Variant report

Variant	rs6922650
Chromosome Location	chr6:163780737-163780738
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs13194411	0.90[ASN][1000 genomes]
rs1737311	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1763999	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4709712	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6905064	0.90[ASN][1000 genomes]
rs6920269	0.90[ASN][1000 genomes]
rs9346957	0.90[ASN][1000 genomes]
rs9347743	0.90[ASN][1000 genomes]
rs9365560	0.90[ASN][1000 genomes]
rs9365561	0.90[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	nsv932127	chr6:163000261-163950870	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv1022610	chr6:163591786-163814041	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv534621	chr6:163731741-163950870	Bivalent/Poised TSS Enhancers Flanking Active TSS Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:163776400-163783400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr6:163777400-163786800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr6:163777400-163787400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr6:163777400-163790000	Weak transcription	Spleen	Spleen
5	chr6:163777400-163791400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr6:163777600-163781400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr6:163778000-163788600	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chr6:163778400-163781400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr6:163778400-163781600	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr6:163778400-163782000	Weak transcription	Fetal Muscle Trunk	muscle
11	chr6:163778400-163783200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr6:163778400-163790800	Weak transcription	Right Atrium	heart
13	chr6:163778600-163782000	Weak transcription	Brain Anterior Caudate	brain
14	chr6:163778600-163783400	Weak transcription	Cortex derived primary cultured neurospheres	brain
15	chr6:163779400-163780800	Enhancers	Fetal Muscle Leg	muscle
16	chr6:163780200-163781400	Weak transcription	Brain Hippocampus Middle	brain
17	chr6:163780400-163782000	Weak transcription	Brain Angular Gyrus	brain
18	chr6:163780400-163782200	Weak transcription	Brain Cingulate Gyrus	brain
19	chr6:163780400-163783400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
20	chr6:163780600-163781600	Weak transcription	Brain Substantia Nigra	brain

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