Variant report

Variant	rs9994834
Chromosome Location	chr4:7399054-7399055
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:7390826..7393048-chr4:7397978..7399599,2	K562	blood:

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:46)

rs_ID	r²[population]
rs10000132	0.95[CEU][hapmap];0.89[YRI][hapmap]
rs10000236	0.95[CEU][hapmap];0.89[YRI][hapmap]
rs10001291	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs10005036	1.00[CEU][hapmap];0.94[YRI][hapmap];0.86[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs10005361	0.95[CEU][hapmap];0.94[YRI][hapmap];0.83[AFR][1000 genomes]
rs10005455	0.94[CEU][hapmap];0.94[YRI][hapmap];0.83[AFR][1000 genomes]
rs10033441	1.00[CEU][hapmap];0.83[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs10516186	1.00[CEU][hapmap];0.96[TSI][hapmap];0.90[EUR][1000 genomes]
rs12500834	1.00[CEU][hapmap];0.88[YRI][hapmap]
rs12512241	0.95[CEU][hapmap];0.89[YRI][hapmap]
rs13103153	0.82[CEU][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes]
rs13105667	1.00[CEU][hapmap]
rs13106023	0.90[EUR][1000 genomes]
rs13113743	0.95[CEU][hapmap];0.84[EUR][1000 genomes]
rs13126413	1.00[CEU][hapmap];0.96[TSI][hapmap];0.90[EUR][1000 genomes]
rs13128656	0.83[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs13139233	0.90[EUR][1000 genomes]
rs13140023	0.90[EUR][1000 genomes]
rs13145868	0.86[EUR][1000 genomes]
rs13146595	1.00[CEU][hapmap]
rs13150726	0.90[EUR][1000 genomes]
rs13151988	0.93[EUR][1000 genomes]
rs28576748	0.91[EUR][1000 genomes]
rs34840766	0.90[EUR][1000 genomes]
rs35211466	0.87[EUR][1000 genomes]
rs35397875	0.87[EUR][1000 genomes]
rs36061257	0.88[EUR][1000 genomes]
rs4234803	0.88[CHB][hapmap];0.90[JPT][hapmap]
rs62277574	0.90[EUR][1000 genomes]
rs62277575	0.90[EUR][1000 genomes]
rs62277576	0.90[EUR][1000 genomes]
rs66506259	0.90[EUR][1000 genomes]
rs68191574	0.90[EUR][1000 genomes]
rs6821857	0.92[EUR][1000 genomes]
rs6835535	0.95[CEU][hapmap];0.92[EUR][1000 genomes]
rs6835739	0.93[EUR][1000 genomes]
rs6847931	0.93[EUR][1000 genomes]
rs6852520	0.92[EUR][1000 genomes]
rs6852909	0.93[EUR][1000 genomes]
rs6854113	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs7700129	1.00[CEU][hapmap];0.89[TSI][hapmap]
rs9995355	0.95[CEU][hapmap];0.94[YRI][hapmap];0.83[AFR][1000 genomes]
rs9997320	1.00[CEU][hapmap];0.94[YRI][hapmap];0.86[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs9997426	0.95[CEU][hapmap];0.94[CHD][hapmap];0.88[GIH][hapmap]
rs9997594	1.00[CEU][hapmap];0.81[YRI][hapmap];0.93[EUR][1000 genomes]
rs9997796	0.86[CEU][hapmap]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv916610	chr4:7238883-7731946	Bivalent Enhancer Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
2	nsv593569	chr4:7291363-7626136	Flanking Active TSS Weak transcription Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
3	nsv1011547	chr4:7318232-7637410	Active TSS ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
4	nsv537017	chr4:7318232-7637410	Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
5	nsv1003679	chr4:7319111-7449262	Bivalent Enhancer Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv469758	chr4:7370083-7546250	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 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	chr4:7384200-7399600	Weak transcription	Right Atrium	heart
2	chr4:7389800-7399800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr4:7391800-7402000	Enhancers	Brain Germinal Matrix	brain
4	chr4:7393600-7400800	Bivalent Enhancer	Fetal Muscle Leg	muscle
5	chr4:7394400-7400000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr4:7395800-7399400	Weak transcription	Brain Anterior Caudate	brain
7	chr4:7395800-7399400	Weak transcription	Brain Substantia Nigra	brain
8	chr4:7396600-7399400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr4:7396800-7401400	Enhancers	Brain Cingulate Gyrus	brain
10	chr4:7397400-7400800	Enhancers	HSMMtube	muscle
11	chr4:7397400-7401200	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr4:7397400-7401800	Enhancers	Breast Myoepithelial Primary Cells	Breast
13	chr4:7397600-7399200	Weak transcription	Fetal Thymus	thymus
14	chr4:7397600-7401600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr4:7398000-7399200	Enhancers	HMEC	breast
16	chr4:7398000-7400400	Enhancers	NH-A	brain
17	chr4:7398200-7399400	Weak transcription	Brain Hippocampus Middle	brain
18	chr4:7398200-7399400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr4:7398200-7400800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr4:7398400-7401200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr4:7398600-7399400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr4:7398600-7400000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr4:7398600-7400000	Enhancers	Fetal Intestine Small	intestine
24	chr4:7398600-7400800	Bivalent Enhancer	Fetal Lung	lung
25	chr4:7398800-7399200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
26	chr4:7398800-7399200	Enhancers	HSMM	muscle
27	chr4:7398800-7399800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr4:7398800-7400200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr4:7398800-7400800	Enhancers	Colon Smooth Muscle	Colon
30	chr4:7398800-7401400	Enhancers	Brain Inferior Temporal Lobe	brain
31	chr4:7399000-7399200	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr4:7399000-7399200	Flanking Active TSS	NHEK	skin
33	chr4:7399000-7399400	Enhancers	Stomach Smooth Muscle	stomach
34	chr4:7399000-7399800	Enhancers	Esophagus	oesophagus
35	chr4:7399000-7399800	Bivalent Enhancer	Fetal Stomach	stomach
36	chr4:7399000-7400200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
37	chr4:7399000-7401200	Enhancers	Fetal Brain Male	brain
38	chr4:7399000-7401400	Enhancers	Brain Angular Gyrus	brain

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