Variant report

Variant	rs17363267
Chromosome Location	chr2:179992205-179992206
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	POLR2A	chr2:179991457-179993112	HepG2	liver:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:179990644..179992721-chr2:180003873..180005520,2	K562	blood:

Variant related genes	Relation type
ENSG00000238339	TF binding region
SESTD1	TF binding region

Extended variants
information (count: 35 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs10084229	1.00[CHB][hapmap];0.89[JPT][hapmap];1.00[ASN][1000 genomes]
rs10084475	1.00[ASN][1000 genomes]
rs10166788	0.88[CEU][hapmap]
rs10197425	0.80[YRI][hapmap]
rs10205477	0.85[ASN][1000 genomes]
rs10208593	1.00[CHB][hapmap];0.89[JPT][hapmap]
rs10930855	1.00[CHB][hapmap];0.89[JPT][hapmap];0.94[ASN][1000 genomes]
rs10930856	1.00[CHB][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10930857	1.00[CHB][hapmap];0.86[JPT][hapmap]
rs12693175	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12693180	0.81[EUR][1000 genomes]
rs12997079	0.88[CEU][hapmap];1.00[CHB][hapmap]
rs13021442	0.87[ASN][1000 genomes]
rs13022867	0.82[CEU][hapmap];1.00[CHB][hapmap];0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13029576	1.00[CEU][hapmap];1.00[CHB][hapmap];0.88[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13396334	1.00[CHB][hapmap];0.89[JPT][hapmap];1.00[ASN][1000 genomes]
rs13403231	0.88[ASN][1000 genomes]
rs13404037	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13420572	1.00[ASN][1000 genomes]
rs17363260	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][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]
rs1900338	1.00[ASN][1000 genomes]
rs2289993	1.00[CHB][hapmap];0.89[JPT][hapmap];1.00[ASN][1000 genomes]
rs2289994	1.00[CHB][hapmap];0.89[JPT][hapmap];1.00[ASN][1000 genomes]
rs28763731	0.88[ASN][1000 genomes]
rs340320	1.00[CHB][hapmap]
rs34728717	1.00[ASN][1000 genomes]
rs55750558	0.82[ASN][1000 genomes]
rs56109193	1.00[ASN][1000 genomes]
rs56181927	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs67028844	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs67312569	0.82[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	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
rs17363267	SESTD1	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:89 , 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	chr2:179972600-180001800	Weak transcription	NHEK	skin
7	chr2:179972800-180014600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
8	chr2:179973000-180007200	Weak transcription	GM12878-XiMat	blood
9	chr2:179973400-180004400	Weak transcription	Pancreas	Pancrea
10	chr2:179973400-180006800	Weak transcription	Small Intestine	intestine
11	chr2:179973400-180012600	Weak transcription	NHLF	lung
12	chr2:179973400-180030200	Weak transcription	Sigmoid Colon	Sigmoid Colon
13	chr2:179974400-179994200	Strong transcription	HepG2	liver
14	chr2:179975800-180047600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
15	chr2:179976000-180004400	Weak transcription	Aorta	Aorta
16	chr2:179977400-180004400	Weak transcription	Lung	lung
17	chr2:179977400-180005000	Weak transcription	Fetal Kidney	kidney
18	chr2:179977400-180049000	Weak transcription	HSMMtube	muscle
19	chr2:179977600-180002000	Weak transcription	Rectal Mucosa Donor 31	rectum
20	chr2:179978200-180014600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr2:179978800-180004400	Weak transcription	Spleen	Spleen
22	chr2:179980000-180038800	Weak transcription	HMEC	breast
23	chr2:179980000-180056800	Weak transcription	HSMM	muscle
24	chr2:179980400-180005200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
25	chr2:179980400-180005600	Weak transcription	Primary T cells fromperipheralblood	blood
26	chr2:179981400-180001800	Weak transcription	Placenta	Placenta
27	chr2:179981400-180005000	Weak transcription	Ovary	ovary
28	chr2:179981400-180016800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
29	chr2:179981600-179997600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
30	chr2:179981600-180004400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr2:179981600-180005000	Weak transcription	Duodenum Mucosa	Duodenum
32	chr2:179981800-180005400	Weak transcription	Osteobl	bone
33	chr2:179982400-180004400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr2:179982800-180004400	Weak transcription	Primary neutrophils fromperipheralblood	blood
35	chr2:179982800-180004600	Weak transcription	Fetal Brain Male	brain
36	chr2:179983600-180005000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
37	chr2:179984600-180003000	Weak transcription	Fetal Lung	lung
38	chr2:179984600-180004600	Weak transcription	HUVEC	blood vessel
39	chr2:179984800-180002000	Weak transcription	Colon Smooth Muscle	Colon
40	chr2:179984800-180004200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr2:179984800-180005200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr2:179985000-180025600	Weak transcription	Fetal Intestine Small	intestine
43	chr2:179985200-180004400	Weak transcription	Fetal Muscle Trunk	muscle
44	chr2:179985200-180004400	Weak transcription	Fetal Stomach	stomach
45	chr2:179985400-180004000	Weak transcription	Dnd41	blood
46	chr2:179985600-179996200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr2:179985600-180005800	Weak transcription	Skeletal Muscle Female	skeletal muscle
48	chr2:179985800-180004000	Weak transcription	Fetal Intestine Large	intestine
49	chr2:179985800-180004400	Weak transcription	Fetal Brain Female	brain
50	chr2:179985800-180004400	Weak transcription	Left Ventricle	heart

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links