Variant report

Variant	rs2716726
Chromosome Location	chr2:39952701-39952702
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr2:39941387..39944301-chr2:39949793..39952707,2	MCF-7	breast:
2	chr2:39949939..39952717-chr2:39956510..39959520,3	K562	blood:
3	chr2:39947562..39949942-chr2:39951658..39954303,2	MCF-7	breast:

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

rSNPs within LD-proxies of this variant (count:35)

rs_ID	r²[population]
rs10193803	1.00[JPT][hapmap]
rs10198734	1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[EUR][1000 genomes]
rs13388310	1.00[CHB][hapmap]
rs13395966	0.96[EUR][1000 genomes]
rs13423235	1.00[JPT][hapmap]
rs17024154	0.91[EUR][1000 genomes]
rs17024276	0.91[EUR][1000 genomes]
rs17024299	1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[EUR][1000 genomes]
rs17024307	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17024325	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];0.96[EUR][1000 genomes]
rs2058621	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2110672	1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[EUR][1000 genomes]
rs2110673	1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[EUR][1000 genomes]
rs2160207	1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[EUR][1000 genomes]
rs2192712	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];0.96[EUR][1000 genomes]
rs2540234	0.80[EUR][1000 genomes]
rs2540243	1.00[JPT][hapmap]
rs2540245	1.00[JPT][hapmap]
rs2716698	1.00[JPT][hapmap]
rs2716706	0.96[EUR][1000 genomes]
rs2716724	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2716734	0.96[EUR][1000 genomes]
rs57704430	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60003713	0.96[EUR][1000 genomes]
rs6708232	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6716262	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6738748	1.00[JPT][hapmap]
rs6745129	0.96[EUR][1000 genomes]
rs73924917	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73924918	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73924919	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73924920	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73924934	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7576551	0.84[EUR][1000 genomes]
rs7604790	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];0.96[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv833870	chr2:39837022-40026024	Flanking Bivalent TSS/Enh Weak transcription Enhancers Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv833881	chr2:39914558-40067256	Weak transcription Enhancers Strong transcription Bivalent Enhancer Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:53 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:39925000-39957600	Weak transcription	Fetal Stomach	stomach
2	chr2:39931400-39957600	Weak transcription	Fetal Muscle Leg	muscle
3	chr2:39938000-39957600	Weak transcription	Fetal Brain Female	brain
4	chr2:39942000-39963000	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr2:39943200-39956200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
6	chr2:39944400-39976600	Weak transcription	Fetal Brain Male	brain
7	chr2:39945200-39954400	Enhancers	Breast Myoepithelial Primary Cells	Breast
8	chr2:39946800-39959600	Weak transcription	Brain Germinal Matrix	brain
9	chr2:39947800-39959800	Weak transcription	Brain Cingulate Gyrus	brain
10	chr2:39948200-39961200	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr2:39948800-39959600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr2:39949000-39960400	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr2:39950000-39953400	Enhancers	NH-A	brain
14	chr2:39950000-39954400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr2:39950600-39953000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr2:39950600-39953000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr2:39950600-39953200	Enhancers	HSMMtube	muscle
18	chr2:39950600-39953200	Enhancers	Osteobl	bone
19	chr2:39950800-39952800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr2:39950800-39953600	Enhancers	HMEC	breast
21	chr2:39951000-39953400	Weak transcription	Left Ventricle	heart
22	chr2:39951000-39956000	Weak transcription	Placenta Amnion	Placenta Amnion
23	chr2:39951000-39957400	Weak transcription	Fetal Muscle Trunk	muscle
24	chr2:39951000-39959400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr2:39951000-39963600	Weak transcription	Pancreas	Pancrea
26	chr2:39951000-39964800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr2:39951200-39952800	Enhancers	HSMM	muscle
28	chr2:39951200-39953200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr2:39951200-39957600	Weak transcription	Fetal Lung	lung
30	chr2:39951200-39964800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr2:39951400-39957800	Weak transcription	Stomach Smooth Muscle	stomach
32	chr2:39951400-39958800	Weak transcription	Aorta	Aorta
33	chr2:39951400-39960200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
34	chr2:39951400-39961400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr2:39951400-39961800	Weak transcription	Colon Smooth Muscle	Colon
36	chr2:39951400-39962000	Weak transcription	HUES48 Cell Line	embryonic stem cell
37	chr2:39951400-39963800	Weak transcription	H9 Cell Line	embryonic stem cell
38	chr2:39951600-39953800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr2:39951800-39953000	Bivalent Enhancer	HepG2	liver
40	chr2:39952000-39956200	Weak transcription	Psoas Muscle	Psoas
41	chr2:39952000-39964800	Weak transcription	Rectal Smooth Muscle	rectum
42	chr2:39952200-39957400	Weak transcription	Skeletal Muscle Female	skeletal muscle
43	chr2:39952200-39960200	Weak transcription	HUES64 Cell Line	embryonic stem cell
44	chr2:39952400-39952800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr2:39952400-39953000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr2:39952400-39953200	Enhancers	Muscle Satellite Cultured Cells	--
47	chr2:39952400-39955400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
48	chr2:39952400-39957400	Weak transcription	Skeletal Muscle Male	skeletal muscle
49	chr2:39952400-39958800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr2:39952400-39962400	Weak transcription	Spleen	Spleen

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