Variant report

Variant	rs7149156
Chromosome Location	chr14:70623885-70623886
allele	A/G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 46 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:44)

rs_ID	r²[population]
rs10444731	1.00[CHB][hapmap]
rs10444732	1.00[CHB][hapmap]
rs10444733	1.00[CHB][hapmap]
rs10483825	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11158839	1.00[CHB][hapmap]
rs1122708	1.00[CHB][hapmap]
rs11846266	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11850592	1.00[CHB][hapmap]
rs11851571	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12147147	1.00[CHB][hapmap]
rs12147341	1.00[CHB][hapmap]
rs12147621	1.00[CHB][hapmap]
rs12147634	1.00[CHB][hapmap]
rs17107920	1.00[CHB][hapmap]
rs17107925	1.00[CHB][hapmap]
rs17175527	1.00[CHB][hapmap]
rs17175597	1.00[CHB][hapmap]
rs17175695	1.00[CHB][hapmap]
rs17175813	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17175834	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17175848	1.00[CHB][hapmap]
rs17175939	1.00[CHB][hapmap]
rs17175960	1.00[CHB][hapmap]
rs17765251	1.00[CHB][hapmap]
rs17765304	1.00[CHB][hapmap]
rs17765376	0.81[CEU][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17765382	1.00[CEU][hapmap];1.00[CHB][hapmap];0.82[JPT][hapmap];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17765449	1.00[CHB][hapmap]
rs17765507	1.00[CEU][hapmap];1.00[CHB][hapmap];0.82[JPT][hapmap];0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17765575	1.00[CHB][hapmap]
rs17765586	1.00[CHB][hapmap]
rs56083999	0.90[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56194332	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61978174	0.90[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs61978179	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61978183	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7140688	1.00[CHB][hapmap]
rs7143465	1.00[CHB][hapmap]
rs7144377	1.00[CHB][hapmap]
rs7159555	1.00[CHB][hapmap]
rs8015011	1.00[CHB][hapmap]
rs8018678	1.00[CHB][hapmap]
rs998306	1.00[CHB][hapmap]
rs999618	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832826	chr14:70559589-70723464	Bivalent/Poised TSS Bivalent Enhancer Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv902075	chr14:70612618-70919016	Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:70604000-70638000	Weak transcription	HSMMtube	muscle
2	chr14:70615800-70632200	Weak transcription	Primary hematopoietic stem cells	blood
3	chr14:70620600-70626200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr14:70621400-70629400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr14:70622400-70626200	Enhancers	Skeletal Muscle Male	skeletal muscle
6	chr14:70622400-70626600	Enhancers	Skeletal Muscle Female	skeletal muscle
7	chr14:70622800-70624600	Enhancers	Psoas Muscle	Psoas
8	chr14:70623200-70624200	Enhancers	Fetal Muscle Leg	muscle

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