Variant report

Variant	rs4944903
Chromosome Location	chr11:74280336-74280337
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr11:74203231..74205154-chr11:74278965..74281872,2	MCF-7	breast:
2	chr11:74163885..74165506-chr11:74280069..74282735,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000077514	Chromatin interaction
ENSG00000254837	Chromatin interaction
ENSG00000175536	Chromatin interaction

Extended variants
information (count: 35 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10501416	0.84[JPT][hapmap];0.90[ASN][1000 genomes]
rs1051076	0.85[JPT][hapmap]
rs12795302	0.90[ASN][1000 genomes]
rs12798723	0.86[ASN][1000 genomes]
rs12801229	0.90[ASN][1000 genomes]
rs12802128	0.90[ASN][1000 genomes]
rs12807883	0.85[CEU][hapmap];0.86[CHB][hapmap];0.84[JPT][hapmap];0.81[ASN][1000 genomes]
rs1433972	0.87[LWK][hapmap];0.93[MKK][hapmap]
rs2298573	0.84[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs34450669	0.81[ASN][1000 genomes]
rs34601749	0.85[ASN][1000 genomes]
rs35167458	0.85[ASN][1000 genomes]
rs35500564	0.85[ASN][1000 genomes]
rs35514423	0.84[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs35778922	0.84[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs35958987	0.90[ASN][1000 genomes]
rs36009269	0.81[AFR][1000 genomes];0.84[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs3902018	0.85[JPT][hapmap];0.90[ASN][1000 genomes]
rs4417306	0.87[LWK][hapmap];0.90[MKK][hapmap]
rs4944902	1.00[ASW][hapmap];0.82[CEU][hapmap];0.86[CHB][hapmap];0.90[CHD][hapmap];0.92[GIH][hapmap];0.85[JPT][hapmap];0.92[MKK][hapmap];0.85[TSI][hapmap];0.91[YRI][hapmap];0.99[AFR][1000 genomes];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4944905	0.96[AFR][1000 genomes];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4944927	0.84[JPT][hapmap]
rs57365763	0.81[AFR][1000 genomes];0.84[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs67575589	0.84[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs7116713	0.99[AFR][1000 genomes];0.84[AMR][1000 genomes];0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7119905	0.95[AFR][1000 genomes];0.84[AMR][1000 genomes];0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71465929	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2757451	chr11:73842609-74545888	Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription Enhancers Genic enhancers Bivalent Enhancer Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	87 gene(s)	inside rSNPs	diseases
2	esv2759837	chr11:73842609-74557597	Flanking Active TSS Enhancers Bivalent/Poised TSS Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	88 gene(s)	inside rSNPs	diseases
3	esv34979	chr11:73878688-74533452	Enhancers Weak transcription Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	85 gene(s)	inside rSNPs	diseases
4	esv2758277	chr11:73887567-74557597	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	85 gene(s)	inside rSNPs	diseases
5	nsv825994	chr11:73936667-74534455	Enhancers Weak transcription Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	83 gene(s)	inside rSNPs	diseases
6	nsv832209	chr11:74155883-74329119	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
7	nsv897914	chr11:74266026-74327614	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	nsv897915	chr11:74269817-74327614	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:74278400-74280400	Weak transcription	Pancreas	Pancrea
2	chr11:74279400-74281800	Weak transcription	Duodenum Mucosa	Duodenum
3	chr11:74279400-74281800	Weak transcription	Fetal Intestine Large	intestine
4	chr11:74279400-74281800	Weak transcription	Stomach Mucosa	stomach
5	chr11:74279400-74281800	Weak transcription	HepG2	liver
6	chr11:74280000-74283000	Enhancers	Fetal Intestine Small	intestine

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links