Variant report

Variant	rs495529
Chromosome Location	chr1:165876705-165876706
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:165876437..165878779-chr1:165881882..165884528,2	K562	blood:
2	chr1:165797327..165800051-chr1:165876668..165879627,3	MCF-7	breast:
3	chr1:165737981..165739699-chr1:165876681..165878558,2	MCF-7	breast:
4	chr1:165735497..165738147-chr1:165876560..165878545,2	K562	blood:
5	chr1:165795932..165799590-chr1:165874555..165878246,4	MCF-7	breast:

Variant related genes	Relation type
ENSG00000224358	Chromatin interaction
ENSG00000143183	Chromatin interaction
ENSG00000143179	Chromatin interaction

Extended variants
information (count: 14 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10800165	0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12080800	0.83[CHD][hapmap];0.93[JPT][hapmap];0.85[TSI][hapmap];0.85[ASN][1000 genomes]
rs12125493	0.83[CHD][hapmap];0.93[JPT][hapmap];0.85[TSI][hapmap];0.85[ASN][1000 genomes]
rs3762365	0.84[CEU][hapmap];0.85[CHB][hapmap];0.81[GIH][hapmap];1.00[JPT][hapmap];0.84[MEX][hapmap];0.83[TSI][hapmap];0.82[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3790659	0.88[CEU][hapmap];0.90[CHB][hapmap];0.90[CHD][hapmap];1.00[JPT][hapmap];0.83[TSI][hapmap];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3806333	0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs485338	1.00[ASW][hapmap];1.00[CEU][hapmap];0.82[CHB][hapmap];0.95[CHD][hapmap];0.94[GIH][hapmap];0.82[JPT][hapmap];0.96[LWK][hapmap];0.84[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.99[AFR][1000 genomes];0.99[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs492467	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs506813	0.90[CHB][hapmap];0.88[CHD][hapmap];0.81[JPT][hapmap];0.86[ASN][1000 genomes]
rs536109	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.97[GIH][hapmap];1.00[JPT][hapmap];0.84[MEX][hapmap];0.93[TSI][hapmap];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs544617	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7519919	0.83[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7543127	0.90[CHB][hapmap];1.00[JPT][hapmap];0.82[EUR][1000 genomes];0.95[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2756102	chr1:165652342-165877342	Weak transcription Strong transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	48 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs495529	USP21	cis	parietal	SCAN

Chromatin state (count:113 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:165854600-165883000	Weak transcription	Colon Smooth Muscle	Colon
2	chr1:165856600-165878800	Weak transcription	Small Intestine	intestine
3	chr1:165858200-165881200	Strong transcription	Dnd41	blood
4	chr1:165858400-165881000	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr1:165858600-165902400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
6	chr1:165859000-165881000	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr1:165859200-165878000	Strong transcription	Hela-S3	cervix
8	chr1:165859200-165880400	Strong transcription	HUES64 Cell Line	embryonic stem cell
9	chr1:165859200-165881000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr1:165859400-165880200	Strong transcription	Monocytes-CD14+_RO01746	blood
11	chr1:165859400-165880400	Strong transcription	Primary monocytes fromperipheralblood	blood
12	chr1:165859400-165880600	Strong transcription	HUES48 Cell Line	embryonic stem cell
13	chr1:165859400-165880600	Strong transcription	iPS-20b Cell Line	embryonic stem cell
14	chr1:165859600-165880600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
15	chr1:165860000-165880200	Strong transcription	H1 Cell Line	embryonic stem cell
16	chr1:165867200-165876800	Weak transcription	Rectal Smooth Muscle	rectum
17	chr1:165868400-165880200	Strong transcription	A549	lung
18	chr1:165870200-165882800	Weak transcription	Fetal Brain Male	brain
19	chr1:165870400-165879400	Weak transcription	Primary T cells fromperipheralblood	blood
20	chr1:165870800-165880800	Strong transcription	HUES6 Cell Line	embryonic stem cell
21	chr1:165871000-165883200	Weak transcription	Primary neutrophils fromperipheralblood	blood
22	chr1:165871800-165877000	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr1:165871800-165880000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr1:165871800-165880800	Strong transcription	Fetal Stomach	stomach
25	chr1:165871800-165882200	Strong transcription	Fetal Brain Female	brain
26	chr1:165872000-165877200	Genic enhancers	HepG2	liver
27	chr1:165872000-165879000	Strong transcription	Rectal Mucosa Donor 31	rectum
28	chr1:165872000-165879200	Strong transcription	Fetal Intestine Small	intestine
29	chr1:165872000-165879600	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
30	chr1:165872000-165879800	Strong transcription	K562	blood
31	chr1:165872200-165879200	Strong transcription	Fetal Intestine Large	intestine
32	chr1:165872400-165883200	Weak transcription	Brain Anterior Caudate	brain
33	chr1:165872400-165883200	Weak transcription	Brain Substantia Nigra	brain
34	chr1:165872800-165883400	Weak transcription	Fetal Kidney	kidney
35	chr1:165873000-165880000	Weak transcription	Placenta Amnion	Placenta Amnion
36	chr1:165873200-165877800	Weak transcription	Aorta	Aorta
37	chr1:165873200-165879600	Strong transcription	Placenta	Placenta
38	chr1:165873200-165881000	Strong transcription	Primary hematopoietic stem cells short term culture	blood
39	chr1:165873400-165879400	Strong transcription	NHLF	lung
40	chr1:165873400-165879600	Strong transcription	HSMMtube	muscle
41	chr1:165873600-165877000	Strong transcription	Primary B cells from cord blood	blood
42	chr1:165873600-165879200	Weak transcription	Stomach Mucosa	stomach
43	chr1:165873600-165879800	Strong transcription	Muscle Satellite Cultured Cells	--
44	chr1:165873600-165879800	Weak transcription	Fetal Heart	heart
45	chr1:165873600-165880400	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr1:165873600-165881000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
47	chr1:165873800-165877000	Genic enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr1:165874000-165879800	Strong transcription	HSMM	muscle
49	chr1:165874000-165881200	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr1:165874000-165881800	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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