relation type
ENSG00000154188	Chromatin interaction

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs12114632	1.00[AMR][1000 genomes]
rs12114634	1.00[AMR][1000 genomes]
rs41474548	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55875407	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56969075	0.89[AFR][1000 genomes]
rs58034973	0.98[AFR][1000 genomes]
rs60186919	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs60876963	1.00[AMR][1000 genomes]
rs73701084	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73701096	0.98[AFR][1000 genomes]
rs73701097	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73701098	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73702003	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73702004	0.85[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73702048	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7837271	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1029202	chr8:107796289-108384241	Enhancers Weak transcription Genic enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv539712	chr8:107796289-108384241	Enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv1034210	chr8:107796489-108384102	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv539713	chr8:107796489-108384102	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv529383	chr8:107796490-108368465	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv915821	chr8:107796490-108393008	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv1028726	chr8:107816841-108392547	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	nsv497805	chr8:107852509-108368371	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	esv2764100	chr8:108220671-108469233	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
10	nsv1030831	chr8:108224295-108466437	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
11	nsv539714	chr8:108224295-108466437	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
12	nsv465760	chr8:108224687-108485912	Weak transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
13	nsv611851	chr8:108224687-108485912	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
14	nsv1027447	chr8:108335387-108365566	Enhancers Flanking Active TSS Weak transcription Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:27 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:108323000-108349000	Weak transcription	HSMM	muscle
2	chr8:108328200-108342600	Weak transcription	Osteobl	bone
3	chr8:108328200-108344000	Weak transcription	Aorta	Aorta
4	chr8:108328400-108344000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr8:108333600-108368800	Weak transcription	Fetal Kidney	kidney
6	chr8:108337000-108344600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr8:108337800-108360200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr8:108340000-108343800	Weak transcription	Rectal Smooth Muscle	rectum
9	chr8:108340000-108344600	Weak transcription	Ovary	ovary
10	chr8:108340200-108343800	Weak transcription	Stomach Smooth Muscle	stomach
11	chr8:108340400-108344600	Weak transcription	Fetal Heart	heart
12	chr8:108340600-108345000	Weak transcription	Skeletal Muscle Male	skeletal muscle
13	chr8:108341800-108343000	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
14	chr8:108342000-108342600	Enhancers	Skeletal Muscle Female	skeletal muscle
15	chr8:108342000-108342800	Enhancers	Adipose Nuclei	Adipose
16	chr8:108342000-108342800	Enhancers	Colon Smooth Muscle	Colon
17	chr8:108342000-108343000	Enhancers	Fetal Lung	lung
18	chr8:108342000-108343800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr8:108342200-108342800	Strong transcription	Primary hematopoietic stem cells	blood
20	chr8:108342200-108343000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr8:108342200-108343000	Enhancers	Duodenum Smooth Muscle	Duodenum
22	chr8:108342200-108343000	Flanking Active TSS	NHLF	lung
23	chr8:108342200-108343200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr8:108342400-108342800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
25	chr8:108342400-108342800	Active TSS	NHDF-Ad	bronchial
26	chr8:108342400-108343000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
27	chr8:108342400-108343000	Transcr. at gene 5' and 3'	K562	blood

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