Variant report

Variant	rs10775165
Chromosome Location	chr15:57801339-57801340
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr15:57801026..57803220-chr15:57837290..57839682,2	K562	blood:

Extended variants
information (count: 68 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:63)

rs_ID	r²[population]
rs10220805	1.00[CEU][hapmap];0.96[CHB][hapmap];0.91[JPT][hapmap];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10518923	0.91[CEU][hapmap];0.87[CHB][hapmap];0.86[JPT][hapmap];0.89[EUR][1000 genomes]
rs10851614	0.91[CEU][hapmap];0.87[CHB][hapmap];0.91[JPT][hapmap];0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10851615	0.92[CEU][hapmap];1.00[CHB][hapmap];0.96[JPT][hapmap];0.95[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10851616	1.00[CEU][hapmap];0.96[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10851617	0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11071323	0.91[CEU][hapmap];0.87[CHB][hapmap];0.95[JPT][hapmap];0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11071324	1.00[CEU][hapmap];1.00[CHB][hapmap];0.96[JPT][hapmap];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11071325	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11071326	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11630712	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11630713	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11630740	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11631943	0.85[CEU][hapmap];0.87[CHB][hapmap];0.82[JPT][hapmap];0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs11634739	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11635065	0.87[ASN][1000 genomes]
rs11637220	0.84[CEU][hapmap];0.87[CHB][hapmap];0.87[JPT][hapmap];0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs11637265	0.91[EUR][1000 genomes]
rs12323972	1.00[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12437888	0.91[CEU][hapmap];0.87[CHB][hapmap];0.86[JPT][hapmap];0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12438901	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12439099	1.00[CEU][hapmap];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12439126	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12440928	0.85[CEU][hapmap];0.88[EUR][1000 genomes]
rs12441608	0.82[EUR][1000 genomes]
rs12442969	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12592077	0.91[CEU][hapmap];0.90[CHB][hapmap];0.89[JPT][hapmap];0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12593650	1.00[CEU][hapmap];0.81[CHB][hapmap];0.86[JPT][hapmap];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12593685	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12593721	0.92[CEU][hapmap];0.84[CHB][hapmap];0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs12594455	0.90[EUR][1000 genomes]
rs12594504	0.85[CEU][hapmap];0.90[EUR][1000 genomes]
rs12595135	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12595169	1.00[CEU][hapmap];0.96[CHB][hapmap];0.91[JPT][hapmap];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1280387	0.92[CEU][hapmap];0.80[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1666567	0.82[JPT][hapmap];0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs16977531	0.85[CEU][hapmap];0.87[CHB][hapmap];0.82[JPT][hapmap];0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs16977534	0.91[CEU][hapmap];0.87[CHB][hapmap];0.91[JPT][hapmap];0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs16977558	1.00[CEU][hapmap];0.83[CHB][hapmap];0.91[JPT][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs16977560	1.00[CEU][hapmap];0.83[CHB][hapmap];0.91[JPT][hapmap];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs16977561	1.00[CEU][hapmap];0.83[CHB][hapmap];0.91[JPT][hapmap];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs16977567	0.91[JPT][hapmap];0.86[AMR][1000 genomes];0.87[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1980048	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1994888	0.92[CEU][hapmap];0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1994889	0.92[CEU][hapmap];0.86[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2087981	0.92[EUR][1000 genomes]
rs2131740	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2172613	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2172614	0.88[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2414510	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2942043	0.91[CEU][hapmap];0.89[EUR][1000 genomes]
rs4545749	1.00[CEU][hapmap];0.96[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs58161678	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs58253526	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7164486	0.92[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7167112	0.84[CEU][hapmap];0.83[ASN][1000 genomes]
