Variant report

Variant	rs2762859
Chromosome Location	chr1:179938798-179938799
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	chr1:179921069..179927710-chr1:179937007..179944258,10	K562	blood:
2	chr1:179937946..179940776-chr1:179952862..179955374,2	K562	blood:

Variant related genes	Relation type
ENSG00000260360	Chromatin interaction
ENSG00000135837	Chromatin interaction

Extended variants
information (count: 99 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:95)

rs_ID	r²[population]
rs10753206	0.80[CEU][hapmap];0.90[MEX][hapmap];0.84[TSI][hapmap]
rs10798729	1.00[ASW][hapmap];0.92[CEU][hapmap];0.88[CHB][hapmap];0.94[CHD][hapmap];0.97[GIH][hapmap];0.96[LWK][hapmap];0.90[MEX][hapmap];1.00[MKK][hapmap];0.98[TSI][hapmap];1.00[YRI][hapmap];0.82[EUR][1000 genomes]
rs10798732	0.88[CEU][hapmap]
rs10913916	0.82[CHB][hapmap];0.93[JPT][hapmap]
rs10913917	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]
rs10913918	0.94[JPT][hapmap]
rs10913927	0.94[ASW][hapmap];1.00[CEU][hapmap];0.94[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];0.87[JPT][hapmap];0.96[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.98[TSI][hapmap];1.00[YRI][hapmap];0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12040314	0.88[CEU][hapmap]
rs12040376	0.88[CEU][hapmap]
rs12075450	0.81[JPT][hapmap]
rs1281384	0.81[JPT][hapmap]
rs1281389	0.81[JPT][hapmap]
rs1292777	0.98[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1297205	0.92[CEU][hapmap];0.87[JPT][hapmap];0.91[YRI][hapmap];0.80[AFR][1000 genomes];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1631932	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1981314	0.81[JPT][hapmap]
rs2281805	0.81[JPT][hapmap]
rs2319676	0.84[JPT][hapmap]
rs2477106	0.94[JPT][hapmap]
rs2477110	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2477111	0.94[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2477112	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2477116	0.82[AFR][1000 genomes];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2477117	0.81[JPT][hapmap]
rs2477118	0.94[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.96[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2477119	0.93[JPT][hapmap]
rs2477120	0.83[AFR][1000 genomes];0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2483621	0.95[EUR][1000 genomes]
rs2483622	0.94[JPT][hapmap]
rs2501607	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];0.94[JPT][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.98[TSI][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2501608	0.94[JPT][hapmap]
rs2501610	0.90[AFR][1000 genomes];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2501611	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.89[AFR][1000 genomes];0.85[AMR][1000 genomes];0.92[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2501613	0.94[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.96[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.98[TSI][hapmap];1.00[YRI][hapmap]
rs2501615	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AFR][1000 genomes];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2501616	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2501617	0.94[ASW][hapmap];0.92[CEU][hapmap];0.94[CHB][hapmap];0.94[CHD][hapmap];0.97[GIH][hapmap];0.94[JPT][hapmap];0.96[LWK][hapmap];0.90[MEX][hapmap];1.00[MKK][hapmap];0.98[TSI][hapmap];1.00[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2501620	0.97[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2501621	0.82[CHB][hapmap];0.94[JPT][hapmap]
rs3767200	0.80[EUR][1000 genomes]
rs3767201	0.81[JPT][hapmap]
rs3767202	0.81[EUR][1000 genomes]
rs3818999	0.94[ASW][hapmap];0.96[CEU][hapmap];0.88[CHB][hapmap];0.94[CHD][hapmap];0.97[GIH][hapmap];0.96[LWK][hapmap];0.90[MEX][hapmap];1.00[MKK][hapmap];0.98[TSI][hapmap];1.00[YRI][hapmap];0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3930305	1.00[CEU][hapmap];0.94[CHB][hapmap];0.87[JPT][hapmap];1.00[YRI][hapmap];0.82[EUR][1000 genomes]
rs4076449	0.94[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.97[GIH][hapmap];0.87[JPT][hapmap];0.92[LWK][hapmap];0.95[MKK][hapmap];0.93[TSI][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4147169	0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4256775	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[JPT][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4263962	0.88[CHB][hapmap];0.81[JPT][hapmap]
