Variant report

Variant	rs10174910
Chromosome Location	chr2:179103773-179103774
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	chr2:179103455..179105342-chr2:179107240..179109495,2	K562	blood:
2	chr2:179084247..179086331-chr2:179102848..179105496,2	K562	blood:

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10205083	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.97[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10497475	1.00[JPT][hapmap]
rs11894754	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11902232	0.85[AFR][1000 genomes]
rs12996084	1.00[JPT][hapmap]
rs13022619	1.00[JPT][hapmap]
rs13398301	0.99[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs168009	1.00[JPT][hapmap]
rs16866058	1.00[JPT][hapmap]
rs16866088	1.00[JPT][hapmap]
rs16866151	1.00[JPT][hapmap]
rs16866156	1.00[JPT][hapmap]
rs16866169	1.00[JPT][hapmap]
rs334007	0.81[YRI][hapmap]
rs334045	0.82[YRI][hapmap]
rs334621	1.00[JPT][hapmap]
rs6433715	0.82[YRI][hapmap]
rs6726222	1.00[JPT][hapmap]
rs73028684	1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1009312	chr2:178924318-179215566	Weak transcription Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
2	nsv536057	chr2:178924318-179215566	Strong transcription Weak transcription Active TSS Bivalent/Poised TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
3	nsv875452	chr2:178963445-179167766	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv1011423	chr2:179084407-179166160	Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr2:179091000-179106400	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr2:179091200-179115000	Weak transcription	Aorta	Aorta
3	chr2:179098600-179106600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr2:179099400-179104200	Enhancers	Skeletal Muscle Male	skeletal muscle
5	chr2:179101000-179103800	Enhancers	Hela-S3	cervix
6	chr2:179101000-179115400	Weak transcription	Gastric	stomach
7	chr2:179101200-179104200	Enhancers	Psoas Muscle	Psoas
8	chr2:179101200-179104200	Enhancers	Skeletal Muscle Female	skeletal muscle
9	chr2:179101400-179107000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr2:179101800-179106600	Weak transcription	Right Atrium	heart
11	chr2:179102400-179104200	Enhancers	Left Ventricle	heart
12	chr2:179103000-179104000	Enhancers	Fetal Heart	heart
13	chr2:179103200-179106600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr2:179103200-179106600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr2:179103200-179106600	Weak transcription	HSMM	muscle
16	chr2:179103200-179106600	Weak transcription	NHEK	skin
17	chr2:179103200-179106600	Weak transcription	NHLF	lung
18	chr2:179103400-179104000	Enhancers	Liver	Liver
19	chr2:179103400-179106600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr2:179103400-179106600	Weak transcription	Osteobl	bone
21	chr2:179103600-179106400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr2:179103600-179106600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr2:179103600-179106600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr2:179103600-179106600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr2:179103600-179106600	Weak transcription	Muscle Satellite Cultured Cells	--
26	chr2:179103600-179106600	Weak transcription	A549	lung
27	chr2:179103600-179106600	Weak transcription	HMEC	breast
28	chr2:179103600-179106600	Weak transcription	K562	blood
29	chr2:179103600-179106600	Weak transcription	NH-A	brain
30	chr2:179103600-179106600	Weak transcription	NHDF-Ad	bronchial

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