Variant report

Variant	rs322811
Chromosome Location	chr7:127744842-127744843
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:127735968..127738181-chr7:127743649..127746341,2	K562	blood:
2	chr7:127735954..127738632-chr7:127744138..127745884,3	MCF-7	breast:

Extended variants
information (count: 44 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs178733	0.81[CEU][hapmap];0.94[CHB][hapmap];0.80[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs184430	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs322738	0.83[ASN][1000 genomes]
rs322752	0.80[ASN][1000 genomes]
rs322756	0.80[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs322760	0.80[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs322761	0.80[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs322762	0.80[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs322765	0.80[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs322766	0.80[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs322768	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs322770	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs322771	0.88[ASN][1000 genomes]
rs322775	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs322778	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs322780	0.94[ASN][1000 genomes]
rs322782	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs322783	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs322784	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs322785	0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs322786	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs322787	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs322790	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs322791	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs322806	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs322807	0.96[CEU][hapmap];1.00[CHB][hapmap];0.86[JPT][hapmap];0.96[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs322808	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs322809	0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs322812	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs322815	0.86[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs322818	1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs5028619	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6467159	0.88[LWK][hapmap];0.83[YRI][hapmap];0.80[AFR][1000 genomes]
rs6467160	0.82[AFR][1000 genomes]
rs6467161	0.82[YRI][hapmap]
rs6467163	0.82[AFR][1000 genomes]
rs6960004	0.94[CHB][hapmap];1.00[CHD][hapmap];0.88[JPT][hapmap];0.97[ASN][1000 genomes]
rs759710	0.82[AFR][1000 genomes]
rs7792971	0.88[LWK][hapmap];0.83[YRI][hapmap];0.81[AFR][1000 genomes]
rs7793071	0.81[AFR][1000 genomes]
rs7803045	0.81[AFR][1000 genomes]
rs7803473	0.82[AFR][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	nsv1022385	chr7:127246656-127971194	Weak transcription Bivalent Enhancer Enhancers Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
2	nsv539120	chr7:127246656-127971194	Enhancers Weak transcription Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs322811	CCDC136	cis	parietal	SCAN
rs322811	EEF2K	trans	cerebellum	SCAN

Chromatin state (count:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:127734400-127748200	Weak transcription	Dnd41	blood
2	chr7:127743400-127745000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
3	chr7:127743400-127745000	Active TSS	Primary T cells from cord blood	blood
4	chr7:127743600-127745000	Bivalent Enhancer	Fetal Brain Male	brain
5	chr7:127743800-127745000	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
6	chr7:127743800-127745000	Flanking Active TSS	Primary B cells from cord blood	blood
7	chr7:127744600-127745000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
8	chr7:127744600-127745000	Bivalent Enhancer	Fetal Muscle Leg	muscle
9	chr7:127744600-127745000	Bivalent Enhancer	Placenta	Placenta
10	chr7:127744600-127745000	Bivalent Enhancer	Stomach Smooth Muscle	stomach
11	chr7:127744600-127745600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr7:127744600-127745800	Enhancers	Spleen	Spleen
13	chr7:127744600-127746000	Enhancers	Primary T killer memory cells from peripheral blood	blood
14	chr7:127744600-127761600	Weak transcription	Right Atrium	heart
15	chr7:127744800-127745000	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr7:127744800-127745000	Enhancers	Primary T helper naive cells from peripheral blood	blood
17	chr7:127744800-127745000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
18	chr7:127744800-127745000	Bivalent Enhancer	Brain Hippocampus Middle	brain
19	chr7:127744800-127745000	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
20	chr7:127744800-127745000	Bivalent Enhancer	Fetal Intestine Small	intestine
21	chr7:127744800-127745000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
22	chr7:127744800-127745000	Bivalent Enhancer	NHDF-Ad	bronchial
23	chr7:127744800-127745200	Enhancers	Primary T helper cells fromperipheralblood	blood
24	chr7:127744800-127745400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
25	chr7:127744800-127745600	Bivalent Enhancer	Fetal Thymus	thymus
26	chr7:127744800-127745800	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
27	chr7:127744800-127746000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
28	chr7:127744800-127746600	Weak transcription	Monocytes-CD14+_RO01746	blood
29	chr7:127744800-127746800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
30	chr7:127744800-127747200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
31	chr7:127744800-127748600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
32	chr7:127744800-127748800	Enhancers	Primary T helper cells PMA-I stimulated	--
33	chr7:127744800-127753200	Enhancers	Primary monocytes fromperipheralblood	blood
34	chr7:127744800-127753400	Enhancers	Primary B cells from peripheral blood	blood

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