Variant report

Variant	rs73852849
Chromosome Location	chr3:111355239-111355240
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 36 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:33)

rs_ID	r²[population]
rs10511300	0.81[AMR][1000 genomes]
rs11914473	0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1513328	0.97[ASN][1000 genomes]
rs1513330	0.87[AMR][1000 genomes]
rs16858329	0.94[ASN][1000 genomes]
rs17202782	0.85[EUR][1000 genomes]
rs2895386	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3733176	1.00[ASN][1000 genomes]
rs4428148	0.87[AMR][1000 genomes]
rs56172864	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56306480	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57067927	1.00[ASN][1000 genomes]
rs57501419	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs57831621	1.00[ASN][1000 genomes]
rs6763322	1.00[ASN][1000 genomes]
rs6765832	0.98[ASN][1000 genomes]
rs6768092	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6770144	1.00[ASN][1000 genomes]
rs6770679	1.00[ASN][1000 genomes]
rs6771309	1.00[ASN][1000 genomes]
rs6780210	1.00[ASN][1000 genomes]
rs6780729	0.98[ASN][1000 genomes]
rs6787870	0.98[ASN][1000 genomes]
rs6801876	1.00[ASN][1000 genomes]
rs6807632	0.87[AMR][1000 genomes]
rs73230132	1.00[ASN][1000 genomes]
rs73230143	1.00[ASN][1000 genomes]
rs73852844	0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7431849	0.94[ASN][1000 genomes]
rs7637536	0.88[ASN][1000 genomes]
rs7639907	0.87[AMR][1000 genomes]
rs9819529	0.99[ASN][1000 genomes]
rs9858544	0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv460821	chr3:110637471-111501097	Enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Weak transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv591275	chr3:110637471-111501097	Strong transcription Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
3	nsv997756	chr3:111226058-111376585	Active TSS Enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:111346400-111357600	Weak transcription	HMEC	breast
2	chr3:111346600-111357600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr3:111346800-111356800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
4	chr3:111346800-111357000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr3:111346800-111357600	Weak transcription	Thymus	Thymus
6	chr3:111346800-111357800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr3:111347000-111356600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr3:111347000-111367200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
9	chr3:111347600-111367800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
10	chr3:111347800-111357000	Weak transcription	Fetal Thymus	thymus
11	chr3:111348000-111355400	Weak transcription	Primary T helper cells PMA-I stimulated	--
12	chr3:111348400-111355400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
13	chr3:111348800-111356600	Weak transcription	Primary B cells from peripheral blood	blood
14	chr3:111351800-111360200	Strong transcription	Primary T cells from cord blood	blood
15	chr3:111353800-111355600	Enhancers	Fetal Intestine Small	intestine
16	chr3:111353800-111356200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr3:111354400-111356800	Strong transcription	Dnd41	blood
18	chr3:111354800-111355600	Enhancers	Fetal Heart	heart
19	chr3:111354800-111359200	Strong transcription	Primary T helper cells fromperipheralblood	blood
20	chr3:111354800-111359600	Strong transcription	Primary T cells fromperipheralblood	blood
21	chr3:111355000-111355400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
22	chr3:111355000-111355600	Enhancers	Fetal Brain Male	brain
23	chr3:111355000-111355800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr3:111355000-111355800	Enhancers	Fetal Lung	lung
25	chr3:111355000-111356200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr3:111355000-111358800	Strong transcription	Primary T helper 17 cells PMA-I stimulated	--
27	chr3:111355000-111359000	Strong transcription	Primary T helper naive cells fromperipheralblood	blood
28	chr3:111355000-111359000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
29	chr3:111355200-111357000	Strong transcription	Primary T killer memory cells from peripheral blood	blood

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