Variant report

Variant	rs10746494
Chromosome Location	chr1:10512390-10512391
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:10512230..10515517-chr1:10533706..10536535,3	K562	blood:
2	chr1:10508493..10514342-chr1:10516490..10519388,5	K562	blood:
3	chr1:10507112..10511032-chr1:10511336..10515640,6	K562	blood:

Variant related genes	Relation type
ENSG00000203469	Chromatin interaction
ENSG00000142655	Chromatin interaction
ENSG00000241563	Chromatin interaction

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs11121579	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1203122	0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12565133	0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1307485	0.84[AFR][1000 genomes];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1307487	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1750349	0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1760664	0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2483684	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2781233	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs36013615	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs475549	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs481571	0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs491880	0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs505141	0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs517241	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs519472	0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs520964	0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs522029	0.90[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs522280	0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs524150	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs528713	0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs579398	0.81[ASN][1000 genomes]
rs583515	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs585703	0.83[ASN][1000 genomes]
rs586223	0.83[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs628462	0.93[ASN][1000 genomes]
rs632690	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs634358	0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs643400	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs649101	0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs649639	0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs655271	0.82[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs663864	0.81[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs666583	0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs667366	0.83[EUR][1000 genomes]
rs670666	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs672606	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs673254	0.81[EUR][1000 genomes]
rs678850	0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs681448	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs681495	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2757722	chr1:10238070-10582554	Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	esv2758920	chr1:10238070-10582554	Strong transcription Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
3	nsv817370	chr1:10305470-10697150	Weak transcription Flanking Active TSS Enhancers Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
4	nsv1008021	chr1:10363794-10802633	Strong transcription Enhancers Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
5	esv2764192	chr1:10383734-10594186	Strong transcription Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
6	nsv1003498	chr1:10445928-10607351	Weak transcription Enhancers Flanking Active TSS Genic enhancers Strong transcription Active TSS Bivalent Enhancer 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	26 gene(s)	inside rSNPs	diseases
7	nsv998731	chr1:10464176-10607351	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
8	esv3416868	chr1:10512210-10512476	Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:96 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:10491400-10519000	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr1:10491400-10521000	Weak transcription	Ovary	ovary
3	chr1:10491400-10521200	Weak transcription	Aorta	Aorta
4	chr1:10491600-10516200	Weak transcription	HMEC	breast
5	chr1:10491600-10517800	Weak transcription	Primary T cells from cord blood	blood
6	chr1:10491600-10518000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr1:10491600-10518000	Weak transcription	Brain Inferior Temporal Lobe	brain
8	chr1:10491600-10519200	Weak transcription	Primary T helper cells PMA-I stimulated	--
9	chr1:10491600-10521200	Weak transcription	Brain Substantia Nigra	brain
10	chr1:10491600-10521200	Weak transcription	Left Ventricle	heart
11	chr1:10491600-10521200	Weak transcription	Sigmoid Colon	Sigmoid Colon
12	chr1:10491600-10521200	Weak transcription	Spleen	Spleen
13	chr1:10491600-10521400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
14	chr1:10491800-10516600	Weak transcription	Primary T helper cells fromperipheralblood	blood
15	chr1:10491800-10516600	Weak transcription	HSMM	muscle
16	chr1:10491800-10520600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr1:10492000-10521200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
18	chr1:10492400-10517200	Weak transcription	Brain Germinal Matrix	brain
19	chr1:10493600-10516800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr1:10494200-10518800	Weak transcription	K562	blood
21	chr1:10494200-10521400	Weak transcription	Primary B cells from peripheral blood	blood
22	chr1:10495400-10519000	Weak transcription	Placenta	Placenta
23	chr1:10499200-10531400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr1:10499400-10519200	Weak transcription	HepG2	liver
25	chr1:10499600-10518200	Weak transcription	Primary B cells from cord blood	blood
26	chr1:10500800-10522800	Weak transcription	Primary hematopoietic stem cells	blood
27	chr1:10501200-10516200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr1:10501200-10519200	Weak transcription	Liver	Liver
29	chr1:10501200-10521400	Weak transcription	Brain Angular Gyrus	brain
30	chr1:10503400-10518000	Weak transcription	Duodenum Mucosa	Duodenum
31	chr1:10503800-10518200	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
32	chr1:10505200-10519200	Weak transcription	Hela-S3	cervix
33	chr1:10505200-10520600	Weak transcription	Lung	lung
34	chr1:10505400-10514600	Weak transcription	Fetal Thymus	thymus
35	chr1:10505400-10518000	Weak transcription	Dnd41	blood
36	chr1:10506000-10514600	Weak transcription	Thymus	Thymus
37	chr1:10507000-10514400	Weak transcription	Fetal Intestine Large	intestine
38	chr1:10507400-10517000	Weak transcription	A549	lung
39	chr1:10508600-10516000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
40	chr1:10508800-10521200	Weak transcription	Pancreas	Pancrea
41	chr1:10509400-10512400	Enhancers	Fetal Brain Male	brain
42	chr1:10509600-10514600	Weak transcription	Fetal Intestine Small	intestine
43	chr1:10509800-10521400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr1:10510000-10512400	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr1:10510600-10514400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr1:10510600-10518000	Weak transcription	H9 Cell Line	embryonic stem cell
47	chr1:10510600-10521200	Weak transcription	Gastric	stomach
48	chr1:10510600-10521400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
49	chr1:10510600-10531600	Weak transcription	Right Atrium	heart
50	chr1:10511000-10512400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links