rs4336810	0.88[CEU][hapmap];0.95[MEX][hapmap];0.88[TSI][hapmap]
rs4379644	0.81[JPT][hapmap]
rs4506429	0.88[CEU][hapmap]
rs4651054	0.85[EUR][1000 genomes]
rs4651055	0.81[JPT][hapmap]
rs4652457	1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4652462	0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4652463	0.82[EUR][1000 genomes]
rs4652465	1.00[CEU][hapmap];0.94[CHB][hapmap];0.87[JPT][hapmap];1.00[YRI][hapmap];0.81[EUR][1000 genomes]
rs4652470	0.80[TSI][hapmap]
rs4652471	0.88[CEU][hapmap]
rs483307	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs498625	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs500371	0.88[CEU][hapmap];0.87[JPT][hapmap];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs504202	0.81[JPT][hapmap]
rs510209	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]
rs521858	0.81[JPT][hapmap]
rs526683	0.86[JPT][hapmap]
rs528350	0.83[ASW][hapmap];0.92[CEU][hapmap];0.89[GIH][hapmap];0.87[JPT][hapmap];0.81[LWK][hapmap];0.95[MEX][hapmap];0.89[TSI][hapmap];0.87[YRI][hapmap];0.80[AFR][1000 genomes];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs533795	0.81[CEU][hapmap];0.81[JPT][hapmap];0.83[EUR][1000 genomes]
rs534168	0.92[CEU][hapmap];0.87[JPT][hapmap];0.91[YRI][hapmap];0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs551607	0.81[JPT][hapmap]
rs552743	0.81[JPT][hapmap]
rs561233	0.81[JPT][hapmap]
rs6425603	1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];0.87[JPT][hapmap];0.98[TSI][hapmap];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6425609	0.96[CEU][hapmap];0.89[GIH][hapmap];0.95[MEX][hapmap];0.84[MKK][hapmap];0.93[TSI][hapmap]
rs6657347	0.94[ASW][hapmap];1.00[CEU][hapmap];0.94[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];0.87[JPT][hapmap];0.95[MEX][hapmap];0.98[MKK][hapmap];0.98[TSI][hapmap];0.81[EUR][1000 genomes]
rs6660984	0.87[JPT][hapmap]
rs6676989	0.80[JPT][hapmap]
rs6691435	0.88[CEU][hapmap];0.95[MEX][hapmap];0.91[TSI][hapmap]
rs6692394	0.82[CHB][hapmap];0.81[JPT][hapmap]
rs7521895	0.81[JPT][hapmap]
rs7521948	0.81[JPT][hapmap]
rs7524849	0.85[AFR][1000 genomes];0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs7551181	0.91[CEU][hapmap]
rs9286932	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];0.87[JPT][hapmap];1.00[LWK][hapmap];1.00[MKK][hapmap];0.98[TSI][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9425481	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs9425482	0.81[EUR][1000 genomes]
rs9425485	0.88[CEU][hapmap];0.89[GIH][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap]
rs9425849	1.00[CEU][hapmap];1.00[CHB][hapmap];0.87[JPT][hapmap];1.00[YRI][hapmap];0.81[AFR][1000 genomes];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9425851	0.84[EUR][1000 genomes]
rs9425853	0.81[JPT][hapmap]
rs9425854	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];0.87[JPT][hapmap];0.96[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.98[TSI][hapmap];1.00[YRI][hapmap];0.83[AFR][1000 genomes];0.82[AMR][1000 genomes];0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9425855	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9425856	0.80[AMR][1000 genomes];0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9425861	1.00[ASW][hapmap];0.96[CEU][hapmap];0.94[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];0.87[JPT][hapmap];0.83[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.98[TSI][hapmap];0.88[YRI][hapmap];0.82[EUR][1000 genomes]
rs9425868	0.88[CEU][hapmap];0.95[MEX][hapmap];0.91[TSI][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	nsv429936	chr1:179790343-180214343	Active TSS Strong transcription Flanking Active TSS Weak transcription Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	72 gene(s)	inside rSNPs	diseases
2	esv1815608	chr1:179813499-180067988	Strong transcription Enhancers Flanking Active TSS Active TSS Weak transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
3	nsv429958	chr1:179814306-179994628	Genic enhancers Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	48 gene(s)	inside rSNPs	diseases
4	nsv872573	chr1:179929388-180093066	Weak transcription Strong transcription Enhancers Genic enhancers ZNF genes & repeats Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs2762859	ASTN1	cis	cerebellum	SCAN

