Variant report

Variant	rs3857075
Chromosome Location	chr4:175416331-175416332
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs11133038	0.81[ASN][1000 genomes]
rs11133040	0.82[ASN][1000 genomes]
rs11133042	0.95[CEU][hapmap];0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs17052166	0.81[ASN][1000 genomes]
rs1816204	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2098948	0.82[ASN][1000 genomes]
rs2555660	0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2612656	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2612665	0.81[ASN][1000 genomes]
rs2612694	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34991202	0.85[ASN][1000 genomes]
rs3846298	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs6419992	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6835564	0.80[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs6838650	0.82[ASN][1000 genomes]
rs7670400	0.82[ASN][1000 genomes]
rs7685956	0.90[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7691986	0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7691993	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869116	chr4:175231090-175801761	Flanking Active TSS Enhancers Genic enhancers Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases
2	nsv525487	chr4:175400104-175470867	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv880289	chr4:175412975-175437117	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv881270	chr4:175413296-175425619	Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:37 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:175396000-175442800	Weak transcription	Esophagus	oesophagus
2	chr4:175409400-175424000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
3	chr4:175410000-175424600	Weak transcription	Fetal Stomach	stomach
4	chr4:175410000-175440800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr4:175410400-175418000	Weak transcription	Rectal Smooth Muscle	rectum
6	chr4:175410800-175417400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
7	chr4:175410800-175420800	Weak transcription	Lung	lung
8	chr4:175410800-175425400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr4:175410800-175430800	Weak transcription	Gastric	stomach
10	chr4:175410800-175440000	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr4:175411000-175418200	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr4:175411600-175416600	Weak transcription	Colon Smooth Muscle	Colon
13	chr4:175412000-175428400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
14	chr4:175412400-175417800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr4:175412600-175418000	Weak transcription	Hela-S3	cervix
16	chr4:175412600-175418400	Strong transcription	Placenta	Placenta
17	chr4:175412800-175417200	Strong transcription	Liver	Liver
18	chr4:175412800-175418200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr4:175413800-175416400	Strong transcription	Primary hematopoietic stem cells	blood
20	chr4:175413800-175418200	Weak transcription	Rectal Mucosa Donor 31	rectum
21	chr4:175414200-175417200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
22	chr4:175414400-175419000	Weak transcription	Sigmoid Colon	Sigmoid Colon
23	chr4:175414400-175428200	Weak transcription	Stomach Smooth Muscle	stomach
24	chr4:175414600-175419000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
25	chr4:175415000-175416600	Strong transcription	Fetal Thymus	thymus
26	chr4:175415200-175416400	Genic enhancers	Fetal Intestine Large	intestine
27	chr4:175415400-175424000	Weak transcription	Muscle Satellite Cultured Cells	--
28	chr4:175415600-175427600	Enhancers	Stomach Mucosa	stomach
29	chr4:175415800-175416600	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr4:175416000-175416400	Enhancers	HUES64 Cell Line	embryonic stem cell
31	chr4:175416000-175416400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr4:175416000-175416600	Weak transcription	Small Intestine	intestine
33	chr4:175416000-175416800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chr4:175416000-175417000	Genic enhancers	Duodenum Mucosa	Duodenum
35	chr4:175416200-175416400	Genic enhancers	A549	lung
36	chr4:175416200-175416800	Genic enhancers	Fetal Intestine Small	intestine
37	chr4:175416200-175417800	Weak transcription	Primary T cells from cord blood	blood

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