Variant report

Variant	rs67560206
Chromosome Location	chr5:75591986-75591987
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:75589308..75591294-chr5:75591949..75593986,2	K562	blood:
2	chr5:75590828..75593662-chr5:75594110..75596646,3	MCF-7	breast:

Extended variants
information (count: 68 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:66)

rs_ID	r²[population]
rs10942765	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13174383	0.85[AMR][1000 genomes]
rs13188781	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1469387	0.91[EUR][1000 genomes]
rs1863919	0.91[EUR][1000 genomes]
rs1971744	0.91[EUR][1000 genomes]
rs1995381	0.86[EUR][1000 genomes]
rs2270927	0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs2358712	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs246813	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs246814	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs246815	0.91[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2913252	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2913255	0.91[EUR][1000 genomes]
rs2913256	0.91[EUR][1000 genomes]
rs2913257	0.91[EUR][1000 genomes]
rs2913258	0.91[EUR][1000 genomes]
rs2913259	0.91[EUR][1000 genomes]
rs2913260	0.91[EUR][1000 genomes]
rs2913262	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2913263	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2913265	0.88[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2913266	0.83[EUR][1000 genomes]
rs2937741	0.91[EUR][1000 genomes]
rs2937742	0.91[EUR][1000 genomes]
rs2937743	0.91[EUR][1000 genomes]
rs2937744	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2937745	0.91[EUR][1000 genomes]
rs2937746	0.91[EUR][1000 genomes]
rs2937747	0.91[EUR][1000 genomes]
rs2937748	0.86[EUR][1000 genomes]
rs2937749	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2937750	0.86[EUR][1000 genomes]
rs2937752	0.86[EUR][1000 genomes]
rs2972836	0.86[EUR][1000 genomes]
rs2972837	0.82[EUR][1000 genomes]
rs2972838	0.86[EUR][1000 genomes]
rs2972839	0.84[EUR][1000 genomes]
rs2972840	0.92[EUR][1000 genomes]
rs2972843	0.91[EUR][1000 genomes]
rs2972846	0.80[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2972847	0.91[EUR][1000 genomes]
rs2972848	0.91[EUR][1000 genomes]
rs2972849	0.91[EUR][1000 genomes]
rs2972850	0.91[EUR][1000 genomes]
rs2972853	0.84[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2972854	0.87[EUR][1000 genomes]
rs31243	0.89[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs31244	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs34596551	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs35662301	0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs35764719	0.92[EUR][1000 genomes]
rs35930860	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs35966882	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs35984318	0.92[EUR][1000 genomes]
rs4352583	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4496693	0.83[AMR][1000 genomes]
rs4546360	0.85[AMR][1000 genomes]
rs4566771	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6453213	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6453214	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs67771044	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6875731	0.85[AMR][1000 genomes]
rs6876070	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6891108	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7730153	0.89[AMR][1000 genomes];0.94[EUR][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	nsv1027368	chr5:74759999-75663712	Active TSS Strong transcription Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
2	nsv870415	chr5:75526088-75738412	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:19 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:75585000-75593400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
2	chr5:75585000-75596000	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr5:75586200-75592400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr5:75587400-75592200	Weak transcription	Liver	Liver
5	chr5:75588200-75599800	Weak transcription	Pancreas	Pancrea
6	chr5:75588400-75599800	Weak transcription	Sigmoid Colon	Sigmoid Colon
7	chr5:75589000-75593400	Weak transcription	Fetal Intestine Small	intestine
8	chr5:75589600-75593200	Weak transcription	Duodenum Mucosa	Duodenum
9	chr5:75590000-75593600	Weak transcription	Stomach Mucosa	stomach
10	chr5:75590600-75593200	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr5:75590800-75595200	Weak transcription	GM12878-XiMat	blood
12	chr5:75591200-75592200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr5:75591200-75592800	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr5:75591200-75592800	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr5:75591400-75592400	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr5:75591400-75593200	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr5:75591400-75594600	Weak transcription	Fetal Thymus	thymus
18	chr5:75591600-75593200	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr5:75591800-75597000	Weak transcription	Primary hematopoietic stem cells	blood

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