Variant report

Variant	rs7542431
Chromosome Location	chr1:224875086-224875087
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr1:224873427..224876593-chr1:224880376..224882893,3	K562	blood:
2	chr1:224874309..224876593-chr1:224880376..224882878,2	K562	blood:
3	chr1:224874942..224876608-chr1:224877645..224880078,2	K562	blood:

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs10915684	0.81[EUR][1000 genomes]
rs10915694	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10915696	0.94[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs10915699	0.81[EUR][1000 genomes]
rs12092438	0.94[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs12130499	0.82[EUR][1000 genomes]
rs12132665	0.82[EUR][1000 genomes]
rs13374487	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1369846	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1369847	0.86[EUR][1000 genomes]
rs1436169	0.86[EUR][1000 genomes]
rs1436171	0.81[EUR][1000 genomes]
rs1561110	0.96[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs169888	0.82[EUR][1000 genomes]
rs1965776	0.94[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1965777	0.81[EUR][1000 genomes]
rs2405525	0.81[EUR][1000 genomes]
rs2648746	0.82[EUR][1000 genomes]
rs2897161	0.80[EUR][1000 genomes]
rs2936575	0.85[EUR][1000 genomes]
rs298732	0.85[EUR][1000 genomes]
rs298733	0.85[EUR][1000 genomes]
rs298734	0.85[EUR][1000 genomes]
rs298735	0.84[EUR][1000 genomes]
rs298738	0.83[EUR][1000 genomes]
rs298739	0.85[EUR][1000 genomes]
rs2993124	0.82[EUR][1000 genomes]
rs3012185	0.85[EUR][1000 genomes]
rs4147293	0.88[EUR][1000 genomes]
rs4653402	0.86[EUR][1000 genomes]
rs4653404	0.86[EUR][1000 genomes]
rs4653591	0.86[EUR][1000 genomes]
rs4653592	0.84[EUR][1000 genomes]
rs56881651	0.93[EUR][1000 genomes]
rs61676104	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6686604	0.94[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs6686633	0.94[AFR][1000 genomes];0.88[EUR][1000 genomes]
rs67817586	0.81[EUR][1000 genomes]
rs713098	0.82[EUR][1000 genomes]
rs7511897	0.82[EUR][1000 genomes]
rs7521396	0.81[EUR][1000 genomes]
rs7535296	0.81[EUR][1000 genomes]
rs7542995	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7543218	0.87[AFR][1000 genomes];0.87[EUR][1000 genomes]
rs7544312	0.82[EUR][1000 genomes]
rs7545574	0.92[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs873594	0.81[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	nsv1014717	chr1:224551939-224885543	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv535311	chr1:224551939-224885543	Strong transcription Genic enhancers Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:224832200-224884400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr1:224861200-224876800	Weak transcription	Ovary	ovary
3	chr1:224862400-224902000	Weak transcription	Pancreas	Pancrea
4	chr1:224864000-224876200	Weak transcription	Cortex derived primary cultured neurospheres	brain
5	chr1:224868400-224875200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr1:224869800-224877200	Weak transcription	Dnd41	blood
7	chr1:224871400-224876400	Strong transcription	NHDF-Ad	bronchial
8	chr1:224871800-224884600	Weak transcription	Fetal Brain Female	brain
9	chr1:224872800-224876000	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr1:224873000-224876800	Weak transcription	Fetal Brain Male	brain
11	chr1:224873000-224884800	Weak transcription	NHLF	lung
12	chr1:224873200-224877000	Strong transcription	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr1:224873400-224884200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chr1:224874400-224876200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr1:224874600-224875600	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr1:224875000-224881600	Weak transcription	NH-A	brain

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