Variant report

Variant	rs11165013
Chromosome Location	chr1:92051419-92051420
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	chr1:92049054..92051542-chr1:92061265..92062961,2	K562	blood:
2	chr1:92040469..92042505-chr1:92051071..92052577,2	K562	blood:

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10458506	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10874794	0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs10874796	0.94[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11164978	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11165002	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs11165008	0.94[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12048543	0.94[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12117800	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4658235	0.94[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs4658236	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6604044	0.94[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6604045	0.94[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6677520	0.94[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs906633	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949516	chr1:91644418-92109261	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv1009560	chr1:91897078-92270781	Enhancers Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:92046000-92055000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr1:92047200-92052000	Enhancers	Fetal Stomach	stomach
3	chr1:92048000-92051800	Enhancers	Colon Smooth Muscle	Colon
4	chr1:92048000-92052200	Enhancers	Stomach Smooth Muscle	stomach
5	chr1:92048400-92054200	Weak transcription	K562	blood
6	chr1:92049400-92056400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
7	chr1:92049600-92061600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr1:92050000-92051600	Enhancers	Fetal Kidney	kidney
9	chr1:92050400-92051800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
10	chr1:92050400-92052200	Enhancers	Primary hematopoietic stem cells	blood
11	chr1:92050400-92052200	Enhancers	Primary hematopoietic stem cells short term culture	blood
12	chr1:92050600-92051600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr1:92050600-92052000	Enhancers	Primary monocytes fromperipheralblood	blood
14	chr1:92050800-92051600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr1:92050800-92051600	Enhancers	Fetal Thymus	thymus
16	chr1:92050800-92054200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr1:92051000-92051600	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
18	chr1:92051000-92051600	Enhancers	Left Ventricle	heart
19	chr1:92051000-92051600	Enhancers	Lung	lung
20	chr1:92051000-92051600	Enhancers	Right Ventricle	heart
21	chr1:92051000-92051800	Enhancers	Placenta	Placenta
22	chr1:92051000-92051800	Weak transcription	Rectal Smooth Muscle	rectum
23	chr1:92051000-92051800	Enhancers	Right Atrium	heart
24	chr1:92051000-92052200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr1:92051000-92052200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr1:92051000-92055400	Weak transcription	Ovary	ovary
27	chr1:92051000-92056400	Weak transcription	Duodenum Smooth Muscle	Duodenum
28	chr1:92051200-92052200	Enhancers	Fetal Heart	heart
29	chr1:92051200-92054600	Weak transcription	Fetal Lung	lung
30	chr1:92051200-92056400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr1:92051400-92051600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr1:92051400-92052000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr1:92051400-92052000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr1:92051400-92052000	Weak transcription	Primary B cells from cord blood	blood
35	chr1:92051400-92053000	Enhancers	Monocytes-CD14+_RO01746	blood
36	chr1:92051400-92056600	Weak transcription	Primary T cells from cord blood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links