Variant report

Variant	rs11711748
Chromosome Location	chr3:141658875-141658876
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:141658582..141660731-chr3:141665381..141667726,2	K562	blood:
2	chr3:141629759..141632331-chr3:141657895..141659555,2	K562	blood:

Variant related genes	Relation type
ENSG00000269905	Chromatin interaction

Extended variants
information (count: 78 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:76)

rs_ID	r²[population]
rs10755098	0.88[CHB][hapmap]
rs10935439	0.83[AFR][1000 genomes]
rs10935440	0.83[AFR][1000 genomes]
rs10935441	0.83[AFR][1000 genomes]
rs10935442	0.88[CHB][hapmap]
rs10935443	0.88[CHB][hapmap]
rs10935445	0.96[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs10935446	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]
rs10935447	1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11569186	1.00[CEU][hapmap]
rs11569190	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];0.88[TSI][hapmap]
rs11569193	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap]
rs11569201	1.00[CEU][hapmap]
rs11569202	1.00[CEU][hapmap]
rs11569205	1.00[CEU][hapmap]
rs11569206	1.00[CEU][hapmap]
rs11569208	1.00[CEU][hapmap]
rs11569209	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap]
rs11569218	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap]
rs11569220	1.00[CEU][hapmap]
rs11569222	1.00[CEU][hapmap]
rs11569223	1.00[CEU][hapmap]
rs11569259	0.91[EUR][1000 genomes]
rs11569262	0.91[EUR][1000 genomes]
rs11569278	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];0.91[EUR][1000 genomes]
rs11569281	0.94[EUR][1000 genomes]
rs11569291	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];0.94[EUR][1000 genomes]
rs11706402	1.00[CEU][hapmap]
rs11706728	1.00[ASW][hapmap];1.00[GIH][hapmap];0.88[TSI][hapmap]
rs11707100	1.00[AFR][1000 genomes];0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11707427	0.83[AFR][1000 genomes]
rs11708301	1.00[CEU][hapmap]
rs11712803	1.00[CEU][hapmap]
rs11713023	1.00[CEU][hapmap];1.00[CHB][hapmap];0.93[JPT][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11716148	1.00[CEU][hapmap]
rs11717517	1.00[CEU][hapmap]
rs11718167	1.00[CEU][hapmap]
rs11719793	1.00[CEU][hapmap]
rs11721024	0.85[CHB][hapmap]
rs11844	1.00[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs12487977	1.00[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs12487983	1.00[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs12490893	1.00[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs12493472	1.00[CEU][hapmap]
rs12493495	1.00[CEU][hapmap]
rs12493643	1.00[CEU][hapmap]
rs12494971	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[TSI][hapmap];1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12497112	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12497443	1.00[CHB][hapmap];0.81[JPT][hapmap];1.00[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs16851892	0.88[CHB][hapmap]
rs1808584	1.00[ASN][1000 genomes]
rs2115935	0.88[CHB][hapmap]
rs2288634	1.00[CHB][hapmap];1.00[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs2288635	1.00[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs2288636	1.00[CHB][hapmap];0.81[JPT][hapmap];1.00[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs34071952	0.83[AFR][1000 genomes]
rs3762726	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs3792411	0.88[CHB][hapmap]
rs3804772	1.00[CHB][hapmap];0.81[JPT][hapmap];1.00[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs3804773	0.88[CHB][hapmap]
rs3828398	1.00[CHB][hapmap];1.00[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs4683412	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4683413	1.00[CEU][hapmap];0.91[EUR][1000 genomes]
rs4683414	0.91[EUR][1000 genomes]
rs4683418	1.00[CEU][hapmap]
rs4683638	0.83[AFR][1000 genomes]
rs4683639	0.88[CHB][hapmap]
rs4683641	0.88[CHB][hapmap]
rs4683649	1.00[AFR][1000 genomes];0.90[EUR][1000 genomes]
rs4683651	1.00[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs4683652	0.90[EUR][1000 genomes]
rs4683659	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap]
rs4683669	1.00[GIH][hapmap]
rs56174413	0.82[AMR][1000 genomes];0.97[ASN][1000 genomes]
rs59122181	0.83[AFR][1000 genomes]
rs745966	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[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	nsv949709	chr3:141295050-142178144	Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	61 gene(s)	inside rSNPs	diseases
2	nsv1013352	chr3:141541105-141870293	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	27 gene(s)	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs11711748	TFDP2	Cis_1M	lymphoblastoid	RTeQTL
rs11711748	ATP1B3	cis	lymphoblastoid	seeQTL