rs7496403	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs878425	0.83[JPT][hapmap]
rs932028	0.91[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.80[AMR][1000 genomes];0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs932029	0.83[CEU][hapmap];0.84[EUR][1000 genomes]
rs955206	0.92[CEU][hapmap];0.84[CHB][hapmap];0.91[JPT][hapmap];0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs966693	0.83[JPT][hapmap];0.82[EUR][1000 genomes]
rs9806311	0.85[CEU][hapmap];0.90[AMR][1000 genomes];0.83[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	nsv1045611	chr15:57350965-58070807	Weak transcription Enhancers Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
2	nsv1054547	chr15:57600488-57977659	Active TSS Weak transcription Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
3	nsv833022	chr15:57657412-57830112	Weak transcription Enhancers Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1045620	chr15:57680733-57804237	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv904255	chr15:57790436-57907574	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:75 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:57787200-57802000	Weak transcription	Aorta	Aorta
2	chr15:57789800-57801600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr15:57790000-57808600	Weak transcription	Fetal Brain Male	brain
4	chr15:57790200-57801400	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr15:57793400-57803200	Enhancers	Placenta	Placenta
6	chr15:57793600-57803200	Enhancers	Fetal Intestine Small	intestine
7	chr15:57793800-57802000	Enhancers	Fetal Intestine Large	intestine
8	chr15:57794200-57808800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr15:57795200-57801600	Weak transcription	Small Intestine	intestine
10	chr15:57797000-57801600	Weak transcription	Right Ventricle	heart
11	chr15:57797000-57814000	Weak transcription	Rectal Smooth Muscle	rectum
12	chr15:57797000-57827200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr15:57797200-57802000	Enhancers	Placenta Amnion	Placenta Amnion
14	chr15:57797200-57802400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr15:57797800-57802600	Weak transcription	Osteobl	bone
16	chr15:57798000-57801800	Weak transcription	Brain Substantia Nigra	brain
17	chr15:57798000-57802000	Weak transcription	Brain Hippocampus Middle	brain
18	chr15:57798000-57802400	Weak transcription	Brain Cingulate Gyrus	brain
19	chr15:57798000-57805200	Enhancers	Fetal Heart	heart
20	chr15:57798400-57809400	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr15:57798600-57801400	Weak transcription	HMEC	breast
22	chr15:57798600-57808600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
23	chr15:57798800-57801400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr15:57798800-57801600	Weak transcription	Fetal Thymus	thymus
25	chr15:57799000-57801400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr15:57799000-57801400	Weak transcription	Ovary	ovary
27	chr15:57799000-57801600	Weak transcription	Left Ventricle	heart
28	chr15:57799000-57801600	Weak transcription	NH-A	brain
29	chr15:57799000-57801600	Weak transcription	NHLF	lung
30	chr15:57799000-57802800	Weak transcription	Brain Anterior Caudate	brain
31	chr15:57799000-57809000	Weak transcription	HepG2	liver
32	chr15:57799400-57801600	Weak transcription	Sigmoid Colon	Sigmoid Colon
33	chr15:57799400-57801800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr15:57799400-57802000	Weak transcription	HUVEC	blood vessel
35	chr15:57799600-57801400	Weak transcription	Fetal Lung	lung
36	chr15:57800000-57801400	Weak transcription	NHEK	skin
37	chr15:57800000-57803400	Enhancers	Primary B cells from peripheral blood	blood
38	chr15:57800200-57801400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr15:57800200-57802200	Weak transcription	Stomach Mucosa	stomach
40	chr15:57800400-57801600	Weak transcription	Rectal Mucosa Donor 31	rectum
41	chr15:57800400-57801800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr15:57800600-57802800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr15:57800600-57802800	Enhancers	Primary B cells from cord blood	blood
44	chr15:57800600-57803200	Enhancers	Pancreas	Pancrea
45	chr15:57800800-57801800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr15:57800800-57801800	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr15:57800800-57801800	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr15:57800800-57801800	Enhancers	Right Atrium	heart
49	chr15:57800800-57802000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr15:57800800-57802000	Enhancers	HUES64 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links