Variant report

Variant	rs73927111
Chromosome Location	chr2:40337791-40337792
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 26 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs5550	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56407349	1.00[AMR][1000 genomes]
rs57032634	1.00[AMR][1000 genomes]
rs60228195	1.00[AMR][1000 genomes]
rs73924751	1.00[AMR][1000 genomes]
rs73924754	1.00[AMR][1000 genomes]
rs73927110	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73927112	1.00[AMR][1000 genomes]
rs73927113	1.00[AMR][1000 genomes]
rs73927114	1.00[AMR][1000 genomes]
rs73927115	1.00[AMR][1000 genomes]
rs73927123	1.00[AMR][1000 genomes]
rs73927125	1.00[AMR][1000 genomes]
rs73927126	1.00[AMR][1000 genomes]
rs73927130	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916300	chr2:40079899-40339019	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv833892	chr2:40188785-40363480	Enhancers Strong transcription Flanking Active TSS Weak transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv529606	chr2:40206280-40896881	Flanking Active TSS Enhancers Active TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv873902	chr2:40231282-40466268	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv1004092	chr2:40264608-40451701	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv1000572	chr2:40271958-40458911	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv535654	chr2:40271958-40458911	Enhancers Weak transcription Genic enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv581502	chr2:40273903-40459645	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv873903	chr2:40285145-40382712	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	nsv873904	chr2:40292289-40466268	Enhancers Strong transcription Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
11	esv275350	chr2:40332851-40338067	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Strong transcription	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:40321200-40354600	Weak transcription	Right Ventricle	heart
2	chr2:40322800-40350200	Weak transcription	Fetal Brain Male	brain
3	chr2:40328000-40365600	Weak transcription	Brain Germinal Matrix	brain
4	chr2:40329000-40341400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
5	chr2:40329600-40341400	Weak transcription	Stomach Smooth Muscle	stomach
6	chr2:40329800-40342400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr2:40329800-40345200	Weak transcription	Fetal Thymus	thymus
8	chr2:40331000-40340800	Weak transcription	Dnd41	blood
9	chr2:40331200-40350200	Weak transcription	Duodenum Smooth Muscle	Duodenum
10	chr2:40331200-40351200	Weak transcription	Fetal Stomach	stomach
11	chr2:40333000-40351000	Weak transcription	Aorta	Aorta
12	chr2:40333200-40342600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr2:40333400-40339000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr2:40333400-40340800	Weak transcription	Psoas Muscle	Psoas
15	chr2:40333400-40354400	Weak transcription	NH-A	brain
16	chr2:40333600-40339000	Weak transcription	NHDF-Ad	bronchial
17	chr2:40333600-40340600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr2:40333800-40340200	Weak transcription	Osteobl	bone
19	chr2:40334600-40354800	Weak transcription	Fetal Brain Female	brain
20	chr2:40336000-40338000	Strong transcription	Primary monocytes fromperipheralblood	blood
21	chr2:40336400-40339200	Strong transcription	HSMM	muscle
22	chr2:40336600-40345600	Strong transcription	Monocytes-CD14+_RO01746	blood
23	chr2:40337400-40338200	Strong transcription	Left Ventricle	heart
24	chr2:40337600-40339800	Enhancers	Fetal Heart	heart

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