Chromatin state (count:102 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:179924800-179963600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr1:179925200-179946200	Weak transcription	Stomach Mucosa	stomach
3	chr1:179925400-179946000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
4	chr1:179925800-179940600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
5	chr1:179926800-179961400	Weak transcription	A549	lung
6	chr1:179927000-179965600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
7	chr1:179927200-179940600	Weak transcription	NHDF-Ad	bronchial
8	chr1:179928000-179939000	Weak transcription	Fetal Heart	heart
9	chr1:179934600-179939200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr1:179934600-179945000	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr1:179936000-179946400	Weak transcription	NHLF	lung
12	chr1:179936200-179939200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
13	chr1:179936200-179946000	Weak transcription	Fetal Lung	lung
14	chr1:179936200-179946000	Weak transcription	HepG2	liver
15	chr1:179936400-179955600	Weak transcription	Dnd41	blood
16	chr1:179936600-179958800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr1:179937200-179938800	Weak transcription	GM12878-XiMat	blood
18	chr1:179937200-179941200	Enhancers	Brain Inferior Temporal Lobe	brain
19	chr1:179937400-179941200	Enhancers	Primary T helper cells PMA-I stimulated	--
20	chr1:179937600-179939200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr1:179937600-179939800	Enhancers	Primary T killer memory cells from peripheral blood	blood
22	chr1:179937600-179939800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
23	chr1:179937600-179939800	Enhancers	Duodenum Smooth Muscle	Duodenum
24	chr1:179937600-179941400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
25	chr1:179937600-179941400	Enhancers	Brain Hippocampus Middle	brain
26	chr1:179937800-179938800	Genic enhancers	Primary hematopoietic stem cells short term culture	blood
27	chr1:179937800-179938800	Strong transcription	Fetal Intestine Large	intestine
28	chr1:179937800-179938800	Enhancers	Right Ventricle	heart
29	chr1:179937800-179939000	Genic enhancers	Primary T cells fromperipheralblood	blood
30	chr1:179937800-179939000	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
31	chr1:179937800-179939000	Enhancers	Left Ventricle	heart
32	chr1:179937800-179939000	Enhancers	Psoas Muscle	Psoas
33	chr1:179937800-179939200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
34	chr1:179937800-179939400	Enhancers	Primary monocytes fromperipheralblood	blood
35	chr1:179937800-179939400	Enhancers	Monocytes-CD14+_RO01746	blood
36	chr1:179937800-179939600	Enhancers	Primary neutrophils fromperipheralblood	blood
37	chr1:179937800-179939800	Enhancers	Primary T helper naive cells from peripheral blood	blood
38	chr1:179937800-179940000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
39	chr1:179937800-179941400	Enhancers	Skeletal Muscle Male	skeletal muscle
40	chr1:179937800-179941600	Enhancers	Brain Angular Gyrus	brain
41	chr1:179937800-179941600	Enhancers	Brain Anterior Caudate	brain
42	chr1:179937800-179946200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr1:179938000-179938800	Genic enhancers	Primary B cells from cord blood	blood
44	chr1:179938000-179938800	Enhancers	Primary B cells from peripheral blood	blood
45	chr1:179938000-179938800	Strong transcription	Rectal Mucosa Donor 29	rectum
46	chr1:179938000-179939000	Genic enhancers	Fetal Muscle Leg	muscle
47	chr1:179938000-179939200	Genic enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
48	chr1:179938000-179939200	Enhancers	Right Atrium	heart
49	chr1:179938000-179939800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr1:179938000-179939800	Enhancers	Colon Smooth Muscle	Colon

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