Variant report

Variant	rs1626923
Chromosome Location	chr14:65246623-65246624
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr14:65243489..65248143-chr14:65249135..65251495,4	K562	blood:

Variant related genes	Relation type
ENSG00000070182	Chromatin interaction

Extended variants
information (count: 23 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs1695764	0.88[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs170684	0.93[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs1741485	1.00[ASW][hapmap];0.88[CHB][hapmap];0.92[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.99[MKK][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs1741486	0.88[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs1741487	1.00[ASW][hapmap];0.88[CHB][hapmap];0.92[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.99[MKK][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs1741488	1.00[ASW][hapmap];0.88[CHB][hapmap];0.89[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.99[MKK][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs1741489	0.82[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs229629	0.91[CEU][hapmap];0.94[CHB][hapmap];0.85[JPT][hapmap];0.89[YRI][hapmap];0.88[AFR][1000 genomes];0.85[AMR][1000 genomes];0.85[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs229635	0.97[AFR][1000 genomes];0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs229638	1.00[ASW][hapmap];0.88[CHB][hapmap];0.92[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.99[MKK][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs229640	0.90[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs229641	1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs229642	0.96[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs229643	0.89[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs2357726	0.94[ASW][hapmap];0.87[CHB][hapmap];0.92[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.99[MKK][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs2357727	1.00[ASW][hapmap];0.88[CHB][hapmap];0.92[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];0.99[MKK][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs2884253	0.90[JPT][hapmap];0.96[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs368194	0.81[CHD][hapmap]
rs3819932	0.88[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs56361624	0.96[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs77806	0.89[YRI][hapmap]

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	esv1818582	chr14:65172898-65256685	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA	11 gene(s)	inside rSNPs	diseases
2	esv1801406	chr14:65193725-65264416	Strong transcription Genic enhancers Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region miRNA	11 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs1626923	WDR89	cis	cerebellum	SCAN

Chromatin state (count:27 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:65228400-65265000	Weak transcription	Aorta	Aorta
2	chr14:65231600-65250600	Weak transcription	Brain Angular Gyrus	brain
3	chr14:65231600-65250600	Weak transcription	Brain Anterior Caudate	brain
4	chr14:65231600-65261400	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr14:65232200-65274200	Weak transcription	Gastric	stomach
6	chr14:65233000-65265600	Weak transcription	Fetal Brain Male	brain
7	chr14:65240400-65262800	Weak transcription	Brain Hippocampus Middle	brain
8	chr14:65242000-65251800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr14:65242200-65250400	Weak transcription	Brain Germinal Matrix	brain
10	chr14:65242400-65252600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr14:65242600-65248800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr14:65243600-65246800	Enhancers	Right Atrium	heart
13	chr14:65243600-65247000	Enhancers	Fetal Heart	heart
14	chr14:65243800-65246800	Enhancers	Left Ventricle	heart
15	chr14:65243800-65247000	Enhancers	Right Ventricle	heart
16	chr14:65244400-65247000	Genic enhancers	Skeletal Muscle Female	skeletal muscle
17	chr14:65244800-65246800	Genic enhancers	Fetal Muscle Trunk	muscle
18	chr14:65244800-65272400	Weak transcription	Brain Cingulate Gyrus	brain
19	chr14:65245200-65248800	Weak transcription	Fetal Brain Female	brain
20	chr14:65245200-65257600	Weak transcription	HSMMtube	muscle
21	chr14:65245800-65247000	Genic enhancers	Skeletal Muscle Male	skeletal muscle
22	chr14:65246200-65246800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr14:65246200-65246800	Enhancers	Psoas Muscle	Psoas
24	chr14:65246400-65246800	Enhancers	Fetal Muscle Leg	muscle
25	chr14:65246400-65253200	Weak transcription	Spleen	Spleen
26	chr14:65246600-65251000	Weak transcription	Pancreatic Islets	Pancreatic Islet
27	chr14:65246600-65251000	Weak transcription	K562	blood

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