Variant report

Variant	rs4309929
Chromosome Location	chr5:179650988-179650989
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	chr5:179636340..179638403-chr5:179650637..179652737,2	K562	blood:
2	chr5:179649668..179652883-chr5:179653368..179656584,4	K562	blood:

Variant related genes	Relation type
ENSG00000229721	Chromatin interaction

Extended variants
information (count: 35 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs10155559	0.85[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs10903250	0.85[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs1127580	0.82[EUR][1000 genomes]
rs17627536	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs3099063	0.84[EUR][1000 genomes]
rs3111536	0.85[EUR][1000 genomes]
rs34763496	0.83[EUR][1000 genomes]
rs35211991	0.86[EUR][1000 genomes]
rs35394934	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs35551113	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs35759987	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4270655	0.96[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4441844	0.89[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4454029	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4469167	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4700728	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4700924	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs55756747	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs56929977	0.86[ASN][1000 genomes]
rs62406982	0.86[EUR][1000 genomes]
rs62406984	0.86[EUR][1000 genomes]
rs62406986	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs62406991	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6864789	0.82[ASN][1000 genomes]
rs6869231	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6874557	0.85[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs6878432	0.80[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6882940	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6894217	0.83[EUR][1000 genomes]

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	nsv948909	chr5:179249099-179772640	Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	175 gene(s)	inside rSNPs	diseases
2	nsv1033706	chr5:179402769-179806356	Strong transcription Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	165 gene(s)	inside rSNPs	diseases
3	esv2758032	chr5:179534477-179729944	Strong transcription Weak transcription Flanking Bivalent TSS/Enh Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
4	esv2759398	chr5:179534477-179729944	Weak transcription Strong transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
5	nsv1023914	chr5:179649883-180040672	Weak transcription Enhancers Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
6	nsv537983	chr5:179649883-180040672	Strong transcription ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:179645600-179660200	Weak transcription	Brain Cingulate Gyrus	brain
2	chr5:179646800-179659200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr5:179647600-179659800	Weak transcription	Brain Angular Gyrus	brain
4	chr5:179647600-179660200	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr5:179647800-179656600	Weak transcription	Brain Anterior Caudate	brain
6	chr5:179649000-179653600	Weak transcription	Right Ventricle	heart
7	chr5:179649600-179657800	Weak transcription	Brain Germinal Matrix	brain
8	chr5:179649600-179660200	Weak transcription	Fetal Brain Female	brain
9	chr5:179650200-179655800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr5:179650200-179669000	Weak transcription	Fetal Brain Male	brain

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