Variant report

Variant	rs875776
Chromosome Location	chr6:114383606-114383607
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs11966557	0.92[JPT][hapmap]
rs12205029	0.92[JPT][hapmap]
rs13195526	0.92[JPT][hapmap]
rs13210690	0.92[JPT][hapmap]
rs1334901	0.92[JPT][hapmap]
rs1334902	0.92[JPT][hapmap]
rs17075821	0.92[JPT][hapmap]
rs17189832	0.92[JPT][hapmap]
rs6926298	0.92[JPT][hapmap]
rs7739597	0.92[JPT][hapmap]
rs7752154	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7766008	0.97[AMR][1000 genomes];1.00[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	nsv1021774	chr6:114063971-114407280	Enhancers Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
2	nsv538422	chr6:114063971-114407280	Genic enhancers Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
3	nsv1024062	chr6:114311029-114679557	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	59 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:114363800-114385000	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr6:114370000-114387000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr6:114370200-114389600	Weak transcription	Fetal Muscle Leg	muscle
4	chr6:114371400-114388200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr6:114379400-114384800	Weak transcription	HSMMtube	muscle
6	chr6:114379600-114390400	Weak transcription	HepG2	liver
7	chr6:114380400-114384600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr6:114380400-114384800	Weak transcription	HSMM	muscle
9	chr6:114380800-114388000	Weak transcription	Psoas Muscle	Psoas
10	chr6:114381200-114386400	Enhancers	Primary monocytes fromperipheralblood	blood
11	chr6:114382600-114384800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr6:114382600-114385000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr6:114383000-114383800	Enhancers	Brain Substantia Nigra	brain
14	chr6:114383200-114384200	Enhancers	Cortex derived primary cultured neurospheres	brain
15	chr6:114383200-114384200	Enhancers	Brain Cingulate Gyrus	brain
16	chr6:114383200-114384200	Enhancers	Brain Hippocampus Middle	brain
17	chr6:114383400-114384000	Enhancers	Brain Inferior Temporal Lobe	brain
18	chr6:114383400-114384200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr6:114383400-114384200	Enhancers	Brain Angular Gyrus	brain
20	chr6:114383400-114390000	Weak transcription	Brain Germinal Matrix	brain
21	chr6:114383600-114384200	Enhancers	Brain Anterior Caudate	brain

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