Variant report

Variant	rs7579536
Chromosome Location	chr2:180029653-180029654
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:180027947..180030148-chr2:180031681..180034023,3	MCF-7	breast:

Extended variants
information (count: 47 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10170520	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10174774	0.95[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10186198	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10192426	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10205390	0.94[JPT][hapmap]
rs10205999	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10439299	0.84[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10930858	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1158872	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.88[YRI][hapmap];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11884516	0.95[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11894870	0.95[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs11898291	0.95[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12997314	1.00[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs13026497	0.95[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs13383965	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs13391602	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs13418701	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1374378	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1374379	0.85[EUR][1000 genomes]
rs1446674	0.95[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap]
rs1907421	0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1979053	0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2008989	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2008999	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2289992	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2847	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[EUR][1000 genomes]
rs4585064	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6433757	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6433760	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AFR][1000 genomes];0.95[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs6433761	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6433764	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[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]
rs6433769	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6707081	0.95[CEU][hapmap];1.00[CHB][hapmap];0.89[JPT][hapmap];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6734121	0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6736098	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6742739	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6743405	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6756326	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7562730	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7585600	0.95[CEU][hapmap];0.90[CHB][hapmap];0.94[JPT][hapmap];0.82[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7608882	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9288022	0.89[EUR][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	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
5	esv1807721	chr2:180024167-180076733	Strong transcription Enhancers ZNF genes & repeats Weak transcription Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs7579536	SESTD1	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:86 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:179973400-180030200	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr2:179975800-180047600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
3	chr2:179977400-180049000	Weak transcription	HSMMtube	muscle
4	chr2:179980000-180038800	Weak transcription	HMEC	breast
5	chr2:179980000-180056800	Weak transcription	HSMM	muscle
6	chr2:179986600-180030400	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr2:179991600-180043200	Weak transcription	Psoas Muscle	Psoas
8	chr2:179996200-180047600	Weak transcription	NH-A	brain
9	chr2:179998000-180060600	Weak transcription	Right Ventricle	heart
10	chr2:180002400-180030200	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr2:180003200-180039800	Weak transcription	Brain Germinal Matrix	brain
12	chr2:180004800-180046000	Weak transcription	Spleen	Spleen
13	chr2:180005600-180040200	Weak transcription	Brain Cingulate Gyrus	brain
14	chr2:180005600-180044400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
15	chr2:180005600-180044400	Weak transcription	Esophagus	oesophagus
16	chr2:180005800-180030200	Weak transcription	Thymus	Thymus
17	chr2:180005800-180043200	Weak transcription	Fetal Brain Male	brain
18	chr2:180005800-180053600	Weak transcription	Primary T cells from cord blood	blood
19	chr2:180006000-180030600	Weak transcription	Fetal Muscle Trunk	muscle
20	chr2:180006000-180044600	Weak transcription	Pancreas	Pancrea
21	chr2:180006200-180031400	Weak transcription	Brain Hippocampus Middle	brain
22	chr2:180006200-180031400	Weak transcription	Fetal Brain Female	brain
23	chr2:180006400-180030200	Weak transcription	Fetal Muscle Leg	muscle
24	chr2:180006600-180042000	Weak transcription	Brain Substantia Nigra	brain
25	chr2:180006600-180051000	Weak transcription	HUVEC	blood vessel
26	chr2:180006800-180031600	Weak transcription	Brain Anterior Caudate	brain
27	chr2:180006800-180054600	Weak transcription	Rectal Mucosa Donor 31	rectum
28	chr2:180007400-180035200	Weak transcription	Colon Smooth Muscle	Colon
29	chr2:180007400-180035600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
30	chr2:180007400-180042200	Weak transcription	Brain Angular Gyrus	brain
31	chr2:180007400-180043000	Weak transcription	Aorta	Aorta
32	chr2:180007600-180030400	Weak transcription	Cortex derived primary cultured neurospheres	brain
33	chr2:180007600-180031000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr2:180007600-180031200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
35	chr2:180008400-180030600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
36	chr2:180008400-180042200	Weak transcription	Brain Inferior Temporal Lobe	brain
37	chr2:180008600-180037600	Weak transcription	Fetal Thymus	thymus
38	chr2:180008600-180038400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
39	chr2:180008600-180048400	Weak transcription	Small Intestine	intestine
40	chr2:180011800-180039400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr2:180013200-180044400	Weak transcription	Fetal Kidney	kidney
42	chr2:180015000-180041600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
43	chr2:180015000-180043200	Weak transcription	Gastric	stomach
44	chr2:180015000-180054800	Weak transcription	Skeletal Muscle Male	skeletal muscle
45	chr2:180015000-180056000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr2:180015000-180060600	Weak transcription	Lung	lung
47	chr2:180015200-180039600	Weak transcription	Fetal Lung	lung
48	chr2:180015200-180046200	Weak transcription	Stomach Smooth Muscle	stomach
49	chr2:180015200-180047200	Weak transcription	Placenta	Placenta
50	chr2:180015400-180035400	Weak transcription	Ovary	ovary

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