Variant report

Variant	rs10423309
Chromosome Location	chr19:39417554-39417555
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr19:39415679..39418451-chr19:39423572..39425396,2	MCF-7	breast:
2	chr19:39416038..39418254-chr19:39423226..39425475,2	K562	blood:
3	chr19:39414900..39416436-chr19:39417401..39420305,2	K562	blood:

Extended variants
information (count: 29 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10411209	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10411301	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13343573	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs16972885	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2070250	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2070251	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2082436	1.00[AMR][1000 genomes]
rs2116853	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2163811	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2304115	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2304116	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs28362605	1.00[ASN][1000 genomes]
rs28808414	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28824318	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28844707	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs28860185	1.00[AMR][1000 genomes]
rs3181068	1.00[ASN][1000 genomes]
rs34264048	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58399999	1.00[ASN][1000 genomes]
rs61194027	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs61232096	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6508826	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6508827	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73537679	1.00[ASN][1000 genomes]
rs73930228	0.82[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs73930229	0.84[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs8113749	0.85[AMR][1000 genomes];1.00[EUR][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	nsv1057899	chr19:39088319-39475493	Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
2	esv1837023	chr19:39190588-39425722	Active TSS Enhancers Weak transcription Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	65 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:39391200-39420800	Weak transcription	Small Intestine	intestine
2	chr19:39391600-39420600	Weak transcription	Right Atrium	heart
3	chr19:39392600-39418800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
4	chr19:39398000-39420600	Weak transcription	Psoas Muscle	Psoas
5	chr19:39402800-39420200	Weak transcription	Colon Smooth Muscle	Colon
6	chr19:39403600-39420400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr19:39403800-39420200	Weak transcription	Fetal Brain Male	brain
8	chr19:39406400-39420000	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr19:39406800-39420200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr19:39409200-39419000	Strong transcription	Fetal Intestine Small	intestine
11	chr19:39409200-39420400	Weak transcription	Stomach Mucosa	stomach
12	chr19:39409600-39418400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
13	chr19:39410200-39417600	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
14	chr19:39411400-39419000	Strong transcription	Fetal Stomach	stomach
15	chr19:39411600-39420400	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr19:39411600-39420400	Weak transcription	Fetal Heart	heart
17	chr19:39412000-39417600	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr19:39412000-39419000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr19:39412000-39419600	Strong transcription	Fetal Muscle Leg	muscle
20	chr19:39412200-39419200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr19:39412800-39420600	Weak transcription	Rectal Smooth Muscle	rectum
22	chr19:39413200-39418800	Weak transcription	GM12878-XiMat	blood
23	chr19:39413200-39420200	Weak transcription	Primary B cells from cord blood	blood
24	chr19:39413200-39420200	Weak transcription	NH-A	brain
25	chr19:39413200-39420200	Weak transcription	NHLF	lung
26	chr19:39413200-39420400	Weak transcription	Primary neutrophils fromperipheralblood	blood
27	chr19:39413200-39420400	Weak transcription	Fetal Kidney	kidney
28	chr19:39413200-39420800	Weak transcription	Aorta	Aorta
29	chr19:39414400-39418600	Strong transcription	HUES6 Cell Line	embryonic stem cell
30	chr19:39414400-39419400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr19:39414800-39419200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
32	chr19:39415200-39418600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
33	chr19:39415400-39420000	Weak transcription	NHEK	skin
34	chr19:39415400-39420200	Weak transcription	NHDF-Ad	bronchial
35	chr19:39415600-39420200	Weak transcription	Brain Angular Gyrus	brain
36	chr19:39415600-39420400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr19:39415600-39420400	Weak transcription	Colonic Mucosa	Colon
38	chr19:39415600-39420600	Weak transcription	Pancreas	Pancrea
39	chr19:39415800-39419600	Weak transcription	K562	blood
40	chr19:39415800-39420200	Weak transcription	Primary T cells from cord blood	blood
41	chr19:39415800-39420200	Weak transcription	HUVEC	blood vessel
42	chr19:39415800-39420400	Weak transcription	HSMM	muscle
43	chr19:39416200-39420200	Weak transcription	Brain Substantia Nigra	brain
44	chr19:39416200-39420200	Weak transcription	Osteobl	bone
45	chr19:39416400-39419800	Weak transcription	Left Ventricle	heart
46	chr19:39416400-39420000	Weak transcription	Primary hematopoietic stem cells	blood
47	chr19:39416400-39420000	Weak transcription	Adipose Nuclei	Adipose
48	chr19:39416400-39420200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
49	chr19:39416400-39420200	Weak transcription	Brain Hippocampus Middle	brain
50	chr19:39416400-39420200	Weak transcription	Duodenum Smooth Muscle	Duodenum

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