Variant report

Variant	rs35354204
Chromosome Location	chr4:158900101-158900102
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr4:158435698..158436662-chr4:158899463..158900935,8	MCF-7	breast:
2	chr4:158138556..158139623-chr4:158899610..158900602,7	MCF-7	breast:
3	chr4:158435706..158436585-chr4:158899459..158900113,2	MCF-7	breast:

Extended variants
information (count: 68 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:65)

rs_ID	r²[population]
rs10517684	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10857307	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10857308	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11100145	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12498860	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12501025	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12504989	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12505752	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12505934	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12510436	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12511544	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12511578	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs12511957	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12512064	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12643255	0.87[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs12644342	0.97[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12650454	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1375138	0.86[EUR][1000 genomes]
rs17036918	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs17036921	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1839129	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1839130	0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2594763	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2594769	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs35146306	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs3934848	0.95[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4129400	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4132016	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4132443	0.95[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs4307005	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4460050	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4464607	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4629502	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4637451	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4691449	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs57156989	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs58762368	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62335304	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs62335305	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs62335306	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs62335307	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs62335308	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs62335310	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs62335311	0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs62335313	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs62335314	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs62335315	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62335316	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62335317	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62335339	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs62335341	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs62335345	0.96[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs62335346	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs62335358	0.95[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs62335359	0.95[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs62336960	0.95[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs62336961	0.95[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs62336984	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs6815131	0.95[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6827475	0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72965897	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72967808	0.97[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs72967836	0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs964237	0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs982239	0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[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	nsv993476	chr4:158550643-159202015	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer 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	nsv1030124	chr4:158758675-159251140	Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
3	nsv881288	chr4:158891733-159028080	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:158893400-158901200	Weak transcription	Aorta	Aorta
2	chr4:158899400-158900200	Flanking Active TSS	HUVEC	blood vessel
3	chr4:158899800-158900200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr4:158899800-158900200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr4:158899800-158900200	Enhancers	Primary monocytes fromperipheralblood	blood
6	chr4:158899800-158900200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
7	chr4:158899800-158900200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
8	chr4:158899800-158900200	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr4:158899800-158900200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr4:158899800-158900200	Active TSS	Brain Cingulate Gyrus	brain
11	chr4:158899800-158900200	Active TSS	Brain Hippocampus Middle	brain
12	chr4:158899800-158900200	Active TSS	Brain Inferior Temporal Lobe	brain
13	chr4:158899800-158900200	Active TSS	Brain Substantia Nigra	brain
14	chr4:158899800-158900200	Active TSS	Duodenum Smooth Muscle	Duodenum
15	chr4:158899800-158900200	Active TSS	Fetal Adrenal Gland	Adrenal Gland
16	chr4:158899800-158900200	Active TSS	Pancreatic Islets	Pancreatic Islet
17	chr4:158899800-158900200	Active TSS	Fetal Lung	lung
18	chr4:158899800-158900200	Active TSS	Ovary	ovary
19	chr4:158899800-158900200	Active TSS	Psoas Muscle	Psoas
20	chr4:158899800-158900200	Active TSS	Rectal Mucosa Donor 29	rectum
21	chr4:158899800-158900200	Active TSS	NH-A	brain
22	chr4:158899800-158900200	Enhancers	NHEK	skin
23	chr4:158899800-158900200	Flanking Active TSS	Osteobl	bone
24	chr4:158899800-158900400	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr4:158899800-158900400	Enhancers	Muscle Satellite Cultured Cells	--
26	chr4:158899800-158900400	Active TSS	Brain Anterior Caudate	brain
27	chr4:158899800-158900400	Flanking Active TSS	Colon Smooth Muscle	Colon
28	chr4:158899800-158900400	Enhancers	Fetal Heart	heart
29	chr4:158899800-158900600	Enhancers	Fetal Brain Male	brain
30	chr4:158900000-158900200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
31	chr4:158900000-158900200	Enhancers	Pancreas	Pancrea
32	chr4:158900000-158900400	Enhancers	Fetal Intestine Small	intestine
33	chr4:158900000-158900400	Enhancers	Monocytes-CD14+_RO01746	blood
34	chr4:158900000-158904400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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