Chromatin state (count:88 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:141621000-141670800	Weak transcription	Small Intestine	intestine
2	chr3:141625600-141668400	Weak transcription	Primary neutrophils fromperipheralblood	blood
3	chr3:141626600-141659000	Weak transcription	Pancreas	Pancrea
4	chr3:141628200-141673600	Weak transcription	Colon Smooth Muscle	Colon
5	chr3:141628600-141669000	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
6	chr3:141628800-141669800	Weak transcription	Fetal Lung	lung
7	chr3:141628800-141674000	Weak transcription	Brain Hippocampus Middle	brain
8	chr3:141629000-141739200	Weak transcription	Psoas Muscle	Psoas
9	chr3:141633000-141659000	Weak transcription	NHLF	lung
10	chr3:141634200-141682000	Weak transcription	Brain Angular Gyrus	brain
11	chr3:141640800-141659200	Weak transcription	Colonic Mucosa	Colon
12	chr3:141640800-141659200	Weak transcription	Rectal Smooth Muscle	rectum
13	chr3:141643000-141675800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr3:141643400-141671200	Weak transcription	Right Ventricle	heart
15	chr3:141644800-141678400	Weak transcription	Primary T helper cells fromperipheralblood	blood
16	chr3:141646800-141659000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr3:141646800-141668200	Weak transcription	H1 Cell Line	embryonic stem cell
18	chr3:141647000-141668400	Weak transcription	HUES48 Cell Line	embryonic stem cell
19	chr3:141647000-141669200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
20	chr3:141647200-141659000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr3:141647200-141669400	Weak transcription	Primary B cells from cord blood	blood
22	chr3:141647400-141668200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
23	chr3:141647400-141670400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chr3:141647600-141659200	Weak transcription	Monocytes-CD14+_RO01746	blood
25	chr3:141647600-141670600	Weak transcription	Duodenum Smooth Muscle	Duodenum
26	chr3:141647800-141659000	Weak transcription	Stomach Smooth Muscle	stomach
27	chr3:141647800-141660800	Weak transcription	Lung	lung
28	chr3:141647800-141664200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr3:141647800-141668200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr3:141647800-141670200	Weak transcription	Adipose Nuclei	Adipose
31	chr3:141648000-141660600	Weak transcription	Gastric	stomach
32	chr3:141648000-141664400	Weak transcription	Primary T cells from cord blood	blood
33	chr3:141648000-141670000	Weak transcription	HUES64 Cell Line	embryonic stem cell
34	chr3:141648000-141670800	Weak transcription	HUES6 Cell Line	embryonic stem cell
35	chr3:141648200-141663400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr3:141648400-141659000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr3:141648600-141660200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
38	chr3:141650000-141664200	Weak transcription	Dnd41	blood
39	chr3:141653200-141664400	Weak transcription	Fetal Stomach	stomach
40	chr3:141653400-141659000	Weak transcription	HSMMtube	muscle
41	chr3:141653400-141664200	Weak transcription	Fetal Muscle Trunk	muscle
42	chr3:141656400-141660200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr3:141656400-141660600	Enhancers	Fetal Brain Male	brain
44	chr3:141656600-141664400	Weak transcription	Esophagus	oesophagus
45	chr3:141656800-141660600	Weak transcription	K562	blood
46	chr3:141656800-141664200	Weak transcription	Thymus	Thymus
47	chr3:141657000-141660800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
48	chr3:141657000-141664600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr3:141657200-141659400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr3:141657200-141659600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin

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