Variant report

Variant	rs10801591
Chromosome Location	chr1:197084143-197084144
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:197080735..197084388-chr1:197109840..197112878,3	K562	blood:
2	chr1:197082888..197084637-chr1:197110135..197112878,2	K562	blood:
3	chr1:197083131..197085209-chr1:197097769..197099515,2	K562	blood:

Extended variants
information (count: 109 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:101)

rs_ID	r²[population]
rs1034162	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10733087	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10737687	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs10754213	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10754214	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10754215	0.87[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10801587	1.00[EUR][1000 genomes]
rs10801588	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10801590	1.00[EUR][1000 genomes]
rs10922165	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10922166	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10922169	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1115246	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1115247	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1170878	0.86[EUR][1000 genomes]
rs1170880	0.86[EUR][1000 genomes]
rs1170881	0.86[EUR][1000 genomes]
rs1170882	0.86[EUR][1000 genomes]
rs1170883	0.86[EUR][1000 genomes]
rs12039586	0.93[EUR][1000 genomes]
rs12092294	0.86[EUR][1000 genomes]
rs12677	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12731209	0.86[EUR][1000 genomes]
rs1332662	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1332663	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1332669	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1412631	0.86[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1412632	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1412633	1.00[EUR][1000 genomes]
rs1412634	1.00[EUR][1000 genomes]
rs1412639	0.96[EUR][1000 genomes]
rs1537319	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1571964	0.88[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1576878	0.96[EUR][1000 genomes]
rs1627765	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1759006	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1759007	1.00[EUR][1000 genomes]
rs1759008	1.00[EUR][1000 genomes]
rs1759009	1.00[EUR][1000 genomes]
rs1759013	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1794003	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1794010	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1855116	0.86[EUR][1000 genomes]
rs1888991	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1953064	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2026429	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2151133	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2151134	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2151135	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2336595	0.96[EUR][1000 genomes]
rs2336597	0.96[EUR][1000 genomes]
rs3891964	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4342879	0.81[EUR][1000 genomes]
rs4350226	0.81[EUR][1000 genomes]
rs4556392	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs4915148	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4915156	1.00[EUR][1000 genomes]
rs4915313	0.91[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4915315	0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4915316	0.93[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4915327	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4915337	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4915345	0.93[EUR][1000 genomes]
rs5997	0.81[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6003	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6428387	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6656858	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6657171	0.86[EUR][1000 genomes]
rs6657246	0.86[EUR][1000 genomes]
rs6671696	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6677082	0.88[AFR][1000 genomes];0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs6679189	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs6680497	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6685259	1.00[EUR][1000 genomes]
rs6694672	0.86[EUR][1000 genomes]
rs6694853	0.86[EUR][1000 genomes]
rs6695300	0.93[EUR][1000 genomes]
rs6702340	0.86[EUR][1000 genomes]
rs6703400	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7411719	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7516700	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7534353	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7539642	0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7541429	0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs7542397	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7554757	0.91[EUR][1000 genomes]
rs857017	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs857020	0.87[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs857021	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs857022	0.96[EUR][1000 genomes]
rs857023	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs857026	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs857027	0.96[EUR][1000 genomes]
rs865071	0.95[EUR][1000 genomes]
rs877897	0.86[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs928439	0.86[EUR][1000 genomes]
rs928440	0.86[EUR][1000 genomes]
rs9427661	0.86[EUR][1000 genomes]
rs9427662	0.86[EUR][1000 genomes]
rs9427942	0.86[EUR][1000 genomes]
rs9726778	0.86[AFR][1000 genomes];0.84[AMR][1000 genomes];0.83[EUR][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	nsv528460	chr1:196542567-197446702	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers 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 miRNA target site	26 gene(s)	inside rSNPs	diseases
2	esv2758990	chr1:196590837-197169772	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
3	nsv427897	chr1:196590837-197169772	Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
4	esv2757767	chr1:196977799-197169772	Weak transcription Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	8 gene(s)	inside rSNPs	diseases
5	nsv873069	chr1:197055925-197109042	Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv873070	chr1:197079671-197165014	Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Enhancers Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
7	nsv873071	chr1:197079671-197187605	Active TSS Flanking Active TSS Strong transcription Weak transcription Bivalent/Poised TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases
8	nsv873072	chr1:197079671-197221248	Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	12 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:68 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:197052200-197106600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr1:197052200-197114200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr1:197054200-197113600	Weak transcription	Fetal Kidney	kidney
4	chr1:197055000-197114200	Weak transcription	Primary B cells from cord blood	blood
5	chr1:197067000-197092200	Weak transcription	Fetal Intestine Large	intestine
6	chr1:197070600-197100000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr1:197070800-197085400	Weak transcription	Osteobl	bone
8	chr1:197071000-197084400	Weak transcription	Fetal Heart	heart
9	chr1:197071000-197105400	Strong transcription	Dnd41	blood
10	chr1:197071400-197095800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
11	chr1:197071800-197104600	Weak transcription	Rectal Mucosa Donor 31	rectum
12	chr1:197072600-197087400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
13	chr1:197072600-197104600	Strong transcription	Monocytes-CD14+_RO01746	blood
14	chr1:197072600-197107400	Weak transcription	Fetal Intestine Small	intestine
15	chr1:197073000-197104000	Strong transcription	Primary monocytes fromperipheralblood	blood
16	chr1:197073000-197115000	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr1:197073600-197098400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr1:197073800-197085200	Weak transcription	GM12878-XiMat	blood
19	chr1:197073800-197091400	Weak transcription	H9 Cell Line	embryonic stem cell
20	chr1:197074000-197085400	Weak transcription	HepG2	liver
21	chr1:197074000-197115000	Weak transcription	Fetal Brain Male	brain
22	chr1:197074200-197085000	Weak transcription	NHDF-Ad	bronchial
23	chr1:197074200-197091400	Weak transcription	NHEK	skin
24	chr1:197074200-197102000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
25	chr1:197076200-197094000	Weak transcription	Muscle Satellite Cultured Cells	--
26	chr1:197076400-197085200	Weak transcription	NH-A	brain
27	chr1:197076400-197096400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr1:197076600-197084200	Weak transcription	H1 Cell Line	embryonic stem cell
29	chr1:197076600-197085200	Weak transcription	HMEC	breast
30	chr1:197077000-197085400	Weak transcription	K562	blood
31	chr1:197077000-197114200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr1:197077200-197090800	Weak transcription	NHLF	lung
33	chr1:197077800-197084400	Weak transcription	HSMM	muscle
34	chr1:197077800-197084800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr1:197078200-197100400	Weak transcription	Rectal Mucosa Donor 29	rectum
36	chr1:197078600-197084600	Weak transcription	Hela-S3	cervix
37	chr1:197079800-197088200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr1:197080000-197084800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr1:197080400-197088000	Strong transcription	Primary neutrophils fromperipheralblood	blood
40	chr1:197080400-197088400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr1:197080400-197092600	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr1:197080600-197105400	Strong transcription	Fetal Thymus	thymus
43	chr1:197080800-197084200	Weak transcription	Brain Germinal Matrix	brain
44	chr1:197081200-197103000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
45	chr1:197081600-197086800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr1:197081800-197090200	Strong transcription	Primary hematopoietic stem cells	blood
47	chr1:197082000-197094600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr1:197082200-197088400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr1:197082400-197084200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
50	chr1:197082600-197084200	Weak transcription	HUES6 Cell Line	embryonic stem cell

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