Variant report

Variant	rs11647818
Chromosome Location	chr16:11927366-11927367
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr16:11925852..11930125-chr16:11943288..11946865,5	K562	blood:
2	chr16:11927157..11932947-chr16:11943372..11947936,7	MCF-7	breast:
3	chr16:11922138..11925096-chr16:11925223..11927674,2	MCF-7	breast:
4	chr16:11926170..11928281-chr16:11932222..11935066,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000262117	Chromatin interaction
ENSG00000263307	Chromatin interaction
ENSG00000171490	Chromatin interaction

Extended variants
information (count: 43 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs10744977	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11075022	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11646545	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11649405	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12925740	0.87[AMR][1000 genomes]
rs153025	0.82[AFR][1000 genomes];0.86[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs154148	0.90[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs171656	0.91[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs2075159	0.83[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs251723	0.91[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs28279	0.84[ASN][1000 genomes]
rs33619	0.81[ASN][1000 genomes]
rs33620	0.81[ASN][1000 genomes]
rs33623	0.81[ASN][1000 genomes]
rs33631	0.83[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs33637	0.85[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs33640	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs33643	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs33645	0.85[AMR][1000 genomes]
rs33647	0.87[AMR][1000 genomes]
rs33649	0.84[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs33651	0.87[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs33652	0.87[AMR][1000 genomes]
rs33653	0.82[AFR][1000 genomes];0.87[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs33655	0.80[AFR][1000 genomes];0.87[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs33660	0.88[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs35153773	0.97[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs40311	0.88[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs4511557	0.90[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs718081	0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7185589	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7193470	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7196913	0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7197111	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7198817	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7202234	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs8046617	0.89[ASN][1000 genomes]
rs8047726	0.86[ASN][1000 genomes]
rs8061189	0.90[AMR][1000 genomes];0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv482288	chr16:11776491-11946429	Flanking Active TSS Strong transcription Genic enhancers Weak transcription Enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	54 gene(s)	inside rSNPs	diseases
2	nsv1043909	chr16:11839910-12007435	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
3	nsv1042660	chr16:11846873-12110435	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	60 gene(s)	inside rSNPs	diseases
4	nsv571458	chr16:11925008-12087282	Weak transcription Genic enhancers Strong transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs11647818	GSPT1	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:11916600-11928800	Weak transcription	Primary B cells from cord blood	blood
2	chr16:11918600-11929600	Weak transcription	Brain Anterior Caudate	brain
3	chr16:11918600-11929800	Weak transcription	Pancreas	Pancrea
4	chr16:11918600-11930000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
5	chr16:11918600-11930200	Weak transcription	Left Ventricle	heart
6	chr16:11918600-11933600	Weak transcription	Stomach Mucosa	stomach
7	chr16:11918600-11943800	Weak transcription	Right Atrium	heart
8	chr16:11918800-11929400	Weak transcription	Duodenum Mucosa	Duodenum
9	chr16:11918800-11930000	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr16:11918800-11930000	Weak transcription	Hela-S3	cervix
11	chr16:11918800-11930200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr16:11918800-11930200	Weak transcription	Colon Smooth Muscle	Colon
13	chr16:11919000-11929600	Weak transcription	Brain Hippocampus Middle	brain
14	chr16:11919000-11929800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr16:11919000-11930000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
16	chr16:11919000-11930000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
17	chr16:11919000-11930200	Weak transcription	Duodenum Smooth Muscle	Duodenum
18	chr16:11919000-11930400	Weak transcription	Right Ventricle	heart
19	chr16:11919000-11931400	Weak transcription	Small Intestine	intestine
20	chr16:11919200-11929400	Weak transcription	Brain Germinal Matrix	brain
21	chr16:11919200-11930000	Weak transcription	Fetal Intestine Large	intestine
22	chr16:11919800-11928600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr16:11920800-11927800	Weak transcription	Monocytes-CD14+_RO01746	blood
24	chr16:11923400-11930400	Weak transcription	Stomach Smooth Muscle	stomach
25	chr16:11923600-11927800	Weak transcription	HepG2	liver
26	chr16:11926200-11928400	Weak transcription	Primary T cells from cord blood	blood
27	chr16:11926200-11930800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr16:11926400-11929400	Weak transcription	Primary T helper cells PMA-I stimulated	--
29	chr16:11926600-11929400	Weak transcription	Fetal Intestine Small	intestine
30	chr16:11926600-11929600	Weak transcription	Rectal Smooth Muscle	rectum
31	chr16:11926600-11930200	Weak transcription	Fetal Brain Male	brain
32	chr16:11927200-11929400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr16:11927200-11930000	Enhancers	Placenta	Placenta
34	chr16:11927200-11930000	Weak transcription	NHLF	lung
35	chr16:11927200-11930200	Weak transcription	Primary T cells fromperipheralblood	blood
36	chr16:11927200-11930400	Weak transcription	Primary T killer memory cells from peripheral blood	blood

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