Variant report

Variant	rs13396334
Chromosome Location	chr2:180002049-180002050
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 41 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs10084229	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10084475	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10170430	0.82[AFR][1000 genomes];0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10196577	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10205477	0.85[ASN][1000 genomes]
rs10208593	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10439300	0.92[CEU][hapmap];0.89[JPT][hapmap]
rs10803924	0.91[CEU][hapmap];0.88[JPT][hapmap]
rs10930855	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[YRI][hapmap];0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs10930856	1.00[CHB][hapmap];0.82[JPT][hapmap];0.88[ASN][1000 genomes]
rs10930857	0.84[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12621023	0.89[JPT][hapmap]
rs12693175	1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[YRI][hapmap];1.00[ASN][1000 genomes]
rs12997079	1.00[CHB][hapmap];0.88[JPT][hapmap]
rs13021442	0.87[ASN][1000 genomes]
rs13022867	1.00[CHB][hapmap];0.85[JPT][hapmap];0.85[ASN][1000 genomes]
rs13029576	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs13403231	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13404037	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs13420572	0.98[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17363260	1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[YRI][hapmap];1.00[ASN][1000 genomes]
rs17363267	1.00[CHB][hapmap];0.89[JPT][hapmap];1.00[ASN][1000 genomes]
rs17454311	0.89[JPT][hapmap]
rs1900338	1.00[ASN][1000 genomes]
rs2289993	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2289994	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28763731	0.88[ASN][1000 genomes]
rs340320	1.00[CHB][hapmap];0.84[JPT][hapmap]
rs340332	0.89[JPT][hapmap]
rs340334	0.89[JPT][hapmap]
rs34728717	1.00[ASN][1000 genomes]
rs55750558	0.89[AFR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs56109193	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56181927	0.88[ASN][1000 genomes]
rs67028844	0.88[ASN][1000 genomes]
rs67312569	0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9288025	0.89[JPT][hapmap]

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	nsv949133	chr2:179711376-180124327	Flanking Active TSS ZNF genes & repeats Active TSS Enhancers Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	5 gene(s)	inside rSNPs	diseases
2	nsv1004693	chr2:179933683-180265288	Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
3	nsv834471	chr2:179974303-180123027	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region miRNA target site	2 gene(s)	inside rSNPs	diseases
4	nsv3060	chr2:179990791-180035511	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs13396334	SESTD1	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:100 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:179967800-180004400	Weak transcription	Esophagus	oesophagus
2	chr2:179970000-180004400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr2:179971600-180012600	Weak transcription	Placenta Amnion	Placenta Amnion
4	chr2:179972000-180005200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr2:179972000-180005200	Weak transcription	Rectal Smooth Muscle	rectum
6	chr2:179972800-180014600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr2:179973000-180007200	Weak transcription	GM12878-XiMat	blood
8	chr2:179973400-180004400	Weak transcription	Pancreas	Pancrea
9	chr2:179973400-180006800	Weak transcription	Small Intestine	intestine
10	chr2:179973400-180012600	Weak transcription	NHLF	lung
11	chr2:179973400-180030200	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr2:179975800-180047600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
13	chr2:179976000-180004400	Weak transcription	Aorta	Aorta
14	chr2:179977400-180004400	Weak transcription	Lung	lung
15	chr2:179977400-180005000	Weak transcription	Fetal Kidney	kidney
16	chr2:179977400-180049000	Weak transcription	HSMMtube	muscle
17	chr2:179978200-180014600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr2:179978800-180004400	Weak transcription	Spleen	Spleen
19	chr2:179980000-180038800	Weak transcription	HMEC	breast
20	chr2:179980000-180056800	Weak transcription	HSMM	muscle
21	chr2:179980400-180005200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
22	chr2:179980400-180005600	Weak transcription	Primary T cells fromperipheralblood	blood
23	chr2:179981400-180005000	Weak transcription	Ovary	ovary
24	chr2:179981400-180016800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr2:179981600-180004400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr2:179981600-180005000	Weak transcription	Duodenum Mucosa	Duodenum
27	chr2:179981800-180005400	Weak transcription	Osteobl	bone
28	chr2:179982400-180004400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr2:179982800-180004400	Weak transcription	Primary neutrophils fromperipheralblood	blood
30	chr2:179982800-180004600	Weak transcription	Fetal Brain Male	brain
31	chr2:179983600-180005000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
32	chr2:179984600-180003000	Weak transcription	Fetal Lung	lung
33	chr2:179984600-180004600	Weak transcription	HUVEC	blood vessel
34	chr2:179984800-180004200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr2:179984800-180005200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr2:179985000-180025600	Weak transcription	Fetal Intestine Small	intestine
37	chr2:179985200-180004400	Weak transcription	Fetal Muscle Trunk	muscle
38	chr2:179985200-180004400	Weak transcription	Fetal Stomach	stomach
39	chr2:179985400-180004000	Weak transcription	Dnd41	blood
40	chr2:179985600-180005800	Weak transcription	Skeletal Muscle Female	skeletal muscle
41	chr2:179985800-180004000	Weak transcription	Fetal Intestine Large	intestine
42	chr2:179985800-180004400	Weak transcription	Fetal Brain Female	brain
43	chr2:179985800-180004400	Weak transcription	Left Ventricle	heart
44	chr2:179985800-180005800	Weak transcription	Skeletal Muscle Male	skeletal muscle
45	chr2:179985800-180010200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr2:179986000-180004400	Weak transcription	Liver	Liver
47	chr2:179986200-180006000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
48	chr2:179986600-180030400	Weak transcription	HUES64 Cell Line	embryonic stem cell
49	chr2:179988600-180003400	Weak transcription	Fetal Muscle Leg	muscle
50	chr2:179990000-180004400	Weak transcription	Muscle Satellite Cultured Cells	--

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