Variant report

Variant	rs6833295
Chromosome Location	chr4:159064672-159064673
allele	G/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:23)

rs_ID	r²[population]
rs10000610	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10003459	0.92[CEU][hapmap];0.94[CHB][hapmap]
rs10013448	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs10027000	0.92[CEU][hapmap];0.87[CHB][hapmap]
rs10049927	0.89[CEU][hapmap];0.81[CHB][hapmap]
rs10517688	0.92[JPT][hapmap]
rs12512643	0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs13126694	0.87[CHB][hapmap];0.85[AMR][1000 genomes]
rs17037241	0.92[JPT][hapmap]
rs2346782	0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4077776	0.89[CEU][hapmap];0.88[CHB][hapmap]
rs4388135	0.85[CEU][hapmap];0.94[CHB][hapmap]
rs4398571	0.92[JPT][hapmap]
rs4574459	0.85[CEU][hapmap];0.81[CHB][hapmap]
rs4631100	0.86[CEU][hapmap];0.82[CHB][hapmap]
rs4691454	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4691460	1.00[CHB][hapmap];0.94[YRI][hapmap];0.93[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6814979	0.96[CEU][hapmap];0.94[CHB][hapmap];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6830475	1.00[CHB][hapmap];0.90[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6843728	0.92[CEU][hapmap];0.94[CHB][hapmap]
rs7657303	0.88[CEU][hapmap];0.81[CHB][hapmap]
rs7692254	0.96[CEU][hapmap];0.94[CHB][hapmap]
rs9968557	0.96[CEU][hapmap];0.94[CHB][hapmap]

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	nsv1021067	chr4:158972282-159175475	Enhancers Flanking Active TSS Active TSS Strong transcription Weak transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:38 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:159042800-159083600	Weak transcription	Fetal Muscle Leg	muscle
2	chr4:159044800-159071000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr4:159044800-159073200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr4:159047000-159080200	Weak transcription	Right Ventricle	heart
5	chr4:159049200-159070000	Weak transcription	Placenta	Placenta
6	chr4:159051800-159070600	Weak transcription	Fetal Intestine Large	intestine
7	chr4:159051800-159073000	Weak transcription	Fetal Stomach	stomach
8	chr4:159051800-159080400	Weak transcription	Duodenum Smooth Muscle	Duodenum
9	chr4:159052000-159071400	Weak transcription	Adipose Nuclei	Adipose
10	chr4:159052200-159071400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr4:159052200-159072800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr4:159052600-159071200	Weak transcription	Fetal Intestine Small	intestine
13	chr4:159052600-159071400	Weak transcription	HSMMtube	muscle
14	chr4:159052600-159080200	Weak transcription	Left Ventricle	heart
15	chr4:159055600-159076200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
16	chr4:159059000-159077800	Weak transcription	Aorta	Aorta
17	chr4:159059400-159071800	Weak transcription	Primary hematopoietic stem cells	blood
18	chr4:159059400-159076600	Weak transcription	Colon Smooth Muscle	Colon
19	chr4:159060400-159066000	Weak transcription	Brain Substantia Nigra	brain
20	chr4:159060600-159070800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr4:159060600-159071200	Weak transcription	Ovary	ovary
22	chr4:159060600-159071400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
23	chr4:159060600-159076600	Weak transcription	HMEC	breast
24	chr4:159060800-159067600	Weak transcription	Brain Anterior Caudate	brain
25	chr4:159061800-159066600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr4:159062000-159065800	Strong transcription	Primary monocytes fromperipheralblood	blood
27	chr4:159062000-159077600	Weak transcription	Rectal Smooth Muscle	rectum
28	chr4:159062600-159077800	Weak transcription	Placenta Amnion	Placenta Amnion
29	chr4:159062600-159083600	Weak transcription	Sigmoid Colon	Sigmoid Colon
30	chr4:159063200-159071600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr4:159063400-159066600	Strong transcription	HUVEC	blood vessel
32	chr4:159063400-159078800	Strong transcription	Monocytes-CD14+_RO01746	blood
33	chr4:159064000-159065600	Weak transcription	HepG2	liver
34	chr4:159064000-159066400	Genic enhancers	Breast Myoepithelial Primary Cells	Breast
35	chr4:159064000-159071800	Weak transcription	Stomach Smooth Muscle	stomach
36	chr4:159064200-159066200	Weak transcription	Brain Hippocampus Middle	brain
37	chr4:159064200-159067600	Weak transcription	HSMM	muscle
38	chr4:159064400-159066400	Enhancers	Fetal Heart	heart

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