Variant report

Variant	rs6877633
Chromosome Location	chr5:177764979-177764980
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:177764211..177766744-chr5:177842337..177844246,2	MCF-7	breast:
2	chr5:177761012..177763612-chr5:177764691..177767517,2	K562	blood:

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

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs17580218	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs17641413	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs2913788	1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs2913789	0.91[ASN][1000 genomes]
rs2913801	0.83[ASN][1000 genomes]
rs2973684	0.82[ASN][1000 genomes]
rs2973685	1.00[JPT][hapmap];0.91[ASN][1000 genomes]
rs2973808	0.90[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs34688771	0.90[ASN][1000 genomes]
rs748083	1.00[JPT][hapmap];0.84[ASN][1000 genomes]
rs7708757	1.00[JPT][hapmap]
rs9329142	1.00[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948342	chr5:177384542-178168737	Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Strong transcription Weak transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	141 gene(s)	inside rSNPs	diseases
2	nsv1029398	chr5:177502106-178070654	Flanking Active TSS Enhancers Weak transcription Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	136 gene(s)	inside rSNPs	diseases
3	nsv1019404	chr5:177507080-177859089	Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Active TSS Weak transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	126 gene(s)	inside rSNPs	diseases
4	nsv1021981	chr5:177620372-177825272	Transcr. at gene 5' and 3' Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Genic enhancers Strong transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	105 gene(s)	inside rSNPs	diseases
5	nsv537967	chr5:177620372-177825272	Active TSS Strong transcription Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	105 gene(s)	inside rSNPs	diseases
6	nsv1024689	chr5:177638936-177926244	Enhancers Bivalent Enhancer Weak transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
7	nsv537968	chr5:177638936-177926244	Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Genic enhancers ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
8	nsv883203	chr5:177682664-177766183	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent/Poised TSS Active TSS	Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
9	nsv883205	chr5:177684682-177777888	Weak transcription ZNF genes & repeats Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
10	nsv883206	chr5:177684682-177796121	Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
11	nsv1027165	chr5:177693601-177843314	Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:22 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:177759200-177765000	Enhancers	Fetal Muscle Leg	muscle
2	chr5:177759400-177783400	Weak transcription	Right Atrium	heart
3	chr5:177759800-177765000	Weak transcription	Left Ventricle	heart
4	chr5:177760600-177766400	Weak transcription	Skeletal Muscle Female	skeletal muscle
5	chr5:177761000-177765200	Weak transcription	Right Ventricle	heart
6	chr5:177762600-177775400	Weak transcription	Thymus	Thymus
7	chr5:177762800-177765200	Enhancers	Fetal Lung	lung
8	chr5:177762800-177766800	Weak transcription	Monocytes-CD14+_RO01746	blood
9	chr5:177763000-177767200	Weak transcription	Primary neutrophils fromperipheralblood	blood
10	chr5:177763200-177766400	Weak transcription	Primary monocytes fromperipheralblood	blood
11	chr5:177763400-177765000	Enhancers	Liver	Liver
12	chr5:177764000-177765200	Enhancers	Spleen	Spleen
13	chr5:177764000-177765400	Bivalent Enhancer	Fetal Muscle Trunk	muscle
14	chr5:177764000-177766000	Enhancers	Fetal Heart	heart
15	chr5:177764000-177767600	Bivalent Enhancer	Fetal Stomach	stomach
16	chr5:177764200-177768400	Enhancers	Breast Myoepithelial Primary Cells	Breast
17	chr5:177764400-177765400	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chr5:177764400-177766600	Enhancers	Fetal Thymus	thymus
19	chr5:177764400-177767200	Enhancers	Skeletal Muscle Male	skeletal muscle
20	chr5:177764600-177765000	Weak transcription	HSMMtube	muscle
21	chr5:177764600-177766000	Weak transcription	Placenta	Placenta
22	chr5:177764800-177768000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links