Variant report

Variant	rs12603197
Chromosome Location	chr17:63125340-63125341
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr17:63123878..63125578-chr17:63133344..63134913,2	MCF-7	breast:
2	chr17:62970667..62973276-chr17:63122835..63125688,2	K562	blood:
3	chr17:63118227..63121662-chr17:63122983..63126434,3	K562	blood:
4	chr17:63051599..63054345-chr17:63124102..63127989,4	MCF-7	breast:
5	chr17:63123841..63126817-chr17:63129572..63131096,2	K562	blood:
6	chr17:63094402..63096834-chr17:63124738..63127386,3	MCF-7	breast:
7	chr17:63117748..63120899-chr17:63122110..63128969,9	MCF-7	breast:

Variant related genes	Relation type
ENSG00000214174	Chromatin interaction
ENSG00000120063	Chromatin interaction
ENSG00000108370	Chromatin interaction

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs1010271	0.81[CEU][hapmap];0.89[JPT][hapmap];0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10853058	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs10853059	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11079557	0.82[AMR][1000 genomes]
rs11079558	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs11079559	0.89[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12450928	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs12451009	0.89[JPT][hapmap];0.82[AMR][1000 genomes]
rs1530352	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1530353	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1554048	0.89[JPT][hapmap];0.84[AMR][1000 genomes]
rs1554049	0.84[AMR][1000 genomes]
rs1561939	0.80[CEU][hapmap];0.88[JPT][hapmap];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs1968573	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs1968574	0.89[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs429583	0.81[CEU][hapmap];0.89[JPT][hapmap];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs4581735	0.84[AMR][1000 genomes]
rs4790958	0.81[CEU][hapmap]
rs4791231	0.85[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7207632	0.82[AMR][1000 genomes]
rs7212241	0.82[AMR][1000 genomes]
rs7215779	0.82[AMR][1000 genomes]
rs7219245	0.82[AMR][1000 genomes]
rs7219799	0.82[AMR][1000 genomes]
rs7219809	0.82[AMR][1000 genomes]
rs8073607	0.82[AMR][1000 genomes]
rs8073924	0.82[AMR][1000 genomes]
rs8075179	0.81[AMR][1000 genomes]
rs8080637	0.84[AMR][1000 genomes]
rs8080746	0.84[AMR][1000 genomes]
rs8081250	0.91[ASN][1000 genomes]
rs8081971	0.84[AMR][1000 genomes]
rs9303478	0.81[CEU][hapmap];0.89[JPT][hapmap];0.84[AMR][1000 genomes]
rs9898914	0.84[AMR][1000 genomes]
rs9899243	0.84[AMR][1000 genomes]
rs9899401	0.84[AMR][1000 genomes]
rs9899628	0.84[AMR][1000 genomes]
rs9912432	0.84[AMR][1000 genomes]
rs9913707	0.84[AMR][1000 genomes]
rs9913725	0.84[AMR][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	nsv530764	chr17:62939944-63278472	Weak transcription Flanking Active TSS Bivalent/Poised TSS Enhancers Strong transcription Bivalent Enhancer Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
2	nsv527042	chr17:63123532-63128261	Bivalent Enhancer Flanking Active TSS Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	3 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	chr17:63118800-63127000	Weak transcription	Spleen	Spleen
2	chr17:63119800-63133600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr17:63120200-63126400	Weak transcription	K562	blood
4	chr17:63124000-63132600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr17:63125000-63126000	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
6	chr17:63125200-63126200	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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