Variant report

Variant	rs648510
Chromosome Location	chr6:140253132-140253133
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:140250688..140253465-chr6:140258352..140260834,2	K562	blood:
2	chr6:139695722..139698010-chr6:140251801..140254360,2	K562	blood:

Variant related genes	Relation type
ENSG00000164442	Chromatin interaction

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs1028469	0.80[EUR][1000 genomes]
rs13204837	0.83[CHB][hapmap];0.86[JPT][hapmap];0.80[YRI][hapmap]
rs1416289	0.83[CHB][hapmap];0.87[JPT][hapmap]
rs584995	0.83[AMR][1000 genomes]
rs586246	0.83[CHB][hapmap];0.86[JPT][hapmap];0.90[YRI][hapmap];0.83[EUR][1000 genomes]
rs587235	0.84[EUR][1000 genomes]
rs592056	0.83[CHB][hapmap];0.86[JPT][hapmap];0.80[YRI][hapmap];0.84[EUR][1000 genomes]
rs592440	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs598498	0.83[EUR][1000 genomes]
rs603310	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs607284	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs609488	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs616279	0.83[EUR][1000 genomes]
rs618515	0.83[CHB][hapmap];0.87[JPT][hapmap];0.84[EUR][1000 genomes]
rs647968	0.83[CHB][hapmap];0.85[JPT][hapmap];0.84[EUR][1000 genomes]
rs650774	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs679849	0.83[EUR][1000 genomes]
rs680290	0.83[EUR][1000 genomes]
rs681235	0.83[EUR][1000 genomes]
rs724061	0.83[CHB][hapmap];0.87[JPT][hapmap]
rs7743374	0.98[AMR][1000 genomes];0.93[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7763294	1.00[CEU][hapmap];0.82[EUR][1000 genomes]
rs856646	0.82[EUR][1000 genomes]
rs9389733	0.83[CHB][hapmap];0.87[JPT][hapmap]
rs9399298	0.83[CHB][hapmap];0.87[JPT][hapmap]
rs9403134	0.83[CHB][hapmap];0.87[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869066	chr6:139777114-140639695	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	26 gene(s)	inside rSNPs	diseases
2	nsv830820	chr6:140059279-140255292	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	n/a
3	nsv1017015	chr6:140084137-140300565	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1019407	chr6:140087307-140304334	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
5	nsv1016532	chr6:140174639-141029988	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:140242400-140254000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr6:140242400-140260200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr6:140242800-140254400	Weak transcription	Monocytes-CD14+_RO01746	blood
4	chr6:140248200-140254000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr6:140249200-140253800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chr6:140249400-140254000	Weak transcription	Osteobl	bone
7	chr6:140250000-140253200	Weak transcription	Fetal Heart	heart
8	chr6:140250000-140254200	Weak transcription	K562	blood
9	chr6:140252000-140253400	Enhancers	Fetal Kidney	kidney
10	chr6:140252400-140253200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr6:140252800-140253200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
12	chr6:140252800-140254800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr6:140253000-140253200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr6:140253000-140253400	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr6:140253000-140253400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr6:140253000-140254600	Enhancers	Muscle Satellite Cultured Cells	--
17	chr6:140253000-140254600	Enhancers	Hela-S3	cervix

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