Variant report

Variant	rs10196577
Chromosome Location	chr2:180100584-180100585
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	chr2:180099965..180101717-chr2:180103234..180105570,2	K562	blood:
2	chr2:180099014..180101971-chr2:180103448..180105283,2	MCF-7	breast:

Extended variants
information (count: 36 )
Associated
traits (count: 1 )

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

rs_ID	r²[population]
rs10084229	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10084475	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10170430	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10194534	0.82[AFR][1000 genomes]
rs10197425	0.91[ASN][1000 genomes]
rs10205477	0.82[ASN][1000 genomes]
rs10208593	0.97[ASN][1000 genomes]
rs10930855	0.84[EUR][1000 genomes]
rs10930856	0.85[ASN][1000 genomes]
rs10930857	0.96[AFR][1000 genomes];0.97[ASN][1000 genomes]
rs12621023	0.91[AFR][1000 genomes]
rs12693180	0.94[ASN][1000 genomes]
rs12989055	0.94[ASN][1000 genomes]
rs13022867	0.82[ASN][1000 genomes]
rs13029576	0.85[ASN][1000 genomes]
rs13389956	0.83[AFR][1000 genomes];0.94[ASN][1000 genomes]
rs13396334	0.87[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs13403231	0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13404037	0.85[ASN][1000 genomes]
rs13420572	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs13420582	0.97[AFR][1000 genomes];0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs13427714	0.81[ASN][1000 genomes]
rs2289993	0.83[EUR][1000 genomes]
rs2289994	0.83[EUR][1000 genomes]
rs28763731	0.85[ASN][1000 genomes]
rs35539795	0.83[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs56109193	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs56181927	0.85[ASN][1000 genomes]
rs58887763	0.82[AFR][1000 genomes]
rs67028844	0.85[ASN][1000 genomes]
rs9288025	0.96[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 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	esv1798738	chr2:180084168-180100584	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv834472	chr2:180091670-180220448	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10196577	SESTD1	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:80 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:180067600-180104600	Weak transcription	Fetal Kidney	kidney
2	chr2:180068000-180103800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr2:180083800-180102200	Weak transcription	HMEC	breast
4	chr2:180089600-180115200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr2:180089800-180102000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
6	chr2:180090000-180102000	Weak transcription	Fetal Muscle Leg	muscle
7	chr2:180090600-180102000	Weak transcription	Psoas Muscle	Psoas
8	chr2:180090600-180102400	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr2:180091200-180102400	Weak transcription	Left Ventricle	heart
10	chr2:180091200-180104600	Weak transcription	Right Ventricle	heart
11	chr2:180091800-180100600	Weak transcription	Brain Angular Gyrus	brain
12	chr2:180091800-180101800	Weak transcription	Pancreatic Islets	Pancreatic Islet
13	chr2:180091800-180102000	Weak transcription	Fetal Brain Male	brain
14	chr2:180091800-180102200	Weak transcription	Fetal Brain Female	brain
15	chr2:180091800-180102200	Weak transcription	Fetal Heart	heart
16	chr2:180091800-180102400	Weak transcription	Colon Smooth Muscle	Colon
17	chr2:180091800-180127200	Weak transcription	Fetal Lung	lung
18	chr2:180092000-180102800	Weak transcription	Fetal Intestine Large	intestine
19	chr2:180092200-180101800	Weak transcription	HUES64 Cell Line	embryonic stem cell
20	chr2:180092200-180102400	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
21	chr2:180092600-180100600	Weak transcription	Aorta	Aorta
22	chr2:180092800-180100600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
23	chr2:180092800-180102000	Weak transcription	Right Atrium	heart
24	chr2:180092800-180102000	Weak transcription	NHLF	lung
25	chr2:180092800-180104600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr2:180092800-180112400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr2:180093000-180107800	Weak transcription	Cortex derived primary cultured neurospheres	brain
28	chr2:180094000-180102000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr2:180094200-180100600	Weak transcription	H9 Cell Line	embryonic stem cell
30	chr2:180094200-180102000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr2:180095200-180104000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr2:180095400-180101800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
33	chr2:180096800-180102200	Weak transcription	HUVEC	blood vessel
34	chr2:180097000-180102800	Weak transcription	Fetal Intestine Small	intestine
35	chr2:180097200-180103600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr2:180098000-180100600	Enhancers	Primary neutrophils fromperipheralblood	blood
37	chr2:180098000-180103400	Enhancers	HepG2	liver
38	chr2:180098000-180105200	Weak transcription	Fetal Thymus	thymus
39	chr2:180098200-180102600	Weak transcription	Primary T cells from cord blood	blood
40	chr2:180098600-180101000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr2:180098600-180102200	Weak transcription	Duodenum Smooth Muscle	Duodenum
42	chr2:180098600-180102400	Weak transcription	Duodenum Mucosa	Duodenum
43	chr2:180098600-180118600	Weak transcription	Pancreas	Pancrea
44	chr2:180098800-180101800	Weak transcription	A549	lung
45	chr2:180098800-180102400	Weak transcription	Stomach Smooth Muscle	stomach
46	chr2:180099000-180100600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr2:180099000-180103400	Weak transcription	Gastric	stomach
48	chr2:180099000-180103800	Weak transcription	Primary B cells from cord blood	blood
49	chr2:180099800-180100800	Enhancers	Brain Substantia Nigra	brain
50	chr2:180099800-180102600	Weak transcription	GM12878-XiMat	blood

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