Variant report

Variant	rs1168736
Chromosome Location	chr12:66572147-66572148
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr12:66568852..66570391-chr12:66571987..66573654,2	K562	blood:
2	chr12:66560846..66563703-chr12:66570897..66572814,2	K562	blood:
3	chr12:66570661..66572865-chr12:66583805..66585652,2	K562	blood:
4	chr12:66570441..66572805-chr12:66575198..66577758,3	K562	blood:
5	chr12:66570441..66574435-chr12:66574821..66579186,5	K562	blood:
6	chr12:66556389..66558004-chr12:66572118..66574414,2	MCF-7	breast:
7	chr12:66562178..66565316-chr12:66569101..66574055,5	MCF-7	breast:

Variant related genes	Relation type
ENSG00000155957	Chromatin interaction

Extended variants
information (count: 45 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:39)

rs_ID	r²[population]
rs1168739	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1168744	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1168757	0.92[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1168758	0.82[ASN][1000 genomes]
rs1168772	0.83[ASN][1000 genomes]
rs1179914	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1185253	0.92[EUR][1000 genomes]
rs12306484	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12578364	0.98[ASN][1000 genomes]
rs12578752	0.99[ASN][1000 genomes]
rs12578801	0.95[ASN][1000 genomes]
rs12578994	0.99[ASN][1000 genomes]
rs12814331	0.99[ASN][1000 genomes]
rs12814606	0.99[ASN][1000 genomes]
rs12823414	0.83[ASN][1000 genomes]
rs1625441	0.99[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs17245364	0.99[ASN][1000 genomes]
rs1732893	0.92[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17825931	0.89[ASN][1000 genomes]
rs17825943	0.93[ASN][1000 genomes]
rs1797410	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1797411	0.87[AFR][1000 genomes]
rs1921082	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2576183	0.99[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2701644	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2701645	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2701653	0.97[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2701654	0.99[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2701655	0.91[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs2917598	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs34406211	0.90[ASN][1000 genomes]
rs34552143	0.93[ASN][1000 genomes]
rs35131575	0.93[ASN][1000 genomes]
rs35187440	0.99[ASN][1000 genomes]
rs35971570	0.99[ASN][1000 genomes]
rs36073795	0.99[ASN][1000 genomes]
rs57825508	0.81[EUR][1000 genomes]
rs59112451	0.93[ASN][1000 genomes]
rs737614	0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1052503	chr12:66293898-67269495	Weak transcription Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
2	nsv541515	chr12:66293898-67269495	Strong transcription Enhancers Active TSS Genic enhancers ZNF genes & repeats Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	51 gene(s)	inside rSNPs	diseases
3	nsv1049537	chr12:66403269-66606174	Strong transcription Genic enhancers Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
4	nsv541516	chr12:66547969-66596036	Flanking Bivalent TSS/Enh Flanking Active TSS Enhancers Active TSS Genic enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region miRNA target site	22 gene(s)	inside rSNPs	diseases
5	nsv899215	chr12:66556960-66594134	Weak transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Active TSS Strong transcription Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region miRNA target site	22 gene(s)	inside rSNPs	n/a
6	nsv899216	chr12:66563835-66716844	Strong transcription Enhancers Genic enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	30 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs1168736	TMBIM4	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:0 , 50 per page) page:

No data

Quick Search:

Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links